Katherine A. Rauen

9.2k total citations · 2 hit papers
86 papers, 4.7k citations indexed

About

Katherine A. Rauen is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Katherine A. Rauen has authored 86 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 29 papers in Genetics and 14 papers in Immunology. Recurrent topics in Katherine A. Rauen's work include Protein Tyrosine Phosphatases (51 papers), Melanoma and MAPK Pathways (19 papers) and PI3K/AKT/mTOR signaling in cancer (14 papers). Katherine A. Rauen is often cited by papers focused on Protein Tyrosine Phosphatases (51 papers), Melanoma and MAPK Pathways (19 papers) and PI3K/AKT/mTOR signaling in cancer (14 papers). Katherine A. Rauen collaborates with scholars based in United States, Germany and Canada. Katherine A. Rauen's co-authors include William E. Tidyman, Frank McCormick, Anne L. Estep, Pablo Rodriguez‐Viciana, Philip D. Cotter, Osamu Tetsu, Dawn H. Siegel, Lauren A. Weiss, Corina Anastasaki and E. Elizabeth Patton and has published in prestigious journals such as Science, Journal of Neuroscience and Nature reviews. Cancer.

In The Last Decade

Katherine A. Rauen

84 papers receiving 4.6k citations

Hit Papers

The RASopathies 2009 2026 2014 2020 2013 2009 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katherine A. Rauen United States 37 3.5k 1.3k 964 920 390 86 4.7k
Lidia Larizza Italy 43 3.7k 1.1× 2.3k 1.8× 577 0.6× 530 0.6× 412 1.1× 271 6.3k
Christel Brou France 33 5.4k 1.5× 1.5k 1.1× 714 0.7× 956 1.0× 745 1.9× 49 6.9k
David T. MacLaughlin United States 47 3.2k 0.9× 1.9k 1.4× 590 0.6× 874 0.9× 169 0.4× 120 7.8k
Anita Rauch Germany 48 4.4k 1.3× 3.4k 2.6× 1.3k 1.3× 501 0.5× 408 1.0× 194 7.5k
Robert J. Lake Canada 22 5.2k 1.5× 645 0.5× 541 0.6× 803 0.9× 803 2.1× 80 6.7k
Hirofumi Ohashi Japan 36 3.1k 0.9× 2.5k 1.9× 546 0.6× 385 0.4× 356 0.9× 165 4.8k
Teresa Druck United States 41 5.1k 1.5× 2.8k 2.1× 728 0.8× 1.2k 1.3× 534 1.4× 87 6.8k
Mark J. Pettenati United States 36 2.1k 0.6× 998 0.8× 397 0.4× 553 0.6× 137 0.4× 148 5.1k
Tetsuya Niihori Japan 27 1.8k 0.5× 495 0.4× 659 0.7× 420 0.5× 175 0.4× 78 2.9k
Arthur M. Buchberg United States 37 3.7k 1.1× 1.3k 1.0× 482 0.5× 702 0.8× 787 2.0× 77 6.3k

Countries citing papers authored by Katherine A. Rauen

Since Specialization
Citations

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

Fields of papers citing papers by Katherine A. Rauen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katherine A. Rauen. 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 Katherine A. Rauen. The network helps show where Katherine A. Rauen may publish in the future.

Co-authorship network of co-authors of Katherine A. Rauen

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

All Works

20 of 20 papers shown
1.
Rauen, Katherine A., et al.. (2023). Melanocytic neoplasms in neurofibromatosis type 1: a systematic review. Melanoma Research. 33(6). 437–446. 4 indexed citations
2.
Vaughn, Alexandra R., et al.. (2023). The association between juvenile xanthogranulomas in neurofibromatosis type 1 patients and the development of leukaemia: A systematic review. Journal of the European Academy of Dermatology and Venereology. 37(12). e1380–e1383. 3 indexed citations
3.
Shankar, Suma P., et al.. (2021). Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development. Ophthalmic Genetics. 43(1). 48–57. 6 indexed citations
4.
Gripp, Karen W., Marni E. Axelrad, Kathryn C. Chatfield, et al.. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics Part A. 179(9). 1725–1744. 72 indexed citations
5.
Gelb, Bruce D., Hélène Cavé, Mitchell W. Dillon, et al.. (2018). ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation. Genetics in Medicine. 20(11). 1334–1345. 90 indexed citations
6.
Rauen, Katherine A., et al.. (2018). RASopathies are associated with a distinct personality profile. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(4). 434–446. 9 indexed citations
7.
Mitra, Ileena, Alinoë Lavillaureix, Erika Yeh, et al.. (2017). Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders. PLoS Genetics. 13(1). e1006516–e1006516. 34 indexed citations
8.
Rauen, Katherine A., Susan Huson, Emma Burkitt‐Wright, et al.. (2014). Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues. American Journal of Medical Genetics Part A. 167(1). 1–10. 36 indexed citations
9.
Goodwin, Alice F., William E. Tidyman, Andrew H. Jheon, et al.. (2013). Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation. Human Molecular Genetics. 23(3). 682–692. 30 indexed citations
10.
Rauen, Katherine A.. (2013). The RASopathies. Annual Review of Genomics and Human Genetics. 14(1). 355–369. 577 indexed citations breakdown →
11.
Kissil, Joseph L., Jaishri O. Blakeley, Rosalie E. Ferner, et al.. (2010). What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: New Frontiers. American Journal of Medical Genetics Part A. 152A(2). 269–283. 22 indexed citations
12.
Yoon, Grace, et al.. (2007). Neurological complications of cardio‐facio‐cutaneous syndrome. Developmental Medicine & Child Neurology. 49(12). 894–899. 96 indexed citations
13.
Rodriguez‐Viciana, Pablo, Osamu Tetsu, William E. Tidyman, et al.. (2006). Germline Mutations in Genes Within the MAPK Pathway Cause Cardio-facio-cutaneous Syndrome. Science. 311(5765). 1287–1290. 418 indexed citations
14.
Korn, W. Michael, Mónica Macal, Christine Christian, et al.. (2006). Expression of the coxsackievirus- and adenovirus receptor in gastrointestinal cancer correlates with tumor differentiation. Cancer Gene Therapy. 13(8). 792–797. 52 indexed citations
15.
Zampino, Giuseppe, Francesca Pantaleoni, Claudio Carta, et al.. (2006). Diversity, parental germline origin, and phenotypic spectrum of de novoHRASmissense changes in Costello syndrome. Human Mutation. 28(3). 265–272. 99 indexed citations
16.
Matsumoto, Kazumasa, Shahrokh F. Shariat, Gustavo E. Ayala, Katherine A. Rauen, & Seth P. Lerner. (2005). Loss of coxsackie and adenovirus receptor expression is associated with features of aggressive bladder cancer. Urology. 66(2). 441–446. 79 indexed citations
17.
Rodriguez‐Viciana, Pablo, et al.. (2005). Cancer Targets in the Ras Pathway. Cold Spring Harbor Symposia on Quantitative Biology. 70(0). 461–467. 86 indexed citations
18.
Glass, Ian A., Katherine A. Rauen, Emily Chen, et al.. (2005). Ring chromosome 15: characterization by array CGH. Human Genetics. 118(5). 611–617. 41 indexed citations
19.
Iglesias, Alejandro, Katherine A. Rauen, Donna G. Albertson, Daniel Pinkel, & Philip D. Cotter. (2005). Duplication of distal 20q: clinical, cytogenetic and array CGH Characterization of a new case. Clinical Dysmorphology. 15(1). 19–23. 6 indexed citations
20.
Albertson, Donna G., Katherine A. Rauen, Philip D. Cotter, et al.. (2003). High-resolution array CGH A validation study for the detection of submicroscopic deletions in DiGeorge and velo-cardio-facial syndromes. The American Journal of Human Genetics. 73(5). 208. 1 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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