Center-Authored Papers

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2012
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, Carlson C, Carty C, Crawford DC, Haessler J, Hindorff LA et al..  2012.  Genotype Imputation of MetabochipSNPs Using a Study-Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women's Health Initiative.. Genetic epidemiology. 36(2):107-17. Abstract
Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, Nalls MA, Zhang G, Franceschini N, Fox K, Lange EM et al..  2012.  Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project.. American journal of human genetics. 91(5):794-808. Abstract
2013
Duan Q, Liu EY, Auer PL, Zhang G, Lange EM, Jun G, Bizon C, Jiao S, Buyske S, Franceschini N et al..  2013.  Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.. Bioinformatics (Oxford, England). 29(21):2744-9. Abstract
Coram MA, Duan Q, Hoffmann TJ, Thornton T, Knowles JW, Johnson NA, Ochs-Balcom HM, Donlon TA, Martin LW, Eaton CB et al..  2013.  Genome-wide Characterization of Shared and Distinct Genetic Components that Influence Blood Lipid Levels in Ethnically Diverse Human Populations.. American journal of human genetics. 92(6):904-916. Abstract
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A et al..  2013.  Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.. American journal of human genetics. 93(3):545-54. Abstract
2014
Franceschini N, Hu Y, Reiner AP, Buyske S, Nalls M, Yanek LR, Li Y, Hindorff LA, Cole SA, Howard BV et al..  2014.  Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.. PloS one. 9(12):e113203. Abstract
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang Z-Z, Bizon C, Lange EM, Smith JD, Turner EH et al..  2014.  Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.. American journal of human genetics. 94(2):233-45. Abstract
2015
Lanktree MB, Elbers CC, Li Y, Zhang G, Duan Q, Karczewski KJ, Guo Y, Tragante V, North KE, Cushman M et al..  2015.  Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration.. Journal of lipid research. Abstract
Coram MA, Candille SI, Duan Q, Chan KHK, Li Y, Kooperberg C, Reiner AP, Tang H.  2015.  Leveraging Multi-ethnic Evidence for Mapping Complex Traits in Minority Populations: An Empirical Bayes Approach.. American journal of human genetics. 96(5):740-52. Abstract
2016
Noordam R, Sitlani CM, Avery CL, Stewart JD, Gogarten SM, Wiggins KL, Trompet S, Warren HR, Sun F, Evans DS et al..  2016.  A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.. Journal of medical genetics. Abstract
Naik RP, Wilson JG, Ekunwe L, Mwasongwe S, Duan Q, Li Y, Correa A, Reiner AP.  2016.  Elevated D-dimer levels in African Americans with sickle cell trait.. Blood.
2017
Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu Y, Auer PL et al..  2017.  Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.. PLoS genetics. 13(4):e1006760. Abstract
Ng MCY, Graff M, Lu Y, Justice AE, Mudgal P, Liu C-T, Young K, Yanek LR, Feitosa MF, Wojczynski MK et al..  2017.  Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African ancestry anthropometry genetics consortium.. PLoS genetics. 13(4):e1006719. Abstract
Christophersen IE, Magnani JW, Yin X, Barnard J, Weng L-C, Arking DE, Niemeijer MN, Lubitz SA, Avery CL, Duan Q et al..  2017.  Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.. Circulation. Cardiovascular genetics. 10(4) Abstract
Quach A, Levine ME, Tanaka T, Lu AT, Chen BH, Ferrucci L, Ritz B, Bandinelli S, Neuhouser ML, Beasley JM et al..  2017.  Epigenetic clock analysis of diet, exercise, education, and lifestyle factors.. Aging. Abstract
Martin JS, Xu Z, Reiner AP, Mohlke KL, Sullivan P, Ren B, Hu M, Li Y.  2017.  HUGIn: Hi-C Unifying Genomic Interrogator.. Bioinformatics (Oxford, England). Abstract
Gondalia R, Avery CL, Napier MD, Méndez-Giráldez R, Stewart JD, Sitlani CM, Li Y, Wilhelmsen KC, Duan Q, Roach J et al..  2017.  Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation.. Environmental health perspectives. 125(6):067002. Abstract
Kerr KF, Avery CL, Lin HJ, Raffield LM, Zhang QS, Browning BL, Browning SR, Conomos MP, Gogarten SM, Laurie CC et al..  2017.  Genome-wide Association Study of Heart Rate and Its Variability in Hispanic/Latino Cohorts.. Heart rhythm. Abstract
Nolte IM, Munoz LM, Tragante V, Amare AT, Jansen R, Vaez A, von der Heyde B, Avery CL, Bis JC, Dierckx B et al..  2017.  Genetic loci associated with heart rate variability and their effects on cardiac disease risk.. Nature communications. 8:15805. Abstract