World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
73
Citations
26135
World Ranking
2017
National Ranking
249

Overview

Nigel K. Spurr is affiliated with GlaxoSmithKline in the United Kingdom. Their professional focus is situated within this major pharmaceutical company's research environment, contributing to the broader field of pharmaceutical science and related disciplines.

While specific details on Nigel K. Spurr's research papers, topics, and fields of study are not available, their association with GlaxoSmithKline indicates involvement in industrial research, likely pertaining to drug development and related biomedical areas.

No detailed records of co-authors or frequent publication venues are provided, suggesting that publicly accessible bibliometric data about their collaborative networks or publication patterns is limited or not disclosed.

Similarly, information regarding awards, major scientific contributions, or book publications has not been documented, which restricts the ability to elaborate on recognitions or broader scholarly impact.

This profile reflects the available factual data concerning Nigel K. Spurr's professional context without speculation or unsupported assumptions.

Best Publications

  • Identification of the breast cancer susceptibility gene BRCA2

    Wooster R;Bignell G;Lancaster J;Swift S

  • A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

    Annelies de Klein;Ad Geurts van Kessel;Gerard Grosveld;Claus R. Bartram

  • Localization of the gene for familial adenomatous polyposis on chromosome 5.

    W F Bodmer;C J Bailey;J Bodmer;H J Bussey

  • Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

    Sunil R. Lakhani;Jocelyne Jacquemier;John P Sloane;Barry A. Gusterson

  • A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

    P M Nolan;J Peters;M Strivens;D Rogers

  • Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.

    John A. Curtin;Elizabeth Quint;Vicky Tsipouri;Ruth M. Arkell

  • An autosomal transcript in skeletal muscle with homology to dystrophin.

    Donald R. Love;Diane F. Hill;George Dickson;Nigel K. Spurr

  • Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer

    S. Zhong;A.H. Wyllie;D. Barnes;C.R. Wolf

  • Identification of transforming gene in two human sarcoma cell lines as a new member of the ras gene family located on chromosome 1

    Alan Hall;Christopher J. Marshall;Nigel K. Spurr;Robin A. Weiss

  • Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

    C.A.D Smith;C.R Wolf;A.C Gough;N.K Spurr

  • Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

    F.J.D. Smith;R.A.J. Eady;I.M. Leigh;J.R. McMillan

  • Structure and polymorphism of human telomere-associated DNA

    William R.A. Brown;Philip J. MacKinnon;Alfredo Villasanté;Nigel Spurr

  • Identification of the primary gene defect at the cytochrome P450 CYP2D locus.

    A C Gough;J S Miles;N K Spurr;J E Moss

  • Chromosomal localization of human cellular homologues of two viral oncogenes.

    Nora Heisterkamp;John Groffen;John R. Stephenson;N. K. Spurr

  • Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility.

    S Zhong;A F Howie;B Ketterer;J Taylor

  • Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts.

    L Roewer;J Arnemann;N K Spurr;K H Grzeschik

  • Loss of the Chromosomal Region 10q23–25 in Prostate Cancer

    Ian C. Gray;Stewart M. A. Phillips;Susan J. Lee;John P. Neoptolemos

  • A First-Generation Whole Genome–Radiation Hybrid Map Spanning the Mouse Genome

    Linda C. McCarthy;Jonathan Terrett;Maria E. Davis;Catherine J. Knights

  • Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.

    Howard P. Stevens;David P. Kelsell;Stephen P. Bryant;D. Timothy Bishop

  • Erratum: Identification of the breast cancer susceptibility gene BRCA2

    Richard Wooster;Graham Bignell;Jonathan Lancaster;Sally Swift

Frequent Co-Authors

Denise Sheer
Denise Sheer Queen Mary University of London
David P. Kelsell
David P. Kelsell Queen Mary University of London
Walter F. Bodmer
Walter F. Bodmer University of Oxford
C. Roland Wolf
C. Roland Wolf University of Dundee
Irene M. Leigh
Irene M. Leigh University of Dundee
Ellen Solomon
Ellen Solomon King's College London
Brunhilde Wirth
Brunhilde Wirth University of Cologne
Jean Weissenbach
Jean Weissenbach Centre national de la recherche scientifique, CNRS
Gabriella Sozzi
Gabriella Sozzi University of Milan

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