Author details

Full Name

Andreas G Chiocchetti

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37448886	Association between Polyunsaturated Fatty Acid Profile and Bronchial Inflammation in Bronchiolitis Obliterans.		2023
36896643	The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing.		2023
36640473	Generation of four human induced pluripotent stem cells derived from ADHD patients carrying different genotypes for the risk SNP rs1397547 in the ADHD-associated gene ADGRL3.	Stem Cell Res	2023
37196654	The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.	Am J Hum Genet	2023
35089926	The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factors.	PLoS ONE	2022
35971782	ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell lines.	Am J Med Genet B Neuropsychiatr Genet	2022
35806391	Effects of Hypoxia on RNA Cargo in Extracellular Vesicles from Human Adipose-Derived Stromal/Stem Cells.	International Journal of Molecular Sciences	2022
36130942	Association of polygenic risk scores and hair cortisol with mental health trajectories during COVID lockdown.	Transl Psychiatry	2022
34856340	Neuroendocrine Stress Response in Female and Male Youths With Conduct Disorder and Associations With Early Adversity.	Journal of the American Academy of Child and Adolescent Psychiatry	2022
34503340	Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder.	Am J Psychiatry	2022
30623719	Knockdown of the ADHD Candidate Gene <i>Diras2</i> in Murine Hippocampal Primary Cells.	J Atten Disord	2021
34128703	[Genetic risk factors and their influence on neural development in autism spectrum disorders].	Zeitschrift fur Kinder- und Jugendpsychiatrie und Psychotherapie	2021
33420481	DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan.	Mol Psychiatry	2021
34561420	SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study.	Translational Psychiatry	2021
34716293	Correction: SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study.	Translational Psychiatry	2021
34828352	Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment.	Genes (Basel)	2021
34638691	The MiR-320 Family Is Strongly Downregulated in Patients with COVID-19 Induced Severe Respiratory Failure.	Int J Mol Sci	2021
32665711	Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.	Nat Neurosci	2020
31698144	A combination of LCPUFAs regulates the expression of miRNA-146a-5p in a murine asthma model and human alveolar cells.	Prostaglandins and Other Lipid Mediators	2020
32545830	Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.	J Clin Med	2020
32758449	Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype.	Am J Hum Genet	2020
33192665	Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults.	Front Psychiatry	2020
33353000	Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD.	J Clin Med	2020
32624584	Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.	Transl Psychiatry	2020
32572023	The role of rare compound heterozygous events in autism spectrum disorder.	Transl Psychiatry	2020
31209396	Recessive gene disruptions in autism spectrum disorder.	Nat Genet	2019
31707462	Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study.	Journal of Neural Transmission	2019
31551911	Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy.	Frontiers in Neurology	2019
29067888	Lithium-induced gene expression alterations in two peripheral cell models of bipolar disorder.	World J Biol Psychiatry	2019
30898465	Corrigendum to "Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient" [Stem Cell Res. 2018 Oct;32:104-109. doi: 10.1016/j.scr.2018.09.008. Epub 2018 Sep 17].	Stem Cell Res	2019
29147782	Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.	J Neural Transm (Vienna)	2018
30266033	Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient.	Stem Cell Res	2018
30443311	Loss of the Chr16p11.2 ASD candidate gene leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model.	Molecular Autism	2018
30343341	Ataxia telangiectasia alters the ApoB and reelin pathway.	Neurogenetics	2018
30288342	A point mutation in the signal peptide impairs the development of innate lymphoid cell subsets.	OncoImmunology	2018
29948230	Conduct disorder in adolescent females: current state of research and study design of the FemNAT-CD consortium.	European Child and Adolescent Psychiatry	2018
29656859	Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.	Am J Hum Genet	2018
27417655	Lack of replication of previous autism spectrum disorder GWAS hits in European populations.	Autism Res	2017
28917501	Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approaches.	Epilepsy Behav	2017
28917498	Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approaches.	Epilepsy Behav	2017
28714951	Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.	Nat Neurosci	2017
26494515	The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2016
26788924	Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder.	Autism Res	2016
27130663	Relationship Between Cortical Gyrification, White Matter Connectivity, and Autism Spectrum Disorder.	Cereb Cortex	2016
27483382	Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.	Transl Psychiatry	2016
25224256	Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.	Molecular Psychiatry	2015
24512814	Protein signatures of oxidative stress response in a patient specific cell line model for autism.	Molecular Autism	2014
25363760	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	2014
24442360	Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.	Human Genetics	2014
24493018	Glutamatergic candidate genes in autism spectrum disorder: an overview.	Journal of Neural Transmission	2014