Hasil Pencarian - Silvia Paracchini

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  1. 1
    Recent Advances in Handedness Genetics

    Recent Advances in Handedness Genetics oleh Silvia Paracchini

    Diterbitkan 2021-09-01
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  2. 2
    Kin selection as a modulator of human handedness: sex-specific, parental and parent-of-origin effects

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

    Diterbitkan 2024-01-01
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  3. 3
    Insights into Dyslexia Genetics Research from the Last Two Decades

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

    Diterbitkan 2021-12-01
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  4. 4
    Auditory Cortex Asymmetry Associations with Individual Differences in Language and Cognition

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

    Diterbitkan 2023-12-01
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  5. 5
    Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively

    Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively oleh Carlos Buenaventura Castillo, Andy G. Lynch, Silvia Paracchini

    Diterbitkan 2020-04-01
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  6. 6
    Identification of loci involved in childhood visual acuity and associations with cognitive skills and educational attainment

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

    Diterbitkan 2023-07-01
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  7. 7
    Handedness in twins: meta-analyses

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

    Diterbitkan 2022-01-01
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  8. 8
    Quantitative multidimensional phenotypes improve genetic analysis of laterality traits

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

    Diterbitkan 2022-02-01
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  9. 9
    KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction

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

    Diterbitkan 2022-01-01
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  10. 10
    Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample

    Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample oleh Mo Zheng, Catherine McBride, Connie Suk-Han Ho, Jonathan Ka-Chun Chan, Kwong Wai Choy, Silvia Paracchini

    Diterbitkan 2020-04-01
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  11. 11
    Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix

    Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix oleh Elisabetta Versace, Paola Sgadò, Julia George, Jasmine L. Loveland, Joseph Ward, Peter Thorpe, Lars Juhl Jensen, Karen A. Spencer, Silvia Paracchini, Giorgio Vallortigara

    Diterbitkan 2022-07-01
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  12. 12
    A common variant associated with dyslexia reduces expression of the KIAA0319 gene.

    A common variant associated with dyslexia reduces expression of the KIAA0319 gene. oleh 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

    Diterbitkan 2009-03-01
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  13. 13
    Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment.

    Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment. oleh Kerry A Pettigrew, Emily Reeves, Ruth Leavett, Marianna E Hayiou-Thomas, Anahita Sharma, Nuala H Simpson, Angela Martinelli, Paul Thompson, Charles Hulme, Margaret J Snowling, Dianne F Newbury, Silvia Paracchini

    Diterbitkan 2015-01-01
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  14. 14
    Identification of candidate genes for dyslexia susceptibility on chromosome 18.

    Identification of candidate genes for dyslexia susceptibility on chromosome 18. oleh 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

    Diterbitkan 2010-10-01
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  15. 15
    Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.

    Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18. oleh 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

    Diterbitkan 2010-01-01
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  16. 16
    A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children

    A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children oleh 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

    Diterbitkan 2024-03-01
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  17. 17
    The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.

    The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. oleh 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

    Diterbitkan 2012-01-01
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  18. 18
    Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.

    Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. oleh 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

    Diterbitkan 2013-01-01
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