A. Craig Chinault - Department of Molecular Genetics, Baylor College of Medicine, Houston, Tex., USA US US

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Confounding by repetitive elements and CpG islands does not explain the association between hypomethylation and genomic instability

R Alan Harris,Chad Shaw,Jian Li,Sau Wai Cheung,Cristian Coarfa,Mira Jeong,Margaret A Goodell,Lisa D White,Ankita Patel,Sung-Hae Kang,A Craig Chinault,Tomasz Gambin,

PLOS GENETICS（2013）

引用11浏览0WOS引用

MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development

Seema R Lalani,Stephanie M Ware,Xueqing Wang,Gladys Zapata,Qi Tian,Luis M Franco,Zhengxin Jiang,Kristine Bucasas,Daryl A Scott,Philippe M Campeau,Neil Hanchard,Luis Umaña,

HUMAN MOLECULAR GENETICS（2013）

引用40浏览0WOS引用

Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome

Jian Li,R Alan Harris,Sau Wai Cheung,Cristian Coarfa,Mira Jeong,Margaret A Goodell,Lisa D White,Ankita Patel,Sung-Hae Kang,Chad Shaw,A Craig Chinault,Tomasz Gambin,

PLOS GENETICS（2012）

引用83浏览0WOS引用

Genomic hypomethylation in the human germline associates with structural mutability in the human genome

Jian Li,R. Alan Harris,Sau Wai Cheung,Cristian Coarfa,Mira Jeong,Margaret A. Goodell,Lisa D. White,Ankita Patel,Sung-Hae Kang,Chad Shaw,A. Craig Chinault,Tomasz Gambin,

semanticscholar（2012）

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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

Patricia B S Celestino-Soper,Chad A Shaw,Stephan J Sanders,Jian Li,Michael T Murtha,A Gulhan Ercan-Sencicek,Lea Davis,Susanne Thomson,Tomasz Gambin,A Craig Chinault,Zhishuo Ou,Jennifer R German,

HUMAN MOLECULAR GENETICS（2011）

引用98浏览0WOS引用

11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity

Marwan Shinawi,Trilochan Sahoo,Bruno Maranda,S A Skinner,Cindy Skinner,Craig Chinault,Roxanne Zascavage,Sarika U Peters,Ankita Patel,Roger E Stevenson,Arthur L Beaudet

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2011）

引用95浏览0WOS引用

Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes

Zhishuo Ou,Paweł Stankiewicz,Zhilian Xia,Amy M Breman,Brian Dawson,Joanna Wiszniewska,Przemyslaw Szafranski,M Lance Cooper,Mitchell Rao,Lina Shao,Sarah T South,Karlene Coleman,

GENOME RESEARCH（2011）

引用83浏览0WOS引用

Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature

A Erez,J Li,M T Geraghty,S Ben-Shachar,M L Cooper, D E Mensing, K D Vonalt,Z Ou, A N Pursley,A C Chinault, A Patel,S W Cheung,

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2010）

引用14浏览0WOS引用

Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results

Sung-Hae L. Kang,Chad Shaw,Zhishuo Ou,Patricia A. Eng,M. Lance Cooper,Amber N. Pursley,Trilochan Sahoo,Carlos A. Bacino,A. Craig Chinault,Pawel Stankiewicz,Ankita Patel,James R. Lupski,

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2010）

引用87浏览0WOS引用

Genomic Duplication Resulting In Increased Copy Number Of Genes Encoding The Sister Chromatid Cohesion Complex Conveys Clinical Consequences Distinct From Cornelia De Lange

J. Yan,F. Zhang, E. Brundage,A. Scheuerle, B. Lanpher,R. P. Erickson, Z. Powis, H. B. Robinson,P. L. Trapane, D. Stachiw-Hietpas,K. M. Keppler-Noreuil, S. R. Lalani,

Journal of medical geneticsno. 9 (2009): 626-634

引用49浏览0WOS引用

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