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Author Details
Full Name
Sharon L R Kardia
Affiliation
School of Public Health, University of Michigan ann arbor
ORCID
Career Start Year
1997
Papers
417
H Index
77
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35943854
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.
Brain
2023
36371759
"Extremely slow and capricious": A qualitative exploration of genetic researcher priorities in selecting shared data resources.
Genet Med
2023
35943854
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.
Brain
2023
36444934
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.
Hum Mol Genet
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
38014529
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.
Circ Genom Precis Med
2023
37904051
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Nat 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
37961350
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
bioRxiv
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
36719719
Policy Preferences Regarding Health Data Sharing Among Patients With Cancer: Public Deliberations.
JMIR Cancer
2023
36716967
DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.
J Thromb Haemost
2023
37403330
Applying anti-racist approaches to informatics: a new lens on traditional frames.
J Am Med Inform Assoc
2023
36645618
Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities.
J Community Genet
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
36702996
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.
Nat Genet
2023
36479596
Epigenome-wide association study of BMI in Black populations from InterGEN and GENOA.
Obesity (Silver Spring)
2023
37126548
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Sci Adv
2023
37180517
Epigenome-Wide Meta-Analysis Reveals Differential DNA Methylation Associated With Estimated Glomerular Filtration Rate Among African American Men With HIV.
Kidney Int Rep
2023
37046083
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
2023
36927883
Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.
Neurology
2023
36736697
US Residents' Preferences for Sharing of Electronic Health Record and Genetic Information: A Discrete Choice Experiment.
Value Health
2023
37169753
meQTL mapping in the GENOA study reveals genetic determinants of DNA methylation in African Americans.
Nat Commun
2023
36791357
Breast Cancer Prevention Misinformation on Pinterest: One Side of a Thick Coin.
Am J Public Health
2023
37425772
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
medRxiv
2023
36670106
Deep phenotyping and genomic data from a nationally representative study on dementia in India.
Sci Data
2023
36782352
Polygenic Risk Scores for Alzheimer's Disease and General Cognitive Function Are Associated With Measures of Cognition in Older South Asians.
J Gerontol A Biol Sci Med Sci
2023
36594825
A Critical Analysis of White Racial Framing and Comfort with Medical Research.
AJOB Empir Bioeth
2023
37961350
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
bioRxiv
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
38014529
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.
Circ Genom Precis Med
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
37904051
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Nat Genet
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37425772
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
medRxiv
2023
37046083
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
2023
37180517
Epigenome-Wide Meta-Analysis Reveals Differential DNA Methylation Associated With Estimated Glomerular Filtration Rate Among African American Men With HIV.
Kidney Int Rep
2023
37403330
Applying anti-racist approaches to informatics: a new lens on traditional frames.
J Am Med Inform Assoc
2023
37169753
meQTL mapping in the GENOA study reveals genetic determinants of DNA methylation in African Americans.
Nat Commun
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
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
36479596
Epigenome-wide association study of BMI in Black populations from InterGEN and GENOA.
Obesity (Silver Spring)
2023
36444934
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.
Hum Mol Genet
2023
36782352
Polygenic Risk Scores for Alzheimer's Disease and General Cognitive Function Are Associated With Measures of Cognition in Older South Asians.
J Gerontol A Biol Sci Med Sci
2023
1 - 50 of 834
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