缩写名/全名 |
MOL CYTOGENET
Molecular Cytogenetics |
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ISSN号 | 1755-8166 | ||||||||||||||||||||||||||||||||||||
研究方向 | GENETICS & HEREDITY- | ||||||||||||||||||||||||||||||||||||
影响因子 | 2015:1.506, 2016:1.455, 2017:1.167, 2018:1.331, 2019:1.233, | ||||||||||||||||||||||||||||||||||||
出版国家 | ENGLAND | ||||||||||||||||||||||||||||||||||||
出版周期 | |||||||||||||||||||||||||||||||||||||
年文章数 | 54 | ||||||||||||||||||||||||||||||||||||
出版年份 | 0 | ||||||||||||||||||||||||||||||||||||
是否OA | Yes | ||||||||||||||||||||||||||||||||||||
审稿周期(仅供参考) | >12周,或约稿 |
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录用比例 | 较易 | ||||||||||||||||||||||||||||||||||||
投稿链接 | https://www.editorialmanager.com/mocy/default.aspx | ||||||||||||||||||||||||||||||||||||
投稿官网 | http://molecularcytogenetics.biomedcentral.com/ | ||||||||||||||||||||||||||||||||||||
h-index | 26 | ||||||||||||||||||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1755-8166%5BISSN%5D | ||||||||||||||||||||||||||||||||||||
中科院SCI期刊分区 ( 2018年新版本) |
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中科院SCI期刊分区 ( 2020年新版本) |
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中国学者近期发表的论文 | |
1. | Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis Author: Huili Xue, Hailong Huang, Yan Wang, Gang An, Min Zhang, Liangpu Xu, Yuan Lin Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-019-0425-5 DOI |
2. | Analysis of meiotic segregation modes in biopsied blastocysts from preimplantation genetic testing cycles of reciprocal translocations Author: Jie Wang, Dong Li, Zhipeng Xu, Zhenyu Diao, Jianjun Zhou, Fei Lin, Ningyuan Zhang Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-019-0423-7 DOI |
3. | The rare mutation in the endosome-associated recycling protein gene <Emphasis Type="Italic">VPS50</Emphasis> is associated with human neural tube defects Author: Zhiwen Shi, Shuxia Chen, Xiao Han, Rui Peng, Jin Luo, Luming Yang, Yufang Zheng, Hongyan Wang Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-019-0421-9 DOI |
4. | Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China Author: Chang Liu, Xiangzhong Zhang, Jicheng Wang, Yan Zhang, Anshi Wang, Jian Lu, Yanlin Huang, Shu Liu, Jing Wu, Li Du, Jie Yang, Hongke Ding, Ling Liu, Xin Zhao, Aihua Yin Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-019-0420-x DOI |
5. | Combined use of bacterial artificial chromosomes-on-beads with karyotype detection improves prenatal diagnosis Author: Zhengyou Miao, Xia Liu, Furong Hu, Ming Zhang, Pingli Yang, Luming Wang Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-019-0416-6 DOI |
6. | Discrepancy of QF-PCR, CMA and karyotyping on a de novo case of mosaic isodicentric Y chromosomes Author: Yuan Liu, Li Guo, Hanbiao Chen, Jian Lu, Jingjing Hu, Xianzheng Li, Xing Li, Ting Wang, Fengzhen Li, Aihua Yin Journal: Molecular Cytogenetics, 2019, Vol.12, , DOI:10.1186/s13039-018-0413-1 DOI |
7. | Chromosomal abnormalities and copy number variations in fetal ventricular septal defects Author: Meiying Cai, Hailong Huang, Linjuan Su, Na Lin, Xiaoqing Wu, Xiaorui Xie, Gang An, Ying Li, Yuan Lin, Liangpu Xu, Hua Cao Journal: Molecular Cytogenetics, 2018, Vol.11, , DOI:10.1186/s13039-018-0408-y DOI |
8. | The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies Author: Hongge Li, Yu Lei, Hui Zhu, Yuqin Luo, Yeqing Qian, Min Chen, Yixi Sun, Kai Yan, Yanmei Yang, Bei Liu, Liya Wang, Yingzhi Huang, Junjie Hu, Jianyun Xu, Minyue Dong Journal: Molecular Cytogenetics, 2018, Vol.11, , DOI:10.1186/s13039-018-0407-z DOI |
9. | A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization Author: Qingwei Qi, Xiya Zhou, Yulin Jiang, Na Hao, Jing Zhou, Liang Zhang Journal: Molecular Cytogenetics, 2013, Vol.6, 11, DOI:10.1186/1755-8166-6-11 DOI |
10. | 19p13.2 Microdeletion including <Emphasis Type="Italic">NFIX</Emphasis> associated with overgrowth and intellectual disability suggestive of Malan syndrome Author: Hai-Yun Dong, Hui Zeng, Yi-Qiao Hu, Li Xie, Jian Wang, Xiu-Ying Wang, Yi-Feng Yang, Zhi-Ping Tan Journal: Molecular Cytogenetics, 2016, Vol.9, , DOI:10.1186/s13039-016-0282-4 DOI |
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