Nancy Rodig, MD
Medical Director, Kidney Transplant Program; Nephrologist, Division of Nephrology
Assistant Professor of Pediatrics, Harvard Medical School
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Nancy Rodig, MD
Medical Director, Kidney Transplant Program; Nephrologist, Division of Nephrology
Assistant Professor of Pediatrics, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
College of the Holy Cross
1990
Worcester
MA
Medical School
Washington University
1995
St. Louis
MO
Internship
Pediatrics
St. Louis Children's Hospital
1996
St. Louis
MO
Residency
Pediatrics
St. Louis Children's Hospital
1998
St. Louis
MO
Fellowship
Pediatric Nephrology
Boston Children's Hospital
2002
Boston
MA
United States
Media
Caregiver Profile
Meet Dr. Nancy Rodig
Certifications
American Board of Pediatrics (General)
American Board of Pediatrics (Nephrology)
Professional History
Dr. Rodig has been with Boston Children's Hospital since 1999. In addition to her role as medical director of the Renal Transplant Program, she is active within the General Renal Program and Dialysis Unit. Her clinical and research interests focus on translational mechanisms related to the outcome and treatment of pediatric patients with chronic kidney disease and end-stage renal disease. Her research interests include growth outcomes in children with chronic kidney disease and general outcomes after kidney transplantation in the context of immunosuppression minimization protocols. In addition to holding an academic appointment as an assistant professor in pediatrics at Harvard Medical School, Dr. Rodig is a member of International Pediatric Nephrology Association, the American Society of Nephrology, the International Society of Nephrology and the American Society of Transplantation.
Publications
Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. View Abstract
Combination Automated Microfluidics Measurement of Urine C-C Motif Ligand 2, CXC-Motif Chemokine 9, CXC-Motif Chemokine 10, and Vascular Endothelial Growth Factor A for Monitoring Patients with a Kidney Transplant. View Abstract
Predictors of Posttransplant Lymphoproliferative Disease in Pediatric Patients. View Abstract
Evaluation for genetic disease in kidney transplant candidates: A practice resource. View Abstract
Pediatric Kidney Transplantation: Cancer and Cancer Risk. View Abstract
Correction to: Outcomes based on induction regimens in pediatric kidney transplantation: a NAPRTCS and PHIS collaborative study. View Abstract
Programmed cell death ligand 1 expression associated with subtypes of post-transplant lymphoproliferative disorder among pediatric kidney transplant recipients. View Abstract
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions. View Abstract
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions. View Abstract
Fecal Microbiota Transplant in Pediatric Solid Organ Transplant Recipients. View Abstract
Outcomes based on induction regimens in pediatric kidney transplantation: a NAPRTCS and PHIS collaborative study. View Abstract
Genetic evaluation of living kidney donor candidates: A review and recommendations for best practices. View Abstract
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis. View Abstract
Associations of body mass index (BMI) and BMI change with progression of chronic kidney disease in children. View Abstract
COVID-19 in pediatric kidney transplantation: a follow-up report of the Improving Renal Outcomes Collaborative. View Abstract
Presentation and outcomes of post-transplant lymphoproliferative disorder at a single institution pediatric transplant center. View Abstract
The development of end stage renal disease in two patients with PMM2-CDG. View Abstract
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. View Abstract
Implementing a regional standardized BK polyomavirus screening protocol across eleven transplant centres. View Abstract
COVID-19 in pediatric kidney transplantation: The Improving Renal Outcomes Collaborative. View Abstract
Longitudinal outcomes of body mass index in overweight and obese children with chronic kidney disease. View Abstract
Incidence and risk factors of kidney allograft loss due to BK nephropathy in the pediatric population: A retrospective analysis of the UNOS/OPTN database. View Abstract
Expecting the unexpected: COVID-19 in Kidney Transplant Recipients within United Network for Organ Sharing Region 1. View Abstract
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. View Abstract
Early outcomes comparing induction with antithymocyte globulin vs alemtuzumab in two steroid-avoidance protocols in pediatric renal transplantation. View Abstract
Perioperative renal transplantation management in small children using adult-sized living or deceased donor kidneys: A single-center experience. View Abstract
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. View Abstract
New England BK consortium: Regional survey of BK screening and management protocols in comparison to published consensus guidelines. View Abstract
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. View Abstract
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. View Abstract
Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1. View Abstract
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. View Abstract
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. View Abstract
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. View Abstract
A Regional Evaluation of Survival of Infants with End-Stage Renal Disease. View Abstract
Urinary NGAL deficiency in recurrent urinary tract infections. View Abstract
Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder. View Abstract
Treatment and outcomes of immune cytopenias following solid organ transplant in children. View Abstract
Methylmalonic acidemia: a megamitochondrial disorder affecting the kidney. View Abstract
Growth in children with chronic kidney disease: a report from the Chronic Kidney Disease in Children Study. View Abstract
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database. View Abstract
Rapid reversal of uremic neuropathy following renal transplantation in an adolescent. View Abstract
Risk factors for urinary tract infection after renal transplantation and its impact on graft function in children and young adults. View Abstract
Central nervous system lymphoproliferative disorder in pediatric kidney transplant recipients. View Abstract
Acute arsenic poisoning in two siblings. View Abstract
Endothelial expression of PD-L1 and PD-L2 down-regulates CD8+ T cell activation and cytolysis. View Abstract
Locations