Wendy Chung
Wendy Chung
Kennedy Professor of Medicine and Pediatrics, Columbia University
Підтверджена електронна адреса в cumc.columbia.edu
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
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
Phenotypes of mouse diabetes and rat fatty due to mutations in the OB (leptin) receptor
SC Chua, WK Chung, XS Wu-Peng, Y Zhang, SM Liu, L Tartaglia, ...
Science 271 (5251), 994-996, 1996
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
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
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
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
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
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
Gene expression patterns in blood leukocytes discriminate patients with acute infections
O Ramilo, W Allman, W Chung, A Mejias, M Ardura, C Glaser, ...
Blood 109 (5), 2066-2077, 2007
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 (1S), S32-S42, 2009
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
A novel channelopathy in pulmonary arterial hypertension
L Ma, D Roman-Campos, ED Austin, M Eyries, KS Sampson, F Soubrier, ...
N Engl J Med 369, 351-361, 2013
Association Between Uncoupling Protein Polymorphisms (UCP2–UCP3) and Energy Metabolism/Obesity in Pima Indians
K Walder, RA Norman, RL Hanson, P Schrauwen, M Neverova, ...
Human Molecular Genetics 7 (9), 1431-1435, 1998
Whole exome sequencing to identify a novel gene (caveolin-1) associated with human pulmonary arterial hypertension
ED Austin, L Ma, C LeDuc, E Berman Rosenzweig, A Borczuk, ...
Circulation: Cardiovascular Genetics 5 (3), 336-343, 2012
The molecular genetics of rodent single gene obesities
RL Leibel, WK Chung, SC Chua
Journal of Biological Chemistry 272 (51), 31937-31940, 1997
Regulation of Fto/Ftm gene expression in mice and humans
G Stratigopoulos, SL Padilla, CA LeDuc, E Watson, AT Hattersley, ...
American Journal of Physiology-Regulatory, Integrative and Comparative …, 2008
Genetics and genomics of pulmonary arterial hypertension
F Soubrier, WK Chung, R Machado, E Grünig, M Aldred, M Geraci, ...
Journal of the American College of Cardiology 62 (25S), D13-D21, 2013
Phenotype of fatty due to Gln269Pro mutation in the leptin receptor (Lepr)
SC Chua, DW White, XS Wu-Peng, SM Liu, N Okada, EE Kershaw, ...
Diabetes 45 (8), 1141-1143, 1996
Male-to-male sexual transmission of Zika virus—Texas, January 2016
DT Deckard, WM Chung, JT Brooks, JC Smith, S Woldai, M Hennessey, ...
Morbidity and Mortality Weekly Report 65 (14), 372-374, 2016
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