DOI,IST REx ID,Research Group,Title of publication
10.1126/scitranslmed.aao0972,702,GaNo,The riddle of CHD8 haploinsufficiency in autism spectrum disorder
10.7554/eLife.25125,713,"GaNo,SiHi",Mapping the mouse Allelome reveals tissue specific regulation of allelic expression
10.1016/j.drugalcdep.2017.04.015,714,GaNo,HIV Tat excites D1 receptor-like expressing neurons from rat nucleus accumbens
10.1126/scitranslmed.aao4218,715,GaNo,More excitation for Rett syndrome
10.1126/scitranslmed.aap8168,731,GaNo,The science of love in ASD and ADHD
10.1016/j.neuroscience.2017.09.034,747,GaNo,Modulation of cardiac vagal tone by bradykinin acting on nucleus ambiguus
10.1186/s13059-016-0873-8,1240,GaNo,Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans
10.1016/j.cell.2016.11.013,1183,GaNo,Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder
10.1093/nar/gkv727,1497,GaNo,"Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data"
10.1038/ejhg.2014.165,1789,GaNo,Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome
10.1126/science.1247363,1916,GaNo,Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders