T. Sander

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

Chromosome Abnormalities and Genetic Counseling

Cohort Profile: The Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort

Dysfunction of the prefrontal cortex in addiction: neuroimaging findings and clinical implications

Stressful life events and the brain-derived neurotrophic factor gene in bipolar disorder

Genetic association study of BDNF in depression: Finding from two cohort studies and a meta‐analysis

Interaction between BDNF Val66Met and Dopamine Transporter Gene Variation Influences Anxiety-Related Traits

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q

Association Between Val66Met Brain‐Derived Neurotrophic Factor (BDNF) Gene Polymorphism and Post‐Treatment Relapse in Alcohol Dependence

Brain-Derived Neurotrophic Factor Val66Met and Psychiatric Disorders: Meta-Analysis of Case-Control Studies Confirm Association to Substance-Related Disorders, Eating Disorders, and Schizophrenia

Orbitofrontal Cortex and Drug Use During Adolescence

Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series

Musical Aptitude Is Associated with AVPR1A-Haplotypes

Juvenile Myoclonic Epilepsy: A 5‐Year Prospective Study

Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies

Health Supervision for Children With Down Syndrome

The Musicality of Non-Musicians: An Index for Assessing Musical Sophistication in the General Population

The molecular neurobiology of depression

GENETICS OF MIGRAINE

Translational Findings on Brain-Derived Neurotrophic Factor and Anxiety: Contributions from Basic Research to Clinical Practice

Is the underlying cause of epilepsy a major prognostic factor for recurrence?

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development

Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications

Whole genome association studies in complex diseases: where do we stand?

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Confirmation of association between the Val66Met polymorphism in the brain‐derived neurotrophic factor (BDNF) gene and bipolar I disorder

Gender-Dependent Association of the Functional Catechol-O-Methyltransferase Val158Met Genotype with Sensation Seeking Personality Trait

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients