Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Sarojini M. Sengupta"'
Autor:
Natalie Grizenko, Aurélie Labbe, Sarojini M. Sengupta, Ridha Joober, Marie-Ève Fortier, Weam Fageera, Boris Chaumette
Publikováno v:
Journal of Psychiatric Research. 135:86-93
Background COMT had been considered a promising candidate gene in pharmacogenetic studies in ADHD; yet the findings from these studies have been inconsistent. Part of these inconsistencies could be related to epigenetic mechanisms (including DNA meth
Publikováno v:
Journal of Attention Disorders. 25:1720-1730
Objective: Examining the joint effect of two functional variants in two dopamine-related genes ( DRD3 and COMT) on ADHD-relevant behaviors under three experimental conditions (EC). Method: 362 children with ADHD were assessed by parents and teachers
Publikováno v:
World Journal of Pediatrics. 16:314-321
This study aims at characterizing the extent of correlation of treatment response (TR) obtained in various observation settings (home, school, clinic) by different observers (parents, teachers, clinicians). Children with attention deficit hyperactivi
Autor:
Ridha Joober, Natalie Grizenko, Gabriel A. Devenyi, Sherif Karama, M. Mallar Chakravarty, Nellie Fotopoulos, Sarojini M. Sengupta, Stephanie Guay
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 31, Iss, Pp 102695-(2021)
NeuroImage: Clinical, Vol 31, Iss, Pp 102695-(2021)
Highlights • Cumulative exposure to ADHD medication characterized as the product of lifetime duration and dose. • Medication effects investigated on 51 subregional volumes. • Smaller hippocampus CA1 volumes associated with higher medication exp
Autor:
Zia Choudhry, Sarojini M Sengupta, Natalie Grizenko, William J Harvey, Marie-Ève Fortier, Norbert Schmitz, Ridha Joober
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e55351 (2013)
Attention-Deficit/Hyperactivity Disorder (ADHD) is a complex and heterogeneous childhood disorder that often coexists with other psychiatric and somatic disorders. Recently, a link between ADHD and body weight dysregulation has been reported and ofte
Externí odkaz:
https://doaj.org/article/6336150359eb43ea9c2dc423978a04ca
Autor:
Oussama Kebir, Marie-Odile Krebs, Sarojini M. Sengupta, Martin Lepage, Ridha Joober, Srividya N. Iyer, Boris Chaumette, Jai Shah, Guy A. Rouleau, Patrick A. Dion, Ashok Malla
Publikováno v:
Schizophrenia Research
Schizophrenia Research, Elsevier, 2020, Online ahead of print. ⟨10.1016/j.schres.2020.06.019⟩
Schizophrenia Research, 2020, Online ahead of print. ⟨10.1016/j.schres.2020.06.019⟩
Schizophrenia Research, Elsevier, 2020, Online ahead of print. ⟨10.1016/j.schres.2020.06.019⟩
Schizophrenia Research, 2020, Online ahead of print. ⟨10.1016/j.schres.2020.06.019⟩
International audience; Schizophrenia is an illness characterized by positive symptoms, negative symptoms, and cognitive impairments. Cognitive impairments occur before the onset of psychosis and could reflect glutamatergic dysregulation. Thus, ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90c0f6facfc261139cffe3ec8c06b603
https://www.hal.inserm.fr/inserm-02892228
https://www.hal.inserm.fr/inserm-02892228
Autor:
Weam Fageera, Ridha Joober, Natalie Grizenko, Svetlana Babienco, Marie-Ève Fortier, Sarojini M. Sengupta, Aurélie Labbe
Publikováno v:
Progress in neuro-psychopharmacologybiological psychiatry. 110
Background Tryptophan hydroxylase 2 (TPH2) is a key enzyme in the biosynthesis of serotonin in the brain. This study aims to investigate the role of a functional variant in TPH2 (rs17110747) in the pathophysiology of ADHD. This variant has been impli
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49616 (2012)
Despite strong pharmacological evidence implicating the norepinephrine transporter in ADHD, genetic studies have yielded largely insignificant results. We tested the association between 30 tag SNPs within the SLC6A2 gene and ADHD, with stratification
Externí odkaz:
https://doaj.org/article/4f5a2de976874ef1b14aa5c465135ef0
Publikováno v:
Psychiatry Research. 256:298-304
Maternal smoking during pregnancy is the most commonly cited risk factor for ADHD. While the causal relation between this factor and ADHD is debated, several lines of evidence suggest that it modulates the severity of ADHD, particularly through highe
Autor:
Ridha Joober, Srividya N. Iyer, Anita Yim, Sarojini M. Sengupta, Ashok Malla, Ferid Fathalli, Kathleen MacDonald, Martin Lepage
Publikováno v:
Schizophrenia Research. 184:116-121
Recent Genome-Wide Association Studies (GWAS) have provided evidence for the involvement of a number of genetic variants in schizophrenia (SCZ). The objective of the current study was to examine the association between these variants and symptom dime