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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 - 4 (of 4 Records)

Query Trace: Disease and SPAG16[original query]
Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants.
PloS one 2018 10 13 (10): e0205422.
Andjelkovic Marina, Minic Predrag, Vreca Misa, Stojiljkovic Maja, Skakic Anita, Sovtic Aleksandar, Rodic Milan, Skodric-Trifunovic Vesna, Maric Nina, Visekruna Jelena, Spasovski Vesna, Pavlovic Son
A transcriptome-wide association study to detect novel genes for volumetric bone mineral density.
Bone 2021 7 153 116106.
Liu Anqi, Liu Yong, Su Kuan-Jui, Greenbaum Jonathan, Bai Yuntong, Tian Qing, Zhao Lan-Juan, Deng Hong-Wen, Shen H
Genetic variant in SPAG16 is associated with the susceptibility of ACPA-positive rheumatoid arthritis possibly via regulation of MMP-3.
Journal of orthopaedic surgery and research 2022 11 17 (1): 511.
Lin Qingxi, Zhou Bingxiang, Song Xiaoxiao, Ye Wei, Li Qinglong, Shi Tong, Cheng Chen, Li Yetian, Wei Xi
Correlation research of susceptibility single nucleotide polymorphisms and the severity of clinical symptoms in attention deficit hyperactivity disorder.
Frontiers in psychiatry 2022 10 13 1003542.
Xu Yunyu, Lin Shuangxiang, Tao Jiejie, Liu Xinmiao, Zhou Ronghui, Chen Shuangli, Vyas Punit, Yang Chuang, Chen Bicheng, Qian Andan, Wang Meih
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