Detalhe da pesquisa
1.
Genetics of Kidney Disease: The Unexpected Role of Rare Disorders.
Annu Rev Med
; 74: 353-367, 2023 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36375470
2.
Targeting WIP1 phosphatase promotes partial remission in experimental collapsing glomerulopathy.
Kidney Int
; 105(5): 980-996, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38423182
3.
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
4.
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
5.
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.
Prenat Diagn
; 44(3): 343-351, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38285371
6.
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
7.
The Clinical Utility of Genetic Testing in the Diagnosis and Management of Adults with Chronic Kidney Disease.
J Am Soc Nephrol
; 34(12): 2039-2050, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794564
8.
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
9.
The effect of genetic education on the referral of patients to genetic evaluation: Findings from a national survey of nephrologists.
Genet Med
; 25(5): 100814, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36789889
10.
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
11.
GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the Ssbp2 Locus.
J Am Soc Nephrol
; 33(1): 108-120, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34893534
12.
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Hum Mol Genet
; 29(22): 3662-3678, 2020 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33276377
13.
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
14.
Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting.
Genet Med
; 24(4): 862-869, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35078725
15.
Do research participants share genomic screening results with family members?
J Genet Couns
; 31(2): 447-458, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665896
16.
Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient.
Ann Intern Med
; 174(4): 540-547, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33460345
17.
COVID-19-Associated Glomerular Disease.
J Am Soc Nephrol
; 32(1): 33-40, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33214201
18.
Medical Records-Based Genetic Studies of the Complement System.
J Am Soc Nephrol
; 32(8): 2031-2047, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941608
19.
Longitudinal Outcomes of COVID-19-Associated Collapsing Glomerulopathy and Other Podocytopathies.
J Am Soc Nephrol
; 32(11): 2958-2969, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34670811
20.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Circulation
; 142(17): 1633-1646, 2020 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32981348