Primary Office

Nemours Children's Hospital, Delaware Nemours Children's Hospital, Delaware 1600 Rockland Road Wilmington, DE 19803 Appointment: (800) 416-4441

Education & Training

Fellowship

  • Medical Genetics - Children's Hospital of Pittsburgh, 2008

Internship

  • Rotating - University Hospital of the West Indies, 1999

Residency

  • Pediatrics - Albert Einstein Medical Center, 2006
  • Internal Medicine/Pediatrics - Albert Einstein Medical Center, 2005

Medical/Dental School

  • MBBS - University of the West Indies, 1998

Board Certifications

  • American Board of Pediatrics/General Pediatrics
  • American Board of Medical Genetics and Genomics/Clinical Genetics and Genomics

Awards & Recognition

  • 2014 Delaware Today magazine, Top Doctors

Insurance Accepted

  • Aetna Better Health PA Kids HMO
  • Aetna HMO
  • Aetna PPO/POS/EPO
  • Amerihealth Caritas Delaware
  • Carefirst MD Community Health Plan Mcaid
  • Cigna/Great West HMO EPO POS
  • Cigna/Great West PPO
  • Delaware First Health
  • Delaware Medicaid/Diamond State
  • Devon Health Services
  • Fidelis Care NJ Medicaid HMO
  • First Health/Affordable PPO
  • Geisinger Health Plan Commercial
  • Global Medical Managment DE/PA
  • Health Partners Medicaid/Kidz Partner HMO
  • Highmark Blue Cross Blue Shield of Delaware
  • Highmark Medicaid Health Options
  • Horizon Blue Cross Blue Shield of New Jersey
  • IBC Amerihealth Keystone HMO/PPO [Delaware Locations]
  • INTEGRA Administrative Group (ClaimsBridge)
  • Keystone First Medicaid HMO
  • Lifetrac Transplant
  • Maryland Medicaid
  • Multiplan PPO
  • New Jersey Medicaid
  • Pennsylvania Medicaid
  • Plan Vista/NPPN PPO
  • Preferred Healthcare PPO
  • Private Health Care Systems (PHCS)
  • Star Healthcare Network
  • Three Rivers Provider Network
  • Tricare/Humana Military Health Services
  • United Healthcare of the Mid-Atlantic
  • UPMC MCAID/CHIP PA DE
  • US Family Health Plan
  • Wellpoint Maryland Medcaid

  • Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.; American journal of medical genetics. Part A; (2021).

    View Full Publication
  • Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors; American Journal of Neuroradiology; (2022).

    View Full Publication
  • Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome; Molecular Psychiatry; (2021).

    View Full Publication
  • Inherited intragenic PBX1 deletion: Expanding the phenotype; American Journal of Medical Genetics, Part A; (2021).

    View Full Publication
  • Newborn Screening; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs; (2020).

  • Genetic and Genomic Testing in the Newborn Period; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs, 8th Edition; (2020).

  • Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients; Science Advances; (2020).

    View Full Publication
  • Multiple Congenital Anomalies: Syndromes, Sequences and Associations; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs, 8th Edition; (2020).

  • Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome; bioRxiv; (2019).

    View Full Publication
  • Chromosome and Gene Anomalies ; The Merck Manual of Diagnosis and Therapy 20th Edition; (2018).

  • HUWE1 variants cause dominant X-linked intellectual disability: A clinical study of 21 patients; European Journal of Human Genetics; (2018).

    View Full Publication
  • Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders; Genome medicine; (2017).

    View Full Publication
  • A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations; American Journal of Human Genetics; (2017).

    View Full Publication
  • A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair; American Journal of Medical Genetics, Part A; (2016).

    View Full Publication
  • Maternal uniparental disomy of chromosome 20: A novel imprinting disorder of growth failure; Genetics in Medicine; (2016).

    View Full Publication
  • Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations; Journal of Neuropathology and Experimental Neurology; (2014).

    View Full Publication

  • English