Mapping rare and common causal alleles for complex human diseases.
about
Molecular mechanisms of disease-causing missense mutationsGenetics and epigenetics of rheumatoid arthritisAssociation, interaction, and replication analysis of genes encoding serotonin transporter and 5-HT3 receptor subunits A and B in alcohol dependenceTargeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseA weighted U-statistic for genetic association analyses of sequencing data.Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's diseaseLaying a solid foundation for Manhattan--'setting the functional basis for the post-GWAS era'.Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.SNPsea: an algorithm to identify cell types, tissues and pathways affected by risk loci.Functional analysis of variance for association studies.Genetics of human cardiovascular diseaseThe marriage of quantitative genetics and cell biology: a novel screening approach reveals people have genetically encoded variation in microtubule stability.Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study.Functional coding variants in SLC6A15, a possible risk gene for major depression.Understanding human variation in infectious disease susceptibility through clinical and cellular GWAS.A genome-wide association study of seed protein and oil content in soybean.Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes.Genomic variations and distinct evolutionary rate of rare alleles in Arabidopsis thaliana.Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility.Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell TraitsConstruction of an integrative regulatory element and variation map of the murine Tst locus.Phenotypic Characterization and Genetic Dissection of Growth Period Traits in Soybean (Glycine max) Using Association Mapping.The eQTL-missense polymorphisms of APOBEC3H are associated with lung cancer risk in a Han Chinese population.Immune system gene dysregulation in autism and schizophrenia.Synthesizing genome-wide association studies and expression microarray reveals novel genes that act in the human growth plate to modulate height.Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity.Hunting human disease genes: lessons from the past, challenges for the future.Multi-Population Selective Genotyping to Identify Soybean [Glycine max (L.) Merr.] Seed Protein and Oil QTLsA genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.Novel CYP2A6 variants identified in African Americans are associated with slow nicotine metabolism in vitro and in vivo.Current understanding of human genetics and genetic analysis of psoriasis.Recent approaches to the prioritization of candidate disease genes.Genome-wide association studies of hematologic phenotypes: a window into human hematopoiesis.Using chromatin marks to interpret and localize genetic associations to complex human traits and diseases.Translating human genetics into mouse: the impact of ultra-rapid in vivo genome editing.Interpreting functional effects of coding variants: challenges in proteome-scale prediction, annotation and assessment.Molecular basis of β thalassemia and potential therapeutic targets.Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†.Role of the p.E66Q variant of GLA in the progression of chronic kidney disease.Complement factor H in AMD: Bridging genetic associations and pathobiology.
P2860
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P2860
Mapping rare and common causal alleles for complex human diseases.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Mapping rare and common causal alleles for complex human diseases.
@en
type
label
Mapping rare and common causal alleles for complex human diseases.
@en
prefLabel
Mapping rare and common causal alleles for complex human diseases.
@en
P2860
P1433
P1476
Mapping rare and common causal alleles for complex human diseases.
@en
P2093
Soumya Raychaudhuri
P2860
P356
10.1016/J.CELL.2011.09.011
P407
P577
2011-09-01T00:00:00Z