Silvia Paracchini

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

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

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

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

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

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

The genetic lexicon of dyslexia.

Alternative splicing in the dyslexia-associated gene KIAA0319.

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

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

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

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.

PCSK6 is associated with handedness in individuals with dyslexia.

Identification of candidate genes for dyslexia susceptibility on chromosome 18.

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

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