Search Results - "Diehl, S R"

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    The Genetics of Schizophrenia: A Current, Genetic-Epidemiologic Perspective by Kendler, Kenneth S., Diehl, Scott R.

    Published in Schizophrenia bulletin (1993)
    “…In the "Special Report on Schizophrenia" published in the Schizophrenia Bulletin in 1987, the genetic basis of schizophrenia was reviewed. Here, we provide our…”
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    Correlates of anti-EBV EBNA1 IgA positivity among unaffected relatives from nasopharyngeal carcinoma multiplex families by Chang, C M, Yu, K J, Hsu, W L, Major, J M, Chen, J Y, Lou, P J, Liu, M Y, Diehl, S R, Goldstein, A M, Chen, C J, Hildesheim, A

    Published in British journal of cancer (03-01-2012)
    “…Background: To determine whether non-viral nasopharyngeal carcinoma (NPC) risk factors might be associated with (and mediated through) Epstein–Barr virus (EBV)…”
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    Factors Associated with Delay in the Diagnosis of Oral Cancer by Pitiphat, W., Diehl, S.R., Laskaris, G., Cartsos, V., Douglass, C.W., Zavras, A.I.

    Published in Journal of dental research (01-03-2002)
    “…Early detection and treatment improve the prognosis for oral cancer. Delays from the onset of symptoms to clinical diagnosis are common. Our aim is to identify…”
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    Smoking and alcohol in the etiology of oral cancer: gender-specific risk profiles in the south of Greece by Zavras, A.I, Douglass, C.W, Joshipura, K, Wu, T, Laskaris, G, Petridou, E, Dokianakis, G, Segas, J, Lefantzis, D, Nomikos, P, Wang, Y.F, Diehl, S.R

    Published in Oral oncology (2001)
    “…Oral and pharyngeal cancer (OC) mortality is very low in Greece, especially among men, compared to other European countries. We conducted a case-control study…”
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    Evidence of a Substantial Genetic Basis for IgG2 Levels in Families with Aggressive Periodontitis by Diehl, S.R., Wu, T., Burmeister, J.A., Califano, J.V., Brooks, C.N., Tew, J.G., Schenkein, H.A.

    Published in Journal of dental research (01-09-2003)
    “…IgG2 is elevated in localized but not in generalized aggressive periodontitis (AgP). Exposure to pathogenic bacteria is essential for disease. Immune responses…”
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    Application of automated DNA sizing technology for genotyping microsatellite loci by Ziegle, J S, Su, Y, Corcoran, K P, Nie, L, Mayrand, P E, Hoff, L B, McBride, L J, Kronick, M N, Diehl, S R

    Published in Genomics (San Diego, Calif.) (01-12-1992)
    “…Highly polymorphic microsatellite loci offer great promise for gene mapping studies, but fulfillment of this potential will require substantial improvements in…”
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    Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24–25 by Geremek, M, Ziętkiewicz, E, Diehl, S R, Alizadeh, B Z, Wijmenga, C, Witt, M

    Published in Journal of medical genetics (01-01-2006)
    “…Background: Primary ciliary dyskinesia (PCD) is a genetic disorder caused by ciliary immotility/dysmotility due to ultrastructural defects of the cilia…”
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    Phenotypic Variation in Waardenburg Syndrome: Mutational Heterogeneity, Modifier Genes or Polygenic Background? by Pandya, Arti, Xia, Xia-Juan, Landa, Barbara L., Arnos, Kathleen S., Israel, Jamie, Lloyd, Joyce, James, Anthony L., Diehl, Scott R., Blanton, Susan H., Nance, Walter E.

    Published in Human molecular genetics (01-04-1996)
    “…We have identified 11 mutational changes in the PAX3 gene in patients with type 1 Waardenburg syndrome (WS1) including three in the paired domain, six within…”
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    Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23 by Wang, S, Detera-Wadleigh, S D, Coon, H, Sun, C E, Goldin, L R, Duffy, D L, Byerley, W F, Gershon, E S, Diehl, S R

    Published in American journal of human genetics (01-09-1996)
    “…Schizophrenia and the closely related phenotype schizo-affective disorder are severe mental illnesses that affect >1.0% of the population. The major role that…”
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    Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome by REYNOLDS, J. E, MARAZITA, M. L, MEYER, J. M, STEVENS, C. A, EAVES, L. J, ARNOS, K. S, PLOUGHMAN, L. M, MACLEAN, C, NANCE, W. E, DIEHL, S. R

    Published in American journal of human genetics (01-02-1996)
    “…We used segregation analysis to investigate the genetic basis of variation in dystopia canthorum, one of the key diagnostic features of Waardenburg syndrome…”
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    Associations Between Serum Antibody Levels to Periodontal Pathogens and Early‐Onset Periodontitis by Albandar, Jasim M., DeNardin, Ann M, Adesanya, Margo R., Diehl, Scott R., Winn, Deborah M.

    Published in Journal of periodontology (1970) (01-11-2001)
    “…Background: The role of antibodies to periodontal microorganisms in the development of periodontal tissue destruction is still unclear. The aim of this study…”
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    Reevaluation of the chromosome 4q candidate region for early onset periodontitis by HART, T. C, MARAZITA, M. L, MCCANNA, K. M, SCHENKEIN, H. A, DIEHL, S. R

    Published in Human genetics (01-06-1993)
    “…Evidence of linkage (lod = 3.1, theta = 0.05) was reported previously in one large kindred (the Brandywine genetic isolate) for an autosomal dominant form of…”
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    Distribution of lod scores under uncertain mode of inheritance by MACLEAN, C. J, BISHOP, D. T, SHERMAN, S. L, DIEHL, S. R

    Published in American journal of human genetics (01-02-1993)
    “…We consider probability distributions of alternative lod statistics, differing in their treatment of segregation parameters when mode of inheritance is…”
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    Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22 by Wang, Shengbiao, Ziegle, Janet S, Goldin, Lynn R, Walczak, Cynthia A, Diehl, Scott R, Kipps, Barbara R, Sun, Cui-e

    Published in Nature genetics (01-05-1995)
    “…We have performed linkage analysis in 186 multiplex families to search for genes that predispose to schizophrenia. Under a model with partially dominant…”
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    Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line by REYNOLDS, J. E, FLETCHER, J. A, LYTLE, C. H, LI NIE, MORTON, C. C, DIEHL, S. R

    Published in Human genetics (01-12-1992)
    “…Malignant schwannomas are soft-tissue neoplasms that occur at increased frequency with germline alterations of the neurofibromatosis-1 (NF1) gene at 17q11.2…”
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    Strategies for Linkage Studies of Schizophrenia: Pedigrees, DNA Markers, and Statistical Analyses by Diehl, Scott R., Kendler, Kenneth S.

    Published in Schizophrenia bulletin (1989)
    “…A current overview of the genetics of schizophrenia is presented. Recently reported linkage studies of schizophrenia using polymorphic DNA markers are…”
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