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Author Details

Jeffrey R O'Connell
University of Maryland School of Medicine
1995
215
67
PMIDPaper TitleJournal TitlePublished Year
36897019SLEMM: million-scale genomic predictions with window-based SNP weighting.Bioinformatics2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37719713Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease.Front Genet2023
37709864Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.Nat Genet2023
36897019SLEMM: million-scale genomic predictions with window-based SNP weighting.Bioinformatics2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37719713Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease.Front Genet2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37709864Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.Nat Genet2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
35393526An Amish founder population reveals rare-population genetic determinants of the human lipidome.Commun Biol2022
35652341Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.Hypertension2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
36220816Whole genome sequence analysis of blood lipid levels in >66,000 individuals.Nat Commun2022
35685441Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort.Front Genet2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
35119614Distribution of 54 polygenic risk scores for common diseases in long lived individuals and their offspring.Geroscience2022
35652341Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.Hypertension2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35393526An Amish founder population reveals rare-population genetic determinants of the human lipidome.Commun Biol2022
35685441Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort.Front Genet2022
36220816Whole genome sequence analysis of blood lipid levels in >66,000 individuals.Nat Commun2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
35119614Distribution of 54 polygenic risk scores for common diseases in long lived individuals and their offspring.Geroscience2022
33189290Major quantitative trait loci influencing milk production and conformation traits in Guernsey dairy cattle detected on Bos taurus autosome 19.J Dairy Sci2021
33859359Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.Mol Psychiatry2021
33856023Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction.Hum Mol Genet2021
34230475Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.Nat Commun2021
33793566Baseline cardiometabolic profiles and SARS-CoV-2 infection in the UK Biobank.PLoS One2021
33846329Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.Nat Commun2021
34214102Identification 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 One2021
33887194Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
33650257Genetic versus stress and mood determinants of sleep in the Amish.Am J Med Genet B Neuropsychiatr Genet2021
34337551BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion.HGG Adv2021
34183656A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.Nat Commun2021
33189290Major quantitative trait loci influencing milk production and conformation traits in Guernsey dairy cattle detected on Bos taurus autosome 19.J Dairy Sci2021
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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