List of works - Silvia Paracchini

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

scientific article

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

scientific article

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

scientific article

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

scientific article published on 10 October 2006

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

scientific article

A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa

scientific article

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N

scientific article

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

scientific article

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

scientific article published on 30 July 2009

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

scientific article

The genetic lexicon of dyslexia

scientific article

Haplotype-specific expression of exon 10 at the human MAPT locus

scientific article published on 3 November 2006

PCSK6 is associated with handedness in individuals with dyslexia

scientific article

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

scientific article

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

scientific article

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

scientific article

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

scientific article

Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry

scientific article

Genome-wide screening for DNA variants associated with reading and language traits

scientific article

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

scientific article published on 6 December 2007

The genetic relationship between handedness and neurodevelopmental disorders

scientific article

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

scientific article published on 11 September 2013

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

scientific article

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

scientific article

Alternative splicing in the dyslexia-associated gene KIAA0319

scientific article

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

scientific article

Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions

article

Reading and language disorders: the importance of both quantity and quality.

scientific article published on 4, Apr, 2014

Dissection of genetic associations with language-related traits in population-based cohorts

scientific article published on September 6, 2011

Y-chromosomal insights into the genetic impact of the caste system in India

scientific article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

scientific article

A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study

scientific article

Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries.

scientific article published on 5 October 2016

A new model organism for studying the catabolism of pyrimidines and purines.

scientific article published on January 1998

Are sequence family variants useful for identifying deletions in the human Y chromosome?

scientific article published on September 2004

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

scientific article published on 11 February 2019

Relationship between Y-chromosomal DNA haplotype and sperm count in Italy

article

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

scientific article published on 14 June 2016

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on

scientific article published on 06 October 2018

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment

scientific article

Human handedness: A meta-analysis

scientific article published on 02 April 2020

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.

scientific article

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

scientific article

The DCDC2 deletion is not a risk factor for dyslexia

scientific article

Papadatou-Pastou, Martin, Munafò, Ntolka, Ocklenburg, & Paracchini. The prevalence of left-handedness: Five meta-analyses of 200 studies totaling 2,396,170 individuals

Y-chromosomal DNA haplotypes in male infertility and cancer

doctoral thesis

An allele-specific gene expression assay to test the functional basis of genetic associations

scientific article

Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness

scientific article published on 02 September 2020

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

scientific article published on 14 October 2020

Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample

scientific article published on 22 April 2020

List of works by Silvia Paracchini

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

The genetic lexicon of dyslexia

Haplotype-specific expression of exon 10 at the human MAPT locus

PCSK6 is associated with handedness in individuals with dyslexia

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry

Genome-wide screening for DNA variants associated with reading and language traits

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

The genetic relationship between handedness and neurodevelopmental disorders

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Alternative splicing in the dyslexia-associated gene KIAA0319

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions

Reading and language disorders: the importance of both quantity and quality.

Dissection of genetic associations with language-related traits in population-based cohorts

Y-chromosomal insights into the genetic impact of the caste system in India

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study

Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries.

A new model organism for studying the catabolism of pyrimidines and purines.

Are sequence family variants useful for identifying deletions in the human Y chromosome?

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Relationship between Y-chromosomal DNA haplotype and sperm count in Italy

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment

Human handedness: A meta-analysis

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

The DCDC2 deletion is not a risk factor for dyslexia

Papadatou-Pastou, Martin, Munafò, Ntolka, Ocklenburg, & Paracchini. The prevalence of left-handedness: Five meta-analyses of 200 studies totaling 2,396,170 individuals

Y-chromosomal DNA haplotypes in male infertility and cancer

An allele-specific gene expression assay to test the functional basis of genetic associations

Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample