Alexandre da Costa Pereira

Possui graduação em Medicina pela Universidade de São Paulo (1999) e doutorado em Cardiologia pela Faculdade de Medicina da Universidade de São Paulo (2008). Atualmente é médico assistente do Instituto do Coração - Hospital das Clinicas - FMUSP. Trabalha no Laboratório de Genética e Cardiologia Molecular do Instituto do Coração (Incor) HC-FMUSP, onde coordena o grupo de genética humana. Seus principais interesses em pesquisa são a identificação e caracterização de fatores genéticos que causem ou modulem fenótipos cardiovasculares.

Informações coletadas do Lattes em 07/06/2023

Acadêmico

Formação acadêmica

Doutorado em Cardiologia

2004 - 2008

Faculdade de Medicina da Universidade de São Paulo
Título: Determinantes Genéticos e Ambientais de Doença Arterial Coronária Precoce
José Eduardo Krieger. Palavras-chave: Cardiologia; Genética.Grande área: Ciências da SaúdeSetores de atividade: Cuidado À Saúde das Populações Humanas.

Especialização - Residência médica

2002 - 2004

Instituto do Coração - Hospital das Clínicas - FMUSP
Residência médica em: CardiologiaNúmero do registro: . Bolsista do(a): Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, CAPES, Brasil. Palavras-chave: Cardiologia.Grande área: Ciências da SaúdeSetores de atividade: Cuidado À Saúde das Populações Humanas.

Especialização - Residência médica

2000 - 2002

Universidade de São Paulo
Residência médica em:Número do registro: . Bolsista do(a): Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, CAPES, Brasil.

Especialização em Research Fellowship

1997 - 1998

Harvard University
Bolsista do(a): Fundação Zerbini, INCOR, Brasil.

Graduação em Medicina

1992 - 1999

Universidade de São Paulo
Bolsista do(a): Fundação de Amparo à Pesquisa do Estado de São Paulo, FAPESP, Brasil.

Idiomas

Inglês

Compreende Bem, Fala Bem, Lê Bem, Escreve Bem.

Áreas de atuação

Grande área: Ciências da Saúde / Área: Medicina / Subárea: Clínica Médica.

Grande área: Ciências da Saúde / Área: Medicina / Subárea: Clínica Médica/Especialidade: Cardiologia.

Grande área: Ciências Biológicas / Área: Genética / Subárea: Genética Humana e Médica.

Grande área: Ciências Biológicas / Área: Genética / Subárea: Genética Quantitativa.

Participação em eventos

ESC Congress 2019. Genetic testing in 101 consecutive lone atrial fibrilation patients is able to identify a subgroup with increased severity. 2019. (Congresso).

XXXVII Congresso da Sociedade de Cardiologia do Estado de São Paulo. Predicação do sucesso da cirurgia de revascularização miocárdica em pacientes com coronariopatia difusa: a contribuição do heart team. 2016. (Congresso).

XXXVII Congresso da Sociedade de Cardiologia do Estado de São Paulo. Cirurgia de revascularização do miocárdio na doença arterial coronariana difusa: resultados clínicos e angiográficos em 1 ano. 2016. (Congresso).

42° Congresso Brasileiro de Análises Clínicas. Doenças metabólicas e marcadores genéticos/ Aspectos fenotípicos das Dislipidemias/ Genes e hipercolesterolemia/ Genes e diabetes. 2015. (Congresso).

XIV Congresso Brasileiro de Insuficiência Cardíaca - DEIC 2015. Perfil dos Pacientes com Cardiomiopatia Chagásica Assistidos em Ambulatório de Hospital Universitário na Região Centro Oeste. 2015. (Congresso).

XV Congresso Brasileiro de Aterosclerose. Diagnóstico Precoce de Aterosclerose: Avanços e Dilemas - Tema: Marcadores Genéticos. 2015. (Congresso).

XXXVI Congresso da Sociedade de Cardiologia do Estado de São Paulo. Hipercolesterolemia Familiar e Hepatite Auto-imune: Relato de Caso. 2015. (Congresso).

XXXVI Congresso da Sociedade de Cardiologia do Estado de São Paulo. Diagnóstico de diabetes tipo I em criança com diagnóstico de hipercolesterolemia familiar em início recente de estatina: relato de caso. 2015. (Congresso).

XXXVI Congresso da Sociedade de Cardiologia do Estado de São Paulo. MC 19 - Marcadores genéticos de doenças cardiovasculares.. 2015. (Congresso).

XXXV Congresso da Sociedade de Cardiologia do Estado de São Paulo. Apnéia Obstrutiva do Sono é extremamente comum e está associada a isquemia miocárdica em pacientes com Angina Refratária.. 2014. (Congresso).

I Simpósio Internacional de Epidemiologia Cardiovascular."Mendellian Randomization: a new tool for observational epidemiology". 2013. (Simpósio).

XXXIV Congresso da Sociedade de Cardiologia do Estado de São Paulo. Fisiologia Cardiovascular, Biologia Molecular e Genética Cardiovascular - MC 19 - O Exercício físico intensifica a hipertrofia miocardica dependente do fumo. 2013. (Congresso).

American College of Cardiology Annual Meeting 2005. Apresentação de Resumo no American College of Cardiology Annual Meeting 2005. 2005. (Congresso).

XXVI Congresso da Sociedade de Cardiologia do Estado de São Paulo. Palestra sobre o tema Epidemiologia Genética na atividade Estado da Arte em Cardiologia. 2005. (Congresso).

.Palestra Técnicas de Biologia Molecular. 2004. (Outra).

Atualização Cardiológica para o Clínico.Palestra: Biologia Molecular em Cardiologia. 2004. (Simpósio).

Curso de Extensão Universitária em Cirurgia Torácica e Cardiovascular.Palestra: Aspectos genéticos das doenças da aorta. 2004. (Seminário).

Curso de Pós-Graduação Distúrbios Metabólicos e Risco Cardiovascular.Palestra Genética e Dislipidemia. 2004. (Simpósio).

Da molécula à clínica: onde estamos e o que esperamos.Simpósio InCor: Da molécula à clínica: onde estamos e o que esperamos. 2004. (Simpósio).

FeSBE 2004. Palestra Investigação fisiológica na era genômica. 2004. (Congresso).

Reunião Científica.Palestra Marcadores Genéticos e Risco Cardiovascular. 2004. (Outra).

Reunião Geral do Instituto do Coração (InCor).Reunião Geral do Instituto do Coração (InCor). 2004. (Seminário).

XXV Congresso da Sociedade de cardiologia do Estado de São Paulo. Palestra Cardiologia Molecular. 2004. (Congresso).

XXVII Congresso Sul Mineiro de Cardiologia. Palestra Mapeando Genes para Doenças Cardiovasculares. 2004. (Congresso).

Participação em bancas

Aluno: Paulo Roberto Xavier Tomaz

PEREIRA, AC; NEGRAO, A. B.; ISSA, J. S.. Distúrbios Genéticos de Desenvolvimento e Metabolismo. 2015. Dissertação (Mestrado em Ciências Médicas) - Faculdade de Medicina da Universidade de São Paulo.

Aluno: Théo Gremen Mimary de Oliveira

Pereira ACJORGE, A. A. L.; MITNE NETO, M.. "Aplicação do sequenciamento de nova geração no diagnóstico molecular de cardiomiopatia hipertrófica.". 2015. Dissertação (Mestrado em Ciências Médicas) - Faculdade de Medicina da Universidade de São Paulo.

Aluno: Cleber Renê Alves

Pereira, Alexandre da Costa. Modulação de vasodilatação mediada por exercício por polimorfismo de receptor de bradicina. 2008. Dissertação (Mestrado em Fisiopatologia Experimental) - Faculdade de Medicina da Universidade de São Paulo.

Aluno: André Luis Brito Querino

ALENCAR, ADRIANO MESQUITA;Pereira AC; GOMES, L. F.; BARBOSA, L. R. S.; ARAUJO, J. M.. Estudo das propriedades mecânicas da contração executada por células cardíacas isoladas aderidas em superfície mimetizada. 2019.

Aluno: Audrey Cecília Tonet Furioso

Pereira AC. Investigação de Associação entre Estimativas de Ancestralidade Genômica e Evolução Clínica Após Infarto Agudo do Miocárdio: Brasília Heart Study.. 2015. Tese (Doutorado em Ciências Médicas) - Universidade de Brasília.

Aluno: José Ribeiro Lemos Junior

Trombetta, I. C.PEREIRA, ACALVES, C. R.OLIVEIRA, E. M.. "Influência da Variante Val66Met na expressão do gene brain-derived neurotrophic factor (BDNF) em resposta ao treinamento físico aeróbico.". 2015. Tese (Doutorado em Programa de Cardiologia) - Faculdade de Medicina da Universidade de São Paulo.

Aluno: aMÍLCAR bERNARDO tOMÉ DA sILVA

Pereira, A C. "Fatores de risco cardiovascular em esclerose pré-púberes de Luanda - Angola". 2015. Tese (Doutorado em Programa de Pós-Graduação em Ciências Fisiológicas) - Universidade Federal do Espírito Santo.

Aluno: Gustavo Nunes de Oliveira Costa

BARRETO, M. L.; RIBEIRO, G. S.; FIACCONE, R. L.; CRUZ, A. A. S.;PEREIRA, AC. Epidemiologia genética dos sintomas de asma e da atopia em crianças de um Centro Urbano da America Latina. 2014. Tese (Doutorado em Programa de Pós-Graduação em Saúde Coletiva) - Universidade Federal da Bahia.

Aluno: Henrique Lane Staniak

SANTOS, R. D.; SPOSITO, A. C.; ROCHITTE, C. E.;Pereira AC; BENSENOR, I. J. M.. "Relação da Lipemia Pós Prandial com Aterosclerose Avaliada pela Angiotomografia Coronária". 2013 - Faculdade de Medicina da Universidade de São Paulo.

Aluno: Thiago Andrade Patente

Pereira, A C. Associação entre polimorfismo em genes que codificam proteínas pró-e antioxidantes e a susceptibilidade à nefropatia em coortes francesas de portadores de diabetes tipo 1: validação de resultados observados em uma casuística brasileira. 2014. Exame de qualificação (Mestrando em Programa de Pós-Graduação em Endocrinologia) - Faculdade de Medicina da Universidade de São Paulo.

Aluno: Larissa Ferreira dos Santos

Pereira, A C. "Controle neurovascular do fluxo sanguíneo muscular e da atividade nervosa simpática durante o exercício em pacientes após síndrome isquêmica miocárdica instável com polimorfismo do receptor beta2-adrenérgico. 2013 - Escola de Educação Física e Esporte da USP.

GOWDAK, L. H. W.;Pereira AC; BUFFOLO, E.; GAIATTO, F. A.; FARSKY, P. S.. "Predição do Sucesso da Cirurgia de Revascularização Miocárdica em Pacientes com Coronaripatia Difusa: A Contribuição do Heart Team.". 2015. Faculdade de Medicina da Universidade de São Paulo.

HUEB, W. A.; LAURINDO, F. R. M.; ALMEIDA, M. F.;Pereira AC; GOLDBAUM, M.. Avaliações das Taxas de Internação por Doença Cardiovascular e Cerebrovascular no Período Anterior e Posterior à Implantação da Lei Antitabaco de Número 13.541/09 na Cidade de São Paulo.". 2015. Faculdade de Medicina da Universidade de São Paulo.

KOIFFMANN, C. P.; KOK, F.; OLIVEIRA, K. G.; MITNE NETO, M.; MINGRONI, R. C.;Pereira AC; CARRAMASHI, L. V. P.. Estudo da Expressão Diferencial de Genes Localizados no Segmento Cromossômico 15q11-q13 em Pacietes com as Síndromes de Angelman e Prader-Willi.". 2015. Instituto de Biociências - Universidade de São Paulo.

PEREIRA, AC. Concurso para contratação de Professor Doutor junto ao Departamento de Biodinâmica do Movimento do Corpo Humano, na área de "Genética da Atividade Motora". 2013. Escola de Educação Física e Esporte da USP.

Orientou

[Nome removido após solicitação do usuário]

"ESTUDO GENÉTICO-QUANTITATIVO DAS PROPRIEDADES BÁSICAS DA PELE"; ; Início: 2015; Dissertação (Mestrado profissional em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP; (Orientador);

Patrícia Schneider Yogi

Identificação de Proteínas Nitradas com Potencial Diagnóstico de Vulnerabilidade de Placas Ateroscleróticas; Início: 2011; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; (Orientador);

Kallyandra Padilha

Estudos de associação genômica ampla do perfil metabólico em uma amostra populacional rural brasileira: Projeto Corações de Baependi; Início: 2016; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; (Orientador);

Francisca Alexandra Gavilanes Oleas

Caracterização genética de pacientes com Hipertensão Arterial Pulmonar associada à Esquistossomose; Início: 2014; Tese (Doutorado em Pneumologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; (Coorientador);

Michelle Sabrina Moreira dos Santos Silva

CARACTERIZAÇÃO DE ASSINATURAS MOLECULARES E ESCORES PREDITORES REPRESENTATIVOS DO NÍVEL DE TREINAMENTO FÍSICO, A PARTIR DE ANÁLISE TRANSCRICIONAL GLOBAL: DO SEDENTÁRIO AO ALTO RENDIMENTO; Início: 2013; Tese (Doutorado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; (Orientador);

André Ramos Vaquero

Comparação de redes gênicas para o entendimento de efeitos tóxicos de glicose e de variantes genéticas no risco de Diabetes Mellitus tipo 2; Início: 2013; Tese (Doutorado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Espírito Santo; (Orientador);

Maria Hellena Chijner Ribeiro do Valle

Identificação de alterações no gene SCN5A, causadoras da síndrome de Brugada e síndrome do QT longo tipo 3 em pacientes do Instituto do Coração HC-FMUSP, São Paulo; Início: 2012; Iniciação científica (Graduando em Ciências Biológicas) - Universidade Presbiteriana Mackenzie; (Orientador);

André Ricardo Martelini

TRIAGEM DE MUTAÇÕES NO GENE NEXN EM PACIENTES COM CARDIOMIOPATIA DILATADA IDIOPÁTICA; Início: 2010; Iniciação científica (Graduando em biologia) - Universidade de São Paulo, Fundação de Amparo à Pesquisa do Estado de São Paulo; (Orientador);

Juliana Morais Alvim

"Efeito da rapamicina na infecção de cardiomiócitos humanos por Trypanosoma cruzi"; 2017; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP,; Orientador: Alexandre da Costa Pereira;

Hadassa Campos Santos

"Associação de etnia auto referida e ancestralidade genética com fatores de risco de doença cardiovascular em uma amostra populacional brasileira: ELSA - Brasil"; 2015; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Vytor Hugo Mendes

"Determinantes genéticos de doença arterial coronária em uma amostra da população brasileira"; 2015; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Gabrielle D'Arezzo Pessente

"Aspectos genéticos da fibrilação atrial isolada"; 2015; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Conselho Nacional de Desenvolvimento Científico e Tecnológico; Orientador: Alexandre da Costa Pereira;

Tamiris Carneiro Gois

Perfis metabolômicos da ingestão de café; 2015; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Orientador: Alexandre da Costa Pereira;

André Ramos Vaquero

Estudo comparativo de redes gênicas de expressão de genes associados à Diabetes Mellitus tipo 2 (DM2) e genótipos de risco da doença; ; 2013; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Bianca Kiers

Correlação de características histológicas de placas ateroscleróticas coronarianas com fatores de risco e a presença de biomarcadores; 2013; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Michelle Sabrina Moreira dos Santos Silva

IDENTIFICAÇÃO, POR MICROARRAY, DE PREDITORES TRANSCRICIONAIS DO GANHO DE CAPACIDADE FUNCIONAL CARDIORRESPIRATÓRIA; 2013; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Hadassa Campos Santos

Associaçao de Ancestralidade com Fatores de Risco de Doenças Cardiovasculares em uma Amostra Populacional Brasileira: ELSA-Brasil; 2012; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Kallyandra Padilha

Herdabilidade de fenótipos metabólicos em uma população brasileira; 2012; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Théo Gremen Mimary de Oliveira

Aplicação do Sequenciamento de Próxima Geração no Diagnóstico Molecular de Cardiomiopatia Hipertrófica; 2012; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Orientador: Alexandre da Costa Pereira;

Vytor Hugo Mendes

DETERMINANTES GENÉTICOS DE DOENÇA ARTERIAL CORONÁRIA EM UMA AMOSTRA DA POPULAÇÃO BRASILEIRA; 2012; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Pamella Araujo Malagrino

Alterações no perfil metabólico em resposta a isquemia/reperfusão renal em modelo suíno de lesão renal aguda; ; 2011; Dissertação (Mestrado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Luciana Oliveira Cascaes Dourado

"Predição do sucesso da cirurgia de revascularização miocárdica em pacientes com coronaripatia difusa: a contribuição do heart team; "; 2015; Tese (Doutorado em Cardiologia) - Faculdade de Medicina da Universidade de São Paulo,; Orientador: Alexandre da Costa Pereira;

Gabriela Venturini da Silva

IDENTIFICAÇÃO DE MARCADORES PROTEICOS DE SHEAR STRESS ALTO E BAIXO; 2014; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Fanny Wulkan

"Análise genética de pacientes portadores de cardiomiopatia arritmogênica do ventrículo direito (CAVD) e caracterização funcional em cardiomiócitos diferenciados (hiPSC-CM)"; 2014; Tese (Doutorado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Pamella Araujo Malagrino

"Perfil proteômico da lesão renal aguda induzida por isquemia e reperfusão"; 2014; Tese (Doutorado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Everton Padilha Gomes

Análise da Associação entre Vegetarianismo e Aterosclerose Subclínica em População no Estado de São Paulo; 2014; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Orientador: Alexandre da Costa Pereira;

Júlia Daher Carneiro Marsiglia

Influência de Variantes Raras em Enhancers Cardíacos de Pacientes Portadores de Cardiopatia Congênita; 2013; Tese (Doutorado em Ciências Médicas) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Orientador: Alexandre da Costa Pereira;

Pãmela Rodrigues de Souza Silva

Programa de seguimento de coorte de pacientes com hipercolesterolemia familiar na região metropolitana de São Paulo; 2013; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Orientador: Alexandre da Costa Pereira;

Rafael de Oliveira Alvim

Associação de Polimorfismos do Gene da Adiponectina (AdipoQ) com o Fenótipo de Pressão Arterial: Projeto Corações de Baependi; 2013; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Carla Luana Dinardo

Variabilidade das propriedades Viscoelásticas de Células de Músculo Liso de Artérias Mamárias entre indivíduos de grupos raciais distintos; 2011; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP,; Orientador: Alexandre da Costa Pereira;

Nilson Tavares Poppi

"Estudo prospectivo em angina refratária: evolução clínica e o papel da troponina ultrassensível"; ; 2011; Tese (Doutorado em Cardiologia) - Instituto do Coração - Hospital das Clinicas - FMUSP,; Orientador: Alexandre da Costa Pereira;

Flávia Laghi Credidio

Padronização da Técnica de Imunoprecipitação da Cromatina (ChIP) para análise da ativação transcricional durante o processo de diferenciação de iPSC em cardiomiócito; 2011; Iniciação Científica; (Graduando em biologia) - Universidade Presbiteriana Mackenzie, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Ashila Garone Cheguri de Almeida

Investigação genética em pacientes com Insuficiência Cardíaca: o papel de polimorfismos associados a modulação da expressão gênica da via de sinalização do cálcio intracelular; 2010; Iniciação Científica - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Léa Ludovico Bozzini

Associação entre níveis de expressão gênica da via de sinalização do cálcio e polimorfismos genéticos; 2010; Iniciação Científica - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Lívia de Paula Marques

Variantes do gene Raldh2 em cardiopatias congênitas; 2009; Iniciação Científica - Instituto do Coração - Hospital das Clinicas - FMUSP, Fundação de Amparo à Pesquisa do Estado de São Paulo; Orientador: Alexandre da Costa Pereira;

Produções bibliográficas

COUTINHO, ELAINE R. ; Miname, Marcio H. ; ROCHA, VIVIANE Z. ; BITTENCOURT, MARCIO S. ; JANNES, CINTHIA E. ; TADA, MAURICIO T. ; LIMA, ISABELLA R. ; FILHO, WILSON SALGADO ; CHACRA, ANA P. ; Pereira, Alexandre C. ; Krieger, Jose E. ; Santos, Raul D. . Familial hypercholesterolemia and cardiovascular disease in older individuals. ATHEROSCLEROSIS , v. 318, p. 32-37, 2021.
IMBIRIBA, LIA ; TESS, BEATRIZ H. ; GRIEP, ROSANE H. ; FONSECA, MARIA J. M. ; Pereira, Alexandre C. ; DINIZ, MARIA F. S. ; Lotufo, Paulo A. ; BENSENOR, ISABELA M. ; SANTOS, ITAMAR S. . Metabolic status is not associated with job stress in individuals with obesity: the ELSA-Brasil baseline. INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH , v. 94, p. 639-646, 2021.
MARCATTO, LEILIANE ; BOER, BRUNO ; SACILOTTO, LUCIANA ; OLIVETTI, NATÁLIA ; DARRIEUX, FRANCISCO CARLOS COSTA ; SCANAVACCA, MAURÍCIO IBRAHIM ; Pereira, Alexandre Costa ; Santos, Paulo Caleb Junior Lima . Impact of adherence to warfarin therapy during 12weeks of pharmaceutical care in patients with poor time in the therapeutic range. JOURNAL OF THROMBOSIS AND THROMBOLYSIS , v. 51, p. 1043-1049, 2021.
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SANTOS, H.C. ; FRAGOSO, T.M. ; MACHADO-COELHO, G.L. ; DO NASCIMENTO, R.M. ; MILL, J.G. ; Krieger, J.E. ; Pereira, A.C. . Self-declared ethnicity associated with risk factors of cardiovascular diseases in an urban sample of the Brazilian population: The role of educational status in the association. International Journal of Cardiology (Print) , v. 168, p. 2973-2975, 2013.
Rodrigues, Sérgio Lamêgo ; Ângelo, Lílian Cláudia Souza ; Baldo, Marcelo Perim ; DANTAS, EDUARDO MIRANDA ; BARCELOS, ALEXANDRE MAULAZ ; Pereira, Alexandre C. ; Krieger, José Eduardo ; MILL, José Geraldo . Detection of left ventricular hypertrophy by the R-wave voltage in lead aVL: population-based study. Clinical Research in Cardiology (Print) , v. 102, p. 653-659, 2013.
de Oliveira Alvim, Rafael ; Santos, Paulo Caleb Junior Lima ; MUSSO, MARIANE ; de Sá Cunha, Roberto ; Krieger, José ; MILL, JOSÉ ; Pereira, Alexandre . Impact of diabetes mellitus on arterial stiffness in a representative sample of an urban Brazilian population. Diabetology & Metabolic Syndrome , v. 5, p. 45, 2013.
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Santos, Paulo Caleb Junior Lima ; Gagliardi, Ana Carolina Moron ; Miname, MÃrcio Hiroshi ; Chacra, Ana Paula ; Santos, Raul Dias ; Krieger, Jose Eduardo ; Pereira, Alexandre Costa . SLCO1B1 haplotypes are not associated with atorvastatin-induced myalgia in Brazilian patients with familial hypercholesterolemia. European Journal of Clinical Pharmacology , v. 68, p. 273-279, 2012.
Carneiro, Marcia M. ; Miname, Marcio H. ; Gagliardi, Ana C. ; Pereira, Carolina ; Pereira, Alexandre C. ; Krieger, Jose E. ; Maranhão, Raul C. ; Santos, Raul D. . The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions. Atherosclerosis (Amsterdam) , v. 221, p. 268-274, 2012.
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ALVIM, RAFAEL DE OLIVEIRA ; Santos, Paulo C. J. L. ; NASCIMENTO, RAIMUNDO M. ; COELHO, GEORGE L. L. M. ; Mill, José G. ; Krieger, José E. ; Pereira, Alexandre C. . BDKRB2 +9/9 Polymorphism Is Associated with Higher Risk for Diabetes Mellitus in the Brazilian General Population. Experimental Diabetes Research (Print) , v. 2012, p. 1-4, 2012.
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BERTOLA, DR ; POPLAWSKI, AB ; TANNURI, U ; LEITE, C ; PEREIRA, AC ; BRASIL, AS ; FALZONI, R ; JANOWSKI, KM ; KIM, CA ; SUZUKI, L ; MESSIAEN, LM . Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship?. Clinical Genetics , v. 81, p. 595-597, 2012.
FERNANDES, FABIO ; Krieger, Jose Eduardo ; Pereira, Alexandre Costa ; BUCK, PAULA ; MATSUMOTO, AFONSO ; Mady, Charles ; ARTEAGA-FERNANDEZ, EDMUNDO ; ANTUNES, MURILLO DE OLIVEIRA ; MARSIGLIA, JULIA DAHER CARNEIRO ; NASTARI, LUCIANO . Plasma Pro-B-Type Natriuretic Peptide Testing as a Screening Method for Hypertrophic Cardiomyopathy. Journal of Cardiac Failure , v. 18, p. 564-568, 2012.
ALVIM, R. D. O. ; Krieger, J. E. ; SANTOS, P. C. J. L. ; Mill, J. G. ; JUNIOR, W. N. ; CUNHA, R. D. S. ; PEREIRA, A. C. ; RODRIGUES, M. V. ; Dias, R. G. . Association between the C242T polymorphism in the p22phox gene with arterial stiffness in the Brazilian population. Physiological Genomics (Online) , v. 10, p. 1-11, 2012.
BRASIL, AMANDA S. ; Malaquias, Alexsandra C. ; Kim, Chong A. ; KRIEGER, José Eduardo ; Jorge, Alexander A.L. ; Pereira, Alexandre C. ; Bertola, Débora R. . KRAS gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G-domain: Report of another family with metopic craniosynostosis. American Journal of Medical Genetics. Part A , v. 158A, p. 1178-1184, 2012.
QUAIO, CAIO R.D.C. ; DA SILVA, CLOVIS A. ; Pereira, Alexandre C. ; Bertola, Débora R. ; BUENO, CLEONICE ; BRASIL, AMANDA S. ; CARVALHO, JOZÉLIO F. ; Jorge, Alexander A.L. ; Kim, Chong A. ; Malaquias, Alexsandra C. . Autoimmune disease and multiple autoantibodies in 42 patients with RASopathies. American Journal of Medical Genetics. Part A , v. 158A, p. 1077-1082, 2012.
PERCY, MELANIE J. ; CHUNG, YU JIN ; MCMULLIN, MARY FRANCES ; MERCIECA, JANE ; HOFFBRAND, A. VICTOR ; HARRISON, CLAIRE ; Santos, Paulo C.J.L. ; Pereira, Alexandre C. ; FONSECA, GUILHERME H.H. ; LEE, FRANK S. ; DINARDO, CARLA L. ; LAPPIN, TERENCE R.J. ; GUALANDRO, SANDRA F.M. . Two new mutations in the HIF2A gene associated with erythrocytosis. American Journal of Hematology (Print) , v. 87, p. 439-442, 2012.
VIEIRA, RICARDO D. ; Pereira, Alexandre C. ; LIMA, EDUARDO G. ; GARZILLO, CIBELE L. ; REZENDE, PAULO CURY ; FAVARATO, DESIDERIO ; HUEB, ALEXANDRE C. ; GERSH, BERNARD J. ; RAMIRES, JOSÉ A.F. ; HUEB, Whady . Cancer-related deaths among different treatment options in chronic coronary artery disease. Coronary Artery Disease , v. 4, p. 1, 2012.
BIAGI, DIOGO G ; MANSUR, Alfredo J ; Mill, Jose G ; Krieger, Jose E ; Pereira, Alexandre C . A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy.. Journal of Negative Results In Biomedicine , v. 11, p. 4, 2012.
Santos, Paulo Caleb Junior Lima ; Krieger, Jose Eduardo ; Pereira, Alexandre Costa . Renin^|^ndash;Angiotensin System, Hypertension, and Chronic Kidney Disease: Pharmacogenetic Implications. Journal of Pharmacological Sciences , v. 120, p. 77-88, 2012.
LIMA SANTOS, PAULO CALEB JÚNIOR D ; DINARDO, CARLA LUANA ; CANÇADO, RODOLFO DELFINI ; SCHETTERT, ISOLMAR TADEU ; KRIEGER, José Eduardo ; Pereira, Alexandre Costa . Non-HFE hemochromatosis. Revista Brasileira de Hematologia e Hemoterapia (Impresso) , v. 34, p. 311-316, 2012.
Soares, Renata Alonso Gadi ; Santos, Paulo Caleb Junior Lima ; Machado-Coelho, George Luiz Lins ; NASCIMENTO, RAIMUNDO MARQUES DO ; MILL, JOSE GERALDO ; KRIEGER, Jose Eduardo ; Pereira, Alexandre Costa . CYP2C9 and VKORC1 Polymorphisms Are Differently Distributed in the Brazilian Population According to Self-Declared Ethnicity or Genetic Ancestry. Genetic Testing and Molecular Biomarkers (Online) , v. 16, p. 957-963, 2012.
Dias, Rodrigo Gonçalves ; Gowdak, Márcia Maria ; Pereira, Alexandre Costa . Genetics and cardiovascular system: influence of human genetic variants on vascular function. Genes & Nutrition: a journal devoted to study of relationship between genetics & nutrition for improvement of human health , v. 6, p. 55-62, 2011.
Pereira, T. V. ; Patsopoulos, N. A. ; PEREIRA, A. C. ; Krieger, J. E. . Strategies for genetic model specification in the screening of genome-wide meta-analysis signals for further replication. International Journal of Epidemiology , v. 40, p. 457-469, 2011.
Tayo, Bamidele O. ; Teil, Marie ; Tong, Liping ; Qin, Huaizhen ; Khitrov, Gregory ; Zhang, Weijia ; Song, Quinbin ; Gottesman, Omri ; Zhu, Xiaofeng ; Pereira, Alexandre C. ; Cooper, Richard S. ; Bottinger, Erwin P. . Genetic Background of Patients from a University Medical Center in Manhattan: Implications for Personalized Medicine. Plos One , v. 6, p. e19166, 2011.
Yugar-Toledo, Juan Carlos ; Martin, José Fernando Vilela ; KRIEGER, José Eduardo ; Pereira, Alexandre C ; Demacq, Caroline ; Coelho, Otávio Rizzi ; Pimenta, Eduardo ; Calhoun, David A. ; Júnior, Heitor Moreno . Gene Variation in Resistant Hypertension: Multilocus Analysis of the Angiotensin 1-Converting Enzyme, Angiotensinogen, and Endothelial Nitric Oxide Synthase Genes. DNA and Cell Biology , v. 30, p. 555-564, 2011.
Almeida, Marcio AA ; Oliveira, Paulo SL ; Pereira, Tiago V ; Krieger, JosÃ E ; Pereira, Alexandre C . An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations. BMC Genetics (Online) , v. 12, p. 10, 2011.
Giolo, Suely R ; Soler, JÃlia M P ; Greenway, Steven C ; Almeida, Marcio A A ; de Andrade, Mariza ; Seidman, J G ; Seidman, Christine E ; Krieger, JosÃ E ; Pereira, Alexandre C . Brazilian urban population genetic structure reveals a high degree of admixture. European Journal of Human Genetics , v. 20, p. 111-116, 2011.
Santos, Paulo CJL ; Soares, Renata AG ; Santos, Diogo BG ; Nascimento, Raimundo M ; Coelho, George LLM ; Nicolau, JosÃ C ; Mill, JosÃ G ; Krieger, JosÃ E ; Pereira, Alexandre C . CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population. BMC Medical Genetics (Online) , v. 12, p. 13, 2011.
SILVA, BRUNO M. ; NEVES, FABRICIA J. ; NEGRÃO, MARCELO V. ; Alves, Cleber R. ; DIAS, RODRIGO G. ; Alves, Guilherme B. ; Pereira, Alexandre C. ; Rondon, Maria U. ; Krieger, José E. ; NEGRÃO, CARLOS E. ; DA NÓBREGA, ANTONIO CLAUDIO LUCAS . Endothelial Nitric Oxide Synthase Polymorphisms and Adaptation of Parasympathetic Modulation to Exercise Training. Medicine and Science in Sports and Exercise , v. 43, p. 1611-1618, 2011.
Sousa, AndrÃ Gustavo P. ; Lopes, Neuza H. ; Hueb, Whady A. ; Krieger, JosÃ Eduardo ; Pereira, Alexandre C. . Genetic Variants of Diabetes Risk and Incident Cardiovascular Events in Chronic Coronary Artery Disease. Plos One , v. 6, p. e16341, 2011.
Santos, Paulo Caleb Junior Lima ; Soares, Renata Alonso Gadi ; Krieger, Jose Eduardo ; Guerra-Shinohara, Elvira Maria ; Pereira, Alexandre Costa . Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000 instrument. Clinical Chemistry and Laboratory Medicine , v. 49, p. 1633-1636, 2011.
Horimoto, AndrÃa RVR ; Giolo, Suely R ; Oliveira, Camila M ; Alvim, Rafael O ; Soler, JÃlia P ; de Andrade, Mariza ; Krieger, JosÃ E ; Pereira, Alexandre C . Heritability of physical activity traits in Brazilian families: the Baependi Heart Study. BMC Medical Genetics (Online) , v. 12, p. 155, 2011.
Medeiros, Alessandra ; Biagi, Diogo G. ; Sobreira, Tiago J.P. ; de Oliveira, Paulo SÃrgio L. ; NegrÃo, Carlos Eduardo ; Mansur, Alfredo J. ; Krieger, JosÃ Eduardo ; Brum, Patricia C. ; Pereira, Alexandre C. . Mutations in the human phospholamban gene in patients with heart failure. The American Heart Journal , v. 162, p. 1088-1095.e1, 2011.
Santos, Paulo CJL ; Soares, Renata AG ; Nascimento, Raimundo M ; Machado-Coelho, George LL ; Mill, JosÃ G ; Krieger, JosÃ E ; Pereira, Alexandre C . SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group. BMC Medical Genetics (Online) , v. 12, p. 136, 2011.
Schreiber, Roberto ; Ferreira-Sae, Maria C ; Ronchi, Juliana A ; Pio-MagalhÃes, JosÃ A ; Cipolli, JosÃ A ; Matos-Souza, JosÃ R ; Mill, JosÃ G ; Vercesi, AnÃ&shy ; Krieger, JosÃ E ; Franchini, Kleber G ; Pereira, Alexandre C ; Nadruz Junior, Wilson . The C242T polymorphism of the p22-phox gene (CYBA) is associated with higher left ventricular mass in Brazilian hypertensive patients. BMC Medical Genetics (Online) , v. 12, p. 114, 2011.
da Rocha Pitta Marin, Lenina ; Bezerra Gaspar Carvalho da Silva, Felipe Theodoro ; Ferreira de SÃ, LuÃ&shy ; Salem Brasil, Amanda ; Pereira, Alexandre ; Mosca Furquim, Isabel ; Kim, Chong Ae ; Romeo Bertola, DÃbora . Ocular manifestations of Noonan syndrome. Ophthalmic Genetics , v. 33, p. 1-5, 2011.
ANGELI, CLÁUDIA B. ; KIMURA, LILIAN ; AURICCHIO, MARIA T. ; VICENTE, JOÃO P. ; MATTEVI, VANESSA S. ; ZEMBRZUSKI, VERÔNICA M. ; HUTZ, MARA H. ; Pereira, Alexandre C. ; PEREIRA, TIAGO V. ; MINGRONI-NETTO, REGINA C. . Multilocus Analyses of Seven Candidate Genes Suggest Interacting Pathways for Obesity-Related Traits in Brazilian Populations. Obesity (Silver Spring Online) , v. 19, p. 1244-1251, 2011.
MAGALHAES, T. A. ; CURY, R. C. ; Pereira, Alexandre Costa ; MOREIRA, V. M. ; Lemos, Pedro A. ; KALIL-FILHO, ROBERTO ; ROCHITTE, CARLOS EDUARDO . Additional value of dipyridamole stress myocardial perfusion by 64-row computed tomography in patients with coronary stents. Journal of Cardiovascular Computed Tomography , v. 5, p. 449-458, 2011.
ALVIM, R O ; SANTOS, P C J L ; FERREIRA, N E ; Mill, J G ; KRIEGER, J e ; Pereira, A C . Thioredoxin interacting protein (TXNIP) rs7212 polymorphism is associated with arterial stiffness in the Brazilian general population. Journal of Human Hypertension , v. 24, p. 1-3, 2011.
GONCALVES, F.T. ; CARDENA, M.M.S.G. ; GONZALEZ, R.S. ; Krieger, J.E. ; Pereira, A.C. ; FRIDMAN, C. . The discrimination power of the hypervariable regions HV1, HV2 and HV3 of mitochondrial DNA in the Brazilian population. Forensic Science International. Genetics Supplement Series (Print) , v. 3, p. e311-e312, 2011.
FRIDMAN, C. ; CARDENA, M.M.S.G. ; Krieger, J.E. ; Pereira, A.C. . Evaluation of the relationship between mitochondrial haplogroup and development of heart failure in Brazilian sample. Forensic Science International. Genetics Supplement Series (Print) , v. 3, p. e77-e78, 2011.
VIANNA, CAIO B. ; MIURA, NANA ; Pereira, Alexandre C. ; JATENE, MARCELO B. . HoltâOram syndrome: novel TBX5 mutation and associated anomalous right coronary artery. Cardiology in the Young , v. 21, p. 351-353, 2011.
Santos, Paulo C.J.L. ; Figueiredo, Maria Stella ; Schettert, Isolmar T. ; Hirata, Mario H. ; SOARES, RENATA A.G. ; Hirata, Rosario D.C. ; Pereira, Alexandre C. ; PAGLIUSI, REGINA A. ; Krieger, Jose E. ; Guerra-Shinohara, Elvira M. ; Chiattone, Carlos S. ; TEIXEIRA, ANA C. ; CANÃADO, RODOLFO D. . Hereditary hemochromatosis: Mutations in genes involved in iron homeostasis in Brazilian patients. Blood Cells, Molecules & Diseases (Print) , v. 46, p. 302-307, 2011.
FRANCO, L.F. ; MOISÃS, R.S. ; Pereira, A.C. ; CRISPIM, F. . Variants of transcription factor 7-like 2 (TCF7L2) gene and incident glucose intolerance in Japanese-Brazilians. Brazilian Journal of Medical and Biological Research , v. 44, p. 240-244, 2011.
SOUSA, ANDRÉ G. ; SELVATICI, LÍVIA ; Krieger, José E. ; Pereira, Alexandre C. . Association Between Genetics of Diabetes, Coronary Artery Disease, and Macrovascular Complications: Exploring a Common Ground Hypothesis. The Review of Diabetic Studies (Print) , v. 8, p. 230-244, 2011.
ALFONSO DE ALMEIDA, MARCIO ; VANÇAN RUSSO HORIMOTO, ANDREA ; LOPES DE OLIVEIRA, PAULO ; Krieger, José ; DA COSTA PEREIRA, ALEXANDRE . Different approaches for dealing with rare variants in family-based genetic studies: application of a Genetic Analysis Workshop 17 problem. BMC PROCEEDINGS , v. 5, p. S78, 2011.
Ferreira, Larissa Gorayb ; Costa Pereira, Alexandre ; Pfeferman Heilberg, Ita . Vitamin D Receptor and Calcium-Sensing Receptor Gene Polymorphisms in Hypercalciuric Stone-Forming Patients. Nephron. Clinical Practice , v. 114, p. c135-c144, 2010.
Schettert, Isolmar T. ; Pereira, Alexandre C. ; Lopes, Neuza H. ; Hueb, Whady A. ; Krieger, Jose E. . Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease. Thrombosis Research , v. 125, p. 61-66, 2010.
MALAFRONTE, P. ; VIEIRA, J. M. ; PEREIRA, A. C. ; Krieger, J. E. ; BARROS, R. T. ; WORONIK, V. . Association of the MCP-1 -2518 A/G Polymorphism and No Association of Its Receptor CCR2 -64 V/I Polymorphism with Lupus Nephritis. Journal of Rheumatology , v. 37, p. 776-782, 2010.
Gowdak, Marcia M.G. ; Laterza, Mateus C. ; Rondon, Maria Urbana P.B. ; Trombetta, Ivani C. ; Pereira, Alexandre C. ; Krieger, Jose Eduardo ; Negrao, Carlos Eduardo . A high-fat meal impairs muscle vasodilatation response to mental stress in humans with Glu27 beta2-adrenoceptor polymorphism. Lipids in health and disease , v. 9, p. 55, 2010.
Sbruzzi, Ivanete C. ; Pereira, Alexandre C. ; Vasconcelos, Beatriz ; Honjo, Raquel S. ; Krieger, José E. ; Kim, Chong A. . Williams-Beuren Syndrome: Diagnosis by Polymorphic Markers. Genetic Testing and Molecular Biomarkers (Print) , v. 14, p. 209-214, 2010.
Santos, Diogo GB ; Resende, Marina F ; Mill, José G ; MANSUR, Alfredo J ; Krieger, José E ; Pereira, Alexandre C . Nuclear Factor (NF) ?B polymorphism is associated with heart function in patients with heart failure. BMC Medical Genetics (Online) , v. 11, p. 89, 2010.
Angelo, Lilian C. ; Vieira, Marcelo L. C. ; Rodrigues, Sergio L. ; Morelato, Renato ; Pereira, Alexandre C. ; Mill, José G. ; Krieger, José E. . Reference Values of Tissue Doppler Imaging and Pulsed Doppler Echocardiography for Analysis of Left Ventricular Diastolic Function in Healthy Adults. Echocardiography (Mount Kisco, N.Y. Print) , v. 27, p. 777-782, 2010.
Brasil, Amanda Salem ; Pereira, Alexandre C. ; Wanderley, Luciana Turolla ; Kim, Chong Ae ; Malaquias, Alexsandra C. ; Jorge, Alexander A.L. ; KRIEGER, José Eduardo ; Bertola, Débora Romeo . and Gene Analysis in Patients with Noonan and Noonan-Like Syndromes. Genetic Testing and Molecular Biomarkers (Print) , v. 14, p. 425-432, 2010.
Negrao, M. V. ; Alves, C. R. ; Alves, G. B. ; PEREIRA, A. C. ; Dias, R. G. ; Laterza, M. C. ; Mota, G. F. ; Oliveira, E. M. ; Bassaneze, V. ; Krieger, J. E. ; Negrao, C. E. ; Rondon, M. U. P. B. . Exercise training improves muscle vasodilatation in individuals with T786C polymorphism of endothelial nitric oxide synthase gene. Physiological Genomics (Print) , v. 42A, p. 71-77, 2010.
Goulart, Alessandra C. ; Bustos, Iara R. ; Abe, Ivana M. ; Pereira, Alexandre C. ; Fedeli, Ligia M. ; Benseor, Isabela M. ; Lotufo, Paulo A. . A stepwise approach to stroke surveillance in Brazil: the EMMA (Estudo de Mortalidade e Morbidade do Acidente Vascular Cerebral) study. International Journal of Stroke , v. 5, p. 284-289, 2010.
Hueb, W. ; Lopes, N. ; Gersh, B. J. ; Soares, P. R. ; Ribeiro, E. E. ; PEREIRA, A. C. ; Favarato, D. ; Rocha, A. S. C. ; Hueb, A. C. ; Ramires, J. A. F. . Ten-Year Follow-Up Survival of the Medicine, Angioplasty, or Surgery Study (MASS II): A Randomized Controlled Clinical Trial of 3 Therapeutic Strategies for Multivessel Coronary Artery Disease. Circulation (New York, N.Y.) , v. 122, p. 949-957, 2010.
Santos, Paulo C.J.L. ; Pereira, Alexandre C. ; Cançado, Rodolfo D. ; Schettert, Isolmar T. ; Sobreira, Tiago J.P. ; Oliveira, Paulo S.L. ; Hirata, Rosario D.C. ; Hirata, Mario H. ; Figueiredo, Maria Stella ; Chiattone, Carlos S. . HFE gene mutations in patients with primary iron overload: Is there a significant improvement in molecular diagnosis yield with HFE sequencing?. Blood Cells, Molecules & Diseases (Print) , v. 45, p. 302-307, 2010.
Hueb, W. ; Lopes, N. H. ; PEREIRA, A. C. ; Hueb, A. C. ; Soares, P. R. ; Favarato, D. ; D&amp ; Lima, E. G. ; Garzillo, C. L. ; da Silva Paulitch, F. ; Cesar, L. A. M. ; Gersh, B. J. ; Ramires, J. A. F. . Five-Year Follow-Up of a Randomized Comparison Between Off-Pump and On-Pump Stable Multivessel Coronary Artery Bypass Grafting. The MASS III Trial. Circulation (New York, N.Y.) , v. 122, p. S48-S52, 2010.
Giolo, Suely R ; Pereira, Alexandre C ; de Andrade, Mariza ; Krieger, Jose E ; Soler, Julia P . Evaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families. BMC Medical Genetics (Online) , v. 11, p. 132, 2010.
HUEB, Whady ; Lopes, Neuza ; SOARES, Paulo R ; GERSH, Bernard J ; Lima, Eduardo GOMES ; Vieira, Ricardo D&amp ; Garzillo, Cibele LARROSA ; Garcia, Rosa RHAMI ; Pereira, Alexandre Costa ; Strunz, Celia MARIA ; Meneguetti, Claudio ; Tsutsui, Jeane ; Parga, Jose ; Lemos, Pedro ; Hueb, Alexandre ; Ushida, Augusto H ; Maranhao, Raul ; Chamone, Dalton A ; Ramires, Jose AF . Hypotheses, rationale, design, and methods for prognostic evaluation in type 2 diabetic patients with angiographically normal coronary arteries. The MASS IV-DM Trial. BMC Cardiovascular Disorders (Online) , v. 10, p. 47, 2010.
de Lima Santos, Paulo Caleb Júnior ; Pereira, Alexandre C. ; Cançado, Rodolfo D. ; Schettert, Isolmar T. ; Hirata, Rosario D.C. ; Hirata, Mario H. ; Figueiredo, Maria Stella ; Chiattone, Carlos S. ; Krieger, Jose E. ; Guerra-Shinohara, Elvira M. . Hemojuvelin and Hepcidin Genes Sequencing in Brazilian Patients with Primary Iron Overload. Genetic Testing and Molecular Biomarkers (Print) , v. 14, p. 803-806, 2010.
Alvim, Rafael O ; Freitas, Silvia RS ; Ferreira, Noely E ; Santos, Paulo CJL ; Cunha, Roberto S ; Mill, José G ; Krieger, José E ; Pereira, Alexandre C . APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population. Lipids in health and disease , v. 9, p. 128, 2010.
Santos, Paulo Caleb J.L. ; Cançado, Rodolfo D. ; Pereira, Alexandre C. ; Chiattone, Carlos S. ; Krieger, Jose Eduardo ; Guerra-Shinohara, Elvira M. . <i>HJV</i> Hemochromatosis, Iron Overload, and Hypogonadism in a Brazilian Man: Treatment with Phlebotomy and Deferasirox. Acta Haematologica , v. 124, p. 204-205, 2010.
Issa, J. S. ; Abe, T. M. O. ; PEREIRA, A. C. ; Megid, M. C. ; Shimabukuro, C. E. ; Valentin, L. S. O. ; Ferreira, M. M. d. C. ; Nobre, M. R. C. ; Lancarotte, I. ; Pereira Barretto, A. C. . The effect of Sao Paulo's smoke-free legislation on carbon monoxide concentration in hospitality venues and their workers. Tobacco Control , v. 20, p. 156-162, 2010.
Sobreira, T. J. P. ; Marletaz, F. ; Simoes-Costa, M. ; Schechtman, D. ; PEREIRA, A. C. ; Brunet, F. ; Sweeney, S. ; Pani, A. ; Aronowicz, J. ; Lowe, C. J. ; Davidson, B. ; Laudet, V. ; Bronner, M. ; de Oliveira, P. S. L. ; Schubert, M. ; Xavier-Neto, J. . Structural shifts of aldehyde dehydrogenase enzymes were instrumental for the early evolution of retinoid-dependent axial patterning in metazoans. Proceedings of the National Academy of Sciences of the United States of America , v. 108, p. 226-231, 2010.
de Lima Santos, Paulo Caleb Júnior ; de Oliveira Alvim, Rafael ; Ferreira, Noely Evangelista ; de Sá Cunha, Roberto ; KRIEGER, José Eduardo ; MILL, José Geraldo ; Pereira, Alexandre Costa . Ethnicity and Arterial Stiffness in Brazil. American Journal of Hypertension , v. 24, p. 278-284, 2010.
Brasil, Amanda Salem ; Malaquias, Alexsandra C. ; Wanderley, Luciana Turolla ; Kim, Chong Ae ; KRIEGER, José Eduardo ; Jorge, Alexander A. L. ; Pereira, Alexandre C. ; Bertola, Débora Romeo . Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?. Arquivos Brasileiros de Endocrinologia e Metabologia (Impresso) , v. 54, p. 717-722, 2010.
Santos, Diogo GB ; Medeiros, Alessandra ; Brum, Patricia C ; Mill, Jose G ; MANSUR, Alfredo J ; Krieger, Jose E ; PEREIRA, A. C. . No evidence for an association between the -36A>C phospholamban gene polymorphism and a worse prognosis in heart failure. BMC Cardiovascular Disorders (Online) , v. 9, p. 33, 2009.
Greenway, Steven C ; Pereira, Alexandre C ; Lin, Jennifer C ; DePalma, Steven R ; Israel, Samuel J ; Mesquita, Sonia M ; Ergul, Emel ; Conta, Jessie H ; Korn, Joshua M ; McCarroll, Steven A ; Gorham, Joshua M ; Gabriel, Stacey ; Altshuler, David M ; de Lourdes Quintanilla-Dieck, Maria ; Artunduaga, Maria Alexandra ; Eavey, Roland D ; Plenge, Robert M ; Shadick, Nancy A ; Weinblatt, Michael E ; De Jager, Philip L ; Hafler, David A ; Breitbart, Roger E ; Seidman, Jonathan G ; Seidman, Christine E . De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. Nature Genetics , v. 41, p. 931-935, 2009.
Alves, Guilherme B. ; Oliveira, Edilamar M. ; Alves, Cleber R. ; Rached, Heron R.S. ; Mota, Glória F.A. ; Pereira, Alexandre C. ; Rondon, Maria U. ; Hashimoto, Nara Y. ; Azevedo, Luciene F. ; KRIEGER, José Eduardo ; Negrão, Carlos Eduardo . Influence of angiotensinogen and angiotensin-converting enzyme polymorphisms on cardiac hypertrophy and improvement on maximal aerobic capacity caused by exercise training. European Journal of Cardiovascular Prevention & Rehabilitation , v. 16, p. 487-492, 2009.
Freitas, S R ; Pereira, A C ; Floriano, M S ; Mill, J G ; KRIEGER, J e . Insertion/deletion polymorphism of the bradykinin type 2 receptor gene influence diastolic blood pressure. Journal of Human Hypertension , v. 23, p. 553-555, 2009.
Ruiz Giolo, Suely ; Costa Pereira, Alexandre ; de Andrade, Mariza ; Maciel de Oliveira, Camila ; Krieger, Jos&amp ; Pavan Soler, J&amp . Genetic Analysis of Age-at-Onset for Cardiovascular Risk Factors in a Brazilian Family Study, v. 68, p. 131-138, 2009.
van Bon, B W M Mefford, H C Menten, B Koolen, D A Sharp, A J Nillesen, W M Innis, J W de Ravel, T J L Mercer, C L Fichera, M Stewart, H Connell, L E Ounap, K Lachlan, K Castle, B Van der Aa, N van Ravenswaaij, C Nobrega, M A Serra-Juhe, C Simonic, I de Leeuw, N Pfundt, R Bongers, E M Baker, C Finnemore, P , et al. Huang, S Maloney, V K Crolla, J A van Kalmthout, M Elia, M Vandeweyer, G Fryns, J P Janssens, S Foulds, N Reitano, S Smith, K Parkel, S Loeys, B Woods, C G Oostra, A Pereira, A C ; Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. Journal of Medical Genetics , v. 46, p. 511-523, 2009.
Vendramini, Marcio F. ; Pereira, Alexandre C. ; Ferreira, Sandra R. ; Kasamatsu, Teresa S. ; Moisés, Regina S. . Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese Brazilians. Journal of Diabetes and its Complications , p. xx-xx, 2009.
Koyama, Renata G. ; Drager, Luciano F. ; Lorenzi-Filho, Geraldo ; Cintra, Fátima D. ; Pereira, Alexandre C. ; Poyares, Dalva ; KRIEGER, José Eduardo ; Castro, Rosa M.R.P.S. ; Tufik, Sérgio ; de Mello, Marco Túlio . Reciprocal interactions of obstructive sleep apnea and hypertension associated with ACE I/D polymorphism in males. Sleep Medicine , p. xx, 2009.
Pires de Sousa, André Gustavo ; Pereira, Alexandre Costa ; Marquezine, Guilherme Figueiredo ; Marques do Nascimento-Neto, Raimundo ; Freitas, Silvia N. ; C. Nicolato, Roney Luiz ; Machado-Coelho, George Luiz Lins ; Rodrigues, Sérgio L. ; Mill, José G. ; KRIEGER, José Eduardo . Derivation and external validation of a simple prediction model for the diagnosis of type 2 Diabetes Mellitus in the Brazilian urban population. European Journal of Epidemiology , v. 24, p. 101-109, 2009.
Dias, R. G. ; Alves, M.-J. N. N. ; PEREIRA, A. C. ; Rondon, M. U. P. B. ; dos Santos, M. R. ; Krieger, J. E. ; Krieger, M. H. ; Negrao, C. E. . Glu298Asp eNOS gene polymorphism causes attenuation in nonexercising muscle vasodilatation. Physiological Genomics , v. 37, p. 99-107, 2009.
SPOSITO, A ; SANTOS, R ; ABDALLA, D ; MOREIRA, A ; LIMA, J ; KRIEGER, J ; MARTINEZ, T ; RAMIRES, J ; PEREIRA, A . Plasma cholesterol is involved in the setting of resting blood pressure: A study in hypercholesterolemic young subjects and in monozygotic twins. International Journal of Cardiology , p. xx, 2009.
Tamanaha, Rosana ; Camacho, Cléber P. ; Pereira, Alexandre C. ; da Silva, Adriana M. Álvares ; Maciel, Rui M. B. ; Cerutti, Janete M. . Evaluation of RET polymorphisms in a six-generation family with G533C RET mutation: specific RET variants may modulate age at onset and clinical presentation. Clinical Endocrinology (Oxford) , v. 71, p. 56-64, 2009.
Rodrigues, Sérgio Lamêgo ; Ângelo, Lílian C.S. ; Pereira, Alexandre C. ; KRIEGER, José Eduardo ; MILL, José Geraldo . Determinants of left ventricular mass and presence of metabolic risk factors in normotensive individuals. International Journal of Cardiology , v. 135, p. 323-330, 2009.
Lopes, Neuza Helena ; da Silva Paulitsch, Felipe ; Pereira, Alexandre ; Garzillo, Cibele Larossa ; Ferreira, João Fernando ; Stolf, Noedir ; HUEB, Whady . Mild chronic kidney dysfunction and treatment strategies for stable coronary artery disease. Journal of Thoracic and Cardiovascular Surgery (Print) , v. 137, p. 1443-1449, 2009.
Maciel, Simone S. ; Pereira, Alexandre da C. ; Silva, Gustavo J.J. ; Rodrigues, Mariliza V. ; Mill, José G. ; Krieger, Jose E. . Association between glutathione S-transferase polymorphisms and triglycerides and HDL-cholesterol. Atherosclerosis (Amsterdam) , v. 206, p. 204-208, 2009.
Sousa, André Gustavo P. ; Marquezine, Guilherme F. ; Lemos, Pedro A. ; Martinez, Eulogio ; Lopes, Neuza ; Hueb, Whady A. ; Krieger, José E. ; Pereira, Alexandre C. . TCF7L2 Polymorphism rs7903146 Is Associated with Coronary Artery Disease Severity and Mortality. Plos One , v. 4, p. e7697, 2009.
Mansur, Alfredo ; Fontes, Rosana ; Canzi, Regina ; Nishimura, Raphael ; Alencar, Airlane ; de Lima, Antonio ; Krieger, José ; Pereira, Alexandre . Beta-2 adrenergic receptor gene polymorphisms Gln27Glu, Arg16Gly in patients with heart failure. BMC Cardiovascular Disorders (Online) , v. 9, p. 50, 2009.
Pavan, Marilene ; Ruiz, Viviane F ; Silva, Fábio A ; Sobreira, Tiago J ; Cravo, Roberta M ; Vasconcelos, Michelle ; Marques, Lívia P ; Mesquita, Sonia MF ; Krieger, José E ; Lopes, Antônio AB ; OLIVEIRA, Paulo S ; Pereira, Alexandre C ; XAVIER-NETO, José . ALDH1A2 (RALDH2) genetic variation in human congenital heart disease. BMC Medical Genetics , v. 10, p. 113, 2009.
Meyerfreund, Diana ; Gonçalves, Christine P ; Cunha, Roberto S ; Pereira, Alexandre C ; Krieger, José E ; Mill, José G . Age-dependent increase in blood pressure in two different Native American communities in Brazil. Journal of Hypertension , v. 27, p. 1753-1760, 2009.
Rodrigues, Sérgio Lamego ; Baldo, Marcelo Perim ; Sá Cunha, Roberto ; Angelo, Lílian CS ; Pereira, Alexandre C ; KRIEGER, José Eduardo ; MILL, José Geraldo . Anthropometric measures of increased central and overall adiposity in association with echocardiographic left ventricular hypertrophy. Hypertension Research , v. 33, p. 83-87, 2009.
Freitas, Silvia R ; Pereira, Alexandre C ; Floriano, Marcilene S ; Mill, José G ; Krieger, José E . Association of alpha1a-adrenergic receptor polymorphism and blood pressure phenotypes in the Brazilian population. BMC Cardiovascular Disorders (Online) , v. 8, p. 40, 2008.
GIOLIPEREIRA, L ; PEREIRA, A ; MESQUITA, S ; XAVIERNETO, J ; LOPES, A ; KRIEGER, J . NKX2.5 mutations in patients with non-syndromic congenital heart disease. International Journal of Cardiology , p. x, 2008.
Marquezine, Guilherme F ; Pereira, Alexandre C ; Sousa, Andre GP ; Mill, Jose G ; Hueb, Whady A ; Krieger, Jose E . TCF7L2 variant genotypes and type 2 diabetes risk in Brazil: significant association, but not a significant tool for risk stratification in the general population. BMC Medical Genetics , v. 9, p. 106, 2008.
Cuoco, Marco Antonio Romeo ; Pereira, Alexandre Costa ; Mota, Glória de Fátima Alves da ; KRIEGER, José Eduardo ; Mansur, Alfredo José . Polimorfismo genético, terapia farmacológica e função cardíaca seqüencial em pacientes com insuficiência cardíaca. Arquivos Brasileiros de Cardiologia , v. 90, p. 252-256, 2008.
de Oliveira, Camila M ; Pereira, Alexandre C ; de Andrade, Mariza ; Soler, Júlia M ; Krieger, José E . Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study. BMC Medical Genetics , v. 9, p. 32, 2008.
Ramasawmy, R. ; Spina, G. S. ; Fae, K. C. ; PEREIRA, A. C. ; Nisihara, R. ; Messias Reason, I. J. ; Grinberg, M. ; Tarasoutchi, F. ; Kalil, J. ; Guilherme, L. . Association of Mannose-Binding Lectin Gene Polymorphism but Not of Mannose-Binding Serine Protease 2 with Chronic Severe Aortic Regurgitation of Rheumatic Etiology. Clinical and Vaccine Immunology , v. 15, p. 932-936, 2008.
Rodrigues, Sérgio Lamêgo ; D?Angelo, Lílian ; Pereira, Alexandre Costa ; KRIEGER, José Eduardo ; MILL, José Geraldo . Revisão dos critérios de Sokolow-Lyon-Rappaport e cornell para hipertrofia do ventrículo esquerdo. Arquivos Brasileiros de Cardiologia , v. 90, p. 46-53, 2008.
LOPES, N ; PAULITSCH, F ; GOIS, A ; PEREIRA, A ; STOLF, N ; DALLAN, L ; RAMIRES, J ; HUEB, W . Impact of number of vessels disease on outcome of patients with stable coronary artery disease: 5-year follow-up of the Medical, Angioplasty, and bypass Surgery Study (MASS). European Journal of Cardio-Thoracic Surgery , v. 33, p. 349-354, 2008.
Pereira, T. V. ; Nunes, A. C.F. ; Rudnicki, M. ; Yamada, Y. ; PEREIRA, A. C. ; Krieger, J. E. . Meta-Analysis of the Association of 4 Angiotensinogen Polymorphisms With Essential Hypertension: A Role Beyond M235T?. Hypertension (Dallas) , v. 51, p. 778-783, 2008.
MARQUEZINE, G ; OLIVEIRA, C ; PEREIRA, A ; KRIEGER, J ; MILL, J . Metabolic syndrome determinants in an urban population from Brazil: Social class and gender-specific interaction?. International Journal of Cardiology , v. 129, p. 259-265, 2008.
GIOLIPEREIRA, L ; PEREIRA, A ; BERGARA, D ; MESQUITA, S ; LOPES, A ; KRIEGER, J . Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases?. International Journal of Cardiology , v. 126, p. 374-378, 2008.
Makdisse, Marcia ; Pereira, Alexandre da Costa ; Brasil, David de Pádua ; Borges, Jairo Lins ; Machado-Coelho, George Luiz Lins ; KRIEGER, José Eduardo ; Nascimento Neto, Raimundo Marques ; Chagas, Antonio Carlos Palandri . Prevalência e fatores de risco associados à doença arterial periférica no projeto corações do Brasil. Arquivos Brasileiros de Cardiologia , v. 91, p. 370-382, 2008.
Girão Faria, Mário Henrique ; Barem Rabenhorst, Silvia Helena ; Pereira, Alexandre da Costa ; KRIEGER, José Eduardo . A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly. International Journal of Cardiology , v. 130, p. 30-35, 2008.
Lopes, Neuza H. ; da Silva Paulitsch, Felipe ; Pereira, A.C. ; GOIS, Aecio ; GAGLIARDI, Antonio ; Garzillo, Cibele Larossa ; Ferreira, João Fernando ; Stolf, Noedir ; Hueb, Whady A . Impact of metabolic syndrome on the outcome of patients with stable coronary artery disease: 2-year follow-up of the MASS II study. Coronary Artery Disease , v. 19, p. 383-388, 2008.
Ângelo, Lílian Cláudia Souza ; Vieira, Marcelo Luiz Campos ; Rodrigues, Sérgio Lamêgo ; Morelato, Renato Lírio ; Pereira, Alexandre C. ; MILL, José Geraldo ; KRIEGER, José Eduardo . Valores de referência de medidas ecocardiográficas em amostra da população brasileira adulta assintomática. Arquivos Brasileiros de Cardiologia , v. 89, p. 184-190, 2007.
Pereira, Tiago V ; Rudnicki, Martina ; Cheung, Bernard MY ; Baum, Larry ; Yamada, Yoshiji ; Oliveira, Paulo SL ; Pereira, Alexandre C ; Krieger, Jos?? E . Three endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication bias. Journal of Hypertension , v. 25, p. 1763-1774, 2007.
BERNARDESSILVA, C ; PEREIRA, A ; DEFATIMAALVESDAMOTA, G ; KRIEGER, J ; LAUDANNA, A . Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients. Clinica Chimica Acta , v. 386, p. 7-11, 2007.
PEREIRA, A ; MIYAKAWA, A ; LOPES, N ; SOARES, P ; DEOLIVEIRA, S ; CESAR, L ; RAMIRES, J ; HUEB, W ; KRIEGER, J . Dynamic regulation of MTHFR mRNA expression and C677T genotype modulate mortality in coronary artery disease patients after revascularization. Thrombosis Research , v. 121, p. 25-32, 2007.
PEREIRA, T ; RUDNICKI, M ; FRANCO, R ; PEREIRA, A ; KRIEGER, J . Effect of the G-308A polymorphism of the tumor necrosis factor ? gene on the risk of ischemic heart disease and ischemic stroke: A meta-analysis. The American Heart Journal , v. 153, p. 821-830, 2007.
CANDIDO, A ; FERREIRA, S ; LIMA, A ; NICOLATO, R ; FREITAS, S ; BRANDAO, P ; PEREIRA, A ; KRIEGER, J ; NASCIMENTONETO, R ; MACHADOCOELHO, G . Lipoprotein(a) as a risk factor associated with ischemic heart disease: Ouro Preto Study. Atherosclerosis (Amsterdam) , v. 191, p. 454-459, 2007.
Silva, Gustavo JJ ; Pereira, Alexandre C ; Krieger, Eduardo M ; Krieger, José E . Genetic mapping of a new heart rate QTL on chromosome 8 of spontaneously hypertensive rats. BMC Medical Genetics , v. 8, p. 17, 2007.
Pereira, Tiago Veiga ; Rudnicki, Martina ; Pereira, Alexandre Costa ; Pombo-de-Oliveira, Maria S. ; Franco, Rendrik França . Do polymorphisms of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene affect the risk of childhood acute lymphoblastic leukemia?. European Journal of Epidemiology , v. 21, p. 885-886, 2007.
HUEB, W ; GERSH, B ; COSTA, F ; LOPES, N ; SOARES, P ; DUTRA, P ; JATENE, F ; PEREIRA, A ; GOIS, A ; OLIVEIRA, S . Impact of Diabetes on Five-Year Outcomes of Patients With Multivessel Coronary Artery Disease. The Annals of Thoracic Surgery , v. 83, p. 93-99, 2007.
DIAS, R ; ALBUQUERQUE, J ; PEREIRA, A ; STOLF, N ; KRIEGER, J ; MADY, C ; OLIVEIRA, S . HoltOram syndrome presenting as agenesis of the left pericardium. International Journal of Cardiology (Print) , v. 114, p. 98-100, 2007.
Bertola, DÃbora Romeo ; Pereira, Alexandre Costa ; Brasil, Amanda Salem ; Albano, Lilian Maria JosÃ ; Kim, Chong Ae ; Krieger, JosÃ Eduardo . Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene. Journal of Human Genetics (Print) , v. 52, p. 521-526, 2007.
Pereira, T. V. ; Rudnicki, M. ; PEREIRA, A. C. ; Pombo-de-Oliveira, M. S. ; Franco, R. F. . 5,10-Methylenetetrahydrofolate Reductase Polymorphisms and Acute Lymphoblastic Leukemia Risk: A Meta-analysis. Cancer Epidemiology, Biomarkers & Prevention , v. 15, p. 1956-1963, 2006.
Bertola, Débora R. ; Pereira, Alexandre C. ; Albano, Lílian Maria José ; Oliveira, Paulo S.L. De ; Kim, Chong A. ; KRIEGER, José Eduardo . Gene Analysis in 74 Brazilian Patients with Noonan Syndrome or Noonan-like Phenotype. Genetic Testing , v. 10, p. 186-191, 2006.
Pereira, Alexandre C. ; Lopes, Neuza H.M. ; Soares, Paulo R. ; Krieger, Jose Eduardo ; de Oliveira, Sergio A. ; Cesar, Luiz A.M. ; Ramires, Jose A.F. ; HUEB, Whady . Clinical Judgment and Treatment Options in Stable Multivessel Coronary Artery DiseaseResults From the One-Year Follow-Up of the MASS II (Medicine, Angioplasty, or Surgery Study II). Journal of the American College of Cardiology (Print) , v. 48, p. 948-953, 2006.
Pereira, T. V. ; Nunes, A. C. F. ; Rudnicki, M. ; Magistroni, R. ; Albertazzi, A. ; PEREIRA, A. C. ; Krieger, J. E. . Influence of ACE I/D gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney disease: a meta-analysis. Nephrology Dialysis Transplantation , v. 21, p. 3155-3163, 2006.
Silva, G. J. J. ; Moreira, E. D. ; PEREIRA, A. C. ; Mill, J. G. ; Krieger, E. M. ; Krieger, J. E. . ACE gene dosage modulates pressure-induced cardiac hypertrophy in mice and men. Physiological Genomics (Print) , v. 27, p. 237-244, 2006.
Errera, F.I.V. ; Silva, M.E.R. ; Yeh, E. ; Maranduba, C.M.C. ; Folco, B. ; Takahashi, W. ; Pereira, A.C. ; Krieger, J.E. ; Passos-Bueno, M.R. . Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients. Brazilian Journal of Medical and Biological Research (Impresso) , v. 39, p. 883-888, 2006.
Soler, Júlia ; Pereira, Alexandre C ; Tôrres, César H ; Krieger, José E . Gene by environment QTL mapping through multiple trait analyses in blood pressure salt-sensitivity: identification of a novel QTL in rat chromosome 5. BMC Medical Genetics , v. 7, p. 47, 2006.
GIOLIPEREIRA, L ; PEREIRA, A ; MESQUITA, S ; LOPES, A ; KRIEGER, J . PCR screening for 22q11.2 microdeletion: Development of a new cost-effective diagnostic tool. Clinica Chimica Acta (Print) , v. 369, p. 78-81, 2006.
Drager, L F ; Pereira, A C ; Barreto-Filho, J A ; Figueiredo, A C ; KRIEGER, J e ; Krieger, E M ; Lorenzi-Filho, G . Phenotypic characteristics associated with hypertension in patients with obstructive sleep apnea. Journal of Human Hypertension , v. 20, p. 523-528, 2006.
ARAUJO, F ; ANTELMI, I ; PEREIRA, A ; LATORRE, M ; GRUPI, C ; KRIEGER, J ; MANSUR, A . Lower heart rate variability is associated with higher serum high-sensitivity C-reactive protein concentration in healthy individuals aged 46 years or more?. International Journal of Cardiology (Print) , v. 107, p. 333-337, 2006.
LANZ, J ; PEREIRA, A ; MARTINEZ, E ; KRIEGER, J . Metabolic syndrome and coronary artery disease: Is there a gender specific effect?. International Journal of Cardiology (Print) , v. 107, p. 317-321, 2006.
Danoviz, Maria E ; Pereira, Alexandre C ; Mill, Jose G ; Krieger, Jose E . HYPERTENSION, OBESITY AND GNB3 GENE VARIANTS. Clinical and Experimental Pharmacology & Physiology , v. 33, p. 248-252, 2006.
SCHETTERT, I ; PEREIRA, A ; LOPES, N ; HUEB, W ; KRIEGER, J . Association between platelet P2Y12 haplotype and risk of cardiovascular events in chronic coronary disease. Thrombosis Research , v. 118, p. 679-683, 2006.
PEREIRA, A ; SPOSITO, A ; MOTA, G ; CUNHA, R ; HERKENHOFF, F ; MILL, J ; KRIEGER, J . Endothelial nitric oxide synthase gene variant modulates the relationship between serum cholesterol levels and blood pressure in the general population: New evidence for a direct effect of lipids in arterial blood pressure. Atherosclerosis (Amsterdam) , v. 184, p. 193-200, 2006.
MONTEIRO, E. J. ; Pereira, A C ; PEREIRA, Aparecido B ; Krieger, J. E. ; MASTROIANNI-KIRSZTAJN, G. . NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis. JN. Journal of Nephrology (Milano) , v. 19, p. 366-371, 2006.
LELIS, R. G. ; Krieger, J. E. ; Pereira, A.C. ; CARMONA, M. J. ; de Oliveira, Sergio A. . Apolipoprotein E4 genotype increases the risk of postoperative cognitive dysfunction in patients undergoing coronary artery bypass graft surgery. Journal of Cardiovascular Surgery (Testo stampato) , v. 47, p. 451-456, 2006.
Nascimento Neto, Raimundo Marques do ; KRIEGER, José Eduardo ; Machado-Coelho, George L ; Pereira, Alexandre da Costa . Projeto Corações do Brasil. Arquivos Brasileiros de Cardiologia , v. 85, p. 218-221, 2005.
Tirone, Adriana Paula ; Arteaga, Edmundo ; Pereira, Alexandre da Costa ; KRIEGER, José Eduardo ; Buck, Paula de Cássia ; Ianni, Barbara Maria ; Mady, Charles . Pesquisa de marcadores para os genes da cadeia pesada da beta-miosina cardíaca e da proteína C de ligação à miosina em familiares de pacientes com cardiomiopatia hipertrófica. Arquivos Brasileiros de Cardiologia , v. 84, p. 467-472, 2005.
Titan, S M O ; Pereira, A C ; Cunha, R S ; Herkenhoff, F L ; Mill, J G ; KRIEGER, J e . Reninangiotensin system polymorphisms interact with blood pressure in the determination of microalbuminuria in the general population. Journal of Human Hypertension , v. 20, p. 235-237, 2005.
PEREIRA, A ; XAVIERNETO, J ; MESQUITA, S ; MOTA, G ; LOPES, A ; KRIEGER, J . Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design. International Journal of Cardiology (Print) , v. 105, p. 15-18, 2005.
Barreto, Alessandra Costa ; Franchi, Sônia Meiken ; Pereira, Alexandre C. ; Lopes, Antonio Augusto . Hipertensão arterial pulmonar: fisiopatologia, aspectos genéticos e resposta ao uso crônico do sildenafil. Arquivos Brasileiros de Cardiologia (Impresso) , v. 85, p. 147, 2005.
LANZ, J ; PEREIRA, A ; LEMOS, P ; MARTINEZ, E ; KRIEGER, J . Angiotensinogen M235T polymorphism is associated with coronary artery disease severity. Clinica Chimica Acta (Print) , v. 362, p. 176-181, 2005.
PEREIRA, A ; MORANDINIFILHO, A ; HEIMANN, A ; RABAK, E ; VIEIRA, A ; MOTA, G ; KRIEGER, J . Serum angiotensin converting enzyme activity association with the I/D polymorphism in an ethnically admixtured population. Clinica Chimica Acta (Print) , v. 360, p. 201-204, 2005.
Bertola, Debora R. ; Pereira, Alexandre C. ; Passetti, Fábio ; de Oliveira, Paulo S.L. ; Messiaen, Ludwine ; Gelb, Bruce D. ; Kim, Chong A. ; KRIEGER, José Eduardo . Neurofibromatosis-Noonan syndrome: Molecular evidence of the concurrence of both disorders in a patient. American Journal of Medical Genetics. Part A , v. 136A, p. 242-245, 2005.
CUOCO, M ; PEREIRA, A ; DEFREITAS, H ; DEFATIMAALVESDAMOTA, G ; FUKUSHIMA, J ; KRIEGER, J ; MANSUR, A . Angiotensin-converting enzyme gene deletion polymorphism modulation of onset of symptoms and survival rate of patients with heart failure. International Journal of Cardiology (Print) , v. 99, p. 97-103, 2005.
ARAUJO, F ; PEREIRA, A ; LATORRE, M ; KRIEGER, J ; MANSUR, A . High-sensitivity C-reactive protein concentration in a healthy Brazilian population. International Journal of Cardiology (Print) , v. 97, p. 433-438, 2004.
ARAUJO, F ; PEREIRA, A ; MOTA, G ; LATORRE, M ; KRIEGER, J ; MANSUR, A . The influence of tumor necrosis factor ?308 and C-reactive protein G1059C gene variants on serum concentration of C-reactive protein: evidence for an age-dependent association. Clinica Chimica Acta (Print) , v. 349, p. 129-134, 2004.
Xavier-Neto, J. ; Pereira, A.C. ; Oliveira, E.M. ; Miyakawa, A.A. ; Junqueira, M.L. ; Krieger, J.E. . Control of the rat angiotensin I converting enzyme gene by CRE-like sequences. Brazilian Journal of Medical and Biological Research (Impresso) , v. 37, p. 1441, 2004.
Bertola, D?bora Romeo ; Pereira, Alexandre C. ; Oliveira, Paulo S.L. De ; Kim, Chong A. ; Krieger, Jos? Eduardo . Clinical variability in a Noonan syndrome family with a newPTPN11 gene mutation. American Journal of Medical Genetics (Print) (Cessou em 2002. Desmembrado em 3: ISSN 1552-4825 American Journal of Medical Genetics. Pt A; ISSN 1552-4 , v. 130A, p. 378-383, 2004.
LOPES, N ; PEREIRA, A ; HUEB, W ; SOARES, P ; LANZ, J ; GERSH, B ; DEOLIVEIRA, S ; CESAR, L ; RAMIRES, J ; KRIEGER, J . Effect of glycoprotein IIIa PlA2 polymorphism on outcome of patients with stable coronary artery disease and effect of smoking1. The American Journal of Cardiology , v. 93, p. 1469-1472, 2004.
Pereira, Alexandre C. ; Pereira, Aparecido B. ; Mota, Gloria F. ; Cunha, Roberto S. ; Herkenhoff, Fernando L. ; Pollak, Martin R. ; Mill, Jose G. ; Krieger, Jose E. . NPHS2 R229Q functional variant is associated with microalbuminuria in the general population. Kidney International , v. 65, p. 1026-1030, 2004.
PEREIRA, A . Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population. Clinica Chimica Acta (Print) , v. 340, p. 99-105, 2004.
Pereira, A.C. ; Corrêa, R.F.R. ; Mota, G.F. ; Kim, C.A. ; Mesquita, S.F. ; Krieger, J.E. . High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups. Brazilian Journal of Medical and Biological Research (Impresso) , v. 36, p. 1359-1365, 2003.
PEREIRA, A. C. . 2 Adrenoceptor Functional Gene Variants, Obesity, and Blood Pressure Level Interactions in the General Population. Hypertension (Dallas, Tex. 1979) , v. 42, p. 685-692, 2003.
Meira-Lima, I V ; Pereira, A C ; Mota, G F ; Floriano, M ; Araújo, F ; Mansur, A J ; KRIEGER, J e ; Vallada, H . Analysis of a polymorphism in the promoter region of the tumor necrosis factor alpha gene in schizophrenia and bipolar disorder: further support for an association with schizophrenia. Molecular Psychiatry , v. 8, p. 718-720, 2003.
PEREIRA, A. C. . Angiotensinogen 235T Allele "Dosage" Is Associated With Blood Pressure Phenotypes. Hypertension (Dallas, Tex. 1979) , v. 41, p. 25-30, 2002.
Nunes, A. B. ; PEREIRA, A. C. . A Novel Val648Ile Substitution in RET Protooncogene Observed in a Cys634Arg Multiple Endocrine Neoplasia Type 2A Kindred Presenting with an Adrenocorticotropin-Producing Pheochromocytoma. The Journal of Clinical Endocrinology and Metabolism , v. 87, p. 5658-5661, 2002.
SYLOS, C. ; PEREIRA, A. C. ; AZEKA, E. ; MIURA, N. ; Mesquita, Sonia M ; EBAID, M. . Arterial Hypertension in a Child with Williams-Beuren Syndrome (7q11.23 Chromosomal Deletion). Arquivos Brasileiros de Cardiologia (Impresso) , v. 79, p. 177-180, 2002.
Pereira, A.C. ; Mota, G.A. ; Benseor, I. ; Lotufo, P.A. ; Krieger, J.E. . Effect of race, genetic population structure, and genetic models in two-locus association studies: clustering of functional renin-angiotensin system gene variants in hypertension association studies. Brazilian Journal of Medical and Biological Research (Impresso) , v. 34, p. 1421-1428, 2001.
PEREIRA, A . Hemochromatosis gene variants in patients with cardiomyopathy. The American Journal of Cardiology , v. 88, p. 388-391, 2001.
Meira-Lima, I V ; Zhao, J ; Sham, P ; Pereira, A C ; KRIEGER, J e ; Vallada, H . Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3. Molecular Psychiatry , v. 6, p. 565-569, 2001.
PEREIRA, A. C. ; Mota, G F ; Krieger, J. E. . Hemochromatosis gene variants in three different ethnic populations: effects of admixture for screening programs. Human Biology (Print) , v. 73, p. 145-151, 2001.
Bertola, D?bora R. ; Kim, Chong A. ; Pereira, Alexandre C. ; Mota, Gl?ria F.A. ; Krieger, Jos? E. ; Vieira, In?s C. ; Valente, Marcelo ; Loreto, Marcos Roberto ; Magalh?es, Roberto P. ; Gonzalez, Claudette H. . Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?. American Journal of Medical Genetics (Print) (Cessou em 2002. Desmembrado em 3: ISSN 1552-4825 American Journal of Medical Genetics. Pt A; ISSN 1552-4 , v. 98, p. 230-234, 2001.
Ribeiro, R. C. J. ; Feng W ; WAGNER, R. ; COSTA, C. ; PEREIRA, A. C. ; APRILETTI, J. ; FLETTERICK, R. ; Baxter, JD . Definition of the Surface in the Thyroid Hormone Receptor Ligand Binding Domain for Association as Homodimers and Heterodimers with Retinoid X Receptor. The Journal of Biological Chemistry (Print) , v. 276, p. 14987-14995, 2001.
Meira-Lima, I ; Pereira, A.C. ; Mota, G F ; Krieger, J. E. ; Vallada, H . Angiotensinogen and angiotensin converting enzyme gene polymorphisms and the risk of bipolar affective disorder in humans. Neuroscience Letters (Print) , v. 293, p. 103-106, 2000.
SOUZA, H ; SOUZA, L ; ANASTACIO, V ; PEREIRA, A ; JUNQUEIRA, M ; KRIEGER, J ; DALUZ, P ; AUGUSTO, O ; LAURINDO, F . Vascular oxidant stress early after balloon injury: evidence for increased NAD(P)H oxidoreductase activity. Free Radical Biology & Medicine , v. 28, p. 1232-1242, 2000.
HUANG, T. ; Yang, W ; Pereira, A.C. ; CRAIGEN, W. J. ; SHIH, V. E. . Cloning and Characterization of a Putative Human ?-2-Hydroxyacid Dehydrogenase in Chromosome 9q. Biochemical and Biophysical Research Communications (Print) , v. 268, p. 298-301, 2000.
XAVIER-NETO, José ; PEREIRA, A. C. ; JUNQUEIRA, Maria de Lourdes ; CARMONA, R. ; KRIEGER, José Eduardo . Rat angiotensin converting enzyme promoter regulation by b adrenergics and cAMP in endothelium. Hypertension (Dallas) , v. 34, p. 31-38, 1999.
BASSON, C. T. ; HUANG, T. ; LIN, R. C. ; BACHINSKI, D. R. ; WEREMOWICZ, S. ; VAGLIO, A. ; BRUZZONES, R. ; PEREIRA, A. C. ; KRIEGER, José Eduardo ; SEIDMAN, C. . Different TBX5 interactions in heart and limb defined by Holt-Oran syndrome mutations. Proceedings of the National Academy of Sciences of the United States of America , v. 96, p. 2919-2924, 1999.
Oliveira, AEA ; MACHADO, O. L. T. ; XAVIER-NETO, José ; PEREIRA, A. C. ; VIEIRA, J. G. H. ; FERNANDES, K. V. S. ; XAVIER-FILHO, J. . Jack Bean Seed Coat Contains a Protein with Complete Sequence Homology to Bovine Insulin. Protein and Peptide Letters , v. 6, p. 15-22, 1999.
XAVIER-NETO, José ; PEREIRA, A. C. ; MOTOYAMA, A. H. ; KRIEGER, José Eduardo . A luciferase-engineered cell line for study of cAMP regulation in endothelial cells. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology , v. 275, p. 75-81, 1998.
AKASHI, D. ; ISSA, F. K. ; PEREIRA, A. C. ; FUCCIOLO, D. Q. ; LOBATO, M. L. ; GALVAO, T. G. ; Benseor, I. ; Lotufo, P.A. . Antihypertensive treatment. Prescription and cost of drugs. Survey in a tertiary care hospital. Arquivos Brasileiros de Cardiologia (Impresso) , v. 71, p. 55-57, 1998.
Benseor, I. ; Pereira, A C ; VALERI, C. M. ; AKASHI, D. ; FUCCIOLO, D. Q. ; ISSA, F. K. ; LOBATO, M. L. ; Titan, S M O ; GALVAO, T. G. ; Lotufo, P.A. . Systemic arterial hypertension and psychiatric morbidity in the outpatient care setting of a tertiary hospital. Arquivos de Neuro-Psiquiatria (Impresso) , v. 56, p. 406-411, 1998.
Benseor, I. ; Lotufo, P.A. ; Pereira, A C ; TANNURI, A. C. ; ISSA, F. K. ; AKASHI, D. ; FUCCIOLO, D. Q. ; KAKUDA, E. S. ; KANASHIRO, H. ; LOBATO, M. L. ; Titan, S M O ; GALVAO, T. G. ; MARTINS, M. A. . Validation of a questionnaire for the diagnosis of headache in an outpatient clinic at a university hospital. Arquivos de Neuro-Psiquiatria (Impresso) , v. 55, p. 364-369, 1997.
SANTOS, P. C. ; FERREIRA, Noely ; DINARDO, C. L. ; SCHETTERT, Isolmar Tadeu ; KRIEGER, Jose Eduardo ; Pereira, Alexandre Costa . Análises Moleculares em Hematologia. In: Alexsandro Macedo Silva; Luciane Maria Ribeiro Neto. (Org.). Hematologia - Métodos e Interpretação. 1ed.São Paulo: Roca, 2013, v. 1, p. 423-438.
PEREIRA, AC ; Santos, Diogo GB ; Marsiglia JDC ; Krieger, J E . Aspectos Genéticos das Doenças Cardiovasculares: cardiopatias isoladas. Genética na Prática Pediátrica. 1ªed.Barueri: Manole, 2010, v. , p. 188-206.
PEREIRA, A. C. ; KRIEGER, José Eduardo . Sal, hipertensão e genética. Hipertensão - Revista da Sociedade Brasileira de Hipertensão, , v. 7, p. 61 - 64, 27 out. 2004.
GOWDAK, Luís Henrique Wolff ; PEREIRA, A. C. ; KRIEGER, José Eduardo . Genética, hipertensão arterial e doença coronária. Hipertensão - Revista da Sociedade Brasileira de Hipertensão, , v. 7, p. 35 - 37.
PEREIRA, A. C. ; LOPES, Neusa H ; SOARES, Paulo R ; KRIEGER, José Eduardo ; OLIVEIRA, Sérgio de ; RAMIREZ, José F ; HUEB, Whady . Clinical judgment and treatment options in stable multivessel coronary artery disease: results from the 1-year follow-up of the MASS II Study. In: American College of Cardiology Annual Scientific Session 2005, 2005, Orlando. Journal of the American College of Cardiology, 2005. v. 45. p. 203A-203A.
LOPES, Neusa H ; GOIS, Aecio ; PEREIRA, A. C. ; GAGLIARDI, Antonio ; BORGES, Jorge ; SOARES, Paulo R ; CESAR, Luiz Antônio M ; HUEB, Whady . Association of the metabolic syndrome with worse outcome of patients with stable coronary disease in the Medicine, Angioplasty or Surgery Study (MASS II). In: American College of Cardiology Annual Scientific Session 2005, 2005, Orlando. Journal of the American College of Cardiology, 2005. v. 45. p. 203A-203A.
CUNHA, Roberto Sá ; PEREIRA, A. C. ; MOTA, Glória Fa ; HERKENHOFF, Fernando F ; MILL, José Geraldo ; KRIEGER, José Eduardo . GLU298ASP ENOS polymorphism genotype and aortic stiffness: results from a population study in Brazil. In: International Congress of Hypertension, 2004, São Paulo. Journal of Hypertension, 2004. v. 22.
BERTOLA, Débora R ; PEREIRA, A. C. ; CARNEIRO, Jda ; KRIEGER, J e ; KIM, Chong A . Further evidence that the T73I PTPN11 gene mutation is associated with a myeloproliferative disorder in Noonan syndrome. In: American College of Medical Genetics Annual Clinical Genetics Meeting, 2004, 2004. p. A41.
BERTOLA, Débora R ; PEREIRA, A. C. ; OLIVEIRA, Paulo S ; MESSIEN, L ; GELB, Bruce D ; KIM, Chong A ; KRIEGER, José Eduardo . Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient. In: The American Society of Human Genetics 54th Annual Meeting, 2004, Toronto, 2004.
KIM, Chong A ; PEREIRA, A. C. ; KRIEGER, José Eduardo ; ALBANO, L M J ; BERTOLA, Débora R . Noonan-like phenotype and PTPN11 gene: study of 15 patients. In: The American Society of Human Genetics 54th Annual Meeting, 2004, Toronto, 2004.
ALMEIDA, ROGÉRIO TOSTA DE ; Pereira, Alexandre da Costa ; FONSECA, MARIA DE JESUS MENDES DA ; MATOS, SHEILA MARIA ALVIM DE ; AQUINO, ESTELA MOTTA LEÃO . Association between body adiposity index and coronary risk in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil). CLINICAL NUTRITION , 2019.
Pereira, A.C. . Implicações genéticas nas doenças do coração. 2015. (Apresentação de Trabalho/Conferência ou palestra).
Pereira, A C . 'Implicações genéticas nas doenças do coração.'. 2014. (Apresentação de Trabalho/Seminário).
Pereira, Alexandre da Costa . Efeitos do treinamento físico no fluxo sanguíneo muscular em indivíduos com polimorfismo do gene da eNOS. 2009. (Apresentação de Trabalho/Congresso).
Pereira, Alexandre da Costa . Influência da circulação extra-corporea na revascularização miocárdica em pacientes do sexo feminino - MASS III. 2008. (Apresentação de Trabalho/Congresso).

Outras produções

Pereira AC . 'Marcadores genéticos e risco cardiovascular: estudos de associação com escores e randomização mendeliana'. 2015. (Curso de curta duração ministrado/Outra).

PEREIRA, AC . 'Importância da Pesquisa de Fatores Genéticos e de Marcadores Biomoleculares na Investigação Clínica'. 2015. (Curso de curta duração ministrado/Outra).

PEREIRA, AC . Metodologia Científica. 2015. (Curso de curta duração ministrado/Outra).

PEREIRA, AC . 'Implicações genéticas nas doenças do coração'. 2014. .

Pereira, Alexandre da Costa . MCP 5820 - Comportamento dos Enxertos Venosos e Arteriais e Correlações Genéticas Moleculares no Tratamento Cirúrgico do Miocárdio Isquêmico. 2009. (Curso de curta duração ministrado/Especialização).

Pereira, Alexandre da Costa . Papel dos marcadores genéticos na avaliação preventiva das dislipidemias, da fibrilação atrial e da insuficiência coronária. 2009. (Curso de curta duração ministrado/Extensão).

Projetos de pesquisa

2013 - Atual

Herdabilidade de Traços Dermatológicos e Correlação com Rigidez Arterial na População Brasileira, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2013 - Atual

Estudo de associação entre Vegetarianismo, Hábitos de Vida e Características da Pele, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2012 - Atual

Associação de Ancestralidade com Fatores de Risco de Doença Cardiovascular em uma Amostra Populacional Brasileira: ELSA Brasil, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2012 - Atual

Herdabilidade de Fenótipos Metabólicos em uma População Brasileira, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2011 - Atual

Sequenciamento do Exoma em Amostras de Pacientes com Sobrecarga Primária de Ferro, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2011 - Atual

Doença Renal Crônica: Determinantes de Progressão e de Risco Cardiovascular. Estudo de Coorte em População Brasileira, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2011 - Atual

Desenvolvimento de Plataforma em Zebrafish para a Caracterização Funcional de Mutações em Cardiopatias Congênitas e Miocardiopatias Hereditárias, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2011 - Atual

Avaliação de Marcadores Moleculares como Preditores para Eventos após Síndrome Coronariana Aguda, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2010 - Atual

Avaliação da Relação entre Haplogrupo Mitocondrial e Desenvolvimento de Insuficiência Cardíaca em Amostra Brasileira, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.
2010 - Atual

Hipercol Brasil Programa de Rastreamento Genético em Cascata na Região Oeste da Cidade de São Paulo, Descrição: Programa de busca ativa de paciente com hipercolesterolemia familiar e realização de teste genético.. , Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador / Cinthia Elim Jannes - Integrante / Raul Dias dos Santos Filho - Integrante.
2008 - Atual

Reprogramação Dirigida de Células Mesenquimais de Tecido Adiposo em CélulasTronco Pluripotentes e Cardiomiócitos, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Alexandre da Costa Pereira - Coordenador.

Prêmios

2020

Prêmio: Melhor Caso Clínico, 37 Congresso Brasileiro de Arritmias Cardíacas ? SOBRAC 2020 ? Virtual; 2020.

2013

Programa de Rastreamento Genético Ativo de Hipercolesterolemia Familiar na Região Metropolitana de São Paulo (Projeto Região Oeste), 9ª Edição do Prêmio Mario Covas.

Histórico profissional

Endereço profissional

Instituto do Coração - Hospital das Clinicas - FMUSP, Laboratório de Genética e Cardiologia Molecular. , Av Dr Eneas de Carvalho Aguiar, 44 - 10º. Andar - Bloco 2, Cerqueira Cesar, 05403000 - São Paulo, SP - Brasil, Telefone: (11) 26615573, Fax: (11) 26615022, URL da Homepage:

Experiência profissional

2004 - Atual

Instituto do Coração - Hospital das Clínicas - FMUSP

Vínculo: Médico Assistente, Enquadramento Funcional: Outro, Carga horária: 40, Regime: Dedicação exclusiva.

Atividades

02/1993
Pesquisa e desenvolvimento, Laboratório de Genética e Cardiologia Molecular.,Linhas de pesquisa