McGovern Medical School

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

Academic Office
713-500-7350


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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. Nguyen J, Lemons J, Crandell S, Northrup H. Efficacy of medical genetics rotation during pediatric training. Genet Med. 2016 Feb;18(2):199-202. doi: 10.1038/gim.2015.65. Epub 2015 May 14. PMID: 25973883.

 

  1. Farach LS, Northrup H. KIAA2022 Nonsense Mutation in a Symptomatic Female. Am J Med Genet A. 2016 Mar;170(3):703-6. doi: 10.1002/ajmg.a.37479. Epub 2015 Nov 17. PMID:26576034.

 

  1. Lalani SR, Liu P, Rosenfeld JA, Watkin LB, Chiang T, Leduc MS, Zhu W, Ding Y, Pan S, Vetrini F, Miyake CY, Shinawi M, Gambin T, Eldomery MK, Akdemir ZH, Emrick L, Wilnai Y, Schelley S, Koenig MK, Memon N, Farach LS, Coe BP, Azamian M, Hernandez P, Zapata G, Jhangiani SN, Muzny DM, Lotze T, Clark G, Wilfong A, Northrup H, Adesina A, Bacino CA, Scaglia F, Bonnen PE, Crosson J, Duis J, Maegawa GH, Coman D, Inwood A, McGill J, Boerwinkle E, Graham B, Beaudet A, Eng CM, Hanchard NA, Xia F, Orange JS, Gibbs RA, Lupski JR, Yang Y. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. Am J Hum Genet. 2016 Feb 4;98(2):347-57. doi: 10.1016/j.ajhg.2015.12.008. Epub 2016 Jan 21. PMID:26805781

 

  1. Fountain MD, Aten E, Cho MT, Juusola J, Walkiewicz MA, Ray JW, Xia F, Yang Y, Graham BH, Bacino CA, Potocki L, van Haeringen A, Ruivenkamp CA, Mancias P, Northrup H, Kukolich MK, Weiss MM, van Ravenswaaij-Arts CM, Mathijssen IB, Levesque S, Meeks N, Rosenfeld JA, Lemke D, Hamosh A, Lewis SK, Race S, Stewart LL, Hay B, Lewis AM, Guerreiro RL, Bras JT, Martins MP, Derksen-Lubsen G, Peeters E, Stumpel C, Stegmann S, Bok LA, Santen GW, Schaaf CP. The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families.  Genet Med. 2016 May 19. doi: 10.1038/gim.2016.53. [Epub ahead of print] PMID:27195816

 

  1. Sahin M, Henske EP, Manning BD, Ess KC, Bissler JJ, Klann E, Kwiatkowski DJ, Roberds SL, Silva AJ, Hillaire-Clarke CS, Young LR, Zervas M, Mamounas LA; Tuberous Sclerosis Complex Working Group to Update the Research Plan. Advances and Future Directions for Tuberous Sclerosis Complex Research: Recommendations From the 2015 Strategic Planning Conference. Pediatr Neurol. 2016 Apr 2. doi: 10.1016/j.pediatrneurol.2016.03.015. [Epub ahead of print] PMID:27267556