Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: CNTN2[original query] |
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Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis.
Ophthalmology 2020 May . Meguro Akira, Yamane Takahiro, Takeuchi Masaki, Miyake Masahiro, Fan Qiao, Zhao Wanting, Wang I-Jong, Mizuki Yuki, Yamada Norihiro, Nomura Naoko, Tsujikawa Akitaka, Matsuda Fumihiko, Hosoda Yoshikatsu, Saw Seang-Mei, Cheng Ching-Yu, Tsai Tzu-Hsun, Yoshida Masao, Iijima Yasuhito, Teshigawara Takeshi, Okada Eiichi, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhi |
Next generation sequencing in children with unexplained epilepsy: A retrospective cohort study. Brain & development 2021 6 43 (10): 1004-1012. Chen Wenjie, Qin Jiong, Shen Yiping, Liang Jingjing, Cui Yanan, Zhang Yi |
Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population.
Journal of clinical periodontology 2021 Mar . de Coo Alicia, Cruz Raquel, Quintela Inés, Herrera David, Sanz Mariano, Diz Pedro, Rodríguez Grandío Segundo, Vallcorba Nuria, Ramos Isabel, Oteo Alfonso, Serrano Cristina, Esmatges Alejandro, Enrile Francisco, Mateos Leopoldo, García Roberto, Álvarez-Novoa Pablo, Noguerol Blas, Zabalegui Ion, Blanco-Moreno José, Alonso Ángel, Lorenzo Ramón, Carracedo Angel, Blanco Ju |
Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry.
Life (Basel, Switzerland) 2022 Aug 12 (9): . Upadhyai Priyanka, Shenoy Pooja U, Banjan Bhavya, Albeshr Mohammed F, Mahboob Shahid, Manzoor Irfan, Das Ranaj |
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders. Human mutation 2022 8 43 (12): 1795-1807. Lieberwirth Johann Kaspar, Büttner Benjamin, Klöckner Chiara, Platzer Konrad, Popp Bernt, Abou Jamra Ra |
A large-scale polygenic risk score analysis identified candidate proteins associated with anxiety, depression and neuroticism. Molecular brain 2022 7 15 (1): 66. Cheng Bolun, Yang Xuena, Cheng Shiqiang, Li Chun'e, Zhang Huijie, Liu Li, Meng Peilin, Jia Yumeng, Wen Yan, Zhang Fe |
Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease. Frontiers in genetics 2022 11 13 995488. Sabotta Caroline M, Kwan Suet-Ying, Petty Lauren E, Below Jennifer E, Joon Aron, Wei Peng, Fisher-Hoch Susan P, McCormick Joseph B, Beretta Lau |
Evaluation of myopia-associated genes in a Han Chinese population with high myopia. Ophthalmic genetics 2023 5 1-5. Zhenzhen Liu, Guangqi An, Yadan Huo, Youmei Xu, Pengyi Zhou, Kunpeng Xie, Haiyan Zhu, Bo Jin, Liping Du, Xuemin J |
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- Page last updated:Apr 16, 2024
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