Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: HPS4[original query] |
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Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type. The Journal of investigative dermatology 2008 Oct 128 (10): 2442-50. Hutton Saunie M, Spritz Richard |
An association study of the Hermansky-Pudlak syndrome type 4 gene in schizophrenic patients. Psychiatric genetics 2013 Aug 23 (4): 163-73. Saito Atsushi, Kuratomi Go, Ito Chihiro, Matsuoka Hiroo, Suzuki Tamio, Ozeki Yuji, Watanabe Takashi, Fujii Kumiko, Shimoda Kazutaka, Fukushima Yasutsugu, Inukai Toshihiko, Ohmori Kenichi, Akiyama Kazufu |
Association of the Hermansky-Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects. BMC psychiatry 2013 13 (1): 276. Kuratomi Go, Saito Atsushi, Ozeki Yuji, Watanabe Takashi, Fujii Kumiko, Shimoda Kazutaka, Inukai Toshihiko, Mori Harunobu, Ohmori Kenichi, Akiyama Kazufu |
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.
Stroke; a journal of cerebral circulation 2015 Aug 46 (8): 2063-8. Carty Cara L, Keene Keith L, Cheng Yu-Ching, Meschia James F, Chen Wei-Min, Nalls Mike, Bis Joshua C, Kittner Steven J, Rich Stephen S, Tajuddin Salman, Zonderman Alan B, Evans Michele K, Langefeld Carl D, Gottesman Rebecca, Mosley Thomas H, Shahar Eyal, Woo Daniel, Yaffe Kristine, Liu Yongmei, Sale Michèle M, Dichgans Martin, Malik Rainer, Longstreth W T, Mitchell Braxton D, Psaty Bruce M, Kooperberg Charles, Reiner Alexander, Worrall Bradford B, Fornage Myriam, |
Instability of BLOC-2 and BLOC-3 in Chinese patients with Hermansky-Pudlak syndrome. Pigment cell & melanoma research 2018 11 32 (3): 373-380. Wei Aihua, Yuan Yefeng, Qi Zhan, Liu Teng, Bai Dayong, Zhang Yingzi, Yu Jiaying, Yang Lin, Yang Xiumin, Li W |
Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising. Orphanet journal of rare diseases 2019 2 14 (1): 52. Power Bradley, Ferreira Carlos R, Chen Dong, Zein Wadih M, O'Brien Kevin J, Introne Wendy J, Stephen Joshi, Gahl William A, Huizing Marjan, Malicdan May Christine V, Adams David R, Gochuico Bernadette |
NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism. BMC genomics 2022 4 23 (1): 332. Xiao Yuanyuan, Zhou Cong, Xie Hanbing, Huang Shuang, Wang Jing, Liu Shanli |
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- Page last updated:Apr 22, 2024
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