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The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axisThe world journal of biological psychiatry
accessLevelRestricted
2014 1,256 8
[Retracted] Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorderBritish journal of psychiatry
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2014 819 111
Neurobiology of suicide: do biomarkers exist?International journal of legal medicine
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2014 171 237
Increased CPA6 promoter methylation in focal epilepsy and in febrile seizuresEpilepsy research
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2014 183 0
EEG anomalies in adult ADHD subjects performing a working memory taskNeuroscience
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2013 793 2
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) ReportPloS one
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2013 1,070 871
Response to psychotherapy in borderline personality disorder and methylation status of the BDNF geneTranslational psychiatry
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2013 245 149
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous familyBMC genetics
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2013 211 91
Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsyJournal of biological chemistry
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2012 149 96
Magnetic resonance imaging correlates of first-episode psychosis in young adult male patients: combined analysis of grey and white matterJournal of psychiatry & neuroscience
accessLevelRestricted
2012 687 2
Genetics of temporal lobe epilepsy: a reviewEpilepsy Research and Treatment
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2012 139 85
Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysisPLoS medicine
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2012 739 461
Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsyHuman mutation
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2012 233 0
Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorderJournal of affective disorders
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2011 720 1,012
War exposure, 5-HTTLPR genotype and lifetime risk of depressionBritish journal of psychiatry
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2011 1,152 452
Replication of association between a SCN1A splice variant and febrile seizuresEpilepsia
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2011 605 329
Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of traumaTranslational psychiatry
accessLevelRestricted
2011 1,457 0
A novel exon 3 mutation in a Tunisian patient with Lafora's diseaseJournal of the neurological sciences
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2011 588 511
Impulsivity, aggression and suicidal behavior in unipolar and bipolar disordersJournal of affective disorders
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2011 839 1,218
Age at onset in bipolar I affective disorder in the USA and EuropeThe world journal of biological psychiatry
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2011 650 1,017
Suicidal behavior is associated with reduced corpus callosum areaBiological psychiatry
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2011 688 1,126
Le projet «SYNAPSY» : un point de rencontre entre clinique et neurosciencesRevue médicale suisse
accessLevelRestricted
2011 621 4
Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victimsNeuropsychobiology
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2011 711 634
Distinguishing the relevant features of frequent suicide attemptersJournal of psychiatric research
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2011 737 1,734
Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphismBrain and behavior
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2011 687 566
Adverse childhood environment and late-life cognitive functioningInternational journal of geriatric psychiatry
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2011 714 803
Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient samplePharmacogenomics
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2011 715 0
BRD2 and TAP-1 genes and juvenile myoclonic epilepsyNeurological sciences
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2010 627 266
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onsetAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
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2010 755 0
Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsiesInternational journal of immunogenetics
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2010 551 0
Gender and genotype modulation of the association between lipid levels and depressive symptomatology in community-dwelling elderly (the ESPRIT study)Biological psychiatry
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2010 649 0
Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorderGenes, brain and behavior
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2010 708 0
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutationEpilepsia
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2010 703 0
Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorderAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
accessLevelRestricted
2010 661 0
Genes, suicide and decisionsEuropean psychiatry
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2010 590 1
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traitsGenes, brain and behavior
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2010 723 2
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresPloS one
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2010 658 341
Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behaviorNeuroImage
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2010 573 0
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian familyEpilepsy research
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2010 628 0
Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victimsAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
accessLevelRestricted
2010 742 1
Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depressionJournal of affective disorders
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2010 626 0
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesPLOS genetics
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2010 704 391
Somatic markers and explicit knowledge are both involved in decision-makingNeuropsychologia
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2009 600 0
Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behaviorAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
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2009 732 1
Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependenceAddictive behaviors
accessLevelRestricted
2009 557 0
Modulation of anger control in suicide attempters by TPH-1Genes, brain and behavior
accessLevelRestricted
2009 592 0
15q13.3 microdeletions increase risk of idiopathic generalized epilepsyNature genetics
accessLevelRestricted
2009 608 2
Childhood trauma as a correlative factor of suicidal behavior - via aggression traits. Similar results in an Italian and in a French sampleEuropean psychiatry
accessLevelRestricted
2009 688 1
Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depressionThe Journal of clinical psychiatry
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2009 709 319
The electroencephalographic fingerprint of sleep is genetically determined: a twin studyAnnals of neurology
accessLevelRestricted
2008 626 0
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attemptGenes, brain and behavior
accessLevelRestricted
2008 696 0
Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter geneBipolar disorders
accessLevelRestricted
2008 647 0
Candidate genes for temporal lobe epilepsy: a replication studyNeurological sciences
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2008 635 271
GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsyEpilepsia
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2005 208 53
Association of the connexin36 gene with juvenile myoclonic epilepsyJournal of medical genetics
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2004 608 0
No association between DUP25 and anxiety disordersAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
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2004 637 0
How mutations in the nAChRs can cause ADNFLE epilepsyEpilepsia
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2002 209 396
Ion channel variation causes epilepsiesBrain Research Reviews
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2001 128 0
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onsetAmerican journal of human genetics
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1998 546 0
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1)American journal of human genetics
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1997 599 0
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsyNature
accessLevelRestricted
1997 654 0
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