Global research landscape on the contribution of de novo mutations to human genetic diseases over the past 20 years: bibliometric analysis

IF 1.8 4区医学 Q3 GENETICS & HEREDITY

Journal of neurogenetics Pub Date : 2024-04-22 DOI:10.1080/01677063.2024.2335171

Jing Guan, Xiaonan Wu, Jiao Zhang, Jin Li, Hongyang Wang, Qiuju Wang

引用次数: 0

Abstract

As the contribution of de novo mutations (DNMs) to human genetic diseases has been gradually uncovered, analyzing the global research landscape over the past 20 years is essential. Because of the l...

查看原文本刊更多论文

过去 20 年全球关于新发基因突变对人类遗传疾病影响的研究概况：文献计量分析

随着新发基因突变（DNM）对人类遗传疾病的影响逐渐被发现，对过去 20 年的全球研究状况进行分析至关重要。由于新基因突变对人类遗传疾病的贡献逐渐被发现，分析过去 20 年的全球研究状况至关重要。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Journal of neurogenetics 医学-神经科学

CiteScore

4.40

自引率

0.00%

发文量

审稿时长

>12 weeks

期刊介绍： The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms