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  1. Article

    Open Access

    The DCDC2 deletion is not a risk factor for dyslexia

    Dyslexia is a specific impairment in learning to read and has strong heritability. An intronic deletion within the DCDC2 gene, with ~8% frequency in European populations, is increasingly used as a marker for dysl...

    T S Scerri, E Macpherson, A Martinelli, W C Wa, A P Monaco… in Translational Psychiatry (2017)

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  2. Article

    Open Access

    Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

    Dyslexia (or reading disability) and specific language impairment (or SLI) are common childhood disorders that show considerable co-morbidity and diagnostic overlaps and have been suggested to share some genet...

    D. F. Newbury, S. Paracchini, T. S. Scerri, L. Winchester, L. Addis… in Behavior Genetics (2011)

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  3. No Access

    Article

    Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia

    D Harold, S Paracchini, T Scerri, M Dennis, N Cope, G Hill… in Molecular Psychiatry (2006)

  4. No Access

    Article

    Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

    The DYX2 locus on chromosome 6p22.2 is the most replicated region of linkage to developmental dyslexia (DD). Two candidate genes within this region have recently been implicated in the disorder: KIAA0319 and DCDC...

    D Harold, S Paracchini, T Scerri, M Dennis, N Cope, G Hill… in Molecular Psychiatry (2006)

  5. No Access

    Article

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

    Forty Italian individuals with sperm counts in the range 20–130×106/ml were typed with eleven Y-specific binary markers. Five Y haplogroups (1, 2, 3, 9 and 21) were present in the sample. In Italy, in contrast to...

    S. Paracchini, L. Stuppia, V. Gatta… in Journal of Endocrinological Investigation (2002)

  6. Article

    Erratum to: Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions

    S. Paracchini, L. Stuppia, V. Gatta, G. Palka… in Journal of Endocrinological Investigation (2001)

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  7. No Access

    Article

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

    We have determined Y-chromosomal DNA haplotypes in 73 infertile European males carrying Y microdeletions and compared them with the haplotypes of 299 infertile males lacking microdeletions. Chromosomes were ty...

    S. Paracchini, L. Stuppia, V. Gatta, G. Palka… in Journal of Endocrinological Investigation (2000)