Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

Avinash V. Dharmadhikari(University of Southern California), Weimin Bi(Zhejiang A & F University), Yaping Yang(Baylor College of Medicine), Carlos A. Bacino(Baylor College of Medicine), Amy M. Breman(Baylor College of Medicine), Alicia Braxton(Baylor College of Medicine), Linyan Meng(Baylor Genetics), Rajarshi Ghosh(University College London), Jennifer Scull(Baylor College of Medicine), Fan Xia(Baylor Genetics), Seema R. Lalani(Baylor College of Medicine), Allen H. Jiang(Dawson Community College), Francesco Vetrini(Indiana University – Purdue University Indianapolis), Shen Gu(Ministry of Education of the People's Republic of China), Richard A. Gibbs(Baylor College of Medicine), Sau Wai Cheung(Chinese University of Hong Kong), Sami Al Masri(Baylor Genetics), Chad A. Shaw(Baylor College of Medicine), Arthur L. Beaudet(Lunar and Planetary Institute), Paweł Stankiewicz(Baylor College of Medicine), Bo Yuan(Second Military Medical University), Theodore Chiang(Hospital for Sick Children), Janice Smith(Baylor Genetics), Hongzheng Dai(Baylor College of Medicine), Pengfei Liu(Macau University of Science and Technology), Xia Wang(Union Hospital), Rui Xiao(Baylor College of Medicine), Ankita Patel(Gujarat University), Chunjing Qu(Baylor Genetics), Christine M. Eng(Baylor College of Medicine), Weimin He(Baylor College of Medicine), Patricia A. Ward(Baylor College of Medicine), James R. Lupski(Baylor College of Medicine), Donna M. Muzny(Baylor College of Medicine), Jennifer E. Posey(Baylor College of Medicine)
Genome Medicine
May 17, 2019
Cited by 70


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