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Author Details
Full Name
Jeffrey R O'Connell
Affiliation
University of Maryland School of Medicine
ORCID
Career Start Year
1995
Papers
215
H Index
67
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36897019
SLEMM: million-scale genomic predictions with window-based SNP weighting.
Bioinformatics
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37662265
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.
medRxiv
2023
37802043
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
2023
37719713
Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease.
Front Genet
2023
37709864
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.
Nat Genet
2023
36897019
SLEMM: million-scale genomic predictions with window-based SNP weighting.
Bioinformatics
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
37126548
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Sci Adv
2023
37046083
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
2023
37425772
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
medRxiv
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37719713
Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease.
Front Genet
2023
37802043
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
2023
37709864
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.
Nat Genet
2023
37662265
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.
medRxiv
2023
37425772
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
medRxiv
2023
37126548
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Sci Adv
2023
37046083
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
34553764
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
2022
35393526
An Amish founder population reveals rare-population genetic determinants of the human lipidome.
Commun Biol
2022
35652341
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Hypertension
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
36220816
Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
Nat Commun
2022
35685441
Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort.
Front Genet
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
34553764
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
2022
35119614
Distribution of 54 polygenic risk scores for common diseases in long lived individuals and their offspring.
Geroscience
2022
35652341
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Hypertension
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
35393526
An Amish founder population reveals rare-population genetic determinants of the human lipidome.
Commun Biol
2022
35685441
Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort.
Front Genet
2022
36220816
Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
Nat Commun
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
35119614
Distribution of 54 polygenic risk scores for common diseases in long lived individuals and their offspring.
Geroscience
2022
33189290
Major quantitative trait loci influencing milk production and conformation traits in Guernsey dairy cattle detected on Bos taurus autosome 19.
J Dairy Sci
2021
33859359
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.
Mol Psychiatry
2021
33856023
Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction.
Hum Mol Genet
2021
34230475
Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33793566
Baseline cardiometabolic profiles and SARS-CoV-2 infection in the UK Biobank.
PLoS One
2021
33846329
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
Nat Commun
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
33887194
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
2021
33558525
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
2021
34087167
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
2021
33650257
Genetic versus stress and mood determinants of sleep in the Amish.
Am J Med Genet B Neuropsychiatr 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
34183656
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.
Nat Commun
2021
33189290
Major quantitative trait loci influencing milk production and conformation traits in Guernsey dairy cattle detected on Bos taurus autosome 19.
J Dairy Sci
2021
1 - 50 of 430
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Fernando Rivadeneira
University Medical Center Rotterdam
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