Nigel K. Spurr - Concepedia

Author

Nigel K. Spurr

The Honourable Society of Lincoln's Inn

Also Known As

N K Spurr, N SPURR, N Spurr, N. K. SPURR, N. K. Spurr, N. SPURR, N. Spurr, N.K Spurr, N.K. SPURR, N.K. Spurr

231

Publications

17.7K

Citations

H-Index

185

Concepts

All Affiliations

The Honourable Society of Lincoln's Inn University College London University of Oxford St James's University Hospital GlaxoSmithKline (United Kingdom)

About

Nigel K. Spurr is an author at The Honourable Society of Lincoln's Inn specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	54	123	15.1K
2	Natural Sciences	14	19	865
3	Engineering	4	4	418
4	Public Health	4	4	105
5	Health Sciences	3	3	1.5K

Nigel K. Spurr

151

Publications

17.3K

Citations

H-Index

Page 1

	Year	Citations
Identification of the breast cancer susceptibility gene BRCA2 Richard Wooster, Graham R. Bignell, Jonathan Lancaster, Nature Breast OncologyCancer GenomicsBreast CancerCancer GeneticsMedicine	1995	3.6K
A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia Annelies de Klein, Ad Geurts van Kessel, Gerard C. Grosveld, Nature Chronic Myelocytic LeukaemiaChromatinCellular OncogeneHematological MalignancyCytogenetics	1982	1.4K
Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations Sunil R. Lakhani, J Jacquemier, J P Sloane, JNCI Journal of the National Cancer Institute	1998	695
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse Patrick M. Nolan, Jo Peters, Mark Strivens, Nature Genetics Knockout MouseTransgenic Mouse ModelsGeneticsPhenotype-driven Mutagenesis ProgrammeGene Characterization	2000	655
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, Current Biology Molecular NeuroscienceDevelopmental BiologyGeneticsMorphogenesisNeurogenetics	2003	617
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, Nature Somatic VariantMedicineGeneticsPathologyCancer Genomics	1983	444
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease Colin Smith, C. Roland Wolf, A C Gough, The Lancet Mendelian DisorderParkinson DiseaseGenetic EpidemiologyHuman PolymorphismPathology	1992	421
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa Frances J.D. Smith, Robin A.J. Eady, I.M. Leigh, Nature Genetics PathologyDegenerative DiseaseGeneral PathologyDermatologyMedicine	1996	391
Structure and polymorphism of human telomere-associated DNA William R. Brown, Philip J. MacKinnon, Alfredo Villasanté, Cell DnaGeneticsHuman PolymorphismGenome StructureMolecular Biology	1990	384
Identification of the primary gene defect at the cytochrome P450 CYP2D locus Alan C. Gough, John S. Miles, Nigel K. Spurr, Nature Genome InstabilityPrimary Gene DefectGenetic DisorderGeneticsBiochemical Genetics	1990	306

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