Laura M. Raffield

University of North Carolina at Chapel Hill

Biochemistry, Genetics and Molecular BiologyMedicine

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

8.3Author DataRank

Indexed papers

22in 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 22 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.

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084

Top 10%

2.1DataRank

Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Papers

Driven by 218 papers — median percentile 35. 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

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Cell(2020)10.1016/j.cell.2020.06.045

N/A

8.3DataRank · unranked

739 citations

Laura M. Raffield, Abdou Mousas, Saori Sakaue, Jennifer E. Huffman, Arden Moscati +95 more

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature Genetics(2022)10.1038/s41588-021-00997-7

N/A

7.2DataRank · unranked

363 citations

Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker +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

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

Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

Aging Cell(2021)10.1111/acel.13366

N/A

3.3DataRank · unranked

134 citations

Ake T. Lu, Alexander G. Bick, Pradeep Natarajan, Joshua Weinstock, Mindy D Szeto +29 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

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084

Top 10%

2.1DataRank

Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 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

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

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

Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression

American Journal of Psychiatry(2023)10.1176/appi.ajp.20230053

N/A

1.3DataRank · unranked

69 citations

Enda M. Byrne, Jacqueline Kiewa, Shuyang Yao, Anna E. Bauer, Karolina A. Åberg +73 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

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature Genetics(2022)10.1038/s41588-022-01225-6

N/A

1.2DataRank · unranked

63 citations

Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +95 more

The trans-ancestral genomic architecture of glycemic traits

Nature Genetics(2021)10.1038/s41588-021-00852-9

N/A

1.0DataRank · unranked

907 citations

Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan +95 more

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Nature Genetics(2022)10.1038/s41588-022-01058-3

N/A

0.994DataRank · unranked

754 citations

Cassandra N. Spracklen, Weihua Zhang, Maggie C. Y. Ng, Lauren E. Petty, Hidetoshi Kitajima +95 more

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Cell(2020)10.1016/j.cell.2020.08.008

N/A

0.988DataRank · unranked

722 citations

Erik L. Bao, Parsa Akbari, Caleb A. Lareau, Abdou Mousas, Tao Jiang +95 more

Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

PLoS Genetics(2023)10.1371/journal.pgen.1010517

N/A

0.970DataRank · unranked

40 citations

François Aguet, Kristin G. Ardlie, Jiawen Chen, Elaine Cornell, Dan Cruz +22 more

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

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.010

N/A

0.893DataRank · unranked

37 citations

Matthew P. Conomos, Sarah C. Nelson, Sally N. Adebamowo, Ananyo Choudhury, David V. Conti +90 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

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

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

Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

Translational Psychiatry(2020)10.1038/s41398-020-00953-9

N/A

0.706DataRank · unranked

110 citations

Dan Liang, Huaigu Sun, Nil Aygün, Jessica C. McAfee, Jessica E. Davis +8 more

TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.006

N/A

0.701DataRank · unranked

106 citations

Jonathan D. Rosen, Quan Sun, Jiawen Chen, Marsha M. Wheeler, Ying Zhou +20 more

Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol

Diabetes Care(2021)10.2337/dc21-1284

N/A

0.700DataRank · unranked

26 citations

Jee‐Young Moon, Iyas Daghlas, Franco Giulianini, Bianca Porneala, Fariba Ahmadizar +47 more

DNAmFitAge: biological age indicator incorporating physical fitness

Aging(2023)10.18632/aging.204538

N/A

0.692DataRank · unranked

100 citations

Zsolt Radak, Ferenc Torma, Matyas Jokai, Ake T. Lu, Daniel W. Belsky +15 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

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

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study

Scientific Reports(2023)10.1038/s41598-023-39936-3

Top 31%

0.641DataRank

Top 31%32 citations

Helena Bui, Roby Joehanes, Jiantao Ma, Chunyu Liu, Tianxiao Huan +31 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

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Malaria is a cause of iron deficiency in African children

Nature Medicine(2021)10.1038/s41591-021-01238-4

N/A

0.626DataRank · unranked

64 citations

Alexander J. Mentzer, Ruth E. Mitchell, Emily L. Webb, Anthony Etyang, Catherine Kyobutungi +39 more

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

Nature Genetics(2023)10.1038/s41588-022-01282-x

N/A

0.606DataRank · unranked

56 citations

Xingyan Wang, Seon-Kyeong Jang, Bryan C. Quach, J. Dylan Weissenkampen, Chachrit Khunsriraksakul +85 more

Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci

Genome Medicine(2021)10.1186/s13073-021-00877-z

N/A

0.606DataRank · unranked

56 citations

Anna Batorsky, Mi Kyeong Lee, Mindy D Szeto, Xiaoguang Xu, Daniel L. McCartney +37 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

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

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

Communications Biology(2022)10.1038/s42003-022-03702-4

Top 34%

0.582DataRank

Top 34%16 citations

Sheila M. Gaynor, Emily M. Russell, Kenneth E. Westerman, Laura M. Raffield, Timothy D. Majarian +88 more

Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

Diabetologia(2021)10.1007/s00125-021-05635-9

N/A

0.553DataRank · unranked

39 citations

Sofia F. Dimos, Stephanie A. Bien, Yao Hu, Burcu F. Darst, Linda M. Polfus +26 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

From GWAS variant to function: A study of ∼148,000 variants for blood cell traits

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100063

N/A

0.523DataRank · unranked

15 citations

Cheynna Crowley, Le Huang, Jia Wen, Jiawen Chen, Erik L. Bao +7 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

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0.505DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 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

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

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Nature Communications(2022)10.1038/s41467-022-28729-3

N/A

0.470DataRank · unranked

22 citations

Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess +91 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

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

Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans

PLoS ONE(2020)10.1371/journal.pone.0231013

N/A

0.442DataRank · unranked

18 citations

Neil A. Zakai, Paul L. Auer, Mary Cushman, Ethan M. Lange, Emily B. Levitan +8 more

Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits

Human Molecular Genetics(2022)10.1093/hmg/ddac011

N/A

0.442DataRank · unranked

18 citations

Sanan Venkatesh, Manuel Tardáguila, Jia Wen, Jonathan D. Rosen, Amanda L. Tapia +13 more

The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes

Diabetologia(2023)10.1007/s00125-023-05912-9

N/A

0.434DataRank · unranked

17 citations

Philip Schroeder, Ravi Mandla, Aaron J. Deutsch, Wanying Zhu, Lauren E. Petty +59 more

Additive Value of Polygenic Risk Score to Family History for Type 2 Diabetes Prediction: Results From the All of Us Research Database

Diabetes Care(2025)10.2337/dc24-1537

Top 43%

0.429DataRank

Top 43%4 citations

Laura M. Raffield, Katherine Kolor, Alain K. Koyama, Ramal Moonesinghe, Meda E. Pavkov +3 more

Investigating Gene–Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits

Diabetes(2023)10.2337/db22-0851

N/A

0.425DataRank · unranked

16 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 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

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Blood(2024)10.1182/blood.2023022596

N/A

0.416DataRank · unranked

15 citations

Jayna Nicholas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

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

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.003

N/A

0.416DataRank · unranked

15 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

Nature Aging(2024)10.1038/s43587-024-00647-7

N/A

0.406DataRank · unranked

14 citations

Michael A. Raddatz, Yash Pershad, Daniel Nachun, Kent D. Taylor, Xiuqing Guo +40 more

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

Cecelia Laurie, Jai Broome, Kent D. Taylor, Xiuqing Guo, Alan R. Shuldiner +82 more

Characterization of the phenotypic consequences of the Duffy-null genotype

Blood Advances(2025)10.1182/bloodadvances.2024014399

N/A

0.373DataRank · unranked

11 citations

Megan M. Shuey, Jennifer E. Huffman, Paul L. Auer, Alex P. Reiner, Laura M. Raffield +1 more

Clonal hematopoiesis is driven by aberrant activation of TCL1A

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.10.471810

N/A

0.360DataRank · unranked

10 citations

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

Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003258

N/A

0.360DataRank · unranked

10 citations

Latchezar Dimitrov, Shyh‐Huei Chen, Lawrence F. Bielak, Joshua C. Bis, Mary F. Feitosa +37 more

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

medRxiv(2020)10.1101/2020.12.09.20246736

N/A

0.360DataRank · unranked

10 citations

Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng +74 more

Rare coding variants in RCN3 are associated with blood pressure

BMC Genomics(2022)10.1186/s12864-022-08356-4

N/A

0.360DataRank · unranked

10 citations

Tanika N. Kelly, Heming Wang, Jingjing Liang, Luke Zhu, Brian E. Cade +72 more

An African ancestry-specific nonsense variant in CD36 is associated with a higher risk of dilated cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02372-2

N/A

0.345DataRank · unranked

9 citations

Liam Gaziano, Zeina R. Al Sayed, Renae Judy, Laura M. Raffield, Kiran J. Biddinger +59 more

Ancestral diversity in lipoprotein(a) studies helps address evidence gaps

Open Heart(2023)10.1136/openhrt-2023-002382

N/A

0.345DataRank · unranked

9 citations

Sofia F. Dimos, Laura M. Raffield, Zhe Wang, Anna F Ballou, Carolina G Downie +29 more

Epigenome-wide DNA methylation association study of CHIP provides insight into perturbed gene regulation

Nature Communications(2025)10.1038/s41467-025-59333-w

N/A

0.345DataRank · unranked

9 citations

Tianxiao Huan, Joseph C. Van Amburg, Roby Joehanes, Md Mesbah Uddin, Ngoc Quynh Nguyen +22 more

Polygenic risk score for type 2 diabetes shows context-dependent effects across populations

Nature Communications(2025)10.1038/s41467-025-63546-4

N/A

0.345DataRank · unranked

9 citations

Yanwei Cai, Daeeun Kim, Roelof A. J. Smit, Zhe Wang, Kruthika R. Iyer +169 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.06.511219

N/A

0.345DataRank · unranked

9 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 more

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1

N/A

0.345DataRank · unranked

9 citations

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

Determinants of mosaic chromosomal alteration fitness

Nature Communications(2024)10.1038/s41467-024-48190-8

N/A

0.345DataRank · unranked

9 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

Type 2 diabetes polygenic risk score demonstrates context-dependent effects and associations with type 2 diabetes-related risk factors and complications across diverse populations

medRxiv(2025)10.1101/2025.02.15.25322341

N/A

0.342DataRank · unranked

4 citations

Yanwei Cai, Daeeun Kim, Roelof A. J. Smit, Zhe Wang, Kruthika Iyer +68 more

A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2023.11.027

N/A

0.330DataRank · unranked

8 citations

Gerard Temprano‐Sagrera, Jara Cárcel‐Márquez, Elena Muiño, Natàlia Cullell, Miquel Lledós +91 more

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

Nature Communications(2024)10.1038/s41467-024-48394-y

N/A

0.330DataRank · unranked

8 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +95 more

Polygenic Risk Prediction using Gradient Boosted Trees Captures Non-Linear Genetic Effects and Allele Interactions in Complex Phenotypes

medRxiv(2021)10.1101/2021.07.09.21260288

N/A

0.315DataRank · unranked

3 citations

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

eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing data

Briefings in Bioinformatics(2021)10.1093/bib/bbab497

N/A

0.312DataRank · unranked

7 citations

Quan Sun, Le Huang, Jai Broome, Adolfo Correa, Alex P. Reiner +4 more

Epigenetic mechanisms underlying variation of IL-6, a well-established inflammation biomarker and risk factor for cardiovascular disease

Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120219

N/A

0.312DataRank · unranked

7 citations

Ulrike Peters, Yao Hu, Farah Ammous, Emelia J. Benjamin, Joshua C. Bis +31 more

Identification of proteins associated with type 2 diabetes risk in diverse racial and ethnic populations

Diabetologia(2024)10.1007/s00125-024-06277-3

N/A

0.292DataRank · unranked

6 citations

Jingjing Zhu, Hua Zhong, Chong Wu, Haoran Xue, Burcu F. Darst +43 more

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

medRxiv(2021)10.1101/2021.12.16.21267871

N/A

0.292DataRank · unranked

6 citations

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

FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

Journal of Thrombosis and Haemostasis(2021)10.1111/jth.15345

N/A

0.292DataRank · unranked

6 citations

Ci Song, Jack Pattee, Benjamin A.T. Rodriguez, Ming‐Huei Chen, Christopher J. O’Donnell +45 more

Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease

EBioMedicine(2025)10.1016/j.ebiom.2025.105790

N/A

0.292DataRank · unranked

6 citations

Satu Strausz, Geetha Chittoor, Shreyash Gupta, Anne E. Justice, Yana Hrytsenko +30 more

Genetic effects on chromatin accessibility uncover mechanisms of liver gene regulation and quantitative traits

Genome Research(2025)10.1101/gr.279741.124

N/A

0.283DataRank · unranked

5 citations

Hannah J. Perrin, Gautam Kumar Pandey, Abdalla A Alkhawaja, Swarooparani Vadlamudi, Annie E Musser +14 more

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

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

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

From GWAS Variant to Function: a Study of ~148,000 Variants for Blood Cell Traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.16.431409

N/A

0.274DataRank · unranked

4 citations

Cheynna Crowley, Le Huang, Jia Wen, Jiawen Chen, Erik L. Bao +7 more

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.18.146423

N/A

0.269DataRank · unranked

5 citations

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

The power of TOPMed imputation for the discovery of Latino enriched rare variants associated with type 2 diabetes

medRxiv(2022)10.1101/2022.09.30.22280535

N/A

0.269DataRank · unranked

5 citations

Philip Schroeder, Ravi Mandla, Aaron J. Deutsch, Wanying Zhu, Lauren E. Petty +57 more

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: The Framingham Heart Study

medRxiv(2022)10.1101/2022.04.13.22273839

Top 60%

0.253DataRank

Top 60%4 citations

Helena Bui, Roby Joehanes, Jiantao Ma, Chunyu Liu, Tianxiao Huan +32 more

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.001

N/A

0.241DataRank · unranked

4 citations

Yingxi Yang, Jonathan D. Rosen, Jiawen Chen, Xihao Li, Wyliena Guan +22 more

Genetic underpinnings of the heterogeneous impact of obesity on lipid levels and cardiovascular disease

Genome Medicine(2025)10.1186/s13073-025-01522-9

N/A

0.241DataRank · unranked

4 citations

Heather M. Highland, Roelof A. J. Smit, Micah R. Hysong, Victoria L. Buchanan, Kristin L. Young +27 more

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

medRxiv(2024)10.1101/2024.04.16.24305851

N/A

0.241DataRank · unranked

4 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +61 more

Genetic architecture and analysis practices of circulating metabolites in the NHLBI Trans-Omics for Precision Medicine Program

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.022

N/A

0.217DataRank · unranked

3 citations

Franklin P Ockerman, Laura Y. Zhou, Megan L. Grove, Taryn Alkis, J. A. Barnard +31 more

The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

medRxiv(2024)10.1101/2024.03.05.24303738

N/A

0.208DataRank · unranked

3 citations

Nuzulul Kurniansyah, Matthew Goodman, Brian Spitzer, Jiongming Wang, Adrienne M. Stilp +27 more

Epigenome-wide DNA Methylation Association Study of CHIP Provides Insight into Perturbed Gene Regulation

Research Square(2024)10.21203/rs.3.rs-4656898/v1

N/A

0.208DataRank · unranked

3 citations

Tianxiao Huan, Joseph C. Van Amburg, Roby Joehanes, Md Mesbah Uddin, Ngoc Quynh Nguyen +21 more

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries

The Lancet Diabetes & Endocrinology(2026)10.1016/s2213-8587(25)00405-x

N/A

0.208DataRank · unranked

3 citations

Joohyun Kim, Ravi Mandla, Yingchang Lu, Ken Suzuki, Lauren E Petty +255 more

Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19

medRxiv(2022)10.1101/2022.02.28.22271562

N/A

0.208DataRank · unranked

3 citations

Quan Sun, Wanjiang Wang, Tyne W. Miller‐Fleming, Nancy J. Cox, Misa Graff +9 more

Genetic underpinnings of regional adiposity distribution in African Americans: Assessments from the Jackson Heart Study

PLoS ONE(2021)10.1371/journal.pone.0255609

N/A

0.208DataRank · unranked

3 citations

Laura M. Raffield, Leslie A. Lange, Adolfo Correa, Kira C. Taylor, Mohammad Yaser Anwar

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

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.07.515222

N/A

0.208DataRank · unranked

3 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +41 more

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

Preprints.org(2021)10.20944/preprints202106.0129.v1

N/A

0.196DataRank · unranked

2 citations

Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Amanda L. Tapia +30 more

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

medRxiv(2022)10.1101/2022.07.26.22278077

N/A

0.182DataRank · unranked

1 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints—A study in asthma

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.008

N/A

0.165DataRank · unranked

2 citations

Quan Sun, Franklin P Ockerman, Brian Chen, Laura Y. Zhou, Micah R. Hysong +12 more

DNA methylation near MAD1L1, KDM2B, and SOCS3 mediates the effect of socioeconomic status on elevated body mass index in African American adults

Human Molecular Genetics(2024)10.1093/hmg/ddae112

N/A

0.165DataRank · unranked

2 citations

Adam G. Lilly, Anne E. Justice, Annie Green Howard, Brooke S. Staley, Yujie Wang +9 more

Prediagnostic Amino Acid Metabolites and Risk of Gout, Accounting for Serum Urate: Prospective Cohort Study and Mendelian Randomization

Arthritis Care & Research(2024)10.1002/acr.25420

Top 70%

0.165DataRank

Top 70%2 citations

Amit D. Joshi, Chio Yokose, Bing Yu, Adrienne Tin, Robert Terkeltaub +9 more

Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.

PubMed(2024)10.1093/hmg/ddae050

N/A

0.165DataRank · unranked

2 citations

Sheila M. Gaynor, Xihao Li, Eric Van Buren, A.M. Stilp, Erin Buth +41 more

Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations

Nature Communications(2025)10.1038/s41467-025-64236-x

N/A

0.165DataRank · unranked

2 citations

Sharjeel A. Chaudhry, Μαρία Ιωάννου, Maria Viskadourou, Paula Reventún, Yasminka A. Jakubek +49 more

Integrating whole genome and transcriptome sequencing to characterize the genetic architecture of isoform variation

Nature Communications(2025)10.1038/s41467-025-64336-8

Top 70%

0.165DataRank

Top 70%2 citations

Roby Joehanes, Jiantao Ma, Jiuyong Xie, Jian Yang, Mengyao Wang +20 more

Mosaic Loss of Y chromosome associates with lung function, emphysema and epigenetic aging

medRxiv(2025)10.1101/2025.07.30.25332379

N/A

0.165DataRank · unranked

2 citations

Kangjin Kim, Yichen Huang, Jeong H. Yun, Xiaolong Ma, Jason Bacon +25 more

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

medRxiv(2023)10.1101/2023.08.14.23294063

N/A

0.165DataRank · unranked

2 citations

Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman +60 more

Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.03.453690

N/A

0.165DataRank · unranked

2 citations

Sanan Venkatesh, Manuel Tardáguila, Jia Wen, Jonathan D. Rosen, Amanda L. Tapia +13 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

medRxiv(2023)10.1101/2023.06.28.23291966

N/A

0.146DataRank · unranked

1 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Proteome‐wide association study using cis and trans variants and applied to blood cell and lipid‐related traits in the Women's Health Initiative study

Genetic Epidemiology(2024)10.1002/gepi.22578

N/A

0.141DataRank · unranked

1 citations

Chanhwa Lee, Amanda L. Tapia, Alex P. Reiner, Hua Tang, Charles Kooperberg +4 more

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

medRxiv(2022)10.1101/2022.10.23.22281418

N/A

0.104DataRank · unranked

1 citations

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

The Relationship of Duffy Gene Polymorphism with High-Sensitivity C-Reactive Protein, Mortality, and Cardiovascular Outcomes in Black Individuals

Genes(2024)10.3390/genes15111382

N/A

0.104DataRank · unranked

1 citations

Jeffery Haessler, Kent D. Taylor, Bjoernar Tuftin, Matthew S. Briggs, Manish A. Parikh +15 more

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

medRxiv(2023)10.1101/2023.06.07.23291095

N/A

0.104DataRank · unranked

1 citations

Jayna Nicolas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

DNA Methylation Signatures of Cardiovascular Health Provide Insights into Diseases

medRxiv(2024)10.1101/2024.11.19.24317587

N/A

0.104DataRank · unranked

1 citations

Yi Li, Yishu Qu, Yinan Zheng, Alexis C. Wood, Mengyao Wang +43 more

A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances

medRxiv(2024)10.1101/2024.09.02.24312466

Top 78%

0.104DataRank

Top 78%1 citations

Wenyi Wang, Pavithra Nagarajan, Heming Wang, Michael R. Brown, Amy R. Bentley +95 more

Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy

Nature Communications(2025)10.1038/s41467-025-65845-2

N/A

0.104DataRank · unranked

1 citations

Kyeezu Kim, Yinan Zheng, Christina A. Castellani, Scott M. Ratliff, Mengyao Wang +41 more

Protein quantitative trait locus analysis in African American and non-Hispanic White individuals

Genome biology(2025)10.1186/s13059-025-03671-x

Top 78%

0.104DataRank

Top 78%1 citations

Mari Johnson, J. Haessler, Aaron J. Molstad, Shih‐Jen Hwang, Roby Joehanes +11 more

A large-scale genome-wide study of gene-sleep duration interactions for blood pressure in 811,405 individuals from diverse populations

Molecular Psychiatry(2025)10.1038/s41380-025-02954-w

Top 78%

0.104DataRank

Top 78%1 citations

Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja, Karen Schwander +95 more

General Kernel Machine Methods for Multi‐Omics Integration and Genome‐Wide Association Testing With Related Individuals

Genetic Epidemiology(2025)10.1002/gepi.22610

N/A

0.104DataRank · unranked

1 citations

Ni Zhao, Anna V. Mikhaylova, Angela Zhang, Wodan Ling, Florian Thibord +25 more

Methylome-wide association analyses of lipids and modifying effects of behavioral factors in diverse race and ethnicity participants

Clinical Epigenetics(2025)10.1186/s13148-025-01859-3

N/A

0.104DataRank · unranked

1 citations

Jeff Haessler, Jessica I. Lundin, Burcu F. Darst, Eric A. Whitsel, Megan L. Grove +32 more

Genome-wide gene by sleepiness interaction analysis for sleep apnea

SLEEP(2025)10.1093/sleep/zsaf212

N/A

0.104DataRank · unranked

1 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +80 more

Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants

Genome Biology(2026)10.1186/s13059-025-03921-y

Top 78%

0.104DataRank

Top 78%1 citations

Xiaowei Hu, Kangjin Kim, Sung Chun, Peter Orchard, Dandi Qiao +65 more

African ancestry genome-wide association study of blood pressure and hypertension identifies 25 novel loci through predicted gene expression

Research Square(2022)10.21203/rs.3.rs-1392991/v1

N/A

0.104DataRank · unranked

1 citations

Jingjing Liang, Ayush Giri, Jacob M. Keaton, Xiao Sun, Eric S. Torstenson +35 more

Determinants of mosaic chromosomal alteration fitness

medRxiv(2023)10.1101/2023.10.20.23297280

N/A

0.104DataRank · unranked

1 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.12.548702

N/A

0.104DataRank · unranked

1 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +93 more

Metabolomic epidemiology offers insights into disease aetiology

UNC Libraries(2024)10.17615/yv8q-st34

N/A

0DataRank · unranked

0 citations

Burcu F. Darst, Sachelly Julián‐Serrano, Afrand K. Sarvestani, Emily Drzymalla, Katherine H. Shutta +9 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

N/A

0DataRank · unranked

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

N/A

0DataRank · unranked

0 citations

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

Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea Subtype

medRxiv(2024)10.1101/2024.10.25.24316158

N/A

0DataRank · unranked

0 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +31 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

0DataRank · unranked

18 citations

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

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

UNC Libraries(2024)10.17615/b6xd-h115

N/A

0DataRank · unranked

0 citations

Eimear E. Kenny, Chunyu Liu, Christy L. Avery, On Behalf of the PAGE Study, Nona Sotoodehnia +35 more

Alterations of T Cell Subsets Associated with Sickle Cell Trait

Blood and genomics discovery.(2024)10.70322/bgd.2025.10001

N/A

0DataRank · unranked

0 citations

Laura M. Raffield, Lynette Ekunwe, Nels C. Olson, Paul L. Auer, Margaret F. Doyle +1 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

UNC Libraries(2024)10.17615/67cq-h633

N/A

0DataRank · unranked

0 citations

John S. Witte, Iman K. Martin, Sally N. Adebamowo, Maggie C. Y. Ng, Eimear E. Kenny +22 more

Optimism and telomere length among African American adults in the Jackson Heart Study

Psychoneuroendocrinology(2020)10.1016/j.psyneuen.2020.105124

N/A

0DataRank · unranked

2 citations

Sakurako S. Okuzono, Eric S. Kim, Immaculata De Vivo, Laura M. Raffield, LáShauntá Glover +4 more

CUE: CpG impUtation ensemble for DNA methylation levels across the human methylation450 (HM450) and EPIC (HM850) BeadChip platforms

Epigenetics(2020)10.1080/15592294.2020.1827716

N/A

0DataRank · unranked

2 citations

Laura M. Raffield, Mark W. Logue, Mark W. Miller, Hudson P. Santos, T. Michael O’Shea +3 more

Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.12100720

N/A

0DataRank · unranked

5 citations

Laura M. Raffield, Nora Franceschini, Paul L. Auer, Ethan M. Lange, Deborah A. Nickerson +4 more

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

PLoS Genetics(2020)10.1371/journal.pgen.1008684

N/A

0DataRank · unranked

33 citations

Mariaelisa Graff, Jeffrey Haessler, Steven Buyske, Stephanie A. Bien, Ran Tao +49 more

Methylation profile of individuals with sickle cell trait

Epigenetics(2025)10.1080/15592294.2025.2539234

N/A

0DataRank · unranked

3 citations

Mari Johnson, Yanwei Cai, Li Hsu, Franceschini, Nora, Paul L. Auer +4 more

Alterations in DNA Methylation, Proteomic, and Metabolomic Profiles in African Ancestry Populations with APOL1 Risk Alleles

Journal of the American Society of Nephrology(2025)10.1681/asn.0000000688

N/A

0DataRank · unranked

2 citations

Ashley W. Scadden, Amarnath Marthi, Victoria L. Buchanan, Yishu Qu, Kendra Ferrier +33 more

Variational autoencoder-based model improves polygenic prediction in blood cell traits

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100490

N/A

0DataRank · unranked

1 citations

Elena Kharitonova, Minxing Pang, Jia Wen, Laura Y. Zhou, Laura M. Raffield +6 more

Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants

Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120603

N/A

0DataRank · unranked

1 citations

Wenyi Wang, Pavithra Nagarajan, Heming Wang, Michael R. Brown, Amy R. Bentley +95 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

N/A

0DataRank · unranked

0 citations

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

Variational Autoencoder-based Model Improves Polygenic Prediction in Blood Cell Traits

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.13.632820

N/A

0DataRank · unranked

2 citations

Minxing Pang, Jia Wen, Laura Y. Zhou, Laura M. Raffield, Haibo Zhou +5 more

Multi-omics integration predicts 17 disease incidences in the UK Biobank

medRxiv(2025)10.1101/2025.08.01.25332841

N/A

0DataRank · unranked

1 citations

Muqing Zhou, Laura M. Raffield, Ruihai Zhou, Yun Li, Can Chen +2 more

Quantifying Social Determinants of Health for Disease Prediction: A Multi-Level Approach Using Healthy People 2030 and All of Us Data

medRxiv(2025)10.1101/2025.09.02.25334565

N/A

0DataRank · unranked

1 citations

Alisa K. Manning, Michael D. Green, Iain R. Konigsberg, Luciana B. Vargas, Jayati Sharma +8 more

A Large-Scale Genome-wide Association Study of Blood Pressure Accounting for Gene-Depressive Symptomatology Interactions in 564,680 Individuals from Diverse Populations

Research Square(2025)10.21203/rs.3.rs-6025759/v1

N/A

0DataRank · unranked

0 citations

Clint L. Miller, Amy R. Bentley, Michael R. Brown, Pavithra Nagarajan, Raymond Noordam +95 more

A multi-ethnic polygenic risk score for chronic kidney disease is associated with increased risk of hypertension in African American individuals

Research Square(2025)10.21203/rs.3.rs-6674221/v1

N/A

0DataRank · unranked

0 citations

Elizabeth Litkowski, Ashley W. Scadden, Mohammad Yaser Anwar, Iain R. Konigsberg, Maggie A. Stanislawski +8 more

African-specific genetic loci determine iron status and risk of severe malaria and bacteremia in African children

Research Square(2025)10.21203/rs.3.rs-6853969/v1

N/A

0DataRank · unranked

0 citations

Alexander J. Mentzer, Gavin Band, Amanda Y. Chong, Alex Macharia, Reagan M. Mogire +21 more

Fibrinogen-Associated Plasma Metabolites and Implications for Coagulation, Inflammation, and Vascular Diseases

medRxiv(2025)10.1101/2025.08.06.25333064

N/A

0DataRank · unranked

0 citations

Taryn Alkis, Joshua C. Bis, Eric Boerwinkle, Jennifer A. Brody, Clary B. Clish +22 more

A multi-ethnic polygenic risk score for chronic kidney disease is associated with increased risk of hypertension in African American individuals

BMC Nephrology(2025)10.1186/s12882-025-04425-4

N/A

0DataRank · unranked

0 citations

Elizabeth Litkowski, Ashley W. Scadden, Mohammad Yaser Anwar, Iain R. Konigsberg, Maggie A. Stanislawski +8 more

Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19

UNC Libraries(2025)10.17615/w64f-zc73

N/A

0DataRank · unranked

0 citations

Annika Faucon, Quan Sun, Misa Graff, Paul L. Auer, Nancy J. Cox +9 more

Nonalcoholic Fatty Liver Disease and Longitudinal Change in Imaging and Plasma Biomarkers of Alzheimer Disease and Vascular Pathology

UNC Libraries(2025)10.17615/a2cm-m654

N/A

0DataRank · unranked

0 citations

James Russell Pike, Yifei Lü, Priya Palta, Elizabeth Selvin, Laura M. Raffield +7 more

Admixture-mapping analysis reveals genetic determinants of the human plasma proteome

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100529

N/A

0DataRank · unranked

0 citations

Shuliang Deng, Usman A. Tahir, Zsu‐Zsu Chen, Mark D. Benson, Bjoernar Tuftin +17 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

UNC Libraries(2025)10.17615/nrrg-ws98

N/A

0DataRank · unranked

0 citations

Laura M. Raffield, Christy L. Avery, Quan Sun, Anna V. Mikhaylova, Tara C. Matise +13 more

Association between neutrophil to lymphocyte ratio and Alzheimer's disease in large biobank cohorts

Journal of Alzheimer s Disease(2025)10.1177/13872877251386813

N/A

0DataRank · unranked

0 citations

Christy L. Avery, Priya Palta, Alex P. Reiner, Quan Sun, Laura M. Raffield +1 more

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study

UNC Libraries(2025)10.17615/408w-ez13

N/A

0DataRank · unranked

0 citations

Jessica Lundin, Dawn L. DeMeo, Daniel Levy, Ramachandran S. Vasan, Shih‐Jen Hwang +31 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

UNC Libraries(2025)10.17615/cdn0-cm52

N/A

0DataRank · unranked

0 citations

Russell P. Tracy, Jill M. Johnsen, Hind Bouzid, Nicholas L. Smith, Katherine P. Prothro +95 more

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

UNC Libraries(2025)10.17615/4609-8b83

N/A

0DataRank · unranked

0 citations

Byron C. Jaeger, Michael J. Bamshad, Alex P. Reiner, Yun Li, Jerome I. Rotter +22 more

Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait

UNC Libraries(2025)10.17615/kwhm-gq49

N/A

0DataRank · unranked

0 citations

Melanie E. Garrett, Morgan E. Grams, Bing Yu, Alex P. Reiner, Genevieve L. Wojcik +17 more

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

UNC Libraries(2025)10.17615/mztm-gw84

N/A

0DataRank · unranked

0 citations

Margaret F. Doyle, Jason Bacon, Xiaolong Ma, Nathan Pankratz, Ramachandran S. Vasan +46 more

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

UNC Libraries(2025)10.17615/yvmq-kt94

N/A

0DataRank · unranked

0 citations

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

Gene expression and splicing QTL analysis of blood cells in African American participants from the Jackson Heart Study

UNC Libraries(2025)10.17615/md8g-4q87

N/A

0DataRank · unranked

0 citations

Lynette Ekunwe, Quan Sun, Lingbo Zhou, Nels C. Olson, Laura M. Raffield +6 more

Association of metabolomics measurements with blood cell phenotypes

Blood Cells Molecules and Diseases(2025)10.1016/j.bcmd.2025.102966

N/A

0DataRank · unranked

0 citations

Amanda L. Tapia, Eric Boerwinkle, Clary B. Clish, Robert E. Gerszten, Misa Graff +15 more

Analysis of left ventricular mass for African American individuals using multi-ancestry polygenic risk scores: the Jackson Heart Study

Open Heart(2025)10.1136/openhrt-2025-003501

N/A

0DataRank · unranked

0 citations

Philip Turk, Olivia Affuso, Laura M. Raffield, Elizabeth Heitman, Douglas M. McLaurin

Integration of genetic risk, cardiometabolic diseases, and cognitive impairment among African American adults

Journal of Stroke and Cerebrovascular Diseases(2025)10.1016/j.jstrokecerebrovasdis.2025.108535

N/A

0DataRank · unranked

0 citations

Nicole D. Armstrong, DaeEun Kim, Laura M. Raffield, Hemant K. Tiwari, Mary Cushman +5 more

The Relationship of Duffy Gene Polymorphism with High-Sensitivity C-Reactive Protein, Mortality, and Cardiovascular Outcomes in Black Individuals

UNC Libraries(2024)10.17615/shas-p528

N/A

0DataRank · unranked

0 citations

Bjoernar Tuftin, Stephen J. Peterson, Laura M. Raffield, KARL T. KELSEY, Manish A. Parikh +15 more

MagicalRsq: Machine-learning-based genotype imputation quality calibration

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.009

N/A

0DataRank · unranked

19 citations

Yingxi Yang, Jonathan D. Rosen, Min-Zhi Jiang, Jiawen Chen, Weifang Liu +14 more

Genetic Landscape of the ACE2 Coronavirus Receptor

Circulation(2022)10.1161/circulationaha.121.057888

N/A

0DataRank · unranked

40 citations

Erin Macdonald-Dunlop, Jiantao Chen, Ranran Zhai, Ting Li, Anne Richmond +64 more

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Nature Methods(2022)10.1038/s41592-022-01640-x

N/A

0DataRank · unranked

109 citations

Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou +95 more

Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types

PLoS Genetics(2022)10.1371/journal.pgen.1009984

N/A

0DataRank · unranked

4 citations

Taylor M. Lagler, Quan Sun, Yuchen Yang, Jiawen Chen, Yuriko Harigaya +6 more

Transcriptome-wide association study of blood cell traits in african ancestry and hispanic/latino populations

UNC Libraries(2021)10.17615/x9y4-pk77

N/A

0DataRank · unranked

0 citations

E. Jorgenson, A.L. Tapia, J.D. Rosen, C.J. Hodonsky, L. Shang +31 more

Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types

UNC Libraries(2022)10.17615/7q9s-be11

N/A

0DataRank · unranked

0 citations

Yuchen Yang, Jia Wen, Ming Hu, Alex P. Reiner, Taylor M. Lagler +6 more

Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.15.435494

N/A

0DataRank · unranked

2 citations

Yuchen Yang, Yuriko Harigaya, Vijay G. Sankaran, Ming Hu, Alexander P. Reiner +4 more

Assay-related Differences in SuPAR Levels: Implications for Measurement and Data Interpretation

medRxiv(2021)10.1101/2021.06.23.21259148

N/A

0DataRank · unranked

4 citations

Laura M. Raffield, Yan Gao, Gunnar Engström, Arshed A. Quyyumi, Alexander P. Reiner +2 more

Metabolomic epidemiology offers insights into disease aetiology

Nature Metabolism(2023)10.1038/s42255-023-00903-x

N/A

0DataRank · unranked

56 citations

Yiwen Zhu, Jayna Nicholas, Haley Chatelaine, Emily Drzymalla, Afrand K. Sarvestani +9 more

Liver integrity and the risk of Alzheimer's disease and related dementias

Alzheimer s & Dementia(2023)10.1002/alz.13601

N/A

0DataRank · unranked

39 citations

James Russell Pike, Ron C. Hoogeveen, Keenan A. Walker, Laura M. Raffield, Elizabeth Selvin +6 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

N/A

0DataRank · unranked

8 citations

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

An epidemiological introduction to human metabolomic investigations

Trends in Endocrinology and Metabolism(2023)10.1016/j.tem.2023.06.006

N/A

0DataRank · unranked

22 citations

Ali Rahnavard, Priyadarshini Kachroo, Kevin Mendez, Wayne R. Lawrence, Sachelly Julián‐Serrano +8 more

A large‐scale transcriptome‐wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine‐mapping

Genetic Epidemiology(2021)10.1002/gepi.22436

N/A

0DataRank · unranked

6 citations

Bryce Rowland, Jonathan D. Rosen, Michael Preuß, Kris Young, Misa Graff +14 more

Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait

Clinical Journal of the American Society of Nephrology(2023)10.2215/cjn.0000000000000257

N/A

0DataRank · unranked

17 citations

Nora Franceschini, Aditya Surapaneni, Melanie E. Garrett, Usman A. Tahir, Li Hsu +17 more

Prediagnostic Glycoprotein Acetyl Levels and Incident and Recurrent Flare Risk Accounting for Serum Urate Levels: A Population‐Based, Prospective Study and Mendelian Randomization Analysis

Arthritis & Rheumatology(2023)10.1002/art.42523

N/A

0DataRank · unranked

17 citations

Natalie McCormick, Chio Yokose, Bing Yu, Adrienne Tin, Robert Terkeltaub +6 more

Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.121.003421

N/A

0DataRank · unranked

15 citations

Laura M. Raffield, Anne H. Moxley, Tyne W. Miller‐Fleming, Paul L. Auer, Franceschini, Nora +12 more

Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche

Human Reproduction(2021)10.1093/humrep/deab086

N/A

0DataRank · unranked

15 citations

Diana L. Cousminer, Nora Franceschini, Laura M. Raffield, Guochong Jia, Lindsay Fernández‐Rhodes +20 more

Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry

Mitochondrion(2021)10.1016/j.mito.2021.07.004

N/A

0DataRank · unranked

23 citations

Jessica L. Fetterman, Yong Qian, Xianbang Sun, Thomas W. Blackwell, Achilleas Pitsillides +14 more

Branched chain amino acids harbor distinct and often opposing effects on health and disease

Communications Medicine(2023)10.1038/s43856-023-00382-x

N/A

0DataRank · unranked

7 citations

Annie Green Howard, Harold Lee, Carolina G Downie, Moa P. Lee, Sarah H. Koenigsberg +8 more

Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19

Blood Cells Molecules and Diseases(2023)10.1016/j.bcmd.2023.102782

N/A

0DataRank · unranked

2 citations

Bryce Rowland, Wanjiang Wang, Tyne W. Miller‐Fleming, Nancy J. Cox, Misa Graff +9 more

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

UNC Libraries(2021)10.17615/e6ew-j192

N/A

0DataRank · unranked

27 citations

NHLBI Trans-Omics for Precision Medicine Consortium, H. Qian, C. Montgomery, T.N. Kelly, M.H. Cho +67 more

Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies

Journal of Human Genetics(2021)10.1038/s10038-021-00968-0

N/A

0DataRank · unranked

55 citations

Misa Graff, Bryce Rowland, Jia Wen, Le Huang, Tyne W. Miller‐Fleming +14 more

Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

UNC Libraries(2023)10.17615/hthq-e624

N/A

0DataRank · unranked

0 citations

David J. Vandenberg, J. Gustav Smith, Tamar Sofer, Yongmei Liu, Peter Durda +23 more

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Nature(2024)10.1038/s41586-024-07019-6

N/A

0DataRank · unranked

537 citations

Konstantinos Hatzikotoulas, Lorraine Southam, Henry J. Taylor, Xianyong Yin, Kimberly Lorenz +95 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

Nature Communications(2024)10.1038/s41467-024-45135-z

N/A

0DataRank · unranked

56 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 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

Top 100%

0DataRank

Top 100%0 citations

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

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

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

Nonalcoholic Fatty Liver Disease and Longitudinal Change in Imaging and Plasma Biomarkers of Alzheimer Disease and Vascular Pathology

Neurology(2024)10.1212/wnl.0000000000209203

N/A

0DataRank · unranked

19 citations

James Russell Pike, Ron C. Hoogeveen, Keenan A. Walker, Laura M. Raffield, Elizabeth Selvin +7 more

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

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

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

eSCAN: Scan Regulatory Regions for Aggregate Association Testing using Whole Genome Sequencing Data

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.30.405266

N/A

0DataRank · unranked

2 citations

Yuchen Yang, Le Huang, Jai Broome, Adolfo Correa, Alex P. Reiner +3 more

Demographic and Clinical Factors Associated With SARS-CoV-2 Spike 1 Antibody Response Among Vaccinated US Adults: the C4R Study

Nature Communications(2024)10.1038/s41467-024-45468-9

N/A

0DataRank · unranked

16 citations

Yifei Sun, Pallavi Balte, Mary Cushman, Rebekah Boyle, Russell P. Tracy +28 more

Presence and Transmission of Mitochondrial Heteroplasmic Mutations in Human Populations of European and African Ancestry

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.13.337071

N/A

0DataRank · unranked

2 citations

Jessica L. Fetterman, Yong Qian, Xianbang Sun, Kaiyu Yan, Thomas W. Blackwell +15 more

Gene expression and splicing QTL analysis of blood cells in African American participants from the Jackson Heart Study

Genetics(2024)10.1093/genetics/iyae098

N/A

0DataRank · unranked

11 citations

Quan Sun, Le Huang, Lingbo Zhou, Margaret F. Doyle, Lynette Ekunwe +6 more

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

Epigenetics(2024)10.1080/15592294.2024.2333668

N/A

0DataRank · unranked

9 citations

Ulrike Peters, Yao Hu, Farah Ammous, Christy L. Avery, Emelia J. Benjamin +35 more

Analyses of Biomarker Traits in Diverse UK Biobank Participants Identify Associations Missed by European-centric Analysis Strategies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.02.279844

N/A

0DataRank · unranked

5 citations

Misa Graff, Bryce Rowland, Jia Wen, Le Huang, Moa P. Lee +6 more

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

Mitochondrion(2024)10.1016/j.mito.2024.101954

N/A

0DataRank · unranked

2 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +19 more

Supplemental Association of Clonal Hematopoiesis With Incident Heart Failure

UNC Libraries(2024)10.17615/apaj-k024

N/A

0DataRank · unranked

10 citations

A. Correa, Michael C. Honigberg, Charles Kooperberg, Eric A. Whitsel, M. R. Brown +21 more

A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations

medRxiv(2024)10.1101/2024.03.07.24303870

N/A

0DataRank · unranked

1 citations

Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja, Karen Schwander +95 more

EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints

medRxiv(2024)10.1101/2024.05.23.24307839

N/A

0DataRank · unranked

1 citations

Quan Sun, Frank Ockerman, Brian Chen, Laura Y. Zhou, Hongyuan Cao +10 more

Association analysis of mitochondrial DNA heteroplasmic variants: methods and application

medRxiv(2024)10.1101/2024.01.12.24301233

N/A

0DataRank · unranked

0 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +20 more

Rare coding variants in RCN3 are associated with blood pressure

UNC Libraries(2024)10.17615/y07d-kq52

N/A

0DataRank · unranked

0 citations

C.-T. Liu, A Furniss, R.S. Vasan, P.A. Peyser, Gao Ya +74 more

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

UNC Libraries(2024)10.17615/hd68-ze50

Top 100%

0DataRank

Top 100%0 citations

B.M. Psaty, Leslie J. Baier, Robert B. Wallace, Anna Köttgen, Jiang He +69 more

A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

UNC Libraries(2024)10.17615/0ea7-3v47

N/A

0DataRank · unranked

0 citations

Nicola L. Hawley, May E. Montasser, P.A. Peyser, Daniel E. Weeks, Braxton D. Mitchell +67 more

Effect of sickle cell trait and apol1 genotype on the association of soluble upar with kidney function measures in black americans

UNC Libraries(2024)10.17615/kd3y-sn92

N/A

0DataRank · unranked

0 citations

Nels C. Olson, A. Correa, A.P. Reiner, Lung National Heart, Laura M. Raffield +5 more

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

UNC Libraries(2024)10.17615/p0b9-dv74

N/A

0DataRank · unranked

0 citations

Berta Almoguera, L.E. Petty, J. Haessler, Christopher J. O’Donnell, Daniel O. Stram +49 more

Genetic discovery and risk characterization in type 2 diabetes across diverse populations

UNC Libraries(2024)10.17615/jc4m-n673

N/A

0DataRank · unranked

0 citations

G.N. Nadkarni, Christopher S. Carlson, H.M. Highland, Maggie Ng, L. Petty +52 more

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

UNC Libraries(2024)10.17615/twaa-ms70

N/A

0DataRank · unranked

0 citations

B.M. Psaty, Juan M. Peralta, R. Graham Barr, B.D. Hobbs, Daniel Levy +85 more

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

UNC Libraries(2024)10.17615/75fz-j027

Top 100%

0DataRank

Top 100%0 citations

J.E. Curran, S.L.R. Kardia, Márcio Rodrigues de Almeida, J.B. Meigs, M.R. Irvin +88 more

A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations

Research Square(2024)10.21203/rs.3.rs-4163414/v1

Top 100%

0DataRank

Top 100%0 citations

Pavithra Nagarajan, Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja +95 more

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

UNC Libraries(2024)10.17615/6n4z-q211

N/A

0DataRank · unranked

0 citations

Jacob C. Ulirsch, Alex P. Reiner, Gonçalo R. Abecasis, Joshua D. Smith, Ethan M. Lange +20 more

eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing data

UNC Libraries(2024)10.17615/7ck5-fq86

N/A

0DataRank · unranked

0 citations

NHLBI Trans-Omics for Precision Medicine Consortium, Adolfo Correa, Yuchen Yang, Quan Sun, Yun Li +5 more

Demographic and Clinical Factors Associated With SARS-CoV-2 Spike 1 Antibody Response Among Vaccinated US Adults: the C4R Study

UNC Libraries(2024)10.17615/b3fj-pt82

N/A

0DataRank · unranked

0 citations

Michaela R. Anderson, John S. Kim, Russell P. Tracy, Elizabeth A. Regan, Prescott G. Woodruff +28 more

Laura M. Raffield

Indexed papers

Top data-sharing exemplar

Papers