Last Updated: 09/26/2026
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Found 23 publications
Association of Rare Variants in Kidney Developmental Genes With Chronic Kidney Disease and Blood Pressure: A UK Biobank Study.
Journal: WMJ : official publication of the State Medical Society of Wisconsin
Published: April 22, 2025
Total plasma cfDNA methylation in pediatric kidney transplant recipients provides insight into acute allograft rejection pathophysiology.
Journal: Clinical immunology (Orlando, Fla.)
Published: December 23, 2024
The methylome and cell-free DNA: current applications in medicine and pediatric disease.
Journal: Pediatric research
Published: May 16, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 15, 2021
Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 23, 2021
Correction to: Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings.
Journal: Neurogenetics
Published: July 12, 2018
Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.
Journal: NPJ genomic medicine
Published: December 22, 2017
Outcomes of infants receiving chronic peritoneal dialysis: an analysis of the USRDS registry.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 27, 2017
The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Journal: NPJ genomic medicine
Published: November 11, 2017
Parents Refusing Dialysis for a 3-Month-Old With Renal Failure.
Journal: Pediatrics
Published: June 21, 2017
Last Updated: 09/26/2026