Human Genetics

The Department of Human Genetics is dedicated to basic scientific research in human genetics and genetic disease, as well as the training of the next generation of scientists and health care providers.

Our faculty explore three broad areas of human genetics: molecular genetics, genetic disease, and statistical/population genetics. Within molecular genetics, research groups study DNA repair and recombination, genome instability, gene function and regulation, epigenetics, RNA modification and control, and genomic systems. Research in human genetic disease emphasizes the genetics of development, neurogenetics, stem cell biology, medical genetics, reproductive sciences, and the genetics of cancer. Evolutionary and population genetics research includes statistical tools for genetics, genetic epidemiology, and genetic mapping of complex traits and diseases.

We invite you to explore our faculty, students, graduate programs, courses, and events/seminars.

 

Featured Publications

Oprescu SN, Griffin LB, Beg AA, Antonellis A. Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations. Methods. 2017 Jan 15;113:139-151. doi: 10.1016/j.ymeth.2016.11.013. Review. PubMed PMID: 27876679 .

Huisman B, Manske G, Carney S, Kalantry S. Functional Dissection of the m6A RNA Modification. Trends Biochem Sci. 2017 Feb;42(2):85-86. doi: 10.1016/j.tibs.2016.12.004. PubMed PMID: 28063638.

Lopez-Santiago LF, Yuan Y, Wagnon JL, Hull JM, Frasier CR, O'Malley HA, Meisler MH, Isom LL. Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy. Proc Natl Acad Sci U S A. 2017 Feb 13. pii: 201616821. doi: 10.1073/pnas.1616821114. [Epub ahead of print] PubMed PMID: 28193882

Varshney A, Scott LJ, Welch RP, Erdos MR, Chines PS, Narisu N, Albanus RD, Orchard P, Wolford BN, Kursawe R, Vadlamudi S, Cannon ME, Didion JP, Hensley J, Kirilusha A; NISC Comparative Sequencing Program., Bonnycastle LL, Taylor DL, Watanabe R, Mohlke KL, Boehnke M, Collins FS, Parker SC, Stitzel ML. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes. Proc Natl Acad Sci U S A. 2017 Feb 13. pii: 201621192. doi: 10.1073/pnas.1621192114. [Epub ahead of print] PubMed PMID: 28193859

Quinonez SC, Gelehrter TD, Uhlmann WR. A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15. Am J Med Genet A. 2017 Jan;173(1):268-273. doi: 10.1002/ajmg.a.38000. PubMed PMID: 27739187

Shukla A, Upadhyai P, Shah J, Neethukrishna K, Bielas S, Girisha KM. Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literature. Eur J Med Genet. 2017 Feb;60(2):118-123. doi: 10.1016/j.ejmg.2016.11.006. PubMed PMID: 27913285

Omenn GS. The proteomes of the human eye, a highly compartmentalized organ. Proteomics. 2017 Jan;17(1-2). doi: 10.1002/pmic.201600340. PubMed PMID: 27860232.

Events

March 8, 2017
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Genetics Training Program / CMB Short Course

3:00 pm

North Lecture Hall, Medical Sciences II

"Exploring the cellular context of risk variants: neurological disorders, non-coding variation and cellular heterogeneity" by Andrew McCallion, Ph.D. (McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine)