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Wendy Chung
Wendy Chung
Boston Children's Hospital, Harvard Medical School
Verified email at cumc.columbia.edu - Homepage
Title
Cited by
Cited by
Year
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
34202007
Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
KB Kuchenbaecker, JL Hopper, DR Barnes, KA Phillips, TM Mooij, ...
Jama 317 (23), 2402-2416, 2017
26472017
Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons
JT Dimos, KT Rodolfa, KK Niakan, LM Weisenthal, H Mitsumoto, W Chung, ...
science 321 (5893), 1218-1221, 2008
25332008
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2. 0): a policy statement of the American College of Medical …
SS Kalia, K Adelman, SJ Bale, WK Chung, C Eng, JP Evans, GE Herman, ...
Genetics in medicine 19 (2), 249-255, 2017
16822017
Phenotypes of Mouse diabetes and Rat fatty Due to Mutations in the OB (Leptin) Receptor
SC Chua Jr, WK Chung, XS Wu-Peng, Y Zhang, SM Liu, L Tartaglia, ...
Science 271 (5251), 994-996, 1996
14911996
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
9842015
Clinical application of whole-exome sequencing across clinical indications
K Retterer, J Juusola, MT Cho, P Vitazka, F Millan, F Gibellini, ...
Genetics in Medicine 18 (7), 696-704, 2016
9802016
Pediatric pulmonary hypertension: guidelines from the American heart association and American thoracic society
SH Abman, G Hansmann, SL Archer, DD Ivy, I Adatia, WK Chung, ...
Circulation 132 (21), 2037-2099, 2015
9702015
De novo mutations in histone-modifying genes in congenital heart disease
S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ...
Nature 498 (7453), 220-223, 2013
9482013
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care
E Mercuri, RS Finkel, F Muntoni, B Wirth, J Montes, M Main, ES Mazzone, ...
Neuromuscular disorders 28 (2), 103-115, 2018
8672018
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ...
Science 350 (6265), 1262-1266, 2015
7482015
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ...
Nature genetics 49 (11), 1593-1601, 2017
7082017
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
7002021
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5702018
A novel channelopathy in pulmonary arterial hypertension
L Ma, D Roman-Campos, ED Austin, M Eyries, KS Sampson, F Soubrier, ...
New England Journal of Medicine 369 (4), 351-361, 2013
5702013
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
5422015
Observational study of spinal muscular atrophy type I and implications for clinical trials
RS Finkel, MP McDermott, P Kaufmann, BT Darras, WK Chung, ...
Neurology 83 (9), 810-817, 2014
5422014
Genetics and genomics of pulmonary arterial hypertension
RD Machado, O Eickelberg, CG Elliott, MW Geraci, M Hanaoka, JE Loyd, ...
Journal of the American College of Cardiology 54 (1_Supplement_S), S32-S42, 2009
5092009
Genetic basis for congenital heart disease: revisited: a scientific statement from the American Heart Association
ME Pierpont, M Brueckner, WK Chung, V Garg, RV Lacro, AL McGuire, ...
Circulation 138 (21), e653-e711, 2018
4692018
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
S Srivastava, JA Love-Nichols, KA Dies, DH Ledbetter, CL Martin, ...
Genetics in Medicine 21 (11), 2413-2421, 2019
4452019
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