<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Davidson CM</submitter><funding>NICHD NIH HHS</funding><pagination>51-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2592548</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>The authors test single nucleotide polymorphisms (SNPs) in coding sequences of 12 candidate genes involved in glucose metabolism and obesity for associations with spina bifida. Genotyping was performed on 507 children with spina bifida and their parents plus anonymous control DNAs from Hispanic and Caucasian individuals. The transmission disequilibrium test was performed to test for genetic associations between transmission of alleles and spina bifida in the offspring (P &lt; .05). A statistically significant association between Lys481 of HK1 (G allele), Arg109Lys of LEPR (G allele), and Pro196 of GLUT1 (A allele) was found ( P = .019, .039, and .040, respectively). Three SNPs on 3 genes involved with glucose metabolism and obesity may be associated with increased susceptibility to spina bifida.</pubmed_abstract><journal>Reproductive sciences (Thousand Oaks, Calif.)</journal><pubmed_title>Genes in glucose metabolism and association with spina bifida.</pubmed_title><pmcid>PMC2592548</pmcid><funding_grant_id>P01 HD035946-10</funding_grant_id><funding_grant_id>P01 HD35946</funding_grant_id><funding_grant_id>P01 HD035946</funding_grant_id><funding_grant_id>P01 HD035946-09</funding_grant_id><pubmed_authors>Tyerman GH</pubmed_authors><pubmed_authors>Davidson CM</pubmed_authors><pubmed_authors>Northrup H</pubmed_authors><pubmed_authors>Fletcher JM</pubmed_authors><pubmed_authors>Townsend I</pubmed_authors><pubmed_authors>Au KS</pubmed_authors><pubmed_authors>King TM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genes in glucose metabolism and association with spina bifida.</name><description>The authors test single nucleotide polymorphisms (SNPs) in coding sequences of 12 candidate genes involved in glucose metabolism and obesity for associations with spina bifida. Genotyping was performed on 507 children with spina bifida and their parents plus anonymous control DNAs from Hispanic and Caucasian individuals. The transmission disequilibrium test was performed to test for genetic associations between transmission of alleles and spina bifida in the offspring (P &lt; .05). A statistically significant association between Lys481 of HK1 (G allele), Arg109Lys of LEPR (G allele), and Pro196 of GLUT1 (A allele) was found ( P = .019, .039, and .040, respectively). Three SNPs on 3 genes involved with glucose metabolism and obesity may be associated with increased susceptibility to spina bifida.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Jan</publication><modification>2021-02-19T19:52:53Z</modification><creation>2020-08-27T07:00:48Z</creation></dates><accession>S-EPMC2592548</accession><cross_references><pubmed>18212354</pubmed><doi>10.1177/1933719107309590</doi></cross_references></HashMap>