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Human Molecular Genetics|November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexiaThomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Transplantation|October 15, 2003
Increased expression of transforming growth factor-beta and eosinophil infiltration is associated with the development of transplant arteriosclerosis in long-term surviving cardiac allograftsBernd M Spriewald, Stephan M Ensminger, J Stephen Billing, et al.
Cytokine|August 30, 2002
Linked unresponsiveness: early cytokine gene expression profiles in cardiac allografts following pretreatment of recipients with bone marrow cells expressing donor MHC alloantigenBernd M Spriewald, J Stephen Billing, Stephan M Ensminger, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean populationPia Villanueva, Dianne F Newbury, Lilian Jara, et al.
Plos Genetics|March 28, 2009
A common variant associated with dyslexia reduces expression of the KIAA0319 geneMegan Y Dennis, Silvia Paracchini, Thomas S Scerri, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 24, 2017
The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 SignalingFilipa Franquinho, Joana Nogueira-Rodrigues, Joana M Duarte, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
CNVs leading to fusion transcripts in individuals with autism spectrum disorderRichard Holt, Nuala H Sykes, Inês C Conceição, et al.
The American Journal of Psychiatry|October 3, 2008
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general populationSilvia Paracchini, Colin D Steer, Lyn-Louise Buckingham, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairmentDianne F Newbury, Pamela C Warburton, Natalie Wilson, et al.
European Journal of Human Genetics : EJHG|April 23, 2009
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collectionNuala H Sykes, Claudio Toma, Natalie Wilson, et al.
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