Wendy Chung
Wendy Chung
Boston Children's Hospital, Harvard Medical School
Verified email at - Homepage
Cited by
Cited by
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
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
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
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
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
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
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
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
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
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
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
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
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
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), 1267-1288, 2018
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
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
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
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
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
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
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