Silvia Paracchini
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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration
S Paracchini, A Thomas, S Castro, C Lai, M Paramasivam, Y Wang, ...
Human molecular genetics 15 (10), 1659-1666, 2006
A 77-kilobase region of chromosome 6p22. 2 is associated with dyslexia in families from the United Kingdom and from the United States
C Francks, S Paracchini, SD Smith, AJ Richardson, TS Scerri, LR Cardon, ...
The American Journal of Human Genetics 75 (6), 1046-1058, 2004
Investigation of dyslexia and SLI risk variants in reading-and language-impaired subjects
DF Newbury, S Paracchini, TS Scerri, L Winchester, L Addis, ...
Behavior genetics 41 (1), 90-104, 2011
A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N
S Fernandes, S Paracchini, LH Meyer, G Floridia, C Tyler-Smith, PH Vogt
The American Journal of Human Genetics 74 (1), 180-187, 2004
A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa
B Arredi, ES Poloni, S Paracchini, T Zerjal, DM Fathallah, M Makrelouf, ...
The American Journal of Human Genetics 75 (2), 338-345, 2004
The genetic lexicon of dyslexia
S Paracchini, T Scerri, AP Monaco
Annual review of genomics and human genetics 8, 2007
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
DF Newbury, L Winchester, L Addis, S Paracchini, LL Buckingham, ...
The American Journal of Human Genetics 85 (2), 264-272, 2009
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
D Harold, S Paracchini, T Scerri, M Dennis, N Cope, G Hill, V Moskvina, ...
Molecular psychiatry 11 (12), 1085-1091, 2006
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
TS Scerri, AP Morris, LL Buckingham, DF Newbury, LL Miller, AP Monaco, ...
Biological psychiatry 70 (3), 237-245, 2011
Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population
S Paracchini D Phil, CD Steer, LL Buckingham, AP Morris, S Ring, ...
American Journal of Psychiatry 165 (12), 1576-1584, 2008
PCSK6 is associated with handedness in individuals with dyslexia
TS Scerri, WM Brandler, S Paracchini, AP Morris, SM Ring, AJ Richardson, ...
Human molecular genetics 20 (3), 608-614, 2011
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
WM Brandler, AP Morris, DM Evans, TS Scerri, JP Kemp, NJ Timpson, ...
PLoS Genet 9 (9), e1003751, 2013
Haplotype-specific expression of exon 10 at the human MAPT locus
TM Caffrey, C Joachim, S Paracchini, MM Esiri, R Wade-Martins
Human molecular genetics 15 (24), 3529-3537, 2006
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
TS Scerri, SE Fisher, C Francks, IL MacPhie, S Paracchini, AJ Richardson, ...
Journal of Medical Genetics 41 (11), 853-857, 2004
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
AT Pagnamenta, E Bacchelli, MV de Jonge, G Mirza, TS Scerri, F Minopoli, ...
Biological psychiatry 68 (4), 320-328, 2010
A common variant associated with dyslexia reduces expression of the KIAA0319 gene
MY Dennis, S Paracchini, TS Scerri, L Prokunina-Olsson, JC Knight, ...
PLoS Genet 5 (3), e1000436, 2009
The genetic relationship between handedness and neurodevelopmental disorders
WM Brandler, S Paracchini
Trends in molecular medicine 20 (2), 83-90, 2014
Genome‐wide screening for DNA variants associated with reading and language traits
A Gialluisi, DF Newbury, EG Wilcutt, RK Olson, JC DeFries, WM Brandler, ...
Genes, Brain and Behavior 13 (7), 686-701, 2014
Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry
S Paracchini, B Arredi, R Chalk, C Tyler-Smith
Nucleic Acids Research 30 (6), e27-e27, 2002
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms
A Velayos-Baeza, C Toma, S Paracchini, AP Monaco
Human molecular genetics 17 (6), 859-871, 2008
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