Francesca Fike

641 total citations
14 papers, 511 citations indexed

About

Francesca Fike is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Francesca Fike has authored 14 papers receiving a total of 511 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Cancer Research. Recurrent topics in Francesca Fike's work include DNA Repair Mechanisms (8 papers), Carcinogens and Genotoxicity Assessment (4 papers) and CRISPR and Genetic Engineering (2 papers). Francesca Fike is often cited by papers focused on DNA Repair Mechanisms (8 papers), Carcinogens and Genotoxicity Assessment (4 papers) and CRISPR and Genetic Engineering (2 papers). Francesca Fike collaborates with scholars based in United States, Canada and Japan. Francesca Fike's co-authors include Richard A. Gatti, Liutao Du, Hailiang Hu, Shareef Nahas, Michael A. Teitell, Refik Kayalı, Nicholas A. Cacalano, Lu Yang, Carmen Bertoni and Mervi Eeva and has published in prestigious journals such as Journal of Clinical Oncology, Journal of Molecular Biology and Clinical Cancer Research.

In The Last Decade

Francesca Fike

14 papers receiving 505 citations

Peers

Countries citing papers authored by Francesca Fike

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Fike

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Fike

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	RNA sequencing for the detection of MET exon 14 skipping in specimens with splice-site mutations. 2018 ·Journal of Clinical Oncology ·(unknown), Durga Cherukuri, (unknown), (unknown), Francesca Fike, Yu Xia, (unknown), (unknown), (unknown), Christopher G. Scott, Gregory E. Sims, Jeffrey Falk, Armin Graber	1
2	Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2 2014 ·Human Molecular Genetics ·Brent L. Fogel, (unknown), Amanda Wahnich, Fuying Gao, Olivier J. Bécherel, (unknown), Francesca Fike, Leslie Chen, Chiara Criscuolo, Giuseppe De Michele, Alessandro Filla, Abigail Collins, Angelika F. Hahn, Richard A. Gatti, Geneviève Konopka, Susan Perlman, Martin F. Lavin, Daniel H. Geschwind, Giovanni Coppola	40
3	A‐T_W_innipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early‐onset dystonia, cancer, and life‐threatening radiotoxicity 2014 ·Molecular Genetics & Genomic Medicine ·Kotoka Nakamura, Francesca Fike, (unknown), Rachel Saunders‐Pullman, Angelika J. Dawson, Thilo Dörk, Richard A. Gatti	12
4	A New Series of Small Molecular Weight Compounds Induce Read Through of All Three Types of Nonsense Mutations in the ATM Gene 2013 ·Molecular Therapy ·Liutao Du, Michael E. Jung, Robert Damoiseaux, Gladys C. Completo, Francesca Fike, Jin‐Mo Ku, Shareef Nahas, (unknown), Hailiang Hu, Richard A. Gatti	44
5	Defective DNA double‐strand break repair in pediatric systemic lupus erythematosus 2011 ·Arthritis & Rheumatism ·(unknown), (unknown), Francesca Fike, Jiexi Wang, Shareef Nahas, (unknown), Hailiang Hu, Richard A. Gatti, Deborah McCurdy	33
6	Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia 2011 ·Human Mutation ·Kotoka Nakamura, Liutao Du, (unknown), Francesca Fike, Simona Cavalieri, Tomohiro Morio, Shuki Mizutani, Alfredo Brusco, Richard A. Gatti	37
7	Arginine-rich cell-penetrating peptide dramatically enhances AMO-mediated ATM aberrant splicing correction and enables delivery to brain and cerebellum 2011 ·Human Molecular Genetics ·Liutao Du, Refik Kayalı, Carmen Bertoni, Francesca Fike, Hailiang Hu, Patrick L. Iversen, Richard A. Gatti	65
8	Assessing ‘radiosensitivity’ with kinetic profiles of γ-H2AX, 53BP1 and BRCA1 foci 2011 ·Radiotherapy and Oncology ·Nathan Martin, Shareef Nahas, (unknown), Francesca Fike, Richard A. Gatti	30
9	Comprehensive Profiling of Radiosensitive Human Cell Lines with DNA Damage Response Assays Identifies the Neutral Comet Assay as a Potential Surrogate for Clonogenic Survival 2011 ·Radiation Research ·Shareef Nahas, (unknown), Francesca Fike, Kotoka Nakamura, Liutao Du, Refik Kayalı, Nathan Martin, Patrick Concannon, Richard A. Gatti	12
10	Radioprotective effects of manganese-containing superoxide dismutase mimics on ataxia–telangiectasia cells 2009 ·Free Radical Biology and Medicine ·Julianne M. Pollard, Júlio S. Rebouças, Armando Durazo, Ivan Kos, Francesca Fike, Moeen K. Panni, Edith Butler Gralla, Joan Selverstone Valentine, Ines Batinić‐Haberle, Richard A. Gatti	63
11	Ataxia-Telangiectasia: Atypical Presentation and Toxicity of Cancer Treatment 2009 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Rochelle Yanofsky, (unknown), Angelika J. Dawson, Kent Stobart, Cheryl R. Greenberg, Frances Booth, Chitra Prasad, Marc R. Del Bigio, (unknown), Francesca Fike, Richard A. Gatti	34
12	Reciprocal Regulation of SOCS 1 and SOCS3 Enhances Resistance to Ionizing Radiation in Glioblastoma Multiforme 2007 ·Clinical Cancer Research ·(unknown), Rika Miki, Mervi Eeva, Francesca Fike, David B. Seligson, Lu Yang, Akihiko Yoshimura, Michael A. Teitell, Christina Jamieson, Nicholas A. Cacalano	93
13	B29 Gene Silencing in Pituitary Cells Is Regulated by Its 3′ Enhancer 2006 ·Journal of Molecular Biology ·Cindy S. Malone, Ali Kuraishy, Francesca Fike, (unknown), (unknown), Michael A. Teitell, Randolph Wall	4
14	Patterned CpG Methylation of Silenced B Cell Gene Promoters in Classical Hodgkin Lymphoma-derived and Primary Effusion Lymphoma Cell Lines 2005 ·Journal of Molecular Biology ·(unknown), Cindy S. Malone, Francesca Fike, Melinda S. Gordon, (unknown), Roman K. Thomas, Qian Tao, Paul G. Murray, Volker Diehl, Michael A. Teitell, Randolph Wall	43

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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