about
Replication of association between working memory and Reelin, a potential modifier gene in schizophreniaGenome-wide association analysis of metabolic traits in a birth cohort from a founder populationEvidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of FinlandHaplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effectsReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesGenome-wide scan for loci of Asperger syndromeMutant CHUK and severe fetal encasement malformationThe genome-wide patterns of variation expose significant substructure in a founder populationA balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysmMolecular genetics of the Finnish disease heritage.Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.Linkage analysis of schizophrenia controlling for population substructure.Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from FinlandA genome-wide screen for acrophobia susceptibility loci in a Finnish isolate.Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?Clinical phenotype of schizophrenia in a Finnish isolate.Prevalence and psychiatric comorbidity of attention-deficit/hyperactivity disorder in an adolescent Finnish population.Impact of the dopamine receptor gene family on temperament traits in a population-based birth cohort.Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.Identification of C12orf4 as a gene for autosomal recessive intellectual disability.Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes.NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease.Association of DISC1 with autism and Asperger syndrome.Affective flattening and alogia associate with the familial form of schizophrenia.Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients.Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohortThe role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in FinlandIdentification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated populationBipolar disorder susceptibility region on Xq24–q27.1 in Finnish familiesThe interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different historiesPhenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population
P50
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P50
description
hulumtues
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onderzoeker
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researcher
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հետազոտող
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name
Teppo Varilo
@ast
Teppo Varilo
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Teppo Varilo
@es
Teppo Varilo
@nl
Teppo Varilo
@sl
type
label
Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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altLabel
Teppo Tapio Varilo
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prefLabel
Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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Teppo Varilo
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P106
P21
P31
P496
0000-0002-5839-8854
P569
2000-01-01T00:00:00Z