复制出版的不同模式:对系统评论中使用的文章进行分析
Erik von Elm1, Greta Poglia, Bernhard Walder
1Division of Anesthesiology, Department of Anesthesiology, Pharmacology, and Surgical Intensive Care, Geneva University Hospitals, Geneva, Switzerland.
JAMA
|February 26, 2004
概括
重复发表,研究结果的重复使用,发生在各种模式. 这项研究确定了六种不同的重复模式,发现重复文章在类似的期刊上发表,并且被引用的频率与原始文章一样多.
科学领域:
- 医学研究的完整性 医学研究的完整性
- 学术出版道德学术出版道德.
背景情况:
- 复制出版,定义为与先前发表的作品的实质性重叠,是科学文献中的一个问题.
- 了解重复出版的模式和普遍性对于保持研究完整性至关重要.
研究的目的:
- 调查科学文献中重复出版的模式.
- 为分类不同类型的重复出版物提出决策树.
主要方法:
- 在1989年至2002年间发表的麻醉和止痛系统评论中,搜索了已识别的重复文章.
- 对复制文章及其对应的主要文章进行了比较,对样本,结果,作者,赞助和出版特征进行比较.
- 根据样本和结果的比较,确定了六种不同的重复模式.
主要成果:
- 在141个系统审查中,56个发现了来自78个主要文章的103个重复文章.
- 确定了六种重复模式,包括相同的样本/结果,相同的样本/不同的结果,以及不同的样本/不同的结果.
- 隐藏的重复文章 (没有交叉引用) 发生在5.3%的案例中. 药品赞助和不同的作者在相当比例的重复中被发现.
结论:
- 复制出版比简单的复制更复杂,基于样本和结果相似性的可识别模式.
- 作者是识别重复的不可靠指标.
- 复制文章出现在具有相似影响因子的期刊中,并且获得与其主要文章相似的引用率.
更多相关视频
04:50Reproducibility and Harmonization in Research Using Biological Standards: The Example of Platelet Agonist Collagen-Related Peptide
Published on: August 4, 2023
07:50Global and Current Research Trends of Single-Cell Sequencing in Cancer: A Bibliometric and Visualization Study
Published on: April 18, 2025
相关概念视频
Pedigree Analysis
Overview
Pleiotropy
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Replication in Eukaryotes
Overview
Fixed Action Patterns
A fixed action pattern (FAP) is a specific, hard-wired sequence of behaviors that occurs in response to an external stimulus, called a sign stimulus. The behavior is “fixed” because it is essentially unchangeable—proceeding similarly across individuals of a species every time it occurs.
Chi-square Analysis
The chi-square test is a statistical hypothesis test. It is used to check whether there is a significant difference between an expected value and an observed value. In the context of genetics, it enables us to either accept or reject a hypothesis, based on how much the observed values deviate from the expected values.
The chi-square test was developed by Pearson in 1990.
The first step of performing a Chi-square analysis is to establish a null hypothesis, which assumes that there is no real...
The chi-square test was developed by Pearson in 1990.
The first step of performing a Chi-square analysis is to establish a null hypothesis, which assumes that there is no real...
Comparing Copy Number Variations and SNPs
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
