Author details

Full Name

Jon Teague

Affiliation

Wellcome Sanger Institute

ORCID

Career Start Year

2002

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36388765	Uncovering novel mutational signatures by <i>de novo</i> extraction with SigProfilerExtractor.	Cell Genom	2022
34663923	Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence.	Nat Genet	2021
34646017	Convergent somatic mutations in metabolism genes in chronic liver disease.	Nature	2021
29656891	Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal.	Cell	2018
30304655	Classification and Personalized Prognosis in Myeloproliferative Neoplasms.	N Engl J Med	2018
29662167	Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.	Nat Genet	2018
29789651	Analysis of the genomic landscape of multiple myeloma highlights novel prognostic markers and disease subgroups.	Leukemia	2018
28643781	Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma.	Nat Commun	2017
29026114	The driver landscape of sporadic chordoma.	Nat Commun	2017
27276561	Genomic Classification and Prognosis in Acute Myeloid Leukemia.	N Engl J Med	2016
27615322	Mutational signatures of ionizing radiation in second malignancies.	Nat Commun	2016
27930809	ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data.	Curr Protoc Bioinformatics	2016
27930805	cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data.	Curr Protoc Bioinformatics	2016
27135926	Landscape of somatic mutations in 560 breast cancer whole-genome sequences.	Nature	2016
25730763	Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.	Nat Genet	2015
26647970	A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.	Nat Commun	2015
26678382	cgpPindel: Identifying Somatically Acquired Insertion and Deletion Events from Paired End Sequencing.	Curr Protoc Bioinformatics	2015
26678383	VAGrENT: Variation Annotation Generator.	Curr Protoc Bioinformatics	2015
26018901	Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.	Nat Genet	2015
24413735	RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.	Nat Genet	2014
25260652	Polygenic in vivo validation of cancer mutations using transposons.	Genome Biol	2014
25271376	Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.	Elife	2014
25082706	Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.	Science	2014
24633157	Recurrent PTPRB and PLCG1 mutations in angiosarcoma.	Nat Genet	2014
24429703	Heterogeneity of genomic evolution and mutational profiles in multiple myeloma.	Nat Commun	2014
23770606	Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.	Nat Genet	2013
24325359	Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2.	N Engl J Med	2013
24162739	Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.	Nat Genet	2013
24148783	The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models.	Genome Biol	2013
24030381	Clinical and biological implications of driver mutations in myelodysplastic syndromes.	Blood	2013
23630320	Single-cell paired-end genome sequencing reveals structural variation per cell cycle.	Nucleic Acids Res	2013
23778141	Whole exome sequencing of adenoid cystic carcinoma.	J Clin Invest	2013
22608083	The life history of 21 breast cancers.	Cell	2012
22722201	The landscape of cancer genes and mutational processes in breast cancer.	Nature	2012
22514011	Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.	J Pathol	2012
22608084	Mutational processes molding the genomes of 21 breast cancers.	Cell	2012
21215367	Massive genomic rearrangement acquired in a single catastrophic event during cancer development.	Cell	2011
21995386	Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.	N Engl J Med	2011
21930507	BioMart Central Portal: an open database network for the biological community.	Database (Oxford)	2011
21248752	Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.	Nature	2011
20016485	A comprehensive catalogue of somatic mutations from a human cancer genome.	Nature	2010
20981101	The patterns and dynamics of genomic instability in metastatic pancreatic cancer.	Nature	2010
20054297	Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes.	Nature	2010
20016488	A small-cell lung cancer genome with complex signatures of tobacco exposure.	Nature	2010
19006239	Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: proposed guidelines for improving data collection, distribution, and integration.	Hum Mutat	2009
19330029	Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.	Nat Genet	2009
19377476	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.	Nat Genet	2009
19306394	Planning the human variome project: the Spain report.	Hum Mutat	2009
18428421	The Catalogue of Somatic Mutations in Cancer (COSMIC).	Curr Protoc Hum Genet	2008
18469813	X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.	Nat Genet	2008

1 - 50 of 74

Ander Diaz-Navarro

Instituto Universitario de Oncologia (IUOPA), Universidad de Oviedo

Career Start Year 2018

Number of shared co-authors 11

Richard de Borja

The Hospital for Sick Children

Career Start Year 2012

Number of shared co-authors 40

Gordon Saksena

Broad Institute of Massachusetts Institute of Technology and Harvard

Career Start Year 2011

Number of shared co-authors 33

Emilie Lalonde

University of Pennsylvania

Career Start Year 2010

Number of shared co-authors 21

Joshua F McMichael

Washington University

Career Start Year 2009

Number of shared co-authors 10

Lixing Yang

University of Chicago, USA University of Chicago Comprehensive Cancer Center

Career Start Year 2008

Number of shared co-authors 15

Kilannin Krysiak

Washington University School of Medicine

Career Start Year 2007

Number of shared co-authors 2

Mark J Cowley

Children's Cancer Institute, Lowy Cancer Research Centre

Career Start Year 2006

Number of shared co-authors 24

Jamie K Teer

H. Lee Moffitt Cancer Center and Research Institute

Career Start Year 2005

Number of shared co-authors 11

Daniel C Koboldt

Institute for Genomic Medicine, Nationwide Children's Hospital

Career Start Year 2005

Number of shared co-authors 15

Robert C Onofrio

The Broad Institute of Harvard and MIT

Career Start Year 2005

Number of shared co-authors 17

Joachim Weischenfeldt

University of Copenhagen

Career Start Year 2004

Number of shared co-authors 44

Chip Stewart

Broad Institute of MIT and Harvard

Career Start Year 2004

Number of shared co-authors 31

David E Larson

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 2003

Number of shared co-authors 6

Michael D McLellan

McDonnell Genome Institute, Washington University in St. Louis

Career Start Year 2003

Number of shared co-authors 15

Olivier Harismendy

University of California

Career Start Year 2003

Number of shared co-authors 6

Trevor J Pugh

Princess Margaret Cancer Centre, University Health Network

Career Start Year 2003

Number of shared co-authors 37

James M Eldred

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 2003

Number of shared co-authors 5

Vladimir Makarov

Center for Immunotherapy and Precision-Immuno-Oncology, Cleveland Clinic

Career Start Year 2001

Number of shared co-authors 6

Nancy F Hansen

National Human Genome Research Institute, National Institutes of Health

Career Start Year 2000

Number of shared co-authors 11

Gad Getz

Broad Institute of the Massachusetts Institute of Technology and Harvard

Career Start Year 2000

Number of shared co-authors 53

Colin C Pritchard

University of Washington, USA Brotman Baty Institute for Precision Medicine

Career Start Year 1999

Number of shared co-authors 14

Michael N Edmonson

St. Jude Children's Research Hospital

Career Start Year 1999

Number of shared co-authors 4

Carrie Sougnez

The Broad Institute of Harvard and MIT

Career Start Year 1998

Number of shared co-authors 36

Li Ding

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 1997

Number of shared co-authors 25

Tom Walsh

University of Washington

Career Start Year 1996

Number of shared co-authors 13

Robert S Fulton

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 1994

Number of shared co-authors 30

Marco A Marra

University of British Columbia

Career Start Year 1993

Number of shared co-authors 67

Elaine R Mardis

The Ohio State University

Career Start Year 1988

Number of shared co-authors 43

Matthew Meyerson

Broad Institute

Career Start Year 1983

Number of shared co-authors 49

row(s) 1 - 30 of 30

Adam Butler

Wellcome Sanger Institute

Co-authored papers 57

Phillip A Futreal

The University of Texas MD Anderson Cancer Center

Co-authored papers 56

Michael R Stratton

Wellcome Sanger Institute

Co-authored papers 53

Andrew Menzies

Wellcome Sanger Institute

Co-authored papers 42

Keiran Raine

Wellcome Sanger Institute

Co-authored papers 41

Peter J Campbell

Wellcome Sanger Institute

Co-authored papers 41

Patrick S Tarpey

Wellcome Trust Sanger Institute

Co-authored papers 39

David Jones

Wellcome Sanger Institute

Co-authored papers 37

Sarah O'Meara

Clinical Research Facility, Mercy University Hospital

Co-authored papers 35

Sarah Edkins

Co-authored papers 28

Laura Mudie

Wellcome Trust Sanger Institute

Co-authored papers 24

David C Wedge

Manchester Cancer Research Centre, University of Manchester

Co-authored papers 24

Jonathan Hinton

Inivata Ltd

Co-authored papers 24

Serena Nik-Zainal

Early Cancer Institute, University of Cambridge

Co-authored papers 23

Chris Greenman

University of East Anglia

Co-authored papers 23

Peter Van Loo

The Francis Crick Institute

Co-authored papers 22

Stuart McLaren

Wellcome Trust Sanger Institute

Co-authored papers 22

Rebecca Shepherd

Murdoch Children's Research Institute, Royal Children's Hospital

Co-authored papers 21

Lucy A Stebbings

Wellcome Trust Sanger Institute

Co-authored papers 17

Ludmil B Alexandrov

Moores Cancer Center, university of california san diego

Co-authored papers 15

Sara Widaa

Co-authored papers 15

Adrienne M Flanagan

University College London, UCL Cancer Institute

Co-authored papers 15

Inigo Martincorena

Wellcome Sanger Institute

Co-authored papers 15

Gemma Buck

Co-authored papers 15

Douglas F Easton

University of Cambridge

Co-authored papers 14

Gunes Gundem

Memorial Sloan Kettering Cancer Center

Co-authored papers 14

Claire Hardy

Wellcome Sanger Institute

Co-authored papers 13

Susanna L Cooke

Institute of Cancer Sciences, University of Glasgow

Co-authored papers 13

Frances Lucy Raymond

University of Cambridge, UK Cambridge University Hospitals NHS Foundation Trust

Co-authored papers 11

Mark Maddison

Wellcome Sanger Institute

Co-authored papers 11

1 - 30

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