Silvia Paracchini Wellcome Trust Centre for Human Genetics University of Oxford Biography Publications Institution JoVE Articles Silvia Paracchini has not added a biography. If you are Silvia Paracchini and would like to personalize this page please email our Author Liaison for assistance. Publications Dissection of Genetic Associations with Language-related Traits in Population-based Cohorts Journal of Neurodevelopmental Disorders. Dec, 2011 | Pubmed ID: 21894572 DCDC2, KIAA0319 and CMIP Are Associated with Reading-related Traits Biological Psychiatry. Aug, 2011 | Pubmed ID: 21457949 PCSK6 is Associated with Handedness in Individuals with Dyslexia Human Molecular Genetics. Feb, 2011 | Pubmed ID: 21051773 Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 PloS One. 2010 | Pubmed ID: 21060895 Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia Biological Psychiatry. Aug, 2010 | Pubmed ID: 20346443 CMIP and ATP2C2 Modulate Phonological Short-term Memory in Language Impairment American Journal of Human Genetics. Aug, 2009 | Pubmed ID: 19646677 A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene PLoS Genetics. Mar, 2009 | Pubmed ID: 19325871 Association of the KIAA0319 Dyslexia Susceptibility Gene with Reading Skills in the General Population The American Journal of Psychiatry. Dec, 2008 | Pubmed ID: 18829873 The Dyslexia-associated Gene KIAA0319 Encodes Highly N- and O-glycosylated Plasma Membrane and Secreted Isoforms Human Molecular Genetics. Mar, 2008 | Pubmed ID: 18063668 Alternative Splicing in the Dyslexia-associated Gene KIAA0319 Mammalian Genome : Official Journal of the International Mammalian Genome Society. Sep, 2007 | Pubmed ID: 17846832 The Genetic Lexicon of Dyslexia Annual Review of Genomics and Human Genetics. 2007 | Pubmed ID: 17444811 Y-chromosomal Insights into the Genetic Impact of the Caste System in India Human Genetics. Mar, 2007 | Pubmed ID: 17075717 Haplotype-specific Expression of Exon 10 at the Human MAPT Locus Human Molecular Genetics. Dec, 2006 | Pubmed ID: 17085483 The Chromosome 6p22 Haplotype Associated with Dyslexia Reduces the Expression of KIAA0319, a Novel Gene Involved in Neuronal Migration Human Molecular Genetics. May, 2006 | Pubmed ID: 16600991 A 77-kilobase Region of Chromosome 6p22.2 is Associated with Dyslexia in Families from the United Kingdom and from the United States American Journal of Human Genetics. Dec, 2004 | Pubmed ID: 15514892 A Predominantly Neolithic Origin for Y-chromosomal DNA Variation in North Africa American Journal of Human Genetics. Aug, 2004 | Pubmed ID: 15202071 Hierarchical High-throughput SNP Genotyping of the Human Y Chromosome Using MALDI-TOF Mass Spectrometry Nucleic Acids Research. Mar, 2002 | Pubmed ID: 11884646 एक ऐल्लि विशिष्ट जीन एक्सप्रेशन आनुवंशिक संघों के कार्यात्मक आधार टेस्ट परख Silvia Paracchini1, Anthony P. Monaco1, Julian C. Knight1 1Wellcome Trust Centre for Human Genetics, University of Oxford JoVE 2279 Biology
एक ऐल्लि विशिष्ट जीन एक्सप्रेशन आनुवंशिक संघों के कार्यात्मक आधार टेस्ट परख Silvia Paracchini1, Anthony P. Monaco1, Julian C. Knight1 1Wellcome Trust Centre for Human Genetics, University of Oxford JoVE 2279 Biology