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Silvia Paracchini

Showing results (31-40 of 60) with videos related to

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American Journal of Human Genetics|June 18, 2004
A predominantly neolithic origin for Y-chromosomal DNA variation in North AfricaBarbara Arredi, Estella S Poloni, Silvia Paracchini, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Human Genetics|September 5, 2023
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twinsCheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, et al.
The Journal of Comparative Neurology|April 6, 2019
The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migrationMonika Gostic, Angela Martinelli, Carl Tucker, et al.
Scientific Reports|July 15, 2022
Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrixElisabetta Versace, Paola Sgadò, Julia George, et al.
Biological Psychiatry|April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traitsTom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Plos Genetics|March 28, 2009
A common variant associated with dyslexia reduces expression of the KIAA0319 geneMegan Y Dennis, Silvia Paracchini, Thomas S Scerri, et al.
The American Journal of Psychiatry|October 3, 2008
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general populationSilvia Paracchini, Colin D Steer, Lyn-Louise Buckingham, et al.
Plos One|August 12, 2015
Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentKerry A Pettigrew, Emily Reeves, Ruth Leavett, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|June 18, 2004
A predominantly neolithic origin for Y-chromosomal DNA variation in North AfricaBarbara Arredi, Estella S Poloni, Silvia Paracchini, et al.
Human Genetics|December 24, 2025
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genesKrzysztof Marianski, Joel B Talcott, John Stein, et al.
Human Genetics|September 5, 2023
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twinsCheuk Yan Chung, Dora Jue Pan, Silvia Paracchini, et al.
The Journal of Comparative Neurology|April 6, 2019
The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migrationMonika Gostic, Angela Martinelli, Carl Tucker, et al.
Scientific Reports|July 15, 2022
Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrixElisabetta Versace, Paola Sgadò, Julia George, et al.
Biological Psychiatry|April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traitsTom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Plos Genetics|March 28, 2009
A common variant associated with dyslexia reduces expression of the KIAA0319 geneMegan Y Dennis, Silvia Paracchini, Thomas S Scerri, et al.
The American Journal of Psychiatry|October 3, 2008
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general populationSilvia Paracchini, Colin D Steer, Lyn-Louise Buckingham, et al.
Plos One|August 12, 2015
Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language ImpairmentKerry A Pettigrew, Emily Reeves, Ruth Leavett, et al.
Pageof 6