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New approaches to investigating heterogeneity in complex traits

New approaches to investigating heterogeneity in complex traits

http://www.wikidata.org/entity/Q35200318

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Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders Three allele combinations associated with multiple sclerosis Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis Polymorphisms in the mu-opioid receptor gene (OPRM1) and the implications for alcohol dependence in humans.Risk conferring genes in multiple sclerosis.A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.Common gene-network signature of different neurological disorders and their potential implications to neuroAIDS.The challenge of implementing genetic tests with clinical utility while avoiding unsound applications.Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity

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P2860

New approaches to investigating heterogeneity in complex traits

http://www.wikidata.org/entity/Q35200318

description

2003 nî lūn-bûn

@nan

2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

New approaches to investigating heterogeneity in complex traits

@ast

New approaches to investigating heterogeneity in complex traits

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type

label

New approaches to investigating heterogeneity in complex traits

@ast

New approaches to investigating heterogeneity in complex traits

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prefLabel

New approaches to investigating heterogeneity in complex traits

@ast

New approaches to investigating heterogeneity in complex traits

@en

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Journal of Medical Genetics

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New approaches to investigating heterogeneity in complex traits

@en

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P E Kovanen

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R Bomprezzi

http://www.w3.org/2001/XMLSchema#string

P2860

Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II

Initial sequencing and comparative analysis of the mouse genome

A comprehensive review of genetic association studies

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

The transmission/disequilibrium test: history, subdivision, and admixture

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling

A gene-expression signature as a predictor of survival in breast cancer

Quantitative monitoring of gene expression patterns with a complementary DNA microarray

Printing proteins as microarrays for high-throughput function determination

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553-559

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8

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