Silvia Paracchini
Silvia Paracchini FRSE is a Professor of Neurogenetics and Genomics at the University of St Andrews. Her research focuses on the genetics of neurodevelopmental traits such as dyslexia and human handedness. Paracchini featured in the Royal Society of Edinburgh's 2019 ''Women in Science in Scotland'' exhibition, which celebrated some of Scotland’s leading female scientists. She is a Fellow of the Royal Society of Biology and of the Royal Society of Edinburgh. Provided by Wikipedia
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Kin selection as a modulator of human handedness: sex-specific, parental and parent-of-origin effects by Bing Dong, Silvia Paracchini, Andy Gardner
Published 2024-01-01
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Insights into Dyslexia Genetics Research from the Last Two Decades by Florina Erbeli, Marianne Rice, Silvia Paracchini
Published 2021-12-01
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Auditory Cortex Asymmetry Associations with Individual Differences in Language and Cognition by Mark A. Eckert, Kenneth I. Vaden, Silvia Paracchini
Published 2023-12-01
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Handedness in twins: meta-analyses by Lena Sophie Pfeifer, Judith Schmitz, Marietta Papadatou-Pastou, Jutta Peterburs, Silvia Paracchini, Sebastian Ocklenburg
Published 2022-01-01
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Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix by Elisabetta Versace, Paola Sgadò, Julia George, Jasmine L. Loveland, Joseph Ward, Peter Thorpe, Lars Juhl Jensen, Karen A. Spencer, Silvia Paracchini, Giorgio Vallortigara
Published 2022-07-01
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A common variant associated with dyslexia reduces expression of the KIAA0319 gene. by Megan Y Dennis, Silvia Paracchini, Thomas S Scerri, Ludmila Prokunina-Olsson, Julian C Knight, Richard Wade-Martins, Penny Coggill, Stephan Beck, Eric D Green, Anthony P Monaco
Published 2009-03-01
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Identification of candidate genes for dyslexia susceptibility on chromosome 18. by Thomas S Scerri, Silvia Paracchini, Andrew Morris, I Laurence MacPhie, Joel Talcott, John Stein, Shelley D Smith, Bruce F Pennington, Richard K Olson, John C DeFries, Anthony P Monaco, Alex J Richardson
Published 2010-10-01
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Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18. by Thomas S. Scerri, Silvia Paracchini, Andrew Morris, I. Laurence MacPhie, Joel Talcott, John Stein, Shelley D. Smith, Bruce F. Pennington, Richard K. Olson, John C. DeFries, Anthony P. Monaco, Alex J. Richardson
Published 2010-01-01
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A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children by Yu-Ping Lin, Yujia Shi, Ruoyu Zhang, Xiao Xue, Shitao Rao, Liangying Yin, Kelvin Fai Hong Lui, Dora Jue PAN, Urs Maurer, Kwong-Wai Choy, Silvia Paracchini, Catherine McBride, Hon-Cheong So
Published 2024-03-01
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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. by Thomas S Scerri, Fahimeh Darki, Dianne F Newbury, Andrew J O Whitehouse, Myriam Peyrard-Janvid, Hans Matsson, Qi W Ang, Craig E Pennell, Susan Ring, John Stein, Andrew P Morris, Anthony P Monaco, Juha Kere, Joel B Talcott, Torkel Klingberg, Silvia Paracchini
Published 2012-01-01
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Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. by William M Brandler, Andrew P Morris, David M Evans, Thomas S Scerri, John P Kemp, Nicholas J Timpson, Beate St Pourcain, George Davey Smith, Susan M Ring, John Stein, Anthony P Monaco, Joel B Talcott, Simon E Fisher, Caleb Webber, Silvia Paracchini
Published 2013-01-01
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