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Patricia weng
Patricia weng
Verified email at mednet.ucla.edu
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Cited by
Cited by
Year
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 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
1942019
Genetic approaches to human renal agenesis/hypoplasia and dysplasia
S Sanna-Cherchi, G Caridi, PL Weng, F Scolari, F Perfumo, AG Gharavi, ...
Pediatric nephrology 22, 1675-1684, 2007
1712007
Mutations in DSTYK and Dominant Urinary Tract Malformations
S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ...
New England Journal of Medicine 369 (7), 621-629, 2013
1482013
A prospective multi-center quality improvement initiative (NINJA) indicates a reduction in nephrotoxic acute kidney injury in hospitalized children
SL Goldstein, D Dahale, ES Kirkendall, T Mottes, H Kaplan, S Muething, ...
Kidney international 97 (3), 580-588, 2020
1362020
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
S Sanna-Cherchi, KE Burgess, SN Nees, G Caridi, PL Weng, M Dagnino, ...
Kidney international 80 (4), 389-396, 2011
952011
Angiotensin II Type 1 receptor antibodies are associated with inflammatory cytokines and poor clinical outcomes in pediatric kidney transplantation
MH Pearl, Q Zhang, MFP Diaz, J Grotts, M Rossetti, D Elashoff, ...
Kidney international 93 (1), 260-269, 2018
702018
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13
PL Weng, S Sanna-Cherchi, T Hensle, E Shapiro, A Werzberger, G Caridi, ...
Journal of the American Society of Nephrology 20 (7), 1633-1640, 2009
552009
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33
S Sanna-Cherchi, G Caridi, PL Weng, M Dagnino, M Seri, A Konka, ...
The American Journal of Human Genetics 80 (3), 539-549, 2007
502007
COVID‐19 in pediatric kidney transplantation: the improving renal outcomes collaborative
C Varnell Jr, LA Harshman, L Smith, C Liu, S Chen, S Al‐Akash, ...
American journal of transplantation 21 (8), 2740-2748, 2021
462021
Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
JH Pelletier, KR Kumar, R Engen, A Bensimhon, JD Varner, MN Rheault, ...
Pediatric Nephrology 33, 1773-1780, 2018
412018
Endothelin type A receptor antibodies are associated with angiotensin II type 1 receptor antibodies, vascular inflammation, and decline in renal function in pediatric kidney …
MH Pearl, L Chen, R ElChaki, D Elashoff, DW Gjertson, M Rossetti, ...
Kidney international reports 5 (11), 1925-1936, 2020
312020
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
K Kiryluk, E Sanchez-Rodriguez, XJ Zhou, F Zanoni, L Liu, N Mladkova, ...
Nature genetics 55 (7), 1091-1105, 2023
302023
State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D’Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG: Mutations in DSTYK and dominant urinary tract …
S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ...
N Engl J Med 369 (7), 621-629, 2013
302013
Endotoxin-neutralizing capacity of serum from cardiac surgical patients
E Bennett-Guerrero, GR Barclay, PL Weng, CA Bodian, DE Feierman, ...
Journal of cardiothoracic and vascular anesthesia 15 (4), 451-454, 2001
282001
An automated histological classification system for precision diagnostics of kidney allografts
D Yoo, V Goutaudier, G Divard, J Gueguen, BC Astor, O Aubert, ...
Nature medicine 29 (5), 1211-1220, 2023
232023
Diagnosis, treatment, and outcomes in children with congenital nephrogenic diabetes insipidus: a pediatric nephrology research consortium study
C D'Alessandri-Silva, M Carpenter, R Ayoob, J Barcia, A Chishti, ...
Frontiers in pediatrics 7, 550, 2020
222020
Cytokine profiles associated with angiotensin II type 1 receptor antibodies
MH Pearl, J Grotts, M Rossetti, Q Zhang, DW Gjertson, P Weng, D Elashoff, ...
Kidney international reports 4 (4), 541-550, 2019
222019
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
PL Weng, AJ Majmundar, K Khan, TY Lim, S Shril, G Jin, J Musgrove, ...
The American Journal of Human Genetics 108 (2), 357-367, 2021
182021
Copy number variant analysis and genome-wide association study identify loci with large effect for vesicoureteral reflux
M Verbitsky, P Krithivasan, E Batourina, A Khan, SE Graham, M Marasà, ...
Journal of the American Society of Nephrology 32 (4), 805-820, 2021
172021
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