Cristen J. Willer

Also affiliated with University of Iceland, Regeneron (United States), University of Michigan, Michigan United, Michigan Medicine, Institute of Human Genetics, Geisinger Health System

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

15.8Author DataRank

Indexed papers

10in 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 10 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.

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Nature Communications(2021)10.1038/s41467-021-24491-0

Top 5%

4.6DataRank

Top 5%327 citations

Yong Li, Pascal Schlosser, Mathias Gorski, Matthias Wuttke, Laurent F. Thomas +20 more

Papers

Driven by 94 papers — median percentile 87. Top paper: “A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease”.

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

Nature Genetics(2021)10.1038/s41588-021-00921-z

N/A

8.0DataRank · unranked

1105 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Dominic Holland +95 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 more

Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence

PLoS Genetics(2011)10.1371/journal.pgen.1002280

N/A

7.5DataRank · unranked

148 citations

Rong Chen, Sergio P. Cordero, Kelly E. Ormond, Colleen Caleshu, Konrad J. Karczewski +33 more

The Power of Meta-Analysis in Genome-Wide Association Studies

Annual Review of Genomics and Human Genetics(2013)10.1146/annurev-genom-091212-153520

N/A

5.9DataRank · unranked

129 citations

Cristen J. Willer, Joel N. Hirschhorn, John P. A. Ioannidis, Orestis A. Panagiotou

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Nature Communications(2021)10.1038/s41467-021-24491-0

Top 5%

4.6DataRank

Top 5%327 citations

Yong Li, Pascal Schlosser, Mathias Gorski, Matthias Wuttke, Laurent F. Thomas +20 more

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

Nature Communications(2020)10.1038/s41467-020-17718-z

N/A

4.0DataRank · unranked

141 citations

Ben Brumpton, Ömer Kabil, Jūlı́us Guðmundsson, Guðmar Þorleifsson, Joshua S. Weinstock +51 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

Evidence of reporting biases in voxel-based morphometry (VBM) studies of psychiatric and neurological disorders

Human Brain Mapping(2013)10.1002/hbm.22384

Top 9%

2.3DataRank

Top 9%60 citations

Joaquim Radua, Marianna Frascarelli, Andrea Mechelli, Stefan Borgwardt, Fabio Di Fabio +5 more

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients

Cell Genomics(2023)10.1016/j.xgen.2023.100257

Top 10%

2.2DataRank

Top 10%98 citations

Lars G. Fritsche, Anita Pandit, Brett Vanderwerff, Snehal Patil, Ellen M. Schmidt +9 more

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Nature Genetics(2023)10.1038/s41588-023-01510-y

N/A

1.6DataRank · unranked

100 citations

Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng +92 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

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

PLoS Genetics(2020)10.1371/journal.pgen.1008725

Top 13%

1.6DataRank

Top 13%57 citations

Judith M. Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua Hoffman +36 more

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 more

Largest GWAS (N=1,126,563) of Alzheimer’s Disease Implicates Microglia and Immune Cells

medRxiv(2020)10.1101/2020.11.20.20235275

N/A

1.5DataRank · unranked

43 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Arvid Rongve +52 more

The HUNT study: A population-based cohort for genetic research

Cell Genomics(2022)10.1016/j.xgen.2022.100193

Top 14%

1.5DataRank

Top 14%108 citations

Sarah E. Graham, Ida Surakka, Anne Heidi Skogholt, Mari Løset, Lars G. Fritsche +25 more

Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

Nature Genetics(2023)10.1038/s41588-023-01420-z

N/A

1.4DataRank · unranked

63 citations

Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen +32 more

Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits

Nature Communications(2022)10.1038/s41467-022-30098-w

N/A

1.2DataRank · unranked

55 citations

Jean‐Tristan Brandenburg, Tinashe Chikowore, Dhriti Sengupta, Palwendé Romuald Boua, Nigel J. Crowther +18 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

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 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

Mitochondrial genome-wide association study of migraine – the HUNT Study

Cephalalgia(2020)10.1177/0333102420906835

Top 19%

1.1DataRank

Top 19%28 citations

John‐Anker Zwart, Anne Heidi Skogholt, Maiken E. Gabrielsen, Laurent F. Thomas, Lars G. Fritsche +13 more

Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.121.003542

N/A

0.934DataRank · unranked

16 citations

Brooke N. Wolford, Scott C. Ritchie, Whitney Hornsby, Nadia R. Sutton, Maiken Elvenstad Gabrielsen +6 more

Publication and other reporting biases in cognitive sciences: detection, prevalence, and prevention

Trends in Cognitive Sciences(2014)10.1016/j.tics.2014.02.010

N/A

0.933DataRank · unranked

503 citations

Marcus Robert Munafo, Brian A. Nosek, Cristen J. Willer, John P. A. Ioannidis, Paolo Fusar‐Poli

Clinical Interpretation and Implications of Whole-Genome Sequencing

JAMA(2014)10.1001/jama.2014.1717

N/A

0.919DataRank · unranked

456 citations

Megan E. Grove, Cuiping Pan, Benjamin A. Goldstein, Jonathan A. Bernstein, Hassan Chaib +26 more

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses

Nature Communications(2020)10.1038/s41467-020-17117-4

N/A

0.909DataRank · unranked

426 citations

Eleanor Sanderson, Karl Heilbron, Fernando Pires Hartwig, Sean Harrison, Gunnhild Åberge Vie +28 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

Genetic mutations associated with susceptibility to perioperative complications in a longitudinal biorepository with integrated genomic and electronic health records

British Journal of Anaesthesia(2020)10.1016/j.bja.2020.08.009

N/A

0.648DataRank · unranked

18 citations

Sachin Kheterpal, Milo Engoren, Michael R. Mathis, George A. Mashour, Whitney Hornsby +3 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0.637DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 more

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools

Brain(2021)10.1093/brain/awab267

N/A

0.633DataRank · unranked

67 citations

Guy Hindley, Bendik Slagsvold Winsvold, Kevin S. O’Connell, Oleksandr Frei, Alexey Shadrin +35 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

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Stroke(2023)10.1161/strokeaha.122.040715

N/A

0.520DataRank · unranked

31 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik Slagsvold Winsvold, John‐Anker Zwart +95 more

Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101430

N/A

0.510DataRank · unranked

29 citations

Arjun Bhattacharya, Wei Zhou, Dan Zhou, Ying Wang, Kristi Läll +31 more

Multi-ancestry meta-analysis identifies 2 novel loci associated with ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

medRxiv(2022)10.1101/2022.02.28.22271647

N/A

0.503DataRank · unranked

18 citations

Kuan-Han H. Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +17 more

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

Cell Genomics(2023)10.1016/j.xgen.2023.100345

N/A

0.483DataRank · unranked

24 citations

Kuan-Han Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +16 more

A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans

Communications Biology(2024)10.1038/s42003-024-06101-z

N/A

0.470DataRank · unranked

22 citations

Ailin Falkmo Hansen, Brooke N. Wolford, Laurent F. Thomas, Humaira Rasheed, Anica Simić +19 more

Variants associated with HHIP expression have sex-differential effects on lung function

Wellcome Open Research(2020)10.12688/wellcomeopenres.15846.1

N/A

0.385DataRank · unranked

12 citations

Ma’en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John +70 more

Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study

Behavior Genetics(2022)10.1007/s10519-022-10116-9

N/A

0.345DataRank · unranked

9 citations

Michel G. Nivard, Laxmi Bhatta, Nicole M. Warrington, Cristen J. Willer, Bjørn Olav Åsvold +3 more

Genome-wide Association Study of Thoracic Aortic Aneurysm and Dissection in the Million Veteran Program

Research Square(2022)10.21203/rs.3.rs-1507463/v1

N/A

0.345DataRank · unranked

9 citations

Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen +29 more

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Human Molecular Genetics(2021)10.1093/hmg/ddab062

N/A

0.312DataRank · unranked

7 citations

Wei Zhou, Yi Fu, Chloe Y. Y. Cheung, Yujun Dong, Min‐Lee Yang +15 more

Differences in Inflammation, Treatment, and Outcomes Between Black and Non-Black Patients Hospitalized for COVID-19: A Prospective Cohort Study

The American Journal of Medicine(2021)10.1016/j.amjmed.2021.10.026

N/A

0.312DataRank · unranked

7 citations

Hanna Berlin, Élizabeth Anderson, Michael Pan, Husam Shadid, Kishan Padalia +12 more

Variants associated with HHIP expression have sex-differential effects on lung function

Wellcome Open Research(2021)10.12688/wellcomeopenres.15846.2

N/A

0.306DataRank · unranked

5 citations

Ma’en Obeidat, Carl Melbourne, Nick Shrine, Anna L. Guyatt, Catherine John +70 more

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

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

N/A

0.277DataRank · unranked

3 citations

Xihao Li, Zilin Li, Akhil Pampana, David Y Zhang, Joseph Park +80 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

Incorporating family disease history and controlling case–control imbalance for population-based genetic association studies

Bioinformatics(2022)10.1093/bioinformatics/btac459

N/A

0.241DataRank · unranked

4 citations

Brooke N. Wolford, Kisung Nam, Wenjian Bi, Wei Zhou, Cristen J. Willer +3 more

Dissecting the Genetic Architecture of Intracranial Aneurysms

Circulation Genomic and Precision Medicine(2025)10.1161/circgen.123.004626

N/A

0.241DataRank · unranked

4 citations

Julie A. Lynch, Ryan Choi, Tanmoy Roychowdhury, Renae Judy, Kaavya Paruchuri +16 more

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

medRxiv(2021)10.1101/2021.09.20.21262960

N/A

0.208DataRank · unranked

3 citations

Ailin Falkmo Hansen, Sarah E. Graham, Sarah A. Gagliano Taliun, Kuan-Han Wu, Wei Zhou +14 more

A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants

UNC Libraries(2021)10.17615/xzx9-fd89

N/A

0.187DataRank · unranked

1 citations

Michael W. Barnhart, Timo T. Valle, Karen L. Mohlke, Michael Boehnke, Heather M. Stringham +36 more

Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish

Blood Advances(2025)10.1182/bloodadvances.2024015790

N/A

0.165DataRank · unranked

2 citations

Yakun Zhao, Kuan-Han H. Wu, Xinge Yu, Catherine E. Richter, Laxmi Bhatta +17 more

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

WOS(2020)10.17615/dkeh-7r02

N/A

0.164DataRank · unranked

1 citations

Jian Yang, Guðmar Þorleifsson, Josine L. Min, Andrew R. Wood, Keri L. Monda +27 more

Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics

UNC Libraries(2020)10.17615/qhxy-td18

N/A

0.104DataRank · unranked

1 citations

Kari E. North, D. Y. Lin, Andrea Ganna, Felix R. Day, Eleanor Wheeler +23 more

Integrating large scale genetic and clinical information to predict cases of heart failure

Communications Medicine(2025)10.1038/s43856-025-01198-7

N/A

0DataRank · unranked

0 citations

Brooke N. Wolford, Jiacong Du, Xianshi Yu, Nicholas J. Douville, Michael R. Mathis +8 more

Causal relationships between NAFLD, T2D and obesity have implications for disease subphenotyping

Journal of Hepatology(2020)10.1016/j.jhep.2020.03.006

N/A

0DataRank · unranked

264 citations

Yang Zhang, Sarah E. Graham, Xiaokun Wang, Defeng Cai, Menghao Huang +6 more

Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

Nature Communications(2020)10.1038/s41467-020-19257-z

N/A

0DataRank · unranked

95 citations

Ben Brumpton, Cristen J. Willer, Bjørn Olav Åsvold, Kåre I. Birkeland, Geng Wang +8 more

Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study)

PLoS Medicine(2020)10.1371/journal.pmed.1003452

N/A

0DataRank · unranked

19 citations

Johan Hå kon Bjø rngaard, Rønnaug Ødegård, Ben Brumpton, George Davey Smith, Bjørn Olav Åsvold +5 more

Gait speed is a preoperative indicator of postoperative events after elective proximal aortic surgery

Journal of Thoracic and Cardiovascular Surgery(2020)10.1016/j.jtcvs.2020.03.165

N/A

0DataRank · unranked

13 citations

Elizabeth L. Norton, Xiaoting Wu, Cristen J. Willer, Scott L. Hummell, Richard L. Prager +4 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 more

A Novel Variant in APOB Gene Causes Extremely Low LDL-C Without Known Adverse Effects

JACC Case Reports(2020)10.1016/j.jaccas.2020.03.016

N/A

0DataRank · unranked

2 citations

Whitney Hornsby, Linda Farhat, Melvyn Rubenfire, Lars G. Fritsche, Kristian Hveem +5 more

Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes

UNC Libraries(2020)10.17615/vz97-xy60

N/A

0DataRank · unranked

10 citations

A. U. Jackson, M. Tong, N. Narisu, Cristen J. Willer, E. W. Pugh +17 more

Common variants associated with plasma triglycerides and risk for coronary artery disease

UNC Libraries(2020)10.17615/3nfp-v503

N/A

0DataRank · unranked

4 citations

Hsing‐Yi Chang, Åsa Johansson, Pierre Fontanillas, Martin L. Buchkovich, Ross M. Fraser +27 more

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

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

N/A

0DataRank · unranked

2 citations

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

Cardiometabolic traits, sepsis and severe covid-19: a Mendelian randomization investigation

medRxiv(2020)10.1101/2020.06.18.20134676

N/A

0DataRank · unranked

20 citations

Apostolos Gkatzionis, Venexia Walker, Andrew J. Grant, Robyn E. Wootton, Luke Moore +16 more

Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study

medRxiv(2020)10.1101/2020.05.04.20091173

N/A

0DataRank · unranked

1 citations

Ben Brumpton, Cristen J. Willer, Bjørn Olav Åsvold, Kåre I. Birkeland, Michael C. Neale +7 more

Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

medRxiv(2020)10.1101/2020.09.04.20187401

N/A

0DataRank · unranked

0 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +22 more

Common variants in the GDF5-UQCC region are associated with variation in human height

UNC Libraries(2020)10.17615/th6f-r873

N/A

0DataRank · unranked

0 citations

Nicholas J. Timpson, Yoav Ben‐Shlomo, Debbie A. Lawlor, Lori L. Bonnycastle, Laura J. Scott +27 more

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

UNC Libraries(2020)10.17615/kr0j-1k09

N/A

0DataRank · unranked

0 citations

Paul Scheet, Inga Prokopenko, Steven A. McCarroll, Nicole Soranzo, Michael N. Weedon +27 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

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

Finding genes and variants for lipid levels after genome-wide association analysis

UNC Libraries(2020)10.17615/1nrs-zs32

N/A

0DataRank · unranked

0 citations

Karen L. Mohlke, Cristen J. Willer

WikiGWA: an open platform for collecting and using genome-wide association results

UNC Libraries(2020)10.17615/jarv-hf24

Top 100%

0DataRank

Top 100%0 citations

Cristen J. Willer, Jie Huang, Lucia A. Hindorff, Eric Y Liu, Yun Li +1 more

Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps

Nature Medicine(2021)10.1038/s41591-021-01549-6

N/A

0DataRank · unranked

445 citations

Adebowale Adeyemo, Mary K. Balaconis, Deanna R. Darnes, Segun Fatumo, Palmira Granados Moreno +22 more

Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.016

N/A

0DataRank · unranked

58 citations

Haocheng Lu, Whitney Hornsby, Bradley Crone, Gao T. Wang, Dongchuan Guo +35 more

Genome-scale CRISPR screening for modifiers of cellular LDL uptake

PLoS Genetics(2021)10.1371/journal.pgen.1009285

N/A

0DataRank · unranked

37 citations

Emily J. Sherman, Paul J. Lascuna, Sarah E. Graham, Cristen J. Willer, David Ginsburg +1 more

Genome-wide association study of cardiac troponin I in the general population

Human Molecular Genetics(2021)10.1093/hmg/ddab124

N/A

0DataRank · unranked

20 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +25 more

Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents

PLoS ONE(2021)10.1371/journal.pone.0246447

N/A

0DataRank · unranked

20 citations

Whitney Hornsby, Bethany Klunder, Amelia Krause, Anisa Driscoll, John Kulka +13 more

Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2

iScience(2021)10.1016/j.isci.2021.103196

N/A

0DataRank · unranked

17 citations

Brooke N. Wolford, Haocheng Lu, Wenying Liang, Jinjian Sun, Wei Zhou +20 more

Translating genetic association of lipid levels for biological and clinical application

Cardiovascular Drugs and Therapy(2021)10.1007/s10557-021-07156-4

N/A

0DataRank · unranked

10 citations

Amelia Krause, Whitney Hornsby, Cristen J. Willer, Ida Surakka, Bradley Crone

Global biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

medRxiv(2021)10.1101/2021.11.18.21266545

N/A

0DataRank · unranked

25 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +25 more

Sex-specific survival bias and interaction modeling in coronary artery disease risk prediction

medRxiv(2021)10.1101/2021.06.23.21259247

N/A

0DataRank · unranked

6 citations

Brooke N. Wolford, Scott C. Ritchie, Whitney Hornsby, Nadia R. Sutton, Maiken Elvenstad Gabrielsen +6 more

Identification of ACE2 modifiers by CRISPR screening

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.10.447768

N/A

0DataRank · unranked

5 citations

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0DataRank · unranked

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0DataRank · unranked

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0DataRank

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0DataRank · unranked

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Communications Biology(2022)10.1038/s42003-022-03529-z

N/A

0DataRank · unranked

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Communications Biology(2022)10.1038/s42003-022-03932-6

N/A

0DataRank · unranked

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N/A

0DataRank · unranked

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medRxiv(2022)10.1101/2022.07.19.22277830

N/A

0DataRank · unranked

0 citations

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0DataRank · unranked

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N/A

0DataRank · unranked

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N/A

0DataRank · unranked

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medRxiv(2023)10.1101/2023.04.25.23289097

N/A

0DataRank · unranked

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0DataRank · unranked

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