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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 17, 2025. (Total: 235411Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Syndrome and IMMP2L[original query]
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
Molecular psychiatry 2010 Jun 15 (6): 637-46.
Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.
European journal of human genetics : EJHG 2014 Nov 22 (11): 1283-9.
Bertelsen Birgitte, Melchior Linea, Jensen Lars R, Groth Camilla, Glenthøj Birte, Rizzo Renata, Debes Nanette Mol, Skov Liselotte, Brøndum-Nielsen Karen, Paschou Peristera, Silahtaroglu Asli, Tümer Zeyn
Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort.
Frontiers in neuroscience 2016 10 531.
Padmanabhuni Shanmukha S, Houssari Rayan, Esserlind Ann-Louise, Olesen Jes, Werge Thomas M, Hansen Thomas F, Bertelsen Birgitte, Tsetsos Fotis, Paschou Peristera, Tümer Zeyn
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Nov .
Zhang Yanqing, Liu Yi, Zarrei Mehdi, Tong Winnie, Dong Rui, Wang Ying, Zhang Haiyan, Yang Xiaomeng, MacDonald Jeffrey R, Uddin Mohammed, Scherer Stephen W, Gai Zhongt
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.
Frontiers in neurology 2020 9 11 803.
Pagliaroli Luca, Vereczkei Andrea, Padmanabhuni Shanmukha Sampath, Tarnok Zsanett, Farkas Luca, Nagy Peter, Rizzo Renata, Wolanczyk Tomasz, Szymanska Urszula, Kapisyzi Mira, Basha Entela, Koumoula Anastasia, Androutsos Christos, Tsironi Vaia, Karagiannidis Iordanis, Paschou Peristera, Barta Csa
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