Silvia Paracchini
University of St Andrews(GB)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Reading and Literacy Development, Hemispheric Asymmetry in Neuroscience, Cognitive and developmental aspects of mathematical skills, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Most-Cited Works
- → Human handedness: A meta-analysis.(2020)467 cited
- → The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration(2006)274 cited
- → A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States(2004)240 cited
- → Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects(2010)227 cited
- → A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa(2004)194 cited
- → CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment(2009)191 cited
- → A Large AZFc Deletion Removes DAZ3/DAZ4 and Nearby Genes from Men in Y Haplogroup N