Detalhe da pesquisa
1.
Disease Heritability Inferred from Familial Relationships Reported in Medical Records.
Cell
; 173(7): 1692-1704.e11, 2018 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29779949
2.
An atlas of healthy and injured cell states and niches in the human kidney.
Nature
; 619(7970): 585-594, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37468583
3.
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Am J Hum Genet
; 110(11): 1950-1958, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37883979
4.
Glomerular transcriptomics predicts long term outcome and identifies therapeutic strategies for patients with assumed benign IgA nephropathy.
Kidney Int
; 105(4): 717-730, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154557
5.
Developing a genetic testing panel for evaluation of morbidities in kidney transplant recipients.
Kidney Int
; 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38521406
6.
Pathologic-genomic correlation identified a novel variant in FN1 and established the diagnosis of recurrent fibronectin glomerulopathy in the kidney allograft.
Am J Transplant
; 24(3): 498-502, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37852577
7.
Genetic versus self-reported African ancestry of the recipient and neighborhood predictors of kidney transplantation outcomes in 2 multiethnic urban cohorts.
Am J Transplant
; 2024 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38331047
8.
Novel EDGE encoding method enhances ability to identify genetic interactions.
PLoS Genet
; 17(6): e1009534, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34086673
9.
Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes.
J Am Soc Nephrol
; 34(5): 909-919, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36758113
10.
Genomic Disorders in CKD across the Lifespan.
J Am Soc Nephrol
; 34(4): 607-618, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36302597
11.
Mendelian randomization for nephrologists.
Kidney Int
; 104(6): 1113-1123, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37783446
12.
Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing Data.
Am J Hum Genet
; 106(4): 513-524, 2020 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32243819
13.
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.
Genet Med
; 25(12): 100983, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37746849
14.
Multiancestral polygenic risk score for pediatric asthma.
J Allergy Clin Immunol
; 150(5): 1086-1096, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35595084
15.
Incorporating genetics services into adult kidney disease care.
Am J Med Genet C Semin Med Genet
; 190(3): 289-301, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161695
16.
Kidney disease progression and collider bias in GWAS.
Kidney Int
; 102(3): 476-478, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35988936
17.
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection.
N Engl J Med
; 380(20): 1918-1928, 2019 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31091373
18.
Diagnostic Utility of Exome Sequencing for Kidney Disease.
N Engl J Med
; 380(2): 142-151, 2019 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30586318
19.
Improving Clinical Trials for Anticomplement Therapies in Complement-Mediated Glomerulopathies: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.
Am J Kidney Dis
; 79(4): 570-581, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34571062
20.
Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis.
Rheumatology (Oxford)
; 61(3): 1204-1210, 2022 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33993232