Caroline Hayward

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 2%percentile

3.1Author 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.

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

Papers

Driven by 86 papers — median percentile 31. Top paper: “Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals”.

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Nature Metabolism(2020)10.1038/s42255-020-00287-2

N/A

10.0DataRank · unranked

782 citations

Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen, Åsa K. Hedman, Andrew J. Schork +78 more

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature Genetics(2022)10.1038/s41588-022-01016-z

N/A

8.1DataRank · unranked

699 citations

Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati +94 more

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

Genome biology(2021)10.1186/s13059-021-02398-9

N/A

5.8DataRank · unranked

307 citations

Josine L. Min, Rebecca Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies +95 more

Genome-wide association study identifies 48 common genetic variants associated with handedness

Nature Human Behaviour(2020)10.1038/s41562-020-00956-y

N/A

3.7DataRank · unranked

157 citations

Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen +95 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0

N/A

2.8DataRank · unranked

151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 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

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

Common Genetic Variants Explain the Majority of the Correlation Between Height and Intelligence: The Generation Scotland Study

Behavior Genetics(2014)10.1007/s10519-014-9644-z

N/A

1.8DataRank · unranked

52 citations

Riccardo E. Marioni, G. David Batty, Caroline Hayward, Shona M. Kerr, Archie Campbell +4 more

Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2020)10.1002/ajmg.b.32807

N/A

1.6DataRank · unranked

65 citations

Jonathan R. I. Coleman, Shing Wan Choi, Héléna A. Gaspar, Mark J. Adams, David M. Howard +43 more

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Nature Human Behaviour(2023)10.1038/s41562-023-01528-6

N/A

1.3DataRank · unranked

59 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Diana van Heemst +92 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

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Nature Genetics(2014)10.1038/ng.2897

N/A

1.0DataRank · unranked

1086 citations

Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E Below, Kyle J Gaulton +327 more

Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma

Nature Communications(2024)10.1038/s41467-023-44380-y

N/A

1.0DataRank · unranked

64 citations

Wenjun Yan, John M. Rouhana, Aboozar Monovarfeshani, Xinyi Jiang, Puja A. Mehta +65 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +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

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

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

N/A

0.606DataRank · unranked

56 citations

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

Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

Nature Communications(2017)10.1038/s41467-017-01525-0

N/A

0.604DataRank · unranked

55 citations

Toma Keser, Annika Wahl, Antti Hassinen, Lin Liu, Genadij Razdorov +26 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

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

Identification of plasma proteins relating to brain neurodegeneration and vascular pathology in cognitively normal individuals

Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring(2021)10.1002/dad2.12240

Top 36%

0.541DataRank

Top 36%11 citations

Colin R. Buchanan, Simon R. Cox, Robert F. Hillary, Riccardo E. Marioni, Archie Campbell +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

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

Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies

PLoS ONE(2013)10.1371/journal.pone.0068604

N/A

0.434DataRank · unranked

17 citations

James Prendergast, Ross M. Fraser, Jennifer E. Huffman, Veronique Vitart, Caroline Hayward +11 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

An Updated Polygenic Index Repository: Expanded Phenotypes, New Cohorts, and Improved Causal Inference

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.14.653986

Top 60%

0.253DataRank

Top 60%4 citations

Anastasia Terskaya, Matthew D. Howell, Junming Guan, Harry Sands, Aaron Kleinman +45 more

Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

Nature Communications(2018)10.1038/s41467-017-02379-2

N/A

0.241DataRank · unranked

4 citations

Toma Keser, Annika Wahl, Antti Hassinen, Lin Liu, Genadij Razdorov +26 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

Preprocessed IgG Fc glycomics data in four Croatian cohorts (LC-ESI-MS)

Figshare(2017)10.6084/m9.figshare.5335861

Top 78%

0.104DataRank

Top 78%1 citations

Maja Pučić‐Baković, Toma Keser, Annika Wahl, Antti Hassinen, Jeong‐Yeh Yang +26 more

Genome-Wide Aggregated Trans Effects Analysis for Circulating Proteins Indicates a Key Role of Immune Checkpoints in Type 1 Diabetes

Diabetes(2025)10.2337/db25-0067

N/A

0.104DataRank · unranked

1 citations

Andrii Iakovliev, Stuart J. McGurnaghan, Buddhiprabha Erabadda, Caroline Hayward, Paul McKeigue +3 more

Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents

American Journal of Psychiatry(2020)10.1176/appi.ajp.2020.19101025

N/A

0DataRank · unranked

128 citations

Andrey A. Shabalin, Emily DiBlasi, Eric T. Monson, Niamh Mullins, Daniel E. Adkins +18 more

Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease

Journal of Human Genetics(2021)10.1038/s10038-020-00895-6

N/A

0DataRank · unranked

77 citations

Sean Bankier, Elisabeth Altmaier, Catriona L. K. Barnes, David W. Clark, Raili Ermel +36 more

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Cell Reports(2021)10.1016/j.celrep.2021.110020

N/A

0DataRank · unranked

47 citations

Jennifer Nguyen, Timothy D. Arthur, Hiroko Matsui, Agnieszka D’Antonio‐Chronowska, Kelly A. Frazer +85 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

Lifestyle and Genetic Factors Modify Parent-of-Origin Effects on the Human Methylome

EBioMedicine(2021)10.1016/j.ebiom.2021.103730

N/A

0DataRank · unranked

16 citations

Carmen Amador, Chenhao Gao, Rosie M. Walker, Stewart W. Morris, Archie Campbell +13 more

Association of low-frequency and rare coding variants with information processing speed

Translational Psychiatry(2021)10.1038/s41398-021-01736-6

N/A

0DataRank · unranked

2 citations

Gail Davies, Albert V. Smith, Yasaman Saba, Joshua C. Bis, Xueqiu Jian +50 more

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Research Square10.21203/rs.3.rs-846265/v1

N/A

0DataRank · unranked

0 citations

Annechien E. G. Haarman, Robert Luben, Jue‐Sheng Ong, Karina Patasova, Rolando Hernandez Trapero +31 more

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

medRxiv(2021)10.1101/2021.04.01.21254789

N/A

0DataRank · unranked

9 citations

Jack Gisby, Artemis Papadaki, Marisa D. Muckian, Erin Macdonald-Dunlop, Jing Hua Zhao +64 more

Copy-Number Variants in The Contactin-5 Gene Are a Potential Risk Factor for Autism Spectrum Disorder

Research Square(2021)10.21203/rs.3.rs-660740/v1

N/A

0DataRank · unranked

0 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +16 more

Epigenetic scores for the circulating proteome as tools for disease prediction

eLife(2022)10.7554/elife.71802

N/A

0DataRank · unranked

139 citations

Robert F. Hillary, Daniel L. McCartney, Shaza B. Zaghlool, Anna J. Stevenson, Yipeng Cheng +23 more

Genetic Associations and Architecture of Asthma-COPD Overlap

CHEST Journal(2022)10.1016/j.chest.2021.12.674

N/A

0DataRank · unranked

45 citations

Anna L. Guyatt, Nick Shrine, Richard Packer, Thorunn A. Olafsdottir, Jiangyuan Liu +49 more

Genetic Landscape of the ACE2 Coronavirus Receptor

Circulation(2022)10.1161/circulationaha.121.057888

N/A

0DataRank · unranked

40 citations

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

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin

Journal of the American Society of Nephrology(2022)10.1681/asn.2021040491

N/A

0DataRank · unranked

31 citations

Marta Mariniello, Ayumi Yoshifuji, Guglielmo Schiano, Jennifer Lake, Jonathan Marten +38 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

0DataRank · unranked

23 citations

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

Identification of influential probe types in epigenetic predictions of human traits: implications for microarray design

Clinical Epigenetics(2022)10.1186/s13148-022-01320-9

N/A

0DataRank · unranked

14 citations

Daniel L. McCartney, Allan F. McRae, Archie Campbell, Rosie M. Walker, Caroline Hayward +5 more

Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder

Research in autism spectrum disorders(2022)10.1016/j.rasd.2022.102055

N/A

0DataRank · unranked

3 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +18 more

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

medRxiv(2022)10.1101/2022.01.11.22268884

N/A

0DataRank · unranked

6 citations

Humaira Rasheed, Paul Remy Jones, Dorret I. Boomsma, David M. Evans, Alexandros Giannelis +23 more

The influence of biological and statistical properties of CpGs on epigenetic predictions of eighteen traits

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.08.479569

N/A

0DataRank · unranked

0 citations

Daniel L. McCartney, Allan F. McRae, Archie Campbell, Rosie M. Walker, Caroline Hayward +5 more

GDF15 linked to maternal risk of nausea and vomiting during pregnancy

Nature(2023)10.1038/s41586-023-06921-9

N/A

0DataRank · unranked

187 citations

Nuno Rocha, Irène Cimino, Sam Lockhart, Clive J. Petry, Richard G. Kay +38 more

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

UNC Libraries(2020)10.17615/2bje-6g29

N/A

0DataRank · unranked

0 citations

Deborah J. Thompson, Hannes Helgason, Timothy M. Frayling, Hilary K. Finucane, Patrick Sulem +211 more

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

International Journal of Epidemiology(2023)10.1093/ije/dyad079

N/A

0DataRank · unranked

39 citations

Humaira Rasheed, Paul Remy Jones, Dorret I. Boomsma, David M. Evans, Alexandros Giannelis +42 more

A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

EBioMedicine(2023)10.1016/j.ebiom.2023.104551

N/A

0DataRank · unranked

33 citations

Samantha Sze‐Yee Lee, Ran Du, Yining Wang, Sander C. M. Kneepkens, Jason Charng +91 more

Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

Cell Metabolism(2020)10.1016/j.cmet.2020.05.007

N/A

0DataRank · unranked

82 citations

Audrey E. Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Julia M. Keogh +16 more

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Communications Biology(2023)10.1038/s42003-022-04323-7

N/A

0DataRank · unranked

10 citations

Annechien E. G. Haarman, Robert Luben, Jue‐Sheng Ong, Karina Patasova, Rolando Hernández Trapero +89 more

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

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

N/A

0DataRank · unranked

8 citations

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

Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans

Genome biology(2023)10.1186/s13059-023-02953-6

N/A

0DataRank · unranked

3 citations

Carmen Amador, Rosie M. Walker, Archie Campbell, Rebecca A. Madden, Mark J. Adams +12 more

Limited overlap between genetic effects on disease susceptibility and disease survival

medRxiv(2023)10.1101/2023.10.10.23296544

N/A

0DataRank · unranked

5 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +19 more

Phenome-wide analysis identifies parent-of-origin effects on the human methylome associated with changes in the rate of aging

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.18.524653

N/A

0DataRank · unranked

0 citations

Carmen Amador, Rosie M. Walker, Archie Campbell, Rebecca A. Madden, Mark J. Adams +12 more

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability

medRxiv(2023)10.1101/2023.11.29.23299190

N/A

0DataRank · unranked

0 citations

Vincent-Raphaël Bourque, Élise Douard, Guillaume Huguet, Cécile Poulain, Jay P. Ross +19 more

A genome-wide association analysis reveals new pathogenic pathways in gout

Nature Genetics(2024)10.1038/s41588-024-01921-5

N/A

0DataRank · unranked

85 citations

Riku Takei, Hirotaka Matsuo, Megan Leask, Nicholas A. Sumpter, Ruth Topless +94 more

Genetic architecture reconciles linkage and association studies of complex traits

Nature Genetics(2024)10.1038/s41588-024-01940-2

N/A

0DataRank · unranked

14 citations

Baptiste Couvy‐Duchesne, Kathryn E. Kemper, Gunn-Helen Moen, Laxmi Bhatta, Bjørn Olav Åsvold +23 more

Genetics of C-Peptide and Age at Diagnosis in Type 1 Diabetes

Diabetes(2024)10.2337/db24-0340

N/A

0DataRank · unranked

4 citations

Athina Spiliopoulou, Stuart J. McGurnaghan, Andrii Iakovliev, Debby Lipschutz, Caroline Hayward +11 more

Family-GWAS reveals effects of environment and mating on genetic associations

medRxiv(2024)10.1101/2024.10.01.24314703

N/A

0DataRank · unranked

39 citations

Hariharan Jayashankar, Junming Guan, Seyed Moeen Nehzati, Mahdi Mir, Michael Bennett +60 more

Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

UNC Libraries(2024)10.17615/36rr-ma25

N/A

0DataRank · unranked

0 citations

Blair Smith, Magnus K. Karlsson, Michelle S. Yau, Frances M. K. Williams, Traci M. Bartz +32 more

Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

UNC Libraries(2024)10.17615/f3mg-7f39

N/A

0DataRank · unranked

0 citations

Jenny Chang‐Claude, Jukka‐Pekka Mecklin, Emily White, Amanda E. Toland, Mireia Obón‐Santacana +95 more

Limited overlap between genetic effects on disease susceptibility and disease survival

Nature Genetics(2025)10.1038/s41588-025-02342-8

N/A

0DataRank · unranked

16 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +20 more

Gene–Environment Interaction Affects Risk of Atopic Eczema: Population and In Vitro Studies

Allergy(2025)10.1111/all.16605

N/A

0DataRank · unranked

9 citations

Ashley Budu‐Aggrey, Luke Johnston, Martina S. Elias, Syed Hasan Arshad, Peter Bager +71 more

An Updated Polygenic Index Repository: Expanded Phenotypes, New Cohorts, and Improved Causal Inference

Research Square(2025)10.21203/rs.3.rs-7828579/v1

Top 100%

0DataRank

Top 100%0 citations

Robel Alemu, Anastasia Terskaya, Matthew Howell, Junming Guan, Harry Sands +45 more

Lifecourse genome-wide association study meta-analysis refines the critical life stages for adiposity’s influence on breast cancer risk

Science Advances(2026)10.1126/sciadv.ady0374

N/A

0DataRank · unranked

0 citations

Laxmi Bhatta, Amanda M. Hughes, Carolina Medina‐Gómez, Anne Richmond, Genevieve M Leyden +18 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

0DataRank · unranked

16 citations

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

Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

The Lancet Respiratory Medicine(2020)10.1016/s2213-2600(20)30101-6

N/A

0DataRank · unranked

126 citations

Phuwanat Sakornsakolpat, Nick Shrine, Brian D. Hobbs, Dawn L. DeMeo, Catherine John +82 more

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

Wellcome Open Research(2020)10.12688/wellcomeopenres.15846.1

N/A

0DataRank · unranked

12 citations

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

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

PLoS ONE(2020)10.1371/journal.pone.0230815

N/A

0DataRank · unranked

45 citations

Denis Rybin, Lawrence F. Bielak, Mary F. Feitosa, Nora Franceschini, Yize Li +53 more

Sex- and age-specific genetic analysis of chronic back pain

Pain(2020)10.1097/j.pain.0000000000002100

N/A

0DataRank · unranked

40 citations

Yakov A. Tsepilov, Ian B. Stanaway, Weihua Meng, Caroline Hayward, Blair Smith +13 more

Polygenic contributions to alcohol use and alcohol use disorders across population-based and clinically ascertained samples

Psychological Medicine(2020)10.1017/s0033291719004045

N/A

0DataRank · unranked

37 citations

Sandra Sanchez-Roige, Laura Ación, Mark J. Adams, Kathleen K. Bucholz, Grace Chan +28 more

Distinguishing pedigree relationships via multi-way identity by descent sharing and sex-specific genetic maps

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.12.004

N/A

0DataRank · unranked

31 citations

Jens Sannerud, Sayantani Basu-Roy, Caroline Hayward, Amy L. Williams, Ying Qiao

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

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

N/A

0DataRank · unranked

5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlap

medRxiv(2020)10.1101/2020.11.26.20236760

N/A

0DataRank · unranked

2 citations

Anna L. Guyatt, Nick Shrine, Richard Packer, Thorunn A. Olafsdottir, Jiangyuan Liu +49 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

Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

UNC Libraries(2020)10.17615/xs3t-3334

N/A

0DataRank · unranked

0 citations

Annette L. Fitzpatrick, Luigi Ferrucci, Paul M. Ridker, Bertram Müller-Myhsok, Arezoo Assareh +95 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

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UNC Libraries(2020)10.17615/y892-y714

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UNC Libraries(2020)10.17615/s8sd-h432

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UNC Libraries(2020)10.17615/nsqr-r935

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UNC Libraries(2020)10.17615/k3vg-tb84

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UNC Libraries(2020)10.17615/tb6e-th27

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