| 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 | 305 | 2006 |
| A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States APM Clyde Francks, Silvia Paracchini, Shelley D Smith, Alex J Richardson ... The American Journal of Human Genetics 75 (6), 1046-1058, 2004 | 278 | 2004 |
| Genetics of developmental dyslexia TS Scerri, G Schulte-Körne European child & adolescent psychiatry 19 (3), 179-197, 2010 | 265 | 2010 |
| 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 | 264 | 2011 |
| The genetic lexicon of dyslexia S Paracchini, T Scerri, AP Monaco Annual review of genomics and human genetics 8, 2007 | 202 | 2007 |
| 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 | 191 | 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 | 183 | 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 | 159 | 2008 |
| An α‐E‐catenin (CTNNA1) mutation in hereditary diffuse gastric cancer IJ Majewski, I Kluijt, A Cats, TS Scerri, D de Jong, RJC Kluin, S Hansford, ... The Journal of pathology 229 (4), 621-629, 2013 | 143 | 2013 |
| 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 | 142 | 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 | 141 | 2013 |
| Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency GB Fliegauf M, L Bryant V, Frede N, Slade C, Woon ST, Lehnert K, Winzer S ... Am J Hum Genet. 97 (3), 389-403, 2015 | 139 | 2015 |
| High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility E Maestrini, AT Pagnamenta, JA Lamb, E Bacchelli, NH Sykes, I Sousa, ... Molecular psychiatry 15 (9), 954-968, 2010 | 137 | 2010 |
| 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 | 131 | 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 | 127 | 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 | 118 | 2009 |
| 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 | 89 | 2014 |
| Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 JC Sim, T Scerri, M Fanjul‐Fernández, JR Riseley, G Gillies, K Pope, ... Annals of neurology 79 (1), 132-137, 2016 | 84 | 2016 |
| Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5 T Scerri, JR Riseley, G Gillies, K Pope, R Burgess, SA Mandelstam, ... Annals of clinical and translational neurology 2 (5), 575-580, 2015 | 74 | 2015 |
| Genome-wide analyses identify common variants associated with macular telangiectasia type 2 TS Scerri, A Quaglieri, C Cai, J Zernant, N Matsunami, L Baird, ... Nature genetics 49 (4), 559-567, 2017 | 63 | 2017 |
Silvia ParacchiniUniversity of St AndrewsVerified email at st-andrews.ac.uk
