Ankana Daga

A national survey of pediatric nephrologists on the treatment of steroid-resistant nephrotic syndrome. Clin Nephrol. 2025 Jun; 103(6):393-403. View A national survey of pediatric nephrologists on the treatment of steroid-resistant nephrotic syndrome. Abstract

Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. Genet Med. 2025 Apr 10; 101432. View Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. Abstract

Advanced CKD of Uncertain Etiology Among Children in Guatemala: Genetic and Clinical Characteristics. Kidney Med. 2024 Dec; 6(12):100910. View Advanced CKD of Uncertain Etiology Among Children in Guatemala: Genetic and Clinical Characteristics. Abstract

Real-world application of the pediatric Glucocorticoid Toxicity Index in childhood-onset lupus. Semin Arthritis Rheum. 2024 Oct; 68:152516. View Real-world application of the pediatric Glucocorticoid Toxicity Index in childhood-onset lupus. Abstract

Underutilization of ambulatory blood pressure monitoring in locally and nationally representative samples of patients with childhood-onset systemic lupus erythematosus. Clin Rheumatol. 2024 Mar; 43(3):1265-1268. View Underutilization of ambulatory blood pressure monitoring in locally and nationally representative samples of patients with childhood-onset systemic lupus erythematosus. Abstract

World Kidney Day 2023: preparing for the unexpected, supporting the vulnerable! Pediatr Nephrol. 2023 06; 38(6):1697-1699. View World Kidney Day 2023: preparing for the unexpected, supporting the vulnerable! Abstract

OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis. Genet Med. 2023 03; 25(3):100351. View OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis. Abstract

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. 2023 05; 38(5):1653-1665. View 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. Abstract

Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism. J Pediatr. 2022 07; 246:116-122.e1. View Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism. Abstract

The scope of treatment of pediatric IgA vasculitis nephritis and its outcome: a Pediatric Nephrology Research Consortium study. Pediatr Nephrol. 2022 Nov; 37(11):2687-2697. View The scope of treatment of pediatric IgA vasculitis nephritis and its outcome: a Pediatric Nephrology Research Consortium study. Abstract

The effect of gender-affirming hormone treatment on serum creatinine in transgender and gender-diverse youth: implications for estimating GFR. Pediatr Nephrol. 2022 09; 37(9):2141-2150. View The effect of gender-affirming hormone treatment on serum creatinine in transgender and gender-diverse youth: implications for estimating GFR. Abstract

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. Genet Med. 2022 02; 24(2):307-318. View Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. Abstract

Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort. Lupus. 2021 Sep; 30(10):1660-1670. View Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort. Abstract

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Am J Hum Genet. 2020 10 01; 107(4):727-742. View Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Abstract

Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome. Kidney Int. 2019 10; 96(4):883-889. View Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome. Abstract

Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Nephrol Dial Transplant. 2019 03 01; 34(3):485-493. View Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Abstract

Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Nephrol Dial Transplant. 2019 03 01; 34(3):474-485. View Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Abstract

Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis. Hum Genet. 2019 Mar; 138(3):211-219. View Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis. Abstract

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. J Am Soc Nephrol. 2019 02; 30(2):201-215. View Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. Abstract

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome. J Clin Invest. 2018 10 01; 128(10):4313-4328. View Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome. Abstract

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. J Am Soc Nephrol. 2018 09; 29(9):2348-2361. View Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. Abstract

Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. Am J Med Genet A. 2018 11; 176(11):2460-2465. View Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. Abstract

GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome. J Am Soc Nephrol. 2018 08; 29(8):2123-2138. View GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome. Abstract

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. Nat Commun. 2018 05 17; 9(1):1960. View Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. Abstract

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. Hypertension. 2018 04; 71(4):691-699. View Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. Abstract

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Clin J Am Soc Nephrol. 2018 01 06; 13(1):53-62. View Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Abstract

Advillin acts upstream of phospholipase C ?1 in steroid-resistant nephrotic syndrome. J Clin Invest. 2017 12 01; 127(12):4257-4269. View Advillin acts upstream of phospholipase C ?1 in steroid-resistant nephrotic syndrome. Abstract

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Kidney Int. 2018 01; 93(1):204-213. View Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Abstract

Transition of Care: Pediatric Ambulatory Center to Emergency Department. Pediatr Emerg Care. 2017 Sep; 33(9):e63-e66. View Transition of Care: Pediatric Ambulatory Center to Emergency Department. Abstract

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat Genet. 2017 Oct; 49(10):1529-1538. View Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Abstract

Diagnosis and Risk Factors of Acute Kidney Injury in Very Low Birth Weight Infants. Pediatr Neonatol. 2017 06; 58(3):258-263. View Diagnosis and Risk Factors of Acute Kidney Injury in Very Low Birth Weight Infants. Abstract

Prevalence of arrhythmias late after the Fontan operation. Am J Cardiol. 2014 Apr 01; 113(7):1184-8. View Prevalence of arrhythmias late after the Fontan operation. Abstract

An international multicenter study comparing arrhythmia prevalence between the intracardiac lateral tunnel and the extracardiac conduit type of Fontan operations. J Thorac Cardiovasc Surg. 2014 Aug; 148(2):576-81. View An international multicenter study comparing arrhythmia prevalence between the intracardiac lateral tunnel and the extracardiac conduit type of Fontan operations. Abstract