1,721,026 research outputs found
Going Beyond Counting First Authors in Author Co-citation Analysis
Get PDFThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
Get PDF“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Get PDFWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Dispelling the Myths Behind First-author Citation Counts
Get PDFWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
Charcot-Marie-Tooth-Neuropathie Typ 2 : neue Myelinprotein-P0-Punktmutationen und Haplotypenanalyse in europäischen Familien
No full textThe dominant forms of hereditary motor and sensory neuropathies of Charcot Marie Tooth type (CMT) are among the most common inherited diseases in humans. With respect to electroneurography and nerve pathology, CMT is subdivided in demyelinating CMT1 and axonal CMT2. Causative gene mutations can be identified in about 80-90% of CMT1 patients while no major CMT2 gene has been identified so far. In the present study, 49 CMT2 patients were tested for mutations in the myelin protein zero (P0, MPZ) gene that had initially been thought to be exclusively involved in the advent of demyelinating hereditary neuropathies. Three heterozygous single nucleotide changes were detected: two novel missense mutations, Asp61Gly and Tyr119Cys, and the known Thr124Met substitution, that had already been reported in several CMT patients from different European countries. Haplotype analysis for the P0 locus proved that the genealogical origin of the 124Met allele is different in the German, Italian, and French/Belgian populations. P0 mutations account for about 5% of CMT2 cases. As the frequency of connexin32 gene mutations is around 10% in CMT2, mutation analysis of both genes is expected to disclose the molecular cause in 1 out of 6 CMT2 patients. Haplotype diversity for the recurrent Thr124Met amino acid substitution suggests a mutation hotspot at the Thr124 codon. This peculiar genotype is presumed to make up a considerable proportion of P0 mutations in CMT2
Charcot-Marie-Tooth-Neuropathie Typ 2 : neue Myelinprotein-P0-Punktmutationen und Haplotypenanalyse in europäischen Familien
No full textThe dominant forms of hereditary motor and sensory neuropathies of Charcot Marie Tooth type (CMT) are among the most common inherited diseases in humans. With respect to electroneurography and nerve pathology, CMT is subdivided in demyelinating CMT1 and axonal CMT2. Causative gene mutations can be identified in about 80-90% of CMT1 patients while no major CMT2 gene has been identified so far. In the present study, 49 CMT2 patients were tested for mutations in the myelin protein zero (P0, MPZ) gene that had initially been thought to be exclusively involved in the advent of demyelinating hereditary neuropathies. Three heterozygous single nucleotide changes were detected: two novel missense mutations, Asp61Gly and Tyr119Cys, and the known Thr124Met substitution, that had already been reported in several CMT patients from different European countries. Haplotype analysis for the P0 locus proved that the genealogical origin of the 124Met allele is different in the German, Italian, and French/Belgian populations. P0 mutations account for about 5% of CMT2 cases. As the frequency of connexin32 gene mutations is around 10% in CMT2, mutation analysis of both genes is expected to disclose the molecular cause in 1 out of 6 CMT2 patients. Haplotype diversity for the recurrent Thr124Met amino acid substitution suggests a mutation hotspot at the Thr124 codon. This peculiar genotype is presumed to make up a considerable proportion of P0 mutations in CMT2
koamabayili/VECTRON-author-checklist: VECTRON author checklist
No full textWe have done our best to complete the author checklist relating to the use of animals in the hut study. Note that the objective for the hut study was to evaluate the IRS treatment applications for residual efficacy against Anopheles mosquitoes, including the local An. coluzzii mosquito population. Cows were only used to attract mosquitoes into the huts and no tests were carried out directly on the cows. The author checklist is intended for use with studies where experiments are carried out on animals, which is why we have had such difficulty in completing this for the hut study, as many of the questions do not relate to how the cows were used
Author-wise bibliometric analysis based on entropy.
No full textAuthor-wise bibliometric analysis based on entropy.</p
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