缩写名/全名 |
AM J HUM GENET
AMERICAN JOURNAL OF HUMAN GENETICS |
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ISSN号 | 0002-9297 | ||||||||||||||||||||
研究方向 | 生物-遗传学 | ||||||||||||||||||||
影响因子 | 2015:10.794, 2016:9.025, 2017:8.855, 2018:9.924, 2019:10.502, | ||||||||||||||||||||
出版国家 | UNITED STATES | ||||||||||||||||||||
出版周期 | Monthly | ||||||||||||||||||||
年文章数 | 192 | ||||||||||||||||||||
出版年份 | 1949 | ||||||||||||||||||||
是否OA | No | ||||||||||||||||||||
审稿周期(仅供参考) | 一般,3-6周 |
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录用比例 | 很难 | ||||||||||||||||||||
投稿链接 | |||||||||||||||||||||
投稿官网 | http://www.cell.com/AJHG/home | ||||||||||||||||||||
h-index | 280 | ||||||||||||||||||||
CiteScore |
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PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0002-9297%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. | Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome Author: Fuxi Zhu, Chao Liu, Fengsong Wang, Xiaoyu Yang, Jingjing Zhang, Huan Wu, Zhiguo Zhang, Xiaojin He, Zhou Zhang, Ping Zhou, Zhaolian Wei, Yongliang Shang, Lina Wang, Ruidan Zhang, Ying-Chun Ouyang, Qing-Yuan Sun, Yunxia Cao, Wei Li Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2018, Vol., , DOI:10.1016/j.ajhg.2018.06.010 DOI |
2. | A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies Author: Yuwen Liu, Yanyu Liang, A. Ercument Cicek, Zhongshan Li, Jinchen Li, Rebecca A. Muhle, Martina Krenzer, Yue Mei, Yan Wang, Nicholas Knoblauch, Jean Morrison, Siming Zhao, Yi Jiang, Evan Geller, Iuliana Ionita-Laza, Jinyu Wu, Kun Xia, James P. Noonan, Zhong Sheng Sun, Xin He Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2018, Vol.102, 1031-1047, DOI:10.1016/j.ajhg.2018.03.023 DOI |
3. | Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese Author: Dong Wang, Yu Fan, Mahadev Malhi, Rui Bi, Yong Wu, Min Xu, Xiu-Feng Yu, Heng Long, Yu-Ye Li, Deng-Feng Zhang, Yong-Gang Yao Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2018, Vol.102, 794-805, DOI:10.1016/j.ajhg.2018.03.006 DOI |
4. | An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation Author: Xiao-Feng Chen, Dong-Li Zhu, Man Yang, Wei-Xin Hu, Yuan-Yuan Duan, Bing-Jie Lu, Yu Rong, Shan-Shan Dong, Ruo-Han Hao, Jia-Bin Chen, Yi-Xiao Chen, Shi Yao, Hlaing Nwe Thynn, Yan Guo, Tie-Lin Yang Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2018, Vol.102, 776-793, DOI:10.1016/j.ajhg.2018.03.001 DOI |
5. | Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility Author: Qing Sang, Bin Li, Yanping Kuang, Xueqian Wang, Zhihua Zhang, Biaobang Chen, Ling Wu, Qifeng Lyu, Yonglun Fu, Zheng Yan, Xiaoyan Mao, Yao Xu, Jian Mu, Qiaoli Li, Li Jin, Lin He, Lei Wang Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2018, Vol.102, 649-657, DOI:10.1016/j.ajhg.2018.02.015 DOI |
6. | Was ADH1B under Selection in European Populations? Author: Quan-Kuan Shen, Xierzhatijiang Sulaiman, Yong-Gang Yao, Min-Sheng Peng, Ya-Ping Zhang Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2016, Vol.99, 1217-1219, DOI:10.1016/j.ajhg.2016.09.017 DOI |
7. | Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome Author: Fuxi Zhu, Fengsong Wang, Xiaoyu Yang, Jingjing Zhang, Huan Wu, Zhou Zhang, Zhiguo Zhang, Xiaojin He, Ping Zhou, Zhaolian Wei, Jozef Gecz, Yunxia Cao Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2016, Vol.99, 942-949, DOI:10.1016/j.ajhg.2016.08.004 DOI |
8. | Ancestral Origins and Genetic History of Tibetan Highlanders Author: Dongsheng Lu, Haiyi Lou, Kai Yuan, Xiaoji Wang, Yuchen Wang, Chao Zhang, Yan Lu, Xiong Yang, Lian Deng, Ying Zhou, Qidi Feng, Ya Hu, Qiliang Ding, Yajun Yang, Shilin Li, Li Jin, Yaqun Guan, Bing Su, Longli Kang, Shuhua Xu Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2016, Vol.99, 580-594, DOI:10.1016/j.ajhg.2016.07.002 DOI |
9. | Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest Author: Yao Xu, Yingli Shi, Jing Fu, Min Yu, Ruizhi Feng, Qing Sang, Bo Liang, Biaobang Chen, Ronggui Qu, Bin Li, Zheng Yan, Xiaoyan Mao, Yanping Kuang, Li Jin, Lin He, Xiaoxi Sun, Lei Wang Journal: AMERICAN JOURNAL OF HUMAN GENETICS, 2016, Vol.99, 744-752, DOI:10.1016/j.ajhg.2016.06.024 DOI |
10. | Whole-Genome Sequencing Reveals Diverse Models of Structural Variations in Esophageal Squamous Cell Carcinoma. Author: Cheng C, Zhou Y, Li H, Xiong T, Li S, Bi Y, Kong P, Wang F, Cui H, Li Y, Fang X, Yan T, Li Y, Wang J, Yang B, Zhang L, Jia Z, Song B, Hu X, Yang J, Qiu H, Zhang G, Liu J, Xu E, Shi R, Zhang Y, Liu H, He C, Zhao Z, Qian Y, Rong R, Han Z, Zhang Y, Luo W, Wang J, Peng S, Yang X, Li X, Li L, Fang H, Liu X, Ma L, Chen Y, Guo S, Chen X, Xi Y, Li G, Liang J, Yang X, Guo J, Jia J, Li Q, Cheng X, Zhan Q, Cui Y. Journal: Am J Hum Genet. 2016 Feb 4;98(2):256-74. doi: 10.1016/j.ajhg.2015.12.013. Epub 2016 Jan 28. PubMed |
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