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Authors
Bruce M. Psaty

Bruce M. Psaty

University of Washington

ORCID: 0000-0002-7278-2190

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

9.2Author DataRank

Indexed papers

20in 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 20 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 →

Top data-sharing exemplar

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

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Nature Communications(2020)10.1038/s41467-020-18367-y

Top 12%

1.8DataRank

Top 12%109 citations

Gennady V. Roshchupkin, Hieab H.H. Adams, Maria J. Knol, Honghuang Lin, Shuo Li +87 more

Papers

Driven by 273 papers — median percentile 52. 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

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Nature Genetics(2021)10.1038/s41588-021-00913-z

N/A

11.2DataRank · unranked

2226 citations

Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng +89 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

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Nature Genetics(2020)10.1038/s41588-020-0676-4

N/A

5.3DataRank · unranked

295 citations

Zilin Li, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +88 more

Cerebral small vessel disease genomics and its implications across the lifespan

Nature Communications(2020)10.1038/s41467-020-19111-2

N/A

4.3DataRank · unranked

209 citations

Hideaki Suzuki, Xueqiu Jian, Chloé Sarnowski, Tavia E. Evans, Joshua C. Bis +94 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

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

Nature Communications(2018)10.1038/s41467-018-03911-8

N/A

3.1DataRank · unranked

104 citations

Amit V. Khera, Mark Chaffin, Derek Klarin, Pradeep Natarajan, Krishna Aragam +43 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Nature Communications(2021)10.1038/s41467-021-23556-4

N/A

2.7DataRank · unranked

110 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Nature Genetics(2024)10.1038/s41588-024-01714-w

N/A

2.4DataRank · unranked

193 citations

Zoha Kamali, Tian Xie, Ahmad Vaez, Ariel Williams, Slavina B. Goleva +95 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

Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury

Nature Medicine(2024)10.1038/s41591-024-02854-6

N/A

1.9DataRank · unranked

76 citations

Cassianne Robinson‐Cohen, Jianchun Chen, Elvis A. Akwo, Alyssa Parker, Samuel A. Silver +26 more

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Nature Communications(2020)10.1038/s41467-020-18367-y

Top 12%

1.8DataRank

Top 12%109 citations

Gennady V. Roshchupkin, Hieab H.H. Adams, Maria J. Knol, Honghuang Lin, Shuo Li +87 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

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

Diabetes(2020)10.2337/db20-0070

N/A

1.5DataRank · unranked

57 citations

Yiying Zhang, Cassandra N. Spracklen, Tugce Karaderi, Lam Opal Huang, Jonathan P. Bradfield +95 more

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002874

N/A

1.4DataRank · unranked

30 citations

Amelia Weber Hall, Seung Hoan Choi, Sean J. Jurgens, Jeffrey Haessler, Nathan A. Bihlmeyer +55 more

A large‐scale exome array analysis of venous thromboembolism

Genetic Epidemiology(2019)10.1002/gepi.22187

N/A

1.4DataRank · unranked

27 citations

Jennifer A. Brody, Constance Turman, Marine Germain, Traci M. Bartz, Erin N. Smith +34 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

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

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

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

PLOS ONE(2017)10.1371/journal.pone.0167742

N/A

1.1DataRank · unranked

50 citations

Maria Sabater-Lleal, Daniel I. Chasman, Stella Trompet, Tarunveer S. Ahluwalia, Alexander Teumer +81 more

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 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

Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study Design

American Journal of Epidemiology(2022)10.1093/aje/kwac032

Top 19%

1.1DataRank

Top 19%36 citations

Akshaya Krishnaswamy, Pallavi Balte, Norrina B. Allen, Tauqeer Ali, Pramod Anugu +81 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

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

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 more

Plasma Trimethylamine‐ N ‐Oxide and Incident Ischemic Stroke: The Cardiovascular Health Study and the Multi‐Ethnic Study of Atherosclerosis

Journal of the American Heart Association(2023)10.1161/jaha.122.029230

N/A

0.821DataRank · unranked

25 citations

Paul N. Jensen, Zeneng Wang, Amanda M. Fretts, Colleen M. Sitlani, Ina Nemet +10 more

Trimethylamine N -Oxide and Related Gut Microbe-Derived Metabolites and Incident Heart Failure Development in Community-Based Populations

Circulation Heart Failure(2024)10.1161/circheartfailure.124.011569

N/A

0.756DataRank · unranked

28 citations

Rozenn N. Lemaître, Paul N. Jensen, Meng Wang, Zeneng Wang, Xinmin S. Li +14 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

Sex-Specific Associations of Cardiovascular Risk Factors and Biomarkers With Incident Heart Failure

Journal of the American College of Cardiology(2020)10.1016/j.jacc.2020.07.044

N/A

0.701DataRank · unranked

106 citations

Emily S. Lau, Michael J. Blaha, Samantha M. Paniagua, Martin G. Larson, Bruce M. Psaty +25 more

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Circulation(2022)10.1161/circulationaha.122.059675

N/A

0.701DataRank · unranked

106 citations

Derek Klarin, Jennifer A. Brody, Ming‐Huei Chen, Michael G. Levin, Daniel I. Chasman +82 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

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

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

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Human Molecular Genetics(2013)10.1093/hmg/ddt588

N/A

0.650DataRank · unranked

75 citations

A. D. Johnson, B. M. Snively, Jarmo Virtamo, P. L. Auer, Jonas B. Nielsen +34 more

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Nature Communications(2024)10.1038/s41467-024-44701-9

N/A

0.648DataRank · unranked

74 citations

Inga Steinbrenner, Yong Li, Melissa Bujnis, Tatsuhiko Naito, Eirini Marouli +95 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

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

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

Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003288

N/A

0.595DataRank · unranked

11 citations

Gina M. Peloso, Mélanie Guirette, Fumiaki Imamura, Traci M. Bartz, Achilleas Pitsillides +51 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

Role of Polyunsaturated Fat in Modifying Cardiovascular Risk Associated With Family History of Cardiovascular Disease: Pooled De Novo Results From 15 Observational Studies

Circulation(2023)10.1161/circulationaha.123.065530

N/A

0.578DataRank · unranked

18 citations

Agneta Åkesson, Matti Marklund, Frank Qian, Bruna Gigante, Traci M. Bartz +46 more

Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.12824

N/A

0.571DataRank · unranked

19 citations

Aïcha Soumaré, Joshua C. Bis, Ida Surakka, Tuuli Jürgenson, Pierre Joly +29 more

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Communications Biology(2022)10.1038/s42003-022-03448-z

N/A

0.553DataRank · unranked

39 citations

Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce Rowan, Kira J. Stanzick +94 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

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 Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.121.003532

Top 38%

0.507DataRank

Top 38%11 citations

Cecelia Laurie, Brandon J. Coombes, Deepti Jain, Matthew P. Conomos, Jennifer A. Brody +30 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

Clinical and biomarker modifiers of vitamin D treatment response: the Multi-Ethnic Study of Atherosclerosis

American Journal of Clinical Nutrition(2021)10.1093/ajcn/nqab390

N/A

0.500DataRank · unranked

10 citations

David K. Prince, Kayleen Williams, Norrina B. Allen, Gregory L. Burke, Andrew N. Hoofnagle +14 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

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data

Human Molecular Genetics(2022)10.1093/hmg/ddac117

N/A

0.455DataRank · unranked

6 citations

Julian Hecker, R. Graham Barr, Eric Boerwinkle, Brian E. Cade, Adolfo Correa +21 more

Cardiac Troponins and Cardiovascular Disease Risk Prediction

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2025.02.016

N/A

0.442DataRank · unranked

18 citations

Spencer Keene, Lisa Pennells, Stephen Kaptoge, Dorien M Kimenai, Matthew R. Walker +57 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

Genome-Wide Association Study of Cardiac Structure and Systolic Function in African Americans: The Candidate Gene Association Resource (CARe) Study

UNC Libraries(2020)10.17615/r6f9-4t91

Top 46%

0.402DataRank

Top 46%6 citations

Ramachandran S. Vasan, Nicole L. Glazer, Susan R. Heckbert, Abdullah Kutlar, Thomas H. Mosley +32 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

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies

Nature Computational Science(2025)10.1038/s43588-024-00764-8

N/A

0.393DataRank · unranked

10 citations

Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang +95 more

Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study Design

medRxiv(2021)10.1101/2021.03.19.21253986

Top 48%

0.380DataRank

Top 48%5 citations

Norrina B. Allen, Tauqeer Ali, Pramod Anugu, Howard Andrews, Alyssa Asaro +77 more

A Polygenic Risk Score of Atrial Fibrillation Improves Prediction of Lifetime Risk for Heart Failure

ESC Heart Failure(2024)10.1002/ehf2.14665

N/A

0.364DataRank · unranked

8 citations

Xi Luo, Katherine Wall, Jennifer A. Brody, Traci M. Bartz, Patricia P. Chang +10 more

Selected social and lifestyle correlates of brain health markers: the Cross‐Cohort Collaboration Consortium

Alzheimer s & Dementia(2025)10.1002/alz.70148

Top 49%

0.363DataRank

Top 49%8 citations

Joshua C. Bis, Stefan Frenzel, Daniel Kojis, Jeannette Simino, Amber Yaqub +29 more

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Research Square(2024)10.21203/rs.3.rs-4535534/v1

N/A

0.331DataRank · unranked

5 citations

Ilana Caro, Daniel Western, Shinichi Namba, Na Sun, Shuji Kawaguchi +52 more

Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function

Scientific Reports(2021)10.1038/s41598-021-98120-7

N/A

0.331DataRank · unranked

5 citations

Victoria E. Jackson, Albert V. Smith, Han Chen, Traci M. Bartz, Colleen M. Sitlani +42 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 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

Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes

Diabetes Care(2024)10.2337/dc23-2274

Top 56%

0.289DataRank

Top 56%5 citations

Ryan B. Hernandez-Cancela, Daniel DiCorpo, David E. Condon, Jordi Merino, Peitao Wu +62 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

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

Oxford University Research Archive (ORA) (University of Oxford)(2020)10.17615/gc55-0r45

N/A

0.221DataRank · unranked

2 citations

Sonsoles Morcillo, Nicholas J. Wareham, Richard A. Jensen, Allan Linnenberg, Josée Dupuis +74 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

Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

Alzheimer s Research & Therapy(2024)10.1186/s13195-023-01376-6

N/A

0.208DataRank · unranked

3 citations

Jeannette Simino, Lianna Li, Fan Jiang, Joshua C. Bis, Gail Davies +62 more

Deep Learning Prediction of Left Atrial Structure and Function from 12-lead Electrocardiograms

medRxiv(2025)10.1101/2025.09.29.25336490

N/A

0.197DataRank · unranked

2 citations

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medRxiv(2022)10.1101/2022.07.26.22278077

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medRxiv(2023)10.1101/2023.08.14.23294063

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UNC Libraries(2020)10.17615/aapr-pr41

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

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medRxiv(2021)10.1101/2021.12.16.21267871

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UNC Libraries(2020)10.17615/s8sd-h432

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

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

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

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European Journal of Heart Failure(2023)10.1002/ejhf.3086

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Diabetes(2023)10.2337/db22-0628

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(2020)10.2337/figshare.12933737.v1

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UNC Libraries(2020)10.17615/ttpw-sn86

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.21.959312

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.03.973420

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

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Journal of Cardiac Failure(2023)10.1016/j.cardfail.2022.12.014

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

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bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.25.550557

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medRxiv(2023)10.1101/2023.01.18.23284671

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medRxiv(2023)10.1101/2023.10.20.23297280

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medRxiv(2023)10.1101/2023.08.01.23293525

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medRxiv(2023)10.1101/2023.09.24.23295485

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medRxiv(2023)10.1101/2023.12.13.23299909

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medRxiv(2020)10.1101/2020.12.09.20246736

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medRxiv(2020)10.1101/2020.09.22.20195529

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PLoS ONE(2020)10.1371/journal.pone.0242062

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Journal of the American Heart Association(2024)10.1161/jaha.124.035710

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