Jennifer A. Brody

Biochemistry, 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

14.5Author DataRank

Indexed papers

17in 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 17 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.

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

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

Top 3%

7.0DataRank

Top 3%2322 citations

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

Papers

Driven by 154 papers — median percentile 62. Top paper: “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations”.

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

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

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

Top 3%

7.0DataRank

Top 3%2322 citations

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

Genetic diversity fuels gene discovery for tobacco and alcohol use

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

N/A

5.9DataRank · unranked

513 citations

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

Clonal haematopoiesis and risk of chronic liver disease

Nature(2023)10.1038/s41586-023-05857-4

N/A

4.5DataRank · unranked

204 citations

Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello +95 more

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Nature Genetics(2022)10.1038/s41588-022-01165-1

N/A

4.4DataRank · unranked

242 citations

Andrew Emmerich, Nicolas J. Pillon, Timothy M. Moore, Daiane Hemerich, Marilyn C. Cornelis +95 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

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +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

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

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

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

N/A

3.0DataRank · unranked

123 citations

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

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

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

N/A

2.3DataRank · unranked

108 citations

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

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

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

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 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

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

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

N/A

1.3DataRank · unranked

70 citations

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

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

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Nature Communications(2022)10.1038/s41467-022-32275-3

N/A

1.1DataRank · unranked

63 citations

Daniel H. Katz, Julián Ávila-Pacheco, Alexander G. Bick, Akhil Pampana, Jeremy Robbins +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

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

A saturated map of common genetic variants associated with human height

Nature(2022)10.1038/s41586-022-05275-y

N/A

1.0DataRank · unranked

911 citations

Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue +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

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 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

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

Molecular Psychiatry(2020)10.1038/s41380-020-0719-3

N/A

0.810DataRank · unranked

25 citations

Yun Ju Sung, Raymond Noordam, Thomas W. Winkler, Mary F. Feitosa, Karen Schwander +95 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

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

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

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

N/A

0.692DataRank · unranked

100 citations

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

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

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

N/A

0.689DataRank · unranked

22 citations

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

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

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

N/A

0.681DataRank · unranked

31 citations

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

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Diabetologia(2023)10.1007/s00125-023-05922-7

N/A

0.676DataRank · unranked

16 citations

Laura Brenner, Varinderpal Kaur, Katherine Figueroa, Philip Schroeder, Alicia Huerta‐Chagoya +95 more

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

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

N/A

0.673DataRank · unranked

88 citations

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

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 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

Population sequencing data reveal a compendium of mutational processes in the human germ line

Science(2021)10.1126/science.aba7408

N/A

0.648DataRank · unranked

74 citations

Ruslan Soldatov, Evan M. Koch, Ryan J. McGinty, Jakob M. Goldmann, Ryan D. Hernandez +38 more

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

Frontiers in Endocrinology(2022)10.3389/fendo.2022.863893

N/A

0.642DataRank · unranked

21 citations

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

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

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

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z

N/A

0.596DataRank · unranked

52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 more

Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations

Nature Communications(2023)10.1038/s41467-023-38800-2

N/A

0.584DataRank · unranked

48 citations

Michael R. Brown, Taryn Alkis, Astrid M. Manuel, Xihao Li, Usman A. Tahir +31 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

Proteomic Prediction of Incident Heart Failure and Its Main Subtypes

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

N/A

0.579DataRank · unranked

18 citations

Brynjolfur G. Jonsson, Thomas R. Austin, Valborg Guðmundsdóttir, G. Axelsson, Elisabet A. Frick +16 more

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

Brain(2022)10.1093/brain/awac290

N/A

0.574DataRank · unranked

45 citations

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

Integrative analysis of clinical and epigenetic biomarkers of mortality

Aging Cell(2022)10.1111/acel.13608

N/A

0.561DataRank · unranked

41 citations

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

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

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

N/A

0.546DataRank · unranked

37 citations

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

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

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

N/A

0.534DataRank · unranked

11 citations

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

The functional impact of rare variation across the regulatory cascade

Cell Genomics(2023)10.1016/j.xgen.2023.100401

N/A

0.526DataRank · unranked

15 citations

Nicole M. Ferraro, Benjamin J. Strober, François Aguet, Silva Kasela, Marios Arvanitis +33 more

Rare genetic variants explain missing heritability in smoking

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

N/A

0.520DataRank · unranked

31 citations

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

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

PLoS ONE(2020)10.1371/journal.pone.0230035

N/A

0.513DataRank · unranked

8 citations

Yi-Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa +40 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

Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing

European Journal of Epidemiology(2022)10.1007/s10654-022-00888-z

N/A

0.505DataRank · unranked

28 citations

Caitlin McHugh, Jennifer A. Brody, Joshua C. Bis, Colleen M. Sitlani, Traci M. Bartz +33 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

Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

EBioMedicine(2024)10.1016/j.ebiom.2024.105233

N/A

0.497DataRank · unranked

15 citations

Chelsea A. Isom, Yangzi Liu, David-Alexandre Trégouët, Sara Lindström, Lu Wang +52 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

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases

JCI Insight(2022)10.1172/jci.insight.157035

N/A

0.477DataRank · unranked

23 citations

Yurong Cheng, Francesco Consolato, Guglielmo Schiano, Michael Chong, Maik Pietzner +38 more

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

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

N/A

0.436DataRank · unranked

7 citations

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

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Human Molecular Genetics(2022)10.1093/hmg/ddac100

N/A

0.434DataRank · unranked

17 citations

Peng Wei, Jennifer A. Brody, Ming‐Huei Chen, Paul S. de Vries, Jennifer E. Huffman +26 more

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Nature Communications(2023)10.1038/s41467-023-36997-w

N/A

0.434DataRank · unranked

17 citations

Jeffrey Haessler, Jan Walter Benjamins, L. Repetto, Jie Yao, Aaron Isaacs +89 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

Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202203-0618oc

N/A

0.414DataRank · unranked

9 citations

Heming Wang, Brian E. Cade, Nuzulul Kurniansyah, Karen He, Jiwon Lee +30 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

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

Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes

Blood(2025)10.1182/blood.2024027879

N/A

0.373DataRank · unranked

11 citations

Florian Thibord, Ohanna Cavalcanti de Lima Bezerra, Jennifer A. Brody, Astrid van Hylckama Vlieg, Lénaïck Gourhant +29 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

Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Nature Communications(2022)10.1038/s41467-022-32009-5

N/A

0.360DataRank · unranked

10 citations

Valerie N. Morrill, Seung Hoan Choi, Sean J. Jurgens, Giorgio Melloni, Nicholas Marston +39 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

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

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0.360DataRank · unranked

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

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0.345DataRank · unranked

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medRxiv(2021)10.1101/2021.07.09.21260288

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0.315DataRank · unranked

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0.312DataRank · unranked

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0.292DataRank · unranked

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0.289DataRank

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bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.11.463514

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0.277DataRank · unranked

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0.277DataRank · unranked

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0.275DataRank

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Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88

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0.269DataRank · unranked

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0.269DataRank · unranked

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0.246DataRank · unranked

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0.241DataRank · unranked

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0.241DataRank · unranked

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0.208DataRank · unranked

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0.197DataRank · unranked

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0.183DataRank · unranked

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0.182DataRank · unranked

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