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Tamison Jewett, M.D.

  • Find a Pediatric Specialist
  • New Patient Appointments

    Locally

    336-716-WAKE

    Toll-free

    888-716-WAKE

  • Additional Information

    For returning patient appointments, contact the clinic directly.


Tamison Jewett, M.D.

Tamison Jewett, M.D.

Professor, Pediatrics - Medical Genetics

Center for Genomics and Personalized Medicine Research

Physician Rating

5.0 out of 5

25 Ratings
11 Comments
contactCONTACT & REFERRAL

Contact Information

Memberships

  • Am Academy Of Pediatrics

  • North Carolina Medical Genetic

  • North Carolina Pediatric Soc

  • Am Soc of Human Genetics

  • NPI: 1770567729

Clinical Interests

  • Connective Tissue Disorders, Fetal Alcohol Syndrome, Dysmorphology

Education & Training

  • B.A.

    1975 - Brown University

  • M.D.

    1984 - University of Arizona College of Medicine

  • Residency

    1987 - Pediatrics: U Arizona Affil Hospitals

  • Fellowship

    1989 - U Iowa Hosps & Clinics

Board Certifications

  • American Board of Medical Genetics and Genomics Clinical Genetics

contactRESEARCH

Research Contact Information

Research Interests

  • Eye Abnormalities, Gene Rearrangement, Congenital Abnormalities, Genes, Essential, Minor Histocompatibility Antigens

Recent Publications

  • Prevalence of fetal alcohol spectrum disorders in 4 US communities May PA, Chambers CD, Kalberg WO, Zellner J, Feldman H, Buckley D, Kopald D, Hasken JM, Xu R, Honerkamp-Smith G, Taras H, Manning MA, Robinson LK, Adam MP, Abdul-Rahman O, Vaux K, Jewett T, Elliott AJ, Kable JA, Akshoomoff N, Falk D,.. JAMA. 2018;319(5):474-482.
  • Adenocarcinoma and polyposis of the colon in a 20-year-old patient with Trisomy 13: a case report Thurtle DP, Huck MB, Zeller KA, Jewett T.. J Med Case Rep. 2018;12(1):56.
  • Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects Seong E, Insolera R, Dulovic M, Kamsteeg EJ, Trinh J, Bruggemann N, Sandford E, Li S, Ozel AB, Li JZ, Jewett T, Kievit AJA, Munchau A, Shakkottai V, Klein C, Collins C, Lohmann K, van de Warrenburg BP, Burmeister M.. Ann Neurol. 2018;83(6):1075-1088.
  • Editorial comment on: prevalence of fetal alcohol spectrum disorders in 4 US communities May PA, Chambers CD, Kalberg WO, Zellner J, Feldman H, Buckley D, Kopald D, Hasken JM, Xu R, Honerkamp-Smith G, Taras H, Manning MA, Robinson LK, Adam MP, Abdul-Rahman O, Vaux K, Jewett T, Elliott AJ, Kable JA, Akshoomoff N, Falk D,.. Obstet Gynecol Surv. 2018;73(7):385-387.
  • The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF,.. Nat Genet. 2017;49(1):36-45.
  • Juvenile muscular atrophy of the distal upper extremities associated with X-linked periventricular heterotopia with features of Ehlers-Danlos syndrome Hommel AL, Jewett T, Mortenson M, Caress JB.. Muscle Nerve. 2016;54(4):794-797.
  • Updated clinical guidelines for diagnosing fetal alcohol spectrum disorders Hoyme HE, Kalberg WO, Elliott AJ, Blankenship J, Buckley D, Marais AS, Manning MA, Robinson LK, Adam MP, Abdul-Rahman O, Jewett T, Coles CD, Chambers C, Jones KL, Adnams CM, Shah PE, Riley EP, Charness ME, Warren KR, May PA.. Pediatrics. 2016;138(2):e20154256.
  • De novo mutations in SON disrupt RNA splicing of genes essential for brain development and metabolism, causing an intellectual-disability syndrome Kim JH, Shinde DN, Reijnders MR, Hauser NS, Belmonte RL, Wilson GR, Bosch DG, Bubulya PA, Shashi V, Petrovski S, Stone JK, Park EY, Veltman JA, Sinnema M, Stumpel CT, Draaisma JM, Nicolai J, Yntema HG, Lindstrom K, de Vries BB, Jewett T,.. Am J Hum Genet. 2016;99(3):711-719.
  • Expanding the phenotype of neural crest cell disorders: hirschsprung disease in branchio-oculo-facial syndrome [abstract] Haldeman-Englert CR, Berry MN, Stamper TH, Jewett T, Argenta LC, Milunsky A.. Am J Med Genet A. 2015;167(8):1702-1703.
  • Kaufman oculocerebrofacial syndrome is caused by mutations in UBE3B and overlaps phenotypically with toriello-carey syndrome [abstract] Jewett T, Mortenson M, Grange DK.. Am J Med Genet A. 2015;167(8):1724.
  • Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations Basel-Vanagaite L, Yilmaz R, Tang S, Reuter MS, Rahner N, Grange DK, Mortenson M, Koty P, Feenstra H, Farwell Gonzalez KD, Sticht H, Boddaert N, Desir J, Anyane-Yeboa K, Zweier C, Reis A, Kubisch C, Jewett T, Zeng W, Borck G.. Hum Genet. 2014;133(7):939-949.
  • Genetics services and children with special health care needs Mendelsohn NJ, Jewett T. In: Saul RA, ed. Medical genetics in pediatric practice. Elk Grove Village (IL): American Academy of Pediatrics;2013: 61-72.
  • De novo 12;17 translocation upstream of SOX9 resulting in 46,XX testicular disorder of sex development Refai O, Friedman A, Terry L, Jewett T, Pearlman A, Perle MA, Ostrer H.. Am J Med Genet A. 2010;152A(2):422-426.

All Publications

For a listing of recent publications, refer to PubMed, a service provided by the National Library of Medicine.

For a list of earlier publications, visit the Carpenter Library Publication Search.

contactPHYSICIAN RATINGS

Doctor Ratings

The overall Patient Rating score is the average of responses to the nine questions listed below. The questions are from the Press Ganey Patient Satisfaction Survey. Responses are measured on a 1 to 5 scale, where 1 represents "very poor" and 5 represents "very good."
Press Ganey Patient Satisfaction Survey

CP concern for questions/worries
5.0
CP efforts to include in decisions
5.0
CP explanations of prob/condition
5.0
CP spoke using clear language
5.0
Friendliness/courtesy of CP
5.0
Likelihood of recommending CP
5.0
Patients' confidence in CP
5.0
Time CP spent with patient
5.0
Wait time at clinic
4.7



Patient Comments

Comments are taken from the Care Provider section of the Press Ganey Patient Satisfaction Survey. Comments are posted exactly as they are written. Comments are added weekly. To protect patient privacy and confidentiality, patient names are not included.

  • 7/24/2018

    Dr. _____ was very professional. She _____ during our discussion to thank me for my service to the country.

  • 7/24/2018

    This provider is the epitome of what doctor should be. The most attentive, "down to earth" and understanding doctor that I believe I have seen. The whole genetics team was wonderful.

  • 7/18/2018

    Dr. Jewett is wonderful; she is thorough and thoughtful.

  • 6/13/2018

    *Dr. Jewett was wonderful! So compassionate and knowledgeable. Only complaint was it took a year to have appt. scheduled, and soonest available appointment was another year out.

  • 5/29/2018

    very impressed with Dr. Jewitt and staff

  • 4/10/2018

    Excellent dr. & team!

  • 3/19/2018

    Dr. Jewett is the absolute best!

  • 1/11/2018

    *Dr. Jewett is wonderful. She is knowledgeable and an ease to talk to. I love *Dr. Jewett.

  • 11/29/2017

    Everyone was very good to us.

  • 10/29/2017

    Dr Jewett is such a great physician. She is such a kind person and an excellent patient advocate.

  • 10/12/2017

    Dr Jewett is very helpful in helping me understand my disease process. She takes her time to rmail me articles about EDS n the organ systems it can affect

contactREQUEST AN APPOINTMENT

We're sorry, Dr. Jewett is not currently accepting new patients. If you are an existing patient, you may contact the office directly at 336-716-2011.

  • Find a Pediatric Specialist
  • New Patient Appointments

    Locally

    336-716-WAKE

    Toll-free

    888-716-WAKE

  • Additional Information

    For returning patient appointments, contact the clinic directly.