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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 31, 2023. (Total: 217454Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Narcolepsy and CHKB[original query]
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. GWAS Catalog
Nature genetics 2008 Nov 40 (11): 1324-8.
Miyagawa Taku, Kawashima Minae, Nishida Nao, Ohashi Jun, Kimura Ryosuke, Fujimoto Akihiro, Shimada Mihoko, Morishita Shinichi, Shigeta Takashi, Lin Ling, Hong Seung-Chul, Faraco Juliette, Shin Yoon-Kyung, Jeong Jong-Hyun, Okazaki Yuji, Tsuji Shoji, Honda Makoto, Honda Yutaka, Mignot Emmanuel, Tokunaga Katsus
Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia).
PloS one 2009 4 (4): e5394.
Miyagawa Taku, Honda Makoto, Kawashima Minae, Shimada Mihoko, Tanaka Susumu, Honda Yutaka, Tokunaga Katsus
TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.
Sleep medicine 2012 Mar 13 (3): 269-72.
Han Fang, Lin Ling, Li Jing, Aran Adi, Dong Song X, An Pei, Zhao Long, Li Qian Y, Yan Han, Wang Jie S, Gao Hui Y, Li Mei, Gao Zhan C, Strohl Kingman P, Mignot Emmanu
Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.
Genetic testing and molecular biomarkers 2014 Apr 18 (4): 261-8.
Cingoz Sultan, Agilkaya Sinem, Oztura Ibrahim, Eroglu Secil, Karadeniz Derya, Evlice Ahmet, Altungoz Oguz, Yilmaz Hikmet, Baklan Bar
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