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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Disease and FNDC3B[original query]
A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland. GWAS Catalog
Molecular neurobiology 2015 Jul .
Hu Yakun, Deng Libing, Zhang Jie, Fang Xin, Mei Puming, Cao Xuebing, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population.
Journal of negative results in biomedicine 2015 14 10.
Abu-Amero Khaled K, Helwa Inas, Al-Muammar Abdulrahman, Strickland Shelby, Hauser Michael A, Allingham R Rand, Liu Yut
Genetic associations for keratoconus: a systematic review and meta-analysis.
Scientific reports 2017 Jul 7 (1): 4620.
Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J
Replication of SNP associations with keratoconus in a Czech cohort.
PloS one 2017 12 (2): e0172365.
Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma. GWAS Catalog
Human molecular genetics 2018 Feb .
Shiga Yukihiro, Akiyama Masato, Nishiguchi Koji M, Sato Kota, Shimozawa Nobuhiro, Takahashi Atsushi, Momozawa Yukihide, Hirata Makoto, Matsuda Koichi, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Oze Isao, Mikami Haruo, Naito Mariko, Wakai Kenji, Yoshikawa Munemitsu, Miyake Masahiro, Yamashiro Kenji, , Kashiwagi Kenji, Iwata Takeshi, Mabuchi Fumihiko, Takamoto Mitsuko, Ozaki Mineo, Kawase Kazuhide, Aihara Makoto, Araie Makoto, Yamamoto Tetsuya, Kiuchi Yoshiaki, Nakamura Makoto, Ikeda Yasuhiro, Sonoda Koh-Hei, Ishibashi Tatsuro, Nitta Koji, Iwase Aiko, Shirato Shiroaki, Oka Yoshitaka, Satoh Mamoru, Sasaki Makoto, Fuse Nobuo, Suzuki Yoichi, Cheng Ching-Yu, Khor Chiea Chuen, Baskaran Mani, Perera Shamira, Aung Tin, Vithana Eranga N, Cooke Bailey Jessica N, Kang Jae H, Pasquale Louis R, Haines Jonathan L, , Wiggs Janey L, Burdon Kathryn P, Gharahkhani Puya, Hewitt Alex W, Mackey David A, MacGregor Stuart, Craig Jamie E, Allingham R Rand, Hauser Micheal, Ashaye Adeyinka, Budenz Donald L, Akafo Stephan, Williams Susan E I, Kamatani Yoichiro, Nakazawa Toru, Kubo Michia
Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China.
Frontiers in cell and developmental biology 2021 9 645501.
Liu Yang, Zhang Jin-Jin, Piao Shun-Yu, Shen Ren-Juan, Ma Ya, Xue Zhong-Qi, Zhang Wen, Liu Juan, Jin Zi-Bing, Zhuang Wen-Ju
Genetic predictors of sick sinus syndrome.
Molecular biology reports 2021 7 48 (6): 5355-5362.
Timasheva Yanina, Badykov Marat, Akhmadishina Leysan, Nasibullin Timur, Badykova Elena, Pushkareva Alfiya, Plechev Vladimir, Sagitov Ildus, Zagidullin Nauf
Sporadic Parkinson's Disease Potential Risk Loci Identified in Han Ancestry of Chinese Mainland.
Frontiers in aging neuroscience 2020 12 603793.
Wang Bo, Liu Xin, Xu Shengyuan, Liu Zheng, Zhu Yu, Zhang Xiong, Xu Rens
Evaluation of ABCA1 and FNDC3B Gene Polymorphisms Associated With Pseudoexfoliation Glaucoma and Primary Angle-Closure Glaucoma in a Saudi Cohort.
Frontiers in genetics 2022 13 877174.
Kondkar Altaf A, Sultan Tahira, Azad Taif A, Osman Essam A, Almobarak Faisal A, Lobo Glenn P, Al-Obeidan Saleh
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