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Nature|May 19, 2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variantChristelle Golzio, Jason Willer, Michael E Talkowski, et al.
European Journal of Human Genetics : EJHG|April 7, 2005
Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage intervalAdi Levi, Yoav Kohn, Kyra Kanyas, et al.
Human Molecular Genetics|August 23, 2013
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste geneticsMirko Ledda, Zoltán Kutalik, Maria C Souza Destito, et al.
Human Molecular Genetics|June 14, 2011
Genome-wide association study identifies two loci strongly affecting transferrin glycosylationZoltán Kutalik, Beben Benyamin, Sven Bergmann, et al.
European Journal of Human Genetics : EJHG|June 15, 2006
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaDaniela Amann-Zalcenstein, Nili Avidan, Kyra Kanyas, et al.
Neuroimage|September 9, 2019
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number VariationsAlonso Cárdenas-de-la-Parra, Sandra Martin-Brevet, Clara Moreau, et al.
Molecular and Cellular Neurosciences|July 17, 2007
SREBP-1c expression in Schwann cells is affected by diabetes and nutritional statusAnne-Sophie de Preux, Katinka Goosen, Weixian Zhang, et al.
American Journal of Medical Genetics. Part A|March 21, 2014
MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr typeLuisa Bonafé, Jinlong Liang, Maria W Gorna, et al.
American Journal of Human Genetics|October 22, 2013
SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variantAndrew Dauber, Christelle Golzio, Cécile Guenot, et al.
Plos One|April 16, 2011
Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanomaArmand Valsesia, Donata Rimoldi, Danielle Martinet, et al.
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