Joan E. Bailey‐Wilson

22.5k total citations
216 papers, 6.9k citations indexed

About

Joan E. Bailey‐Wilson is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Joan E. Bailey‐Wilson has authored 216 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Genetics, 71 papers in Molecular Biology and 31 papers in Epidemiology. Recurrent topics in Joan E. Bailey‐Wilson's work include Genetic Associations and Epidemiology (77 papers), Genetic Mapping and Diversity in Plants and Animals (36 papers) and Genetic and phenotypic traits in livestock (31 papers). Joan E. Bailey‐Wilson is often cited by papers focused on Genetic Associations and Epidemiology (77 papers), Genetic Mapping and Diversity in Plants and Animals (36 papers) and Genetic and phenotypic traits in livestock (31 papers). Joan E. Bailey‐Wilson collaborates with scholars based in United States, Canada and Finland. Joan E. Bailey‐Wilson's co-authors include Robert C. Elston, Jeffrey M. Trent, Alexander F. Wilson, Priya Duggal, Elizabeth M. Gillanders, Taura N. Holmes, Wee Lock Ooi, Francis S. Collins, Teri A. Manolio and Kevin G. Becker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Statistical Association and Bioinformatics.

In The Last Decade

Joan E. Bailey‐Wilson

210 papers receiving 6.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Joan E. Bailey‐Wilson United States	44	2.5k	2.1k	1.1k	982	957	216	6.9k
Mary J. Emond United States	44	2.0k 0.8×	4.1k 2.0×	944 0.9×	872 0.9×	1.1k 1.2×	117	10.0k
Jane Worthington United Kingdom	56	1.9k 0.8×	1.8k 0.9×	925 0.9×	897 0.9×	500 0.5×	215	9.7k
Shigenobu Nagataki Japan	54	1.8k 0.7×	2.9k 1.4×	1.1k 1.0×	1.0k 1.1×	1.2k 1.3×	548	12.1k
Ryo Yamada Japan	44	1.2k 0.5×	1.9k 0.9×	623 0.6×	530 0.5×	1.1k 1.2×	173	7.0k
Marta E. Alarcón‐Riquelme Sweden	49	2.0k 0.8×	2.2k 1.1×	1.3k 1.2×	695 0.7×	641 0.7×	218	9.4k
Sharon E. Plon United States	50	3.4k 1.4×	3.8k 1.8×	1.3k 1.2×	1.1k 1.1×	533 0.6×	187	8.4k
Paolo Beck‐Peccoz Italy	63	1.9k 0.8×	2.6k 1.3×	662 0.6×	1.3k 1.3×	1.5k 1.6×	239	12.0k
Mark Lathrop France	58	3.7k 1.5×	5.8k 2.8×	918 0.9×	1.1k 1.1×	671 0.7×	207	14.0k
Anne Barton United Kingdom	55	1.4k 0.6×	2.4k 1.2×	1.1k 1.1×	901 0.9×	498 0.5×	326	11.2k
Christian Ingvar Sweden	48	900 0.4×	2.0k 1.0×	3.9k 3.6×	825 0.8×	713 0.7×	221	7.3k

Countries citing papers authored by Joan E. Bailey‐Wilson

Since Specialization

Citations

This map shows the geographic impact of Joan E. Bailey‐Wilson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Joan E. Bailey‐Wilson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joan E. Bailey‐Wilson more than expected).

Fields of papers citing papers by Joan E. Bailey‐Wilson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joan E. Bailey‐Wilson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Joan E. Bailey‐Wilson. The network helps show where Joan E. Bailey‐Wilson may publish in the future.

Co-authorship network of co-authors of Joan E. Bailey‐Wilson

This figure shows the co-authorship network connecting the top 25 collaborators of Joan E. Bailey‐Wilson. A scholar is included among the top collaborators of Joan E. Bailey‐Wilson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Joan E. Bailey‐Wilson. Joan E. Bailey‐Wilson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Simpson, Claire L., Settara C. Chandrasekharappa, Emily Holzinger, et al.. (2023). A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly. Molecular Genetics & Genomic Medicine. 11(8). e2179–e2179. 2 indexed citations

Cannon‐Albright, Lisa, Craig C. Teerlink, Jeff Stevens, et al.. (2023). A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall‐cell lung cancer. International Journal of Cancer. 153(2). 364–372. 1 indexed citations

Guggenheim, Jeremy A., Louise Terry, Karina Patasova, et al.. (2022). EUR Research Repository (Erasmus University Rotterdam). 12 indexed citations

Patasova, Karina, Annechien E. G. Haarman, Anthony M. Musolf, et al.. (2022). Association analyses of rare variants identify two genes associated with refractive error. PLoS ONE. 17(9). e0272379–e0272379. 2 indexed citations

Musolf, Anthony M., Claire L. Simpson, Claudio W. Pikielny, et al.. (2021). Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. Cancer Research. 81(12). 3162–3173. 7 indexed citations

Middlebrooks, Candace D., Qing Li, Carrie Snyder, et al.. (2019). Analysis of the CDKN2A Gene in FAMMM Syndrome Families Reveals Early Age of Onset for Additional Syndromic Cancers. Cancer Research. 79(11). 2992–3000. 9 indexed citations

Musolf, Anthony M., Haiming Sun, Claudio W. Pikielny, et al.. (2019). Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. Cancer Epidemiology Biomarkers & Prevention. 29(2). 434–442. 10 indexed citations

Shane, Barry, Faith Pangilinan, James L. Mills, et al.. (2018). The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. American Journal of Clinical Nutrition. 108(6). 1334–1341. 20 indexed citations

Cropp, Cheryl D., et al.. (2018). ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available. Genetic Epidemiology. 43(1). 102–111. 7 indexed citations

10.

Middlebrooks, Candace D., Claire L. Simpson, Anthony M. Musolf, et al.. (2018). Family-Based Association Tests of Myopia reveal a potentially hidden association signal upstream of two GABA receptor genes. Investigative Ophthalmology & Visual Science. 59(9). 702–702. 1 indexed citations

11.

Wassif, Christopher A., James Iben, Luis Sánchez‐Pulido, et al.. (2015). High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets. Genetics in Medicine. 18(1). 41–48. 156 indexed citations

12.

Verhoeven, Virginie J. M., Pirro G. Hysi, Robert Wojciechowski, et al.. (2013). Genome-wide Meta-Analyses Of Multi-Ethnic Cohorts Identify Multiple New Susceptibility Loci For Refractive Error And Myopia. Investigative Ophthalmology & Visual Science. 54(15). 1736–1736. 2 indexed citations

13.

Liu, Pengyuan, Haris G. Vikis, Yan Lü, et al.. (2010). Cumulative Effect of Multiple Loci on Genetic Susceptibility to Familial Lung Cancer. Cancer Epidemiology Biomarkers & Prevention. 19(2). 517–524. 26 indexed citations

14.

Fang, Shenying, Susan M. Pinney, Joan E. Bailey‐Wilson, et al.. (2010). Ordered Subset Analysis Identifies Loci Influencing Lung Cancer Risk on Chromosomes 6q and 12q. Cancer Epidemiology Biomarkers & Prevention. 19(12). 3157–3166. 7 indexed citations

15.

Amos, Christopher I., Susan M. Pinney, Yafang Li, et al.. (2010). A Susceptibility Locus on Chromosome 6q Greatly Increases Lung Cancer Risk among Light and Never Smokers. Cancer Research. 70(6). 2359–2367. 37 indexed citations

16.

Jun, Gyungah, Hong Guo, Ronald Klein, et al.. (2009). EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and Humans. PLoS Genetics. 5(7). e1000584–e1000584. 119 indexed citations

17.

Cheng, Ching‐Yu, Kristine E. Lee, Priya Duggal, et al.. (2009). Genome‐wide Linkage Analysis of Multiple Metabolic Factors: Evidence of Genetic Heterogeneity. Obesity. 18(1). 146–152. 5 indexed citations

18.

Beckmann, Lars, Andreas Ziegler, Priya Duggal, & Joan E. Bailey‐Wilson. (2005). Haplotypes and haplotype-tagging single-nucleotide polymorphism: Presentation Group 8 of Genetic Analysis Workshop 14. Genetic Epidemiology. 29(S1). S59–S71. 9 indexed citations

19.

Arcos‐Burgos, Mauricio, F. Xavier Castellanos, David Pineda, et al.. (2004). Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11. The American Journal of Human Genetics. 75(6). 998–1014. 150 indexed citations

20.

Korczak, Jeannette F., et al.. (1995). Effects of marker information on sib‐pair linkage analysis of a rare disease. Genetic Epidemiology. 12(6). 625–630. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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