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Wellcome Trust Centre for Human Genetics
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Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry.
Nucleic acids research Mar, 2002 | Pubmed ID: 11884646
A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa.
American journal of human genetics Aug, 2004 | Pubmed ID: 15202071
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
American journal of human genetics Dec, 2004 | Pubmed ID: 15514892
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Human molecular genetics May, 2006 | Pubmed ID: 16600991
Y-chromosomal insights into the genetic impact of the caste system in India.
Human genetics Mar, 2007 | Pubmed ID: 17075717
Haplotype-specific expression of exon 10 at the human MAPT locus.
Human molecular genetics Dec, 2006 | Pubmed ID: 17085483
The genetic lexicon of dyslexia.
Annual review of genomics and human genetics , 2007 | Pubmed ID: 17444811
Alternative splicing in the dyslexia-associated gene KIAA0319.
Mammalian genome : official journal of the International Mammalian Genome Society Sep, 2007 | Pubmed ID: 17846832
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.
Human molecular genetics Mar, 2008 | Pubmed ID: 18063668
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
The American journal of psychiatry Dec, 2008 | Pubmed ID: 18829873
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
PLoS genetics Mar, 2009 | Pubmed ID: 19325871
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
American journal of human genetics Aug, 2009 | Pubmed ID: 19646677
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
Biological psychiatry Aug, 2010 | Pubmed ID: 20346443
PCSK6 is associated with handedness in individuals with dyslexia.
Human molecular genetics Feb, 2011 | Pubmed ID: 21051773
Identification of candidate genes for dyslexia susceptibility on chromosome 18.
PloS one , 2010 | Pubmed ID: 21060895
DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
Biological psychiatry Aug, 2011 | Pubmed ID: 21457949
Dissection of genetic associations with language-related traits in population-based cohorts.
Journal of neurodevelopmental disorders Dec, 2011 | Pubmed ID: 21894572
University of Oxford
Silvia Paracchini1,
Anthony P. Monaco1,
Julian C. Knight1
1Wellcome Trust Centre for Human Genetics, University of Oxford
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