Evaluating the current state of the art of Huntington disease research: a scientometric analysis

Huntington disease (HD) is an incurable neurodegenerative disorder caused by a dominant mutation on the 4th chromosome. We aim to present a scientometric analysis of the extant scientific undertakings devoted to better understanding HD. Therefore, a quantitative study was performed to examine the cu...

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Main Authors: L.A. Barboza, N.C. Ghisi
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2018-01-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2018000300402&lng=en&tlng=en
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spelling doaj-7a7d8ed5c2d44203ac12acdd180733b62020-11-24T23:07:26ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2018-01-0151310.1590/1414-431x20176299S0100-879X2018000300402Evaluating the current state of the art of Huntington disease research: a scientometric analysisL.A. BarbozaN.C. GhisiHuntington disease (HD) is an incurable neurodegenerative disorder caused by a dominant mutation on the 4th chromosome. We aim to present a scientometric analysis of the extant scientific undertakings devoted to better understanding HD. Therefore, a quantitative study was performed to examine the current state-of-the-art approaches that foster researchers’ understandings of the current knowledge, research trends, and research gaps regarding this disorder. We performed literature searches of articles that were published up to September 2016 in the “ISI Web of Science™” (http://apps.webofknowledge.com/). The keyword used was “Huntington disease”. Of the initial 14,036 articles that were obtained, 7732 were eligible for inclusion in the study according to their relevance. Data were classified according to language, country of publication, year, and area of concentration. The country leader regarding the number of studies published on HD is the United States, accounting for nearly 30% of all publications, followed by England and Germany, who have published 10 and 7% of all publications, respectively. Regarding the language in which the articles were written, 98% of publications were in English. The first publication to be found on HD was published in 1974. A surge of publications on HD can be seen from 1996 onward. In relation to the various knowledge areas that emerged, most publications were in the fields of neuroscience and neurology, likely because HD is a neurodegenerative disorder. Publications written in areas such as psychiatry, genetics, and molecular biology also predominated.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2018000300402&lng=en&tlng=enGenetic diseaseChoreaCAG repeatNeurodegenerationHD gene
collection DOAJ
language English
format Article
sources DOAJ
author L.A. Barboza
N.C. Ghisi
spellingShingle L.A. Barboza
N.C. Ghisi
Evaluating the current state of the art of Huntington disease research: a scientometric analysis
Brazilian Journal of Medical and Biological Research
Genetic disease
Chorea
CAG repeat
Neurodegeneration
HD gene
author_facet L.A. Barboza
N.C. Ghisi
author_sort L.A. Barboza
title Evaluating the current state of the art of Huntington disease research: a scientometric analysis
title_short Evaluating the current state of the art of Huntington disease research: a scientometric analysis
title_full Evaluating the current state of the art of Huntington disease research: a scientometric analysis
title_fullStr Evaluating the current state of the art of Huntington disease research: a scientometric analysis
title_full_unstemmed Evaluating the current state of the art of Huntington disease research: a scientometric analysis
title_sort evaluating the current state of the art of huntington disease research: a scientometric analysis
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 1414-431X
publishDate 2018-01-01
description Huntington disease (HD) is an incurable neurodegenerative disorder caused by a dominant mutation on the 4th chromosome. We aim to present a scientometric analysis of the extant scientific undertakings devoted to better understanding HD. Therefore, a quantitative study was performed to examine the current state-of-the-art approaches that foster researchers’ understandings of the current knowledge, research trends, and research gaps regarding this disorder. We performed literature searches of articles that were published up to September 2016 in the “ISI Web of Science™” (http://apps.webofknowledge.com/). The keyword used was “Huntington disease”. Of the initial 14,036 articles that were obtained, 7732 were eligible for inclusion in the study according to their relevance. Data were classified according to language, country of publication, year, and area of concentration. The country leader regarding the number of studies published on HD is the United States, accounting for nearly 30% of all publications, followed by England and Germany, who have published 10 and 7% of all publications, respectively. Regarding the language in which the articles were written, 98% of publications were in English. The first publication to be found on HD was published in 1974. A surge of publications on HD can be seen from 1996 onward. In relation to the various knowledge areas that emerged, most publications were in the fields of neuroscience and neurology, likely because HD is a neurodegenerative disorder. Publications written in areas such as psychiatry, genetics, and molecular biology also predominated.
topic Genetic disease
Chorea
CAG repeat
Neurodegeneration
HD gene
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2018000300402&lng=en&tlng=en
work_keys_str_mv AT labarboza evaluatingthecurrentstateoftheartofhuntingtondiseaseresearchascientometricanalysis
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