Adapting PRISMA Guidelines to Enhance Reporting Quality in Genetic Association Studies: A Framework Proposal [0.03%]
适应PRISMA指南以提高遗传关联研究的报告质量：框架提案
Rezvan Nezameslami,Alireza Nezameslami,Bahareh Mehdikhani et al.
Rezvan Nezameslami et al.
Objective: To propose a framework for enhancing the reporting quality of genetic association studies by adapting the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. ...
Unveiling Novel Genetic Loci and Superior Alleles for Nickel Accumulation in Wheat via Genome-Wide Association Study [0.03%]
利用全基因组关联分析在小麦中发掘镍累积的新位点及优良等位变异
Xia Shi,Shenghui Geng,Jinna Hou et al.
Xia Shi et al.
Nickel (Ni) pollution poses significant threats to human health and crop development through the food chain. This study aimed to identify the novel genomic regions and superior alleles associated with Ni accumulation in wheat (Triticum aest...
Spontaneous Coronary Artery Dissection and a Family History of Aortic Dissection: A Genetic Association Study [0.03%]
冠状动脉夹层和主动脉夹层的家族史：一项基因相关性研究
Lucy McGrath-Cadell,Stephanie Hesselson,Ingrid Tarr et al.
Lucy McGrath-Cadell et al.
Background: Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndrome or sudden cardiac death, primarily affecting relatively young women (median age, 51 years) without t...
Genetic association studies in critically ill patients: a systematic review [0.03%]
危重患者中的遗传关联研究：系统回顾
Wenbo Zhang,Nam Nguyen-Hoang,Sean C S Rivrud et al.
Wenbo Zhang et al.
Background: Critical illness is complex, and genetic research holds the potential to uncover underlying disease mechanisms. However, existing research results have not been systematically summarized. This study aims to co...
Novel ABCD1 and MTHFSD Variants in Taiwanese Bipolar Disorder: A Genetic Association Study [0.03%]
台湾地区双相情感障碍的新ABCD1和MTHFSD基因变异：一项基因关联研究
Yi-Guang Wang,Chih-Chung Huang,Ta-Chuan Yeh et al.
Yi-Guang Wang et al.
Background and Objectives: In recent years, bipolar disorder (BD), a multifaceted mood disorder marked by severe episodic mood fluctuations, has been shown to have an impact on disability-adjusted life years (DALYs). The increasing prevalen...
Association of Genes TRH, PRL and PRLR with Milk Performance, Reproductive Traits and Heat Stress Response in Dairy Cattle [0.03%]
与奶牛乳用性能、繁殖性状和热应激反应相关的TRH、PRL和PRLR基因关联研究
Qianhai Fang,Hailiang Zhang,Qing Gao et al.
Qianhai Fang et al.
In our previous study, we found that changes in plasma prolactin (PRL) concentration were significantly associated with heat stress in dairy cows, and that PRL plays an important role in milk performance. Microarray sequencing revealed that...
Myoung Keun Lee,Noah Herrick,Mary L Marazita et al.
Myoung Keun Lee et al.
Background: Fifth finger clinodactyly describes the conspicuous curvature of the fifth digit toward the other digits of the hand. Phenotypic expression can range from mild and almost imperceptible to severe, where functio...
Initial Genome-Wide Case-Control Study for Genetic Background of Retinal Dysplasia in Czechoslovakian Wolfdog [0.03%]
捷克斯洛伐克狼犬视网膜发育不良遗传背景的初期全基因关联研究
Michal Gábor,Juraj Candrák,Martina Miluchová et al.
Michal Gábor et al.
Retinal dysplasia is a genetically heterogeneous ocular disorder in dogs, characterized by abnormal retinal development, resulting in a range of visual impairments from mild to complete blindness. The objective of this study was to investig...
Genetic association studies using disease liabilities from deep neural networks [0.03%]
使用深度神经网络疾病的易感性进行基因关联研究
Lu Yang,Marie C Sadler,Russ B Altman
Lu Yang
The case-control study is a widely used method for investigating the genetic underpinnings of binary traits. However, long-term, prospective cohort studies often grapple with absent or evolving health-related outcomes. Here, we propose two ...
Association of Genetic Polymorphisms in SLC45A2, TYR, HERC2, and SLC24A in African Women with Melasma: A Pilot Study [0.03%]
非洲女性中SLC45A2、TYR、HERC2和SLC24A基因多态性与黄褐斑关联的初步研究
Nomakhosi Mpofana,Zinhle Pretty Mlambo,Mokgadi Ursula Makgobole et al.
Nomakhosi Mpofana et al.
Melasma is a chronic skin disorder characterized by hyperpigmentation, predominantly affecting women with darker skin types, including those of African descent. This study investigates the association between genetic variants in SLC45A2, TY...
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