Detalhe da pesquisa
1.
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Hum Mol Genet
; 21(24): 5359-72, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22949513
2.
Childhood maltreatment and methylation of the glucocorticoid receptor gene NR3C1 in bipolar disorder.
Br J Psychiatry
; 204(1): 30-5, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23743517
3.
Neurobiology of suicide: do biomarkers exist?
Int J Legal Med
; 128(1): 73-82, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23430141
4.
Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder.
Am J Med Genet B Neuropsychiatr Genet
; 165B(1): 77-83, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24339138
5.
Naturally occurring carboxypeptidase A6 mutations: effect on enzyme function and association with epilepsy.
J Biol Chem
; 287(51): 42900-9, 2012 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23105115
6.
A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family.
BMC Genet
; 14: 93, 2013 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24067191
7.
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.
PLoS Genet
; 6(5): e1000962, 2010 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-20502679
8.
Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy.
Hum Mutat
; 33(1): 124-35, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21922598
9.
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 Med
; 9(10): e1001326, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23091423
10.
Magnetic resonance imaging correlates of first-episode psychosis in young adult male patients: combined analysis of grey and white matter.
J Psychiatry Neurosci
; 37(5): 305-12, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22748698
11.
War exposure, 5-HTTLPR genotype and lifetime risk of depression.
Br J Psychiatry
; 199(1): 43-8, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21593514
12.
Replication of association between a SCN1A splice variant and febrile seizures.
Epilepsia
; 52(10): e135-8, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21762453
13.
Alterations in phosphatidylinositol 3-kinase activity and PTEN phosphatase in the prefrontal cortex of depressed suicide victims.
Neuropsychobiology
; 63(4): 224-31, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21422769
14.
Adverse childhood environment and late-life cognitive functioning.
Int J Geriatr Psychiatry
; 26(5): 503-10, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21445999
15.
[The "SYNAPSY" project: where psychiatrists and neuroscientists meet]. / Le projet "SYNAPSY": un point de rencontre entre clinique et neurosciences.
Rev Med Suisse
; 7(309): 1818-20, 1822-3, 2011 Sep 21.
Artigo
em Francês
| MEDLINE | ID: mdl-22016937
16.
Decreased activation of lateral orbitofrontal cortex during risky choices under uncertainty is associated with disadvantageous decision-making and suicidal behavior.
Neuroimage
; 51(3): 1275-81, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20302946
17.
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation.
Epilepsia
; 51(9): 1915-8, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20738378
18.
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy.
Neurol Sci
; 31(1): 53-6, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19953286
19.
Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims.
Am J Med Genet B Neuropsychiatr Genet
; 153B(4): 909-18, 2010 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20052688
20.
Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder.
Am J Med Genet B Neuropsychiatr Genet
; 153B(8): 1494-7, 2010 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20862697