Concepedia

Silvia Paracchini

SP

54

Publications

4.1K

Citations

32

H-Index

1998

Active since

Affiliations

University of Oxford(Current)

Centre for Human Genetics

University of St Andrews

Aston University

University of Bristol

Silvia Paracchini is an author at University of Oxford specializing in medicine, genetics, and neuroscience.

ORCID

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Publications per year

1998–2022

54

Publications

54

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

Silvia Paracchini, Ankur Thomas, Sandra C. de Castro et al. · Human Molecular Genetics · 2006 · 274 citations · Full text

A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States

Clyde Francks, Silvia Paracchini, Shelley D. Smith et al. · The American Journal of Human Genetics · 2004 · 240 citations · Full text

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

Dianne F. Newbury, Silvia Paracchini, Tom S. Scerri et al. · Behavior Genetics · 2010 · 227 citations · Full text

A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa

Barbara Arredi, Estella S. Poloni, Silvia Paracchini et al. · The American Journal of Human Genetics · 2004 · 194 citations · Full text

, , +10

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

Dianne F. Newbury, Laura Winchester, Laura Addis et al. · The American Journal of Human Genetics · 2009 · 191 citations · Full text

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