| The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis | The world journal of biological psychiatry | | | 2014 | 1,273 | 8 |
|
| [Retracted] Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorder | British journal of psychiatry | | | 2014 | 835 | 111 |
|
| Neurobiology of suicide: do biomarkers exist? | International journal of legal medicine | | | 2014 | 179 | 346 |
|
| Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures | Epilepsy research | | | 2014 | 195 | 0 |
|
| EEG anomalies in adult ADHD subjects performing a working memory task | Neuroscience | | | 2013 | 815 | 2 |
|
| Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report | PloS one | | | 2013 | 1,081 | 967 |
|
| Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene | Translational psychiatry | | | 2013 | 258 | 232 |
|
| A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family | BMC genetics | | | 2013 | 220 | 120 |
|
| Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy | The Journal of biological chemistry | | | 2012 | 159 | 204 |
|
| Magnetic resonance imaging correlates of first-episode psychosis in young adult male patients: combined analysis of grey and white matter | Journal of psychiatry & neuroscience | | | 2012 | 701 | 2 |
|
| Genetics of temporal lobe epilepsy: a review | Epilepsy Research and Treatment | | | 2012 | 148 | 176 |
|
| Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis | PLoS medicine | | | 2012 | 753 | 480 |
|
| Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy | Human mutation | | | 2012 | 242 | 0 |
|
| Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder | Journal of affective disorders | | | 2011 | 730 | 1,147 |
|
| War exposure, 5-HTTLPR genotype and lifetime risk of depression | British journal of psychiatry | | | 2011 | 1,163 | 484 |
|
| Replication of association between a SCN1A splice variant and febrile seizures | Epilepsia | | | 2011 | 615 | 346 |
|
| Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma | Translational psychiatry | | | 2011 | 1,470 | 0 |
|
| A novel exon 3 mutation in a Tunisian patient with Lafora's disease | Journal of the neurological sciences | | | 2011 | 597 | 607 |
|
| Impulsivity, aggression and suicidal behavior in unipolar and bipolar disorders | Journal of affective disorders | | | 2011 | 848 | 1,403 |
|
| Age at onset in bipolar I affective disorder in the USA and Europe | The world journal of biological psychiatry | | | 2011 | 660 | 1,209 |
|
| Suicidal behavior is associated with reduced corpus callosum area | Biological psychiatry | | | 2011 | 700 | 1,228 |
|
| Le projet «SYNAPSY» : un point de rencontre entre clinique et neurosciences | Revue médicale suisse | | | 2011 | 633 | 4 |
|
| Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victims | Neuropsychobiology | | | 2011 | 722 | 703 |
|
| Distinguishing the relevant features of frequent suicide attempters | Journal of psychiatric research | | | 2011 | 747 | 1,891 |
|
| Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism | Brain and behavior | | | 2011 | 699 | 597 |
|
| Adverse childhood environment and late-life cognitive functioning | International journal of geriatric psychiatry | | | 2011 | 726 | 940 |
|
| Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample | Pharmacogenomics | | | 2011 | 726 | 0 |
|
| BRD2 and TAP-1 genes and juvenile myoclonic epilepsy | Neurological sciences | | | 2010 | 645 | 350 |
|
| European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset | American journal of medical genetics. Part B, Neuropsychiatric genetics | | | 2010 | 765 | 0 |
|
| Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies | International journal of immunogenetics | | | 2010 | 559 | 0 |
|
| Gender and genotype modulation of the association between lipid levels and depressive symptomatology in community-dwelling elderly (the ESPRIT study) | Biological psychiatry | | | 2010 | 660 | 0 |
|
| Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder | Genes, brain and behavior | | | 2010 | 719 | 0 |
|
| A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation | Epilepsia | | | 2010 | 713 | 0 |
|
| Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder | American journal of medical genetics. Part B, Neuropsychiatric genetics | | | 2010 | 674 | 0 |
|
| Genes, suicide and decisions | European psychiatry | | | 2010 | 598 | 1 |
|
| COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits | Genes, brain and behavior | | | 2010 | 732 | 2 |
|
| Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures | PloS one | | | 2010 | 675 | 388 |
|
| Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behavior | NeuroImage | | | 2010 | 587 | 0 |
|
| Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family | Epilepsy research | | | 2010 | 638 | 0 |
|
| Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims | American journal of medical genetics. Part B, Neuropsychiatric genetics | | | 2010 | 750 | 1 |
|
| Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depression | Journal of affective disorders | | | 2010 | 635 | 0 |
|
| Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies | PLOS genetics | | | 2010 | 721 | 543 |
|
| Somatic markers and explicit knowledge are both involved in decision-making | Neuropsychologia | | | 2009 | 616 | 0 |
|
| Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior | American journal of medical genetics. Part B, Neuropsychiatric genetics | | | 2009 | 750 | 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 dependence | Addictive behaviors | | | 2009 | 572 | 0 |
|
| Modulation of anger control in suicide attempters by TPH-1 | Genes, brain and behavior | | | 2009 | 600 | 0 |
|
| 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy | Nature genetics | | | 2009 | 628 | 2 |
|
| Childhood trauma as a correlative factor of suicidal behavior - via aggression traits. Similar results in an Italian and in a French sample | European psychiatry | | | 2009 | 696 | 1 |
|
| Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression | The Journal of clinical psychiatry | | | 2009 | 721 | 382 |
|
| The electroencephalographic fingerprint of sleep is genetically determined: a twin study | Annals of neurology | | | 2008 | 636 | 0 |
|
| Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt | Genes, brain and behavior | | | 2008 | 714 | 0 |
|
| Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter gene | Bipolar disorders | | | 2008 | 662 | 0 |
|
| Candidate genes for temporal lobe epilepsy: a replication study | Neurological sciences | | | 2008 | 650 | 311 |
|
| GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsy | Epilepsia | | | 2005 | 216 | 79 |
|
| Association of the connexin36 gene with juvenile myoclonic epilepsy | Journal of medical genetics | | | 2004 | 617 | 0 |
|
| No association between DUP25 and anxiety disorders | American journal of medical genetics. Part B, Neuropsychiatric genetics | | | 2004 | 649 | 0 |
|
| How mutations in the nAChRs can cause ADNFLE epilepsy | Epilepsia | | | 2002 | 218 | 576 |
|
| Ion channel variation causes epilepsies | Brain research reviews | | | 2001 | 135 | 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 onset | American journal of human genetics | | | 1998 | 557 | 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 | | | 1997 | 613 | 0 |
|
| Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy | Nature | | | 1997 | 666 | 0 |
|
