Lista de obras - Peristera Paschou - Dominio Público Uruguay

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

artículo científico publicado en 2016

A Brief History of the European Society for the Study of Tourette Syndrome

artículo científico publicado en 2013

A European population in Minoan Bronze Age Crete ⬇️

artículo científico publicado el 1 de enero de 2013

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Ancestry informative markers for fine-scale individual assignment to worldwide populations

artículo científico publicado en 2010

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

artículo científico publicado en 2015

COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

artículo científico publicado en 2004

Comment: Dissecting the genetic architecture of Tourette syndrome into subphenotypes

artículo científico publicado en 2016

Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

Efficient genomewide selection of PCA-correlated tSNPs for genotype imputation

artículo científico publicado en 2011

Epigenome-Wide Association Study of Tic Disorders

artículo científico

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome

artículo científico publicado en 2012

Exploring Genomic Structure Differences and Similarities between the Greek and European HapMap Populations: Implications for Association Studies

artículo científico publicado en 2012

Familial early-onset dementia with complex neuropathologic phenotype and genomic background

artículo científico

G894T polymorphism ofeNOSgene is a predictor of response to combination of inhaled corticosteroids with long-lasting β2-agonists in asthmatic children

artículo científico publicado en 2012

Genetic association signal near NTN4 in Tourette syndrome

artículo científico publicado en 2014

Genetic history of the population of Crete

artículo científico publicado en 2019

Genetic screening for individuals at high risk for type 1 diabetes in the general population using HLA Class II alleles as disease markers. A comparison between three European populations with variable rates of disease incidence

artículo científico publicado en 2004

Genetic susceptibility and neurotransmitters in Tourette syndrome

artículo científico publicado en 2013

Genetic variation in the visfatin (PBEF1/NAMPT) gene and type 2 diabetes in the Greek population

artículo científico publicado en 2010

Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks

artículo científico publicado en 2017

Gilles de la Tourette syndrome

artículo científico publicado en 2017

HLA alleles and type 1 diabetes mellitus in low disease incidence populations of Southern Europe: a comparison of Greeks and Albanians

artículo científico publicado en 2004

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

artículo científico publicado en 2004

Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers

artículo científico publicado en 2010

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

artículo científico publicado en 2019

Intra- and interpopulation genotype reconstruction from tagging SNPs

artículo científico publicado en 2006

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

artículo científico publicado en 2014

Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort

artículo científico publicado en 2016

Maritime route of colonization of Europe

artículo científico publicado en 2014

Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis

artículo científico publicado en 2016

PCA-correlated SNPs for structure identification in worldwide human populations

artículo científico publicado en 2007

Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe

scientific article published on 04 September 2019

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

artículo científico publicado en 2011

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

artículo científico publicado en 2013

TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome

artículo científico publicado en 2016

Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology

artículo científico publicado en 2016

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

scientific article published on 03 August 2016

The distribution and most recent common ancestor of the 17q21 inversion in humans

artículo científico publicado en 2010

The genetic basis of Gilles de la Tourette Syndrome.

artículo científico publicado en 2013

Tracing cattle breeds with principal components analysis ancestry informative SNPs

artículo científico publicado en 2011

Tracing sub-structure in the European American population with PCA-informative markers

artículo científico publicado en 2008

Lista de obras de Peristera Paschou

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

A Brief History of the European Society for the Study of Tourette Syndrome

A European population in Minoan Bronze Age Crete ⬇️

Analysis of shared heritability in common disorders of the brain

Ancestry informative markers for fine-scale individual assignment to worldwide populations

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

Comment: Dissecting the genetic architecture of Tourette syndrome into subphenotypes

Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

Efficient genomewide selection of PCA-correlated tSNPs for genotype imputation

Epigenome-Wide Association Study of Tic Disorders

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome

Exploring Genomic Structure Differences and Similarities between the Greek and European HapMap Populations: Implications for Association Studies

Familial early-onset dementia with complex neuropathologic phenotype and genomic background

G894T polymorphism ofeNOSgene is a predictor of response to combination of inhaled corticosteroids with long-lasting β2-agonists in asthmatic children

Genetic association signal near NTN4 in Tourette syndrome

Genetic history of the population of Crete

Genetic screening for individuals at high risk for type 1 diabetes in the general population using HLA Class II alleles as disease markers. A comparison between three European populations with variable rates of disease incidence

Genetic susceptibility and neurotransmitters in Tourette syndrome

Genetic variation in the visfatin (PBEF1/NAMPT) gene and type 2 diabetes in the Greek population

Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks

Gilles de la Tourette syndrome

HLA alleles and type 1 diabetes mellitus in low disease incidence populations of Southern Europe: a comparison of Greeks and Albanians

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

Intra- and interpopulation genotype reconstruction from tagging SNPs

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort

Maritime route of colonization of Europe

Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis

PCA-correlated SNPs for structure identification in worldwide human populations

Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome

Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

The distribution and most recent common ancestor of the 17q21 inversion in humans

The genetic basis of Gilles de la Tourette Syndrome.

Tracing cattle breeds with principal components analysis ancestry informative SNPs

Tracing sub-structure in the European American population with PCA-informative markers