AS
Salzmann, Annick
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsy | PloS one |  | 2015 | 262 | 170 | ||
| Galanin pathogenic mutations in temporal lobe epilepsy | Human molecular genetics |  | 2015 | 556 | 0 | ||
| DAT1 and DRD4 genes involved in key dimensions of adult ADHD | Neurological sciences | | 2015 | 681 | 1 | ||
| Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures | Epilepsy research | | 2014 | 193 | 0 | ||
| Response to psychotherapy in borderline personality disorder and methylation status of the BDNF gene | Translational psychiatry | | 2013 | 255 | 206 | ||
| 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 | 217 | 114 | ||
| Naturally occurring Carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy | The Journal of biological chemistry | | 2012 | 157 | 161 | ||
| Genetics of temporal lobe epilepsy: a review | Epilepsy Research and Treatment | | 2012 | 145 | 135 | ||
| 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 | 239 | 0 | ||
| Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder | Journal of affective disorders | | 2011 | 728 | 1,110 | ||
| Replication of association between a SCN1A splice variant and febrile seizures | Epilepsia | | 2011 | 613 | 343 | ||
| 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 | 1,468 | 0 | ||
| Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism | Brain and behavior | | 2011 | 697 | 594 | ||
| 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 | 672 | 0 | ||
| Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures | PloS one | | 2010 | 672 | 381 | ||
| Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family | Epilepsy research | | 2010 | 636 | 0 | ||
| Caractérisation de nouveaux variants génétiques dans les convulsions fébriles et syndromes associés | | 2008 | 837 | 2,781 | |||
| Candidate genes for temporal lobe epilepsy: a replication study | Neurological sciences | | 2008 | 648 | 295 | ||
| GABAB receptor 1 polymorphism (G1465A) and temporal lobe epilepsy | Epilepsia | | 2005 | 214 | 73 |
