| Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsy | PloS one |  | | 2015 | 265 | 178 |
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| Galanin pathogenic mutations in temporal lobe epilepsy | Human molecular genetics |  | | 2015 | 558 | 0 |
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| DAT1 and DRD4 genes involved in key dimensions of adult ADHD | Neurological sciences | | | 2015 | 683 | 1 |
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| Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures | Epilepsy research | | | 2014 | 195 | 0 |
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| Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene | Translational psychiatry | | | 2013 | 258 | 232 |
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| 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 |
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| Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy | The Journal of biological chemistry | | | 2012 | 159 | 204 |
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| Genetics of temporal lobe epilepsy: a review | Epilepsy Research and Treatment | | | 2012 | 148 | 186 |
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| 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 |
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| Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder | Journal of affective disorders | | | 2011 | 730 | 1,147 |
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| Replication of association between a SCN1A splice variant and febrile seizures | Epilepsia | | | 2011 | 615 | 346 |
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| 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 |
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| Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism | Brain and behavior | | | 2011 | 699 | 600 |
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| 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 |
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| Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures | PloS one | | | 2010 | 675 | 389 |
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| Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family | Epilepsy research | | | 2010 | 638 | 0 |
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| Caractérisation de nouveaux variants génétiques dans les convulsions fébriles et syndromes associés | | | | 2008 | 839 | 2,859 |
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| Candidate genes for temporal lobe epilepsy: a replication study | Neurological sciences | | | 2008 | 650 | 311 |
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| GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsy | Epilepsia | | | 2005 | 216 | 79 |
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