Human Genetics And Genomics Advances

Human Genetics And Genomics Advances

人类遗传学和基因组学进展

  • 2区 中科院分区
  • Q2 JCR分区

期刊简介

《Human Genetics And Genomics Advances》是由Elsevier出版社创办的英文国际期刊(ISSN: 2666-2477),该期刊长期致力于遗传学领域的创新研究,主要研究方向为GENETICS & HEREDITY。作为SCIE收录期刊(JCR分区 Q2,中科院 2区),本刊采用OA未开放获取模式以发表遗传学领域等方向的原创性研究为核心(研究类文章占比98.50%%)。凭借严格的同行评审与高效编辑流程,期刊年载文量精选控制在133篇,确保学术质量与前沿性。成果覆盖Web of Science、Scopus等国际权威数据库,为学者提供推动生物领域高水平交流平台。

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投稿提示

Human Genetics And Genomics Advances审稿周期约为14 Weeks。该刊近年未被列入国际预警名单,年发文量约133篇,录用竞争适中,主题需确保紧密契合生物前沿。投稿策略提示:避开学术会议旺季投稿以缩短周期,语言建议专业润色提升可读性。

  • 生物 大类学科
  • English 出版语言
  • 是否预警
  • SCIE 期刊收录
  • 133 发文量

中科院分区

《新锐期刊分区表》(2026年3月发布)

Top期刊 综述期刊 大类学科 小类学科
生物学
2区
GENETICS & HEREDITY 遗传学
2区

期刊分区表(2025年3月升级版)

Top期刊 综述期刊 大类学科 小类学科
生物学
2区
GENETICS & HEREDITY 遗传学
3区

JCR分区

2025-2026年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:GENETICS & HEREDITY ESCI Q2 74 / 192

61.7

学科:GENETICS & HEREDITY ESCI Q1 47 / 192

75.78

2023-2024年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:GENETICS & HEREDITY ESCI Q2 64 / 191

66.8

学科:GENETICS & HEREDITY ESCI Q1 28 / 191

85.6

CiteScore(2026年6月最新版)

CiteScore SJR SNIP CiteScore 排名
CiteScore: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%

期刊发文

  • 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

    Journal: HUMAN GENETICS AND GENOMICS ADVANCES. 2026; Vol. 7, Issue 2, pp. -. DOI: 10.1016/j.xhgg.2026.100574

  • 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

    Journal: HUMAN GENETICS AND GENOMICS ADVANCES. 2026; Vol. 7, Issue 2, pp. -. DOI: 10.1016/j.xhgg.2026.100566

  • 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

    Journal: HUMAN GENETICS AND GENOMICS ADVANCES. 2026; Vol. 7, Issue 2, pp. -. DOI: 10.1016/j.xhgg.2026.100563

  • 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

    Journal: HUMAN GENETICS AND GENOMICS ADVANCES. 2025; Vol. 6, Issue 1, pp. -. DOI: 10.1016/j.xhgg.2024.100375

  • Togaram1 is expressed in the neural tube and its absence causes neural tube closure defect

    Author: Wang, Yanyan; Kraemer, Nadine; Schneider, Joanna; Ninnemann, Olaf; Weng, Kai; Hildebrand, Michael; Reid, Joshua; Li, Na; Hu, Hao; Mani, Shyamala; Kaindl, Angela M.

    Journal: HUMAN GENETICS AND GENOMICS ADVANCES. 2025; Vol. 6, Issue 1, pp. -. DOI: 10.1016/j.xhgg.2024.100363