Nigel K. Spurr

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Nigel K. Spurr

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Nigel K. Spurr

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Philosophy
Biology

Nigel K. Spurr's Degrees

Doctorate Medicine Harvard University

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Nigel K. Spurr's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Identification of the breast cancer susceptibility gene BRCA2 (1995) (2451)
Identification of the breast cancer susceptibility gene BRCA2 (1996) (1451)
Localization of the gene for familial adenomatous polyposis on chromosome 5 (1987) (1379)
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. (1998) (700)
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse (2000) (682)
Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse (2003) (607)
An autosomal transcript in skeletal muscle with homology to dystrophin (1989) (490)
Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer. (1993) (447)
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease (1992) (435)
Identification of transforming gene in two human sarcoma cell lines as a new member of the ras gene family located on chromosome 1 (1983) (409)
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa (1996) (390)
Structure and polymorphism of human telomere-associated DNA (1990) (365)
Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. (1989) (340)
Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism. (1996) (310)
Identification of the primary gene defect at the cytochrome P450 CYP2D locus (1990) (308)
Chromosomal localization of human cellular homologues of two viral oncogenes (1982) (286)
Multiplexed SNP genotyping using the Qbead system: a quantum dot-encoded microsphere-based assay. (2003) (264)
Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility. (1991) (263)
Single nucleotide polymorphisms as tools in human genetics. (2000) (255)
Loss of the chromosomal region 10q23-25 in prostate cancer. (1995) (248)
Abnormal expression of wild type p53 protein in normal cells of a cancer family patient (1992) (204)
A first-generation whole genome-radiation hybrid map spanning the mouse genome. (1997) (189)
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. (1996) (178)
A gene-driven ENU-based approach to generating an allelic series in any gene (2004) (178)
Regulated expression and phosphorylation of a possible mammalian cell-cycle control protein (1988) (171)
Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN. (1998) (169)
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16 (1991) (160)
The human IL-1 receptor antagonist gene (IL1RN) maps to chromosome 2q14–q21, in the region of the IL-1α and IL-1β loci (1992) (153)
RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome. (2012) (149)
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts (1992) (148)
A single-nucleotide polymorphism tagging set for human drug metabolism and transport (2005) (147)
Chromosomal localisation of the human homologues to the oncogenes erbA and B. (1984) (146)
Cloning and mapping of a testis-specific gene with sequence similarity to a sperm-coating glycoprotein gene. (1989) (145)
Expression of the PAX2 gene in human fetal kidney and Wilms' tumor. (1992) (141)
Germline mutations of the CDKN2 gene in UK melanoma families. (1997) (139)
The Lutheran blood group glycoprotein, another member of the immunoglobulin superfamily, is widely expressed in human tissues and is developmentally regulated in human liver. (1995) (123)
A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24. (1995) (123)
Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression. (1992) (118)
Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource (2000) (118)
High allele loss rates at I7q I2‐q2I in breast and ovarian tumors from BRCAI‐linked families (1995) (118)
Characterization and chromosomal localization of the gene encoding the human cell adhesion molecule uvomorulin. (1988) (114)
Molecular features of CD34: a hemopoietic progenitor cell-associated molecule. (1992) (113)
Chromosomal localization of human genes for arylamine N-acetyltransferase. (1994) (113)
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee. (1997) (104)
Alpha 2-chimerin, an SH2-containing GTPase-activating protein for the ras-related protein p21rac derived by alternate splicing of the human n-chimerin gene, is selectively expressed in brain regions and testes (1993) (95)
The human Thy-1 gene: structure and chromosomal location. (1985) (92)
cDNA cloning and chromosomal assignment of the human O6-methylguanine-DNA methyltransferase. cDNA expression in Escherichia coli and gene expression in human cells. (1990) (84)
The Murine GABAA Receptor δ-Subunit Gene: Structure and Assignment to Human Chromosome 1 (1990) (84)
Val64Ile Polymorphism in the C-C Chemokine Receptor 2 Is Associated With Reduced Coronary Artery Calcification (2002) (81)
Chromosomal localization of the human c-fms oncogene. (1983) (81)
The hemopoietic stem cell antigen, CD34, is encoded by a gene located on chromosome 1. (1989) (79)
Immunoglobulin heavy chain genes in humans are located on chromosome 14 (1981) (77)
Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10. (1988) (77)
Localization of brain nitric oxide synthase (NOS) to human chromosome 12. (1992) (77)
Human cardiac troponin T: identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q. (1994) (77)
Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping (1995) (75)
Msp-1 polymorphism detected with a cDNA probe for the P-450 I family on chromosome 15. (1987) (73)
Chromosomal assignment of the human genes coding for the major proteins of the desmosome junction, desmoglein DGI (DSG), desmocollins DGII/III (DSC), desmoplakins DPI/II (DSP), and plakoglobin DPIII (JUP). (1991) (70)
A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse (2003) (70)
Novel phenotypes identified by plasma biochemical screening in the mouse (2002) (70)
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia (2004) (70)
Genetic analysis of the BRCA1 region in a large breast/ovarian family: refinement of the minimal region containing BRCA1. (1993) (69)
Chromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene family. (1985) (67)
Three genes for protein phosphatase 1 map to different human chromosomes: sequence, expression and gene localisation of protein serine/threonine phosphatase 1 beta (PPP1CB). (1994) (65)
Localization of the CYP2D gene locus to human chromosome 22q13.1 by polymerase chain reaction, in situ hybridization, and linkage analysis. (1993) (64)
Genetic heterogeneity in familial malignant melanoma. (1994) (64)
The oncogene associated with human papillary thyroid carcinoma (PTC) is assigned to chromosome 10 q11-q12 in the same region as multiple endocrine neoplasia type 2A (MEN2A). (1989) (63)
Complete sequence of human vinculin and assignment of the gene to chromosome 10. (1990) (63)
The human homologue of the mouse t‐complex gene, TCP1, is located on chromosome 6 but is not near the HLA region. (1987) (62)
A novel human cytochrome P450 gene (P450IIB): chromosomal localization and evidence for alternative splicing (1988) (62)
Molecular analysis of 9p deletions associated with XY sex reversal: refining the localization of a sex-determining gene to the tip of the chromosome. (1998) (61)
Overexpression of the oncoprotein p53 in primary hepatic tumors of childhood does not correlate with gene mutations. (1994) (61)
Localization of the gene encoding a type I protein phosphatase catalytic subunit to human chromosome band 11q13. (1990) (60)
Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations (1998) (59)
Report of the committee on the genetic constitution of chromosome 6. (1988) (59)
Wnt-16a, a novel Wnt-16 isoform, which shows differential expression in adult human tissues. (2000) (59)
The human IL-1 receptor antagonist gene (IL1RN) maps to chromosome 2q14-q21, in the region of the IL-1 alpha and IL-1 beta loci. (1992) (59)
Sequence of human protein serine/threonine phosphatase 1 gamma and localization of the gene (PPP1CC) encoding it to chromosome bands 12q24.1-q24.2. (1993) (58)
Report of the Fourth International Workshop on Human Chromosome 2 Mapping 1996 (1992) (58)
The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37 (1987) (57)
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland (2001) (55)
Cloning of the cDNA (DSC1) coding for human type 1 desmocollin and its assignment to chromosome 18. (1993) (53)
Gene structure of semenogelin I and II. The predominant proteins in human semen are encoded by two homologous genes on chromosome 20. (1992) (52)
The human heat-shock genes HSPA6 and HSPA7 are both expressed and localize to chromosome 1. (1992) (52)
p53 protein detected by immunohistochemical staining is not always mutant. (1993) (52)
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC). (1996) (51)
Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11. (1988) (51)
Germline BRCA2 mutations in men with breast cancer. (1997) (51)
Polymorphisms in drug-metabolizing enzymes as modifiers of cancer risk. (1995) (50)
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy (2000) (48)
Deduced amino acid sequence, gene structure and chromosomal location of a novel human class Mu glutathione S-transferase, GSTM4. (1993) (48)
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene. (2004) (48)
The human T-cell receptor α-chain gene maps to chromosome 14 (1985) (47)
Human cellular retinol-binding protein gene organization and chromosomal location. (1988) (42)
Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene 2 (ACTBP2) detected using the polymerase chain reaction. (1991) (41)
Immunohistochemical expression of BRCA2 protein and allelic loss at the BRCA2 locus in prostate cancer (1998) (41)
Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13. (1996) (40)
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region (1997) (40)
Human TRK proto-oncogene maps to chromosome 1q32-q41. (1990) (40)
Detection of debrisoquine hydroxylation phenotypes (1990) (39)
Molecular genetic analysis of the cytochrome P450-debrisoquine hydroxylase locus and association with cancer susceptibility. (1992) (38)
Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25. (1999) (37)
Chromosomal assignment of genes encoding the α, β, and γ subunits of human complement protein C8: Identification of a close physical linkage between the α and the β loci (1989) (36)
Erratum: Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease (The Lancet, vol. 339/8806 (1375-1377)) (1992) (36)
Molecular cloning and chromosomal assignment of human calbindin-D9k. (1992) (36)
Genetic analysis of cytochrome P450 system. (1991) (36)
The human gene (DSG2) coding for HDGC, a second member of the desmoglein subfamily of the desmosomal cadherins, is, like DSG1 coding for desmoglein DGI, assigned to chromosome 18. (1992) (36)
Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity. (1995) (36)
Localization of the gene for human simple epithelial keratin 18 to chromosome 12 using polymerase chain reaction. (1990) (34)
Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study (1999) (33)
A human T‐cell antigen receptor beta chain gene maps to chromosome 7. (1984) (33)
The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon (2003) (32)
European Gene Mapping Project (EUROGEM): Genetic Maps based on the CEPH reference families (1994) (32)
Association between loss of heterozygosity of BRCA1 and BRCA2 and morphological attributes of sporadic breast cancer (2000) (31)
Some oral carcinomas from Sri Lankan betel/tobacco chewers overexpress p53 oncoprotein but lack mutations in exons 5-9. (1993) (31)
Cloning of the mouse homologue of the yeast cell cycle control gene cdc2. (1990) (30)
REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996 (1997) (30)
Combined loss of BRCA1/BRCA2 in grade 3 breast carcinomas (1996) (28)
Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3. (1992) (28)
Identification of multiple forms of 180-kDa ribosome receptor in human cells. (1998) (28)
The human tropomyosin gene involved in the generation of the TRK oncogene maps to chromosome 1q31. (1991) (28)
Activation of the met oncogene in the human MNNG-HOS cell line involves a chromosomal rearrangement. (1986) (27)
Assignment of tissue-type plasminogen activator to chromosome 8 in man and identification of a common restriction length polymorphism within the gene. (1984) (27)
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy. (2001) (27)
A novel dystrophin/utrophin-associated protein is an enzymatically inactive member of the phosphoglucomutase superfamily. (1996) (27)
Report of the first international workshop on human chromosome 10 mapping 1995. (1996) (27)
Localization of the genes encoding the catalytic subunits of protein phosphatase 2A to human chromosome bands 5q23-->q31 and 8p12-->p11.2, respectively. (1993) (26)
Human N-CAM gene: mapping to chromosome 11 by analysis of somatic cell hybrids with mouse and human cDNA probes. (1986) (25)
Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders (2004) (25)
Guidelines for conducting and reporting whole genome/large-scale association studies. (2005) (24)
Chromosomal assignment and linkage analysis of the human glutathione S-transferase μ gene (GSTM1) using intron specific polymerase chain reaction (1992) (24)
Chromosomal assignment of the gene encoding the human tissue inhibitor of metalloproteinases to Xp11.1–p11.4 (1987) (24)
CYP2D6 genotyping and the association with lung cancer susceptibility. (1994) (24)
Isolation and characterization of a cDNA clone corresponding to bovine cellular retinoic-acid-binding protein and chromosomal localization of the corresponding human gene. (1988) (23)
Further support for the association of CCR5 allelic variants with asthma susceptibility. (2002) (22)
The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter (2004) (22)
A human sequence homologous to v-sea maps to chromosome 11, band q13. (1988) (22)
Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4. (1993) (21)
Localisation of the gene encoding the catalytic gamma subunit of phosphorylase kinase to human chromosome bands 7p12-q21. (1990) (21)
Molecular genetics of calcium sensing in bone cells. (2002) (20)
Assignment of the chromosomal locus of the human 30-kDal Rh (rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13----p34. (1992) (20)
A novel family of cathepsin L-like (CTSLL) sequences on human chromosome 10q and related transcripts. (1994) (20)
The plakophilin 1 (PKP1) and plakoglobin (JUP) genes map to human chromosomes 1q and 17, respectively (1997) (20)
An integrated physical and genetic map spanning chromosome band 10q24. (1997) (20)
Report and abstracts of the Second International Workshop on Human Chromosome 2 Mapping. (1993) (20)
Report and abstracts of the Third International Workshop on Human Chromosome 2 Mapping 1994. Aarhus, Denmark, June 24-26, 1994. (1994) (19)
Making drug discovery a SN(i)P (2000) (18)
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables (1999) (18)
Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical staining. (1995) (18)
Detection of transforming genes by transfection of DNA from primary soft-tissue tumours. (1991) (18)
Genomic organization, chromosomal mapping, and analysis of the 5’ promoter region of the human MAdCAM-1 gene (1997) (18)
Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region (1997) (17)
Molecular genetics of the human cytochrome P-450 system. (1990) (16)
Cloning and characterisation of ITGAV, the genomic sequence for human cell adhesion protein (vitronectin) receptor alpha subunit, CD51 (2000) (16)
The human T-cell receptor alpha-chain gene maps to chromosome 14. (1985) (15)
The human LFA-3 gene is located at the same chromosome band as the gene for its receptor CD2 (2004) (15)
Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17. (1993) (15)
Genomic organization and chromosomal localization of the human CTP synthetase gene (CTPS). (1991) (15)
Chromosomal assignment of 311 sequences transcribed in human adult testis. (1997) (15)
Evidence for the absence of intron H of the histidine-rich glycoprotein (HRG) gene: genetic mapping and in situ localization of HRG to chromosome 3q28-q29. (1994) (15)
Assignment of the human gene for beta-microseminoprotein (MSMB) to chromosome 10 and demonstration of related genes in other vertebrates. (1991) (14)
The genetic analysis of prostate carcinoma. (1997) (14)
CEPH consortium map of chromosome 14. (1995) (14)
Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy. (1988) (13)
The fibroblast growth factor receptor 3 gene (FGFR3) is assigned to human chromosome 4. (1993) (13)
Second International Workshop on Human Chromosome 8 Mapping 1994. Eynsham Hall, Oxford, UK, 16-18 September, 1994 (1994) (13)
Mapping of mouse carbonic anhydrase-3, Car-3: another locus in the homologous region of mouse chromosome 3 and human chromosome 8. (1990) (13)
Chromosomal assignment of c-MEL, a human transforming oncogene, to chromosome 19 (p13.2-q13.2) (1986) (13)
Chromosomal assignment of seven human genomic DNA sequences associated with restriction fragment length polymorphisms (1986) (13)
The murine GABAA receptor delta-subunit gene: structure and assignment to human chromosome 1. (1990) (12)
Chromosomal locations of the gene coding for the CD3 (T3) γ subunit of the human and mouse CD3/T-cell antigen receptor complexes (2004) (12)
Genetics of calcium-sensing--regulation of calcium levels in the body. (2003) (12)
The human myoglobin gene: a third dispersed globin locus in the human genome. (1984) (12)
The human cardiac troponin I locus: assignment to chromosome 19p13.2–19q13.2 (1991) (12)
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3 (1996) (12)
Localization of a second NM23 gene, NME2, to chromosome 17q21-q22. (1993) (12)
Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia (1992) (11)
Assignment of the Hepatocyte Growth Factor (HGF) to chromosome 7q22‐qter (1991) (11)
Chromosome mapping of the human gene encoding the 68-kDa nuclear antigen (p68) by using the polymerase chain reaction. (1989) (11)
Integrated Radiation Hybrid and Yeast Artificial Chromosome Map of Chromosome 9p (1997) (11)
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding region. (1995) (11)
Isolation and mapping to 17p12-13 of the human homologous of the murine growth arrest specific Gas-3 gene. (1992) (11)
RFLP of the human placental alkaline phosphatase gene (PLAP). (1987) (11)
The gene coding for the p68 calcium-binding protein is localised to bands q32–q34 of human chromosome 5, and to mouse chromosome 11 (1989) (10)
Chromosomal assignment of human uracil-DNA glycosylase to chromosome 12. (1990) (10)
Localisation of the gene coding for the haemopoietic stem cell antigen CD34 to chromosome 1q32 (1991) (10)
Concomitant reversion of the characteristic phenotypic properties of a cell line of Bloom's syndrome origin. (1989) (10)
Val 64 Ile Polymorphism in the C-C Chemokine Receptor 2 Is Associated With Reduced Coronary Artery Calcification (2002) (10)
Report of the committee on the genetic constitution of chromosome 2. (1990) (10)
Construction of a radiation hybrid map of chromosome 9p. (1996) (10)
Dinucleotide repeat polymorphism in the human coagulation factor XI gene, intron B (F11), detected using the polymerase chain reaction. (1991) (9)
Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP. (1998) (9)
The human chromosome content in human x rodent somatic cell hybrids analyzed by a screening technique using Alu PCR. (1991) (9)
Sph I restriction fragment length polymorphism on human chromosome 16 detected with an APRT gene probe. (1987) (9)
Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11 (1995) (9)
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region. (1997) (8)
ICRF handbook of genome analysis (1998) (8)
Glutathione S-transferase mu locus (1991) (8)
An XmnI RFLP detected with a probe for the CYP2E gene locus on chromosome 10. (1990) (8)
N‐ras‐like sequences on chromosomes 9, 6 and 22 with a polymorphism at the chromosome 9 locus (1988) (8)
European Gene Mapping Project (EUROGEM): Breakpoint panels for human chromosomes based on the CEPH reference families (1996) (7)
A BamHI RFLP recognised by an anonymous chromosome 20 probe, p4.8 (D20S14). (1987) (7)
A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders (1998) (7)
Localisation of the human gene encoding the cytoskeletal protein talin to chromosome 9p (1995) (7)
Report and abstracts of the second international workshop on human chromosome 8 mapping 1994. Oxford, United Kingdom, September 16-18, 1994. (1995) (6)
Chromosomal localization of a cytochrome b5 gene to human chromosome 18 and a cytochrome b5 pseudogene to the X chromosome. (1991) (6)
Evolutionary conservation of the human homologue of the yeast cell cycle control gene cdc2 and assignment of Cd2 to chromosome 10 (1988) (6)
Dinucleotide repeat polymorphism at the human erythroid alpha-spectrin (SPTA1) mRNA gene detected using PCR. (1992) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
CD8B, the human equivalent of the mouse Ly-3 gene is localized on chromosome 2 (2004) (6)
The human gene (DSG3) coding for the pemphigus vulgaris antigen is, like the genes coding for the other two known desmogleins, assigned to chromosome 18 (1992) (6)
Chromosomal ocations fo the genes coding for the integrin β6 and β7 subunits (2004) (6)
Gene mapping using somatic cell hybrids. (1997) (5)
Mapping And Characterization of the Eukaryotic Early Pregnancy Factor/Chaperonin 10 Gene Family (1998) (5)
Standards for reporting alleles at highly polymorphic loci: a proposal. (1992) (5)
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p (1987) (5)
Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization (1991) (5)
Chromosomal assignment of genes encoding the alpha, beta, and gamma subunits of human complement protein C8: identification of a close physical linkage between the alpha and the beta loci. (1989) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Chromosomal locations of the genes coding for the integrin beta 6 and beta 7 subunits. (1992) (5)
Dinucleotide repeat polymorphism in the human alpha-cardiac actin gene, intron IV (ACTC), detected using the polymerase chain reaction. (1991) (5)
Immunoglobulin heavy chain genes in humans are located on chromosome. (1981) (5)
Chromosomal localization of three human genes coding for A15, L6, and S5.7(TAPA1): all members of the transmembrane 4 superfamily of proteins (2004) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
The CEPH consortium linkage map of human chromosome 2. (1992) (4)
GENETICS OF THE T-CELL RECEPTOR (1985) (4)
The molecular basis of parathyroid tumours in multiple endocrine neoplasia type 1 (1990) (4)
A MspI-RFLP in the C-terminal part of the gene for desmoglein DGI (DSG). (1991) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Propping Mapping of the human adenosine A 2 a receptor gene : relationship to potential schizophrenia loci on chromosome 22 q and exclusion from the CATCH 22 region (4)
Localization of the cellular retinoic acid binding protein (CRABP) gene relative to the acute promyelocytic leukemia-associated breakpoint on human chromosome 15 (1991) (4)
The polymorphic human DNA sequence D8S8 assigned to 8ql3‐21.1, close to the carbonic anhydrase gene cluster, by isotopic and non‐isotopic in situ hybridization and by linkage analysis (1990) (4)
Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes. (1997) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Chromosome analysis protocols. Methods in molecular biology, volume 29. JOHN R. GOSDEN, (Ed.) Humana Press, Price: $69.50 (paperback). ISBN: 0 896 03289 2 (1994) (3)
TheCG-1 gene, a member of the kinectin and ES/130 family, maps to human chromosome band 14q22 (2004) (3)
Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse (2004) (3)
Pharmacogenetic studies of epilepsy drugs: are we there yet? (2006) (3)
Chromosome assignment of the human glutathione S-transferase mu 3 gene (GSTM3) to chromosome 1 by gene specific polymerase chain reaction. (1994) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Prediction of debrisoquine phenotype (1991) (2)
Report on the 1996 International chromosome 9 workshop (1997) (2)
Regional chromosomal assignment of the Kell blood group locus (KEL) to chromosome 7q33-q35 by fluorescence in situ hybridization: evidence for the polypeptide nature of antigenic variation (1993) (2)
Isolation of a polymorphic DNA sequence (lambda EMBL3.287, D8S8) from chromosome 8. (1986) (2)
Molecular genetics of the human cytochrome P450-dependent monooxygenases. (1992) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Isolation of a polymorphic DNA sequence (λEMBL3.121, D14S12) from chromosome 14 (1986) (2)
Identification of genetic differences in debrisoquine hydroxylase activity (1992) (2)
First international workshop on human chromosome 8 mapping 1993 (1993) (2)
A TaqI RFLP in the N-terminal part of the gene for desmocollins DGII/III (psc). (1991) (2)
Chromosomal assignment of 79 cDNAs from a range of human tissues. (1996) (2)
Bioinformatics – from genomes to drugs (2 volumes) (2002) (1)
Isolation of a polymorphic DNA sequence (λEMBL3.303, D2S14) from chromosome 2 (1986) (1)
Isolation of a polymorphic DNA sequence (lambda EMBL3.121, D14S12) from chromosome 14. (1986) (1)
The Integrated Genomic Database (IGD)s (1997) (1)
The EUROGEM map of human chromosome 8. (1993) (1)
Guidelines for Human Gene Mapping (1997) (1)
Mapmakers--progress in the human genome project. (1996) (1)
An integrated genetic map of Chromosome 6 (1996) (1)
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse: Short Communications (2004) (1)
Contents Vol. 55, 1990 (1990) (1)
Report of the First International Workshop on Human Chromosome 2 mapping 1991. (1992) (1)
Atypical CTSK Transcripts and ARNT Transcription Read-Through Into CTSK (2005) (1)
Serendipitous cloning of a mitochondrial cDNA and its polymorphism. (1984) (1)
THE INTEGRATED GENOMIC DATABASE (IGD)S Enhancing the Productivity of Gene Mapping Projects (1997) (1)
Genetic heterogeneity in families with non-epidermolytic palmar plantar keratosis (1994) (0)
Confirmation of the assignment of the vitronectin (VNRA) and fibronectin (FNRA) receptor alpha-subunits. (1991) (0)
Studies on the immunohistochemical demonstration of P53 protein in inherited breast cancers correlated with evidence of mutation in the P53 gene (1992) (0)
Subject Index, Vol. 69, 1995 (2004) (0)
Subject Index, Vol. 68, 1995 (1995) (0)
“Take a break — have a quick map” (1995) (0)
Genetic test for cytochrome P450 (1991) (0)
Focal palmoplantar keratodermas (PPK): Segregation analysis and immunofluorescence (1994) (0)
British Society for Investigative Dermatology Annual Meeting, Bath, 15–16 September 1994 (1994) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
Basic and applied research in human genetics: Advances in Human Genetics edited by H. Harris and K. Hirschhorn, Plenum Press, 1990. $65.00 (xix + 339 pages) ISBN 0 306 43298 6 (1991) (0)
An XmnI RFLP detected with a cDNA probe for the CYP2C gene locus on chromosome 10. (1989) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
ICRF handbook of genome analysis. Volumes 1 and 2 (1998) (0)
Irish Association for Cancer Research (1995) (0)
Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphisms (1991) (0)
Dinucleotide repeat polymorphism at the D5S214 locus. (1993) (0)
ASSIGNMENT OF THE DESMOGLEIN AND DESMOCOLLIN GENES, CODING FOR CADHERIN-LIKE CELL-ADHESION MOLECULES OF THE DESMOSOME-TYPE OF CELL JUNCTION, TO CHROMOSOME-18 (1994) (0)
CHROMOSOME-11 ABNORMALITIES IN PARATHYROID TUMORS OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-I (MENTI) (1989) (0)
Molecular Genetic Analysis of the Cytochrome P450-Debrisoquine Hydroxylase (2016) (0)
Contents Vol. 89, 2000 (2000) (0)
Mechanisms regulating the initiation of neural tube closure (2004) (0)
Isolation of a DNA sequence (lambda EMBL3.123, D4S64) from chromosome 4 showing a BglII polymorphism. (1987) (0)
Germline mutations in the CDKN2 and CDK4 genes are rare in melanoma families in the UK (1997) (0)
Summaries of Papers (1993) (0)
Integrated radiation hybrid and YAC map of chromosome 9p. (1997) (0)
Index by Keyword (1989) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Identification of novel behavioural mutations using ENU mutagenesis. (2000) (0)
Non-epidermolytic palmoplantar keratoderma (NEPPK): Segregation analysis and immunofluorescence (1994) (0)
Contents Vol. 68, 1999 (1999) (0)
Isolation of a polymorphic DNA sequence (lambda EMBL3.303, D2S14) from chromosome 2. (1987) (0)
Molecular cloning and analysis of human cardiac troponin I gene expression (1991) (0)
Subject Index, Vol. 73, 1996 (1996) (0)
Dinucleotide repeat polymorphism at the D12S371 locus. (1993) (0)
Punctate palmoplantar keratoderma (PPPK) associated with malignancy: Immunofluorescence and segregation analysis (1994) (0)
Twenty different alleles at the locus D5S683 on 5q23-31. (1993) (0)
Chromosomal assignments ofthegenescoding forhumantypes II, III, andIVcollagen: A dispersed genefamily (1985) (0)
Chromosomal mapping of the human interleukin-1 receptor antagonist gene (IL-1RN) and isolation of specific YAC clones (2005) (0)
Cloning in higher organisms. (1993) (0)
Molecular genetic approaches to the analysis of colorectal cancer. (1990) (0)
Genetic Aberrations in Prostate Tumours (2003) (0)
Monochromosomal Somatic Cell Hybrids (2001) (0)
Assignment of an anonymous DNA sequence IB/D22 (DXS371) to XP11.1-11.4. (1989) (0)
Debrisoquine metabolism status as a risk factor of bladder cancer. (1992) (0)
Atypical CTSK transcripts and ARNT transcription read-through into CTSK: Research Articles (2005) (0)
Isolation of a DNA sequence (lambda EMBL 3.93, D9S37) from chromosome 9cen-qter detecting polymorphisms with TaqI and MspI. (1989) (0)
Report of the committee on the genetic constitution on chromosome 6. (1988) (0)
Index by Abstract Number (1989) (0)
Subject Index Vol. 89, 2000 (2000) (0)
Probe mapping and tumour breakpoint characterisation on chromosome 11. (1991) (0)
Studies in oncogenes. (1991) (0)
Localisation of human hepatocyte growth factor gene to chromosome 7 (1991) (0)

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