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Jaclyn B. Murry, Ph.D.

Jaclyn B. Murry, Ph.D.

Headshot of Jaclyn B. Murry
  • Assistant Director, Cytogenetics Laboratory
  • Assistant Professor of Pathology


Jaclyn Murry is from Houston, TX where she also received her PhD from Baylor College of Medicine in the Department of Molecular and Human Genetics in 2016. Prior to that, she received a Bachelor of Science degree from Texas A&M University at College Station. After completing her PhD, Jaclyn completed her postdoctoral training at Brigham and Women's Hospital in the Laboratory for Molecular Medicine, which was followed by a Laboratory Genetics and Genomics Fellowship at the University of California, Los Angeles. She is board-certified in Laboratory Genetics and Genomics by the American Board of Medical Genetics and Genomics.

Dr. Murry joined the faculty as Assistant Professor of Pathology in July 2021, where she is serving as the Assistant Director of the Cytogenomics laboratory. Her areas of clinical expertise include cytogenetics and cytogenomics as well as molecular genetics, and her research interests include chromosomal disorders as well as the mechanisms of structural aberrations and copy number variation. more


  • Assistant Director, Cytogenetics Laboratory
  • Assistant Professor of Pathology
  • Assistant Professor of Genetic Medicine

Departments / Divisions



  • Ph.D.; Baylor College of Medicine - Houston (Texas) (2016)
  • B.Sc.; Texas A&M University (Texas) (2007)

Research & Publications

Selected Publications

Mannucci, I., Dang, N.D.P., Huber, H., Murry, JB. et al. Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders. Genome Med 13, 90 (2021)

Ceyhan-Birsoy O, Murry JB, et al. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. Am J Hum Genet. 2019 Jan 3;104(1):76-93

Murry JB, Machini K, et al. Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Cold Spring Harb Mol Case Stud. 2018 Aug 1;4(4):a002873

Murry JB, Santos XM, et al. A genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies. Fertil Steril. 2015 Feb;103(2):487-93

Ramocki MB, Bartnik M, Szafranski P, Kołodziejska KE, Xia Z, Bravo J, et al. Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems. Am J Hum Genet. 2010 Dec 10;87(6):857-65

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