Keiran Raine

69.2k total citations · 1 hit paper
17 papers, 1.5k citations indexed

About

Keiran Raine is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Keiran Raine has authored 17 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Cancer Research and 4 papers in Genetics. Recurrent topics in Keiran Raine's work include Cancer Genomics and Diagnostics (14 papers), Genomics and Phylogenetic Studies (6 papers) and DNA Repair Mechanisms (3 papers). Keiran Raine is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Genomics and Phylogenetic Studies (6 papers) and DNA Repair Mechanisms (3 papers). Keiran Raine collaborates with scholars based in United Kingdom, United States and Spain. Keiran Raine's co-authors include Peter J. Campbell, Michael R. Stratton, Helen Davies, Peter Van Loo, Kerstin Haase, Moritz Gerstung, Iñigo Martincorena, Kevin J. Dawson, Serena Nik‐Zainal and Yee Ling Wu and has published in prestigious journals such as Cell, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Keiran Raine

17 papers receiving 1.5k 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.

Universal Patterns of Selection in Cancer and Somatic Tissues

2017 802 citations Iñigo Martincorena, Keiran Raine et al. Cell profile →

Peers

Countries citing papers authored by Keiran Raine

Since Specialization

Citations

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

Fields of papers citing papers by Keiran Raine

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keiran Raine

This figure shows the co-authorship network connecting the top 25 collaborators of Keiran Raine. A scholar is included among the top collaborators of Keiran Raine 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 Keiran Raine. Keiran Raine 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:

17 of 17 papers shown

#	Work	Indexed citations
1	Haplotype-specific assembly of shattered chromosomes in esophageal adenocarcinomas 2024 ·Cell Genomics ·(unknown), Edward Harry, Keiran Raine, Andrew Menzies, Kathryn Beal, Michael A. Quail, Sonia Zumalave, Hyunchul Jung, Tim Coorens, Andrew Lawson, Daniel Leongamornlert, Hayley E. Francies, Mathew J. Garnett, Zemin Ning, Peter J. Campbell	5
2	Framework for quality assessment of whole genome cancer sequences 2020 ·Nature Communications ·Justin P. Whalley, Ivo Buchhalter, Esther Rheinbay, Keiran Raine, Miranda D. Stobbe, Kortine Kleinheinz, Johannes Werner, Sergi Beltrán, Marta Gut, Daniel Hübschmann, Barbara Hutter, Dimitri Livitz, Marc D. Perry, Mara Rosenberg, Gordon Saksena, Jean-Rémi Trotta, Roland Eils, Daniela S. Gerhard, Peter J. Campbell, Matthias Schlesner	4
3	Split-Read Indel and Structural Variant Calling Using PINDEL 2018 ·Methods in molecular biology ·Kai Ye, Li Guo, Xiaofei Yang, (unknown), Keiran Raine, Zemin Ning	13
4	Universal Patterns of Selection in Cancer and Somatic Tissues breakdown → 2017 ·Cell ·Iñigo Martincorena, Keiran Raine, Moritz Gerstung, Kevin J. Dawson, Kerstin Haase, Peter Van Loo, Helen Davies, Michael R. Stratton, Peter J. Campbell	802
5	A DNA target-enrichment approach to detect mutations, copy number changes and immunoglobulin translocations in multiple myeloma 2016 ·Blood Cancer Journal ·Niccolò Bolli, (unknown), Vijitha Sathiaseelan, Keiran Raine, David Jones, Peter Ganly, Federica Cocito, Graham R. Bignell, Michael A. Chapman, Adam S. Sperling, Kenneth C. Anderson, Hervé Avet‐Loiseau, Stéphane Minvielle, Peter J. Campbell, Nikhil C. Munshi	44
6	cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data 2016 ·Current Protocols in Bioinformatics ·David Jones, Keiran Raine, Helen Davies, Patrick Tarpey, Adam P. Butler, Jon W. Teague, Serena Nik‐Zainal, Peter J. Campbell	82
7	ascatNgs: Identifying Somatically Acquired Copy‐Number Alterations from Whole‐Genome Sequencing Data 2016 ·Current Protocols in Bioinformatics ·Keiran Raine, Peter Van Loo, David C. Wedge, David Jones, Andrew Menzies, Adam P. Butler, Jon W. Teague, Patrick Tarpey, Serena Nik‐Zainal, Peter J. Campbell	57
8	cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing 2015 ·Current Protocols in Bioinformatics ·Keiran Raine, Jonathan Hinton, Adam P. Butler, Jon W. Teague, Helen Davies, Patrick Tarpey, Serena Nik‐Zainal, Peter J. Campbell	44
9	Polygenic in vivovalidation of cancer mutations using transposons 2014 ·Genome biology ·Su Kit Chew, Dong Lu, Lia S. Campos, Kenneth L. Scott, Abdel Saci, Juexuan Wang, (unknown), Keiran Raine, Jonathan Hinton, Jon W. Teague, David Jones, Andrew Menzies, Adam P. Butler, John Gamble, Sarah O’Meara, Stuart McLaren, Lynda Chin, Pentao Liu, P. Andrew Futreal	3
10	C. eleganswhole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency 2014 ·Genome Research ·Bettina Meier, Susanna L. Cooke, (unknown), Aymeric Bailly, Ludmil B. Alexandrov, John Marshall, Keiran Raine, Mark Maddison, Elizabeth Anderson, Michael R. Stratton, Anton Gartner, Peter J. Campbell	126
11	DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis 2013 ·eLife ·Ben Taylor, Serena Nik‐Zainal, Yee Ling Wu, Lucy Stebbings, Keiran Raine, Peter J. Campbell, Cristina Rada, Michael R. Stratton, Michael S. Neuberger	276
12	604 Cancer Genomics, Epigenetics and Genomic Instability. Mutational Processes Shaping the Genomes of Twenty-one Breast Cancers 2012 ·European Journal of Cancer ·Serena Nik‐Zainal, Ludmil B. Alexandrov, David C. Wedge, Peter Van Loo, Keiran Raine, (unknown), PA Futreal, (unknown), Michael R. Stratton	1
13	Identification of mutations of the SWI/SNF complex gene PBRM1 by exome sequencing in renal carcinoma. 2011 ·Journal of Clinical Oncology ·Bin Tean Teh, Ignacio Varela, Patrick Tarpey, Keiran Raine, Danqing Huang, Choon Kiat Ong, Kyle A. Furge, (unknown), Michael R. Stratton, PA Futreal	1
14	The Genomic Landscape of TEL-AML1+ (ETV6-RUNX1) Acute Lymphoblastic Leukaemia 2011 ·Blood ·Elli Papaemmanuil, Inmaculada Rapado, Anthony M. Ford, Keiran Raine, Jonathan Hinton, David Jones, John Marshall, Laura Mudie, Jan Zuna, Giovanni Cazzaniga, Helena Kempski, Maria S. Pombo‐de‐Oliveira, Mike Stratton, P. Andrew Futreal, Peter J. Campbell, Mel Greaves	2
15	Abstract 93: COSMIC: The catalogue of somatic mutations in cancer receives full genome variant annotations 2010 ·Cancer Research ·Simon Forbes, Nidhi Bindal, (unknown), Sally Bamford, Elisabeth Dawson, Charlotte G. Cole, Rebecca Shepherd, Andrew Menzies, Keiran Raine, Mingming Jia, Chai Yin Kok, Jon W. Teague, Michael R. Stratton, P. Andrew Futreal	1
16	Abstract 90: Mining for cancer causing mutations in whole genome sequence data 2010 ·Cancer Research ·Andrew Menzies, Philip J. Stephens, David Beare, Adam P. Butler, Simon Forbes, Mingming Jia, David Jones, Catherine Leroy, John Marshall, Keiran Raine, Lucy Stebbings, Jon W. Teague, P. Andrew Futreal, Michael R. Stratton, Peter J. Campbell	1
17	AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes 2007 ·Bioinformatics ·Ed Dicks, Jon W. Teague, Philip Stephens, Keiran Raine, Andrew Yates, C. Mattocks, Patrick Tarpey, Adam P. Butler, Andrew Menzies, David Richardson, Andy Jenkinson, Helen Davies, Sarah Edkins, Simon Forbes, Kristian Gray, Chris Greenman, Rebecca Shepherd, Michael R. Stratton, P. Andrew Futreal, Richard Wooster	8

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.

Explore authors with similar magnitude of impact