These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
183 related articles for article (PubMed ID: 23349736)
1. Sequencing ASMT identifies rare mutations in Chinese Han patients with autism. Wang L; Li J; Ruan Y; Lu T; Liu C; Jia M; Yue W; Liu J; Bourgeron T; Zhang D PLoS One; 2013; 8(1):e53727. PubMed ID: 23349736 [TBL] [Abstract][Full Text] [Related]
3. Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Etain B; Dumaine A; Bellivier F; Pagan C; Francelle L; Goubran-Botros H; Moreno S; Deshommes J; Moustafa K; Le Dudal K; Mathieu F; Henry C; Kahn JP; Launay JM; Mühleisen TW; Cichon S; Bourgeron T; Leboyer M; Jamain S Hum Mol Genet; 2012 Sep; 21(18):4030-7. PubMed ID: 22694957 [TBL] [Abstract][Full Text] [Related]
4. Association between ASMT and autistic-like traits in children from a Swedish nationwide cohort. Jonsson L; Anckarsäter H; Zettergren A; Westberg L; Walum H; Lundström S; Larsson H; Lichtenstein P; Melke J Psychiatr Genet; 2014 Feb; 24(1):21-7. PubMed ID: 23995775 [TBL] [Abstract][Full Text] [Related]
5. Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. Pagan C; Botros HG; Poirier K; Dumaine A; Jamain S; Moreno S; de Brouwer A; Van Esch H; Delorme R; Launay JM; Tzschach A; Kalscheuer V; Lacombe D; Briault S; Laumonnier F; Raynaud M; van Bon BW; Willemsen MH; Leboyer M; Chelly J; Bourgeron T BMC Med Genet; 2011 Jan; 12():17. PubMed ID: 21251267 [TBL] [Abstract][Full Text] [Related]
6. Single-nucleotide polymorphisms and mRNA expression for melatonin synthesis rate-limiting enzyme in recurrent depressive disorder. Gałecki P; Szemraj J; Bartosz G; Bieńkiewicz M; Gałecka E; Florkowski A; Lewiński A; Karbownik-Lewińska M J Pineal Res; 2010 May; 48(4):311-7. PubMed ID: 20433639 [TBL] [Abstract][Full Text] [Related]
7. Mutation screening of melatonin-related genes in patients with autism spectrum disorders. Jonsson L; Ljunggren E; Bremer A; Pedersen C; Landén M; Thuresson K; Giacobini M; Melke J BMC Med Genomics; 2010 Apr; 3():10. PubMed ID: 20377855 [TBL] [Abstract][Full Text] [Related]
8. Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway. Botros HG; Legrand P; Pagan C; Bondet V; Weber P; Ben-Abdallah M; Lemière N; Huguet G; Bellalou J; Maronde E; Beguin P; Haouz A; Shepard W; Bourgeron T J Pineal Res; 2013 Jan; 54(1):46-57. PubMed ID: 22775292 [TBL] [Abstract][Full Text] [Related]
9. Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population. Wang L; Li J; Shuang M; Lu T; Wang Z; Zhang T; Yue W; Jia M; Ruan Y; Liu J; Wu Z; Zhang D; Wang L Transl Psychiatry; 2018 Aug; 8(1):152. PubMed ID: 30108208 [TBL] [Abstract][Full Text] [Related]
10. Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay. Veatch OJ; Pendergast JS; Allen MJ; Leu RM; Johnson CH; Elsea SH; Malow BA J Autism Dev Disord; 2015 Jan; 45(1):100-10. PubMed ID: 25059483 [TBL] [Abstract][Full Text] [Related]
11. An ASMT variant associated with bipolar disorder influences sleep and circadian rhythms: a pilot study. Geoffroy PA; Boudebesse C; Henrion A; Jamain S; Henry C; Leboyer M; Bellivier F; Etain B Genes Brain Behav; 2014 Mar; 13(3):299-304. PubMed ID: 24308489 [TBL] [Abstract][Full Text] [Related]
12. Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. Toma C; Rossi M; Sousa I; Blasi F; Bacchelli E; Alen R; Vanhala R; Monaco AP; Järvelä I; Maestrini E; Mol Psychiatry; 2007 Nov; 12(11):977-9. PubMed ID: 17957233 [No Abstract] [Full Text] [Related]
13. Mutation analysis of the NRXN1 gene in a Chinese autism cohort. Liu Y; Hu Z; Xun G; Peng Y; Lu L; Xu X; Xiong Z; Xia L; Liu D; Li W; Zhao J; Xia K J Psychiatr Res; 2012 May; 46(5):630-4. PubMed ID: 22405623 [TBL] [Abstract][Full Text] [Related]
14. Lack of evidence to support the glyoxalase 1 gene (GLO1) as a risk gene of autism in Han Chinese patients from Taiwan. Wu YY; Chien WH; Huang YS; Gau SS; Chen CH Prog Neuropsychopharmacol Biol Psychiatry; 2008 Oct; 32(7):1740-4. PubMed ID: 18721844 [TBL] [Abstract][Full Text] [Related]
15. The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population. Yang W; Liu J; Zheng F; Jia M; Zhao L; Lu T; Ruan Y; Zhang J; Yue W; Zhang D; Wang L PLoS One; 2013; 8(4):e61021. PubMed ID: 23620727 [TBL] [Abstract][Full Text] [Related]
16. ASMT gene polymorphisms have no association with schizophrenia in a Han Chinese sample. Cong Z; Li X; Lin A; Zhu G; Peng M; Wang Y; Huang Y; Jiang W; Zhao X; Peng L; Ma H Psychiatry Res; 2015 Aug; 228(3):969-71. PubMed ID: 26154813 [No Abstract] [Full Text] [Related]
17. Association of oligodendrocytes differentiation regulator gene DUSP15 with autism. Tian Y; Wang L; Jia M; Lu T; Ruan Y; Wu Z; Wang L; Liu J; Zhang D World J Biol Psychiatry; 2017 Mar; 18(2):143-150. PubMed ID: 27223645 [TBL] [Abstract][Full Text] [Related]
18. Cloning and functional characterization of the Arabidopsis N-acetylserotonin O-methyltransferase responsible for melatonin synthesis. Byeon Y; Lee HJ; Lee HY; Back K J Pineal Res; 2016 Jan; 60(1):65-73. PubMed ID: 26484897 [TBL] [Abstract][Full Text] [Related]
19. Mutation screening of the UBE3A gene in Chinese Han population with autism. Zhao X; Zhang R; Yu S BMC Psychiatry; 2020 Dec; 20(1):589. PubMed ID: 33308194 [TBL] [Abstract][Full Text] [Related]
20. PVRL1 as a candidate gene for nonsyndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in southern Han Chinese patients. Cheng HQ; Huang EM; Xu MY; Shu SY; Tang SJ DNA Cell Biol; 2012 Jul; 31(7):1321-7. PubMed ID: 22455396 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]