Tanya Noelle Eble, M.S., C.G.C.

Assistant Professor

(713) 798-8321

Request Clinical Appointment

Email

teble@bcm.edu

Positions

Assistant Professor: Mol. & Human Gen./Clinic. Prgm
Baylor College of Medicine
Houston, TX, US

Addresses

Lee and Joe Jamail Specialty Care Center (Clinic): 1977 Butler Blvd.
Room: E5.128
Houston, TX, 77030
United States
Phone: (713) 798-8321
teble@bcm.edu

Education

MS from University Of Pittsburgh: 01/2004 - Pittsburgh, Pennsylvania, United States

BS from Pennsylvania State University: 06/2002 - State College, Pennsylvania, United States; Biology

Certifications

Certified Genetic Counselor: American Board of Genetic Counseling

Professional Interests

Adult Genetic Counseling
Cancer Genetic Counseling
Ehlers Danlos Syndrome
Medical Ethics

Professional Statement

As the manager of the adult genetics service at BCM and a certified genetic counselor I am dedicated to providing the highest level of patient care. I find great fulfillment in helping patients to better understand information about their genetic risks, testing options, diagnosis, and plans for management. I have experience with prenatal genetics, cancer genetics, and general adult genetics. I also have a keen interest in medical ethics and am an affiliated member of the BCM Center of Medical Ethics and Health Policy.

Websites

VIICTR Publications List

Adult Genetics Clinic

Department of Molecular and Human Genetics

Selected Publications

Wang X, Sutton VR, Eble TN, Lewis RA, Gunaratne P, Patel A, Van den Veyver IB. " A genome-wide screen for copy number alterations in Aicardi syndrome. " Am. J. Med. Genet. A. 2009 Oct ; 149 (10) : 2113-21.
Pubmed PMID: 19760649.
Burrage LC, Eble TN, Hixson PM, Roney EK, Cheung SW, Franco LM. " A mosaic 2q24.2 deletion narrows the critical region to a 0.4?Mb interval that includes TBR1, TANK, and PSMD14. " Am. J. Med. Genet. A. 2013 Apr ; 161 (4) : 841-4.
Pubmed PMID: 23444363.
Sutton VR, Hopkins BJ, Eble TN, Gambhir N, Lewis RA, Van den Veyver IB. " Facial and physical features of Aicardi syndrome: infants to teenagers. " Am. J. Med. Genet. A. 2005 Oct 15; 138 (3) : 254-8.
Pubmed PMID: 16158440.
Wang X, Reid Sutton V, Omar Peraza-Llanes J, Yu Z, Rosetta R, Kou YC, Eble TN, Patel A, Thaller C, Fang P, Van den Veyver IB. " Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia. " Nat. Genet.. 2007 Jul ; 39 (7) : 836-8.
Pubmed PMID: 17546030.
Fruhman G, Eble TN, Gambhir N, Sutton VR, Van den Veyver IB, Lewis RA. " Ophthalmologic findings in Aicardi syndrome. " J AAPOS. 2012 Jun ; 16 (3) : 238-41.
Pubmed PMID: 22681940.
Eble TN, Sutton VR, Sangi-Haghpeykar H, Wang X, Jin W, Lewis RA, Fang P, Van den Veyver IB. " Non-random X chromosome inactivation in Aicardi syndrome. " Hum. Genet.. 2009 Mar ; 125 (2) : 211-6.
Pubmed PMID: 19116729.
Glasmacher MA, Sutton VR, Hopkins B, Eble T, Lewis RA, Park Parsons D, Van den Veyver IB. " Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children. " J. Child Neurol.. 2007 Feb ; 22 (2) : 176-84.
Pubmed PMID: 17621479.
Bekheirnia MR, Zhang W, Eble T, Willis A, Shaibani A, Wong LJ, Scaglia F, Dhar SU. " POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria. " Gene. 2012 May 10; 499 (1) : 209-12.
Pubmed PMID: 22405928.
Eble TN, Nagamani SC, Franco LM, Plon SE, Blazo M, Dhar SU. " The practice of adult genetics: A 7-year experience from a single center. " Am. J. Med. Genet. A. 2013 Jan ; 161 (1) : 89-93.
Pubmed PMID: 23239603.

Memberships

National Society of Genetic Counselors

Texas Society of Genetic Counselors