DOI,IST REx ID,Research Group,Title of publication
10.15479/AT:ISTA:th_992,395,GaNo,The branched chain amino acids in autism spectrum disorders 
10.1111/ejn.13418,1228,GaNo,Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence
10.1371/journal.ppat.1006758,540,GaNo,Characterization of host proteins interacting with the lymphocytic choriomeningitis virus L protein
10.1007/978-3-319-52498-6_9,623,GaNo,Extracerebral dysfunction in animal models of autism spectrum disorder
10.1007/978-3-319-52498-6_10,634,GaNo,Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder
10.1126/scitranslmed.aam9867,656,GaNo,Modeling Alzheimer's disease in mice with human neurons
10.1126/scitranslmed.aan2786,667,GaNo,The antisocial side of antibiotics
10.1126/scitranslmed.aan8196,689,GaNo,Rett syndrome modeling goes simian
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