Sharon Kardia
#85,420
Most Influential Person Now
American epidemiologist
Sharon Kardia's AcademicInfluence.com Rankings
Sharon Kardiamedical Degrees
Medical
#1060
World Rank
#1355
Historical Rank
Epidemiology
#455
World Rank
#477
Historical Rank
Download Badge
Medical
Why Is Sharon Kardia Influential?
(Suggest an Edit or Addition)According to Wikipedia, Sharon Lee Reilly Kardia is an American epidemiologist. She is the Millicent W. Higgins Collegiate Professor of Epidemiology and Associate Dean for Education at the University of Michigan School of Public Health. Her research interests involve genetic epidemiology of common chronic diseases.
Sharon Kardia's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Gene-expression profiles predict survival of patients with lung adenocarcinoma (2002) (1982)
- Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
- Discordant Protein and mRNA Expression in Lung Adenocarcinomas * (2002) (922)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2018) (914)
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
- A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
- New loci associated with kidney function and chronic kidney disease (2010) (754)
- Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries (2018) (735)
- Epigenetic Signatures of Cigarette Smoking (2016) (574)
- Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. (2005) (564)
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Synergistic Polymorphisms of β1- and α2C-Adrenergic Receptors and the Risk of Congestive Heart Failure (2002) (495)
- The transcriptional landscape of age in human peripheral blood (2015) (450)
- Gene expression in ovarian cancer reflects both morphology and biological behavior, distinguishing clear cell from other poor-prognosis ovarian carcinomas. (2002) (447)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) (417)
- A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. (2001) (391)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- A GRK5 polymorphism that inhibits β-adrenergic receptor signaling is protective in heart failure (2008) (339)
- Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) (2015) (328)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- Proteomic analysis of lung adenocarcinoma: identification of a highly expressed set of proteins in tumors. (2002) (307)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
- Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction (2011) (286)
- Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism (2015) (276)
- Protein profiles associated with survival in lung adenocarcinoma (2003) (265)
- Exploring the Public Understanding of Basic Genetic Concepts (2004) (257)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry (2013) (244)
- A Bivariate Genome-Wide Approach to Metabolic Syndrome (2011) (235)
- Genes, Environment, and Cardiovascular Disease (2003) (234)
- GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. (2015) (229)
- Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males. (1998) (224)
- Organ-specific molecular classification of primary lung, colon, and ovarian adenocarcinomas using gene expression profiles. (2001) (215)
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (215)
- Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci (2016) (214)
- CUBN is a gene locus for albuminuria. (2011) (214)
- Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP). (2002) (202)
- The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop (2009) (196)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
- Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
- Inherited Causes of Clonal Hematopoiesis in 97,691 TOPMed Whole Genomes (2020) (184)
- Positional genomic analysis identifies the beta(2)-adrenergic receptor gene as a susceptibility locus for human hypertension. (2000) (181)
- Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function (2012) (180)
- Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. (2013) (176)
- Synergistic polymorphisms of beta1- and alpha2C-adrenergic receptors and the risk of congestive heart failure. (2002) (173)
- A Genome-Wide Association Study of Depressive Symptoms (2013) (166)
- Ethnic and sex differences in the prevalence, treatment, and control of dyslipidemia among hypertensive adults in the GENOA study. (2004) (166)
- A meta-analysis of genome-wide association studies identifies multiple longevity genes (2019) (158)
- Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
- Ethnic differences in peripheral arterial disease in the NHLBI Genetic Epidemiology Network of Arteriopathy (GENOA) study (2003) (153)
- The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
- 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 (2019) (151)
- Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
- Novel candidate targets of beta-catenin/T-cell factor signaling identified by gene expression profiling of ovarian endometrioid adenocarcinomas. (2003) (150)
- Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits (2017) (149)
- Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways (2011) (149)
- Life course socioeconomic status and DNA methylation in genes related to stress reactivity and inflammation: The multi-ethnic study of atherosclerosis (2015) (145)
- Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2017) (145)
- Directional dominance on stature and cognition in diverse human populations (2015) (144)
- Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI (2015) (139)
- Epigenomic association analysis identifies smoking-related DNA methylation sites in African Americans (2013) (134)
- DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. (2017) (132)
- Characterization of european ancestry nonalcoholic fatty liver disease‐associated variants in individuals of african and hispanic descent (2013) (129)
- Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci (2013) (129)
- The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
- GWAS for executive function and processing speed suggests involvement of the CADM2 gene (2016) (125)
- Heterogeneity in polygenic scores for common human traits (2017) (121)
- Pleiotropic genes for metabolic syndrome and inflammation. (2014) (118)
- Clinical and genetic modifiers of long-term survival in heart failure. (2009) (118)
- Familial aggregation of hypertension treatment and control in the Genetic Epidemiology Network of Arteriopathy (GENOA) study. (2004) (117)
- Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function (2011) (117)
- Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity (2017) (117)
- A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. (2003) (117)
- Genome-wide association study of kidney function decline in individuals of European descent (2014) (114)
- Multiple genes for essential-hypertension susceptibility on chromosome 1q. (2007) (114)
- Recombination rates in admixed individuals identified by ancestry-based inference (2011) (110)
- SNP Set Association Analysis for Familial Data (2012) (110)
- Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium (2017) (102)
- Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies (2012) (102)
- A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. (2018) (100)
- Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation (2016) (100)
- Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension (2002) (97)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (93)
- GENOME‐WIDE ASSOCIATION STUDY (GWAS) AND GENOME‐WIDE BY ENVIRONMENT INTERACTION STUDY (GWEIS) OF DEPRESSIVE SYMPTOMS IN AFRICAN AMERICAN AND HISPANIC/LATINA WOMEN (2016) (90)
- Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans (2006) (89)
- Risk of lung cancer among white and black relatives of individuals with early-onset lung cancer. (2005) (89)
- Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women (2010) (89)
- An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype (2017) (89)
- Neighborhood characteristics influence DNA methylation of genes involved in stress response and inflammation: The Multi-Ethnic Study of Atherosclerosis (2017) (88)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- Family-centered approaches to understanding and preventing coronary heart disease. (2003) (87)
- Overexpression of Oncoprotein 18 Correlates with Poor Differentiation in Lung Adenocarcinomas* (2003) (87)
- Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism. (2002) (84)
- Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
- Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. (2011) (80)
- Current Applications of Genetic Risk Scores to Cardiovascular Outcomes and Subclinical Phenotypes (2015) (80)
- Accurate molecular classification of human cancers based on gene expression using a simple classifier with a pathological tree-based framework. (2003) (79)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
- Proteomic analysis of cytokeratin isoforms uncovers association with survival in lung adenocarcinoma. (2002) (77)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (77)
- Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. (2019) (77)
- Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. (2019) (77)
- Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3. (2004) (75)
- A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. (2016) (75)
- Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (2015) (75)
- Genome-Wide Linkage Analysis Reveals Evidence of Multiple Regions That Influence Variation in Plasma Lipid and Apolipoprotein Levels Associated With Risk of Coronary Heart Disease (2001) (74)
- Combinations of glutathione S-transferase genotypes and risk of early-onset lung cancer in Caucasians and African Americans: a population-based study. (2005) (73)
- Public preferences regarding informed consent models for participation in population-based genomic research (2013) (73)
- A database of protein expression in lung cancer (2001) (73)
- Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. (2019) (73)
- A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE). (2001) (72)
- Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
- Association of the Vitamin D Metabolism Gene CYP24A1 With Coronary Artery Calcification (2010) (71)
- Identification and prevention of a GC content bias in SAGE libraries. (2001) (70)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (68)
- PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
- Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. (2012) (67)
- Application of machine learning algorithms to predict coronary artery calcification with a sibship‐based design (2008) (66)
- A saturated map of common genetic variants associated with human height (2022) (65)
- The Perennial Debate: Nature, Nurture, or Choice? Black and White Americans’ Explanations for Individual Differences (2009) (65)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
- Education and Lifestyle Factors Are Associated with DNA Methylation Clocks in Older African Americans (2019) (64)
- The Genomic Applications in Practice and Prevention Network (2009) (63)
- Ethnicity and human genetic linkage maps. (2005) (62)
- 5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk: a hypothesis-generating study. (2006) (62)
- Meta-analysis of epigenome-wide association studies of cognitive abilities (2018) (62)
- The Glutathione S-Transferase-μ and -θ Genotypes in the Etiology of Prostate Cancer: Genotype-Environment Interactions with Smoking (2000) (61)
- A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants. (2016) (61)
- Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects (2022) (59)
- Public Trust in Health Information Sharing: Implications for Biobanking and Electronic Health Record Systems (2015) (58)
- Within-sibship GWAS improve estimates of direct genetic effects (2021) (58)
- Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
- Association of parental smoking history with nicotine dependence, smoking rate, and psychological cofactors in adult smokers. (2003) (58)
- Genome-wide linkage analyses for hypertension genes in two ethnically and geographically diverse populations. (2003) (57)
- New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders (2019) (57)
- Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform (2011) (56)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (55)
- The relationship between risk factor levels and presence of coronary artery calcification is dependent on apolipoprotein E genotype. (1999) (55)
- Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes (2010) (55)
- Patient-Reported Experiences of Discrimination in the US Health Care System (2020) (54)
- Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin. (2016) (54)
- Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
- Genome-Wide Association Study of Cardiac Structure and Systolic Function in African Americans: The Candidate Gene Association Resource (CARe) Study (2013) (54)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
- Genetic Variation in NCAM1 Contributes to Left Ventricular Wall Thickness in Hypertensive Families (2011) (52)
- Aromatase gene (CYP 19) polymorphisms and endogenous androgen concentrations in a multiracial/multiethnic, multisite study of women at midlife. (2006) (52)
- The relationship of high sensitivity C-reactive protein to percent body fat mass, body mass index, waist-to-hip ratio, and waist circumference in a Taiwanese population (2010) (52)
- Context-dependent genetic effects in hypertension (2000) (51)
- A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study. (2006) (51)
- CYP1A1 and CYP1B1 polymorphisms and their association with estradiol and estrogen metabolites in women who are premenopausal and perimenopausal. (2006) (50)
- New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
- Endogenous estradiol and its association with estrogen receptor gene polymorphisms. (2006) (49)
- Research and Practice Opportunities at the Intersection of Health Education, Health Behavior, and Genomics (2005) (49)
- Meta-analysis of loci associated with age at natural menopause in African-American women. (2014) (49)
- Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging (2021) (48)
- Disproportionate Sterilization of Latinos Under California’s Eugenic Sterilization Program, 1920-1945 (2018) (48)
- Facebook Advertising Across an Engagement Spectrum: A Case Example for Public Health Communication (2016) (48)
- Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration (2019) (47)
- Public Trust in Health Information Sharing: A Measure of System Trust (2018) (47)
- Genomic Susceptibility Loci for Brain Atrophy in Hypertensive Sibships From the GENOA Study (2005) (46)
- An Empirical Comparison of Meta‐analysis and Mega‐analysis of Individual Participant Data for Identifying Gene‐Environment Interactions (2014) (46)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
- Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
- California's Sterilization Survivors: An Estimate and Call for Redress (2017) (45)
- Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. (2015) (45)
- Association and linkage analysis of the α-adducin gene and blood pressure (2000) (45)
- Genome-Wide Association Study of Gene by Smoking Interactions in Coronary Artery Calcification (2013) (45)
- Sex steroid hormone pathway genes and health-related measures in women of 4 races/ethnicities: the Study of Women's Health Across the Nation (SWAN). (2006) (44)
- DNA mismatch repair gene MSH6 implicated in determining age at natural menopause (2013) (44)
- SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. (2017) (44)
- Evidence for Consistent Intragenic and Intergenic Interactions between SNP Effects in the APOA1/C3/A4/A5 Gene Cluster (2006) (43)
- Dynamic relationships between the genome and exposures to environments as causes of common human diseases. (2004) (43)
- Religion as a Health Promoter During the 2019/2020 COVID Outbreak: View from Detroit (2020) (42)
- Interactions between metallopeptidase 3 polymorphism rs679620 and BMI in predicting blood pressure in African–American women with hypertension (2008) (42)
- GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium (2016) (42)
- Sex difference in the association of metabolic syndrome with high sensitivity C-reactive protein in a Taiwanese population (2010) (42)
- Influence of genomic loci on measures of chronic kidney disease in hypertensive sibships. (2006) (42)
- Association of novel risk factors with the ankle brachial index in African American and non-Hispanic white populations. (2007) (41)
- A model-based scan statistic for identifying extreme chromosomal regions of gene expression in human tumors (2005) (41)
- Gene-Specific DNA Methylation Association with Serum Levels of C-Reactive Protein in African Americans (2013) (40)
- Sex steroid hormone polymorphisms, high-density lipoprotein cholesterol, and apolipoprotein A-1 from the Study of Women's Health Across the Nation (SWAN). (2006) (39)
- Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis (2016) (39)
- Testing an Online, Dynamic Consent Portal for Large Population Biobank Research (2014) (38)
- Genetic Architecture of Gene Expression in European and African Americans: An eQTL Mapping Study in GENOA. (2020) (38)
- Bayesian Shrinkage Estimation of High Dimensional Causal Mediation Effects in Omics Studies (2018) (38)
- Classification of rheumatoid arthritis status with candidate gene and genome-wide single-nucleotide polymorphisms using random forests (2007) (37)
- A scan statistic for identifying chromosomal patterns of SNP association (2006) (37)
- Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans (2016) (37)
- Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking (2019) (36)
- Admixture Mapping of Quantitative Trait Loci for BMI in African Americans: Evidence for Loci on Chromosomes 3q, 5q, and 15q (2009) (35)
- Syndrome X: Is it for real? (1998) (35)
- Hypertension in Pregnancy Is a Risk Factor for Microalbuminuria Later in Life (2013) (35)
- Hypertrophy‐Associated Polymorphisms Ascertained in a Founder Cohort Applied to Heart Failure Risk and Mortality (2011) (35)
- Hypertension in pregnancy is a risk factor for peripheral arterial disease decades after pregnancy. (2013) (35)
- Common variants in Mendelian kidney disease genes and their association with renal function. (2013) (35)
- Metabolic syndrome is associated with change in subclinical arterial stiffness - A community-based Taichung Community Health Study (2011) (34)
- Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health (2014) (34)
- Association of polymorphisms in NOS3 with the ankle-brachial index in hypertensive adults. (2008) (34)
- Synergistic polymorphisms of the β1- and α2c-adrenergic receptors and the risk of congestive heart failure ☆ (2003) (34)
- Novel DNA methylation sites associated with cigarette smoking among African Americans (2019) (33)
- Multivariate linkage analysis of blood pressure and body mass index (2004) (33)
- Insulin Resistance Exacerbates Genetic Predisposition to Nonalcoholic Fatty Liver Disease in Individuals Without Diabetes (2019) (33)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (33)
- Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships. (2009) (33)
- The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment (2008) (32)
- Utility of the predictors of coronary heart disease mortality in a longitudinal study of elderly Finnish men aged 65 to 84 years is dependent on context defined by Apo E genotype and area of residence (1999) (32)
- The glutathione S-transferase-mu and -theta genotypes in the etiology of prostate cancer: genotype-environment interactions with smoking. (2000) (32)
- Imputing missing genotypic data of single-nucleotide polymorphisms using neural networks (2008) (32)
- Association of plasma homocysteine with coronary artery calcification in different categories of coronary heart disease risk. (2006) (32)
- Complexity in the genetic architecture of leukoaraiosis in hypertensive sibships from the GENOA Study (2009) (31)
- Population sequencing data reveal a compendium of mutational processes in human germline (2020) (31)
- Genome-Wide Association Analysis of Plasma B–Type Natriuretic Peptide in Blacks: The Jackson Heart Study (2015) (31)
- Gene-Environment Interaction for Hypertension Among African American Women Across Generations (2010) (30)
- Associations between self-referral and health behavior responses to genetic risk information (2015) (29)
- Characterizing variation in sex steroid hormone pathway genes in women of 4 races/ethnicities: the Study of Women's Health Across the Nation (SWAN). (2006) (29)
- A comparison of serum creatinine-based methods for identifying chronic kidney disease in hypertensive individuals and their siblings. (2006) (29)
- Genetic Variations Associated With Echocardiographic Left Ventricular Traits in Hypertensive Blacks (2007) (29)
- Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury (2006) (29)
- A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. (2019) (28)
- A Peripheral Blood DNA Methylation Signature of Hepatic Fat Reveals a Potential Causal Pathway for Nonalcoholic Fatty Liver Disease (2019) (28)
- Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships. (2005) (28)
- Heritability of urinary traits that contribute to nephrolithiasis. (2014) (28)
- Laying Anchor: Inserting Precision Health into a Public Health Genetics Policy Course (2018) (28)
- A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction (2016) (27)
- Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families. (2011) (27)
- Matrix Gla Protein Gene Polymorphism Is Associated With Increased Coronary Artery Calcification Progression (2013) (26)
- Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits (2017) (26)
- Considerations for Designing a Prototype Genetic Test for Use in Translational Research (2009) (26)
- Novel DNA methylation signatures of tobacco smoking with trans-ethnic effects (2021) (26)
- Novel Genomic Loci Influencing Plasma Homocysteine Levels (2006) (25)
- Lack of association between lipoprotein(a) and coronary artery calcification in the Genetic Epidemiology Network of Arteriopathy (GENOA) study. (2004) (25)
- The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region (2015) (25)
- The complex genetics of gait speed: genome-wide meta-analysis approach (2017) (25)
- Identification of epistatic effects using a protein-protein interaction database. (2010) (25)
- Genomic Loci with Pleiotropic Effects on Coronary Artery Calcification in Hypertensive Sibships (2004) (25)
- An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP) (2007) (25)
- Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose (2020) (24)
- Association and linkage analysis of the alpha-adducin gene and blood pressure. (2000) (24)
- Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects (2009) (24)
- A functional polymorphism of the Galphaq (GNAQ) gene is associated with accelerated mortality in African-American heart failure. (2007) (23)
- Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes (2019) (23)
- ChromoScan: a scan statistic application for identifying chromosomal regions in genomic studies (2006) (23)
- Investigating the complex genetic architecture of ankle-brachial index, a measure of peripheral arterial disease, in non-Hispanic whites (2008) (23)
- Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
- A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships. (2005) (22)
- A statistical approach for rare-variant association testing in affected sibships. (2015) (22)
- Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
- An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene‐Lifestyle Interactions Working Group (2016) (21)
- Encouraging Participation And Transparency In Biobank Research. (2018) (21)
- Expert and Advocacy Group Consensus Findings on the Horizon of Public Health Genetic Testing (2016) (21)
- Correlates of family history of coronary artery disease in children. (1998) (21)
- Multiple interactions between the alpha2C- and beta1-adrenergic receptors influence heart failure survival (2008) (21)
- Genetic polymorphisms and obesity influence estradiol decline during the menopause (2011) (20)
- Modeling the Causal Role of DNA Methylation in the Association Between Cigarette Smoking and Inflammation in African Americans: A 2-Step Epigenetic Mendelian Randomization Study (2017) (20)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
- Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program. (2010) (20)
- Epigenetic age acceleration is associated with cardiometabolic risk factors and clinical cardiovascular disease risk scores in African Americans (2021) (20)
- ‘Born in Michigan? You're in the Biobank': Engaging Population Biobank Participants through Facebook Advertisements (2013) (19)
- Key influence of sex on urine volume and osmolality (2016) (19)
- A Peripheral Blood DNA Methylation Signature of Hepatic Fat Reveals a Potential Causal Pathway for Nonalcoholic Fatty Liver Disease. (2019) (19)
- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- Genome sequencing unveils a regulatory landscape of platelet reactivity (2019) (18)
- Glycemic control paradox: Poor glycemic control associated with higher one-year and eight-year risks of all-cause hospitalization but lower one-year risk of hypoglycemia in patients with type 2 diabetes. (2015) (18)
- Hypertension in pregnancy is associated with elevated homocysteine levels later in life. (2013) (18)
- Heterogeneity in phenotypes based on smoking status in the Great Lakes Smoker Sibling Registry. (2004) (18)
- Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. (2021) (18)
- NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality. (2017) (18)
- ‘Cool! and creepy’: engaging with college student stakeholders in Michigan’s biobank (2014) (18)
- Evaluating the Context-Dependent Effect of Family History of Stroke in a Genome Scan for Hypertension (2003) (17)
- Intrinsic and extrinsic epigenetic age acceleration are associated with hypertensive target organ damage in older African Americans (2019) (17)
- Menstrual cycle markers of ovarian aging and sex steroid hormone genotypes. (2006) (17)
- Contribution of regulatory and structural variations in APOE to predicting dyslipidemia Published, JLR Papers in Press, November 29, 2005. (2006) (17)
- Gene-environment effects of SLC4A5 and skin color on blood pressure among African American women. (2012) (17)
- Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential (2022) (17)
- Relation of C-reactive protein and fibrinogen to coronary artery calcium in subjects with systemic hypertension. (2003) (17)
- Blood Pressure Sunday: Introducing Genomics to the Community Through Family History (2005) (17)
- Set-Based Tests for the Gene–Environment Interaction in Longitudinal Studies (2017) (17)
- Risk factor profile for chronic kidney disease is similar to risk factor profile for small artery disease (2011) (16)
- SNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in african-americans of the GENOA study (2010) (16)
- Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry (2017) (16)
- Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure (2017) (16)
- Identification of correlated genetic variants jointly associated with rheumatoid arthritis using ridge regression (2009) (16)
- Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies (2016) (16)
- Model-based assessment of replicability for genome-wide association meta-analysis (2021) (15)
- Copy number variations associated with obesity related traits in African Americans: a joint analysis between GENOA and HyperGEN (2012) (15)
- Hypertension in pregnancy is associated with elevated C-reactive protein levels later in life (2013) (15)
- Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease (2018) (15)
- A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program (2021) (15)
- Lack of genetic linkage evidence for a trans-acting factor having a large effect on plasma lipoprotein[a] levels in African Americans Published, JLR Papers in Press, May 1, 2003. DOI 10.1194/jlr.M300163-JLR200 (2003) (15)
- Epigenomic Indicators of Age in African Americans (2014) (15)
- Hormone therapy and urine protein excretion: a multiracial cohort study, systematic review, and meta-analysis (2018) (15)
- Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed (2022) (15)
- Genomics and Public Health: Development of Web-based Training Tools for Increasing Genomic Awareness (2005) (14)
- DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis. (2018) (14)
- Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention (2022) (14)
- Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population (2014) (14)
- Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data (2019) (14)
- The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program (2006) (14)
- The Role of Health Education and Behavior in Public Health Genetics (2005) (14)
- A Common Copy Number Variation on Chromosome 6 Association With the Gene Expression Level of Endothelin 1 in Transformed B Lymphocytes From Three Racial Groups (2009) (14)
- Heritability of cardiovascular risk factors in a Chinese population--Taichung Community Health Study and Family Cohort. (2014) (14)
- Low-density lipoprotein particle size and coronary atherosclerosis in subjects belonging to hypertensive sibships. (2004) (14)
- Genome-wide linkage analysis for smoking-related regions, with replication in two ethnically diverse populations. (2007) (13)
- Uric Acid: A Missing Link Between Hypertensive Pregnancy Disorders and Future Cardiovascular Disease? (2015) (13)
- The public’s trust and information brokers in health care, public health and research (2019) (13)
- Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging (2018) (13)
- Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the multi-ethnic study of atherosclerosis (2015) (13)
- Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study (2015) (12)
- Epistatic effects between two genes in the renin-angiotensin system and systolic blood pressure and coronary artery calcification. (2006) (12)
- Introduction to the featured section: genetic research on smoking. (1999) (12)
- The public’s comfort with sharing health data with third-party commercial companies (2020) (12)
- Family History of Stroke among Mexican-American and Non-Hispanic White Patients with Stroke and TIA: Implications for the Feasibility and Design of Stroke Genetics Research (2004) (12)
- KGraph: a system for visualizing and evaluating complex genetic associations (2007) (12)
- Set‐based tests for genetic association in longitudinal studies (2015) (12)
- Social regulation of inflammation related gene expression in the multi-ethnic study of atherosclerosis (2020) (12)
- The Role of Religious Values in Decisions About Genetics and the Public’s Health (2014) (12)
- Meta-analyses identify DNA methylation associated with kidney function and damage (2021) (12)
- Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing (2020) (12)
- Effect of Demographics on Excretion of Key Urinary Factors Related to Kidney Stone Risk. (2015) (12)
- Variants for HDL-C, LDL-C, and Triglycerides Identified from Admixture Mapping and Fine-Mapping Analysis in African American Families (2015) (12)
- The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3 (2014) (12)
- Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360) (2017) (12)
- Interaction between Social/Psychosocial Factors and Genetic Variants on Body Mass Index: A Gene-Environment Interaction Analysis in a Longitudinal Setting (2017) (11)
- Joint relationship between renal function and proteinuria on mortality of patients with type 2 diabetes: The Taichung Diabetes Study (2012) (11)
- A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids (2021) (11)
- Influence of apolipoprotein E genotype variation on the means, variances, and correlations of plasma lipids and apolipoproteins in children (1999) (11)
- Negotiating Deliberative Ideals in Theory and Practice: A Case Study in “Hybrid Design” (2016) (11)
- Interactions between the adducin 2 gene and antihypertensive drug therapies in determining blood pressure in people with hypertension (2007) (11)
- Allele Specific Variation at APOE Increases Non-alcoholic Fatty Liver Disease and Obesity but Decreases Risk of Alzheimer's Disease and Myocardial Infarction. (2021) (11)
- Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts (2022) (11)
- Epigenetic Markers of Renal Function in African Americans (2013) (11)
- Erratum: Combinations of glutathione S-transferase genotypes and risk of early-onset lung cancer in Caucasians and African Americans: A population-based study (Carcinogenesis (2005) 26 (811-819)) (2005) (10)
- Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels (2020) (10)
- The response of renal plasma flow to angiotensin II infusion in a population‐based sample and its association with the parental history of essential hypertension (1997) (10)
- Linkage analysis of plasma ApoE in three ethnic groups: multiple genes with context-dependent effects. (2005) (10)
- Fast implementation of a scan statistic for identifying chromosomal patterns of genome wide association studies (2009) (10)
- SLC2A9 Genotype Is Associated with SLC2A9 Gene Expression and Urinary Uric Acid Concentration (2015) (10)
- Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. (2021) (10)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
- The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus (2019) (9)
- Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
- Differences in accuracy of offspring assessment based on parental smoking status. (2005) (9)
- Bayesian sparse mediation analysis with targeted penalization of natural indirect effects (2020) (9)
- Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
- Genetic diversity is a predictor of mortality in humans (2014) (9)
- Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes (2021) (9)
- Genome‐wide survey in African Americans demonstrates potential epistasis of fitness in the human genome (2017) (9)
- Epigenome-wide association study identifies DNA methylation sites associated with target organ damage in older African Americans (2020) (9)
- Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus (2020) (9)
- Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci (2020) (9)
- Heritability of dietary traits that contribute to nephrolithiasis in a cohort of adult sibships (2016) (9)
- A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program (2020) (8)
- Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2018) (8)
- The Glutathione S-Transferase-m andu Genotypes in the Etiology of Prostate Cancer : Genotype-Environment Interactions with Smoking 1 (2000) (8)
- Willingness to Participate in Health Information Networks with Diverse Data Use: Evaluating Public Perspectives (2019) (8)
- Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
- Classification and Clustering Methods for Multiple Environmental Factors in Gene-Environment Interaction: Application to the Multi-Ethnic Study of Atherosclerosis. (2016) (8)
- A noncoding variant near PPP1R3B promotes liver glycogen storage and MetS, but protects against myocardial infarction. (2020) (8)
- Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2019) (7)
- Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices (2021) (7)
- Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity (2017) (7)
- Genetic research on complex behaviors: an examination of attempts to identify genes for smoking. (2007) (7)
- Association Between Episodic Memory and Genetic Risk Factors for Alzheimer's Disease in South Asians from the Longitudinal Aging Study in India-Diagnostic Assessment of Dementia (LASI-DAD). (2020) (7)
- Whole genome sequence analysis of blood lipid levels in >66,000 individuals (2021) (7)
- Applying Novel Methods for Assessing Individual- and Neighborhood-Level Social and Psychosocial Environment Interactions with Genetic Factors in the Prediction of Depressive Symptoms in the Multi-Ethnic Study of Atherosclerosis (2016) (7)
- Association between Stress Response Genes and Features of Diurnal Cortisol Curves in the Multi-Ethnic Study of Atherosclerosis: A New Multi-Phenotype Approach for Gene-Based Association Tests (2015) (7)
- An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
- Bayesian hierarchical models for high‐dimensional mediation analysis with coordinated selection of correlated mediators (2020) (7)
- Hypertension in Pregnancy and Future Cardiovascular Event Risk in Siblings. (2016) (7)
- Expression of socially sensitive genes: The multi-ethnic study of atherosclerosis (2019) (6)
- Linkage Analysis of Plasma ApoE in Three Ethnic Groups: Multiple Genes with Context‐Dependent Effects (2005) (6)
- Epigenetic loci for blood pressure are associated with hypertensive target organ damage in older African Americans from the genetic epidemiology network of Arteriopathy (GENOA) study (2020) (6)
- Genetic and Social Environment Interactions and Their Impact on Health Policy (2007) (6)
- Do people have an ethical obligation to share their health information? Comparing narratives of altruism and health information sharing in a nationally representative sample (2020) (6)
- Hidden Markov model for defining genomic changes in lung cancer using gene expression data. (2006) (6)
- Evaluating the Influence of Quality Control Decisions and Software Algorithms on SNP Calling for the Affymetrix 6.0 SNP Array Platform (2011) (6)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
- Joint Influence of SNPs and DNA Methylation on Lipids in African Americans From Hypertensive Sibships (2018) (6)
- Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma. (2019) (6)
- Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies (2018) (6)
- Stakeholder consultation insights on the future of genomics at the clinical-public health interface. (2014) (6)
- Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program (2007) (5)
- Polymorphisms in Renal Ammonia Metabolism Genes Correlate With 24-Hour Urine pH (2017) (5)
- Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed (2019) (5)
- A Bayesian method for finding interactions in genomic studies (2004) (5)
- Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus (2021) (5)
- Gene-by-Psychosocial Factor Interactions Influence Diastolic Blood Pressure in European and African Ancestry Populations: Meta-Analysis of Four Cohort Studies (2017) (5)
- Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA) (2022) (5)
- Clonal hematopoiesis is driven by aberrant activation of TCL1A (2021) (5)
- Associations between polygenic risk score for age at menarche and menopause, reproductive timing, and serum hormone levels in multiple race/ethnic groups (2021) (5)
- Rare Variants in Genes Encoding Subunits of the Epithelial Na+ Channel Are Associated With Blood Pressure and Kidney Function (2022) (5)
- Association of urinary citrate excretion, pH, and net gastrointestinal alkali absorption with diet, diuretic use, and blood glucose concentration (2017) (5)
- Integrative biology and the developing limb bud 1 (2002) (5)
- Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program (2020) (5)
- Association of the Vitamin D Metabolism Gene CYP 24 A 1 With Coronary Artery Calcification (2010) (5)
- Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders (2018) (5)
- Phase Changes in the BRCA Policy Domain (2014) (4)
- Testing cross‐phenotype effects of rare variants in longitudinal studies of complex traits (2018) (4)
- Ethical, legal, and social implications of learning health systems (2018) (4)
- Accelerated DNA methylation age and medication use among African Americans (2021) (4)
- Cumulative Genetic Risk and APOE ε4 Are Independently Associated With Dementia Status in a Multiethnic, Population-Based Cohort (2021) (4)
- Role of Rare and Low Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels (2018) (4)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
- Rare genetic variants explain missing heritability in smoking (2022) (4)
- Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
- When Genetics Meets Religion: What Scientists and Religious Leaders Can Learn from Each Other (2019) (4)
- The Combinatorial Partitioning Method (2000) (4)
- METRO: Multi-ancestry transcriptome-wide association studies for powerful gene-trait association detection. (2022) (3)
- Data Related to Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (3)
- Are we teaching our students visual communication? Evaluation of writing assignments in public health (2019) (3)
- Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
- The ecological model in genetics and religion (2013) (3)
- Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke (2022) (3)
- Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151 (2017) (3)
- Engaging a state: Facebook comments on a large population biobank (2017) (3)
- Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate (2022) (3)
- Genome-wide association study of kidney function decline in individuals of European descent: the CKDGen Consortium. (2015) (3)
- Genome‐wide meta‐analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans (2019) (3)
- Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 (2018) (3)
- Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 (2012) (3)
- Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program (2021) (3)
- Shared Genetic Effects among Measures of Cognitive Function and Leukoaraiosis (2012) (2)
- Identification of genes associated with complex traits by testing the genetic dissimilarity between individuals (2011) (2)
- Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension (2022) (2)
- REPORTS : CARDIOVASCULAR DISEASE AND RISK FACTORS GENE-ENVIRONMENT EFFECTS OF SLC 4 A 5 AND SKIN COLOR ON BLOOD PRESSURE AMONG AFRICAN AMERICAN WOMEN (2012) (2)
- Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes (2021) (2)
- Association of low-frequency and rare coding variants with information processing speed (2016) (2)
- Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids (2019) (2)
- DNA Methylation Mediates the Association Between Individual and Neighborhood Social Disadvantage and Cardiovascular Risk Factors (2022) (2)
- Innovating consent for pediatric HCT patients (2016) (2)
- Public Deliberation Process on Patient Perspectives on Health Information Sharing: Evaluative Descriptive Study (2022) (2)
- Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning (2022) (2)
- Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging (2021) (2)
- Discrimination, trust, and withholding information from providers: Implications for missing data and inequity (2022) (2)
- Testing departure from additivity in Tukey's model using shrinkage: application to a longitudinal setting (2014) (2)
- Relationship between renal plasma flow response to angiotensin II and blood pressure in a population‐based sample (1997) (2)
- Gene–Environment Interaction (2006) (2)
- Using Genetic Burden Scores for Gene-by-Methylation Interaction Analysis on Metabolic Syndrome in African Americans (2019) (2)
- The relative role of invariant and context dependent genetic effects in predicting cardiovascular disease (2000) (2)
- Long-term risk of reproductive cancer among Vietnamese women using the quinacrine hydrochloride pellet system vs. intrauterine devices or tubal ligation for contraception (2017) (2)
- Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples. (2020) (2)
- Detecting fitness epistasis in recently admixed populations with genome-wide data (2019) (1)
- Regulations and Norms for Reuse of Residual Clinical Biospecimens and Health Data (2021) (1)
- Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease. (2022) (1)
- A Novel Apolipoprotein A-IV Polymorphism is Associated with Lipoprotein Metabolism and Response to Fenofibrate (2006) (1)
- Physical activity and sedentary behavior; mechanistic insights and role in disease prevention (2021) (1)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
- Distinctive features of public health ethics in the domain of expanded genetic screening and population biobanking (2015) (1)
- Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease (2021) (1)
- Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
- Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI (2022) (1)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (1)
- Rare‐variant association tests in longitudinal studies, with an application to the Multi‐Ethnic Study of Atherosclerosis (MESA) (2017) (1)
- Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile (2019) (1)
- The cis and trans effects of the risk variants of coronary artery disease in the Chr 9 p 21 region (2015) (1)
- Enlarging the social definition of harm to include genetics (2015) (1)
- "Extremely slow and capricious": A qualitative exploration of genetic researcher priorities in selecting shared data resources. (2022) (1)
- Short Communication Organ-Specific Molecular Classification of Primary Lung, Colon, and Ovarian Adenocarcinomas Using Gene Expression Profiles (2001) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Abstract 32: Novel Genetic Loci for Blood Pressure Regulation Identified by the Analysis of DNA Methylation (2016) (1)
- Correction: The complex genetics of gait speed: genome-wide meta-analysis approach (2017) (1)
- Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing (2023) (1)
- Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes (2021) (1)
- Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid (2019) (1)
- Long-term risk of hysterectomy and ectopic pregnancy among Vietnamese women using the quinacrine hydrochloride pellet system vs. intrauterine devices or tubal ligation for contraception (2018) (1)
- Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population (2014) (1)
- Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior (2017) (1)
- Lessons Learned for Identifying and Annotating Permissions in Clinical Consent Forms (2021) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization (2018) (1)
- Linear dynamic features of ambulatory blood pressure in a population-based study (2004) (1)
- Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health (2013) (1)
- A non-APOE Polygenic score for Alzheimer’s disease and APOE-ε4 have independent associations with dementia in the Health and Retirement Study (2020) (1)
- Abstract 2001: Genetic {beta}-Blockade: A G-Protein Coupled Receptor Kinase-5 Polymorphism That Inhibits Beta-Adrenergic Receptor Signaling is Protective in Heart Failure (2006) (1)
- Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
- Evaluating and extending the Informed Consent Ontology for representing permissions from the clinical domain (2022) (1)
- Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids (2021) (1)
- Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
- Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos (2017) (0)
- Public willingness to share networked health information (2018) (0)
- US residents' preferences for sharing of electronic health record and genetic information: a discrete choice experiment. (2023) (0)
- Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants (2022) (0)
- Abstract MP071: Genetic Modification of Triggers of Acute Myocardial Infarction: Results From a Case-crossover Study in Costa Rica (2017) (0)
- Author's response to reviews Title: Metabolic syndrome is associated with change in subclinical arterial stiffness - A community-based Taichung Community Health Study Authors: (2011) (0)
- Providing context and interpretability to genetic association analysis results using the KGraph. (2010) (0)
- Genome-Wide Association Analysis of Plasma B-Type Natriuretic Peptide in African Americans : The Jackson Heart Study Running title : (2015) (0)
- G-Protein Receptor Kinase-5 Polymorphism Influences Therapeutic Efficacy of β-Blockers in Heart Failure (2006) (0)
- Interactions between a dducin 2 and antihypertensive drug therapies in determining blood pressure in hypertensives (2007) (0)
- University of Groningen Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking Sikdar, (2019) (0)
- Reviewer Acknowledgment (2008) (0)
- National Institute on Aging Using Genome-Wide Association Studies ( GWAS ) to Explore Fundamental Questions About Aging in the Health and Retirement Study ( HRS ) Sample Summary of an Expert Meeting (2011) (0)
- Differential relationship of C-reactive protein and fibrinogen to coronary artery calcification in individuals at intermediate risk of cardiovascular events (2003) (0)
- GENE-ENVIRONMENT INTERACTION FOR HYPERTENSION AMONG AFRICAN AMERICAN WOMEN (2011) (0)
- Abstract 4881: Interaction of Genetic and Pharmacologic {beta}-adrenergic Signaling Inhibitors Determines Long-term Mortality after Acute Coronary Ischemia (2008) (0)
- Abstract P091: Ethnic Disparities in Social and Psychosocial Factors Modify the Effect of Genes on Body Mass Index (2016) (0)
- ‘Cool! and creepy’: engaging with college student stakeholders in Michigan’s biobank (2014) (0)
- in A measure of system trust (2016) (0)
- Sub-clinical atherosclerosis in hypertensive individuals: the role of conditional risk factors (2002) (0)
- 1093-146 The association of plasma homocysteine with coronary artery atherosclerosis is modified by conventional risk factors (2004) (0)
- A: The location of the 11 SNPs on the gene (2011) (0)
- A Response to ‘Why Realistic Test Scenarios in Translational Research Remain Hypothetical’ (2009) (0)
- Society for Vascular Medicine and Biology abstracts (2003) (0)
- W14.342 Variation in 5′ region contributes significantly to pleoiotropic effects of the APOE gene on multiple measures of lipid metabolism (2004) (0)
- Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies. (2017) (0)
- Abstract P530: Pleiotropic Effects on Blood Pressure Traits Using Genome-wide Analysis of Gene-alcohol Interactions (2017) (0)
- Common and rare variants in Alzheimer’s disease genes are associated with episodic memory in South Asians from the LASI‐DAD study (2020) (0)
- Abstract 2073: Genome-wide Association Studies of the Ankle-brachial Index: A Meta-analysis of 12 Cohorts Including 28083: Participants (2009) (0)
- Examining the Distribution of Services: How Hospital Chaplaincy Screens the Religiously Unaffiliated (2020) (0)
- Endometrioid Adenocarcinomas Identified by Gene Expression Profiling of Ovarian-Catenin / T-cell Factor Signaling β Novel Candidate Targets of Updated (2003) (0)
- Autosomal genomewide linkage scan for coronary artery calcification loci. (2001) (0)
- Detecting fitness epistasis in recently admixed populations with genome-wide data (2020) (0)
- Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA) (2022) (0)
- Genetic Contributions to Early and Late Onset Ischemic Stroke (2021) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
- SupplementalMaterials-2016-03-29-complete-FINALv2 (2016) (0)
- Abstract P076: Genetic Factors Modify the Triggering of Acute Myocardial Infarction by Transient Exposure to Coffee Intake (2012) (0)
- Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits (2020) (0)
- Engaging a state: Facebook comments on a large population biobank (2017) (0)
- Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function (2023) (0)
- The Interplay of Epigenetic, Genetic, and Traditional Risk Factors on Blood Pressure: Findings from the Health and Retirement Study (2022) (0)
- Intrinsic and extrinsic epigenetic age acceleration are associated with hypertensive target organ damage in older African Americans (2019) (0)
- Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 (2018) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
- Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2019) (0)
- Abstract P207: Gene-by-Psychosocial Factor Interactions on Blood Pressure in Older Non-hispanic Whites and African Americans: A Genomic Region-level Analysis (2016) (0)
- Ankle-Brachial Index , a Measure of Peripheral Arterial Disease , in non-Hispanic Whites (2008) (0)
- Are Americans confident in their ability to manage their health information? (2020) (0)
- Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
- Polygenic risk score for general cognitive function is associated with measures of cognition in South Asians from the LASI‐DAD Study (2021) (0)
- Genetic diversity is a predictor of mortality in humans (2014) (0)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
- Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis (2023) (0)
- The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region (2015) (0)
- The public’s comfort with sharing health data with third-party commercial companies (2020) (0)
- Abstract 3507: Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing (2023) (0)
- Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data (2019) (0)
- Common and rare variants in topologically associated domains for cognitive function in South Asians from the LASI‐DAD Study (2021) (0)
- Reviewer Acknowledgment (2005) (0)
- The most recent and extensive genome-wide human genetic linkage maps (2005) (0)
- Novel coronary heart disease markers many years after hypertensive pregnancy (2013) (0)
- identifies 148 independent genetic loci influencing general cognitive function Permalink (2018) (0)
- SNP Set Association Analysis for Familial Data Running Title: SNP Set Analysis for Familial Data (2012) (0)
- Novel DNA methylation signatures of tobacco smoking with trans-ethnic effects (2021) (0)
- Identification of ABCA7 SNP‐by‐CpG interactions associated with cognition in older African Americans (2022) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
- Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities (2023) (0)
- Open Novel DNA methylation signatures of tobacco smoking with trans-ethnic effects (2022) (0)
- Policy Preferences Regarding Health Data Sharing Among Patients With Cancer: Public Deliberations (2023) (0)
- Genetic variants predictive of reproductive aging are associated with vasomotor symptoms in a multiracial/ethnic cohort (2021) (0)
- A network of pleiotropic genes for metabolic syndrome and inflammation (2013) (0)
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (0)
- Polygenic risk scores for Alzheimer's disease and general cognitive function are associated with measures of cognition in older South Asians from LASI-DAD. (2023) (0)
- Epigenomic association analysis identifies smoking-related DNA methylation sites in African Americans (2013) (0)
- Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
- Breast Cancer Prevention Misinformation on Pinterest: One Side of a Thick Coin. (2023) (0)
- Abstract 057: Epigenome Wide Association Study Identifies DNA Methylation Sites Associated With Target Organ Damage in Elderly African Americans (2019) (0)
- Reported Interest in Notification Regarding Use of Health Information and Biospecimens. (2022) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
- Heart Disease Variation in Plasma Lipid and Apolipoprotein Levels Associated With Risk of Coronary Genome-Wide Linkage Analysis Reveals Evidence of Multiple Regions That Influence (2001) (0)
- Applying Novel Methods for Assessing Individual- and Neighborhood-Level Social and Psychosocial Environment Interactions with Genetic Factors in the Prediction of Depressive Symptoms in the Multi-Ethnic Study of Atherosclerosis (2015) (0)
- Deep phenotyping and genomic data from a nationally representative study on dementia in India (2023) (0)
- Epigenome‐wide association study of BMI in Black populations from InterGEN and GENOA (2022) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
- Epigenome-wide meta-analysis reveals differential DNA methylation associated with estimated glomerular filtration rate among African American men with HIV (2023) (0)
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) (0)
- Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study (2022) (0)
- Correction: Association of low-frequency and rare coding variants with information processing speed (2022) (0)
- Associations between self-referral and health behavior responses to genetic risk information (2015) (0)
- Genome-wide association and functional follow-up reveals new loci for kidney function | NOVA. The University of Newcastle's Digital Repository (2012) (0)
- Contribution of Regulatory and Structural Variations in the APOE Gene to Predicting Dyslipidemia (2005) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- SNP-by-CpG Site Interactions in ABCA7 Are Associated with Cognition in Older African Americans (2022) (0)
- Abstract P185: Novel Loci for Blood Pressure Using Gene-alcohol Interactions and 1000g Imputed Data (2016) (0)
- Epigenetic age acceleration is associated with cardiometabolic risk factors and clinical cardiovascular disease risk scores in African Americans (2021) (0)
- Epigenetic loci for blood pressure are associated with hypertensive target organ damage in older African Americans from the genetic epidemiology network of Arteriopathy (GENOA) study (2020) (0)
- The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus (2019) (0)
- Rare coding variants in RCN3 are associated with blood pressure (2022) (0)
- The genetic determinants of recurrent somatic mutations in 43,693 blood genomes (2023) (0)
- Contents Vol. 71, 2011 (2011) (0)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
- A067: Antihypertensive drug therapy and its efficacy in the GENOA study: Do ends justify means? (2000) (0)
- ’ s response to reviews Title : Intrinsic and Extrinsic Epigenetic Age Acceleration are associated with Hypertensive Target Organ Damage in Older African Americans (2019) (0)
- Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the multi-ethnic study of atherosclerosis (2015) (0)
- A Critical Analysis of White Racial Framing and Comfort with Medical Research. (2023) (0)
- Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing (2022) (0)
- Multivariate, region‐based genetic analyses of facets of reproductive aging in White and Black women (2022) (0)
- Key influence of sex on urine volume and osmolality (2016) (0)
- DNA methylation analysis identifies novel genetic loci associated with circulating fibrinogen levels in blood. (2023) (0)
- Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium (2022) (0)
- ' s response to reviews Title : Investigating the complex genetic architecture of ankle-brachial index , a measure of peripheral arterial disease , in non-Hispanic whites (2008) (0)
This paper list is powered by the following services:
Other Resources About Sharon Kardia
What Schools Are Affiliated With Sharon Kardia?
Sharon Kardia is affiliated with the following schools:
