Shashi Nagaraj

Medicine · Health Sciences

16h-index1.5kcitations36works0.02yr avg
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Research Topics

Renal Diseases and Glomerulopathies(11), Pediatric Urology and Nephrology Studies(6), Renal Transplantation Outcomes and Treatments(4), Complement system in diseases(4), Adenosine and Purinergic Signaling(4)

Publications35 total

Corrigendum to “Rondeau E, Scully M, Ariceta G, Barbour T, Cataland S, Heyne N, Miyakawa Y, Ortiz S, Swenson E, Vallee M, Yoon S-S, Kavanagh D and Haller H; on behalf of the 311 Study Group. The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment.” Kidney Int. 2020;97:1287–1296
Kidney International·2021· 3 citedOpen Access
Long-Term Efficacy and Safety of the Long-Acting Complement C5 Inhibitor Ravulizumab for the Treatment of Atypical Hemolytic Uremic Syndrome in Adults
Kidney International Reports·2021· 63 citedOpen Access
Erratum to “Rondeau E, Scully M, Ariceta G, Barbour T, Cataland S, Heyne N, Miyakawa Y, Ortiz S, Swenson E, Vallee M, Yoon S-S, Kavanagh D, Haller H; on behalf of the 311 Study Group. The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment” Kidney Int. 2020;97:1287–1296
Kidney International·2020· 3 citedOpen Access
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux
UNC Libraries·2020Open Access
The long-acting C5 inhibitor, Ravulizumab, is effective and safe in adult patients with atypical hemolytic uremic syndrome naïve to complement inhibitor treatment
Kidney International·2020· 204 citedOpen Access
Tailored use of belatacept in adolescent kidney transplantation
American Journal of Transplantation·2019· 16 citedOpen Access
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
Journal of Clinical Investigation·2019· 91 citedOpen Access
Psychosocial Assessment of Candidates for Transplantation (PACT) Score Identifies High Risk Patients in Pediatric Renal Transplantation
Frontiers in Pediatrics·2019· 19 citedOpen Access
Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
Pediatric Nephrology·2018· 4 cited
Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
Pediatric Nephrology·2018· 42 citedOpen Access
Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases
Genetics in Medicine·2017· 52 citedOpen Access
Neutropenic enterocolitis (typhlitis) in a pediatric renal transplant patient. A case report and review of the literature
Pediatric Transplantation·2017· 9 cited
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux
Pediatric Nephrology·2015· 13 citedOpen Access
Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation
Clinical Kidney Journal·2015· 13 citedOpen Access
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
Journal of the American Society of Nephrology·2014· 145 citedOpen Access
Efficacy of Antibiotic Prophylaxis in Children with Vesicoureteral Reflux: Systematic Review and Meta-Analysis
The Journal of Urology·2014· 97 citedOpen Access
Neurogenic Bladder Dysfunction Presenting as Urinary Retention in Neuronopathic Gaucher Disease
JIMD Reports·2014· 3 citedOpen Access
A de novo novel missense mutation in AVPR2 with severe nephrogenic diabetes insipidus
Clinical Kidney Journal·2010· 2 citedOpen Access
Potential Donor–Recipient MYH9 Genotype Interactions in Posttransplant Nephrotic Syndrome After Pediatric Kidney Transplantation
American Journal of Transplantation·2009· 18 citedOpen Access
Management patterns of childhood-onset nephrotic syndrome
Pediatric Nephrology·2009· 53 cited
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Frequent Co-authors

Delbert R. Wigfall(11), Rasheed Gbadegesin(10), John W. Foreman(9), Larry A. Greenbaum(5), Vandana Shashi(5), Debbie S. Gipson(4), Éric Rondeau(4), Marie Scully(4), Gema Ariceta(4), Thomas Barbour(4), Spero Cataland(4), Nils Heyne(4), Yoshitaka Miyakawa(4), David Kavanagh(4), Sunil Babu(4), Nilüfer Broeders(4), Nicole Lietar(4), Fiona G. Brown(4), Paramit Chowdhury(4), Theo Kasimatis(4)