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Silvia Paracchini

Showing results (41-50 of 60) with videos related to

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Human Molecular Genetics|February 25, 2016
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcriptsRobert Shore, Laura Covill, Kerry A Pettigrew, et al.
NPJ Science of Learning|March 28, 2024
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese childrenYu-Ping Lin, Yujia Shi, Ruoyu Zhang, et al.
Plos One|November 10, 2010
Identification of candidate genes for dyslexia susceptibility on chromosome 18Thomas S Scerri, Silvia Paracchini, Andrew Morris, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2019
A novel mutation in <i>SPART</i> gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismChiara Diquigiovanni, Christian Bergamini, Rebeca Diaz, et al.
Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.
American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.
Human Molecular Genetics|April 8, 2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationSilvia Paracchini, Ankur Thomas, Sandra Castro, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|February 25, 2016
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcriptsRobert Shore, Laura Covill, Kerry A Pettigrew, et al.
NPJ Science of Learning|March 28, 2024
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese childrenYu-Ping Lin, Yujia Shi, Ruoyu Zhang, et al.
Plos One|November 10, 2010
Identification of candidate genes for dyslexia susceptibility on chromosome 18Thomas S Scerri, Silvia Paracchini, Andrew Morris, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2019
A novel mutation in <i>SPART</i> gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismChiara Diquigiovanni, Christian Bergamini, Rebeca Diaz, et al.
Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.
American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.
Human Molecular Genetics|April 8, 2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationSilvia Paracchini, Ankur Thomas, Sandra Castro, et al.
Pageof 6