Catherine E. Cottrell

2.6k total citations
69 papers, 1.1k citations indexed

About

Catherine E. Cottrell is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Catherine E. Cottrell has authored 69 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 22 papers in Genetics and 19 papers in Cancer Research. Recurrent topics in Catherine E. Cottrell's work include Cancer Genomics and Diagnostics (18 papers), Genomics and Rare Diseases (14 papers) and Glioma Diagnosis and Treatment (11 papers). Catherine E. Cottrell is often cited by papers focused on Cancer Genomics and Diagnostics (18 papers), Genomics and Rare Diseases (14 papers) and Glioma Diagnosis and Treatment (11 papers). Catherine E. Cottrell collaborates with scholars based in United States, Canada and Jordan. Catherine E. Cottrell's co-authors include Eric J. Duncavage, John D. Pfeifer, Christina M. Lockwood, Ian S. Hagemann, Jonathan W. Heusel, Andrew J. Bredemeyer, Haley Abel, Ramaswamy Govindan, Samantha N. McNulty and Katinka A. Vigh‐Conrad and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer.

In The Last Decade

Catherine E. Cottrell

62 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine E. Cottrell United States	19	389	367	316	295	202	69	1.1k
Emma Tham Sweden	19	373 1.0×	470 1.3×	138 0.4×	223 0.8×	359 1.8×	59	1.2k
Jana Fassunke Germany	16	318 0.8×	468 1.3×	268 0.8×	85 0.3×	244 1.2×	53	956
Sana Yokoi Japan	21	297 0.8×	870 2.4×	378 1.2×	150 0.5×	498 2.5×	43	1.4k
Helen J. Huang United States	19	418 1.1×	689 1.9×	157 0.5×	340 1.2×	336 1.7×	47	1.3k
Nicola MacDonald United Kingdom	15	369 0.9×	633 1.7×	107 0.3×	276 0.9×	313 1.5×	42	1.6k
JS Reis‐Filho United Kingdom	10	409 1.1×	412 1.1×	147 0.5×	150 0.5×	377 1.9×	22	897
Gayatry Mohapatra United States	14	320 0.8×	743 2.0×	486 1.5×	107 0.4×	517 2.6×	26	1.4k
Daniel C. Koboldt United States	9	247 0.6×	313 0.9×	202 0.6×	121 0.4×	461 2.3×	19	804
Marc Hotfilder Germany	19	254 0.7×	695 1.9×	294 0.9×	87 0.3×	389 1.9×	40	1.3k
Valérie Panet-Raymond Canada	16	220 0.6×	306 0.8×	414 1.3×	195 0.7×	306 1.5×	50	1.4k

Countries citing papers authored by Catherine E. Cottrell

Since Specialization

Citations

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

Fields of papers citing papers by Catherine E. Cottrell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine E. Cottrell. 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 Catherine E. Cottrell. The network helps show where Catherine E. Cottrell may publish in the future.

Co-authorship network of co-authors of Catherine E. Cottrell

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine E. Cottrell. A scholar is included among the top collaborators of Catherine E. Cottrell 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 Catherine E. Cottrell. Catherine E. Cottrell 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

Schieffer, Kathleen M., Bhuvana A. Setty, Margot Lazow, et al.. (2025). Comprehensive Genomic Characterization of Congenital and Infantile Cancers Reveals High Yield of Medically Meaningful Findings. JCO Precision Oncology. 9(9). e2400910–e2400910.

Koboldt, Daniel C., Hui Mei, Ying‐Chen Claire Hou, et al.. (2024). Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing. Molecular Genetics & Genomic Medicine. 12(3). e2349–e2349. 3 indexed citations

Lazow, Margot, Diana Thomas, Catherine E. Cottrell, et al.. (2023). LGG-14. TREATMENT OF TWO PEDIATRIC FGFR-ALTERED LOW-GRADE GLIONEURONAL TUMORS WITH MEK INHIBITION. Neuro-Oncology. 25(Supplement_1). i58–i58. 3 indexed citations

Konczyk, Dennis J., Jeremy A. Goss, Brian I. Labow, et al.. (2023). Papillary Hemangioma Harbors Somatic GNA11 and GNAQ Mutations. The American Journal of Surgical Pathology. 48(1). 106–111. 4 indexed citations

Schieffer, Kathleen M., et al.. (2023). CHEK2 Alterations in Pediatric Malignancy: A Single-Institution Experience. Cancers. 15(6). 1649–1649. 6 indexed citations

Koo, Selene C., Kathleen M. Schieffer, Kristy Lee, et al.. (2022). EGFR internal tandem duplications in fusion‐negative congenital and neonatal spindle cell tumors. Genes Chromosomes and Cancer. 62(1). 17–26. 3 indexed citations

Ramesh, Naveen, Min Hu, Sayaka Hashimoto, et al.. (2022). A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. Journal of Molecular Diagnostics. 24(9). 1031–1040. 3 indexed citations

Halsey, Jordan N., Esteban Fernández Faith, Suzanna Logan, et al.. (2022). Syringocystadenocarcinoma Papilliferum in a Fifteen-Year-Old Girl: A Case Report and Review of the Literature. Case Reports in Dermatological Medicine. 2022. 1–5. 7 indexed citations

Kautto, Esko A., Kathleen M. Schieffer, Sean McGrath, et al.. (2022). Expanding the Clinical Phenotype of FGFR1 Internal Tandem Duplication. Molecular Case Studies. 8(2). mcs.a006174–mcs.a006174. 5 indexed citations

10.

Li, Marilyn M., Catherine E. Cottrell, Somak Roy, et al.. (2022). Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines. Journal of Molecular Diagnostics. 25(2). 69–86. 17 indexed citations

11.

Hunter, Jesse M., Lauren Massingham, Kandamurugu Manickam, et al.. (2022). Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder. Molecular Case Studies. 8(2). mcs.a006180–mcs.a006180. 10 indexed citations

12.

Miller, Anthony R., Saranga Wijeratne, Sean McGrath, et al.. (2022). Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome–Based Resolution of Isoform Complexity. Journal of Molecular Diagnostics. 24(12). 1292–1306. 6 indexed citations

13.

Schieffer, Kathleen M., et al.. (2022). Alternative RNA splicing defects in pediatric cancers: new insights in tumorigenesis and potential therapeutic vulnerabilities. Annals of Oncology. 33(6). 578–592. 31 indexed citations

14.

Garzón, Maria C., Ilona J. Frieden, Catherine E. Cottrell, et al.. (2021). Cutaneous vascular anomalies associated with a mosaic variant of AKT3: Genetic analysis continues to refine the diagnosis, nomenclature, and classification of vascular anomalies. Journal of the American Academy of Dermatology. 87(1). 162–164. 7 indexed citations

15.

Darby, Charlotte A., James Fitch, Patrick J. Brennan, et al.. (2019). Samovar: Single-Sample Mosaic Single-Nucleotide Variant Calling with Linked Reads. iScience. 18. 1–10. 5 indexed citations

16.

Barrie, Elizabeth S., Catherine E. Cottrell, Julie M. Gastier‐Foster, et al.. (2019). Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene. European Journal of Medical Genetics. 63(3). 103735–103735. 11 indexed citations

17.

Schieffer, Kathleen M., Liz Varga, Katherine E. Miller, et al.. (2019). Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma. European Journal of Medical Genetics. 62(8). 103701–103701. 11 indexed citations

18.

Carter, Jamal, Catherine E. Cottrell, Samantha N. McNulty, et al.. (2017). FGFR2 amplification in colorectal adenocarcinoma. Molecular Case Studies. 3(6). a001495–a001495. 23 indexed citations

19.

Hagemann, Ian S., Ramaswamy Govindan, Cylen Javidan-Nejad, John D. Pfeifer, & Catherine E. Cottrell. (2014). Stabilization of Disease after Targeted Therapy in a Thymic Carcinoma with KIT Mutation Detected by Clinical Next-Generation Sequencing. Journal of Thoracic Oncology. 9(2). e12–e16. 14 indexed citations

20.

Hagemann, Ian S., Catherine E. Cottrell, & Christina M. Lockwood. (2013). Design of targeted, capture-based, next generation sequencing tests for precision cancer therapy. Cancer Genetics. 206(12). 420–431. 39 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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