DANA C. CRAWFORD, PHD

Associate Director for Population and Diversity Research

Dana Craw­ford, PhD, is Pro­fes­sor in the Department of Population and Quantitative Health Sciences and Associate Director for Population and Diversity Research in the Cleveland Insti­tute for Com­pu­ta­tional Biol­ogy. She also has a secondary appointment in the Department of Genetics and Genome Sciences. Dr. Craw­ford received her Ph.D. at Emory Uni­ver­sity in genet­ics and mol­e­c­u­lar biol­ogy in 2000 and then trained as a post-doctoral fel­low as an Epi­demic Intel­li­gence Ser­vice Offi­cer at the Cen­ters for Dis­ease Con­trol and Pre­ven­tion (2000–2002) and as a senior fel­low at the Uni­ver­sity of Washington’s Depart­ment of Genome Sci­ences (2002–2006). Prior to her most cur­rent posi­tion, Dr. Craw­ford spent eight years as tenure-track fac­ulty in the Depart­ment of Mol­e­c­u­lar Phys­i­ol­ogy and Bio­physics and Inves­ti­ga­tor in the Cen­ter for Human Genet­ics Research at Van­der­bilt Uni­ver­sity. As a genetic epi­demi­ol­o­gist at CWRU, Dr. Crawford’s broad research inter­ests include apply­ing genetic vari­a­tion data to large-scale epi­demi­o­logic and clin­i­cal cohorts to bet­ter under­stand human genotype-phenotype asso­ci­a­tions with an empha­sis on diverse populations.

Recent Publications

  1. Drouet, DE, Liu, S, Crawford, DC. Assessment of multi-population polygenic risk scores for lipid traits in African Americans. PeerJ 2023; 11 : e14910. PubMed PMID:37214096 PubMed Central PMC10198155.
  2. Cruz, LA, Bailey, JNC, Crawford, DC. Importance of Diversity in Precision Medicine: Generalizability of Genetic Associations Across Ancestry Groups Toward Better Identification of Disease Susceptibility Variants. Annu Rev Biomed Data Sci 2023; : . PubMed PMID:37196357 .
  3. Nealon, CL, Halladay, CW, Gorman, BR, Simpson, P, Roncone, DP, Canania, RL, Anthony, SA, Sawicki Rogers, LR, Leber, JN, Dougherty, JM et al.. Association Between Fuchs Endothelial Corneal Dystrophy, Diabetes Mellitus, and Multimorbidity. Cornea 2023; : . PubMed PMID:37170406 .
  4. Chen, F, Madduri, RK, Rodriguez, AA, Darst, BF, Chou, A, Sheng, X, Wang, A, Shen, J, Saunders, EJ, Rhie, SK et al.. Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. Eur Urol 2023; : . PubMed PMID:36872133 .
  5. Waksmunski, AR, Kinzy, TG, Cruz, LA, Nealon, CL, Halladay, CW, Anthony, SA, Greenberg, PB, Sullivan, JM, Wu, WC, Iyengar, SK et al.. Diversity is key for cross-ancestry transferability of glaucoma genetic risk scores in Hispanic Veterans in the Million Veteran Program. Pac Symp Biocomput 2023; 28 : 413-424. PubMed PMID:36540996 PubMed Central PMC9997528.
  6. Liu, J, Nair, V, Zhao, YY, Chang, DY, Limonte, C, Bansal, N, Fermin, D, Eichinger, F, Tanner, EC, Bellovich, KA et al.. Multi-Scalar Data Integration Links Glomerular Angiopoietin-Tie Signaling Pathway Activation With Progression of Diabetic Kidney Disease. Diabetes 2022; 71 (12): 2664-2676. PubMed PMID:36331122 PubMed Central PMC9750948.
  7. Yang, HT, Crawford, DC, Abazeed, ME. Editorial: Translating clinical genomics and health informatics into precision oncology. Front Genet 2022; 13 : 1029212. PubMed PMID:36263433 PubMed Central PMC9574329.
  8. Lutnick, B, Manthey, D, Becker, JU, Ginley, B, Moos, K, Zuckerman, JE, Rodrigues, L, Gallan, AJ, Barisoni, L, Alpers, CE et al.. A user-friendly tool for cloud-based whole slide image segmentation with examples from renal histopathology. Commun Med (Lond) 2022; 2 : 105. PubMed PMID:35996627 PubMed Central PMC9391340.
  9. Liu, S, Bush, WS, Miskimen, K, Gonzalez-Vicente, A, Bailey, JNC, Konidari, I, McCauley, JL, Sedor, JR, O'Toole, JF, Crawford, DC et al.. T-cell receptor diversity in minimal change disease in the NEPTUNE study. Pediatr Nephrol 2023; 38 (4): 1115-1126. PubMed PMID:35943576 PubMed Central PMC10037226.
  10. Waksmunski, AR, Kinzy, TG, Cruz, LA, Nealon, CL, Halladay, CW, Simpson, P, Canania, RL, Anthony, SA, Roncone, DP, Sawicki Rogers, L et al.. Glaucoma Genetic Risk Scores in the Million Veteran Program. Ophthalmology 2022; 129 (11): 1263-1274. PubMed PMID:35718050 PubMed Central PMC9997524.
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Featured Publications

Using Electronic Health Records to Generate Phenotypes for Research

Sarah A. Pendergrass and Dana C. Crawford Electronic health records contain patient-level data collected during and for clinical care. Data within the electronic health record include diagnostic billing codes, procedure codes, vital signs, laboratory test results, clinical imaging, and physician notes. With repeated clinic visits, these data are longitudinal, providing important information on disease development, […]

Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records.

Restrepo NA, Laper S, Farber-Eger E, Crawford DC. Glaucoma is a leading cause of blindness in developed countries. Primary open-angle glaucoma (POAG), the most prevalent clinical subtype of glaucoma in the United States, affects African Americans at a higher rate compared with European Americans. Risk factors identified for POAG include increased age and family history, […]

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