Myriam Fornage

The University of Texas Health Science Center at Houston

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

23.3Author DataRank

Indexed papers

26in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 26 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association

Circulation(2020)10.1161/cir.0000000000000757

Top 2%

9.1DataRank

Top 2%9396 citations

Jesus Ramon Castro, Emelia J. Benjamin, Marcio S. Bittencourt, Clifton W. Callaway, April P. Carson +45 more

Papers

Driven by 223 papers — median percentile 53. Top paper: “Inherited causes of clonal haematopoiesis in 97,691 whole genomes”.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Nature(2020)10.1038/s41586-020-2819-2

N/A

11.6DataRank · unranked

748 citations

Joshua S. Weinstock, Satish K. Nandakumar, Charles P. Fulco, Erik L. Bao, Seyedeh M. Zekavat +95 more

Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association

Circulation(2020)10.1161/cir.0000000000000757

Top 2%

9.1DataRank

Top 2%9396 citations

Jesus Ramon Castro, Emelia J. Benjamin, Marcio S. Bittencourt, Clifton W. Callaway, April P. Carson +45 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 more

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

Genome biology(2021)10.1186/s13059-021-02398-9

N/A

5.8DataRank · unranked

307 citations

Josine L. Min, Rebecca Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies +95 more

Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium

PLoS Genetics(2011)10.1371/journal.pgen.1001371

N/A

5.4DataRank · unranked

140 citations

Noah Zaitlen, Guillaume Lettre, Gary K. Chen, Arti Tandon, W. H. Linda Kao +40 more

Large-scale plasma proteomic analysis identifies proteins and pathways associated with dementia risk

Nature Aging(2021)10.1038/s43587-021-00064-0

N/A

4.1DataRank · unranked

211 citations

Jingsha Chen, Jingning Zhang, Myriam Fornage, Yunju Yang, Linda Zhou +20 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Genome Medicine(2020)10.1186/s13073-020-00778-7

N/A

3.0DataRank · unranked

123 citations

Ryan J. Longchamps, Jason A. Sumpter, Charles Newcomb, John Lane, Megan L. Grove +19 more

Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations

Communications Biology(2022)10.1038/s42003-022-03812-z

N/A

2.3DataRank · unranked

108 citations

Genevieve Lyons, Santiago Romero‐Brufau, Nuzulul Kurniansyah, Jennifer A. Brody, Xiuqing Guo +17 more

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Nature Communications(2022)10.1038/s41467-022-31080-2

N/A

2.1DataRank · unranked

80 citations

Matthew Goodman, Tanika N. Kelly, Tali Elfassy, Kerri L. Wiggins, Joshua C. Bis +32 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Nature(2023)10.1038/s41586-023-05806-1

N/A

2.1DataRank · unranked

107 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk

Diabetes Care(2023)10.2337/dc23-0805

N/A

1.5DataRank · unranked

71 citations

Alisa K. Manning, Jennifer Wessel, Sridharan Raghavan, Kenneth E. Westerman, Alexander G. Bick +27 more

Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure

Hypertension(2020)10.1161/hypertensionaha.120.14973

N/A

1.4DataRank · unranked

87 citations

Miina Ollikainen, Maheswary Muniandy, Tao Zhang, Jenny van Dongen, Guang Hao +47 more

Association of mitochondrial DNA copy number with cardiometabolic diseases

Cell Genomics(2021)10.1016/j.xgen.2021.100006

N/A

1.4DataRank · unranked

62 citations

Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao +33 more

Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

Stroke(2021)10.1161/strokeaha.120.031792

Top 16%

1.3DataRank

Top 16%38 citations

Jeffrey W. Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser +34 more

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.011

N/A

1.1DataRank · unranked

34 citations

Anne E. Justice, Kristin L. Young, Eirini Marouli, Xinruo Zhang, Rebecca S. Fine +220 more

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

Nature Communications(2021)10.1038/s41467-021-23899-y

N/A

1.1DataRank · unranked

45 citations

Michael Mendelson, Rory Wilson, Rahul Gondalia, Roby Joehanes, Elias Salfati +59 more

Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood

Cell(2019)10.1016/j.cell.2019.03.028

N/A

1.0DataRank · unranked

842 citations

Mark Chaffin, Kaitlin H. Wade, Sohail Zahid, Joseph Brancale, Rui Xia +14 more

Single-Nucleotide Polymorphism Genotyping for Disease Association Studies

Hypertension10.1385/1-59259-850-1:159

N/A

1.0DataRank · unranked

13 citations

Peter A. Doris, Myriam Fornage

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

Journal of the American Heart Association(2023)10.1161/jaha.122.029090

N/A

0.920DataRank · unranked

30 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, M M Lai, Kerri L. Wiggins +40 more

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Hypertension(2022)10.1161/hypertensionaha.122.19324

Top 24%

0.842DataRank

Top 24%29 citations

Xiao Sun, Karen He, Michael R. Brown, Sarah A. Gagliano Taliun, Jacklyn N. Hellwege +95 more

Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

Stroke(2021)10.1161/strokeaha.121.037388

N/A

0.801DataRank · unranked

208 citations

Seyedeh M. Zekavat, Jeffrey Haessler, Myriam Fornage, Laura M. Raffield, Md Mesbah Uddin +28 more

Clonal hematopoiesis is associated with protection from Alzheimer’s disease

Nature Medicine(2023)10.1038/s41591-023-02397-2

N/A

0.755DataRank · unranked

152 citations

Julia A. Belk, Max Jan, Yanyan Qi, Chloé Sarnowski, Sara A. Wirth +23 more

Genome-wide association analysis identifies six new loci associated with forced vital capacity

Nature Genetics(2014)10.1038/ng.3011

N/A

0.754DataRank · unranked

151 citations

María Soler Artigas, Sina A Gharib, Louise V Wain, Nora Franceschini, Beate Koch +155 more

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Nature Genetics(2023)10.1038/s41588-023-01518-4

N/A

0.753DataRank · unranked

150 citations

Maxime M. Bos, Hanna J. Barnes, Christian L. Lino Cardenas, Doris Wong, Haojie Lu +84 more

Proteomics analysis of plasma from middle-aged adults identifies protein markers of dementia risk in later life

Science Translational Medicine(2023)10.1126/scitranslmed.adf5681

N/A

0.738DataRank · unranked

136 citations

Jingsha Chen, Shi Liu, Yunju Yang, Myriam Fornage, Linda Zhou +20 more

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428

Top 27%

0.737DataRank

Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

Nature Genetics(2023)10.1038/s41588-023-01338-6

N/A

0.727DataRank · unranked

126 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +24 more

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

Human Molecular Genetics(2021)10.1093/hmg/ddab252

Top 28%

0.724DataRank

Top 28%20 citations

Yao Hu, Quan Sun, Deepti Jain, Jai Broome, Ming‐Huei Chen +62 more

Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

Brain(2021)10.1093/brain/awab432

N/A

0.696DataRank · unranked

35 citations

Cécile Duplàa, Dina Vojinović, Hideaki Suzuki, Nuno R. Zilhäo, Shuo Li +61 more

Methylome-Wide Association Study of Central Adiposity Implicates Genes Involved in Immune and Endocrine Systems

Epigenomics(2020)10.2217/epi-2019-0276

Top 29%

0.694DataRank

Top 29%16 citations

Geetha Chittoor, Rahul Gondalia, Phillip E. Melton, Elise Lim, Megan L. Grove +23 more

Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease

Nature Communications(2022)10.1038/s41467-022-33093-3

N/A

0.692DataRank · unranked

100 citations

Ngoc Quynh Nguyen, Bing Yu, Jennifer A. Brody, Akhil Pampana, Tetsushi Nakao +27 more

Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

Communications Biology(2023)10.1038/s42003-023-05454-1

N/A

0.689DataRank · unranked

22 citations

Alison E. Fohner, Qiong Yang, Jennifer A. Brody, Gail Davies, Jie Yao +52 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature Genetics(2023)10.1038/s41588-023-01553-1

N/A

0.681DataRank · unranked

31 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +46 more

Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes

Cerebral Cortex(2020)10.1093/cercor/bhaa035

Top 30%

0.676DataRank

Top 30%26 citations

Shaojie Ma, Edith Hofer, Yash Patel, Daniel E. Vosberg, Steven Tilley +64 more

Whole Blood DNA Methylation Signatures of Diet Are Associated With Cardiovascular Disease Risk Factors and All-Cause Mortality

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002766

N/A

0.673DataRank · unranked

88 citations

Casey M. Rebholz, Kim V.E. Braun, Lindsay M. Reynolds, Stella Aslibekyan, Rui Xia +45 more

Longitudinal change in blood DNA epigenetic signature after smoking cessation

Epigenetics(2021)10.1080/15592294.2021.1985301

N/A

0.649DataRank · unranked

19 citations

Roby Joehanes, Weihua Guan, Tianxiao Huan, Dawn L. DeMeo, Megan L. Grove +4 more

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

Human Genetics(2021)10.1007/s00439-021-02394-w

N/A

0.648DataRank · unranked

74 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, Jon D. Lane, Megan L. Grove +47 more

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

Frontiers in Endocrinology(2022)10.3389/fendo.2022.863893

N/A

0.642DataRank · unranked

21 citations

Shing Wan Choi, Nathalie Chami, Eric Boerwinkle, Myriam Fornage, Susan Redline +36 more

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

Stroke(2020)10.1161/strokeaha.120.029123

N/A

0.637DataRank · unranked

69 citations

Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng +43 more

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

American Journal of Epidemiology(2021)10.1093/aje/kwab115

N/A

0.631DataRank · unranked

66 citations

Leslie S. Emery, Jai Broome, Erin Buth, Alyna Khan, Cecelia Laurie +67 more

MRI free water as a biomarker for cognitive performance: Validation in the MarkVCID consortium

Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring(2022)10.1002/dad2.12362

N/A

0.617DataRank · unranked

22 citations

Laura J. Hillmer, Hanzhang Lu, Konstantinos Arfanakis, Brian T. Gold, Christopher E. Bauer +19 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.014

N/A

0.605DataRank · unranked

14 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +64 more

Circulating trimethylamine N-oxide in association with diet and cardiometabolic biomarkers: an international pooled analysis

American Journal of Clinical Nutrition(2020)10.1093/ajcn/nqaa430

N/A

0.604DataRank · unranked

55 citations

Xiao‐Ou Shu, David M. Herrington, Steven C. Moore, Katie A. Meyer, Jennifer Ose +21 more

A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

Blood(2024)10.1182/blood.2023021452

N/A

0.601DataRank · unranked

23 citations

Paula Reventún, Michael R. Brown, Adam S. Heath, Jennifer E. Huffman, Ngoc‐Quynh Le +90 more

Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

Nature Communications(2023)10.1038/s41467-023-38990-9

N/A

0.578DataRank · unranked

46 citations

Matthew Goodman, Alyna Khan, Jiongming Wang, Elena V. Feofanova, Joshua C. Bis +38 more

Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI

Brain(2022)10.1093/brain/awac290

N/A

0.574DataRank · unranked

45 citations

Maria J. Knol, Ruiqi Wang, Aniket Mishra, Dan Liu, Michelle Luciano +47 more

A population‐based meta‐analysis of circulating GFAP for cognition and dementia risk

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51652

N/A

0.564DataRank · unranked

42 citations

Crystal Wiedner, Chen‐Pin Wang, Qianqian Liu, Joshua C. Bis, Chi Kong Li +27 more

Unsupervised deep representation learning enables phenotype discovery for genetic association studies of brain imaging

Communications Biology(2024)10.1038/s42003-024-06096-7

N/A

0.561DataRank · unranked

41 citations

Ziqian Xie, Hao Yuan, Sheikh Muhammad Saiful Islam, Yaochen Xie, Wei He +10 more

Integrative analysis of clinical and epigenetic biomarkers of mortality

Aging Cell(2022)10.1111/acel.13608

N/A

0.561DataRank · unranked

41 citations

Steve Nguyen, Elena Colicino, Carolina Ochoa‐Rosales, W. David Hill, Jennifer A. Brody +43 more

Investigating Associations of Omega-3 Fatty Acids, Lung Function Decline, and Airway Obstruction

American Journal of Respiratory and Critical Care Medicine(2023)10.1164/rccm.202301-0074oc

N/A

0.561DataRank · unranked

41 citations

Pallavi Balte, Traci M. Bartz, R. Graham Barr, Myriam Fornage, Mariaelisa Graff +19 more

Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202108-1907oc

N/A

0.546DataRank · unranked

37 citations

Tianxiao Huan, Daniel L. McCartney, Geetha Chittoor, Maaike de Vries, Lies Lahousse +57 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0.534DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

Genomic and phenomic landscape of clonal hematopoiesis in over a million ancestrally diverse participants

medRxiv(2022)10.1101/2022.07.29.22278015

Top 37%

0.528DataRank

Top 37%13 citations

Zhi Yu, Joshua S. Weinstock, Abhishek Niroula, Satoshi Koyama, Tetsushi Nakao +83 more

Genetic associations between sleep traits and cognitive ageing outcomes in the Hispanic Community Health Study/Study of Latinos

EBioMedicine(2022)10.1016/j.ebiom.2022.104393

N/A

0.524DataRank · unranked

32 citations

Michael Elgart, Einat Granot‐Hershkovitz, Heming Wang, Wassim Tarraf, Alberto R. Ramos +14 more

Rare genetic variants explain missing heritability in smoking

Nature Human Behaviour(2022)10.1038/s41562-022-01408-5

N/A

0.520DataRank · unranked

31 citations

Luke M. Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes +85 more

Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

BMC Genomics(2020)10.1186/s12864-020-6626-9

N/A

0.515DataRank · unranked

30 citations

Antoine Baldassari, Stephanie A. Bien, Laura M. Raffield, Heather M. Highland, Colleen M. Sitlani +16 more

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +95 more

Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer’s disease etiopathogenesis

Aging(2021)10.18632/aging.202950

N/A

0.510DataRank · unranked

29 citations

Alzheimer’s Disease Neuroimaging Initiative (ADNI)*, Sonia Moreno–Grau, Shahzad Ahmad, Antonio González-Pérez, Itziar de Rojas +32 more

Association of Plasma YKL-40 With MRI, CSF, and Cognitive Markers of Brain Health and Dementia

Neurology(2024)10.1212/wnl.0000000000208075

N/A

0.505DataRank · unranked

28 citations

Jayandra J. Himali, Raquel Puerta, Alexa Beiser, Mitzi M. Gonzales, Claudia L. Satizábal +21 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.007

N/A

0.494DataRank · unranked

26 citations

Caitlin McHugh, Linda M. Polfus, Laura M. Raffield, Meher Preethi Boorgula, Thomas W. Blackwell +88 more

Leukocyte Traits and Exposure to Ambient Particulate Matter Air Pollution in the Women’s Health Initiative and Atherosclerosis Risk in Communities Study

Environmental Health Perspectives(2020)10.1289/ehp5360

N/A

0.489DataRank · unranked

25 citations

Katelyn M. Holliday, Antoine Baldassari, Anne E. Justice, James D. Stewart, Duanping Liao +18 more

Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.007

N/A

0.489DataRank · unranked

25 citations

Dandi Qiao, Wonji Kim, Matthew Moll, Pallavi Balte, Leslie A. Lange +46 more

Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.02.013

N/A

0.484DataRank · unranked

12 citations

Genevieve L. Wojcik, Mariaelisa Graff, Katherine K. Nishimura, Chani J. Hodonsky, Antoine Baldassari +31 more

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

BMC Genomics(2021)10.1186/s12864-021-07745-5

N/A

0.477DataRank · unranked

23 citations

Stephanie A. Bien, Katherine K. Nishimura, Jeffrey Haessler, Chani J. Hodonsky, Antoine Baldassari +29 more

Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

Nature Genetics(2024)10.1038/s41588-024-01951-z

N/A

0.470DataRank · unranked

22 citations

Adrián I. Campos, Santiago Díaz‐Torres, Jill A. Rabinowitz, Zuriel Ceja, Brittany L. Mitchell +95 more

Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

Genes(2021)10.3390/genes12071049

N/A

0.457DataRank · unranked

20 citations

Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Jiawen Chen +31 more

Gaseous air pollutants and DNA methylation in a methylome-wide association study of an ethnically and environmentally diverse population of U.S. adults

Environmental Research(2022)10.1016/j.envres.2022.113360

N/A

0.457DataRank · unranked

20 citations

Rahul Gondalia, Antoine Baldassari, Anne E. Justice, James D. Stewart, Duanping Liao +26 more

Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos

Translational Psychiatry(2020)10.1038/s41398-020-00930-2

N/A

0.457DataRank · unranked

20 citations

Tamar Sofer, Wassim Tarraf, Jan Bressler, Jessica D. Faul, Wei Zhao +15 more

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

Cell Genomics(2023)10.1016/j.xgen.2023.100468

N/A

0.457DataRank · unranked

20 citations

Amy R. Bentley, Charles E. Breeze, François Aguet, Xiaoguang Xu, Girish N. Nadkarni +69 more

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7

N/A

0.442DataRank · unranked

18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores

Scientific Reports(2024)10.1038/s41598-024-62945-9

N/A

0.436DataRank · unranked

7 citations

Benjamin Shea, Michael Elgart, Nuzulul Kurniansyah, Genevieve Lyons, Alanna C. Morrison +32 more

Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.012

N/A

0.431DataRank · unranked

8 citations

Xinyue Rui, David V. Conti, Myriam Fornage, Mariaelisa Graff, Jeffrey Haessler +13 more

Genetic risk factors underlying white matter hyperintensities and cortical atrophy

Nature Communications(2024)10.1038/s41467-024-53689-1

N/A

0.425DataRank · unranked

16 citations

Jean Shin, Eeva Sliz, Ariana Tang, Aniket Mishra, Rui Xia +35 more

Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease

Human Molecular Genetics(2022)10.1093/hmg/ddac290

N/A

0.416DataRank · unranked

15 citations

Xiao Sun, Xuenan Mi, Zhijie Huang, Y.Y. Hsu, James E. Hixson +47 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

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BMC Genomic Data(2025)10.1186/s12863-025-01360-z

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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

UNC Libraries(2025)10.17615/cdn0-cm52

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UNC Libraries(2025)10.17615/mztm-gw84

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UNC Libraries(2025)10.17615/yvmq-kt94

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0 citations

Xiaoguang Xu, Jason G. Umans, Thomas Gilliland, Charles Kooperberg, Mariah Meyer +69 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

UNC Libraries(2025)10.17615/5tss-f273

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Eric Boerwinkle, Yash Pershad, K.E. North, Fulong Yu, Center, Regeneron Genetics +66 more

Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

10.1101/2025.06.11.25329426

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Mohsen Sharifitabar, Alexa Beiser, Claudia L. Satizábal, Thomas H. Mosley, Joanne E. Curran +34 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

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0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

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Briefings in Bioinformatics(2026)10.1093/bib/bbag142

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0 citations

Kent D Taylor, Jerome I. Rotter, Stephen S Rich, Yinan Zheng, Lifang Hou +12 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

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Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

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medRxiv(2021)10.1101/2021.06.16.21258702

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8 citations

Einat Granot‐Hershkovitz, Ying Zhang, Jan Bressler, Wassim Tarraf, Bing Yu +16 more

Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.25.428086

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8 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, John Lane, ML Grove +47 more

Plasma metabolites associated with cognitive function across race/ethnicities affirming the importance of healthy nutrition

Alzheimer s & Dementia(2022)10.1002/alz.12786

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0DataRank · unranked

15 citations

Shan He, Jan Bressler, Bing Yu, Wassim Tarraf, Casey M. Rebholz +13 more

Blood metabolites predicting mild cognitive impairment in the study of Latinos‐investigation of neurocognitive aging (HCHS/SOL)

Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring(2022)10.1002/dad2.12259

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16 citations

Einat Granot‐Hershkovitz, Ying Zhang, Jan Bressler, Wassim Tarraf, Bing Yu +16 more

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Annals of Neurology(2022)10.1002/ana.26569

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11 citations

Myriam Fornage, Lenore J. Launer, Mohamad Habes, Christos Davatzikos, Kristine Yaffe +1 more

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Epigenetics(2022)10.1080/15592294.2022.2026591

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11 citations

Yue Lu, Myriam Fornage, Li Jiao, Jianjun Shen, Donghui Li +2 more

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American Journal of Clinical Nutrition(2021)10.1093/ajcn/nqab152

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49 citations

Jae Jeong Yang, Xiao‐Ou Shu, Steven C. Moore, Nicholette D Palmer, Marta Guasch‐Ferré +23 more

Epigenome-wide association meta-analysis of DNA methylation with coffee and tea consumption

Nature Communications(2021)10.1038/s41467-021-22752-6

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56 citations

Eliana Portilla-Fernández, Yang Li, Jiantao Ma, Silvana C. E. Maas, Daokun Sun +45 more

Epigenetic Age and the Risk of Incident Atrial Fibrillation

Circulation(2021)10.1161/circulationaha.121.056456

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0DataRank · unranked

118 citations

Eric Vittinghoff, Ake T. Lu, Álvaro Alonso, Biqi Wang, Colleen M. Sitlani +23 more

Plasma metabolites associated with cognitive function across race/ethnicities affirming the importance of healthy nutrition

medRxiv(2022)10.1101/2022.03.09.22271910

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2 citations

Shan He, Jan Bressler, Bing Yu, Wassim Tarraf, Casey M. Rebholz +13 more

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

UNC Libraries(2020)10.17615/jcdv-pt45

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0 citations

Wei Zhao, Cathryn M. Lewis, Thomas G. Schulze, Philip L. De Jager, Markus M. Nöthen +95 more

Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection

UNC Libraries(2020)10.17615/hjj0-4367

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0 citations

Pardis C. Sabeti, Leslie A. Lange, Josyf C. Mychaleckyj, George Papanicolaou, Noah Zaitlen +27 more

Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults

UNC Libraries(2020)10.17615/6xbd-1w54

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0 citations

Gorka Alkorta‐Aranburu, Xuemei Huang, Nora Franceschini, Steven R. Cummings, Honglei Chen +19 more

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

UNC Libraries(2020)10.17615/wn5h-av49

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0 citations

David Couper, Struan F.A. Grant, Tamara B. Harris, Santhi K. Ganesh, Sampath Arepalli +27 more

Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study

UNC Libraries(2020)10.17615/0bgd-vd04

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0 citations

Myriam Fornage, Kari E. North, Molly S. Bray, Bruce D. Hammock, John W. Newman +5 more

Mendelian randomization of blood lipids for coronary heart disease

Utrecht University Repository (Utrecht University)(2020)10.17615/vm5z-r604

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0 citations

Reecha Sofat, Sonia Shah, Suthesh Sivapalaratnam, Daniel I. Swerdlow, Jon White +27 more

Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium

UNC Libraries(2020)10.17615/3jdw-6426

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0 citations

Leslie A. Lange, Michael F. Press, Elisa V. Bandera, L. Adrienne Cupples, Solomon K. Musani +27 more

Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

UNC Libraries(2020)10.17615/bzpx-ja61

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0 citations

James S. Pankow, Megan L. Grove, Yi‐Hui Zhou, Åsa K. Hedman, Marguerite R. Irvin +19 more

The landscape of recombination in African Americans

UNC Libraries(2020)10.17615/hgd9-hc10

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0 citations

W. Ryan Diver, Sarah G. Buxbaum, Sue A. Ingles, Sonja I. Berndt, Boerwinkle, Eric +27 more

A Phenomics-Based Strategy Identifies Loci on APOC1, BRAP, and PLCG1 Associated with Metabolic Syndrome Phenotype Domains

UNC Libraries(2020)10.17615/j176-x981

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0 citations

Kari E. North, Sarah A. Pendergrass, José Luis Ambite, Lynne R. Wilkens, Charles Kooperberg +13 more

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

UNC Libraries(2020)10.17615/d3kg-q519

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0 citations

Patricia A. Cassano, Jing Zhao, Guðný Eiríksdóttir, Gauti Kjartan Gíslason, Jennifer E. Huffman +27 more

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Publisher(2020)10.17615/tme1-9982

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0 citations

Keolu Fox, Ping An, Li Li, Marie‐France Hivert, Laura J. Rasmussen‐Torvik +27 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

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Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

UNC Libraries(2020)10.17615/hx9s-wm59

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0 citations

Devin Absher, Petra Bůžková, Wayne H.-H. Sheu, Wen‐Jane Lee, Ran Tao +52 more

Genome-wide association study of selenium concentrations

UNC Libraries(2020)10.17615/vcdg-ss44

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0 citations

Pengcheng Xun, Myriam Fornage, Joanne M. Jordan, Millennia Foy, Frank B. Hu +8 more

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

Genetics(2023)10.1093/genetics/iyad115

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10 citations

Dafni A. Glinos, Eric Boerwinkle, Peter J. Castaldi, Dawood Darbar, Mariza de Andrade +28 more

Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults

UNC Libraries(2020)10.17615/v0aq-7b55

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0 citations

Lynne J. Hocking, Najaf Amin, Lori L. Bonnycastle, Ching‐Ti Liu, Inês Barroso +95 more

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

UNC Libraries(2020)10.17615/sbz9-wg52

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0 citations

Rebecca D. Jackson, Valeska Redon, Gina M. Peloso, Joshua C. Bis, Arend Voorman +27 more

Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study

PLoS ONE(2023)10.1371/journal.pone.0285259

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7 citations

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Scientific Reports(2023)10.1038/s41598-023-32028-2

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7 citations

Rui Xia, Yunju Yang, Brian Spitzer, Wassim Tarraf, Priscilla M. Vásquez +10 more

Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

MURAL - Maynooth University Research Archive Library (National University of Ireland, Maynooth)(2020)10.17615/8trn-p892

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0 citations

W. T. Longstreth, Reinhold Schmidt, Paul Freudenberger, Pamela J. Schreiner, Stella Trompet +95 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

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0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

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medRxiv(2023)10.1101/2023.01.31.23285251

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4 citations

Farid Khasiyev, Sanjeev Sariya, Antonio Spagnolo‐Allende, Danurys Sanchez, Howard Andrews +18 more

Epigenome-wide association study of incident type 2 diabetes in Black and White participants from the Atherosclerosis Risk in Communities Study

medRxiv(2023)10.1101/2023.08.09.23293896

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4 citations

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Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study

UNC Libraries(2023)10.17615/g0mj-1s30

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0 citations

Alanna C. Morrison, Paul S. de Vries, Natalie R. Hasbani, David Couper, Vijay Nambi +6 more

Associations of cardiometabolic polygenic risk scores with cardiovascular disease in African Americans

Research Square(2023)10.21203/rs.3.rs-3228815/v1

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0 citations

Jian Ying, Berhanu Gebremeskel G., Tianyuan Lu, April F. Mohanty, Tali Elfassy +15 more

Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores

medRxiv(2023)10.1101/2023.12.13.23299909

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0 citations

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Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study

UNC Libraries(2020)10.17615/3pkd-qx31

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0 citations

Elisa T. Lee, Myriam Fornage, José Luis Ambite, Fredrick R. Schumacher, Lucia A. Hindorff +27 more

Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

UNC Libraries(2020)10.17615/xs3t-3334

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0 citations

Annette L. Fitzpatrick, Luigi Ferrucci, Paul M. Ridker, Bertram Müller-Myhsok, Arezoo Assareh +95 more

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

UNC Libraries(2020)10.17615/9842-r797

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0 citations

Jeffrey Haessler, Rebecca Rohde, Lynne R. Wilkens, Peters, Ulrike, Christopher S. Carlson +27 more

find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.23.394296

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0 citations

Florian Thibord, Paul L. Auer, John Blangero, Zeynep Coban‐Akdemir, James S. Floyd +11 more

Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations

UNC Libraries(2020)10.17615/408q-rq81

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1 citations

Angelo Gaffo, Nancy S. Jenny, Jason G. Umans, Anna Köttgen, Tara C. Matise +17 more

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

UNC Libraries(2020)10.17615/003k-2b61

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2 citations

Cristen J. Willer, Jennifer A. Brody, Eric Boerwinkle, Joshua C. Bis, Jeffery Haessler +27 more

Intracranial Volume Is Driven by Both Genetics and Early Life Exposures: The SOL-INCA-MRI Study

Ethnicity & Disease(2024)10.18865/ed.34.2.103

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3 citations

Einat Granot‐Hershkovitz, Wassim Tarraf, Paola Filigrana, Carmen R. Isasi, Shakira F. Suglia +10 more

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

UNC Libraries(2020)10.17615/vygp-he02

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7 citations

Richard S. Cooper, Michele K. Evans, Hua Tang, Alex P. Reiner, Colin A. McKenzie +74 more

Genome-Wide Association Study Meta-Analysis Uncovers Novel Genetic Variants Associated with Olfactory Dysfunction

View(2024)10.1101/2024.08.09.24311665

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1 citations

Konstantinos Melas, Adrienne Tin, Valentina Talevi, Honglei Chen, Myriam Fornage +13 more

Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

UNC Libraries(2024)10.17615/a7t8-mf18

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0 citations

Stephen S. Rich, Xin Hu, B.E Cade, TOPMed Lung Working Group, Shannon Dugan‐Perez +47 more

Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease

UNC Libraries(2024)10.17615/6p0e-2r19

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0 citations

N Sotoodehnia, Siddhartha Jaiswal, J.M Murabito, Jerome I. Rotter, E.A. Whitsel +27 more

Integrative analysis of clinical and epigenetic biomarkers of mortality

UNC Libraries(2024)10.17615/xaw2-3j65

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0 citations

Jian Ma, James S. Pankow, M Waldenberger, Yao, C, Annette Peters +43 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

UNC Libraries(2024)10.17615/vs68-ca81

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0 citations

Ryan L. Minster, Fernando D. Martínez, Dawood Darbar, Juan M. Peralta, Barbara A. Konkle +93 more

Determinants of mosaic chromosomal alteration fitness

UNC Libraries(2024)10.17615/yx5k-ka41

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0 citations

Taralynn Mack, Margaret F. Doyle, Yash Pershad, Paul L. Auer, Jeong H. Yun +39 more

Association of blood pressure with cognitive function at midlife: a Mendelian randomization study

BMC Medical Genomics(2020)10.1186/s12920-020-00769-y

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21 citations

Emy A. Thomas, Lenore J. Launer, Stephen Sidney, Kristine Yaffe, Myriam Fornage +1 more

APOE alleles’ association with cognitive function differs across Hispanic/Latino groups and genetic ancestry in the study of Latinos‐investigation of neurocognitive aging (HCHS/SOL)

Alzheimer s & Dementia(2020)10.1002/alz.12205

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75 citations

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