Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.
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CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMDMaternal and fetal genetic associations of PTGER3 and PON1 with preterm birthAsthma and genes encoding components of the vitamin D pathwayA CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritisKynurenine 3-monooxygenase polymorphisms: relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controlsThe role of LTA4H and ALOX5AP genes in the risk for asthma in LatinosConfirmation of association between multiple sclerosis and CYP27B1A genome-wide association study of autism reveals a common novel risk locus at 5p14.1Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaDisruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lipTwo variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorderFine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritisAn imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingGenetic association analysis of ATP binding cassette protein family reveals a novel association of ABCB1 genetic variants with epilepsy risk, but not with drug-resistanceRestless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonTwo new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groupsA comprehensive family-based replication study of schizophrenia genesOligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes.Common variants of the G protein-coupled receptor type 4 are associated with human essential hypertension and predict the blood pressure response to angiotensin receptor blockade.Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music.Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.Susceptibility locus in neurokinin-1 receptor gene associated with alcohol dependence.Transcription factor SP4 is a susceptibility gene for bipolar disorderHigh-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesANK3 as a risk gene for schizophrenia: new data in Han Chinese and meta analysis.Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior.Comparison of methods to account for relatedness in genome-wide association studies with family-based data.Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiologyTesting for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traitsSNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children.Missing data imputation and haplotype phase inference for genome-wide association studies.Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche.Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.A new method to account for missing data in case-parent triad studies.Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia.
P2860
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P2860
Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.
description
2008 nî lūn-bûn
@nan
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Likelihood-based association a ...... ts with missing genotype data.
@ast
Likelihood-based association a ...... ts with missing genotype data.
@en
type
label
Likelihood-based association a ...... ts with missing genotype data.
@ast
Likelihood-based association a ...... ts with missing genotype data.
@en
prefLabel
Likelihood-based association a ...... ts with missing genotype data.
@ast
Likelihood-based association a ...... ts with missing genotype data.
@en
P2860
P356
P1433
P1476
Likelihood-based association a ...... ts with missing genotype data.
@en
P2860
P356
10.1159/000119108
P577
2008-03-31T00:00:00Z