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Authors: Thomas Sander
Journal Article
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy Get access
Human Molecular Genetics, Volume 23, Issue 22, 15 November 2014, Pages 6069–6080, https://doi.org/10.1093/hmg/ddu306
Published: 16 June 2014
Journal Article
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Get access
Human Molecular Genetics, Volume 21, Issue 24, 15 December 2012, Pages 5359–5372, https://doi.org/10.1093/hmg/dds373
Published: 04 September 2012
Journal Article
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance Get access
Human Molecular Genetics, Volume 18, Issue 19, 1 October 2009, Pages 3626–3631, https://doi.org/10.1093/hmg/ddp311
Published: 10 July 2009
Journal Article
Association of attentional network function with exon 5 variations of the CHRNA4 gene Open Access
Human Molecular Genetics, Volume 16, Issue 18, 15 September 2007, Pages 2165–2174, https://doi.org/10.1093/hmg/ddm168
Published: 05 July 2007
Journal Article
Genome search for susceptibility loci of common idiopathic generalised epilepsies Get access
Human Molecular Genetics, Volume 9, Issue 10, 12 June 2000, Pages 1465–1472, https://doi.org/10.1093/hmg/9.10.1465
Published: 12 June 2000
