Takip et
Ali G. Gharavi
Ali G. Gharavi
Professor of Medicine & Chair, Department of Medicine, Columbia University
columbia.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Genetic studies of body mass index yield new insights for obesity biology
AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ...
Nature 518 (7538), 197-206, 2015
49752015
Molecular mechanisms of human hypertension
RP Lifton, AG Gharavi, DS Geller
Cell 104 (4), 545-556, 2001
23092001
New genetic loci link adipose and insulin biology to body fat distribution
D Shungin, TW Winkler, DC Croteau-Chonka, T Ferreira, AE Locke, ...
Nature 518 (7538), 187-196, 2015
17282015
The pathophysiology of IgA nephropathy
H Suzuki, K Kiryluk, J Novak, Z Moldoveanu, AB Herr, MB Renfrow, ...
Journal of the American Society of Nephrology 22 (10), 1795-1803, 2011
9402011
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
8432021
Genome-wide association study identifies susceptibility loci for IgA nephropathy
AG Gharavi, K Kiryluk, M Choi, Y Li, P Hou, J Xie, S Sanna-Cherchi, ...
Nature genetics 43 (4), 321-327, 2011
7072011
Diagnostic utility of exome sequencing for kidney disease
EE Groopman, M Marasa, S Cameron-Christie, S Petrovski, VS Aggarwal, ...
New England Journal of Medicine 380 (2), 142-151, 2019
7032019
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
K Kiryluk, Y Li, F Scolari, S Sanna-Cherchi, M Choi, M Verbitsky, D Fasel, ...
Nature genetics 46 (11), 1187-1196, 2014
6782014
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
LM Boyden, M Choi, KA Choate, CJ Nelson-Williams, A Farhi, HR Toka, ...
Nature 482 (7383), 98-102, 2012
6752012
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23
AG Gharavi, Y Yan, F Scolari, FP Schena, GM Frasca, GM Ghiggeri, ...
Nature genetics 26 (3), 354-357, 2000
4562000
Kidney biopsy findings in patients with COVID-19
S Kudose, I Batal, D Santoriello, K Xu, J Barasch, Y Peleg, P Canetta, ...
Journal of the American Society of Nephrology 31 (9), 1959-1968, 2020
4542020
Presentation and outcomes of patients with ESKD and COVID-19
AM Valeri, SY Robbins-Juarez, JS Stevens, W Ahn, MK Rao, ...
Journal of the american society of nephrology 31 (7), 1409-1415, 2020
4312020
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis
K Kiryluk, Y Li, S Sanna-Cherchi, M Rohanizadegan, H Suzuki, F Eitner, ...
PLoS genetics 8 (6), e1002765, 2012
4172012
Current understanding of the role of complement in IgA nephropathy
N Maillard, RJ Wyatt, BA Julian, K Kiryluk, A Gharavi, V Fremeaux-Bacchi, ...
Journal of the American Society of Nephrology 26 (7), 1503-1512, 2015
3822015
Mutations in SEC63 cause autosomal dominant polycystic liver disease
S Davila, L Furu, AG Gharavi, X Tian, T Onoe, Q Qian, A Li, Y Cai, ...
Nature genetics 36 (6), 575-577, 2004
3482004
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy
AG Gharavi, Z Moldoveanu, RJ Wyatt, CV Barker, SY Woodford, RP Lifton, ...
Journal of the American Society of Nephrology 19 (5), 1008-1014, 2008
3332008
Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch–Schönlein purpura nephritis
K Kiryluk, Z Moldoveanu, JT Sanders, TM Eison, H Suzuki, BA Julian, ...
Kidney international 80 (1), 79-87, 2011
3062011
Acute kidney injury due to collapsing glomerulopathy following COVID-19 infection
Y Peleg, S Kudose, V D’Agati, E Siddall, S Ahmad, T Nickolas, S Kisselev, ...
Kidney international reports 5 (6), 940-945, 2020
3002020
The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression
N Zhao, P Hou, J Lv, Z Moldoveanu, Y Li, K Kiryluk, AG Gharavi, J Novak, ...
Kidney international 82 (7), 790-796, 2012
2742012
Copy-number disorders are a common cause of congenital kidney malformations
S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ...
The American Journal of Human Genetics 91 (6), 987-997, 2012
2582012
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