Benjamin F. Voight

Also affiliated with Translational Therapeutics (United States), University of Pennsylvania

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

5.5Author DataRank

Indexed papers

8in 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 8 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.

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

Science(2024)10.1126/science.adj1182

Top 7%

3.2DataRank

Top 7%377 citations

Jennifer E. Huffman, Alex A Rodriguez, Mitchell Conery, Molei Liu, Yuk‐Lam Ho +66 more

Papers

Driven by 84 papers — median percentile 30. Top paper: “Large-scale genome-wide association study of coronary artery disease in genetically diverse populations”.

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Nature Medicine(2022)10.1038/s41591-022-01891-3

N/A

6.8DataRank · unranked

363 citations

Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma +78 more

Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual

Genome Biology(2021)10.1186/s13059-020-02207-9

N/A

4.2DataRank · unranked

149 citations

Yadav Wagley, James A. Pippin, Ahmed Elhakeem, Gregory P. Way, Matthew C. Pahl +29 more

Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations

American Journal of Epidemiology(2009)10.1093/aje/kwp145

N/A

4.0DataRank · unranked

67 citations

Lorraine Southam, David Altshuler, Kristin G. Ardlie, Inês Barroso, Michael Boehnke +27 more

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

Science(2024)10.1126/science.adj1182

Top 7%

3.2DataRank

Top 7%377 citations

Jennifer E. Huffman, Alex A Rodriguez, Mitchell Conery, Molei Liu, Yuk‐Lam Ho +66 more

A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program

PLoS Genetics(2022)10.1371/journal.pgen.1010193

Top 17%

1.2DataRank

Top 17%22 citations

Jie Huang, Catherine Tcheandjieu, Jennifer E. Huffman, Elizabeth Litkowski, Chang Liu +20 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Confounding from Cryptic Relatedness in Case-Control Association Studies

PLoS Genetics(2005)10.1371/journal.pgen.0010032

N/A

0.820DataRank · unranked

236 citations

Jonathan K. Pritchard, Benjamin F. Voight

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z

N/A

0.793DataRank · unranked

197 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes

Nature Communications(2021)10.1038/s41467-021-22338-2

N/A

0.731DataRank · unranked

130 citations

Marijana Vujković, Joshua Elliott, Evangelos Evangelou, Dipender Gill, Mohsen Ghanbari +95 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

Characterization of the genome and silk-gland transcriptomes of Darwin’s bark spider (Caerostris darwini)

PLoS ONE(2022)10.1371/journal.pone.0268660

N/A

0.630DataRank · unranked

16 citations

Matjaž Gregorič, Nicholas F. Lahens, David N. Nicholson, Cheryl Y. Hayashi, Linden Higgins +4 more

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Science(2025)10.1126/science.adp4753

N/A

0.587DataRank · unranked

49 citations

Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng, Bernhard Dumoulin +94 more

Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.09.375592

Top 34%

0.576DataRank

Top 34%14 citations

Ziyuan Ma, Junnan Wu, Hongbo Liu, Chengxiang Qiu, Zhen Miao +14 more

A large-scale multi-ethnic genome-wide association study of coronary artery disease

Research Square(2021)10.21203/rs.3.rs-275591/v1

N/A

0.561DataRank · unranked

11 citations

Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni +77 more

Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis

Diabetologia(2023)10.1007/s00125-023-05925-4

N/A

0.553DataRank · unranked

39 citations

Emmanouil Bouras, Andrei‐Emil Constantinescu, Kimberley Burrows, Caroline J. Bull, Emma E. Vincent +92 more

Type 1 diabetes in Africa: an immunogenetic study in the Amhara of North-West Ethiopia

Diabetologia(2020)10.1007/s00125-020-05229-x

N/A

0.553DataRank · unranked

39 citations

Abayneh Girma Demisse, Rajashree Mishra, Tanwi Vartak, Diana L. Cousminer, Kenyaita M. Hodge +13 more

A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

medRxiv(2021)10.1101/2021.05.18.21257396

N/A

0.506DataRank · unranked

8 citations

Noah L. Tsao, Lauren O. Thomann, Yuk‐Lam Ho, Sudha K. Iyengar, Shiuh‐Wen Luoh +32 more

A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

PLoS Genetics(2022)10.1371/journal.pgen.1010113

N/A

0.500DataRank · unranked

27 citations

Noah L. Tsao, Lauren O. Thomann, Yuk‐Lam Ho, Sudha K. Iyengar, Shiuh‐Wen Luoh +32 more

Multi-omics characterization of type 2 diabetes associated genetic variation

medRxiv(2024)10.1101/2024.07.15.24310282

Top 41%

0.470DataRank

Top 41%12 citations

Kimberly Lorenz, Xianyong Yin, Ozvan Bocher, Alicia Huerta‐Chagoya, Ana Luiza Arruda +27 more

Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction–associated steatotic liver disease

Hepatology Communications(2024)10.1097/hc9.0000000000000487

N/A

0.434DataRank · unranked

17 citations

Craig C. Teerlink, Tae‐Hwi Schwantes‐An, Trina M. Norden‐Krichmar, Scott L. DuVall, Timothy R. Morgan +6 more

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491

N/A

0.425DataRank · unranked

16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 more

Regularized sequence-context mutational trees capture variation in mutation rates across the human genome

PLoS Genetics(2023)10.1371/journal.pgen.1010807

N/A

0.385DataRank · unranked

12 citations

Mitchell Conery, Benjamin J. Auerbach, Shane T. Jensen, Iain Mathieson, Benjamin F. Voight +1 more

Prioritizing the Role of Major Lipoproteins and Subfractions as Risk Factors for Peripheral Artery Disease

medRxiv(2021)10.1101/2021.01.11.21249148

N/A

0.330DataRank · unranked

8 citations

Verena Zuber, Venexia Walker, Derek Klarin, Julie A. Lynch, Rainer Malik +12 more

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum

medRxiv(2023)10.1101/2023.07.16.23292724

N/A

0.292DataRank · unranked

6 citations

Kathleen M. Cardone, David Y. Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +30 more

Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual through variant-to-gene mapping

medRxiv(2020)10.1101/2020.02.17.20024133

N/A

0.290DataRank · unranked

5 citations

Yadav Wagley, James A. Pippin, Ahmed Elhakeem, Gregory P. Way, Shana E. McCormack +28 more

Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.05.450786

N/A

0.208DataRank · unranked

3 citations

Sumei Lu, Binglan Li, Chun Su, Matthew E. Johnson, Wei-Qi Wei +14 more

Multi-ancestry Multivariate Genome-Wide Analysis Highlights the Role of Common Genetic Variation in Cardiac Structure, Function, and Heart Failure-related Traits

medRxiv(2021)10.1101/2021.08.03.21261508

N/A

0.104DataRank · unranked

1 citations

Noah L. Tsao, Tiffany R. Bellomo, William P. Bone, Krishna G. Aragam, Yifan Yang +11 more

Characterization of non-coding variants associated with transcription factor binding through ATAC-seq-defined footprint QTLs in liver

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.24.614730

N/A

0.104DataRank · unranked

1 citations

Brandon M. Wenz, Christopher D. Brown, Benjamin F. Voight, Laura Almasy, Struan F.A. Grant +1 more

Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach

BMC Bioinformatics(2022)10.1186/s12859-022-04977-4

N/A

0DataRank · unranked

0 citations

Marylyn D. Ritchie, Benjamin F. Voight, Wei‐Ting Hwang, Zhuoran Ding

Genetically-proxied anti-diabetic drug target perturbation and risk of cancer: a Mendelian randomization analysis

medRxiv(2022)10.1101/2022.10.24.22281370

N/A

0DataRank · unranked

0 citations

Emmanouil Bouras, Andrei‐Emil Constantinescu, Kimberley Burrows, Caroline J. Bull, Emma E. Vincent +21 more

Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms

Nature Communications(2023)10.1038/s41467-023-41057-4

N/A

0DataRank · unranked

24 citations

Sumei Lu, Binglan Li, Chun Su, Matthew E. Johnson, Wei‐Qi Wei +12 more

Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets

medRxiv(2023)10.1101/2023.11.30.23299247

N/A

0DataRank · unranked

15 citations

Sile Hu, Lingyan Chen, Charlotte Daly, Cesar A. Prada‐Medina, Tom G. Richardson +15 more

Deciphering the genetic architecture of atrial fibrillation offers insights into disease prediction, pathophysiology and downstream sequelae

medRxiv(2023)10.1101/2023.07.20.23292938

N/A

0DataRank · unranked

7 citations

Yuying Li, Lijuan Wang, Fengzhe Xu, Jie Chen, Michael G. Levin +11 more

Evaluation of the Performance of the RECODe Equation with the Addition of Polygenic Risk Scores for Adverse Cardiovascular Outcomes in Individuals with Type II Diabetes

medRxiv(2023)10.1101/2023.05.03.23289457

N/A

0DataRank · unranked

4 citations

Renae Judy, Michael G. Levin, Gabrielle Shakt, Penn Medicine BioBank, Benjamin F. Voight +3 more

G6PC2 controls glucagon secretion by defining the setpoint for glucose in pancreatic α-cells

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.23.541901

N/A

0DataRank · unranked

2 citations

Eric Waite, Reut Rifkind, Zenab Hamdan, Catherine Lee May, Elisabetta Manduchi +8 more

Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores

JAMA(2024)10.1001/jama.2024.23784

N/A

0DataRank · unranked

60 citations

Kristin Boulier, Karl Keat, Katie M. Cardone, Manu Shivakumar, John DePaolo +35 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

UNC Libraries(2024)10.17615/8zyz-p282

Top 100%

0DataRank

Top 100%0 citations

Shining Ma, J.C. Bis, Noah L. Tsao, Philip S. Tsao, Yi‐Lwun Ho +81 more

Genomics and phenomics of body mass index reveals a complex disease network

RePEc: Research Papers in Economics(2024)10.17615/jxxp-qf89

N/A

0DataRank · unranked

0 citations

X. Mai Nguyen, Yan V. Sun, Ítalo Faria do Valle, Dan Rader, Julie A. Lynch +33 more

A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program

UNC Libraries(2024)10.17615/gaa4-wv47

Top 100%

0DataRank

Top 100%0 citations

Yuk Lam Ho, Huijie Zhao, Eirini Marouli, S. Raghavan, Haley Hunter-Zinck +19 more

Mendelian randomization analyses clarify the effects of height on cardiovascular diseases

PLoS ONE(2024)10.1371/journal.pone.0298786

N/A

0DataRank · unranked

0 citations

Eric Sanford, Kimberly Lorenz, Scott M. Damrauer, Themistocles L. Assimes, Christopher S. Thom +2 more

Genotype inference from aggregated chromatin accessibility data reveals genetic regulatory mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.04.610850

Top 100%

0DataRank

Top 100%0 citations

Yuan He, Nae-Chyun Chen, Joseph K. Pickrell, Jeremiah H. Li, Max F. Dudek +6 more

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

UNC Libraries(2024)10.17615/c75g-gz70

N/A

0DataRank · unranked

0 citations

Maties Torrent, Struan F.A. Grant, Jonathan A. Mitchell, Joseph M. Kindler, Emily Oken +95 more

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02140-2

N/A

0DataRank · unranked

33 citations

Kathleen M. Cardone, David Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +35 more

Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation

Nature Communications(2025)10.1038/s41467-025-61720-2

N/A

0DataRank · unranked

17 citations

Jie Chen, Xixian Ruan, Yuying Li, Sarah Abramowitz, Lijuan Wang +12 more

The effect of type 2 diabetes genetic predisposition on non-cardiovascular comorbidities

Nature Communications(2025)10.1038/s41467-025-64927-5

N/A

0DataRank · unranked

6 citations

Ozvan Bocher, Henry J. Taylor, Davis Cammann, Satoshi Yoshiji, Xianyong Yin +14 more

Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population

Nature Communications(2025)10.1038/s41467-025-64659-6

N/A

0DataRank · unranked

7 citations

Kazuo Miyazawa, Satoshi Koyama, Ryo Kurosawa, Hirotaka Ieki, Hiroki Yoshida +26 more

G6PC2 controls glucagon secretion by defining the set point for glucose in pancreatic α cells

Science Translational Medicine(2025)10.1126/scitranslmed.adi6148

N/A

0DataRank · unranked

7 citations

Reut Rifkind, Eric Waite, Zenab Hamdan, Catherine Lee May, Elisabetta Manduchi +8 more

Characterization of non-coding variants associated with transcription-factor binding through ATAC-seq-defined footprint QTLs in liver

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.019

N/A

0DataRank · unranked

3 citations

Brandon M. Wenz, Christopher D. Brown, Benjamin F. Voight, Laura Almasy, Struan F.A. Grant +1 more

Methylation-associated mutagenesis underlies variation in the mutation spectrum across eukaryotes

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.28.656604

N/A

0DataRank · unranked

2 citations

Ziyue Gao, Benjamin F. Voight, Iain Mathieson, Fabián Ramos-Almodóvar

A multi-trait genome-wide association study of coronary artery disease and subclinical atherosclerosis traits

Research Square(2025)10.21203/rs.3.rs-6456056/v1

N/A

0DataRank · unranked

1 citations

Adam S. Heath, Chani J. Hodonsky, Julie Hahn, Devendra Meena, Haojie Lu +10 more

Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissues

medRxiv(2025)10.1101/2025.05.05.25326880

N/A

0DataRank · unranked

1 citations

Ana Luiza Arruda, Satoshi Yoshiji, Chi Zhao, Chen‐Yang Su, Xianyong Yin +19 more

Expanded Chromatin Accessibility Mapping Explains Genetic Variation Associated with Complex Traits in Liver

medRxiv(2025)10.1101/2025.09.15.25335593

N/A

0DataRank · unranked

1 citations

Max F. Dudek, Shweta Ramdas, Kate Townsend Creasy, Xin Dong, Kim M. Olthoff +5 more

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways

medRxiv(2025)10.1101/2025.09.16.25335186

N/A

0DataRank · unranked

1 citations

David E. Kaplan, Jonas Ghouse, Bao‐Li Loza, Joseph Brancale, Adam Lewis +68 more

The effect of type 2 diabetes genetic predisposition on non-cardiovascular comorbidities

medRxiv(2025)10.1101/2025.05.05.25326966

N/A

0DataRank · unranked

0 citations

Ozvan Bocher, Henry J. Taylor, Davis Cammann, Satoshi Yoshiji, Xianyong Yin +13 more

Protocol for discovering genetic variants associated with ATAC-seq footprint-inferred transcription factor binding

STAR Protocols(2025)10.1016/j.xpro.2025.104148

N/A

0DataRank · unranked

0 citations

Brandon M. Wenz, Benjamin F. Voight, Laura Almasy, Struan F.A. Grant, Max F. Dudek

Expanded chromatin accessibility mapping explains genetic variation associated with complex traits in liver

The American Journal of Human Genetics(2026)10.1016/j.ajhg.2026.01.003

N/A

0DataRank · unranked

0 citations

Max F. Dudek, Shweta Ramdas, Kate Townsend Creasy, Dong Xin, Kim M. Olthoff +7 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

PLoS Genetics(2020)10.1371/journal.pgen.1008629

N/A

0DataRank · unranked

169 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study

PLoS Medicine(2020)10.1371/journal.pmed.1003302

N/A

0DataRank · unranked

131 citations

Katherine M. Siewert, Derek Klarin, Scott M. Damrauer, the VA Million Veteran Program, Kyong-Mi Chang +5 more

BetaScan2: Standardized Statistics to Detect Balancing Selection Utilizing Substitution Data

Genome Biology and Evolution(2020)10.1093/gbe/evaa013

N/A

0DataRank · unranked

106 citations

Benjamin F. Voight, Katherine M. Siewert

Genetic determinants of increased body mass index mediate the effect of smoking on increased risk for type 2 diabetes but not coronary artery disease

Human Molecular Genetics(2020)10.1093/hmg/ddaa193

N/A

0DataRank · unranked

11 citations

Zhuoran Ding, Michael G. Levin, Scott M. Damrauer, Kyung Min Lee, Julie A. Lynch +11 more

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.06.146951

N/A

0DataRank · unranked

5 citations

Claudia A. Doege, Kenyaita M. Hodge, Sheridan H. Littleton, Michelle E. Leonard, Sumei Lu +16 more

Genetically determined body mass index mediates the effect of smoking on type 2 diabetes risk, but not coronary artery disease risk

medRxiv(2020)10.1101/2020.01.30.20019737

N/A

0DataRank · unranked

3 citations

Zhuoran Ding, Michael G. Levin, Scott M. Damrauer, Benjamin F. Voight, Christopher S. Thom

Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits

medRxiv(2020)10.1101/2020.08.26.20179366

N/A

0DataRank · unranked

2 citations

Katherine M. Siewert, Anupama Jha, Derek Klarin, Scott M. Damrauer, the VA Million Veteran Project +6 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

Apollo (University of Cambridge)(2020)10.17863/cam.52580

N/A

0DataRank · unranked

0 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

UNC Libraries(2020)10.17615/55vz-3f21

N/A

0DataRank · unranked

0 citations

Richard N. Bergman, Katherine S. Elliott, Harald Grallert, Eleftheria Zeggini, Peter Almgren +27 more

Common variants at 30 loci contribute to polygenic dyslipidemia

UNC Libraries(2020)10.17615/wktm-vc19

N/A

0DataRank · unranked

0 citations

Pilar Galán, Serkalem Demissie, Eric E. Schadt, Aarti Surti, Luigi Ferrucci +27 more

Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases

UNC Libraries(2020)10.17615/9k4n-rx53

N/A

0DataRank · unranked

0 citations

Francis S. Collins, Christian Gieger, Martha Ganser, Valgerður Steinthórsdóttir, Eric Boerwinkle +27 more

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

UNC Libraries(2020)10.17615/p2f9-t736

N/A

0DataRank · unranked

0 citations

Jeff K. Trimmer, Pål R. Njølstad, Allan Linneberg, Kāri Stefánsson, David R. Cox +16 more

Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study

UNC Libraries(2020)10.17615/xgey-c257

Top 100%

0DataRank

Top 100%0 citations

Charles B. Eaton, Hyun Min Kang, Logan Dumitrescu, Themistocles L. Assimes, Jeffrey Haessler +27 more

A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis

Nature Communications(2021)10.1038/s41467-021-25377-x

N/A

0DataRank · unranked

83 citations

Xiujie Liang, Ziyuan Ma, Hailong Hu, Hongbo Liu, Zhen Miao +5 more

Prioritizing the Role of Major Lipoproteins and Subfractions as Risk Factors for Peripheral Artery Disease

Circulation(2021)10.1161/circulationaha.121.053797

N/A

0DataRank · unranked

67 citations

Verena Zuber, Venexia Walker, Derek Klarin, Julie A. Lynch, Rainer Malik +13 more

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits

Nature Communications(2021)10.1038/s41467-021-27001-4

N/A

0DataRank · unranked

50 citations

Claudia A. Doege, Kenyaita M. Hodge, Sheridan H. Littleton, Michelle E. Leonard, Sumei Lu +18 more

Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits

Alzheimer s Research & Therapy(2021)10.1186/s13195-021-00773-z

N/A

0DataRank · unranked

38 citations

William P. Bone, Katherine M. Siewert, Anupama Jha, Derek Klarin, Scott M. Damrauer +6 more

Evaluation of height as a disease risk factor through a phenome-wide association study of genetically-predicted height

medRxiv(2021)10.1101/2021.08.29.21262793

N/A

0DataRank · unranked

2 citations

Jie Huang, Catherine Tcheandjieu, Jennifer E. Huffman, Elizabeth Litkowski, Yuk‐Lam Ho +19 more

Mendelian randomization analyses clarify the effects of height on cardiovascular diseases

medRxiv(2021)10.1101/2021.12.16.21267869

N/A

0DataRank · unranked

1 citations

Eric Sanford, Kimberly Lorenz, Scott M. Damrauer, Themistocles L. Assimes, Christopher S. Thom +2 more

Obesity and adiposity have opposing genetic impacts on human blood traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.05.467482

N/A

0DataRank · unranked

0 citations

Madison B Wilken, Stella T. Chou, Benjamin F. Voight, Christopher S. Thom

Identification of ten loci associated with height highlights new biological pathways in human growth

UNC Libraries(2021)10.17615/jwbr-0w10

N/A

0DataRank · unranked

0 citations

Frank B. Hu, Peter Kraft, S. Eyheramendy, Candace Guiducci, H.‐Erich Wichmann +26 more

Genomics and phenomics of body mass index reveals a complex disease network

Nature Communications(2022)10.1038/s41467-022-35553-2

N/A

0DataRank · unranked

188 citations

Jennifer E. Huffman, Yunfeng Huang, Ítalo Faria do Valle, Themistocles L. Assimes, Sridharan Raghavan +34 more

Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

Nature Communications(2022)10.1038/s41467-022-34216-6

N/A

0DataRank · unranked

150 citations

Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe +38 more

ColocQuiaL: a QTL-GWAS colocalization pipeline

Bioinformatics(2022)10.1093/bioinformatics/btac512

N/A

0DataRank · unranked

24 citations

William P. Bone, Kim Lorenz, Michael G. Levin, Marylyn D. Ritchie, Benjamin F. Voight +1 more

Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci

Frontiers in Genetics(2022)10.3389/fgene.2021.787545

N/A

0DataRank · unranked

9 citations

William P. Bone, Brian Y. Chen, Katerina A.B. Gawronski, David Zhang, Joseph Park +18 more

Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetes

Diabetologia(2022)10.1007/s00125-022-05653-1

N/A

0DataRank · unranked

12 citations

Marijana Vujković, Alice R Carter, Neil M. Davies, Miriam S. Udler, Michael G. Levin +5 more

Regularized sequence-context mutational trees capture variation in mutation rates across the human genome

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.14.512160

N/A

0DataRank · unranked

1 citations

Mitchell Conery, Benjamin J. Auerbach, Shane T. Jensen, Iain Mathieson, Benjamin F. Voight +1 more

Benjamin F. Voight

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