Author details

Full Name

Eftichia Duketis

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
32624584	Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.	Transl Psychiatry	2020
29147782	Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.	J Neural Transm (Vienna)	2018
27417655	Lack of replication of previous autism spectrum disorder GWAS hits in European populations.	Autism Res	2017
26788924	Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder.	Autism Res	2016
25224256	Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.	Molecular Psychiatry	2015
24768552	Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.	Am J Hum Genet	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
23933821	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.	Nat Genet	2013
21996756	A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.	Hum Genet	2012
22843504	Individual common variants exert weak effects on the risk for autism spectrum disorders.	Hum Mol Genet	2012
22346768	Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.	PLoS Genet	2012
21656903	No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.	Am J Med Genet B Neuropsychiatr Genet	2011
21454389	Sex differences in cognitive domains and their clinical correlates in higher-functioning autism spectrum disorders.	Autism	2011
21567917	Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder.	American Journal of Medical Genetics, Part A	2011
20663923	A genome-wide scan for common alleles affecting risk for autism.	Hum Mol Genet	2010
19564046	Severe affective and behavioral dysregulation in youth is associated with increased serum TSH.	Journal of Affective Disorders	2010
20402708	Bipolar disorder in children and adolescents in Germany: national trends in the rates of inpatients, 2000-2007.	Bipolar Disorders	2010
19941018	Genetics of autistic disorders: review and clinical implications.	European Child and Adolescent Psychiatry	2010
20531469	Functional impact of global rare copy number variation in autism spectrum disorders.	Nature	2010
19328541	Validation of the Hypomania Checklist (HCL-32) in a nonclinical sample of German adolescents.	Journal of Adolescence	2009
19165532	Pilot evaluation of the Frankfurt Social Skills Training for children and adolescents with autism spectrum disorder.	European Child and Adolescent Psychiatry	2009
19724983	A 16-year-old boy with severe gamma-butyrolactone (GBL) withdrawal delirium.	Pharmacopsychiatry	2009
19739059	[Withdrawal syndrome after abuse of GHB (Gamma-Hydroxybutyrate) and its physiological precursors - its relevance for child and adolescent psychiatrists].	Z Kinder Jugendpsychiatr Psychother	2009
19050728	A 15q13.3 microdeletion segregating with autism.	Eur J Hum Genet	2009