User profiles for S. Jamain
Stéphane JamainUniv Paris Est Créteil, Inserm, IMRB Verified email at inserm.fr Cited by 17451 |
[HTML][HTML] La génétique de l'autisme
… Ce rapport s’élève à 23 garçons pour une fille dans une population d’individus autistes
sans anomalie morphologique et présentant une IRM (imagerie par résonance magnétique) …
sans anomalie morphologique et présentant une IRM (imagerie par résonance magnétique) …
Genome-wide association study identifies 30 loci associated with bipolar disorder
Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide
association study (GWAS) including 20,352 cases and 31,358 controls of European descent, …
association study (GWAS) including 20,352 cases and 31,358 controls of European descent, …
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Bipolar disorder is a heritable mental illness with complex etiology. We performed a genome-wide
association study of 41,917 bipolar disorder cases and 371,549 controls of European …
association study of 41,917 bipolar disorder cases and 371,549 controls of European …
[HTML][HTML] The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study
…, E González, K Hubbard, S Jamain… - The Lancet …, 2019 - thelancet.com
Background Cannabis use is associated with increased risk of later psychotic disorder but
whether it affects incidence of the disorder remains unclear. We aimed to identify patterns of …
whether it affects incidence of the disorder remains unclear. We aimed to identify patterns of …
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
S Jamain, K Radyushkin… - Proceedings of the …, 2008 - National Acad Sciences
… Considerable effort is expended to protect today’s children from lead exposure, but there
is little evidence on the harms past lead exposures continue to hold for yesterday’s children, …
is little evidence on the harms past lead exposures continue to hold for yesterday’s children, …
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Background Lithium is a first-line treatment in bipolar disorder, but individual response is
variable. Previous studies have suggested that lithium response is a heritable trait. However, …
variable. Previous studies have suggested that lithium response is a heritable trait. However, …
[PDF][PDF] Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
…, B Müller-Myhsok, S Lucae, S Jamain… - The American Journal of …, 2011 - cell.com
We conducted a genome-wide association study (GWAS) and a follow-up study of bipolar
disorder (BD), a common neuropsychiatric disorder. In the GWAS, we investigated 499,494 …
disorder (BD), a common neuropsychiatric disorder. In the GWAS, we investigated 499,494 …
[PDF][PDF] Early onset bipolar disorder: validation from admixture analyses and biomarkers
… La recherche bibliographique s’est arrêtée le 3 février 2012 et portait jusqu’à l’année 1990.
Les termes Mesh « bipolar disorder » et « admixture » ont été utilisés, obtenant 21 résultats. …
Les termes Mesh « bipolar disorder » et « admixture » ont été utilisés, obtenant 21 résultats. …
Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia
Bipolar disorder and schizophrenia are two often severe disorders with high heritabilities.
Recent studies have demonstrated a large overlap of genetic risk loci between these disorders …
Recent studies have demonstrated a large overlap of genetic risk loci between these disorders …
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
Many studies have supported a genetic etiology for autism. Here we report mutations in two
X-linked genes encoding neuroligins NLGN3 and NLGN4 in siblings with autism-spectrum …
X-linked genes encoding neuroligins NLGN3 and NLGN4 in siblings with autism-spectrum …