Adam Campbell Smith

Pós-doutorado

Formação complementar

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Participação em eventos

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Orientou

Produções bibliográficas

• DAHER-REYES, GEORGINA KIM, TAEHYUNG NOVITZKY-BASSO, IGOR KIM, KYUOUNG HA Smith, Adam STOCKLEY, TRACY CAPOCHICHI, JOSE-MARIO AL-SHAIBANI, ZEYAD PASIC, IVAN LAW, ARJUN LAM, WILSON MICHELIS, FOTIOS V. GERBITZ, ARMIN VISWABANDYA, AURO LIPTON, JEFFREY KUMAR, RAJAT MATTSSON, JONAS SCHIMMER, AARON MCNAMARA, CAROLINE MURPHY, TRACY MAZE, DAWN GUPTA, VIKAS SIBAI, HASSAN CHAN, STEVEN YEE, KAREN , et al. MINDEN, MARK ZHANG, ZHAOLEI SCHUH, ANDRE KIM, DENNIS D. H. ; Prognostic impact of the adverse molecular-genetic profile on long-term outcomes following allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia. BONE MARROW TRANSPLANTATION , v. 56, p. 1908-1918, 2021.

• MAKAREM, MAISAM ; EZEIFE, DOREEN A. ; Smith, Adam C. ; LI, JANICE J. N. ; LAW, JENNIFER H. ; TSAO, MING-SOUND ; LEIGHL, NATASHA B. . Reflex ROS1 IHC Screening with FISH Confirmation for Advanced Non-Small Cell Lung Cancer-A Cost-Efficient Strategy in a Public Healthcare System. Current Oncology , v. 28, p. 3268-3279, 2021.

• CHEUNG, CAROL C. Smith, Adam C. ALBADINE, ROULA BIGRAS, GILBERT BOJARSKI, ANNA COUTURE, CHRISTIAN CUTZ, JEAN-CLAUDE HUANG, WEEI-YUAN IONESCU, DIANA ITANI, DOHA IZEVBAYE, IYARE KARSAN, ALY KELLY, MARGARET M. KNOLL, JOAN KWAN, KEITH NASR, MICHEL R. QING, GEFEI RASHID-KOLVEAR, FARIBOZ SEKHON, HARMANJATINDER S. SPATZ, ALAN STOCKLEY, TRACY TRAN-THANH, DANH TUCKER, TRACY WAGHRAY, RANJIT WANG, HANGJUN , et al. XU, ZHAOLIN YATABE, YASUSHI TORLAKOVIC, EMINA E. TSAO, MING-SOUND ; Canadian ROS proto-oncogene 1 study (CROS) for multi-institutional implementation of ROS1 testing in non-small cell lung cancer. LUNG CANCER , v. 160, p. 127-135, 2021.

• KIM, JAESEUNG C. ; ZUZARTE, PHILIP C. ; MURPHY, TRACY ; CHAN-SENG-YUE, MICHELLE ; BROWN, ANDREW M. K. ; KRZYZANOWSKI, PAUL M. ; Smith, Adam C. ; NOTTA, FAIYAZ ; MINDEN, MARK D. ; MCPHERSON, JOHN D. . Cryptic genomic lesions in adverse-risk acute myeloid leukemia identified by integrated whole genome and transcriptome sequencing. LEUKEMIA , v. 34, p. 306-311, 2020.

• QUEVEDO, RENE ; SPREAFICO, ANNA ; BRUCE, JEFF ; DANESH, ARNAVAZ ; EL GHAMRASNI, SAMAH ; GIESLER, AMANDA ; HANNA, YOUSTINA ; HAVE, CHERRY ; LI, TIANTIAN ; YANG, S. Y. CINDY ; ZHANG, TONG ; ASA, SYLVIA L. ; HAIBE-KAINS, BENJAMIN ; KRZYZANOWSKA, MONIKA ; Smith, Adam C. ; SINGH, SIMRON ; SIU, LILLIAN L. ; PUGH, TREVOR J. . Centromeric cohesion failure invokes a conserved choreography of chromosomal mis-segregations in pancreatic neuroendocrine tumor. Genome Medicine , v. 12, p. 38, 2020.

• GARG, SWATI ; NAGARIA, TEDDY S. ; CLARKE, BLAISE ; FREEDMAN, ORIT ; KHAN, ZANOBIA ; SCHWOCK, JOERG ; BERNARDINI, MARCUS Q. ; OZA, AMIT M. ; HAN, KATHY ; Smith, Adam C. ; STOCKLEY, TRACY L. ; ROUZBAHMAN, MARJAN . Molecular characterization of gastric-type endocervical adenocarcinoma using next-generation sequencing. MODERN PATHOLOGY , v. 32, p. 1823-1833, 2019.

• FISET, PIERRE O. ; LABBÉ, CATHERINE ; YOUNG, KELVIN ; CRADDOCK, KENNETH J. ; Smith, Adam C. ; TANGUAY, JEFFREY ; PINTILIE, MELANIA ; WANG, RI ; TORLAKOVIC, EMINA ; CHEUNG, CAROL ; SANTOS, GILDA ; KO, HYANG'MI ; BOERNER, SCOTT L. ; HWANG, DAVID M. ; LEIGHL, NATASHA B. ; TSAO, MING'SOUND . Anaplastic lymphoma kinase 5A4 immunohistochemistry as a diagnostic assay in lung cancer: A Canadian reference testing center's results in population-based reflex testing. CANCER , v. 125, p. 4043-4051, 2019.

• WASSERMAN, JASON K. ; DICKSON, BRENDAN C. ; Smith, Adam ; SWANSON, DAVID ; PURGINA, BIBIANNA M. ; WEINREB, ILAN . Metastasizing Pleomorphic Adenoma. AMERICAN JOURNAL OF SURGICAL PATHOLOGY , v. 43, p. 1145-1151, 2019.

• BEBB, D. G. ; AGULNIK, J. ; ALBADINE, R. ; BANERJI, S. ; BIGRAS, G. ; BUTTS, C. ; COUTURE, C. ; CUTZ, J. C. ; DESMEULES, P. ; IONESCU, D. N. ; LEIGHL, N. B. ; MELOSKY, B. ; MORZYCKI, W. ; RASHID-KOLVEAR, F. ; SEKHON, H. S. ; SMITH, A. C. ; STOCKLEY, T. L. ; TORLAKOVIC, E. ; XU, Z. ; TSAO, M. S. . Crizotinib inhibition of ROS1-positive tumours in advanced non-small-cell lung cancer: a Canadian perspective. Current Oncology , v. 26, p. e551-e557, 2019.

• BARGHOUT, SAMIR H. ; PATEL, PARASVI S. ; WANG, XIAOMING ; XU, G. WEI ; KAVANAGH, SIMON ; HALGAS, ONDREJ ; ZARABI, SARA F. ; GRONDA, MARCELA ; HURREN, ROSE ; JEYARAJU, DANNY V. ; MACLEAN, NEIL ; BRENNAN, SHAWN ; HYER, MARC L. ; BERGER, ALLISON ; TRAORE, TARY ; MILHOLLEN, MICHAEL ; Smith, Adam C. ; MINDEN, MARK D. ; PAI, EMIL F. ; HAKEM, RAZQ ; SCHIMMER, AARON D. . Preclinical evaluation of the selective small-molecule UBA1 inhibitor, TAK-243, in acute myeloid leukemia. LEUKEMIA , v. June, p. 10.1038/s41375-, 2018.

• HUANG, STEVEN J. ; LEE, LAUREN J. ; GERRIE, ALINA S. ; GILLAN, TANYA L. ; BRUYERE, HELENE ; HRYNCHAK, MONICA ; Smith, Adam C. ; KARSAN, ALY ; RAMADAN, KHALED M. ; JAYASUNDARA, KAVISHA S. ; TOZE, CYNTHIA L. . Characterization of treatment and outcomes in a population-based cohort of patients with chronic lymphocytic leukemia referred for cytogenetic testing in British Columbia, Canada. Leukemia Research , v. 55, p. 79-90, 2017.

• ABEKHOUKH, SABIHA ; SAHIN, H BAHAR ; GROSSI, MAURO ; ZONGARO, SAMANTHA ; MAURIN, THOMAS ; MADRIGAL, IRENE ; KAZUE-SUGIOKA, DANIELE ; RAAS-ROTHSCHILD, ANNICK ; DOULAZMI, MOHAMED ; CARRERA, PILAR ; STACHON, ANDREA ; SCHERER, STEVEN ; NASCIMENTO, MARIA RITA DRULA DO ; TREMBLEAU, ALAIN ; ARROYO, IGNACIO ; PETER, SZATMARI ; SMITH, ISABEL M. ; MILÀ, MONTSERRAT ; Smith, Adam C. ; GIANGRANDE, ANGELA ; CAILLÉ, ISABELLE ; BARDONI, BARBARA . New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes. DISEASE MODELS & MECHANISMS , v. 10, p. dmm.025809-474, 2017.

• KAO, K R ; HASAN, T ; BAPTISTA, A ; TRUONG, T ; GAI, L ; SMITH, A C ; LI, S ; GONZALES, P ; VOISEY, K ; ERIWVO, P ; POWER, J ; DENIC, N . Effect of fixation time on breast biomarker expression: a controlled study using cell line-derived xenografted (CDX) tumours. JOURNAL OF CLINICAL PATHOLOGY , v. 1, p. jclinpath-2017-204381, 2017.

• HUANG, STEVEN J. ; BERGIN, KRYSTAL ; Smith, Adam C. ; GERRIE, ALINA S. ; BRUYERE, HELENE ; DALAL, CHINMAY B. ; SUGIOKA, DANIELE K. ; HRYNCHAK, MONICA ; RAMADAN, KHALED M. ; KARSAN, ALY ; GILLAN, TANYA L. ; TOZE, CYNTHIA L. . Clonal evolution as detected by interphase fluorescence in situ hybridization is associated with worse overall survival in a population-based analysis of patients with chronic lymphocytic leukemia in British Columbia, Canada. CANCER GENETICS , v. 210, p. 1-8, 2017.

• HUANG, STEVEN J. T. ; GILLAN, TANYA L. ; GERRIE, ALINA S. ; HRYNCHAK, MONICA ; KARSAN, ALY ; RAMADAN, KHALED ; Smith, Adam C. ; TOZE, CYNTHIA L. ; BRUYERE, HELENE . Influence of clone and deletion size on outcome in chronic lymphocytic leukemia patients with an isolated deletion 13q in a population-based analysis in British Columbia, Canada. Genes Chromosomes & Cancer (Print) , v. 55, p. 16-24, 2016.

• GERRIE, ALINA S. ; HUANG, STEVEN J.T. ; BRUYERE, HELENE ; DALAL, CHINMAY ; HRYNCHAK, MONICA ; KARSAN, ALY ; RAMADAN, KHALED M. ; Smith, Adam C. ; TYSON, CHRISTINE ; TOZE, CYNTHIA L. ; GILLAN, TANYA L. . Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization. Cancer Genetics , v. 1, p. 1, 2014.

• Lee, Anna F. ; Yip, Stephen ; Smith, Adam C. ; Hayes, Malcolm M. ; Nielsen, Torsten O. ; O'Connell, John X. . Low-grade fibromyxoid sarcoma of the perineum with heterotopic ossification: case report and review of the literature. Human Pathology (Print) , p. epub, 2011.

• Smith, Adam C. ; Suzuki, Masako ; Thompson, Reid ; Choufani, Sanaa ; Higgins, Michael J. ; Chiu, Idy W. ; Squire, Jeremy A. ; Greally, John M. ; Weksberg, Rosanna . Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression. Genomics (San Diego, Calif.) , v. Nov3, p. 1, 2011.

• Horike, Shin-Ichi ; Ferreira, Jose Carlos P. ; Meguro-Horike, Makiko ; Choufani, Sanaa ; Smith, Adam C. ; Shuman, Cheryl ; Meschino, Wendy ; Chitayat, David ; Zackai, Elaine ; Scherer, Stephen W. ; Weksberg, Rosanna . Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome. American Journal of Medical Genetics. Part A , v. 149A, p. 2415-2423, 2009.

• GUO, L ; CHOUFANI, S ; FERREIRA, J ; SMITH, A. C. ; CHITAYAT, D ; SHUMAN, C ; UXA, R ; KEATING, S ; KINGDOM, J ; WEKSBERG, R . Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae. Developmental Biology (Print) , v. 320, p. 79-91, 2008.

• Stachon, Andrea C. ; Baskin, Berivan ; Smith, Adam C. ; Shugar, Andrea ; Cytrynbaum, Cheryl ; Fishman, Leona ; Mendoza-Londono, Roberto ; Klatt, Regan ; Teebi, Ahmed ; Ray, Peter N. ; Weksberg, Rosanna . Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification. American Journal of Medical Genetics. Part A , v. 143A, p. 2924-2930, 2007.

• Smith, Adam C. ; Shuman, Cheryl ; Chitayat, David ; Steele, Leslie ; Ray, Peter N. ; Bourgeois, Jaqueline ; Weksberg, Rosanna . Severe presentation of BeckwithWiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15. American Journal of Medical Genetics. Part A , v. 143A, p. 3010-3015, 2007.

• Smith, Adam C. ; Choufani, Sanaa ; FERREIRA, JOSE C. ; Weksberg, Rosanna . Growth Regulation, Imprinted Genes, and Chromosome 11p15.5. Pediatric Research , v. 61, p. 43R-47R, 2007.

• Shuman, Cheryl ; Smith, Adam C. ; Steele, Leslie ; Ray, Peter N. ; Clericuzio, Carol ; Zackai, Elaine ; Parisi, Melissa A. ; Meadows, Anna T. ; Kelly, Thaddeus ; Tichauer, David ; Squire, Jeremy A. ; Sadowski, Paul ; Weksberg, Rosanna . Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies. American Journal of Medical Genetics. Part A , v. 140A, p. 1497-1503, 2006.

• Smith, A.C. ; Rubin, T. ; Shuman, C. ; Estabrooks, L. ; Aylsworth, A.S. ; McDonald, M.T. ; Steele, L. ; Ray, P.N. ; Weksberg, R. . New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome. Cytogenetic and Genome Research (Online) , v. 113, p. 313-317, 2006.

• McMinn, J. ; Wei, M. ; Schupf, N. ; Cusmai, J. ; Johnson, E.B. ; Smith, A.C. ; Weksberg, R. ; Thaker, H.M. ; Tycko, B. . Unbalanced Placental Expression of Imprinted Genes in Human Intrauterine Growth Restriction. Placenta (Eastbourne) , v. 27, p. 540-549, 2006.

• Weksberg, Rosanna ; Shuman, Cheryl ; Smith, Adam C. . Beckwith-Wiedemann syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics , v. 137C, p. 12-23, 2005.

• CYTRYNBAUM, CHERYL S ; SMITH, ADAM C ; RUBIN, TAMAR ; Weksberg, Rosanna . Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome. Current Opinion in Pediatrics , v. 17, p. 740-746, 2005.

• WEKSBERG, R ; Smith, A.C. ; Squire, Jeremy A. ; Sadowski, Paul . Beckwith-Wiedemann Syndrome Demonstrates a Role for Epigenetic Control of Normal Development.. Human Molecular Genetics (Print) , v. 12, p. R61-R68, 2003.

• Weksberg, R. ; Shuman, C. ; Caluseriu, O ; Smith, A.C. ; Fei, YL ; Nishikawa, J. ; Stockley, T ; Best, L ; CHITAYAT, D ; Olney, A ; Ives, E ; Schneider, A ; Bestor, TL ; Li, M ; Sadowski, Paul ; Squire, Jeremy A. . Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.. Human Molecular Genetics (Print) , v. 11, p. 1317-1325, 2002.

• GOLDMAN, M. ; SMITH, A. ; Shuman, C. ; CALUSERIU, O. ; WEI, C. ; Steele, L. ; RAY, P. ; SADOWSKI, P. ; SQUIRE, J. ; Weksberg, R. ; ROSENBLUM, N. D. . Renal Abnormalities in Beckwith-Wiedemann Syndrome Are Associated with 11p15.5 Uniparental Disomy. Journal of the American Society of Nephrology , v. 13, p. 2077-2084, 2002.

• Li, M ; Squire, Jeremy A. ; SHUMAN, C ; Fei, YL ; Atkin, J ; Pauli, R ; SMITH, A ; CHITAYAT, D ; Weksberg, R. . Imprinting Status of 11p15 Genes in BeckwithWiedemann Syndrome Patients with CDKN1C Mutations. Genomics (San Diego, Calif.) , v. 74, p. 370-376, 2001.

• WEKSBERG, R ; Nishikawa, J. ; Caluseriu, O ; Fei, YL ; Shuman, C. ; Wei, C ; Steele, L. ; Cameron, J ; SMITH, A ; Ambus, I ; Li, M ; Ray, P.N. ; Sadowski, Paul ; Squire, Jeremy A. . Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.. Human Molecular Genetics (Print) , v. 10, p. 2989-3000, 2001.

• SMITH, A. C. ; Squire, Jeremy A. ; Thorner, P ; Zielenska, M ; Shuman, C. ; Grant, R ; Chitayat, David ; Nishikawa, J. ; Weksberg, R. . Association of Alveolar Rhabdomyosarcoma with the Beckwith-Wiedemann Syndrome. Pediatric and Developmental Pathology (Print) , v. 4, p. 550-558, 2001.

• HINEK, A ; SMITH, A ; CUTIONGCO, E ; CALLAHAN, J ; GRIPP, K ; WEKSBERG, R . Decreased Elastin Deposition and High Proliferation of Fibroblasts from Costello Syndrome Are Related to Functional Deficiency in the 67-kD Elastin-Binding Protein. American Journal of Human Genetics , v. 66, p. 859-872, 2000.

• HINEK, A ; Zhang, S ; Smith, A.C. ; CALLAHAN, J . Impaired Elastic-Fiber Assembly by Fibroblasts from Patients with Either Morquio B Disease or Infantile GM1-Gangliosidosis Is Linked to Deficiency in the 67-kD Spliced Variant of Î-Galactosidase. American Journal of Human Genetics , v. 67, p. 23-36, 2000.

• Weksberg, Rosanna ; Sadowski, Paul ; Smith, Adam C. ; Tycko, B. . Epigenetics. In: Alan E.H. Emery, David L. Rimoin. (Org.). Emery and Rimoin's Principles and Practice of Medical Genetics. 5thed.Philadelphia: Elsevier, 2006, v. 1, p. 81-100.

• Krystal Bergin ; GERRIE, A. S. ; HUANG, S. J. T. ; RAMADAN, K. M. ; Aly Karsan ; HRYNCHAK, M. A. ; DALAL, C. B. ; BRUYERE, H. ; Smith, A.C. ; TOZE, C. L. ; Gillan, T. . Clonal Evolution Predicts Poor Prognosis in Chronic Lymphocytic Leukaemia and Is Possibly a Worse Prognostic Factor Than 17p Deletion: A Population Based Cohort study of FISH Testing in British Columbia, Canada. In: American Society of Hematology Annual Meeting, 2012, Altanta, GA, USA. 2012 ASH Annual Meeting Abstract Book, 2012.

• GERRIE, A. S. ; HUANG, S. J. T. ; BRUYERE, H. ; DALAL, C. B. ; HRYNCHAK, M. A. ; Aly Karsan ; RAMADAN, K. M. ; SMITH, A. C. ; Gillan, T. ; TOZE, C. L. . Comprehensive Assessment of Clinical Outcomes for CLL Patients with Trisomy 12 (+12): Results of a Population-Based Analysis of 822 CLL Patients in British Columbia (BC), Canada. In: American Society of Hematology Annual Meeting, 2012, Atlanta, GA, USA. 2012 ASH Annual Meeting Abstract Book, 2012.

• Horike, Shin-Ichi ; Meguro-Horike, Makiko ; FERREIRA, JOSE C. ; Smith, A.C. ; SHUMAN, C ; Meschino, Wendy ; Scherer, Stephen W. ; Zackai, Elaine ; WEKSBERG, R . Complex epigenetic abnormalities are not detected by targeted methylation analysis.. In: American Society of Human Genetics Annual Meeting, 2008, Philadelphia, USA. American Society of Human Genetics Abstract Book, 2008.

• SMITH, A ; C. Shuman ; Steele, Leslie ; Ray, Peter N. ; WEKSBERG, R . Severe phenotypic expression of Beckwith-Wiedemann syndrome associated with high levels of paternal uniparental disomy for chromosome 11p15.. In: American Society of Human Genetics Annual Meeting, 2006, New Orleans, USA. American Society of Human Genetics Abstract Book, 2006.

• SHUMAN, C ; Steele, L. ; SMITH, A ; Ray, Peter N. ; Zackai, Elaine ; Parisi, Melissa A. ; Clericuzio, Carol ; Meadows, Anna T. ; Kelly, Thaddeus ; Tichauer, David ; Squire, Jeremy A. ; WEKSBERG, R . Increased Tumor Frequency in Individuals with Isolated Hemihyperplasia and Molecular Alterations at 11p15.. In: American Society of Human Genetics Annual Meeting, 2005, Salt Lake City, USA. American Society of Human Genetics Abstract Book, 2005.

• SMITH, A. C. ; Squire, Jeremy A. ; SHUMAN, C ; WEKSBERG, R . Disruption of epigenetic regulatory elements and chromosomal aberrations in patients with Beckwith-Wiedemann syndrome.. In: American Society of Human Genetics Annual Meeting, 2004, Toronto, Canada. American Society of Human Genetics Abstract Book, 2004.

• Nakabayashi, K. ; Minagawa, S ; Bentley, L ; He, L ; Kapur, R ; SMITH, A. C. ; Bamforth, JS ; Oshimura, M ; WEKSBERG, R ; Moore, GE ; Scherer, Stephen W. . Chromosome-wide discovery of imprinted and differentially expressed genes for disease study.. In: American Society of Human Genetics Annual Meeting, 2002, Baltimore, USA. American Society of Human Genetics Abstract Book, 2002.

• Goy, J ; Gillan, T. ; HUANG, S. J. T. ; BRUYERE, H. ; HRYNCHAK, MONICA ; KARSAN, ALY ; RAMADAN, KHALED M. ; SMITH, ADAM C ; TOZE, CYNTHIA L. ; GERRIE, ALINA S. . Clinical outcomes for Chronic Lymphocytic Leukemia (CLL) patients with 11q deletion in British Columbia (BC), Canada: Results of an observational population-based cohort. 2014. (Apresentação de Trabalho/Simpósio).

• Smith, Adam C. . ICF Syndrome. 2010. (Apresentação de Trabalho/Conferência ou palestra).

• SMITH, A. C. . Genomic Rearrangements in Beckwith-Wiedemann Syndrome: The Genetic and Epigenetic Consequences. 2009. (Apresentação de Trabalho/Comunicação).

• SMITH, A. C. . Genomic Rearrangements in Beckwith-Wiedemann Syndrome: The Genetic and Epigenetic Consequences. 2009. (Apresentação de Trabalho/Comunicação).

• SMITH, A. C. . Prenatal diagnosis of a maternally derived unbalanced der(4)t(4;11) leading to an overlapping phenotype of Wolf-Hirschhorn and Russell-Silver syndromes in two siblings: novel recurrent translocation, aCGH and molecular cytogenetic analyses.. 2009. (Apresentação de Trabalho/Comunicação).

• SMITH, A. C. . Genomic Rearrangements in Beckwith-Wiedemann Syndrome: The Genetic and Epigenetic Consequences. 2009. (Apresentação de Trabalho/Comunicação).

• Smith, Adam C. . Mosaic Variegated Aneuploidy. 2009. (Apresentação de Trabalho/Comunicação).

• Smith, Adam C. . Introduction to the Cytogenetic Diagnostic Lab for Medical Residents. 2009. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. . Cancer Epigenetics. 2009. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. . Syndromes with Defects in Chromosome Cohesion. 2009. (Apresentação de Trabalho/Comunicação).

• Smith, Adam C. . Marker Chromosomes - Emanuel Syndrome. 2009. (Apresentação de Trabalho/Comunicação).

• Smith, Adam C. . Sex Chromosome Mosaicism. 2009. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. . Uniparental Disomy and Diagnostic Testing. 2009. (Apresentação de Trabalho/Conferência ou palestra).

• SMITH, A. C. . Epigenetics and Psychiatry. 2008. (Apresentação de Trabalho/Simpósio).

• Smith, Adam C. . A Primer on Epigenetics. 2008. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. . Array Complete Genomic Hybridization for the Detection of Complex Chromosome Abnormalties. 2008. (Apresentação de Trabalho/Comunicação).

• Smith, A.C. ; Weksberg, Rosanna ; Shuman, Cheryl . Severe Uniparental Disomy in Beckwith-Wiedemann Syndrome. 2006. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, A.C. ; Weksberg, Rosanna ; Ray, Peter N. ; Squire, Jeremy A. ; Shuman, Cheryl . Epigenetic Alterations in Patient with Tranlocations and Inversions with the Beckwith-Wiedemann Syndrome. 2005. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. ; Squire, Jeremy A. ; Shuman, Cheryl ; Weksberg, Rosanna . Disruption of epigenetic regulatory elements and chromosomal aberrations in patients with Beckwith-Wiedemann syndrome.. 2004. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. ; Squire, Jeremy A. ; Weksberg, Rosanna ; Shuman, Cheryl ; Ray, Peter N. . Methylation Abnormalties of the H19 DMR in Patients with the Beckwith-Wiedemann Syndrome. 2003. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. ; Squire, Jeremy A. ; Shuman, Cheryl ; Ray, Peter N. ; Weksberg, Rosanna . Methylation Abnormalities in Patients with the Beckwith-Wiedemann Syndrome. 2002. (Apresentação de Trabalho/Conferência ou palestra).

• Smith, Adam C. ; HINEK, A ; Weksberg, Rosanna . Elastin Deficiency in the Costello Syndrome. 2001. (Apresentação de Trabalho/Congresso).

• Shuman, Cheryl ; J. Bruce Beckwith ; Smith, Adam C. ; Weksberg, Rosanna . Beckwith-Wiedemann Syndrome. Seattle, Washington, USA: Edited by Roberta A Pagon, Editor-in-chief, Thomas D Bird, Cynthia R Dolan, Karen Stephens, and Marg, 2010 (Capitulo no Livro Online).

Outras produções

Projetos de pesquisa

• 2014 - 2018

  Role of Genomic Alterations in Intellectual Disability and Autism., Situação: Concluído; Natureza: Pesquisa. , Alunos envolvidos: Mestrado acadêmico: (1) Doutorado: (1) . , Integrantes: Adam Campbell Smith - Coordenador / Stachon, Andrea C. - Integrante / Barbara Bardoni - Integrante., Financiador(es): Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Auxílio financeiro.

• 2011 - 2013

  Determination of the Prognostic Significance of IGH Translocations in CLL patients in BC, Descrição: Using a samples of almost 800 patients from British Columbia involving three cytogenetic laboratories the retrospective analysis of the prognostic significance of IGH translocations and other genetic abnormalities involving IGH will be examined.. , Situação: Concluído; Natureza: Pesquisa. , Alunos envolvidos: Graduação: (1) . , Integrantes: Adam Campbell Smith - Integrante / Gillan, Tanya - Coordenador., Financiador(es): Vancouver Coastal Health Research Foundation - Auxílio financeiro.

Prêmios