Nina N Powell-Hamilton, MD
GeneticsInsurance 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
- Independance Blue Cross/Amerihealth/Keystone Health Plan
- 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/CHAMPVA
- United Healthcare of the Mid-Atlantic
- UPMC MCAID/CHIP PA DE
- US Family Health Plan
- Wellpoint Maryland Medcaid
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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).
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Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome; Molecular Psychiatry; (2021).
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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).
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Inherited intragenic PBX1 deletion: Expanding the phenotype; American Journal of Medical Genetics, Part A; (2021).
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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).
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Genetic and Genomic Testing in the Newborn Period; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs, 8th Edition; (2020).
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Newborn Screening; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs; (2020).
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Multiple Congenital Anomalies: Syndromes, Sequences and Associations; Gomella's Neonatology: Management, Procedures, On-Call Problems, Diseases and Drugs, 8th Edition; (2020).
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Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome; bioRxiv; (2019).
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HUWE1 variants cause dominant X-linked intellectual disability: A clinical study of 21 patients; European Journal of Human Genetics; (2018).
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Chromosome and Gene Anomalies ; The Merck Manual of Diagnosis and Therapy 20th Edition; (2018).
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Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders; Genome medicine; (2017).
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A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations; American Journal of Human Genetics; (2017).
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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).
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Maternal uniparental disomy of chromosome 20: A novel imprinting disorder of growth failure; Genetics in Medicine; (2016).
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Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations; Journal of Neuropathology and Experimental Neurology; (2014).
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- English