Search Results - "Hill, Lori D"

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  1. 1

    Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study by Hill, Lori D, Hilliard, DaShaunda D, York, Timothy P, Srinivas, Sindhu, Kusanovic, Juan P, Gomez, Ricardo, Elovitz, Michal A, Romero, Roberto, Strauss, 3rd, Jerome F

    Published in BMC medical genetics (11-05-2011)
    “…Preeclampsia affects 3-8% of pregnancies and is a major cause of maternal and perinatal morbidity and mortality worldwide. This complex disorder is…”
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    Journal Article
  2. 2

    Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse? by Chen, Chen, MD, Hill, Lori D., BS, Schubert, Christine M., PhD, Strauss, Jerome F., MD, PhD, Matthews, Catherine A., MD

    “…Objective We sought to determine allele frequencies of 3 LAMC1 single nucleotide polymorphisms (SNPs) in Caucasian and African American (AA) women with stage >…”
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    Journal Article Conference Proceeding
  3. 3

    Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia by Hill, Lori D, York, Timothy P, Kusanovic, Juan P, Gomez, Ricardo, Eaves, Lindon J, Romero, Roberto, Strauss, 3rd, Jerome F

    Published in PloS one (31-01-2011)
    “…Preeclampsia is a leading cause of perinatal morbidity and mortality. This disorder is thought to be multifactorial in origin, with multiple genes,…”
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    Journal Article
  4. 4

    Genetic variation in SPAG16 regions encoding the WD40 repeats is not associated with reduced sperm motility and axonemal defects in a population of infertile males by Nagarkatti-Gude, David R, Collodel, Giulia, Hill, Lori D, Moretti, Elena, Geminiani, Michela, Zhang, Zhibing, Strauss, 3rd, Jerome F

    Published in BMC urology (10-09-2012)
    “…SPAG16 is a critical structural component of motile cilia and flagella. In the eukaryotic unicellular algae Chlamydomonas, loss of gene function causes…”
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    Journal Article
  5. 5

    Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome by Hill, Lori D., Ewens, Kathryn G., Maher, Brion S., York, Timothy P., Legro, Richard S., Dunaif, Andrea, Strauss, Jerome F.

    Published in Molecular and cellular endocrinology (05-03-2012)
    “…► Catechol-O-methyltransferase gene (COMT) variants are not significantly associated with polycystic ovary syndrome. ► No significant correlations between COMT…”
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    Journal Article
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    Connective Tissue and Related Disorders and Preterm Birth: Clues to Genes Contributing to Prematurity by Anum, E.A, Hill, L.D, Pandya, A, Strauss, J.F

    Published in Placenta (Eastbourne) (01-03-2009)
    “…Abstract To identify candidate genes contributing to preterm birth, we examined the existing literature on the association between known disorders of…”
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    Journal Article
  11. 11

    Racial differences in the genetics of preeclampsia by Hill, Lori D

    Published 01-01-2011
    “…Preeclampsia (PE), characterized by hypertension and proteinuria after 20 weeks of gestation, affects 5-8% of pregnancies worldwide. Although preeclampsia is a…”
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    Dissertation