Wendy Roeb

1.6k total citations · 1 hit paper
7 papers, 1.1k citations indexed

About

Wendy Roeb is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Wendy Roeb has authored 7 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Sensory Systems. Recurrent topics in Wendy Roeb's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), BRCA gene mutations in cancer (2 papers) and FOXO transcription factor regulation (2 papers). Wendy Roeb is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), BRCA gene mutations in cancer (2 papers) and FOXO transcription factor regulation (2 papers). Wendy Roeb collaborates with scholars based in United States, Israel and Palestinian Territory. Wendy Roeb's co-authors include Mary‐Claire King, Tom Walsh, Ming K. Lee, Anne Thornton, Alex S. Nord, Sunday M. Stray, Silvia Casadei, Elizabeth M. Swisher, Kathy Agnew and Kathryn P. Pennington and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Wendy Roeb

7 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

2011 662 citations Tom Walsh, Silvia Casadei et al. Proceedings of the National Academy of Sciences profile →

Peers

Wendy Roeb

GENET

MB

RM

ONCOL

CR

James Lespinasse France

Veronique Duke United Kingdom

Florence Dastot‐Le Moal France

Elizabeth Ives Canada

Susanne Morlot Germany

Silvestre Oltra Spain

Jan Murken Germany

K. O. J. Simola Finland

Ryoji Morita Japan

Milhan Telatar United States

James Lespinasse France

Wendy Roeb

619 ×1.0

GENET

702 ×1.3

MB

327 ×1.2

RM

133 ×0.5

ONCOL

132 ×0.6

CR

Citations per year, relative to Wendy Roeb Wendy Roeb (= 1×) peers James Lespinasse

Countries citing papers authored by Wendy Roeb

Since Specialization

Citations

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

Fields of papers citing papers by Wendy Roeb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wendy Roeb

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Roeb, Wendy, Jake Higgins, & Mary‐Claire King. (2012). Response to DNA damage of CHEK2 missense mutations in familial breast cancer. Human Molecular Genetics. 21(12). 2738–2744. 63 indexed citations

2.

Walsh, Tom, Silvia Casadei, Ming K. Lee, et al.. (2011). Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proceedings of the National Academy of Sciences. 108(44). 18032–18037. 662 indexed citations breakdown →

3.

Nord, Alex S., Wendy Roeb, Diane E. Dickel, et al.. (2011). Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. European Journal of Human Genetics. 19(6). 727–731. 89 indexed citations

4.

Walsh, Tom, Hashem Shahin, T. Elkan Miller, et al.. (2010). Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. The American Journal of Human Genetics. 87(1). 90–94. 198 indexed citations

5.

Walsh, Tom, Sarah B. Pierce, Danielle R. Lenz, et al.. (2010). Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51. The American Journal of Human Genetics. 87(1). 101–109. 74 indexed citations

6.

Roeb, Wendy, Antonia Boyer, Webster K. Cavenee, & Karen C. Arden. (2008). Guilt by association: PAX3-FOXO1 regulates gene expression through selective destabilization of the EGR1 transcription factor. Cell Cycle. 7(7). 837–841. 13 indexed citations

7.

Roeb, Wendy, Antonia Boyer, Webster K. Cavenee, & Karen C. Arden. (2007). PAX3-FOXO1 controls expression of the p57Kip2 cell-cycle regulator through degradation of EGR1. Proceedings of the National Academy of Sciences. 104(46). 18085–18090. 43 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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