about
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosisPolymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophreniaGenomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesGenome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair StudyLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseNo significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric geneticsNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesComprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studySingle-marker and multi-marker mixed models for polygenic score analysis in family-based dataHomozygosity at the dopamine D3 receptor locus is not associated with schizophrenia.No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.Comparative study of statistical methods for detecting association with rare variants in exome-resequencing dataCooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.Summary of contributions to GAW Group 15: family-based samples are useful in identifying common polymorphisms associated with complex traitsBivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD.No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseA pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.Genetic comorbidities in Parkinson's disease.New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study.Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis.Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk.Sampling strategies for linkage studies.Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis.Evidence for caveolin-1 as a new susceptibility gene regulating tissue fibrosis in systemic sclerosis.The p.Asp216His TOR1A allele effect is not found in the French population.Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: evidence for genetic heterogeneity.WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.Long-term stability of diagnosis and symptom dimensions in a systematic sample of patients with onset of schizophrenia in childhood and early adolescence. I: nosology, sex and age of onset.Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities.Power of the linkage test for a heterogeneous disorder due to two independent inherited causes: a simulation study.Long-term stability of diagnosis and symptom dimensions in a systematic sample of patients with onset of schizophrenia in childhood and early adolescence. II: Postnegative distinction and childhood predictors of adult outcome.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Maria Martinez
@ast
Maria Martinez
@en
Maria Martinez
@es
Maria Martinez
@nl
type
label
Maria Martinez
@ast
Maria Martinez
@en
Maria Martinez
@es
Maria Martinez
@nl
altLabel
M Martinez
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maria martinez
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prefLabel
Maria Martinez
@ast
Maria Martinez
@en
Maria Martinez
@es
Maria Martinez
@nl
P1053
B-3111-2013
P106
P21
P31
P496
0000-0003-2180-4537