Jennifer Madeoy

1.8k total citations
11 papers, 923 citations indexed

About

Jennifer Madeoy is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Jennifer Madeoy has authored 11 papers receiving a total of 923 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Jennifer Madeoy's work include Genetic Associations and Epidemiology (3 papers), Genetic and phenotypic traits in livestock (3 papers) and Evolution and Genetic Dynamics (2 papers). Jennifer Madeoy is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Genetic and phenotypic traits in livestock (3 papers) and Evolution and Genetic Dynamics (2 papers). Jennifer Madeoy collaborates with scholars based in United States, Sweden and Denmark. Jennifer Madeoy's co-authors include Joshua M. Akey, Mark M. Wurfel, John D. Storey, James Ronald, Caitlin Connelly, Willie J. Swanson, John C. Calhoun, Joanna L. Kelley, Dayna T. Akey and Mark W. Neff and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Clinical Cancer Research.

In The Last Decade

Jennifer Madeoy

10 papers receiving 905 citations

Peers

Jennifer Madeoy

GENET

ECOLO

Thomas J. Nicholas United States

Rick Tearle Australia

Sara E. Kalla United States

Jessica Alföldi United States

Suzanne J. Rowe New Zealand

Huayu Qi China

Gaudenz Dolf Switzerland

Liu Yan-hu China

Nima Rafati Sweden

Alison L. Ruhe United States

Thomas J. Nicholas United States

Jennifer Madeoy

493 ×0.9

GENET

388 ×0.9

78 ×0.7

181 ×2.6

35 ×0.6

ECOLO

Citations per year, relative to Jennifer Madeoy Jennifer Madeoy (= 1×) peers Thomas J. Nicholas

Countries citing papers authored by Jennifer Madeoy

Since Specialization

Citations

This map shows the geographic impact of Jennifer Madeoy'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 Jennifer Madeoy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennifer Madeoy more than expected).

Fields of papers citing papers by Jennifer Madeoy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer Madeoy. 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 Jennifer Madeoy. The network helps show where Jennifer Madeoy may publish in the future.

Co-authorship network of co-authors of Jennifer Madeoy

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer Madeoy. A scholar is included among the top collaborators of Jennifer Madeoy 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 Jennifer Madeoy. Jennifer Madeoy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Vermulst, Marc, Nigel Clegg, Jennifer Madeoy, et al.. (2024). MADDD-seq, a novel massively parallel sequencing tool for simultaneous detection of DNA damage and mutations. Nucleic Acids Research. 52(16). e76–e76.

Gittelman, Rachel M., Ferhat Ay, Jennifer Madeoy, et al.. (2015). Comprehensive identification and analysis of human accelerated regulatory DNA. Genome Research. 25(9). 1245–1255. 72 indexed citations

Skelly, Daniel A., Marnie Johansson, Jennifer Madeoy, Jon Wakefield, & Joshua M. Akey. (2011). A powerful and flexible statistical framework for testing hypotheses of allele-specific gene expression from RNA-seq data. Genome Research. 21(10). 1728–1737. 130 indexed citations

Lambert, Charla, Caitlin Connelly, Jennifer Madeoy, et al.. (2010). Highly Punctuated Patterns of Population Structure on the X Chromosome and Implications for African Evolutionary History. The American Journal of Human Genetics. 86(1). 34–44. 19 indexed citations

Tennessen, Jacob A., Jennifer Madeoy, & Joshua M. Akey. (2010). Signatures of positive selection apparent in a small sample of human exomes. Genome Research. 20(10). 1327–1334. 15 indexed citations

Akey, Joshua M., Alison L. Ruhe, Dayna T. Akey, et al.. (2010). Tracking footprints of artificial selection in the dog genome. Proceedings of the National Academy of Sciences. 107(3). 1160–1165. 247 indexed citations

Yatsenko, Andriy S., Mariya M. Kucherenko, Karin A. Fischer, et al.. (2009). The conserved WW-domain binding sites in Dystroglycan C-terminus are essential but partially redundant for Dystroglycan function. BMC Developmental Biology. 9(1). 18–18. 10 indexed citations

Scheinfeldt, Laura, Shameek Biswas, Jennifer Madeoy, et al.. (2009). Population Genomic Analysis of ALMS1 in Humans Reveals a Surprisingly Complex Evolutionary History. Molecular Biology and Evolution. 26(6). 1357–1367. 20 indexed citations

Storey, John D., et al.. (2007). Gene-Expression Variation Within and Among Human Populations. The American Journal of Human Genetics. 80(3). 502–509. 226 indexed citations

10.

Kelley, Joanna L., Jennifer Madeoy, John C. Calhoun, Willie J. Swanson, & Joshua M. Akey. (2006). Genomic signatures of positive selection in humans and the limits of outlier approaches. Genome Research. 16(8). 980–989. 169 indexed citations

11.

Zuhlke, Kimberly A., Jennifer Madeoy, Jennifer Beebe‐Dimmer, et al.. (2004). Truncating BRCA1 Mutations Are Uncommon in a Cohort of Hereditary Prostate Cancer Families with Evidence of Linkage to 17q Markers. Clinical Cancer Research. 10(18). 5975–5980. 15 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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