AM
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
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The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis | The world journal of biological psychiatry | 2014 | 941 | 7 | |||
[Retracted] Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorder | British journal of psychiatry | 2014 | 722 | 111 | |||
Neurobiology of suicide: do biomarkers exist? | International journal of legal medicine | 2014 | 113 | 149 | |||
Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures | Epilepsy research | 2014 | 131 | 0 | |||
EEG anomalies in adult ADHD subjects performing a working memory task | Neuroscience | 2013 | 712 | 2 | |||
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report | PloS one | 2013 | 1 026 | 834 | |||
Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene | Translational psychiatry | 2013 | 170 | 90 | |||
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 | 148 | 59 | |||
Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy | Journal of biological chemistry | 2012 | 96 | 50 | |||
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 | 642 | 2 | |||
Genetics of temporal lobe epilepsy: a review | Epilepsy Research and Treatment | 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-analysis | PLoS medicine | 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 epilepsy | Human mutation | 2012 | 162 | 0 | |||
Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder | Journal of affective disorders | 2011 | 652 | 825 | |||
War exposure, 5-HTTLPR genotype and lifetime risk of depression | British journal of psychiatry | 2011 | 1 108 | 439 | |||
Replication of association between a SCN1A splice variant and febrile seizures | Epilepsia | 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 trauma | Translational psychiatry | 2011 | 1 317 | 0 | |||
A novel exon 3 mutation in a Tunisian patient with Lafora's disease | Journal of the neurological sciences | 2011 | 543 | 401 | |||
Impulsivity, aggression and suicidal behavior in unipolar and bipolar disorders | Journal of affective disorders | 2011 | 771 | 1 080 | |||
Age at onset in bipolar I affective disorder in the USA and Europe | The world journal of biological psychiatry | 2011 | 578 | 942 | |||
Suicidal behavior is associated with reduced corpus callosum area | Biological psychiatry | 2011 | 603 | 1 037 | |||
Le projet «SYNAPSY» : un point de rencontre entre clinique et neurosciences | Revue médicale suisse | 2011 | 576 | 4 | |||
Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victims | Neuropsychobiology | 2011 | 659 | 573 | |||
Distinguishing the relevant features of frequent suicide attempters | Journal of psychiatric research | 2011 | 676 | 1 625 | |||
Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism | Brain and behavior | 2011 | 631 | 550 | |||
Adverse childhood environment and late-life cognitive functioning | International journal of geriatric psychiatry | 2011 | 643 | 696 | |||
Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample | Pharmacogenomics | 2011 | 649 | 0 | |||
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy | Neurological sciences | 2010 | 574 | 220 | |||
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 | 592 | 0 | |||
Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies | International journal of immunogenetics | 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 | 2010 | 558 | 0 | |||
Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder | Genes, brain and behavior | 2010 | 630 | 0 | |||
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation | Epilepsia | 2010 | 611 | 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 | 584 | 0 | |||
Genes, suicide and decisions | European psychiatry | 2010 | 547 | 1 | |||
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits | Genes, brain and behavior | 2010 | 649 | 2 | |||
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures | PloS one | 2010 | 579 | 319 | |||
Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behavior | NeuroImage | 2010 | 529 | 0 | |||
Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family | Epilepsy research | 2010 | 579 | 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 | 655 | 1 | |||
Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depression | Journal of affective disorders | 2010 | 581 | 0 | |||
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies | PLOS genetics | 2010 | 610 | 352 | |||
Somatic markers and explicit knowledge are both involved in decision-making | Neuropsychologia | 2009 | 536 | 0 | |||
Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior | American journal of medical genetics. Part B, Neuropsychiatric genetics | 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 dependence | Addictive behaviors | 2009 | 503 | 0 | |||
Modulation of anger control in suicide attempters by TPH-1 | Genes, brain and behavior | 2009 | 538 | 0 | |||
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy | Nature genetics | 2009 | 527 | 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 | 585 | 1 | |||
Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression | The Journal of clinical psychiatry | 2009 | 642 | 295 | |||
The electroencephalographic fingerprint of sleep is genetically determined: a twin study | Annals of neurology | 2008 | 555 | 0 | |||
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt | Genes, brain and behavior | 2008 | 632 | 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 | 596 | 0 | |||
Candidate genes for temporal lobe epilepsy: a replication study | Neurological sciences | 2008 | 568 | 234 | |||
GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsy | Epilepsia | 2005 | 146 | 29 | |||
Association of the connexin36 gene with juvenile myoclonic epilepsy | Journal of medical genetics | 2004 | 554 | 0 | |||
No association between DUP25 and anxiety disorders | American journal of medical genetics. Part B, Neuropsychiatric genetics | 2004 | 594 | 0 | |||
How mutations in the nAChRs can cause ADNFLE epilepsy | Epilepsia | 2002 | 133 | 275 | |||
Ion channel variation causes epilepsies | Brain Research Reviews | 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 onset | American journal of human genetics | 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 | 1997 | 552 | 0 | |||
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy | Nature | 1997 | 601 | 0 |