缩写名/全名 |
CANCER GENET-NY
Cancer Genetics |
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ISSN号 | 2210-7762 | ||||||||||||||||||||||||
研究方向 | ONCOLOGY-GENETICS & HEREDITY | ||||||||||||||||||||||||
影响因子 | 2015:2.333, 2016:1.93, 2017:2.351, 2018:2.183, 2019:3.105, | ||||||||||||||||||||||||
出版国家 | UNITED STATES | ||||||||||||||||||||||||
出版周期 | |||||||||||||||||||||||||
年文章数 | 73 | ||||||||||||||||||||||||
出版年份 | 2011 | ||||||||||||||||||||||||
是否OA | No | ||||||||||||||||||||||||
审稿周期(仅供参考) | 较慢,6-12周 |
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录用比例 | 较易 | ||||||||||||||||||||||||
投稿链接 | http://ees.elsevier.com/cg/ | ||||||||||||||||||||||||
投稿官网 | http://www.cancergeneticsjournal.org/ | ||||||||||||||||||||||||
h-index | 35 | ||||||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=2210-7762%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. | STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients Author: Yu-Liang Jiang, Zi-Ye Zhao, Bai-Rong Li, Hao Wang, En-Da Yu, Shou-Bin Ning Journal: Cancer Genetics, 2018, Vol.230, 47-57, DOI:10.1016/j.cancergen.2018.11.008 DOI |
2. | Genome-wide isoform-level analysis reveals tumor-specific isoforms for lung adenocarcinoma diagnosis and prognosis Author: Hu Zhuhong, Bai Zhenyu, Chen Xiangyuan, Xu Tingzhen, Song Libin Journal: Cancer Genetics, 2018, Vol.230, 58-65, DOI:10.1016/j.cancergen.2018.11.004 DOI |
3. | Correlations between microsatellite instability, ERCC1/XRCC1 polymorphism and clinical characteristics, and FOLFOX adjuvant chemotherapy effect of colorectal cancer patients Author: Liping Zhang, Jiangman Zhao, Bin Yu, Xinjiang Song, Guogang Sun, Lijiang Han, Lu Wang, Shu Dong Journal: Cancer Genetics, 2017, Vol.218-219, 51-57, DOI:10.1016/j.cancergen.2017.09.004 DOI |
4. | Regulatory mechanisms of long noncoding RNAs on gene expression in cancers Author: Weiliang Sun, Yunben Yang, Chunjing Xu, Junming Guo Journal: Cancer Genetics, 2017, Vol.216-217, 105-110, DOI:10.1016/j.cancergen.2017.06.003 DOI |
5. | Identification of a novel CSF3R-SPTAN1 fusion gene in an atypical chronic myeloid leukemia patient with t(1;9)(p34;q34) by RNA-Seq Author: Guangying Sheng, Jian Zhang, Zhao Zeng, Jinlan Pan, Qinrong Wang, Lijun Wen, Yang Xu, Depei Wu, Suning Chen Journal: Cancer Genetics, 2017, Vol.216-217, 16-19, DOI:10.1016/j.cancergen.2017.05.002 DOI |
6. | Six generations of epidermolytic palmoplantar keratoderma, associated with a KRT9 R163W mutation Author: Peng Wang, Xiao-Jing Kang, Xiao-Hui Tang, Jian-Yong Liu, Wen-Zheng Li, Wei-Jia Wang, Sheng-Nan Liang, Yan-Yan Feng, Yuan Ding, Wen-Jing Chen Journal: Cancer Genetics, 2016, Vol.209, 515-524, DOI:10.1016/j.cancergen.2016.10.002 DOI |
7. | Clinical and molecular cytogenetic studies in ten patients with hematological malignancies characterized by t(20;21)(q11;q11) resulted from del(20q) Author: Chunxiao Wu, Jun Zhang, Shuxiao Bai, Jianxin Yao, Huiying Qiu, Yongquan Xue, Suning Chen, Yafang Wu, Juan Shen, Jinlan Pan Journal: Cancer Genetics, 2016, Vol.209, 456-462, DOI:10.1016/j.cancergen.2016.09.006 DOI |
8. | Association between microRNA-27a rs895819 polymorphism and risk of colorectal cancer: A meta-analysis Author: Feifei Liu, Keith Dear, Lei Huang, Li Liu, Yun Shi, Shaofa Nie, Yisi Liu, Yuanan Lu, Hao Xiang Journal: Cancer Genetics, 2016, Vol.209, 388-394, DOI:10.1016/j.cancergen.2016.08.003 DOI |
9. | Papillary renal cell carcinoma with a somatic mutation in MET in a patient with autosomal dominant polycystic kidney disease. Author: Zhang W, Tan AY, Blumenfeld J, Liu G, Michaeel A, Zhang T, Robinson BD, Salvatore SP, Kapur S, Donahue S, Bobb WO, Rennert H. Journal: Cancer Genet. 2016 Jan-Feb;209(1-2):11-20. doi: 10.1016/j.cancergen.2015.11.002. Epub 2015 Dec 1. PubMed |
10. | Distinct set of chromosomal aberrations in childhood hepatocellular carcinoma is correlated to hepatitis B virus infection. Author: Tan L, Meier T, Kuhlmann M, Xie F, Baier C, Zhu Z, Cong WM, Wilkens L. Journal: Cancer Genet. 2016 Mar;209(3):87-96. doi: 10.1016/j.cancergen.2015.12.010. Epub 2016 Jan 12. PubMed |
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