Publications

Crosslin D.R., Shah S.H., Nelson S.C., et al., Hauser E.R., 2009: “Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis,” Human Genetics, 125:217-229. (PMCID: PMC2759090.)

Crosslin D.R., McDavid A., Weston N., et al., Jarvik G.P., 2012: “Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network,” Human Genetics, 131(4):639-652. (PMCID: PMC3640990.)

Crosslin D.R., Carrell D.S., Burt A., et al., Jarvik G.P., 2014: “Genetic variation in the HLA region is associated with susceptibility to herpes zoster,” Genes & Immunity, 16(1):1-7. (PMCID: PMC4308645.)

Crosslin D.R., Tromp G., Burt A., et al., Jarvik G.P., 2014: “Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to Electronic Health Records” Frontiers in Genetics, 5:352, eCollection. (PMCID: PMC4220165.)

Crosslin D.R., Robertson P.D., Carrell D.S., et al., Jarvik G.P., 2015: “Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network,” Genome Medicine, 7(1):67, eCollection. (PMCID: PMC4517371.)

Stanaway I.B., Hall T.O., Rosenthal E.A., et al., Crosslin D.R. “The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype” Genet Epidemiol. 2018 Oct 8. (PMCID: PMC6375696.)

Hall T.O., Stanaway I.B., Carrell D.S., et al., Crosslin, D.R., 2018: “Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling,” Genes & Immunity, (PMCID: PMC6541537.)

Linder J., et al., Crosslin D.R., 2021: “Lessons from the eMERGE Network: Balancing genomics in discovery and in practice,” Human Genetics and Genomics Advances, 2(1).

Muenzen K.D. et al., Crosslin D.R. (2022) “Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience,” Human Genetics and Genomics Advances, 3(3).

Muenzen K.D. et al., Crosslin D.R. (2023) “Genetic variation in the regulatory region of HLA- DRB1*15:01-HLA-DRB5*01:01 confers susceptibility to Clostridioides difficile infection in European ancestry participants from the eMERGE Network,” Scientific Reports, 13, Article number: 18532.

Xian, S., Grabowska, M.E., Kullo, I.J. et al. “Transformer patient embedding using electronic health records enables patient stratification and progression analysis.” npj Digit. Med. 8, 521 (2025). https://doi.org/10.1038/s41746-025-01872-z

​​Most of Professor Crosslin’s publications can be found here at PubMed.