Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: RB1CC1[original query] |
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RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism. Molecular genetics & genomic medicine 2020 12 9 (1): e1561. Errichiello Edoardo, Giorda Roberto, Gambale Antonella, Iolascon Achille, Zuffardi Orsetta, Giglio Sabri |
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population. Psychiatric genetics 2022 Oct 32 (5): 188-193. Guo Aiguo, Lun Peng, Chen Jianhua, Li Qinghua, Chang Kaihui, Li Teng, Pan Dun, Zhang Jinmai, Zhou Juan, Wang Ke, Zhang Qian, Yang Qiangzhen, Gao Chengwen, Wu Chuanhong, Jian Xuemin, Wen Yanqin, Wang Zhuo, Shi Yongyong, Zhao Xiangzhong, Sun Peng, Li Zhiqia |
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis. Psychiatric genetics 2022 Jun . Curtis Dav |
Rare genetic variants impact muscle strength. Nature communications 2023 6 14 (1): 3449. Yunfeng Huang, Dora Bodnar, Chia-Yen Chen, Gabriela Sanchez-Andrade, Mark Sanderson, , Jun Shi, Katherine G Meilleur, Matthew E Hurles, Sebastian S Gerety, Ellen A Tsai, Heiko Ru |
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