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| 36809323 | Association of African Ancestry-Specific APOE Missense Variant R145C With Risk of Alzheimer Disease. | JAMA | 2023 |
| 36778409 | X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease. | | 2023 |
| 37333771 | Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. | HGG Adv | 2023 |
| 34553764 | Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative. | Hum Mol Genet | 2022 |
| 35385699 | Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. | Am J Hum Genet | 2022 |
| 35917738 | Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort. | Parkinsonism and Related Disorders | 2022 |
| 32972274 | Maternal-fetal genetic interactions, imprinting, and risk of placental abruption. | Journal of Maternal-Fetal and Neonatal Medicine | 2022 |
| 34798387 | Sleep problems and risk of cancer incidence and mortality in an older cohort: The Cardiovascular Health Study (CHS). | Cancer Epidemiology | 2022 |
| 35034197 | Associating sleep problems with advanced cancer diagnosis, and immune checkpoint treatment outcomes: a pilot study. | Supportive Care in Cancer | 2022 |
| 34670813 | Genome-Wide Admixture Mapping of Estimated Glomerular Filtration Rate and Chronic Kidney Disease Identifies European and African Ancestry-of-Origin Loci in Hispanic and Latino Individuals in the United States. | J Am Soc Nephrol | 2022 |
| 34582791 | Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 33910371 | Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants. | Arteriosclerosis, Thrombosis, and Vascular Biology | 2021 |
| 33632714 | In Vivo Functional Effects of a Novel and Common Variant in the Yup'ik Alaska Native Population. | Drug Metabolism and Disposition | 2021 |
| 34227697 | Characterizing the Genetic Architecture of Parkinson's Disease in Latinos. | Annals of Neurology | 2021 |
| 34217363 | Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics. | Alzheimers Res Ther | 2021 |
| 34270706 | Genome-wide association study in the Taiwan Biobank identifies four novel genes for human height: NABP2, RASA2, RNF41 and SLC39A5. | Human Molecular Genetics | 2021 |
| 33567186 | Embracing Genetic Diversity to Improve Black Health. | New England Journal of Medicine | 2021 |
| 33503331 | Characterization of CYP3A pharmacogenetic variation in American Indian and Alaska Native communities, targeting CYP3A4*1G allele function. | Clin Transl Sci | 2021 |
| 33150996 | Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients. | Movement Disorders | 2021 |
| 32966694 | Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women. | Alzheimers Dement | 2021 |
| 33418499 | Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. | EBioMedicine | 2021 |
| 34520119 | Nicotine metabolism and its association with CYP2A6 genotype among Indigenous people in Alaska who smoke. | Clinical and Translational Science | 2021 |
| 34658056 | REHE: Fast variance components estimation for linear mixed models. | Genetic Epidemiology | 2021 |
| 34706549 | Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults. | Circ Genom Precis Med | 2021 |
| 31536170 | Interrogation of CYP2D6 Structural Variant Alleles Improves the Correlation Between CYP2D6 Genotype and CYP2D6-Mediated Metabolic Activity. | Clin Transl Sci | 2020 |
| 32240245 | Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans. | PLoS One | 2020 |
| 31985870 | Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African Americans. | J Thromb Haemost | 2020 |
| 32797036 | On the cross-population generalizability of gene expression prediction models. | PLoS Genet | 2020 |
| 30773276 | Genome-wide Significance Thresholds for Admixture Mapping Studies. | American Journal of Human Genetics | 2019 |
| 31869403 | Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. | PLoS Genet | 2019 |
| 31606368 | Local ancestry at APOE modifies Alzheimer's disease risk in Caribbean Hispanics. | Alzheimers Dement | 2019 |
| 30403821 | Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans. | Hum Mol Genet | 2019 |
| 30368908 | Generalizing polygenic risk scores from Europeans to Hispanics/Latinos. | Genetic Epidemiology | 2019 |
| 31040861 | New Genetic Loci Associated With Chronic Kidney Disease in an Indigenous Australian Population. | Front Genet | 2019 |
| 30821933 | VKORC1 and Novel CYP2C9 Variation Predict Warfarin Response in Alaska Native and American Indian People. | Clin Transl Sci | 2019 |
| 31217584 | Genetic analyses of diverse populations improves discovery for complex traits. | Nature | 2019 |
| 31251759 | GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations. | PLoS One | 2019 |
| 31001318 | Accuracy of Gene Expression Prediction From Genotype Data With PrediXcan Varies Across and Within Continental Populations. | Frontiers in Genetics | 2019 |
| 31329242 | Genetic association testing using the GENESIS R/Bioconductor package. | | 2019 |
| 29590102 | Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. | PLoS Genet | 2018 |
| 29045054 | Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease. | Genes Brain Behav | 2018 |
| 29884306 | Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies. | Placenta | 2018 |
| 30194050 | Abruptio placentae risk and genetic variations in mitochondrial biogenesis and oxidative phosphorylation: replication of a candidate gene association study. | American Journal of Obstetrics and Gynecology | 2018 |
| 29862559 | Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. | Genet Epidemiol | 2018 |
| 30569016 | Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. | Neurol Genet | 2018 |
| 29094808 | Dietary Vitamin K and Association with Hepatic Vitamin K Status in a Yup'ik Study Population from Southwestern Alaska. | Molecular Nutrition and Food Research | 2018 |
| 29486463 | Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. | Dement Geriatr Cogn Disord | 2018 |
| 29343609 | Polymorphic Human Sulfotransferase 2A1 Mediates the Formation of 25-Hydroxyvitamin D<sub>3</sub>-3-<i>O</i>-Sulfate, a Major Circulating Vitamin D Metabolite in Humans. | Drug Metab Dispos | 2018 |
| 29436156 | Cytochrome P450 Genetic Variation Associated with Tamoxifen Biotransformation in American Indian and Alaska Native People. | Clin Transl Sci | 2018 |
| 29602798 | Hepatic Abundance and Activity of Androgen- and Drug-Metabolizing Enzyme UGT2B17 Are Associated with Genotype, Age, and Sex. | Drug Metab Dispos | 2018 |