Joan E. Bailey-Wilson

National Human Genome Research Institute

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

2.7Author DataRank

Indexed papers

4in 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 4 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.

IMI 2021 Yearly Digest

Investigative Ophthalmology & Visual Science(2021)10.1167/iovs.62.5.7

Top 9%

2.5DataRank

Top 9%68 citations

Jost B. Jonas, James S. Wolffsohn, David A. Berntsen, Pauline Cho, Danielle Clarkson-Townsend +20 more

Papers

Driven by 35 papers — median percentile 18. Top paper: “What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics”.

What makes a good prediction? Feature importance and beginning to open the black box of machine learning in genetics

Human Genetics(2021)10.1007/s00439-021-02402-z

N/A

3.4DataRank · unranked

127 citations

Emily Holzinger, James D. Malley, Joan E. Bailey-Wilson, Anthony M. Musolf

IMI 2021 Yearly Digest

Investigative Ophthalmology & Visual Science(2021)10.1167/iovs.62.5.7

Top 9%

2.5DataRank

Top 9%68 citations

Jost B. Jonas, James S. Wolffsohn, David A. Berntsen, Pauline Cho, Danielle Clarkson-Townsend +20 more

Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa609

N/A

1.0DataRank · unranked

24 citations

Adam Burkholder, Christopher A. Lavender, Lacey Plummer, Verónica Mericq, Paulina M. Merino +12 more

Rare deleterious germline variants and risk of lung cancer

npj Precision Oncology(2021)10.1038/s41698-021-00146-7

N/A

1.0DataRank · unranked

34 citations

Jun Xia, James McKay, Spiridon Tsavachidis, Xiangjun Xiao, Margaret R. Spitz +42 more

Sterol and lipid analyses identifies hypolipidemia and apolipoprotein disorders in autism associated with adaptive functioning deficits

Translational Psychiatry(2021)10.1038/s41398-021-01580-8

N/A

0.856DataRank · unranked

23 citations

Alan T. Remaley, Audrey Thurm, Leah R. Jager, Christopher A. Wassif, Lisa E. Kratz +8 more

Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk

Human Molecular Genetics(2022)10.1093/hmg/ddac030

N/A

0.395DataRank · unranked

7 citations

Xiangjun Xiao, Jianrong Li, Jinyoung Byun, Chao Cheng, Yohan Bossé +50 more

Association analyses of rare variants identify two genes associated with refractive error

PLOS ONE(2022)10.1371/journal.pone.0272379

N/A

0.208DataRank · unranked

3 citations

Annechien E. G. Haarman, Anthony M. Musolf, Omar A. Mahroo, Jugnoo S. Rahi, Mario Falchi +9 more

Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka

BMC Research Notes(2022)10.1186/s13104-022-06081-5

Top 65%

0.206DataRank

Top 65%2 citations

Anthony M. Musolf, Joan E. Bailey-Wilson, T. Kalum Wetthasinghe, Vajira H. W. Dissanayake, Prabhavi Wijesiriwardhana

Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk

Research Square(2021)10.21203/rs.3.rs-647012/v1

N/A

0.175DataRank · unranked

2 citations

Xiangjun Xiao, Jianrong Li, Jinyoung Byun, Chao Cheng, Yohan Bossé +50 more

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

UNC Libraries(2020)10.17615/azx9-qr47

N/A

0DataRank · unranked

0 citations

Fredrik Wiklund, Michael J. Ackerman, Kathleen A. Cooney, Zsofia Kote‐Jarai, Elaine A. Ostrander +27 more

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

UNC Libraries(2020)10.17615/gd7n-3n77

Top 100%

0DataRank

Top 100%0 citations

Olivier Cussenot, Diptasri Mandal, Nilah M. Ioannidis, Graham G. Giles, Shannon K. McDonnell +36 more

Admixture Mapping of Obesity-related Traits in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study*

UNC Libraries(2020)10.17615/9r37-4f65

N/A

0DataRank · unranked

0 citations

Eric Boerwinkle, W. H.Linda Kao, Arti Tandon, Kari E. North, Joan E. Bailey-Wilson +6 more

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses

UNC Libraries(2020)10.17615/cv63-ck59

N/A

0DataRank · unranked

0 citations

Ingrid Oakley‐Girvan, Douglas F. Easton, Gianluca Severi, Stephen N. Thibodeau, Alice S. Whittemore +27 more

A powerful new method for rare-variant analysis of quantitative traits in families

European Journal of Human Genetics(2020)10.1038/s41431-020-00731-7

N/A

0DataRank · unranked

0 citations

Joan E. Bailey-Wilson

Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer

European Urology(2020)10.1016/j.eururo.2020.07.038

N/A

0DataRank · unranked

42 citations

Shannon K. McDonnell, Liesel M. FitzGerald, Lissa DeRycke, Zachary C. Fogarty, Graham G. Giles +34 more

Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

Cancer Research(2021)10.1158/0008-5472.can-20-3196

N/A

0DataRank · unranked

11 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 more

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

UNC Libraries(2021)10.17615/ktmt-6886

N/A

0DataRank · unranked

6 citations

Kimberly A. Zuhlke, Nicola J. Camp, Zsofia Kote‐Jarai, Lingyi Lu, Nancy Hamel +45 more

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Communications Biology(2020)10.1038/s42003-020-0802-y

N/A

0DataRank · unranked

42 citations

Alfred Pozarickij, Nicholas Y.Q. Tan, Xiaobo Guo, Virginie J. M. Verhoeven, Véronique Vitart +94 more

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

Nature Genetics(2022)10.1038/s41588-022-01115-x

N/A

0DataRank · unranked

123 citations

Younghun Han, Yafang Li, Jun Xia, Erping Long, Jiyeon Choi +80 more

Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia

Human Molecular Genetics(2022)10.1093/hmg/ddac004

N/A

0DataRank · unranked

22 citations

Rosie Clark, Jiangtian Cui, Louise Terry, Karina Patasova, Annechien E. G. Haarman +7 more

Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration

Journal of the American Statistical Association(2020)10.1080/01621459.2020.1799809

N/A

0DataRank · unranked

9 citations

Chi‐Yang Chiu, Qi Yan, Wei Chen, Michael B. Gorin, Yvette P. Conley +13 more

Complex N-Linked Glycosylation: A Potential Modifier of Niemann–Pick Disease, Type C1 Pathology

International Journal of Molecular Sciences(2022)10.3390/ijms23095082

N/A

0DataRank · unranked

8 citations

A. Lyons, Daniel Abebe, Rachel Luke, Julia C. Yerger, Rebecca Telese +4 more

Gene‐level association analysis of ordinal traits with functional ordinal logistic regressions

Genetic Epidemiology(2022)10.1002/gepi.22451

N/A

0DataRank · unranked

5 citations

Shuqi Wang, Bingsong Zhang, Yutong Luo, Claire L. Simpson, Wei Zhang +8 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

Entanglement Mapping: A Novel Method to Detect Interacting SNPs in Genome-Wide Studies

(2022)10.1109/cibcb55180.2022.9863029

N/A

0DataRank · unranked

1 citations

Anthony M. Musolf, James D. Malley, Daniel S. Kiser, Dwight Stambolian, Qing Li +2 more

A Novel de novo TP63 Mutation in Whole Exome Sequencing of a Syrian Family with Oral Cleft and Ectrodactyly

medRxiv(2022)10.1101/2022.02.10.21265142

N/A

0DataRank · unranked

0 citations

Danielle C. Kimble, Settara C. Chandrasekharappa, NISC Comparative Sequencing Program, Khalid Alqosayer, Emily Holzinger +7 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

Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus

Genes and Immunity(2023)10.1038/s41435-023-00214-x

N/A

0DataRank · unranked

7 citations

Anthony M. Musolf, Joan E. Bailey-Wilson, Linda T. Hiraki, Earl D. Silverman, Christiaan Scott +6 more

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer

International Journal of Cancer(2023)10.1002/ijc.34510

N/A

0DataRank · unranked

3 citations

Craig C. Teerlink, Jeff Stevens, Julio C. Facelli, Shamus R. Carr, Kristina Allen-Brady +5 more

A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly

Molecular Genetics & Genomic Medicine(2023)10.1002/mgg3.2179

N/A

0DataRank · unranked

3 citations

Danielle C. Kimble, Settara C. Chandrasekharappa, NISC Comparative Sequencing Program, Khalid Alqosayer, Emily Holzinger +7 more

Data from Haplotype and Cell Proliferation Analyses of Candidate Lung Cancer Susceptibility Genes on Chromosome 15q24-25.1

(2023)10.1158/0008-5472.c.6500087.v1

Top 100%

0DataRank

Top 100%0 citations

Pengyuan Liu, Weidong Wen, Michael A. James, Yian Wang, Joan E. Bailey-Wilson +19 more

Data from Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

(2023)10.1158/0008-5472.c.6513273.v1

N/A

0DataRank · unranked

0 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 more

Data from Fine Mapping of Chromosome 6q23-25 Region in Familial Lung Cancer Families Reveals RGS17 as a Likely Candidate Gene

(2023)10.1158/1078-0432.c.6517600.v1

N/A

0DataRank · unranked

0 citations

Daolong Wang, Pengyuan Liu, Haris G. Vikis, Michael James, Yan Lü +37 more

Lung Cancer in Ever- and Never-Smokers: Findings from Multi-Population GWAS Studies

Cancer Epidemiology Biomarkers & Prevention(2024)10.1158/1055-9965.epi-23-0613

N/A

0DataRank · unranked

10 citations

Xiangjun Xiao, Jianrong Li, Younghun Han, Chao Cheng, Gail Fernandes +53 more

High-Penetrance Rare Variants Underlying Familial Lung Cancer Risk: Insights From Genetic Epidemiology of Lung Cancer Consortium

Journal of Thoracic Oncology(2025)10.1016/j.jtho.2025.12.004

N/A

0DataRank · unranked

3 citations

Yafang Li, Jinyoung Byun, Vikram R. Shaw, Claudio W. Pikielny, Bo Peng +29 more

Joan E. Bailey-Wilson

Indexed papers

Top data-sharing exemplar

Papers