|
| 36463326 | Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. | Int J Obes (Lond) | 2023 |
| 37601969 | Multiset correlation and factor analysis enables exploration of multi-omics data. | Cell Genom | 2023 |
| 37662416 | Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies. | bioRxiv | 2023 |
| 36463326 | Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. | Int J Obes (Lond) | 2023 |
| 37425716 | Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects. | bioRxiv | 2023 |
| 36721044 | An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling. | Commun Biol | 2023 |
| 37662416 | Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies. | bioRxiv | 2023 |
| 37601969 | Multiset correlation and factor analysis enables exploration of multi-omics data. | Cell Genom | 2023 |
| 37425716 | Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects. | bioRxiv | 2023 |
| 36721044 | An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling. | Commun Biol | 2023 |
| 35134542 | CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project. | J Mol Diagn | 2022 |
| 35134542 | CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project. | J Mol Diagn | 2022 |
| 35087136 | Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study. | Sci Rep | 2022 |
| 35346344 | Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program. | Genome Med | 2022 |
| 35346344 | Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program. | Genome Med | 2022 |
| 35087136 | Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study. | Sci Rep | 2022 |
| 34015820 | Benchmarking association analyses of continuous exposures with RNA-seq in observational studies. | Brief Bioinform | 2021 |
| 34015820 | Benchmarking association analyses of continuous exposures with RNA-seq in observational studies. | Brief Bioinform | 2021 |
| 33679876 | Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. | Front Genet | 2021 |
| 33679876 | Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. | Front Genet | 2021 |
| 30510241 | Discovery of common and rare genetic risk variants for colorectal cancer. | Nat Genet | 2019 |
| 30510241 | Discovery of common and rare genetic risk variants for colorectal cancer. | Nat Genet | 2019 |
| 30820706 | Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 30806792 | Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders. | Hum Genet | 2019 |
| 31215115 | Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. | Hum Mutat | 2019 |
| 30951678 | De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism. | Am J Hum Genet | 2019 |
| 31254090 | Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 31328417 | Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. | Birth Defects Res | 2019 |
| 31328417 | Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. | Birth Defects Res | 2019 |
| 31215115 | Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. | Hum Mutat | 2019 |
| 31254090 | Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 30951678 | De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism. | Am J Hum Genet | 2019 |
| 30806792 | Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders. | Hum Genet | 2019 |
| 30820706 | Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. | Hum Genet | 2019 |
| 29168297 | Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. | Am J Med Genet A | 2018 |
| 30537273 | Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290-300. | Am J Med Genet A | 2018 |
| 29168297 | Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. | Am J Med Genet A | 2018 |
| 29590102 | Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. | PLoS Genet | 2018 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 29805042 | Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate. | Am J Hum Genet | 2018 |
| 29805042 | Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate. | Am J Hum Genet | 2018 |
| 30537273 | Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290-300. | Am J Med Genet A | 2018 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 29590102 | Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. | PLoS Genet | 2018 |
| 26927283 | Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner. | Pharmacogenomics J | 2017 |
| 28912365 | D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study. | Arterioscler Thromb Vasc Biol | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28332277 | Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder. | Am J Med Genet B Neuropsychiatr Genet | 2017 |
| 29257133 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2017 |
| 29161273 | Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data. | PLoS One | 2017 |