UTHealth Medical School

hope-northrup
Contact Info
Hope.Northrup@uth.tmc.edu

Academic Office
713-500-5760


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Professor,
Director, Division of Medical Genetics

Education & Background

Graduate School
Medical University of South Carolina
Charleston, South Carolina
1983
Residency
Children’s Medical Center Southwestern Medical School
Dallas, Texas
1983-1986
Fellowship
Institute for Molecular Genetics (now Department of Molecular and Human Genetics) Baylor College of Medicine
Houston, Texas
1986-1989

Certifications

American Academy of Pediatrics, 1988 (permanent certificate)
American Board of Medical Genetics (Biochemical, Clinical, and Molecular), 1990


Publications

 

  1. Soler-Alfonso C, Enns GM, Koenig MK, Saavedra H, Northrup H. Identification of HIBCH gene mutations causing autosomal recessive Leigh syndrome: A unique gene involved in valine metabolism. Pediatric Neurology. 2015 Mar, 52(3): 361-5. PMID: 25591832.

 

  1. Nguyen J, Lemons J, Crandell S, Northrup H. Efficacy of medical genetics rotation during pediatric training. Genet Med. 2015 May 14. PMID: 25973883

 

  1. Ruggiero J, Northrup H, Au KS. Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotype. Birth Defects Res Part A. 2015 Jun: 103(6): 479-87. PMID: 25776730.

 

  1. Wu JY, Peters JM, Goyal M, Krueger D, Sahin M, Northrup H, Au KS, Cutter G, Bebin EM. Clinical Electroencephalographic Biomarker for Impending Epilepsy in Asymptomatic Tuberous Sclerosis Complex Infants. Pediat Neurol. 2015 Sept. pii: S0887-8995(15) 30076-X. [Epub ahead of print] PMID: 26498039.

 

  1. Farach, LS, Northrup H. KIAA2022 nonsense mutation in a symptomatic female. Am J Med Genet A. 2015 Nov 17. doi: 10.1002/ajmg.a.37479. [Epub ahead of print] PMID: 26576034