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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Apr 25, 2024
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Sleep and meta-analysis and ACE[original query]
The association of angiotensin-converting enzyme gene insertion/deletion polymorphisms with OSA: a meta-analysis.
The European respiratory journal 2012 Aug 40 (2): 394-9.
Lee Peilin, Douglas Neil J, Riha Renata
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A review of genetic association studies of obstructive sleep apnea: field synopsis and meta-analysis.
Sleep 2011 Nov 34 (11): 1461-8.
Varvarigou Vasileia, Dahabreh Issa J, Malhotra Atul, Kales Stefanos
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The association of angiotensin-converting enzyme gene insertion/deletion polymorphisms with acute mountain sickness susceptibility: a meta-analysis.
High altitude medicine & biology 2012 Dec 13 (4): 4.
Luo Y, Chen Y, Zhang Y, Gao Y
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Association of ACE I/D polymorphism with obstructive sleep apnea susceptibility: evidence based on 2,228 subjects.
Sleep & breathing = Schlaf & Atmung 2013 Nov .
Lin H, Lin D, Zheng C, Li J, Fang L
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Meta-analysis demonstrates lack of association between the ACE gene I/D polymorphism and obstructive sleep apnea-hypopnea syndrome occurrence and severity.
Genetics and molecular research : GMR 2013 12 (1): 1.
Feng Y, Ri J, Wan HY, Shi GC, Li QY, Fan L
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Obstructive sleep apnea syndrome susceptible genes in the Chinese population: a meta-analysis of 21 case-control studies.
Sleep & breathing = Schlaf & Atmung 2015 Apr .
Lan Fen, Cao Chao, Liu Jinkai, Li W
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Genetically-reduced serum ACE activity might be a causal risk factor for obstructive sleep apnea syndrome: A meta-analysis.
Scientific reports 2015 5 15267.
He Lan, Wang Bin, Lang Wei-Ya, Xue Jing, Zhao Da-Long, Li Guo-Feng, Zheng Li-Hong, Pan Hong-Mi
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Association of angiotensin-converting enzyme gene insertion/deletion polymorphism and obstructive sleep apnoea in a Chinese population: A meta-analysis.
Journal of the renin-angiotensin-aldosterone system : JRAAS 2021 5 21 (2): 1470320320934716.
Xu Jian, Chen Jiming, Li Yilu, Zhang Dandan, Li Xiao
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 22, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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