Thomas Scerri
Thomas Scerri
Postdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical Research
Verified email at wehi.edu.au
Title
Cited by
Cited by
Year
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
3052006
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
2782004
Genetics of developmental dyslexia
TS Scerri, G Schulte-Körne
European child & adolescent psychiatry 19 (3), 179-197, 2010
2652010
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
2642011
The genetic lexicon of dyslexia
S Paracchini, T Scerri, AP Monaco
Annual review of genomics and human genetics 8, 2007
2022007
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
1912006
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
1832011
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
1592008
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
1432013
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
1422011
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
1412013
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
1392015
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
1372010
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
1312004
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
1272010
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
1182009
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
892014
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
842016
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
742015
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
632017
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