Center-Authored Papers

Filters: Author is Haessler, Jeff  [Clear All Filters]
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Zhou Y, Nair B, Shaughnessy JD, Cartron M-A, Haessler J, Anaissie E, van Rhee F, Crowley J, Barlogie B.  2009.  Cytogenetic abnormalities in multiple myeloma: poor prognosis linked to concomitant detection in random and focal lesion bone marrow samples and associated with high-risk gene expression profile.. British journal of haematology. 145(5):637-41. Abstract
Zheng H-F, Forgetta V, Hsu Y-H, Estrada K, Rosello-Diez A, Leo PJ, Dahia CL, Park-Min KH, Tobias JH, Kooperberg C et al..  2015.  Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.. Nature. 526(7571):112-7. Abstract
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Taylor KC, Carty CL, Dumitrescu L, Bůžková P, Cole SA, Hindorff L, Schumacher FR, Wilkens LR, Shohet RV, Quibrera MP et al..  2013.  Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study.. BMC genetics. 14:33. Abstract
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Shaughnessy JD, Zhou Y, Haessler J, van Rhee F, Anaissie E, Nair B, Waheed S, Alsayed Y, Epstein J, Crowley J et al..  2009.  TP53 deletion is not an adverse feature in multiple myeloma treated with total therapy 3.. British journal of haematology. 147(3):347-51. Abstract
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Peters U, North KE, Sethupathy P, Buyske S, Haessler J, Jiao S, Fesinmeyer MD, Jackson RD, Kuller LH, Rajkovic A et al..  2013.  A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study.. PLoS genetics. 9(1):e1003171. Abstract
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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
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Haiman CA, Fesinmeyer MD, Spencer KL, Buzková P, Voruganti SV, Wan P, Haessler J, Franceschini N, Monroe KR, Howard BV et al..  2012.  Consistent Directions of Effect for Established Type 2 Diabetes Risk Variants Across Populations: The Population Architecture using Genomics and Epidemiology (PAGE) Consortium.. Diabetes. 61(6):1642-1647. Abstract
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Graff M, Gordon-Larsen P, Lim U, Fowke JH, Love S-A, Fesinmeyer M, Wilkens LR, Vertilus S, Ritchie MD, Prentice RL et al..  2013.  The Influence of Obesity-Related Single Nucleotide Polymorphisms on BMI Across the Life Course: The PAGE Study.. Diabetes. 62(5):1763-7. Abstract
Gong J, Schumacher F, Lim U, Hindorff LA, Haessler J, Buyske S, Carlson CS, Rosse S, Bůžková P, Fornage M et al..  2013.  Fine Mapping and Identification of BMI Loci in African Americans.. American journal of human genetics. 93(4):661-71. Abstract
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Franceschini N, Carty CL, Lu Y, Tao R, Sung YJ, Manichaikul A, Haessler J, Fornage M, Schwander K, Zubair N et al..  2016.  Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.. PloS one. 11(10):e0164132. Abstract
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Dumitrescu L, Carty CL, Franceschini N, Hindorff LA, Cole SA, Bůžková P, Schumacher FR, Eaton CB, Goodloe RJ, Duggan DJ et al..  2013.  Post-Genome-Wide Association Study Challenges for Lipid Traits: Describing Age as a Modifier of Gene-Lipid Associations in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.. Annals of human genetics. 77(5):416-25. Abstract
Dumitrescu L, Carty CL, Taylor K, Schumacher FR, Hindorff LA, Ambite JL, Anderson G, Best LG, Brown-Gentry K, Bůžková P et al..  2011.  Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.. PLoS genetics. 7(6):e1002138. Abstract
Dumitrescu L, Carty CL, Franceschini N, Hindorff LA, Cole SA, Bůžková P, Schumacher FR, Eaton CB, Goodloe RJ, Duggan DJ et al..  2013.  No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.. Human genetics. 132(12):1427-31. Abstract
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Carty CL, Bhattacharjee S, Haessler J, Cheng I, Hindorff LA, Aroda V, Carlson CS, Hsu C-N, Wilkens L, Liu S et al..  2014.  Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study.. Circulation. Cardiovascular genetics. Abstract
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Bartel TB, Haessler J, Brown TLY, Shaughnessy JD, van Rhee F, Anaissie E, Alpe T, Angtuaco E, Walker R, Epstein J et al..  2009.  F18-fluorodeoxyglucose positron emission tomography in the context of other imaging techniques and prognostic factors in multiple myeloma.. Blood. 114(10):2068-76. Abstract
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Auer PL, Teumer A, Schick U, O'Shaughnessy A, Lo KS, Chami N, Carlson C, de Denus S, Dubé M-P, Haessler J et al..  2014.  Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.. Nature genetics. 46(6):629-34. Abstract