Published in Genes Brain Behav on September 18, 2007
Gene × environment interaction studies have not properly controlled for potential confounders: the problem and the (simple) solution. Biol Psychiatry (2013) 1.88
Imaging phenotypes of major depressive disorder: genetic correlates. Neuroscience (2009) 1.49
Brain-derived neurotrophic factor: role in depression and suicide. Neuropsychiatr Dis Treat (2009) 1.48
Brain-derived neurotrophic factor signaling and subgenual anterior cingulate cortex dysfunction in major depressive disorder. Am J Psychiatry (2012) 1.28
Association between Val66Met brain-derived neurotrophic factor (BDNF) gene polymorphism and post-treatment relapse in alcohol dependence. Alcohol Clin Exp Res (2009) 1.16
Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression. J Clin Psychiatry (2009) 1.11
The BDNF gene Val66Met polymorphism as a modifier of psychiatric disorder susceptibility: progress and controversy. Mol Psychiatry (2015) 1.02
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits. Genes Brain Behav (2009) 0.94
Brain-derived neurotrophic factor and suicide pathogenesis. Ann Med (2010) 0.91
Childhood Maltreatment, Depression, and Suicidal Ideation: Critical Importance of Parental and Peer Emotional Abuse during Developmental Sensitive Periods in Males and Females. Front Psychiatry (2015) 0.86
GABAergic control of depression-related brain states. Adv Pharmacol (2015) 0.86
Suicidality: risk factors and the effects of antidepressants. The example of parallel reduction of suicidality and other depressive symptoms during treatment with the SNRI, milnacipran. Neuropsychiatr Dis Treat (2010) 0.82
Brain-derived neurotrophic factor val66met genotype and early life stress effects upon bipolar course. J Psychiatr Res (2012) 0.81
Brain-derived neurotrophic factor (BDNF) Val66Met and adulthood chronic stress interact to affect depressive symptoms. J Psychiatr Res (2012) 0.81
Gene-environment studies and borderline personality disorder: a review. Curr Psychiatry Rep (2013) 0.80
Altered DNA methylation status of human brain derived neurotrophis factor gene could be useful as biomarker of depression. Am J Med Genet B Neuropsychiatr Genet (2014) 0.79
Combined effect of TLR2 gene polymorphism and early life stress on the age at onset of bipolar disorders. PLoS One (2015) 0.79
Genetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future Directions. Front Psychiatry (2016) 0.77
Dysfunctional Attitudes and Affective Responses to Daily Stressors: Separating Cognitive, Genetic, and Clinical Influences on Stress Reactivity. Cognit Ther Res (2014) 0.76
Understanding Suicide Risk within the Research Domain Criteria (RDoC) Framework: Insights, Challenges, and Future Research Considerations. Clin Psychol Sci (2017) 0.76
Neuropathology of suicide: recent findings and future directions. Mol Psychiatry (2017) 0.75
The complement system: a gateway to gene-environment interactions in schizophrenia pathogenesis. Mol Psychiatry (2017) 0.75
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet (2000) 5.05
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet (1999) 3.93
Diagnosing autism: analyses of data from the Autism Diagnostic Interview. J Autism Dev Disord (1997) 3.45
Association between the tryptophan hydroxylase gene and manic-depressive illness. Arch Gen Psychiatry (1998) 2.55
Linkage and association of the glutamate receptor 6 gene with autism. Mol Psychiatry (2002) 2.51
Tyrosine hydroxylase polymorphisms associated with manic-depressive illness. Lancet (1990) 2.38
Genetic determinants of sleep regulation in inbred mice. Sleep (1999) 2.18
Sleep in patients with remitted bipolar disorders: a meta-analysis of actigraphy studies. Acta Psychiatr Scand (2014) 2.10
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy. Nature (1997) 2.09
Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker. Lancet (1995) 2.07
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1. Psychiatry Res (1998) 1.95
Autism, language delay and mental retardation in a patient with 7q11 duplication. J Med Genet (2007) 1.86
Genetic variation in EEG activity during sleep in inbred mice. Am J Physiol (1998) 1.79
Abnormal melatonin synthesis in autism spectrum disorders. Mol Psychiatry (2007) 1.79
Early and late onset bipolar disorders: two different forms of manic-depressive illness? J Affect Disord (2000) 1.71
Psychiatric genetics: search for phenotypes. Trends Neurosci (1998) 1.68
Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma. Transl Psychiatry (2011) 1.60
Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry (2012) 1.57
Prevalence of DSM-IV psychiatric disorder in the French elderly population. Br J Psychiatry (2004) 1.54
Antidepressant-induced mania in bipolar patients: identification of risk factors. J Clin Psychiatry (2001) 1.53
Neuropsychological testing of cognitive impairment in euthymic bipolar disorder: an individual patient data meta-analysis. Acta Psychiatr Scand (2013) 1.52
Increased white matter connectivity in euthymic bipolar patients: diffusion tensor tractography between the subgenual cingulate and the amygdalo-hippocampal complex. Mol Psychiatry (2007) 1.50
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder. Mol Psychiatry (2011) 1.44
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder. Mol Psychiatry (2011) 1.43
Suicidal behaviors and the tryptophan hydroxylase gene. Arch Gen Psychiatry (1995) 1.40
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33. Am J Hum Genet (1999) 1.30
How mutations in the nAChRs can cause ADNFLE epilepsy. Epilepsia (2002) 1.27
Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene. Transl Psychiatry (2013) 1.17
Admixture analysis of age at onset in bipolar I affective disorder. Arch Gen Psychiatry (2001) 1.16
Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Mol Psychiatry (2002) 1.15
Feasibility, reproducibility, risks and benefits of face transplantation: a prospective study of outcomes. Am J Transplant (2011) 1.15
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q. Hum Mol Genet (1997) 1.13
Towards a cognitive phenotype for autism: increased prevalence of executive dysfunction and superior spatial span amongst siblings of children with autism. J Child Psychol Psychiatry (1999) 1.13
Executive function in parents of children with autism. Psychol Med (1997) 1.12
Automatic fiber bundle segmentation in massive tractography datasets using a multi-subject bundle atlas. Neuroimage (2012) 1.11
Do the treasures of 'big data' combined with behavioural intervention therapies contain the key to the mystery of large psychiatric issues? Acta Psychiatr Scand (2014) 1.09
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. Transl Psychiatry (2012) 1.08
Influence of cigarette smoking on the levels of DNA adducts in human bronchial epithelium and white blood cells. Int J Cancer (1990) 1.07
Genetics of circadian rhythms and mood spectrum disorders. Eur Neuropsychopharmacol (2011) 1.05
The neuroscience of suicidal behaviors: what can we expect from endophenotype strategies? Transl Psychiatry (2011) 1.04
Relationship of HLA to schizophrenia not supported in multiplex families. Psychiatry Res (1992) 1.03
Antidepressant-induced mania, rapid cycling and the serotonin transporter gene polymorphism. Pharmacogenomics J (2003) 1.02
32P-postlabelling detection of aromatic DNA adducts in peripheral blood lymphocytes from aluminium production plant workers. Mutat Res (1991) 1.01
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14. Mol Psychiatry (2006) 1.01
Staging systems in bipolar disorder: an International Society for Bipolar Disorders Task Force Report. Acta Psychiatr Scand (2014) 0.99
Duration of untreated bipolar disorder: missed opportunities on the long road to optimal treatment. Acta Psychiatr Scand (2012) 0.99
Decision making and problem solving in adolescents who deliberately self-harm. Psychol Med (2008) 0.98
Effectiveness and tolerance of anti-inflammatory drugs' add-on therapy in major mental disorders: a systematic qualitative review. Acta Psychiatr Scand (2013) 0.98
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder. Mol Psychiatry (2005) 0.97
Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression. Neurosci Lett (1998) 0.97
SPECT of the brain in childhood autism: evidence for a lack of normal hemispheric asymmetry. Dev Med Child Neurol (1995) 0.96
Memory tests in first-degree adult relatives of schizophrenic patients: a meta-analysis. Schizophr Res (2005) 0.96
Family cancer history and risk of childhood acute leukemia (France). Cancer Causes Control (2001) 0.95
COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits. Genes Brain Behav (2009) 0.94
Pharmacological properties of acetorphan, a parenterally active "enkephalinase" inhibitor. J Pharmacol Exp Ther (1986) 0.94
A SNAP25 promoter variant is associated with early-onset bipolar disorder and a high expression level in brain. Mol Psychiatry (2009) 0.94
Deficit of cognitive inhibition in depressed elderly: a neurocognitive marker of suicidal risk. J Affect Disord (2012) 0.94
Performance of linkage analysis under misclassification error when the genetic model is unknown. Genet Epidemiol (1989) 0.93
Two TaqI dimorphic sites at the human beta-hydroxylase locus. Nucleic Acids Res (1989) 0.93
Opiate antagonists in children and adolescents. Eur Child Adolesc Psychiatry (2000) 0.93
Ion channel variation causes epilepsies. Brain Res Brain Res Rev (2001) 0.93
Gender and age at onset in schizophrenia: impact of family history. Am J Psychiatry (1995) 0.92
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1). Am J Hum Genet (1997) 0.92
Psychiatric diagnoses and personality traits associated with disadvantageous decision-making. Eur Psychiatry (2007) 0.92
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis. Can J Neurol Sci (1998) 0.92
Association of the connexin36 gene with juvenile myoclonic epilepsy. J Med Genet (2004) 0.92