21 results for author:"Haites N." in Literature citations
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| A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions. De Palma G., Dick F.D., Calzetti S., Scott N.W., Prescott G.J., Osborne A., Haites N., Mozzoni P., Negrotti A., Scaglioni A. et al. Mov. Disord. 25:912-919(2010) · Mapped (104) |
| Oral contraceptive use and BRCA penetrance: a case-only study. Pasanisi P., Hedelin G., Berrino J., Chang-Claude J., Hermann S., Steel M., Haites N., Hart J., Peled R., Gafa L. et al. Cancer Epidemiol. Biomarkers Prev. 18:2107-2113(2009) · Mapped (18) |
| No evidence that GATA3 rs570613 SNP modifies breast cancer risk. Breast Cancer Association Consortium and Consortium of Investigators of Modifiers of BRCA1/2 Breast Cancer Res. Treat. 117:371-379(2009) · Mapped (55) |
| Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene, intakes of folate and related B vitamins and colorectal cancer: a case-control study in a population with relatively low folate intake. Sharp L., Little J., Brockton N.T., Cotton S.C., Masson L.F., Haites N.E., Cassidy J. Br. J. Nutr. 99:379-389(2008) · Mapped (6) |
| Gene-environment interactions in parkinsonism and Parkinson's disease: the Geoparkinson study. Dick F.D., De Palma G., Ahmadi A., Osborne A., Scott N.W., Prescott G.J., Bennett J., Semple S., Dick S., Mozzoni P. et al. Occup Environ Med 64:673-680(2007) · Mapped (103) |
| Colorectal cancer and genetic polymorphisms of CYP1A1, GSTM1 and GSTT1: a case-control study in the Grampian region of Scotland. Little J., Sharp L., Masson L.F., Brockton N.T., Cotton S.C., Haites N.E., Cassidy J. Int. J. Cancer 119:2155-2164(2006) · Mapped (21) |
| Effect of B vitamins and genetics on success of in-vitro fertilisation: prospective cohort study. Haggarty P., McCallum H., McBain H., Andrews K., Duthie S., McNeill G., Templeton A., Haites N., Campbell D., Bhattacharya S. Lancet 367:1513-1519(2006) · Mapped (6) |
| Length and somatic mosaicism of CAG and GGN repeats in the androgen receptor gene and the risk of prostate cancer in men with benign prostatic hyperplasia. Tayeb M.T., Clark C., Murray G.I., Sharp L., Haites N.E., McLeod H.L. Ann Saudi Med 24:21-26(2004) · Mapped (11) |
| Vitamin D receptor, HER-2 polymorphisms and risk of prostate cancer in men with benign prostate hyperplasia. Tayeb M.T., Clark C., Haites N.E., Sharp L., Murray G.I., McLeod H.L. Saudi Med J 25:447-451(2004) · Mapped (14) |
| A rapid method of screening for N-acetyltransferase (NAT2) phenotype by use of the WAVE DNA fragment analysis system. Osborne A., Bell C., Grant F., Dick F., Seaton A., Haites N. Biochem. Genet. 41:405-411(2003) · Mapped (18) |
| Folate and breast cancer: the role of polymorphisms in methylenetetrahydrofolate reductase (MTHFR). Sharp L., Little J., Schofield A.C., Pavlidou E., Cotton S.C., Miedzybrodzka Z., Baird J.O., Haites N.E., Heys S.D., Grubb D.A. Cancer Lett. 181:65-71(2002) · Mapped (6) |
| Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy. Moller P., Borg A., Evans D.G., Haites N., Reis M.M., Vasen H., Anderson E., Steel C.M., Apold J., Goudie D. et al. Int. J. Cancer 101:555-559(2002) · Mapped (18) |
| Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review. Morrison E.R., Miedzybrodzka Z.H., Campbell D.M., Haites N.E., Wilson B.J., Watson M.S., Greaves M., Vickers M.A. Thromb. Haemost. 87:779-785(2002) · Mapped (35) |
| CYP3A4 promoter variant is associated with prostate cancer risk in men with benign prostate hyperplasia. Tayeb M.T., Clark C., Sharp L., Haites N.E., Rooney P.H., Murray G.I., Payne S.N., McLeod H.L. Oncol. Rep. 9:653-655(2002) · Mapped (8) |
| Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1alpha gene: implications for predictive testing. Miedzybrodzka Z., Hattersley A.T., Ellard S., Pearson D., de Silva D., Harvey R., Haites N. Eur. J. Hum. Genet. 7:729-732(1999) · UniProtKB (1) |
| Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. Nelis E., Haites N., van Broeckhoven C. Hum. Mutat. 13:11-28(1999) · UniProtKB (3) |
| ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Stankovic T., Kidd A.M.J., Sutcliffe A., McGuire G.M., Robinson P., Weber P., Bedenham T., Bradwell A.R., Easton D.F., Lennox G.G. et al. Am. J. Hum. Genet. 62:334-345(1998) · UniProtKB (1) |
| Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. Wicking C., Shanley S., Smyth I., Gillies S., Negus K., Graham S., Suthers G., Haites N., Edwards M., Wainwright B.J. et al. Am. J. Hum. Genet. 60:21-26(1997) · UniProtKB (1) |
| Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposis. de Silva D.C., Wright M.F., Stevenson D.A., Clark C., Gray E.S., Holmes J.D., Dean J.C., Haites N.E., Dunlop M.G. Cancer 77:972-976(1996) · Mapped (10) |
| Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1). Fairweather N., Bell C., Cochrane S., Chelly J., Wang S., Mostacciuolo M.L., Monaco A.P., Haites N.E. Hum. Mol. Genet. 3:29-34(1994) · UniProtKB (1) |
| Nitric oxide production by human proximal tubular cells: a novel immunomodulatory mechanism? McLay J.S., Chatterjee P., Nicolson A.G., Jardine A.G., McKay N.G., Ralston S.H., Grabowski P., Haites N.E., Macleod A.M., Hawksworth G.M. Kidney Int. 46:1043-1049(1994) · UniProtKB (1) |