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期刊名字 | Molecular Autism MOL AUTISM (此期刊被最新的JCR期刊SCIE收录) LetPub评分 7.3
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声誉 8.3 影响力 6.4 速度 7.1 | |||||||||||||||||||||||||||||||
期刊ISSN | 2040-2392 | 微信扫码收藏此期刊 | ||||||||||||||||||||||||||||||
2023-2024最新影响因子 (数据来源于搜索引擎) | 6.3 点击查看影响因子趋势图 | |||||||||||||||||||||||||||||||
实时影响因子 | 截止2024年10月29日:3.979 | |||||||||||||||||||||||||||||||
2023-2024自引率 | 3.20%点击查看自引率趋势图 | |||||||||||||||||||||||||||||||
五年影响因子 | 6.5 | |||||||||||||||||||||||||||||||
JCI期刊引文指标 | 1.46 | |||||||||||||||||||||||||||||||
h-index | 44 | |||||||||||||||||||||||||||||||
CiteScore ( 2024年最新版) |
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期刊简介 |
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期刊官方网站 | https://www.springer.com/journal/13229 | |||||||||||||||||||||||||||||||
期刊投稿网址 | https://www.editorialmanager.com/MOLA | |||||||||||||||||||||||||||||||
期刊语言要求 | 经LetPub语言功底雄厚的美籍native English speaker精心编辑的稿件,不仅能满足Molecular Autism的语言要求,还能让Molecular Autism编辑和审稿人得到更好的审稿体验,让稿件最大限度地被Molecular Autism编辑和审稿人充分理解和公正评估。LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)帮助作者准备稿件,已助力全球15万+作者顺利发表论文。部分发表范例可查看:服务好评 论文致谢(1篇) 。
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是否OA开放访问 | Yes | |||||||||||||||||||||||||||||||
OA期刊相关信息 | 文章处理费:需要( GBP2590; USD3790; EUR2990; ) 文章处理费豁免:查看说明 其他费用:没有 期刊主题关键词:autism、neurodevelopmental conditions、asperger syndrome 相关链接:Aims & ScopeAuthor InstructionsEditorial BoardAnonymous peer review | |||||||||||||||||||||||||||||||
通讯方式 | CAMPUS, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW | |||||||||||||||||||||||||||||||
出版商 | BioMed Central | |||||||||||||||||||||||||||||||
涉及的研究方向 | GENETICS & HEREDITY-NEUROSCIENCES | |||||||||||||||||||||||||||||||
出版国家或地区 | ENGLAND | |||||||||||||||||||||||||||||||
出版语言 | English | |||||||||||||||||||||||||||||||
出版周期 | ||||||||||||||||||||||||||||||||
出版年份 | 2010 | |||||||||||||||||||||||||||||||
年文章数 | 45点击查看年文章数趋势图 | |||||||||||||||||||||||||||||||
Gold OA文章占比 | 99.38% | |||||||||||||||||||||||||||||||
研究类文章占比: 文章 ÷(文章 + 综述) | 93.33% | |||||||||||||||||||||||||||||||
WOS期刊SCI分区 ( 2023-2024年最新版) | WOS分区等级:1区
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中国科学院《国际期刊预警 名单(试行)》名单 | 2024年02月发布的2024版:不在预警名单中 2023年01月发布的2023版:不在预警名单中 2021年12月发布的2021版:不在预警名单中 2020年12月发布的2020版:不在预警名单中 | |||||||||||||||||||||||||||||||
中国科学院SCI期刊分区 ( 2023年12月最新升级版) | 点击查看中国科学院SCI期刊分区趋势图
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中国科学院SCI期刊分区 ( 2022年12月升级版) |
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中国科学院SCI期刊分区 ( 2021年12月旧的升级版) |
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SCI期刊收录coverage | Science Citation Index Expanded (SCIE) (2020年1月,原SCI撤销合并入SCIE,统称SCIE) Scopus (CiteScore) Directory of Open Access Journals (DOAJ) | |||||||||||||||||||||||||||||||
PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=2040-2392%5BISSN%5D | |||||||||||||||||||||||||||||||
平均审稿速度 | 网友分享经验: 17 Weeks | |||||||||||||||||||||||||||||||
平均录用比例 | 网友分享经验: | |||||||||||||||||||||||||||||||
版面费/APC文章处理费信息 | 文章处理费:需要( GBP2590; USD3790; EUR2990; ) 文章处理费豁免:查看说明 其他费用:没有 LetPub提供文章处理费(APC)支持服务,可以用人民币支付版面费啦! | |||||||||||||||||||||||||||||||
LetPub助力发表 | 经LetPub编辑的稿件平均录用比例是未经润色的稿件的1.5倍,平均审稿时间缩短40%。众多作者在使用LetPub的专业SCI论文编辑服务(包括SCI论文英语润色,同行资深专家修改润色,SCI论文专业翻译,SCI论文格式排版,专业学术制图等)后论文在Molecular Autism顺利发表。
快看看作者怎么说吧:服务好评 论文致谢 | |||||||||||||||||||||||||||||||
期刊常用信息链接 |
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中国学者近期发表的论文 | |
1. | Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model Author: Hui Guo, Tianyun Wang, Huidan Wu, Min Long, Bradley P. Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Lian Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael A. Bernier, Evan E. Eichler, Kun Xia Journal: Molecular Autism, 2018, Vol.9, , DOI:10.1186/s13229-018-0247-z DOI |
2. | Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons Author: Qiong Xu, Yuan-yuan Liu, Xiaoming Wang, Guo-he Tan, Hui-ping Li, Samuel W. Hulbert, Chun-yang Li, Chun-chun Hu, Zhi-qi Xiong, Xiu Xu, Yong-hui Jiang Journal: Molecular Autism, 2018, Vol.9, , DOI:10.1186/s13229-018-0244-2 DOI |
3. | CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors Author: Chun-xue Liu, Chun-yang Li, Chun-chun Hu, Yi Wang, Jia Lin, Yong-hui Jiang, Qiang Li, Xiu Xu Journal: Molecular Autism, 2018, Vol.9, , DOI:10.1186/s13229-018-0204-x DOI |
4. | Network-specific sex differentiation of intrinsic brain function in males with autism Author: Dorothea L. Floris, Meng-Chuan Lai, Tanmay Nath, Michael P. Milham, Adriana Di Martino Journal: Molecular Autism, 2018, Vol.9, , DOI:10.1186/s13229-018-0192-x DOI |
5. | Statistical analysis of twenty years (1993 to 2012) of data from mainland China’s first intervention center for children with autism spectrum disorder Author: Wei-Zhen Zhou, Adam Ye, Zhong-Kai Sun, Hope Tian, Tad Pu, Yu-Yu Wu, Dan-Dan Wang, Ming-Zhen Zhao, Shu-Juan Lu, Chang-Hong Yang, Liping Wei Journal: Molecular Autism, 2014, Vol.5, 52, DOI:10.1186/2040-2392-5-52 DOI |
6. | The association between maternal use of folic acid supplements during pregnancy and risk of autism spectrum disorders in children: a meta-analysis Author: Meiyun Wang, Kaiqin Li, Dongmei Zhao, Ling Li Journal: Molecular Autism, 2017, Vol.8, , DOI:10.1186/s13229-017-0170-8 DOI |
7. | Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism Author: Kit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, Christopher Chun Yu Mak, Gordon Ka Chun Leung, Mandy Ho Yin Tsang, Dingge Ying, Steven Lim Cho Pei, So Lun Lee, Wanling Yang, Brian Hon-Yin Chung Journal: Molecular Autism, 2017, Vol.8, , DOI:10.1186/s13229-017-0182-4 DOI |
8. | Prenatal levonorgestrel exposure induces autism-like behavior in offspring through ERβ suppression in the amygdala Author: Yuanlin Zou, Qiaomei Lu, Dan Zheng, Zhigang Chu, Zhaoyu Liu, Haijia Chen, Qiongfang Ruan, Xiaohu Ge, Ziyun Zhang, Xiaoyan Wang, Wenting Lou, Yongjian Huang, Yifei Wang, Xiaodong Huang, Zhengxiang Liu, Weiguo Xie, Yikai Zhou, Paul Yao Journal: Molecular Autism, 2017, Vol.8, , DOI:10.1186/s13229-017-0159-3 DOI |
9. | Identification of autism-related <Emphasis Type="Italic">MECP2</Emphasis> mutations by whole-exome sequencing and functional validation Author: Zhu Wen, Tian-Lin Cheng, Gai-zhi Li, Shi-Bang Sun, Shun-Ying Yu, Yi Zhang, Ya-Song Du, Zilong Qiu Journal: Molecular Autism, 2017, Vol.8, , DOI:10.1186/s13229-017-0157-5 DOI |
10. | Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder—implications of a copy number variation involving <Emphasis Type="Italic">DPP10</Emphasis> Author: Annisa Shui Lam Mak, Annie Ting Gee Chiu, Gordon Ka Chun Leung, Christopher Chun Yu Mak, Yoyo Wing Yiu Chu, Gary Tsz Kin Mok, Wing Fai Tang, Kelvin Yuen Kwong Chan, Mary Hoi Yin Tang, Elizabeth Tak-Kwong Lau Yim, Kin Wai So, Victoria Qinchen Tao, Cheuk Wing Fung, Virginia Chun Nei Wong, Mohammed Uddin, So Lun Lee, Christian R. Marshall, Stephen W. Scherer, Anita Sik Yau Kan, Brian Hon Yin Chung Journal: Molecular Autism, 2017, Vol.8, , DOI:10.1186/s13229-017-0136-x DOI |
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