Thomas Scerri
Thomas Scerri
Postdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical Research
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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
APM Clyde Francks, Silvia Paracchini, Shelley D Smith, Alex J Richardson ...
The American Journal of Human Genetics 75 (6), 1046-1058, 2004
Genetics of developmental dyslexia
TS Scerri, G Schulte-Körne
European child & adolescent psychiatry 19 (3), 179-197, 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
The genetic lexicon of dyslexia
S Paracchini, T Scerri, AP Monaco
Annual review of genomics and human genetics 8, 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
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
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
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
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
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
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
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
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
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
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
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