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| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37582364 | Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma. | Cell Metab | 2023 |
| 36713248 | Beyond the exome: what's next in diagnostic testing for Mendelian conditions. | ArXiv | 2023 |
| 37278509 | Enhanced Quantum Anomalous Hall Effect with an Active Capping Layer. | | 2023 |
| 36960714 | Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program. | Circ Genom Precis Med | 2023 |
| 37192819 | Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research. | J Am Med Inform Assoc | 2023 |
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| 34814699 | Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. | Circulation | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 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 |
| 35501457 | Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program. | Commun Biol | 2022 |
| 36070237 | Superconducting Fourfold Fe(Te,Se) Film on Sixfold Magnetic MnTe via Hybrid Symmetry Epitaxy. | Nano Letters | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 34855941 | Association of clonal hematopoiesis with chronic obstructive pulmonary disease. | Blood | 2022 |
| 34553764 | Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative. | Hum Mol Genet | 2022 |
| 34582791 | Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34265206 | Spacer-Layer-Tunable Magnetism and High-Field Topological Hall Effect in Topological Insulator Heterostructures. | Nano Letters | 2021 |
| 34214102 | Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. | PLoS One | 2021 |
| 34087167 | Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34337551 | BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion. | HGG Adv | 2021 |
| 34319741 | Hybrid Symmetry Epitaxy of the Superconducting Fe(Te,Se) Film on a Topological Insulator. | Nano Letters | 2021 |
| 33038041 | JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation. | Genet Epidemiol | 2021 |
| 33231305 | Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program. | Transfusion | 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 |
| 34868058 | A Model of Minor Histocompatibility Antigens in Allogeneic Hematopoietic Cell Transplantation. | Front Immunol | 2021 |
| 33057025 | Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants. | Nat Commun | 2020 |
| 31883642 | Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. | Am J Hum Genet | 2020 |
| 31665830 | Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico. | Pediatr Pulmonol | 2020 |
| 32459537 | Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth. | Am J Respir Crit Care Med | 2020 |
| 32327564 | Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand <i>KITLG/SCF</i> and Gene-By-Air-Pollution Interaction. | Genetics | 2020 |
| 31259439 | Quantum-Hall to Insulator Transition in Ultra-Low-Carrier-Density Topological Insulator Films and a Hidden Phase of the Zeroth Landau Level. | Advanced Materials | 2019 |
| 31564435 | Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. | Am J Hum Genet | 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 |
| 32454741 | Intrinsic Stability Study and Forced Degradation Profiling of Olopatadine Hydrochloride by RP-HPLC-DAD-HRMS Method. | | 2019 |
| 30452639 | Genomic analyses in African populations identify novel risk loci for cleft palate. | Hum Mol Genet | 2019 |
| 30431558 | Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males. | Pain | 2019 |
| 31185718 | Record High-Proximity-Induced Anomalous Hall Effect in (BiSb)Te Thin Film Grown on CrGeTe Substrate. | Nano Letters | 2019 |
| 31388106 | Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. | Sci Rep | 2019 |
| 29590102 | Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease. | PLoS Genet | 2018 |
| 30390057 | Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. | Nat Genet | 2018 |
| 30141273 | Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts. | Mol Genet Genomic Med | 2018 |
| 28081371 | GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos. | J Dent Res | 2017 |
| 28453575 | Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. | PLoS Genet | 2017 |
| 28334935 | Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? | Human Molecular Genetics | 2017 |
| 28374190 | A genome-wide study of Hardy-Weinberg equilibrium with next generation sequence data. | Hum Genet | 2017 |
| 28610988 | Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. | Heart Rhythm | 2017 |
| 28158719 | Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. | Human Molecular Genetics | 2017 |
| 27668658 | Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. | Nat Genet | 2016 |
| 27018472 | A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. | Am J Hum Genet | 2016 |