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| 基本信息 | 登录收藏 | |||||||||||||||||||||
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期刊名字 | AMERICAN JOURNAL OF HUMAN GENETICS AM J HUM GENET （此期刊被最新的JCR期刊SCIE收录） LetPub评分 9.1
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声誉 9.8 影响力 8.6 速度 9.5 | |||||||||||||||||||||
| 期刊ISSN | 0002-9297 | 安装APP，查看期刊最新消息
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| E-ISSN | 1537-6605 | |||||||||||||||||||||
| 2025-2026最新IF （数据来源于网友提供） | 注册或登录后，查看IF | |||||||||||||||||||||
| 实时影响因子 | 截止2026年9月20日：4.235 | |||||||||||||||||||||
| 2025-2026自引率 | 5.2%点击查看自引率趋势图 | |||||||||||||||||||||
| 五年IF （数据来源于网友提供） | 9.303数据由网友[crystal_lotus]收集提供 | |||||||||||||||||||||
| h-index | 280 | |||||||||||||||||||||
| CiteScore （ 2026年6月最新版） |
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| 期刊简介 |
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| 期刊官方网站 | http://www.cell.com/AJHG/home | |||||||||||||||||||||
期刊投稿格式模板 VIP专享 |
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| 期刊投稿网址 | ||||||||||||||||||||||
| 该期刊中国学者近期发文 - New | Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia Author: Terkelsen, Thorkild; Yumiceba, Veronica; Kim, Joshua; Melo, Uira Souto; Axelgaard, Esben; Febbraro, Fabia; Gunnarsson, Anders Vermelin; Balachandran, Saranya; Dahl-Jessen, Mikkel; Christensen, Rikke; Peters, Brock Andrew; Asan; Thelle, Thomas; Nyegaard, Mette; Bak, Rasmus O.; Denham, Mark; Spielmann, Malte; Jensen, Uffe Birk Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 8, pp. 1736-1753. DOI: 10.1016/j.ajhg.2026.07.001 Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity Author: Cao, Qiaoyu; Zhao, Anqi; Wang, Jianbo; Lin, Xinjie; Long, Zhoukai; Pan, Chaolan; Yang, Kai; Gu, Chun; Wang, Yumeng; Li, Lu; Wang, Xiaoxiao; Lin, Jinran; Wu, Wenyu; Xia, Rushan; Li, Ming Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 8, pp. 1719-1735. DOI: 10.1016/j.ajhg.2026.06.013 Integrative analysis of gastric tissue transcriptomes and gastric cancer GWAS implicates candidate susceptibility genes Author: Hu, Beiping; Zhang, Min; Yu, Yuhui; Liu, Yongchao; Wang, Jiawei; Zhang, Aiping; Li, Qian; Gao, Yun; Li, Zhe; Bian, Lijun; Gu, Yuanliang; Zhu, Xia; She, Qiang; Gao, Xuefeng; Deng, Bin; Fang, Haisheng; Hu, Caihong; Chen, Yuheng; Chen, Yan; Wang, Xinya; Yin, Xianyong; Zhu, Meng; Wang, Lu; Jiang, Yue; Chen, Jiaping; Dai, Juncheng; Ma, Hongxia; Ding, Yanbing; Yan, Caiwang; Jin, Guangfu Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 7, pp. 1521-1542. DOI: 10.1016/j.ajhg.2026.06.002 Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder Author: Chan, Sock Hoai; Iness, Audra N.; Rosenfeld, Jill A.; Bekheirnia, Mir Reza; Burrage, Lindsay C.; Chau, Matthew Hoi Kin; Htoo, Chaerish Eint Myet Chae; Kao, Eric C.; Ketkar, Shamika; Lim, Wan Wan; Luo, Xi; Mazlan, Rifhan; Mizerik, Elizabeth; Mun, Kein Seong; Patel, Kalyani R.; Potocki, Lorraine; Rapp, Christina K.; Roca, Xavier; Saianda, Ana; Iglesias-Serrano, Ignacio; Siew, Everlyn C.; Sim, Donald Yuhui; Spielberg, David R.; Tae, Sok-Kun; Teo, Jing Xian; Warfsmann, Julian; Xia, Fan; Jamuar, Saumya S.; Tan, Ee Shien; Griese, Matthias; Lim, Weng Khong; Thong, Meow-Keong; Machol, Keren Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 7, pp. 1558-1569. DOI: 10.1016/j.ajhg.2026.05.008 | |||||||||||||||||||||
| 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AMERICAN JOURNAL OF HUMAN GENETICS的语言要求，还能让AMERICAN JOURNAL OF HUMAN GENETICS编辑和审稿人得到更好的审稿体验，让稿件最大限度地被AMERICAN JOURNAL OF HUMAN GENETICS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 。
提交文稿 | |||||||||||||||||||||
| 是否OA开放访问 | No | |||||||||||||||||||||
| 通讯方式 | CELL PRESS, 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, USA, MA, 02139 | |||||||||||||||||||||
| 出版商 | Cell Press | |||||||||||||||||||||
| 涉及的研究方向 | 生物-遗传学 | |||||||||||||||||||||
| 出版国家或地区 | UNITED STATES | |||||||||||||||||||||
| 出版语言 | English | |||||||||||||||||||||
| 出版周期 | Monthly | |||||||||||||||||||||
| 出版年份 | 1949 | |||||||||||||||||||||
| 年文章数 | 191点击查看年文章数趋势图 | |||||||||||||||||||||
| Gold OA文章占比 | 33.90% | |||||||||||||||||||||
| 研究类文章占比： 文章 ÷（文章 + 综述） | 89.53% | |||||||||||||||||||||
| WOS期刊JCR分区 （ 2025-2026年最新版） | 注册或登录后，查看WOS分区等级 | |||||||||||||||||||||
| 期刊分区表预警名单 | 2026年03月发布的新锐学术版：不在预警名单中 2025年03月发布的2025版：不在预警名单中 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 | |||||||||||||||||||||
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| 《新锐期刊分区表》 （ 2026年3月发布） | 点击查看期刊分区表趋势图
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| 期刊分区表 （ 2025年3月升级版） |
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| 期刊分区表 （ 2023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) | |||||||||||||||||||||
| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0002-9297%5BISSN%5D | |||||||||||||||||||||
| 平均审稿速度 | 网友分享经验： 一般,3-6周 | |||||||||||||||||||||
| 平均录用比例 | 网友分享经验： 很难 | |||||||||||||||||||||
| 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AMERICAN JOURNAL OF HUMAN GENETICS顺利发表。
快看看作者怎么说吧：服务好评 论文致谢 。 提交文稿 | |||||||||||||||||||||
| 期刊常用信息链接 |
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| 中国学者近期发表的论文 | |
| 1. | Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia Author: Terkelsen, Thorkild; Yumiceba, Veronica; Kim, Joshua; Melo, Uira Souto; Axelgaard, Esben; Febbraro, Fabia; Gunnarsson, Anders Vermelin; Balachandran, Saranya; Dahl-Jessen, Mikkel; Christensen, Rikke; Peters, Brock Andrew; Asan; Thelle, Thomas; Nyegaard, Mette; Bak, Rasmus O.; Denham, Mark; Spielmann, Malte; Jensen, Uffe Birk Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 8, pp. 1736-1753. DOI: 10.1016/j.ajhg.2026.07.001 PubMed DOI |
| 2. | Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity Author: Cao, Qiaoyu; Zhao, Anqi; Wang, Jianbo; Lin, Xinjie; Long, Zhoukai; Pan, Chaolan; Yang, Kai; Gu, Chun; Wang, Yumeng; Li, Lu; Wang, Xiaoxiao; Lin, Jinran; Wu, Wenyu; Xia, Rushan; Li, Ming Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 8, pp. 1719-1735. DOI: 10.1016/j.ajhg.2026.06.013 PubMed DOI |
| 3. | Integrative analysis of gastric tissue transcriptomes and gastric cancer GWAS implicates candidate susceptibility genes Author: Hu, Beiping; Zhang, Min; Yu, Yuhui; Liu, Yongchao; Wang, Jiawei; Zhang, Aiping; Li, Qian; Gao, Yun; Li, Zhe; Bian, Lijun; Gu, Yuanliang; Zhu, Xia; She, Qiang; Gao, Xuefeng; Deng, Bin; Fang, Haisheng; Hu, Caihong; Chen, Yuheng; Chen, Yan; Wang, Xinya; Yin, Xianyong; Zhu, Meng; Wang, Lu; Jiang, Yue; Chen, Jiaping; Dai, Juncheng; Ma, Hongxia; Ding, Yanbing; Yan, Caiwang; Jin, Guangfu Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 7, pp. 1521-1542. DOI: 10.1016/j.ajhg.2026.06.002 PubMed DOI |
| 4. | Bi-allelic loss-of-function variants in TMEM63B cause syndromic surfactant dysfunction disorder Author: Chan, Sock Hoai; Iness, Audra N.; Rosenfeld, Jill A.; Bekheirnia, Mir Reza; Burrage, Lindsay C.; Chau, Matthew Hoi Kin; Htoo, Chaerish Eint Myet Chae; Kao, Eric C.; Ketkar, Shamika; Lim, Wan Wan; Luo, Xi; Mazlan, Rifhan; Mizerik, Elizabeth; Mun, Kein Seong; Patel, Kalyani R.; Potocki, Lorraine; Rapp, Christina K.; Roca, Xavier; Saianda, Ana; Iglesias-Serrano, Ignacio; Siew, Everlyn C.; Sim, Donald Yuhui; Spielberg, David R.; Tae, Sok-Kun; Teo, Jing Xian; Warfsmann, Julian; Xia, Fan; Jamuar, Saumya S.; Tan, Ee Shien; Griese, Matthias; Lim, Weng Khong; Thong, Meow-Keong; Machol, Keren Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 7, pp. 1558-1569. DOI: 10.1016/j.ajhg.2026.05.008 PubMed DOI |
| 5. | Signatures of pathogen-driven selection and Austronesian gene flow of Papua New Guinea HLA alleles Author: Font-Porterias, Neus; Nemat-Gorgani, Neda; Kichula, Katherine M.; Al-Hindi, Dana R.; Harrison, Genelle F.; Tao, Sudan; Zhu, Faming; Montero-Martin, Gonzalo; Fernandez-Vina, Marcelo A.; Guethlein, Lisbeth A.; Parham, Peter; Oppenheimer, Stephen J.; Ioannidis, Alexander G.; Moreno-Estrada, Andres; Pomat, William; Mentzer, Alexander J.; Henn, Brenna M.; Norman, Paul J Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 6, pp. 1175-1193. DOI: 10.1016/j.ajhg.2026.04.006 PubMed DOI |
| 6. | A next-generation episignature for Kabuki syndrome enables fine mapping of the impact of KMT2D variants to inform precision medicine Author: Wang, Mengqi; Helal, Shaimaa; Torabi-Marashi, Arteen; Goodman, Sarah; Kallurkar, Prajkta; Truong, Tina K.; Mizrahi-Powell, Emma; Evrony, Gilad D.; Chacon-Fonseca, Inara; Palafoll, Irene Valenzuela; Kannu, Peter; Piton, Amelie; Chitayat, David; Boerkoel, Cornelius F.; Mendoza-Londono, Robert; Ortigoza-Escobar, Juan Dario; Kwint, Michael; Rots, Dmitrijs; Kleefstra, Tjitske; Wojcik, Monica H.; Scherer, Stephen W.; Chung, Brian Hon-Yin; Ko, Jung Min; Bjornsson, Hans T.; Harris, Jacqueline R.; Choufani, Sanaa; Weksberg, Rosanna Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 6, pp. 1233-1252. DOI: 10.1016/j.ajhg.2026.04.010 PubMed DOI |
| 7. | PACells identifies phenotype-associated cell states from single-cell chromatin accessibility profiles Author: Hua, Jiao; Sheng, Qiongyu; Xiao, Shutong; Zhou, Yang; Qi, Jing; Jin, Shuilin Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 5, pp. 929-949. DOI: 10.1016/j.ajhg.2026.03.012 PubMed DOI |
| 8. | Associations of genetic variants with gene expression factors reveal biological pathways underlying complex traits Author: Sun, Xiaotong; LaPierre, Nathan; Gu, Jing; Tan, Wenchang; He, Xin Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 4, pp. 852-867. DOI: 10.1016/j.ajhg.2026.03.004 PubMed DOI |
| 9. | Genetics of skeletal proportions across two different populations Author: Bartell, Eric; Lin, Kuang; Tsuo, Kristin; Gan, Wei; Vedantam, Sailaja; Cole, Joanne B.; Baronas, John M.; Yengo, Loic; Marouli, Eirini; Amariuta, Tiffany; Chen, Zhengming; Li, Liming; Renthal, Nora E.; Jacobsen, Christina M.; Salem, Rany M.; Walters, Robin G.; Hirschhorn, Joel N Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 4, pp. 794-808. DOI: 10.1016/j.ajhg.2026.02.015 PubMed DOI |
| 10. | Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies Author: Di Donato, Nataliya; Thom, Andrew; Rump, Andreas; Greve, Johannes N.; Cadinanos, Juan; Calabro, Rocco Salvatore; Cathey, Sara; Chung, Brian; Cope, Heidi; Costales, Maria; Cuvertino, Sara; Dinkel, Philine; Erripi, Kalliopi; Fry, Andrew E.; Garavelli, Livia; Hoffjan, Sabine; Janzarik, Wibke G.; Kreimer, Insa; Mancini, Grazia; Marin-Reina, Purificacion; Meinhardt, Andrea; Niehaus, Indra; Pilz, Daniela; Ricca, Ivana; Simarro, Fernando Santos; Schrock, Evelin; Marquardt, Anja; Taft, Manuel H.; Tezcan, Kamer; Thunstrom, Sofia; Verhagen, Judith; Verloes, Alain; Wollnik, Bernd; Krawitz, Peter; Hsieh, Tzung-Chien; Seifert, Michael; Heide, Michael; Lawrence, Catherine B.; Roberts, Neil A.; Manstein, Dietmar J.; Woolf, Adrian S.; Banka, Siddharth Journal: AMERICAN JOURNAL OF HUMAN GENETICS. 2026; Vol. 113, Issue 2, pp. -. DOI: 10.1016/j.ajhg.2025.12.007 PubMed DOI |
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