Jaclyn B. Murry, Ph.D.

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

Background

Jaclyn is from Houston, TX, and received her Ph.D. from Baylor College of Medicine in the Department of Molecular and Human Genetics in 2016. Before that, she received a Bachelor of Science degree from Texas A&M University at College Station. After completing her Ph.D., Jaclyn completed her postdoctoral training at the Brigham and Women's Hospital in the Laboratory for Molecular Medicine. She then completed her Laboratory Genetics and Genomics Fellowship at the University of California, Los Angeles.

Dr. Murry joined the faculty as an 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 and the mechanisms of structural aberrations and copy number variation.

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Titles

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

Departments / Divisions

Education

Degrees

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

Research & Publications

Selected Publications

Zou, Y.S.; Morsberger, L.; Hardy, M.; Ghabrial, J.; Stinnett, V.; Murry, J.B.; Long, P.; Kim, A.; Pratilas, C.A.; Llosa, N.J.; et al. Complex/cryptic EWSR1::FLI1/ERG Gene Fusions and 1q Jumping Translocation in Pediatric Ewing Sarcomas. Genes 2023, 14, 1139. https://doi.org/10.3390/genes14061139

Bi W, Yuan B, Liu P, Murry JB, Qin X, Xia F, Quach T, Cooper LM, Wiszniewska J, Hixson P, Peacock S, Tonk VS, Huff RW, Ortega V, Lupski JR, Scherer SE, Littlejohn RO, Velagaleti GVN, Roeder ER, Cheung SW. Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences. J Med Genet. 2023 Jun;60(6):547-556. doi: 10.1136/jmg-2022-108586. Epub 2022 Sep 23. PMID: 36150828

Murry JB, Zou YS. Live-Born Double Aneuploidy at the Johns Hopkins Cytogenomics Laboratory: Case Report and Review of the Literature. OBM Genetics 2022; 6(4): 168; doi:10.21926/obm.genet.2204168

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

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

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