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Title Published in Access level OA Policy Year Views Downloads
The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axisThe world journal of biological psychiatry
accessLevelRestricted
2014 941 7
[Retracted] Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorderBritish journal of psychiatry
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2014 722 111
Neurobiology of suicide: do biomarkers exist?International journal of legal medicine
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2014 113 149
Increased CPA6 promoter methylation in focal epilepsy and in febrile seizuresEpilepsy research
accessLevelRestricted
2014 131 0
EEG anomalies in adult ADHD subjects performing a working memory taskNeuroscience
accessLevelRestricted
2013 712 2
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) ReportPloS one
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2013 1 026 834
Response to psychotherapy in borderline personality disorder and methylation status of the BDNF geneTranslational psychiatry
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2013 170 90
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 148 59
Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsyJournal of biological chemistry
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2012 96 50
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 642 2
Genetics of temporal lobe epilepsy: a reviewEpilepsy Research and Treatment
accessLevelPublic
2012 100 51
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 646 448
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 162 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 651 824
War exposure, 5-HTTLPR genotype and lifetime risk of depressionBritish journal of psychiatry
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2011 1 108 439
Replication of association between a SCN1A splice variant and febrile seizuresEpilepsia
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2011 560 322
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 1 317 0
A novel exon 3 mutation in a Tunisian patient with Lafora's diseaseJournal of the neurological sciences
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2011 543 401
Impulsivity, aggression and suicidal behavior in unipolar and bipolar disordersJournal of affective disorders
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2011 771 1 079
Age at onset in bipolar I affective disorder in the USA and EuropeThe world journal of biological psychiatry
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2011 578 942
Suicidal behavior is associated with reduced corpus callosum areaBiological psychiatry
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2011 603 1 037
Le projet «SYNAPSY» : un point de rencontre entre clinique et neurosciencesRevue médicale suisse
accessLevelRestricted
2011 576 4
Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victimsNeuropsychobiology
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2011 659 573
Distinguishing the relevant features of frequent suicide attemptersJournal of psychiatric research
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2011 676 1 625
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 631 550
Adverse childhood environment and late-life cognitive functioningInternational journal of geriatric psychiatry
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2011 643 696
Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient samplePharmacogenomics
accessLevelPrivate
2011 649 0
BRD2 and TAP-1 genes and juvenile myoclonic epilepsyNeurological sciences
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2010 574 220
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
accessLevelRestricted
2010 591 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 501 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 558 0
Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorderGenes, brain and behavior
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2010 629 0
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutationEpilepsia
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2010 611 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 584 0
Genes, suicide and decisionsEuropean psychiatry
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2010 547 1
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traitsGenes, brain and behavior
accessLevelRestricted
2010 649 2
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizuresPloS one
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2010 579 319
Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behaviorNeuroImage
accessLevelRestricted
2010 529 0
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian familyEpilepsy research
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2010 579 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 655 1
Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depressionJournal of affective disorders
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2010 581 0
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesPLOS genetics
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2010 610 352
Somatic markers and explicit knowledge are both involved in decision-makingNeuropsychologia
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2009 536 0
Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behaviorAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
accessLevelRestricted
2009 655 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 503 0
Modulation of anger control in suicide attempters by TPH-1Genes, brain and behavior
accessLevelRestricted
2009 538 0
15q13.3 microdeletions increase risk of idiopathic generalized epilepsyNature genetics
accessLevelRestricted
2009 527 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 585 1
Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depressionThe Journal of clinical psychiatry
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2009 642 295
The electroencephalographic fingerprint of sleep is genetically determined: a twin studyAnnals of neurology
accessLevelRestricted
2008 555 0
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attemptGenes, brain and behavior
accessLevelRestricted
2008 632 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 596 0
Candidate genes for temporal lobe epilepsy: a replication studyNeurological sciences
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2008 568 234
GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsyEpilepsia
accessLevelPublic
2005 146 29
Association of the connexin36 gene with juvenile myoclonic epilepsyJournal of medical genetics
accessLevelRestricted
2004 554 0
No association between DUP25 and anxiety disordersAmerican journal of medical genetics. Part B, Neuropsychiatric genetics
accessLevelRestricted
2004 594 0
How mutations in the nAChRs can cause ADNFLE epilepsyEpilepsia
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2002 133 275
Ion channel variation causes epilepsiesBrain Research Reviews
accessLevelRestricted
2001 89 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
accessLevelRestricted
1998 494 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
accessLevelRestricted
1997 552 0
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsyNature
accessLevelRestricted
1997 601 0
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