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Search Results to Susannah Spiess

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One or more keywords matched the following items that are connected to Spiess, Susannah

Item TypeName
Concept European Continental Ancestry Group
Academic Article Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Academic Article Genome-wide screen for atopy susceptibility alleles in the Hutterites.
Academic Article Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Academic Article Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom.
Academic Article Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians.
Academic Article Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene.
Academic Article Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians.
Academic Article Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses.
Academic Article Population-specific GSTM1 copy number variation.
Academic Article Identification of genetic variants and gene expression relationships associated with pharmacogenes in humans.
Academic Article Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines.
Academic Article Identification of common genetic variants that account for transcript isoform variation between human populations.
Academic Article Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.
Academic Article Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome.
Academic Article Population differences in microRNA expression and biological implications.
Academic Article Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.
Academic Article The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy.
Academic Article Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects.
Academic Article HLA-DR typing "at the DNA level": RFLPs and subtypes detected with a DR beta cDNA probe.
Academic Article Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry.
Academic Article Genetic architecture of transcript-level variation in humans.
Academic Article Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from the International Association of Diabetes and Pregnancy Study Groups.
Academic Article A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
Academic Article Identification of novel germline polymorphisms governing capecitabine sensitivity.
Academic Article The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships.
Academic Article Variation in the calpain-10 gene affects blood glucose levels in the British population.
Academic Article Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21.
Academic Article A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
Academic Article Genome-wide association study of Tourette's syndrome.
Academic Article Genome-wide association study of obsessive-compulsive disorder.
Academic Article Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival.
Academic Article Genome-wide interrogation of longitudinal FEV1 in children with asthma.
Academic Article A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
Academic Article The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.

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  • European Continental Ancestry Group