Search Results - "Jammulapati, S"

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  1. 1

    Patterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancer by Abkevich, V, Timms, K M, Hennessy, B T, Potter, J, Carey, M S, Meyer, L A, Smith-McCune, K, Broaddus, R, Lu, K H, Chen, J, Tran, T V, Williams, D, Iliev, D, Jammulapati, S, FitzGerald, L M, Krivak, T, DeLoia, J A, Gutin, A, Mills, G B, Lanchbury, J S

    Published in British journal of cancer (06-11-2012)
    “…Background: Defects in BRCA1 , BRCA2 , and other members of the homologous recombination pathway have potential therapeutic relevance when used to support…”
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  2. 2

    Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression by Neff, C D, Abkevich, V, Packer, J C L, Chen, Y, Potter, J, Riley, R, Davenport, C, DeGrado Warren, J, Jammulapati, S, Bhathena, A, Choi, W S, Kroeger, P E, Metzger, R E, Gutin, A, Skolnick, M H, Shattuck, D, Katz, D A

    Published in Molecular psychiatry (01-06-2009)
    “…The HTR1A −1019C>G genotype was associated with major depression in the Utah population. Linkage analysis on Utah pedigrees with strong family histories of…”
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    Abstract P5-10-02: Development and validation of a polygenic score to predict breast cancer risk in unaffected Hispanic women negative for mutations on a multi-gene hereditary cancer panel by Hughes, ER, Wagner, S, Pruss, D, Gallagher, SK, Swedlund, B, Bulka, K, Hoff, R, Jammulapati, S, Morris, B, Perry, T, Lanchbury, JS, Gutin, A

    Published in Cancer research (Chicago, Ill.) (15-02-2019)
    “…Abstract Background: Breast cancer (BC) is the most commonly diagnosed cancer and the leading cause of cancer-related death among Hispanic women in the United…”
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  6. 6

    A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree by TIMMS, Kirsten M, WAGNER, Susanne, SAMUELS, Mark E, FORBEY, Kristian, GOLDFINE, Howard, JAMMULAPATI, Srikanth, SKOLNICK, Mark H, HOPKINS, Paul N, HUNT, Steve C, SHATTUCK, Donna M

    Published in Human genetics (01-03-2004)
    “…Familial hypercholesterolemia results from mutations in the low-density lipoprotein (LDL) receptor or apolipoprotein B genes. We have previously reported the…”
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    Low incidence of BRCA2 mutations in breast carcinoma and other cancers by Teng, David H.-R, Bogden, Robert, Mitchell, Jeffrey, Baumgard, Michelle, Bell, Russell, Berry, Simin, Davis, Thaylon, Ha, Phuong C, Kehrer, Robert, Jammulapati, Srikanth, Chen, Qian, Offit, Kenneth, Skolnick, Mark H, Tavtigian, Sean V, Jhanwar, Suresh, Swedlund, Brad, Wong, Alexander K.C, Kamb, Alexander

    Published in Nature genetics (01-06-1996)
    “…Inherited mutant alleles of familial tumour suppressor genes predispose individuals to particular types of cancer. In addition to an involvement in inherited…”
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