Search details
1.
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.
Genet Med
; 25(3): 100351, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36571463
2.
Acute kidney injury requiring kidney replacement therapy in childhood lupus nephritis: a cohort study of the Pediatric Nephrology Research Consortium and Childhood Arthritis and Rheumatology Research Alliance.
Pediatr Nephrol
; 38(5): 1653-1665, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36251074
3.
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Genet Med
; 24(2): 307-318, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34906515
4.
Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism.
J Pediatr
; 246: 116-122.e1, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35358588
5.
The effect of gender-affirming hormone treatment on serum creatinine in transgender and gender-diverse youth: implications for estimating GFR.
Pediatr Nephrol
; 37(9): 2141-2150, 2022 09.
Article
in English
| MEDLINE | ID: mdl-35083530
6.
The scope of treatment of pediatric IgA vasculitis nephritis and its outcome: a Pediatric Nephrology Research Consortium study.
Pediatr Nephrol
; 37(11): 2687-2697, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-35233641
7.
Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort.
Lupus
; 30(10): 1660-1670, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34219529
8.
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
J Am Soc Nephrol
; 30(2): 201-215, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30655312
9.
Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome.
Kidney Int
; 96(4): 883-889, 2019 10.
Article
in English
| MEDLINE | ID: mdl-31472902
10.
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis.
Hum Genet
; 138(3): 211-219, 2019 Mar.
Article
in English
| MEDLINE | ID: mdl-30778725
11.
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
Nephrol Dial Transplant
; 34(3): 485-493, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-29534211
12.
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children.
Nephrol Dial Transplant
; 34(3): 474-485, 2019 03 01.
Article
in English
| MEDLINE | ID: mdl-30295827
13.
GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.
J Am Soc Nephrol
; 29(8): 2123-2138, 2018 08.
Article
in English
| MEDLINE | ID: mdl-29959197
14.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
J Am Soc Nephrol
; 29(9): 2348-2361, 2018 09.
Article
in English
| MEDLINE | ID: mdl-30143558
15.
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
Kidney Int
; 93(1): 204-213, 2018 01.
Article
in English
| MEDLINE | ID: mdl-28893421
16.
Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.
Am J Med Genet A
; 176(11): 2460-2465, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30079490
17.
World Kidney Day 2023: preparing for the unexpected, supporting the vulnerable!
Pediatr Nephrol
; 38(6): 1697-1699, 2023 06.
Article
in English
| MEDLINE | ID: mdl-36941486
18.
Transition of Care: Pediatric Ambulatory Center to Emergency Department.
Pediatr Emerg Care
; 33(9): e63-e66, 2017 Sep.
Article
in English
| MEDLINE | ID: mdl-26466144
19.
Underutilization of ambulatory blood pressure monitoring in locally and nationally representative samples of patients with childhood-onset systemic lupus erythematosus.
Clin Rheumatol
; 43(3): 1265-1268, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-37991677
20.
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
Hypertension
; 71(4): 691-699, 2018 04.
Article
in English
| MEDLINE | ID: mdl-29483232