| Human handedness: A meta-analysis. M Papadatou-Pastou, E Ntolka, J Schmitz, M Martin, MR Munafò, ... Psychological bulletin, 2020 | 604 | 2020 |
| 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 | 386 | 2006 |
| 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 | 351 | 2011 |
| 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 | 346 | 2004 |
| 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 | 266 | 2009 |
| 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 | 266 | 2004 |
| 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 | 254 | 2011 |
| The genetic lexicon of dyslexia S Paracchini, T Scerri, AP Monaco Annu. Rev. Genomics Hum. Genet. 8 (1), 57-79, 2007 | 254 | 2007 |
| 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 | 250 | 2004 |
| 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 | 231 | 2006 |
| The genetic relationship between handedness and neurodevelopmental disorders WM Brandler, S Paracchini Trends in molecular medicine 20 (2), 83-90, 2014 | 200 | 2014 |
| 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 genetics 9 (9), e1003751, 2013 | 194 | 2013 |
| 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 | 193 | 2008 |
| 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 | 187 | 2006 |
| 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 | 184 | 2010 |
| 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 | 176 | 2011 |
| Discovery of 42 genome-wide significant loci associated with dyslexia C Doust, P Fontanillas, E Eising, SD Gordon, Z Wang, G Alagöz, B Molz, ... Nature Genetics, 1-9, 2022 | 168 | 2022 |
| Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia A Gialluisi, TFM Andlauer, N Mirza-Schreiber, K Moll, J Becker, ... Molecular psychiatry 26 (7), 3004-3017, 2021 | 167 | 2021 |
| 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 | 158 | 2014 |
| 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 | 150 | 2004 |
Anthony P MonacoUniversity Professor and President emeritus, Tufts UniversityVerified email at tufts.edu
