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A. Chiocchetti · SciRah

Researcher profile · Semantic Scholar

A. Chiocchetti

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A. Chiocchetti — researcher profile on SciRah

h-index: 27
Works: 84
Citations: 5,413

Most-cited papers

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
D. Pinto, Elsa Delaby, D. Merico, M. Barbosa +108 more
2014American Journal of Human Genetics936 citations Open access
Semantic Scholar
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
C. Leblond, J. Heinrich, R. Delorme, C. Proepper +56 more
2012PLoS Genetics401 citations Open access
Semantic Scholar
The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms
R. Waltes, A. Chiocchetti, C. Freitag
2016American Journal of Medical Genetics Part B: Neuropsychiatric Genetics168 citations Open access
Semantic Scholar
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
A. Pagnamenta, E. Bacchelli, M. D. de Jonge, G. Mirza +23 more
2010Biological Psychiatry152 citations Open access
Semantic Scholar
Recessive gene disruptions in autism spectrum disorder
Ryan N. Doan, Elaine T. Lim, S. de Rubeis, C. Betancur +10 more
2019Nature Genetics140 citations Open access
Semantic Scholar
Ribosomal proteins Rpl10 and Rps6 are potent regulators of yeast replicative life span.
A. Chiocchetti, Jia Zhou, Hua-Shun Zhu, T. Karl +8 more
2007Experimental Gerontology132 citations
Semantic Scholar
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism
S. Klauck, B. Felder, A. Kolb-Kokocinski, C. Schuster +7 more
2006Molecular Psychiatry112 citations Open access
Semantic Scholar
Relationship Between Cortical Gyrification, White Matter Connectivity, and Autism Spectrum Disorder
C. Ecker, D. Andrews, F. Dell'Acqua, E. Daly +13 more
2016Cerebral Cortex83 citations Open access
Semantic Scholar
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.
C. Guissart, X. Latypova, Paul Rollier, Tahir N. Khan +55 more
2018American Journal of Human Genetics73 citations Open access
Semantic Scholar
Conduct disorder in adolescent females: current state of research and study design of the FemNAT-CD consortium
C. Freitag, K. Konrad, C. Stadler, S. De Brito +8 more
2018European Child and Adolescent Psychiatry72 citations
Semantic Scholar
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
R. Waltes, E. Duketis, M. Knapp, R. Anney +16 more
2014Human Genetics72 citations
Semantic Scholar
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +153 more
2018bioRxiv60 citations Open access
Semantic Scholar
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
D. Hadley, Zhi-Liang Wu, Charlly Kao, A. Kini +94 more
2014Nature Communications59 citations Open access
Semantic Scholar
Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder.
C. Ecker, C. Pretzsch, Anke Bletsch, C. Mann +35 more
2021American Journal of Psychiatry53 citations Open access
Semantic Scholar
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype.
M. Breen, Paras Garg, Lara Tang, Danielle Mendonca +25 more
2020American Journal of Human Genetics49 citations Open access
Semantic Scholar
Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach
A. Chiocchetti, Marnie Kopp, R. Waltes, Denise Haslinger +9 more
2014Molecular Psychiatry48 citations
Semantic Scholar
Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model
Denise Haslinger, R. Waltes, Afsheen Yousaf, Silvia Lindlar +12 more
2018Molecular Autism37 citations Open access
Semantic Scholar
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder
S. Curran, P. Bolton, K. Rozsnyai, A. Chiocchetti +22 more
2011American Journal of Medical Genetics Part B: Neuropsychiatric Genetics37 citations
Semantic Scholar
The MiR-320 Family Is Strongly Downregulated in Patients with COVID-19 Induced Severe Respiratory Failure
R. Duecker, E. Adam, Sarah Wirtz, Lucia Gronau +10 more
2021International Journal of Molecular Sciences36 citations Open access
Semantic Scholar
Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder
A. Chiocchetti, G. Pakalapati, Eftichia Duketis, Stefan Wiemann +3 more
2011American Journal of Medical Genetics. Part A36 citations
Semantic Scholar
Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders
A. Chiocchetti, Denise Haslinger, J. Stein, L. de la Torre-Ubieta +7 more
2016Translational Psychiatry30 citations Open access
Semantic Scholar
Glutamatergic candidate genes in autism spectrum disorder: an overview
A. Chiocchetti, H. Bour, C. Freitag
2014Journal of neural transmission30 citations
Semantic Scholar
Dual Role of microRNA-146a in Experimental Inflammation in Human Pulmonary Epithelial and Immune Cells and Expression in Inflammatory Lung Diseases
Lucia Gronau, R. Duecker, S. Jerkic, O. Eickmeier +5 more
2024International Journal of Molecular Sciences28 citations Open access
Semantic Scholar
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
D. Rots, Taryn E. Jakub, Crystal Keung, A. Jackson +113 more
2023American Journal of Human Genetics28 citations Open access
Semantic Scholar
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder
Afsheen Yousaf, R. Waltes, Denise Haslinger, S. Klauck +11 more
2020Translational Psychiatry28 citations Open access
Semantic Scholar
DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan
J. van Dongen, F. Hagenbeek, M. Suderman, Peter J. Roetman +85 more
2020bioRxiv27 citations Open access
Semantic Scholar
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approaches.
F. Rosenow, Natascha van Alphen, A. Becker, A. Chiocchetti +30 more
2017Epilepsy & Behavior27 citations
Semantic Scholar
Protein signatures of oxidative stress response in a patient specific cell line model for autism
A. Chiocchetti, Denise Haslinger, M. Boesch, T. Karl +11 more
2014Molecular Autism25 citations Open access
Semantic Scholar
Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range
R. Waltes, Johannes Gfesser, Denise Haslinger, K. Schneider-Momm +4 more
2014Journal of neural transmission22 citations
Semantic Scholar
Proteomic profiling reveals a catalogue of new candidate proteins for human skin aging
M. Laimer, T. Kocher, A. Chiocchetti, A. Trost +5 more
2010Experimental Dermatology22 citations
Semantic Scholar
Lithium-induced gene expression alterations in two peripheral cell models of bipolar disorder
S. Kittel-Schneider, M. Hilscher, C. Scholz, H. Weber +4 more
2019World Journal of Biological Psychiatry19 citations Open access
Semantic Scholar
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses
B. Torrico, Ester Antón-Galindo, N. Fernàndez-Castillo, Eva Rojo-Francàs +17 more
2020Journal of Clinical Medicine18 citations Open access
Semantic Scholar
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approaches.
S. Bauer, Natascha van Alphen, A. Becker, A. Chiocchetti +30 more
2017Epilepsy & Behavior17 citations
Semantic Scholar
Neuroendocrine Stress Response in Females and Males With Conduct Disorder and Associations With Early Adversity.
A. Bernhard, K. Ackermann, A. Martinelli, A. Chiocchetti +12 more
2021Journal of the American Academy of Child and Adolescent Psychiatry16 citations Open access
Semantic Scholar
Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD
V. S. Palladino, A. Chiocchetti, Lukas Frank, Denise Haslinger +10 more
2020Journal of Clinical Medicine16 citations Open access
Semantic Scholar
Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy
Sarah Martin, A. Strzelczyk, Silvia Lindlar, K. Krause +6 more
2019Frontiers in Neurology15 citations Open access
Semantic Scholar
Effects of Hypoxia on RNA Cargo in Extracellular Vesicles from Human Adipose-Derived Stromal/Stem Cells
Benjamin Koch, Alec Geßner, Samira Farmand, D. Fuhrmann +3 more
2022International Journal of Molecular Sciences14 citations Open access
Semantic Scholar
Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment
V. Vasić, Matt Jones, Denise Haslinger, L. Knaus +3 more
2021Genes14 citations Open access
Semantic Scholar
A point mutation in the Ncr1 signal peptide impairs the development of innate lymphoid cell subsets
F. F. Almeida, S. Tognarelli, A. Marçais, A. Kueh +28 more
2018Oncoimmunology12 citations Open access
Semantic Scholar
Ataxia telangiectasia alters the ApoB and reelin pathway
J. Canet-Pons, R. Schubert, R. Duecker, R. Schrewe +7 more
2018Neurogenetics12 citations Open access
Semantic Scholar
Psychoneuroendocrine stress response in female and male youth with major depressive disorder
A. Bernhard, Nikola Fann, A. Chiocchetti, K. Ackermann +2 more
2025Journal of Child Psychology and Psychiatry and Allied Disciplines8 citations Open access
Semantic Scholar
The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing
Sophie von Brauchitsch, Denise Haslinger, Silvia Lindlar, H. Thiele +12 more
2023Epilepsia Open8 citations Open access
Semantic Scholar
SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study
Elizabeth Farrow, A. Chiocchetti, J. Rogers, Ruth Pauli +11 more
2021Translational Psychiatry8 citations Open access
Semantic Scholar
Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults
Silvia Biere, T. Kranz, S. Matura, Kristiyana Petrova +12 more
2020Frontiers in Psychiatry8 citations Open access
Semantic Scholar
[Genetic analyses for identifying molecular mechanisms in autism spectrum disorders].
A. Chiocchetti, S. Klauck
2011Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie8 citations
Semantic Scholar
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines
F. Radtke, V. S. Palladino, R. McNeill, A. Chiocchetti +12 more
2022American Journal of Medical Genetics Part B: Neuropsychiatric Genetics7 citations Open access
Semantic Scholar
The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factors
A. Chiocchetti, Afsheen Yousaf, R. Waltes, A. Bernhard +11 more
2022PLoS ONE7 citations Open access
Semantic Scholar
Knockdown of the ADHD Candidate Gene Diras2 in Murine Hippocampal Primary Cells
L. Grünewald, A. Chiocchetti, H. Weber, C. Scholz +3 more
2019Journal of Attention Disorders7 citations
Semantic Scholar
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities
A. Chiocchetti, Afsheen Yousaf, H. Bour, Denise Haslinger +12 more
2018Journal of neural transmission7 citations
Semantic Scholar

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