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.
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
3.
Genetic evaluation of living kidney donor candidates: A review and recommendations for best practices.
Am J Transplant
; 23(5): 597-607, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36868514
4.
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
5.
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
6.
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
7.
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
; 24(5): 1130-1138, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216901
8.
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
9.
Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.
Am J Med Genet A
; 185(2): 508-516, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36046768
10.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(5): 789-802, 2017 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29100090
11.
Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience.
Genet Med
; 22(10): 1667-1672, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32555418
12.
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Ann Intern Med
; 170(1): 11-21, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30476936
13.
Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.
Genet Med
; 21(10): 2407, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31040387
14.
Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease.
Kidney Int
; 90(6): 1262-1273, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27591083
15.
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet
; 101(6): 1034, 2017 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29220675
16.
ZEB2 controls kidney stromal progenitor differentiation and inhibits abnormal myofibroblast expansion and kidney fibrosis.
JCI Insight
; 8(1)2023 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36445780
17.
Genomic medicine for kidney disease.
Nat Rev Nephrol
; 14(2): 83-104, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29307893
18.
SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion.
JCI Insight
; 1(19): e86934, 2016 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27882344
19.
Lower urinary tract development and disease.
Wiley Interdiscip Rev Syst Biol Med
; 5(3): 307-42, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23408557
20.
Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.
Cell Rep
; 2(1): 52-61, 2012 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-22840396