研究论文开放获取
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E. Ramensky, Anna V Gerasimova, Peer Bork, Alexey S. Kondrashov, Shamil R. Sunyaev
Brigham and Women's Hospital Harvard University Max Planck Institute for Developmental Biology Center for Systems Biology
阅读操作
确认中在文库中上传 PDF 后可生成中文音频讲解。
摘要与影响
摘要 · 节选
暂未获取摘要。可打开原文或 PDF，后续可基于全文生成更完整的速读。
逐年被引趋势
1,1725860
17
18
19
20
1,17221
22
23
24
25
26
关键指标
13,768
被引次数 · OpenAlex
311.14
领域内被引倍数
同类平均 = 1
同类平均 = 1
前 0.1%
引用位次
同领域 · 同年份 · 同类型
同领域 · 同年份 · 同类型
7
参考文献
Google Scholar 与 OpenAlex 的被引统计范围不同，数值存在差异属正常。
AI 辅助阅读
依据：文献信息
论文问答
当前基于文献信息回答
可就本文提问；依据不足时会说明。
学术脉络
学科主题
生物医学Genomics and Rare Diseases
Genomics and Phylogenetic Studies · RNA and protein synthesis mechanisms
参考文献 7
Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information
被引 976Emidio Capriotti, Remo Calabrese, Rita Casadio · Bioinformatics · 2006
Human non-synonymous SNPs: server and survey
被引 2,324Vasily E. Ramensky · Nucleic Acids Research · 2002
SNPs3D: Candidate gene and SNP selection for association studies
被引 466Peng Yue, Eugene Melamud, John Moult · BMC Bioinformatics · 2006
此处列出前 3 条
引用本文 13,768
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
被引 33,515Sue M. Richards, Nazneen Aziz, Sherri J. Bale · Genetics in Medicine · 2015
The Phyre2 web portal for protein modeling, prediction and analysis
被引 10,433Lawrence A. Kelley, Stefans Mezulis, Christopher M. Yates · Nature Protocols · 2015
The Ensembl Variant Effect Predictor
被引 9,004William M. McLaren, Laurent Gil, Sarah E Hunt · Genome biology · 2016
按被引量排序，此处列出前 3 条