Rex L. Chisholm

Affiliations: 
Northwestern University, Evanston, IL 
Area:
Cell Biology
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"Rex Chisholm"
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Pottinger TD, Puckelwartz MJ, Pesce LL, et al. (2020) Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants. Journal of the American Heart Association. 9: e013808
Manolio TA, Rowley R, Williams MS, et al. (2019) Opportunities, resources, and techniques for implementing genomics in clinical care. Lancet (London, England)
Rasmussen LV, Smith ME, Almaraz F, et al. (2019) An ancillary genomics system to support the return of pharmacogenomic results. Journal of the American Medical Informatics Association : Jamia
Stanaway IB, Hall TO, Rosenthal EA, et al. (2018) The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype. Genetic Epidemiology
Manolio TA, Fowler DM, Starita LM, et al. (2017) Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 169: 6-12
Simonti CN, Vernot B, Bastarache L, et al. (2016) The phenotypic legacy of admixture between modern humans and Neandertals. Science (New York, N.Y.). 351: 737-41
Bush WS, Crosslin DR, Obeng AO, et al. (2016) Genetic Variation among 82 Pharmacogenes: the PGRN-Seq data from the eMERGE Network. Clinical Pharmacology and Therapeutics
Van Driest SL, Wells QS, Stallings S, et al. (2016) Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records. Jama. 315: 47-57
Basu S, Fey P, Jimenez-Morales D, et al. (2015) dictyBase 2015: Expanding data and annotations in a new software environment. Genesis (New York, N.Y. : 2000)
Manolio TA, Abramowicz M, Al-Mulla F, et al. (2015) Global implementation of genomic medicine: We are not alone. Science Translational Medicine. 7: 290ps13
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