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List of works by Teppo Varilo

A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm

scientific article

A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate

scientific article published on 20 December 2016

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia

scientific article published in December 2005

ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.

scientific article published in December 2007

Affective flattening and alogia associate with the familial form of schizophrenia

scientific article published in February 2006

Association of DISC1 with autism and Asperger syndrome

scientific article published on 19 June 2007

Bipolar disorder susceptibility region on Xq24–q27.1 in Finnish families

scientific article published on 01 January 2002

Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes.

scientific article published on 23 November 2017

Clinical phenotype of schizophrenia in a Finnish isolate.

scientific article published in April 2004

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

scientific article published on 04 August 2013

Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?

scientific article published on 22 October 2012

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

scientific article (publication date: October 2003)

Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients

scientific article published in September 2003

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

scientific article

Genome-wide scan for loci of Asperger syndrome

scientific article (publication date: February 2004)

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

scientific article (publication date: December 2003)

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia

scientific article

Identification of C12orf4 as a gene for autosomal recessive intellectual disability.

scientific article

Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population

Impact of the dopamine receptor gene family on temperament traits in a population-based birth cohort

scientific article

Linkage analysis of schizophrenia controlling for population substructure

scientific article

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

scientific article published on 19 May 2009

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

scientific article published on 2 April 2006

Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis

scientific article

Molecular genetics of the Finnish disease heritage.

scientific article

Mutant CHUK and severe fetal encasement malformation

scientific article

NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease.

scientific article published on 8 February 2018

Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

scientific article published on 26 March 2019

Prevalence and psychiatric comorbidity of attention-deficit/hyperactivity disorder in an adolescent Finnish population

scientific article published in December 2007

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia

scientific article

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families

scientific article (publication date: July 2008)

Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.

scientific article published on 15 June 2004

Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort

scientific article published on 01 August 2012

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.

scientific article published on 13 September 2013

The genome-wide patterns of variation expose significant substructure in a founder population

scientific article (publication date: December 2008)

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

scientific article published on 01 January 2003

The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland

article

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus

scientific article published in September 1996

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