Search Results - Silvia Paracchini

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
Refine Results
  1. 1
    The genetic relationship between handedness and neurodevelopmental disorders

    The genetic relationship between handedness and neurodevelopmental disorders by William M. Brandler, Silvia Paracchini

    Published 2013
    Get full text
    Revisão
    Save to List
    Saved in:
  2. 2
    Insights into Dyslexia Genetics Research from the Last Two Decades

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

    Published 2021
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  3. 3
    The Genetic Lexicon of Dyslexia

    The Genetic Lexicon of Dyslexia by Silvia Paracchini, Thomas Scerri, Anthony P. Monaco

    Published 2007
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  4. 4
    Reading and Language Disorders: The Importance of Both Quantity and Quality

    Reading and Language Disorders: The Importance of Both Quantity and Quality by Dianne F. Newbury, Anthony P. Monaco, Silvia Paracchini

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Genetics of human handedness: microtubules and beyond

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

    Published 2025
    Get full text
    Revisão
    Save to List
    Saved in:
  6. 6
    The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

    The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms by Antonio Velayos‐Baeza, Claudio Toma, Silvia Paracchini, Anthony P. Monaco

    Published 2007
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Haplotype-specific expression of exon 10 at the human MAPT locus

    Haplotype-specific expression of exon 10 at the human MAPT locus by Tara M. Caffrey, Catharine Joachim, Silvia Paracchini, Margaret M. Esiri, Richard Wade‐Martins

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    A Large AZFc Deletion Removes DAZ3/DAZ4 and Nearby Genes from Men in Y Haplogroup N

    A Large AZFc Deletion Removes DAZ3/DAZ4 and Nearby Genes from Men in Y Haplogroup N by Susana Fernandes, Silvia Paracchini, Lukas Meyer, Giovanna Floridia, Chris Tyler‐Smith, P. H. Vogt

    Published 2004
    Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    Human handedness: A meta-analysis.

    Human handedness: A meta-analysis. by Μαριέττα Παπαδάτου-Παστού, Eleni Ntolka, Judith Schmitz, Maryanne Martin, Marcus R. Munafò, Sebastian Ocklenburg, Silvia Paracchini

    Published 2020
    Get full text
    Revisão
    Save to List
    Saved in:
  10. 10
    Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness

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

    Published 2020
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  11. 11
    Elevated levels of mixed-hand preference in dyslexia: Meta-analyses of 68 studies

    Elevated levels of mixed-hand preference in dyslexia: Meta-analyses of 68 studies by Julian Packheiser, Μαριέττα Παπαδάτου-Παστού, Angeliki Koufaki, Silvia Paracchini, Clara C. Stein, Judith Schmitz, Sebastian Ocklenburg

    Published 2023
    Get full text
    Revisão
    Save to List
    Saved in:
  12. 12
    Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

    Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population by Silvia Paracchini, Q. W. Ang, F Stanley, Anthony P. Monaco, Craig E. Pennell, Andrew J. O. Whitehouse

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on

    The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on by Luiz G. Guidi, Antonio Velayos‐Baeza, Isabel Martínez‐Garay, Anthony P. Monaco, Silvia Paracchini, Dorothy Bishop, Zoltán Molnár

    Published 2018
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  14. 14
    DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits

    DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits by Tom S. Scerri, Andrew P. Morris, Lyn-Louise Buckingham, Dianne F. Newbury, Laura L. Miller, Anthony P. Monaco, Dorothy Bishop, Silvia Paracchini

    Published 2011
    Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa

    A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa by Barbara Arredi, Estella S. Poloni, Silvia Paracchini, Tatiana Zerjal, Dahmani M. Fathallah, Mohamed Makrelouf, Vincenzo L. Pascali, Andrea Novelletto, Chris Tyler‐Smith

    Published 2004
    Get full text
    Artigo
    Save to List
    Saved in:
  16. 16
    PCSK6 is associated with handedness in individuals with dyslexia

    PCSK6 is associated with handedness in individuals with dyslexia by Thomas Scerri, William M. Brandler, Silvia Paracchini, Andrew P. Morris, Susan M. Ring, A.J. Richardson, Joel B. Talcott, John Stein, Anthony P. Monaco

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  17. 17
    Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

    Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects by Dianne F. Newbury, Silvia Paracchini, Tom S. Scerri, Laura Winchester, Laura Addis, A.J. Richardson, Janet G. Walter, John Stein, Joel B. Talcott, Anthony P. Monaco

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

    A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene by Megan Y. Dennis, Silvia Paracchini, Thomas Scerri, Ludmila Prokunina‐Olsson, Julian C. Knight, Richard Wade‐Martins, Penny Coggill, Stephan Beck, Eric D. Green, Anthony P. Monaco

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  19. 19
    Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

    Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia by Denise Harold, Silvia Paracchini, Thomas Scerri, Megan Y. Dennis, Natalie Cope, Gary Hill, Valentina Moskvina, Janet G. Walter, A.J. Richardson, Mike Owen, John Stein, E D Green, Michael O’Donovan, Julie Williams, Anthony P. Monaco

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  20. 20
    Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment

    Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment by Ron Nudel, Nuala H. Simpson, G. Baird, Anne O’Hare, Gina Conti‐Ramsden, Patrick Bolton, Elizabeth R Hennessy, Susan M. Ring, George Davey Smith, Clyde Francks, Silvia Paracchini, Anthony P. Monaco, Simon E. Fisher, Dianne F. Newbury

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: