PUBLICATIONS

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  1. Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. Genet Med. 2021 Nov 16. View abstract
  2. Implementing a regional standardized BK polyomavirus screening protocol across eleven transplant centres. Transpl Int. 2021 Dec; 34(12):2680-2685. View abstract
  3. COVID-19 in pediatric kidney transplantation: The Improving Renal Outcomes Collaborative. Am J Transplant. 2021 08; 21(8):2740-2748. View abstract
  4. Longitudinal outcomes of body mass index in overweight and obese children with chronic kidney disease. Pediatr Nephrol. 2021 07; 36(7):1851-1860. View abstract
  5. Incidence and risk factors of kidney allograft loss due to BK nephropathy in the pediatric population: A retrospective analysis of the UNOS/OPTN database. Pediatr Transplant. 2021 Aug; 25(5):e13927. View abstract
  6. Expecting the unexpected: COVID-19 in Kidney Transplant Recipients within United Network for Organ Sharing Region 1. Transpl Int. 2020 12; 33(12):1843-1844. View abstract
  7. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Am J Hum Genet. 2020 10 01; 107(4):727-742. View abstract
  8. Early outcomes comparing induction with antithymocyte globulin vs alemtuzumab in two steroid-avoidance protocols in pediatric renal transplantation. Pediatr Transplant. 2020 05; 24(3):e13685. View abstract
  9. Perioperative renal transplantation management in small children using adult-sized living or deceased donor kidneys: A single-center experience. Pediatr Transplant. 2019 11; 23(7):e13553. View abstract
  10. Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. J Am Soc Nephrol. 2019 02; 30(2):201-215. View abstract
  11. New England BK consortium: Regional survey of BK screening and management protocols in comparison to published consensus guidelines. Transpl Infect Dis. 2018 Dec; 20(6):e12985. View abstract
  12. 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 abstract
  13. 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 abstract
  14. Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1. Pediatr Nephrol. 2018 05; 33(5):881-887. View abstract
  15. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Clin J Am Soc Nephrol. 2018 01 06; 13(1):53-62. View abstract
  16. Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Kidney Int. 2018 01; 93(1):204-213. View abstract
  17. Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. Pediatr Nephrol. 2018 02; 33(2):305-314. View abstract
  18. A Regional Evaluation of Survival of Infants with End-Stage Renal Disease. Neonatology. 2017; 112(1):73-79. View abstract
  19. Urinary NGAL deficiency in recurrent urinary tract infections. Pediatr Nephrol. 2017 06; 32(6):1077-1080. View abstract
  20. Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder. Pediatr Nephrol. 2015 Jul; 30(7):1197-202. View abstract
  21. Treatment and outcomes of immune cytopenias following solid organ transplant in children. Pediatr Blood Cancer. 2015 02; 62(2):214-218. View abstract
  22. Methylmalonic acidemia: a megamitochondrial disorder affecting the kidney. Pediatr Nephrol. 2014 Nov; 29(11):2139-46. View abstract
  23. Growth in children with chronic kidney disease: a report from the Chronic Kidney Disease in Children Study. Pediatr Nephrol. 2014 Oct; 29(10):1987-95. View abstract
  24. Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database. Hum Mutat. 2012 Mar; 33(3):457-66. View abstract
  25. Rapid reversal of uremic neuropathy following renal transplantation in an adolescent. Pediatr Transplant. 2012 Nov; 16(7):E296-300. View abstract
  26. Risk factors for urinary tract infection after renal transplantation and its impact on graft function in children and young adults. J Urol. 2010 Oct; 184(4):1462-7. View abstract
  27. Central nervous system lymphoproliferative disorder in pediatric kidney transplant recipients. Pediatr Transplant. 2006 Jun; 10(4):505-12. View abstract
  28. Acute arsenic poisoning in two siblings. Pediatrics. 2005 Jul; 116(1):249-57. View abstract
  29. Endothelial expression of PD-L1 and PD-L2 down-regulates CD8+ T cell activation and cytolysis. Eur J Immunol. 2003 Nov; 33(11):3117-26. View abstract