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Andrew T. DeWan

Affiliations: 
Chronic Disease Epidemiology Yale University, New Haven, CT 
Area:
Epidemiology, Genetics
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"Andrew DeWan"
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Linlu Zhao grad student 2012 Yale

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Cahill ME, Loeb M, Dewan AT, et al. (2020) In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease. Vaccines. 8
Rogne T, Damås JK, Solligård E, et al. (2020) Genome-Wide Linkage Analysis of the Risk of Contracting a Bloodstream Infection in 47 Pedigrees Followed for 23 Years Assembled From a Population-Based Cohort (the HUNT Study). Critical Care Medicine
Salinas YD, Wang Z, DeWan AT. (2020) Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2. American Journal of Epidemiology
Rogne T, Damås JK, Flatby HM, et al. (2020) The Role of FER rs4957796 in the Risk of Developing and Dying from a Bloodstream Infection: A 23-Year Follow-up of the Population-based Nord-Trøndelag Health Study. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America
Streicher SA, Klein AP, Olson SH, et al. (2020) A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population. Human Genetics
Brown AL, de Smith AJ, Gant VU, et al. (2019) Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. Blood
de Smith AJ, Walsh KM, Morimoto LM, et al. (2019) Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. Leukemia
Spector LG, DeWan AT, Pankratz ND, et al. (2019) Race/ethnicity, socioeconomic position, and childhood acute lymphoblastic leukemia. American Journal of Epidemiology
Monin JK, Goktas SO, Kershaw T, et al. (2019) Associations between spouses' oxytocin receptor gene polymorphism, attachment security, and marital satisfaction. Plos One. 14: e0213083
He Z, DeWan AT, Leal SM. (2018) MendelProb: Probability and sample size calculations for Mendelian studies of exome and whole genome sequence data. Bioinformatics (Oxford, England)
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