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Spiess, Susannah

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

Item Type	Name
Concept	Polymorphism, Single Nucleotide
Academic Article	Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
Academic Article	A statistical method for identification of polymorphisms that explain a linkage result.
Academic Article	Methods for analysis and visualization of SNP genotype data for complex diseases.
Academic Article	Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population.
Academic Article	Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
Academic Article	Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33.
Academic Article	Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene.
Academic Article	Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
Academic Article	Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses.
Academic Article	Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.
Academic Article	Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
Academic Article	SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report.
Academic Article	Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1.
Academic Article	Interpreting P values in pharmacogenetic studies: a call for process and perspective.
Academic Article	Evaluation of genetic variation contributing to differences in gene expression between populations.
Academic Article	Population-specific GSTM1 copy number variation.
Academic Article	SNPinProbe_1.0: a database for filtering out probes in the Affymetrix GeneChip human exon 1.0 ST array potentially affected by SNPs.
Academic Article	Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans.
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	The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution.
Academic Article	The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
Academic Article	Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes.
Academic Article	Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci.
Academic Article	SCAN: SNP and copy number annotation.
Academic Article	Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS.
Academic Article	Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci.
Academic Article	Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping.
Academic Article	Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.
Academic Article	Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia.
Academic Article	The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
Academic Article	Population differences in microRNA expression and biological implications.
Academic Article	Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients.
Academic Article	Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
Academic Article	Genome-wide meta-analysis for severe diabetic retinopathy.
Academic Article	Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry.
Academic Article	Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.
Academic Article	Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium.
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	Replication analysis for severe diabetic retinopathy.
Academic Article	Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.
Academic Article	Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture?
Academic Article	Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
Academic Article	Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer.
Academic Article	Genetic architecture of transcript-level variation in humans.
Academic Article	PACdb: a database for cell-based pharmacogenomics.
Academic Article	Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas.
Academic Article	Power and sample size calculations for SNP association studies with censored time-to-event outcomes.
Academic Article	Clinical translation of cell-based pharmacogenomic discovery.
Academic Article	Copy number polymorphisms and anticancer pharmacogenomics.
Academic Article	Variants affecting exon skipping contribute to complex traits.
Academic Article	Concordant gene expression in leukemia cells and normal leukocytes is associated with germline cis-SNPs.
Academic Article	FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3.
Academic Article	Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility.
Academic Article	A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.
Academic Article	Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset.
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 study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
Academic Article	The use of genomic information to optimize cancer chemotherapy.
Academic Article	Identification of novel germline polymorphisms governing capecitabine sensitivity.
Academic Article	A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
Academic Article	Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
Academic Article	Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
Academic Article	Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.
Academic Article	Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans.
Academic Article	Genetic architecture of microRNA expression: implications for the transcriptome and complex traits.
Academic Article	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Academic Article	Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
Academic Article	Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy.
Academic Article	Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
Academic Article	Genome-wide association study of Tourette's syndrome.
Academic Article	Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.
Academic Article	A genome-wide association study of breast cancer in women of African ancestry.
Academic Article	Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases.
Academic Article	Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients.
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	A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.
Academic Article	A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
Academic Article	Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.
Academic Article	Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Academic Article	Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients.
Academic Article	Genome wide association studies for diabetes: perspective on results and challenges.

Search Criteria

Polymorphism Single Nucleotide