Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: ASMT[original query] |
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Single-nucleotide polymorphisms and mRNA expression for melatonin synthesis rate-limiting enzyme in recurrent depressive disorder. Journal of pineal research 2010 May 48 (4): 311-7. Ga?ecki Piotr, Szemraj Janusz, Bartosz Grzegorz, Bie?kiewicz Ma?gorzata, Ga?ecka Elzbieta, Florkowski Antoni, Lewi?ski Andrzej, Karbownik-Lewi?ska Ma?gorza |
Mutation screening of melatonin-related genes in patients with autism spectrum disorders. BMC medical genomics 2010 Apr 3 (1): 1. Jonsson L, Ljunggren E, Bremer A, Pedersen C, Landen M, Thuresson K, Giacobini M, Melke J |
Polymorphisms in melatonin synthesis pathways: possible influences on depression. Journal of circadian rhythms 2011 9 (1): 8. Kripke Daniel F, Nievergelt Caroline M, Tranah Greg J, Murray Sarah S, McCarthy Michael J, Rex Katharine M, Parimi Neeta, Kelsoe John |
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. Journal of pineal research 2011 Nov 51 (4): 394-9. Chaste Pauline, Clement Nathalie, Botros Hany Goubran, Guillaume Jean-Luc, Konyukh Marina, Pagan Cécile, Scheid Isabelle, Nygren Gudrun, Anckarsäter Henrik, Rastam Maria, Ståhlberg Ola, Gillberg I Carina, Melke Jonas, Delorme Richard, Leblond Claire, Toro Roberto, Huguet Guillaume, Fauchereau Fabien, Durand Christelle, Boudarene Lydia, Serrano Emilie, Lemière Nathalie, Launay Jean Marie, Leboyer Marion, Jockers Ralf, Gillberg Christopher, Bourgeron Thom |
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. BMC medical genetics 2011 1 12 17. Pagan Cecile, Botros Hany Goubran, Poirier Karine, Dumaine Anne, Jamain Stéphane, Moreno Sarah, de Brouwer Arjan, Van Esch Hilde, Delorme Richard, Launay Jean-Marie, Tzschach Andreas, Kalscheuer Vera, Lacombe Didier, Briault Sylvain, Laumonnier Frédéric, Raynaud Martine, van Bon Bregje W, Willemsen Marjolein H, Leboyer Marion, Chelly Jamel, Bourgeron Thom |
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Human molecular genetics 2012 Sep 21 (18): 4030-7. Etain Bruno, Dumaine Anne, Bellivier Frank, Pagan Cécile, Francelle Laetitia, Goubran-Botros Hany, Moreno Sarah, Deshommes Jasmine, Moustafa Khaled, Le Dudal Katia, Mathieu Flavie, Henry Chantal, Kahn Jean-Pierre, Launay Jean-Marie, Mühleisen Thomas W, Cichon Sven, Bourgeron Thomas, Leboyer Marion, Jamain Stépha |
Association between ASMT and autistic-like traits in children from a Swedish nationwide cohort. Psychiatric genetics 2013 Aug . Jonsson L, Anckarsäter H, Zettergren A, Westberg L, Walum H, Lundström S, Larsson H, Lichtenstein P, Melke J |
An ASMT variant associated with bipolar disorder influences sleep and circadian rhythms: a pilot study. Genes, brain, and behavior 2014 Mar 13 (3): 299-304. Geoffroy P A, Boudebesse C, Henrion A, Jamain S, Henry C, Leboyer M, Bellivier F, Etain |
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism. PloS one 2013 8 (1): 1. Wang L, Li J, Ruan Y, Lu T, Liu C, Jia M, Yue W, Liu J, Bourgeron T, Zhang D |
Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay. Journal of autism and developmental disorders 2015 Jan 45 (1): 100-10. Veatch Olivia J, Pendergast Julie S, Allen Melissa J, Leu Roberta M, Johnson Carl Hirschie, Elsea Sarah H, Malow Beth |
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): e001527. Li Changwei, Kim Yun Kyoung, Dorajoo Rajkumar, Li Huaixing, Lee I-Te, Cheng Ching-Yu, He Meian, Sheu Wayne H-H, Guo Xiuqing, Ganesh Santhi K, He Jiang, Lee Juyoung, Liu Jianjun, Hu Yao, Rao Dabeeru C, Tsai Fuu-Jen, Koh Jia Yu, Hu Hua, Liang Kae-Woei, Palmas Walter, Hixson James E, Han Sohee, Teo Yik-Ying, Wang Yiqin, Chen Jing, Lu Chieh Hsiang, Zheng Yingfeng, Gui Lixuan, Lee Wen-Jane, Yao Jie, Gu Dongfeng, Han Bok-Ghee, Sim Xueling, Sun Liang, Zhao Jinying, Chen Chien-Hsiun, Kumari Neelam, He Yunfeng, Taylor Kent D, Raffel Leslie J, Moon Sanghoon, Rotter Jerome I, Ida Chen Yii-der, Wu Tangchun, Wong Tien Yin, Wu Jer-Yuarn, Lin Xu, Tai E-Shyong, Kim Bong-Jo, Kelly Tanika |
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC medical genetics 2018 3 19 (1): 46. Prasad Aparna, Sdano Matthew A, Vanzo Rena J, Mowery-Rushton Patricia A, Serrano Moises A, Hensel Charles H, Wassman E Robe |
[Association of polymorphic variants of DDC (AADC), AANAT and ASMT genes encoding enzymes for melatonin synthesis with the higher risk of neuropsychiatric disorders]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2021 121 (5): 151-157. Moskaleva P V, Shnayder N A, Nasyrova R |
Association between the Arylalkylamine N-Acetyltransferase (AANAT) Gene and Seasonality in Patients with Bipolar Disorder. Psychiatry investigation 2021 5 18 (5): 453-462. Yang So Yung, Hong Kyung Sue, Cho Youngah, Cho Eun-Young, Choi Yujin, Kim Yongkang, Park Taesung, Ha Kyooseob, Baek Ji Hy |
Molecular Regulation of the Melatonin Biosynthesis Pathway in Unipolar and Bipolar Depression. Frontiers in pharmacology 2021 5 12 666541. Dmitrzak-Weglarz Monika, Banach Ewa, Bilska Karolina, Narozna Beata, Szczepankiewicz Aleksandra, Reszka Edyta, Jablonska Ewa, Kapelski Pawe?, Skibinska Maria, Pawlak Joan |
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach. Psychiatric genetics 2022 3 32 (3): 91-104. Mpoulimari Ioanna, Zintzaras Eli |
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- Page last updated:Mar 25, 2024
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