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University of Alabama Hospital (Birmingham) Medical Genetics and Genomics/Pediatrics

Residency · Birmingham, AL

Sponsored by University of Alabama Hospital

People

Everyone 22Leadership 3Faculty 15Residents 4
  • Anna Hurst, MD, MS

    Program Directors

    Clinical genetics and genomics physician, Associate Professor at University of Alabama Hospital

    Clinical Genetics (Dysmorphology; Undiagnosed Disease Program

  • Michele Nichols, MD

    Program Directors

    Emergency physician, Vice-Chair for Academic Affairs at University of Alabama Hospital

    Injury Prevention, Community Outreach and Advocacy / Coat of Arms, Medical Education, Pediatric Emergency Medicine

  • Nathaniel Robin, MD

    Clinical Division Director

    Clinical genetics and genomics physician, Professor at University of Alabama Hospital

    Clinical Genetics (Craniofacial Genetics, Syndrome identification, Craniofacial Genetics, Medial Education

  • Akila Subramaniam, MD, MPH

    Faculty

    Clinical genetics and genomics physician, Associate Professor at University of Alabama Hospital

    Fetal ultrasound, prenatal genetic diagnosis, complicated twin pregnancies

  • Alexis Heatherly, MS

    Faculty

    Orthopaedic Surgery resident, University of Alabama Hospital

  • Amitha Ananth, MD

    Faculty

    Clinical genetics and genomics physician, Assistant Professor at University of Alabama Hospital

    Neurometabolic disorders, neurodegenerative disorders, Rett Syndrome and other childhood degenerative and genetic disorders, Neurometabolic disorders and neurodegenerative disorders.

  • Andrew Carroll, PhD

    Faculty

    Professor at University of Alabama Hospital

    Cancer cytogenetics, chromosome polymorphisms, clinical cytogenetics

  • Brian Kirmse, MD

    Faculty

    Medical genetics and genomics physician, Assistant Professor at University of Alabama Hospital

  • Bruce Korf, MD, PhD

    Faculty

    Pediatric medicine physician, Professor at University of Alabama Hospital

    Neurofibromatosis; Undiagnosed Disease Program, Neurofibromatosis type 1

  • Carley King, MD

    PGY-3

    Pediatrics resident, University of Alabama Hospital

  • Caterina Abdala-Villa, MD

    Faculty

    Clinical genetics and genomics physician, Assistant Professor at University of Alabama Hospital

  • CW
    C-H Wu, MD, PhD

    Faculty

    Clinical biochemical genetics physician at UAB Heersink School of Medicine

  • Dana Goodloe, MPH, MS

    Faculty

    Supervisor - Genetic Counselors at University of Alabama Hospital

  • Dan Sharer, PhD

    Faculty

    Associate Professor at University of Alabama Hospital

    Rare childhood metabolic disorders of carnitine and other metabolic disorders of childhood

  • Fady Mikhail, MD, PhD

    Faculty

    Medical genetics / clinical cytogenetics physician, Associate Professor at University of Alabama Hospital

    Clinical cytogenetics

  • FB
    Fallon Brewer, MS

    Faculty

    Lead Genetic Counselor at University of Alabama Hospital

  • Kiley Lawrence, MD

    PGY-2

    Pediatrics resident, University of Alabama Hospital

  • Kristin Linscott, MD, PhD

    Faculty

    Clinical biochemical genetics physician, Assistant Professor at University of Alabama Hospital

  • Lindsay Jenkins, MD

    PGY-4

    Pediatrics resident, University of Alabama Hospital

  • PL
    Pongtawat Lertwilaiwittaya, MD

    Faculty

    Clinical genetics and genomics physician, Assistant Professor at University of Alabama Hospital

  • Victoria Ourso, MD

    PGY-1

    Pediatrics resident, University of Alabama Hospital

  • Yunjia Chen, PhD, MBA

    Faculty

    Assistant Professor at University of Alabama Hospital

    Clinical cytogenetics, cancer cytogenetics, clinical molecular genetics, neurofibromatosis/schwannomatosis