Design of Case-controls Studies with Unscreened Controls
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Lung cancer susceptibility model based on age, family history and genetic variantsThe Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophreniaA genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisConvergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaIndividual and cumulative effects of GWAS susceptibility loci in lung cancer: associations after sub-phenotyping for COPDGenome-wide association study of Alzheimer's disease with psychotic symptomsUsing public control genotype data to increase power and decrease cost of case-control genetic association studies.Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locusCommon Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of EndometriosisCommon variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical resultsOn the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3.Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility geneStrong evidence that GNB1L is associated with schizophrenia.Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.Genome-wide association scan for variants associated with early-onset prostate cancerThirty-five common variants for coronary artery disease: the fruits of much collaborative labourMeta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder.Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder.The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma riskGenetic evidence linking lung cancer and COPD: a new perspectiveAssociation of bone morphogenetic proteins with otosclerosis.Regulatory regions of the paraoxonase 1 (PON1) gene are associated with neovascular age-related macular degeneration (AMD).Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.The Machado-Joseph disease-associated mutant form of ataxin-3 regulates parkin ubiquitination and stability.Designing case-control studies: decisions about the controls.GSTM1 null genotype in COPD and lung cancer: evidence of a modifier or confounding effect?FAM13A locus in COPD is independently associated with lung cancer - evidence of a molecular genetic link between COPD and lung cancer.An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction.IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.On rare-variant analysis in population-based designs: decomposing the likelihood to two informative components.Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries.Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions.
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Design of Case-controls Studies with Unscreened Controls
description
im September 2005 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у вересні 2005
@uk
name
Design of Case-controls Studies with Unscreened Controls
@en
Design of Case-controls Studies with Unscreened Controls
@nl
type
label
Design of Case-controls Studies with Unscreened Controls
@en
Design of Case-controls Studies with Unscreened Controls
@nl
prefLabel
Design of Case-controls Studies with Unscreened Controls
@en
Design of Case-controls Studies with Unscreened Controls
@nl
P2093
P2860
P1476
Design of Case-controls Studies with Unscreened Controls
@en
P2093
K. M. Schmidt
N. Craddock
V. Moskvina
P2860
P304
P356
10.1111/J.1529-8817.2005.00175.X
P407
P577
2005-09-01T00:00:00Z