Human Genetics And Genomics Advances
收藏杂志
  • 数据库收录SCIE
  • 年发文量133

Human Genetics And Genomics Advances

期刊中文名:人类遗传学和基因组学进展ISSN:2666-2477

该杂志国际简称:HUM GENET GENOM ADV,是由出版商Elsevier出版的一本致力于发布生物研究新成果的的专业学术期刊。该杂志以遗传学研究为重点,主要发表刊登有创见的学术论文文章、行业最新科研成果,扼要报道阶段性研究成果和重要研究工作的最新进展,选载对学科发展起指导作用的综述与专论,促进学术发展,为广大读者服务。该刊是一本国际优秀杂志,在国际上有很高的学术影响力。

基本信息:
期刊简称:HUM GENET GENOM ADV
是否OA:未开放
是否预警:
Gold OA文章占比:100.00%
出版信息:
出版地区:United States
出版语言:English
出版商:Elsevier
评价信息:
中科院分区:2区
JCR分区:Q2
影响因子:3.1
CiteScore:6.1
杂志介绍 中科院JCR分区 JCR分区 CiteScore 投稿经验

杂志介绍

Human Genetics And Genomics Advances杂志介绍

《Human Genetics And Genomics Advances》是一本以English为主的未开放获取国际优秀期刊,中文名称人类遗传学和基因组学进展,本刊主要出版、报道生物-遗传学领域的研究动态以及在该领域取得的各方面的经验和科研成果,介绍该领域有关本专业的最新进展,探讨行业发展的思路和方法,以促进学术信息交流,提高行业发展。该刊已被国际权威数据库SCIE收录,为该领域相关学科的发展起到了良好的推动作用,也得到了本专业人员的广泛认可。该刊最新影响因子为3.1,最新CiteScore 指数为6.1。

本刊近期中国学者发表的论文主要有:

  • Application of the STAAR framework in detecting rare variant associations with Alzheimer disease and related dementias: Insights and implication

    Author: Wang, Dongyu; Abbruzzese, Sabrina; Heard-Costa, Nancy; Rampersaud, Andy; Martin, Eden; Naj, Adam; Akgun, Bilcag; Kunkle, Brian; Seshadri, Sudha; Peloso, Gina; Destefano, Anita L.; Li, Zilin; Li, Xihao; Choi, Seung Hoan

  • Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse population

    Author: Lee, Songmi; Miller, Clint L.; Bentley, Amy R.; Brown, Michael R.; Nagarajan, Pavithra; Noordam, Raymond; Morrison, John L.; Schwander, Karen; Westerman, Kenneth; Kho, Minjung; Kraja, Aldi T.; de Vries, Paul S.; Ammous, Farah; Aschard, Hughes; Bartz, Traci M.; Do, Anh; Dupont, Charles T.; Feitosa, Mary F.; Gudmundsdottir, Valborg; Guo, Xiuqing; Harris, Sarah E.; Hikino, Keiko; Huang, Zhijie; Lefevre, Christophe; Lyytikainen, Leo-Pekka; Milaneschi, Yuri; Nardone, Giuseppe Giovanni; Santin, Aurora; Schmidt, Helena; Shen, Botong; Sofer, Tamar; Sun, Quan; Tan, Ye An; Tang, Jingxian; Theriault, Sebastien; van der Most, Peter J.; Ware, Erin B.; Weiss, Stefan; Xing, Wang Ya; Yu, Chenglong; Zhao, Wei; Ansari, Md Abu Yusuf; Anugu, Pramod; Attia, John R.; Bazzano, Lydia A.; Bis, Joshua C.; Breyer, Max; Cade, Brian; Chen, Guanjie; Collins, Stacey; Corley, Janie; Davies, Gail; Doerr, Marcus; Du, Jiawen; Edwards, Todd L.; Faquih, Tariq; Faul, Jessica D.; Fohner, Alison E.; Fretts, Amanda M.; Gangireddy, Srushti; Gepner, Adam; Graff, MariaElisa; Hofer, Edith; Homuth, Georg; Hood, Michelle M.; Jie, Xu; Kahonen, Mika; Kardia, Sharon L. R.; Karvonen-Gutierrez, Carrie A.; Launer, Lenore J.; Levy, Daniel; Maheshwari, Maitreiyi; Martin, Lisa W.; Matsuda, Koichi; McNeil, John J.; Nolte, Ilja M.; Okochi, Tomo; Raffield, Laura M.; Raitakari, Olli T.; Risch, Lorenz; Risch, Martin; Roux, Ana Diez; Ruiz-Narvaez, Edward A.; Russ, Tom C.; Saito, Takeo; Schreiner, Pamela J.; Scott, Rodney J.; Shikany, James; Smith, Jennifer A.; Snieder, Harold; Spedicati, Beatrice; Tai, E. Shyong; Taylor, Adele M.; Taylor, Kent D.; Tesolin, Paola; van Dam, Rob M.; Wang, Rujia; Wei Wenbin; Xie, Tian; Yao, Jie; Young, Kristin L.; Zhang, Ruiyuan; Zonderman, Alan B.; Concas, Maria Pina; Conen, David; Cox, Simon R.; Evans, Michele K.; Fox, Ervin R.; de las Fuentes, Lisa; Giri, Ayush; Girotto, Giorgia; Grabe, Hans J.; Gu, Charles; Gudnason, Vilmundur; Harlow, Sioban D.; Holliday, Elizabeth; Jost, Jonas B.; Lacaze, Paul; Lee, Seunggeun; Lehtimaki, Terho; Li, Changwei; Liu, Ching-Ti; Morrison, Alanna C.; North, Kari E.; Penninx, Brenda W. J. H.; Peyser, Patricia A.; Province, Michael M.; Psaty, Bruce M.; Redline, Susan; Rosendaal, Frits R.; Rotimi, Charles N.; Rotter, Jerome I.; Schmidt, Reinhold; Sim, Xueling; Terao, Chikashi; Weir, David R.; Zhu, Xiaofeng; Franceschini, Nora; O'Connell, Jeffrey R.; Jaquish, Cashell E.; Wang, Heming; Manning, Alisa; Munroe, Patricia B.; Rao, Dabeeru C.; Chen, Han; Gauderman, W. James; Bierut, Laura J.; Winkler, Thomas W.; Fornage, Myriam

  • EEFSEC deficiency underlies a human selenopathy with primary neurodevelopmental origins via midbrain-hindbrain hypoplasi

    Author: Xia, Zhiyi; Liu, Hui; Guo, Pengbo; Chen, Chongfen; Ge, Lili; Tang, Longfei; Zhang, Yaodong; Ma, Yanli

  • Functional genomics implicates natural killer cells in the pathogenesis of ankylosing spondyliti

    Author: Chinas, Marcos; Fernandez-Salinas, Daniela; Aguiar, Vitor R. C.; Nieto-Caballero, Victor E.; Lefton, Micah; Nigrovic, Peter A.; Ermann, Joerg; Gutierrez-Arcelus, Maria

英文介绍

Human Genetics And Genomics Advances杂志英文介绍

Human Genetics and Genomics Advances is an academic journal dedicated to the fields of human genetics and genomics. This journal is dedicated to publishing the latest research achievements in the fields of human genetics and genomics, including research progress in gene variation, genetic diseases, genetic diversity, genome structure and function, and more. The magazine covers various aspects from basic research to clinical applications, providing readers with a comprehensive platform to understand the latest developments in the fields of human genetics and genomics. It focuses on hot topics such as the relationship between genes and diseases, gene therapy, personalized medicine, and explores the impact of these studies on human health and society.

The readership of the magazine mainly includes geneticists, molecular biologists, doctors, medical researchers, and others. This journal provides a platform for professionals to exchange and share the latest research findings, promoting academic exchange and collaboration. Intended to provide a high-quality academic journal for researchers in the fields of human genetics and genomics, promoting the development of academic research and technological innovation in this field. By publishing high-quality research papers and review articles, this journal promotes academic exchanges and practical applications in the fields of human genetics and genomics.

中科院SCI分区

Human Genetics And Genomics Advances杂志中科院分区信息

《新锐期刊分区表》
2026年3月发布
综述:
TOP期刊:
大类:生物学 2区
小类:

GENETICS & HEREDITY
遗传学 2区

中科院SCI分区:是中国科学院文献情报中心科学计量中心的科学研究成果。期刊分区表自2004年开始发布,延续至今;2019年推出升级版,实现基础版、升级版并存过渡,2022年只发布升级版,期刊分区表数据每年底发布。 中科院分区为4个区。中科院分区采用刊物前3年影响因子平均值进行分区,即前5%为该类1区,6%~20%为2区、21%~50%为3区,其余的为4区。1区和2区杂志很少,杂志质量相对也高,基本都是本领域的顶级期刊。

JCR分区

Human Genetics And Genomics Advances杂志 JCR分区信息

2025-2026年最新版
按JCI指标学科分区
学科:GENETICS & HEREDITY
收录子集:ESCI
分区:Q2
排名:74 / 192
百分位:

61.7

学科:GENETICS & HEREDITY
收录子集:ESCI
分区:Q1
排名:47 / 192
百分位:

75.78

JCR分区:JCR分区来自科睿唯安公司,JCR是一个独特的多学科期刊评价工具,为唯一提供基于引文数据的统计信息的期刊评价资源。每年发布的JCR分区,设置了254个具体学科。JCR分区根据每个学科分类按照期刊当年的影响因子高低将期刊平均分为4个区,分别为Q1、Q2、Q3和Q4,各占25%。JCR分区中期刊的数量是均匀分为四个部分的。

CiteScore 评价数据(2026年6月最新版)

Human Genetics And Genomics Advances杂志CiteScore 评价数据

  • CiteScore 值:6.1
  • SJR:1.761
  • SNIP:1.144
学科类别 分区 排名 百分位
大类:Medicine 小类:Genetics (clinical) Q2 28 / 100

72%

大类:Medicine 小类:Molecular Medicine Q2 79 / 179

56%

历年影响因子和期刊自引率

投稿经验

Human Genetics And Genomics Advances杂志投稿经验

该杂志是一本国际优秀杂志,在国际上有较高的学术影响力,行业关注度很高,已被国际权威数据库SCIE收录,该杂志在遗传学综合专业领域专业度认可很高,对稿件内容的创新性和学术性要求很高,作为一本国际优秀杂志,一般投稿过审时间都较长,投稿过审时间平均14 Weeks,如果想投稿该刊要做好时间安排。版面费不祥。该杂志近两年未被列入预警名单,建议您投稿。如您想了解更多投稿政策及投稿方案,请咨询客服。

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