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| 37181330 | Cloud-based biomedical data storage and analysis for genomic research: Landscape analysis of data governance in emerging NIH-supported platforms. | HGG Adv | 2023 |
| 36483158 | Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos. | HGG Adv | 2022 |
| 36119389 | Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program. | Cell Genom | 2022 |
| 36055210 | Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience. | Am J Hum Genet | 2022 |
| 34720558 | Consent for Use of Genetic Data among US Hispanics/Latinos: Results from the Hispanic Community Health Study/ Study of Latinos. | Ethn Dis | 2021 |
| 31402353 | Who's on third? Regulation of third-party genetic interpretation services. | Genet Med | 2020 |
| 32687560 | Recipient and donor genetic variants associated with mortality after allogeneic hematopoietic cell transplantation. | Blood advances | 2020 |
| 30431558 | Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males. | Pain | 2019 |
| 31217584 | Genetic analyses of diverse populations improves discovery for complex traits. | Nature | 2019 |
| 31204012 | Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior. | Am J Hum Genet | 2019 |
| 30510241 | Discovery of common and rare genetic risk variants for colorectal cancer. | Nat Genet | 2019 |
| 30452639 | Genomic analyses in African populations identify novel risk loci for cleft palate. | Hum Mol Genet | 2019 |
| 29411211 | "Bridge to the Literature"? Third-Party Genetic Interpretation Tools and the Views of Tool Developers. | J Genet Couns | 2018 |
| 30608210 | A content analysis of the views of genetics professionals on race, ancestry, and genetics. | AJOB Empir Bioeth | 2018 |
| 29924316 | Genome-wide association study of familial lung cancer. | Carcinogenesis | 2018 |
| 29454384 | APPLaUD: access for patients and participants to individual level uninterpreted genomic data. | Hum Genomics | 2018 |
| 29417738 | Genetic variants in sex hormone pathways and the risk of type 2 diabetes among African American, Hispanic American, and European American postmenopausal women in the US. | J Diabetes | 2018 |
| 27872059 | Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease. | Blood | 2017 |
| 28553957 | Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. | Nat Genet | 2017 |
| 26718567 | Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. | Neurology | 2016 |
| 27808206 | Geneticists should offer data to participants. | Nature | 2016 |
| 27346520 | Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). | Human Molecular Genetics | 2016 |
| 26822973 | Use of metaphors about exome and whole genome sequencing. | Am J Med Genet A | 2016 |
| 26805783 | Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans. | Am J Hum Genet | 2016 |
| 26748518 | Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos. | Am J Hum Genet | 2016 |
| 26632368 | How Metaphors About the Genome Constrain CRISPR Metaphors: Separating the "Text" From Its "Editor". | Am J Bioeth | 2015 |
| 26377959 | Exact Inference for Hardy-Weinberg Proportions with Missing Genotypes: Single and Multiple Imputation. | G3 (Bethesda) | 2015 |
| 25748358 | Characterization of large structural genetic mosaicism in human autosomes. | Am J Hum Genet | 2015 |
| 24613276 | Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participants. | Cancer Genet | 2014 |
| 24651765 | Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. | PLoS Genet | 2014 |
| 23979933 | Imputation-based genomic coverage assessments of current human genotyping arrays. | G3 (Bethesda) | 2013 |
| 23936524 | Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. | PLoS One | 2013 |
| 23912340 | Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis. | Hum Mol Genet | 2013 |
| 22037903 | Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. | Hum Genet | 2012 |
| 23259602 | Genome-wide association scan of dental caries in the permanent dentition. | BMC Oral Health | 2012 |
| 23052040 | GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies. | Bioinformatics | 2012 |
| 22829776 | A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation. | PLoS Genet | 2012 |
| 22658725 | Is 'forward' the same as 'plus'?⿦and other adventures in SNP allele nomenclature. | Trends Genet | 2012 |
| 22561516 | Detectable clonal mosaicism from birth to old age and its relationship to cancer. | Nat Genet | 2012 |
| 22065088 | Branched-chain amino acid levels are associated with improvement in insulin resistance with weight loss. | Diabetologia | 2012 |
| 21298289 | Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. | Hum Genet | 2011 |
| 22384361 | Genome-wide association analysis of ischemic stroke in young adults. | G3 (Bethesda) | 2011 |
| 20187133 | Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family. | Arthritis Rheum | 2010 |
| 20421368 | Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies. | Hum Mol Genet | 2010 |
| 19119412 | Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. | PLoS Genet | 2009 |
| 19403457 | A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease. | Hum Genomics | 2009 |
| 19130089 | Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis. | Hum Genet | 2009 |
| 18204052 | Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets. | Hum Mol Genet | 2008 |
| 18430236 | Genetic and functional association of FAM5C with myocardial infarction. | BMC Med Genet | 2008 |
| 18374923 | ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention. | Atherosclerosis | 2008 |