21 results for author:"Green J.S." in Literature citations
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| Inherited deleterious variants in GALNT12 are associated with CRC susceptibility. Clarke E., Green R.C., Green J.S., Mahoney K., Parfrey P.S., Younghusband H.B., Woods M.O. |
| Increased cancer predisposition in family members of colorectal cancer patients harboring the p.V600E BRAF mutation: a population-based study. Wish T.A., Hyde A.J., Parfrey P.S., Green J.S., Younghusband H.B., Simms M.I., Fontaine D.G., Dicks E.L., Stuckless S.N., Gallinger S. et al. Cancer Epidemiol. Biomarkers Prev. 19:1831-1839(2010) · Mapped (26) |
| Short-term residential cardiac rehabilitation reduces B-type natriuretic peptide. Berent R., von Duvillard S.P., Crouse S.F., Auer J., Green J.S., Sinzinger H., Schmid P. Eur J Cardiovasc Prev Rehabil 16:603-608(2009) · Mapped (1) |
| Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. Doucette L., Merner N.D., Cooke S., Ives E., Galutira D., Walsh V., Walsh T., MacLaren L., Cater T., Fernandez B. et al. Eur. J. Hum. Genet. 17:554-564(2009) · Mapped (10) |
| The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome. Stuckless S., Parfrey P.S., Woods M.O., Cox J., Fitzgerald G.W., Green J.S., Green R.C. Fam. Cancer 6:1-12(2007) · Mapped (12) |
| Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies. Green R.C., Green J.S., Buehler S.K., Robb J.D., Daftary D., Gallinger S., McLaughlin J.R., Parfrey P.S., Younghusband H.B. Fam. Cancer 6:53-62(2007) · Mapped (22) |
| High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes. Woods M.O., Hyde A.J., Curtis F.K., Stuckless S., Green J.S., Pollett A.F., Robb J.D., Green R.C., Croitoru M.E., Careen A. et al. Clin. Cancer Res. 11:6853-6861(2005) · Mapped (48) |
| Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet-Biedl syndrome 1 critical interval. Fan Y., Green J.S., Ross A.J., Beales P.L., Parfrey P.S., Davidson W.S. Hum. Genet. 116:62-71(2005) · Mapped (8) |
| Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome. Fan Y., Esmail M.A., Ansley S.J., Blacque O.E., Boroevich K., Ross A.J., Moore S.J., Badano J.L., May-Simera H., Compton D.S. et al. |
| Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Li J.B., Gerdes J.M., Haycraft C.J., Fan Y., Teslovich T.M., May-Simera H., Li H., Blacque O.E., Li L., Leitch C.C. et al. |
| Bardet-Biedl syndrome 1 genotype and obesity in the Newfoundland population. Fan Y., Rahman P., Peddle L., Hefferton D., Gladney N., Moore S.J., Green J.S., Parfrey P.S., Davidson W.S. Int. J. Obes. Relat. Metab. Disord. 28:680-684(2004) · Mapped (9) |
| Germline hMLH1 promoter mutation in a Newfoundland HNPCC kindred. Green R.C., Green A.G., Simms M., Pater A., Robb J.D., Green J.S. Clin. Genet. 64:220-227(2003) · Mapped (30) |
| Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1. Eichers E.R., Green J.S., Stockton D.W., Jackman C.S., Whelan J., McNamara J.A., Johnson G.J., Lupski J.R., Katsanis N. Am. J. Hum. Genet. 70:955-964(2002) · UniProtKB (1) |
| Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci. Beales P.L., Katsanis N., Lewis R.A., Ansley S.J., Elcioglu N., Raza J., Woods M.O., Green J.S., Parfrey P.S., Davidson W.S. et al. Am. J. Hum. Genet. 68:606-616(2001) · UniProtKB (1) |
| Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome. Katsanis N., Beales P.L., Woods M.O., Lewis R.A., Green J.S., Parfrey P.S., Ansley S.J., Davidson W.S., Lupski J.R. |
| Mutations in MKKS cause Bardet-Biedl syndrome. Slavotinek A.M., Stone E.M., Mykytyn K., Heckenlively J.R., Green J.S., Heon E., Musarella M.A., Parfrey P.S., Sheffield V.C., Biesecker L.G. Nat. Genet. 26:15-16(2000) · UniProtKB (1) |
| Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity. Oh J., Ho L., Ala-Mello S., Amato D., Armstrong L., Bellucci S., Carakushansky G., Ellis J.P., Fong C.-T., Green J.S. et al. Am. J. Hum. Genet. 62:593-598(1998) · UniProtKB (1) |
| Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Agarwal S.K., Kester M.B., Debelenko L.V., Heppner C., Emmert-Buck M.R., Skarulis M.C., Doppman J.L., Kim Y.S., Lubensky I.A., Zhuang Z. et al. Hum. Mol. Genet. 6:1169-1175(1997) · UniProtKB (1) |
| Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. Maher E.R., Webster A.R., Richards F.M., Green J.S., Crossey P.A., Payne S.J., Moore A.T. J. Med. Genet. 33:328-332(1996) · UniProtKB (1) |
| Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. Crossey P.A., Richards F.M., Foster K., Green J.S., Prowse A., Latif F., Lerman M.I., Zbar B., Affara N.A., Ferguson-Smith M.A. et al. Hum. Mol. Genet. 3:1303-1308(1994) · UniProtKB (1) |
| Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype. Chen F., Kishida T., Yao M., Hustad T., Glavac D., Dean M., Gnarra J.R., Orcutt M.L., Duh F.-M., Glenn G. et al. Hum. Mutat. 5:66-75(1995) · UniProtKB (1) |