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Andreas G Chiocchetti
Andreas G Chiocchetti
Prof Translational Child Psychiatry, Goethe University Frankfurt
Verified email at kgu.de - Homepage
Title
Cited by
Cited by
Year
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
27412014
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
16932020
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
10642014
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ...
PLoS genetics 8 (2), e1002521, 2012
4712012
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
4612017
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Molecular autism 8, 1-17, 2017
3312017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
ET Lim, M Uddin, S De Rubeis, Y Chan, AS Kamumbu, X Zhang, ...
Nature neuroscience 20 (9), 1217-1224, 2017
2652017
The neurobiological basis of human aggression: a review on genetic and epigenetic mechanisms
R Waltes, AG Chiocchetti, CM Freitag
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 …, 2016
2092016
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
AT Pagnamenta, E Bacchelli, MV de Jonge, G Mirza, TS Scerri, F Minopoli, ...
Biological psychiatry 68 (4), 320-328, 2010
1702010
Recessive gene disruptions in autism spectrum disorder
RN Doan, ET Lim, S De Rubeis, C Betancur, DJ Cutler, AG Chiocchetti, ...
Nature genetics 51 (7), 1092-1098, 2019
1412019
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism
SM Klauck, B Felder, A Kolb-Kokocinski, C Schuster, A Chiocchetti, ...
Molecular psychiatry 11 (12), 1073-1084, 2006
1292006
Ribosomal proteins Rpl10 and Rps6 are potent regulators of yeast replicative life span
A Chiocchetti, J Zhou, H Zhu, T Karl, O Haubenreisser, M Rinnerthaler, ...
Experimental gerontology 42 (4), 275-286, 2007
1272007
Relationship between cortical gyrification, white matter connectivity, and autism spectrum disorder
C Ecker, D Andrews, F Dell'Acqua, E Daly, C Murphy, M Catani, ...
Cerebral Cortex 26 (7), 3297-3309, 2016
912016
Conduct disorder in adolescent females: current state of research and study design of the FemNAT-CD consortium
CM Freitag, K Konrad, C Stadler, SA De Brito, A Popma, SC Herpertz, ...
European child & adolescent psychiatry 27 (9), 1077-1093, 2018
772018
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
D Hadley, Z Wu, C Kao, A Kini, A Mohamed-Hadley, K Thomas, ...
Nature communications 5 (1), 1-10, 2014
732014
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
R Waltes, E Duketis, M Knapp, RJL Anney, G Huguet, S Schlitt, ...
Human genetics 133 (6), 781-792, 2014
672014
Dual molecular effects of dominant RORA mutations cause two variants of syndromic intellectual disability with either autism or cerebellar ataxia
C Guissart, X Latypova, P Rollier, TN Khan, H Stamberger, K McWalter, ...
The American Journal of Human Genetics 102 (5), 744-759, 2018
612018
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, SD Rubeis, JY An, ...
BioRxiv, 484113, 2018
492018
Meta‐analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder
TM Kranz, M Kopp, R Waltes, M Sachse, E Duketis, TA Jarczok, ...
Autism Research 9 (10), 1036-1045, 2016
492016
Lack of replication of previous autism spectrum disorder GWAS hits in European populations
B Torrico, AG Chiocchetti, E Bacchelli, E Trabetti, A Hervás, B Franke, ...
Autism research 10 (2), 202-211, 2017
462017
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