Related Experiment Video
Updated: Apr 22, 2026

04:18
Author Spotlight: Exploring Cloning Techniques for Full-Length DNA Fragments
Published on: May 17, 2024
1.3K
[A unique author ID is a possible solution to the name ambiguity problem].
Andreas Qwist Fenger1, Hans-Christian Pommergaard, Jakob Burcharth
1Kirurgisk Sektion, Herlev Hospital, Herlev Ringvej 75, 2730 Herlev.
Ugeskrift for Laeger
|October 9, 2014
Summary
Open Researcher and Contributor ID (ORCID) provides unique 16-digit IDs to scholars, solving author name ambiguity. This initiative aims to centralize scientific work validation and test its adoption in research communities.
Area of Science:
- Bibliometrics
- Scholarly Communication
- Information Science
Background:
- Author name ambiguity poses challenges in connecting researchers with their scholarly contributions.
- Distinguishing between individuals with identical names is crucial for accurate academic attribution.
Purpose of the Study:
- To introduce Open Researcher and Contributor ID (ORCID) as a solution to author name ambiguity.
- To establish ORCID as a central hub for validating scientific work.
- To assess the adoption and impact of ORCID within scientific communities.
Main Methods:
- Implementation of a unique 16-digit identifier for each scholar.
- Development of a non-profit organization to manage and promote the ORCID initiative.
- Monitoring the integration of ORCID into scholarly workflows and validation processes.
Main Results:
- ORCID successfully provides a persistent, unique identifier for researchers.
- The system addresses the critical issue of distinguishing authors with similar names.
- The initiative serves as a test case for the broader acceptance of standardized research identification.
Conclusions:
- ORCID offers a robust solution to author name disambiguation in scholarly publishing.
- The widespread adoption of ORCID is key to improving the integrity of scientific record-keeping.
- The success of ORCID will indicate the scientific community's readiness for standardized research identification systems.
Related Concept Videos
Second Uniqueness Theorem
1.4K
Consider a region consisting of several individual conductors with a definite charge density in the region between these conductors. The second uniqueness theorem states that if the total charge on each conductor and the charge density in the in-between region are known, then the electric field can be uniquely determined.
In contrast, consider that the electric field is non-unique and apply Gauss's law in divergence form in the region between the conductors and the integral form to the surface...
In contrast, consider that the electric field is non-unique and apply Gauss's law in divergence form in the region between the conductors and the integral form to the surface...
1.4K
Multiple Allele Traits
32.4K
The Concept of Multiple Allelism
32.4K
Nondisjunction
67.4K
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
67.4K
Nondisjunction
4.4K
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
4.4K
X-linked Traits
45.4K
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
45.4K
Sex-linked Disorders
93.2K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
93.2K

