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Medicine
UK
2026
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Genetics
UK
2024

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Genetics

D-Index
167
Citations
155894
World Ranking
73
National Ranking
12

Medicine

D-Index
167
Citations
156950
World Ranking
578
National Ranking
71

Research.com Recognitions

  • 2026 - Research.com Medicine in United Kingdom Leader Award
  • 2025 - Research.com Medicine in United Kingdom Leader Award
  • 2024 - Research.com Genetics in United Kingdom Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in United Kingdom Leader Award
  • 2023 - Research.com Genetics in United Kingdom Leader Award

Overview

Peter J. Campbell is affiliated with the Wellcome Sanger Institute in the United Kingdom. Their research primarily focuses on biochemistry, genetics, and molecular biology, with significant contributions to medicine.

The main fields of study in their work include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

The subfields closely associated with their research are:

  • Molecular Biology
  • Cancer Research
  • Genetics
  • Pathology and Forensic Medicine
  • Hematology

Their research also covers key scientific topics such as:

  • Cancer Genomics and Diagnostics
  • Genetic factors in colorectal cancer
  • Single-cell and spatial transcriptomics
  • Acute Myeloid Leukemia Research
  • DNA Repair Mechanisms
  • Epigenetics and DNA Methylation
  • CRISPR and Genetic Engineering

Peter J. Campbell has an extensive publication record. Recent papers include:

  • Patterns of somatic structural variation in human cancer genomes, 2020, Nature
  • Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution, 2020, Nature Genetics
  • Somatic mutation landscapes at single-molecule resolution, 2021, Nature
  • Tobacco smoking and somatic mutations in human bronchial epithelium, 2020, Nature
  • Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes, 2021, Cell

The frequent co-authors with whom Peter J. Campbell has collaborated are:

  • Iñigo Martincorena
  • Tim Coorens
  • Michael R. Stratton
  • Jyoti Nangalia
  • Emily Mitchell

They commonly publish in the following venues:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature
  • Nature Communications
  • Nature Genetics
  • Blood

Best Publications

  • Signatures of mutational processes in human cancer

    Ludmil B. Alexandrov;Serena Nik-Zainal;Serena Nik-Zainal;David C. Wedge;Samuel A. J. R. Aparicio

  • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.

    E Joanna Baxter;Linda M Scott;Peter J Campbell;Clare East

  • The cancer genome

    Michael R. Stratton;Michael R. Stratton;Peter J. Campbell;Peter J. Campbell;P. Andrew Futreal

  • COSMIC: the Catalogue Of Somatic Mutations In Cancer

    John G Tate;Sally Bamford;Harry C Jubb;Harry C Jubb;Zbyslaw Sondka

  • Genomic Classification and Prognosis in Acute Myeloid Leukemia

    Elli Papaemmanuil;Moritz Gerstung;Lars Bullinger;Verena I Gaidzik

  • Patterns of somatic mutation in human cancer genomes

    Christopher Greenman;Philip Stephens;Raffaella Smith;Gillian L. Dalgliesh

  • Pan-cancer analysis of whole genomes

    Peter J. Campbell;Gad Getz;Jan O. Korbel;Joshua M. Stuart

  • COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer.

    Simon A. Forbes;Nidhi Bindal;Sally Bamford;Charlotte Cole

  • COSMIC: exploring the world's knowledge of somatic mutations in human cancer

    Simon A. Forbes;David Beare;Prasad Gunasekaran;Kenric Leung

  • Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development

    Philip J. Stephens;Chris D. Greenman;Beiyuan Fu;Fengtang Yang

  • International network of cancer genome projects

    Thomas J. Hudson;Thomas J. Hudson;Warwick Anderson;Axel Aretz;Anna D. Barker

  • Origins and functional impact of copy number variation in the human genome

    Donald F. Conrad;Dalila Pinto;Richard Redon;Richard Redon;Lars Feuk;Lars Feuk

  • Landscape of somatic mutations in 560 breast cancer whole-genome sequences

    Serena Nik-Zainal;Serena Nik-Zainal;Helen Davies;Johan Staaf;Manasa Ramakrishna

  • Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2

    J. Nangalia;C.E. Massie;E.J. Baxter;F.L. Nice

  • Mutational Processes Molding the Genomes of 21 Breast Cancers

    Serena Nik-Zainal;Ludmil B. Alexandrov;David C. Wedge;Peter Van Loo;Peter Van Loo;Peter Van Loo

  • A comprehensive catalogue of somatic mutations from a human cancer genome

    Erin D. Pleasance;R. Keira Cheetham;Philip J. Stephens;David J. Mcbride

  • COSMIC: somatic cancer genetics at high-resolution.

    Simon A. Forbes;David Beare;Harry Boutselakis;Sally Bamford

  • Clinical and biological implications of driver mutations in myelodysplastic syndromes.

    Elli Papaemmanuil;Moritz Gerstung;Luca Malcovati;Sudhir Tauro

  • The landscape of cancer genes and mutational processes in breast cancer

    Philip J. Stephens;Patrick S. Tarpey;Helen Davies;Peter Van Loo;Peter Van Loo

  • Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

    Xose S. Puente;Magda Pinyol;Víctor Quesada;Laura Conde

Frequent Co-Authors

Michael R. Stratton
Michael R. Stratton Wellcome Sanger Institute
Peter Van Loo
Peter Van Loo The Francis Crick Institute
David C. Wedge
David C. Wedge University of Manchester
Jon W. Teague
Jon W. Teague Wellcome Sanger Institute
Keiran Raine
Keiran Raine Wellcome Sanger Institute
Inigo Martincorena
Inigo Martincorena Wellcome Sanger Institute
Anthony R. Green
Anthony R. Green University of Cambridge
Ludmil B. Alexandrov
Ludmil B. Alexandrov University of California, San Diego
Patrick S. Tarpey
Patrick S. Tarpey Wellcome Sanger Institute
Nikhil C. Munshi
Nikhil C. Munshi Harvard University

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