Center-Authored Papers
Filters: Author is Haessler, Jeffrey [Clear All Filters]
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2012.
HNF1B and endometrial cancer risk: results from the PAGE study.. PloS one. 7(1):e30390. Abstract
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2012.
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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
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2013.
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2013.
Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.. Carcinogenesis. 35(9):2068-73. Abstract
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2014.
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.. Human molecular genetics. 23(24):6607-15. Abstract
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2014.
Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract
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2014.
Genetic studies of body mass index yield new insights for obesity biology.. Nature. 518(7538):197-206. Abstract
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2015.
Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.. PloS one. 11(12):e0167758. Abstract
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2016.
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-wide Association Studies.. Gastroenterology. 151(2):351-363. Abstract
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2016.
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.. American journal of human genetics. 99(3):636-46. Abstract
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2016.
Discovery of novel heart rate-associated loci using the Exome Chip.. Human molecular genetics. Abstract
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2017.
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2017.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.. Nature genetics. 49(6):946-952. Abstract
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2017.
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.. PLoS genetics. 13(3):e1006678. Abstract
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2017. Doing Business with Arnold Library
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