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Krzysztof Kiryluk, MD
Krzysztof Kiryluk, MD
Associate Professor, Columbia University
在 columbia.edu 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
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
47102015
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
16282015
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
8462011
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
7412021
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
6732011
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
6352014
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
6142019
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
3992012
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
3552015
New developments in the genetics, pathogenesis, and therapy of IgA nephropathy
R Magistroni, VD D’Agati, GB Appel, K Kiryluk
Kidney international 88 (5), 974-989, 2015
2962015
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
2932011
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
2562012
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
2542012
The genetics and immunobiology of IgA nephropathy
K Kiryluk, J Novak
The Journal of clinical investigation 124 (6), 2325-2332, 2014
2492014
Assessment of network module identification across complex diseases
S Choobdar, ME Ahsen, J Crawford, M Tomasoni, T Fang, D Lamparter, ...
Nature methods 16 (9), 843-852, 2019
2472019
An atlas of healthy and injured cell states and niches in the human kidney
BB Lake, R Menon, S Winfree, Q Hu, R Melo Ferreira, K Kalhor, ...
Nature 619 (7970), 585-594, 2023
2032023
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
1972019
Predicting progression of IgA nephropathy: new clinical progression risk score
J Xie, K Kiryluk, W Wang, Z Wang, S Guo, P Shen, H Ren, X Pan, X Chen, ...
PloS one 7 (6), e38904, 2012
1922012
Whole-exome sequencing in adults with chronic kidney disease: a pilot study
S Lata, M Marasa, Y Li, DA Fasel, E Groopman, V Jobanputra, H Rasouly, ...
Annals of internal medicine 168 (2), 100-109, 2018
1912018
An eQTL landscape of kidney tissue in human nephrotic syndrome
CE Gillies, R Putler, R Menon, E Otto, K Yasutake, V Nair, P Hoover, ...
The American Journal of Human Genetics 103 (2), 232-244, 2018
1662018
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