Publications by authors named "Silvia Paracchini"

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Toward an Improved Understanding of Dyslexia: Reflections on a New Consensus Definition and Its Implications.
Kinga Morsanyi, Silvia Paracchini, Saloni Krishnan, Catherine Manning, Jennifer Milne

Dyslexia· February 2026

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Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Krzysztof Marianski, Joel B Talcott, John Stein, Anthony P Monaco, Simon E Fisher, Silvia Paracchini

Hum Genet· December 2025

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Genetics of human handedness: microtubules and beyond.
Sebastian Ocklenburg, Annakarina Mundorf, Jutta Peterburs, Silvia Paracchini

Trends Genet· June 2025

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Bonn: Prof. Silvia Paracchini, PhD, Professor of Neurodevelopmental Genomics.
Silvia Paracchini

Med Genet· December 2024

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A GWAS for grip strength in cohorts of children-Advantages of analysing young participants for this trait.
Filippo Abbondanza, Carol A Wang, Judith Schmitz, Krzysztof Marianski, Craig E Pennell, Silvia Paracchini

Genes Brain Behav· October 2024

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Kin selection as a modulator of human handedness: sex-specific, parental and parent-of-origin effects.
Bing Dong, Silvia Paracchini, Andy Gardner

Evol Hum Sci· August 2024

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A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children.
Yu-Ping Lin, Yujia Shi, Ruoyu Zhang, Xiao Xue, Shitao Rao, Silvia Paracchini

NPJ Sci Learn· March 2024

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Auditory Cortex Asymmetry Associations with Individual Differences in Language and Cognition.
Mark A Eckert, Kenneth I Vaden, Silvia Paracchini

Brain Sci· December 2023

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Elevated levels of mixed-hand preference in dyslexia: Meta-analyses of 68 studies.
Julian Packheiser, Marietta Papadatou-Pastou, Angeliki Koufaki, Silvia Paracchini, Clara C Stein

Neurosci Biobehav Rev· November 2023

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Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twins.
Cheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, Wenxuan Jiang, Hon-Cheong So

Hum Genet· October 2023

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Identification of loci involved in childhood visual acuity and associations with cognitive skills and educational attainment.
Judith Schmitz, Filippo Abbondanza, Krzysztof Marianski, Michelle Luciano, Silvia Paracchini

NPJ Sci Learn· July 2023

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Language and reading impairments are associated with increased prevalence of non-right-handedness.
Filippo Abbondanza, Philip S Dale, Carol A Wang, Marianna E Hayiou-Thomas, Umar Toseeb, Silvia Paracchini

Child Dev· June 2023

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Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
Catherine Doust, Pierre Fontanillas, Else Eising, Scott D Gordon, Zhengjun Wang, Silvia Paracchini

Nat Genet· March 2023

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Discovery of 42 genome-wide significant loci associated with dyslexia.
Catherine Doust, Pierre Fontanillas, Else Eising, Scott D Gordon, Zhengjun Wang, Silvia Paracchini

Nat Genet· November 2022

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Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Else Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, Carol A Wang, Dongnhu T Truong, Silvia Paracchini

Proc Natl Acad Sci U S A· August 2022

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Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix.
Elisabetta Versace, Paola Sgadò, Julia George, Jasmine L Loveland, Joseph Ward, Silvia Paracchini

Sci Rep· July 2022

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Quantitative multidimensional phenotypes improve genetic analysis of laterality traits.
Judith Schmitz, Mo Zheng, Kelvin F H Lui, Catherine McBride, Connie S-H Ho, Silvia Paracchini

Transl Psychiatry· February 2022

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KIAA0319 influences cilia length, cell migration and mechanical cell-substrate interaction.
Rebeca Diaz, Nils M Kronenberg, Angela Martinelli, Philipp Liehm, Andrew C Riches, Silvia Paracchini

Sci Rep· January 2022

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Handedness in twins: meta-analyses.
Lena Sophie Pfeifer, Judith Schmitz, Marietta Papadatou-Pastou, Jutta Peterburs, Silvia Paracchini

BMC Psychol· January 2022

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Insights into Dyslexia Genetics Research from the Last Two Decades.
Florina Erbeli, Marianne Rice, Silvia Paracchini

Brain Sci· December 2021

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Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature.
Marietta Papadatou-Pastou, Despoina-Athanasia Panagiotidou, Filippo Abbondanza, Ursula Fischer, Silvia Paracchini

Laterality· September 2021

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Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, Kristina Moll, Jessica Becker, Silvia Paracchini

Mol Psychiatry· July 2021

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Genome-wide association study and polygenic risk score analysis for hearing measures in children.
Judith Schmitz, Filippo Abbondanza, Silvia Paracchini

Am J Med Genet B Neuropsychiatr Genet· July 2021

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A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.
Angela Martinelli, Mabel L Rice, Joel B Talcott, Rebeca Diaz, Shelley Smith, Silvia Paracchini

Hum Mol Genet· June 2021

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Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness.
Julian Packheiser, Judith Schmitz, Gesa Berretz, David P Carey, Silvia Paracchini

Sci Rep· September 2020

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