"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits. - Wikidata - wikimedia - TriplyDB

"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.

"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.

http://www.wikidata.org/entity/Q30334349

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The use of racial, ethnic, and ancestral categories in human genetics research USF1 on trial Functional consequences of PRODH missense mutations Epidemiological evidence for Mycobacterium avium subspecies paratuberculosis as a cause of Crohn's disease Comprehensive testing of positionally cloned asthma genes in two populations Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata Genetics and functional genomics of type 2 diabetes mellitus Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies Farm animal genomics and informatics: an update Bridging the gap between statistical and biological epistasis in Alzheimer's disease Recent Advances and Emerging Applications in Text and Data Mining for Biomedical Discovery Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease Accounting for population stratification in practice: a comparison of the main strategies dedicated to genome-wide association studies Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence Detection of gene x gene interactions in genome-wide association studies of human population data.Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.Reporting of human genome epidemiology (HuGE) association studies: an empirical assessment.Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.Do allelic variants of SLC6A14 predispose to obesity?Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.The future of association studies: gene-based analysis and replication.Recent developments in genomewide association scans: a workshop summary and review Association between HLA-DRB1 polymorphisms and pemphigus vulgaris: a meta-analysis Mycobacterium avium paratuberculosis and the etiology of Crohn's disease: a review of the controversy from the clinician's perspective Obesity-susceptibility loci and their influence on adiposity-related traits in transition from adolescence to adulthood--the HUNT study The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.Prevalence of disorders recorded in dogs attending primary-care veterinary practices in England.A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population Genetics and public health--evolution, or revolution?Factors affecting statistical power in the detection of genetic association.Genetic variations of tubular sodium reabsorption leading to "primary" hypertension: from gene polymorphism to clinical symptoms.Genomics and cardiovascular disease.Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer.Case-control genetic association studies in gastrointestinal disease: review and recommendations.Characterizing differential individual response to porcine reproductive and respiratory syndrome virus infection through statistical and functional analysis of gene expression.Pharmacology and statistics: recommendations to strengthen a productive partnership.Apolipoprotein E ε4 Allele was Associated With Nonlesional Mesial Temporal Lobe Epilepsy in Han Chinese Population.On the synthesis and interpretation of consistent but weak gene-disease associations in the era of genome-wide association studies.Recent development in pharmacogenomics: from candidate genes to genome-wide association studies.

P2860

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P2860

"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.

http://www.wikidata.org/entity/Q30334349

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2003 nî lūn-bûn

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2003 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2003 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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American Journal of Human Genetics

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"Are we there yet?": Deciding ...... eases and quantitative traits.

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P2093

Grier P Page

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Patricia Z Page

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Rodney C Go

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Varghese George

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P2860

Control of confounding of genetic associations in stratified populations

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.

Viruses and Koch's Postulates

Sequence-based identification of microbial pathogens: a reconsideration of Koch's postulates

Sequential tests for the detection of linkage

Statistical significance for genomewide studies

The environment and disease: association or causation? 1965.

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Point: population stratification: a problem for case-control studies of candidate-gene associations?

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10.1086/378900

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David B. Allison

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2003-09-17T00:00:00Z

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9885602

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