publication venue for
- Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity.. 109:223-239. 2022
- Genetic control of the human brain proteome.. 108:400-410. 2021
- The Genetic Landscape of Diamond-Blackfan Anemia.. 104:-. 2019
- The Genetic Landscape of Diamond-Blackfan Anemia.. 103:930-947. 2018
- Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function.. 103:100-114. 2018
- A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.. 102:375-400. 2018
- Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.. 100:51-63. 2016
- Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.. 99:56-75. 2016
- Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.. 96:695-708. 2015
- A novel test for recessive contributions to complex diseases implicates Bardet-Biedl syndrome gene BBS10 in idiopathic type 2 diabetes and obesity.. 95:509-20. 2014
- Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.. 95:183-93. 2014
- GeMes, clusters of DNA methylation under genetic control, can inform genetic and epigenetic analysis of disease.. 94:485-95. 2014
- An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases.. 94:437-52. 2014
- Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.. 94:223-32. 2014
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.. 94:233-45. 2014
- Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.. 93:1035-45. 2013
- Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.. 93:545-54. 2013
- Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.. 93:398-404. 2013
- Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.. 91:823-38. 2012
- A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.. 91:202-8. 2012
- Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.. 86:229-39. 2010
- Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.. 80:650-63. 2007
- A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.. 75:436-47. 2004
- Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics.. 70:237-43. 2001
- Relative risk of Alzheimer disease and age-at-onset distributions, based on APOE genotypes among elderly African Americans, Caucasians, and Hispanics in New York City.. 58:574-84. 1996