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以下是对 MOL CYTOGENET 杂志介绍 收藏
缩写名/全名
MOL CYTOGENET
Molecular Cytogenetics
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
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
CiteScoreSJRSNIPCiteScore排名
1.500.7020.624
学科分区排名
大类:Medicine
小类:Biochemistry, medical
Q332 / 51
大类:Medicine
小类:Genetics(clinical)
Q368 / 91
大类:Biochemistry, Genetics and Molecular Biology
小类:Molecular Medicine
Q3123 / 165
大类:Biochemistry, Genetics and Molecular Biology
小类:Genetics
Q3226 / 318
大类:Biochemistry, Genetics and Molecular Biology
小类:Biochemistry
Q3294 / 407
大类:Biochemistry, Genetics and Molecular Biology
小类:Molecular Biology
Q3304 / 375

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)
大类学科小类学科Top期刊综述期刊
生物 3区4区2区
GENETICS & HEREDITY
遗传学
1区3区4区
中科院SCI期刊分区
( 2020年新版本)
大类学科小类学科Top期刊综述期刊
生物学 1区4区1区
GENETICS & HEREDITY
遗传学
1区3区4区
  • 该杂志上中国学者近期发表的论文
  • 同领域相关期刊
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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NATURE REVIEWS MICROBIOLOGY25014.70
NATURE REVIEWS GENETICS32016.63
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Annual Review of Biochemistry26825.59
Cell Metabolism21914.42
Cell Stem Cell21212.13
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS280978
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APPLIED AND ENVIRONMENTAL MICROBIOLOGY185964
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JOURNAL OF EXPERIMENTAL BOTANY163533