《Human Genetics And Genomics Advances》期刊

杂志介绍

JCR分区

中科院分区

2区

影响因子

3.1

CiteScore

6.1

期刊收录

SCIE

Human Genetics And Genomics Advances（中文译名：《人类遗传学和基因组学进展》），ISSN：2666-2477，是Elsevier出版的国际性学术期刊，2026年总发文量约133篇。该刊采用非OA开放访问，学科归属为GENETICS & HEREDITY。该刊是生物、遗传学领域的国际权威刊物，已被SCIE（科学引文索引扩展版）等国际主流学术数据库收录。2026年期刊影响因子达3.1，2025年期刊CiteScore为6.1，2025年期刊自引率约6.5%，在中科院期刊分区体系中位列生物学大类2区，在所属学科领域具备高学术影响力与国际认可度。Human Genetics And Genomics Advances长期聚焦生物、遗传学及相关产业的技术应用前沿，平均审稿周期14 Weeks，审稿流程高效稳定。在稿件录用评判中，该刊将创新性与前沿性作为核心遴选标准，重点收录能够对生物、遗传学领域的落地与发展产生实质性推动价值的研究成果。

期刊评价

名词解释：

影响因子（Impact Factor, IF）：指该期刊前两年发表的文章，在第三年的平均被引用次数。它反映了期刊的近期平均影响力和热度。

中科院分区：中科院分区表是国内主流的学术期刊分级评价工具，核心意义是建立跨学科可比的统一评价标尺，为职称评审、学位授予、科研立项等科研管理工作提供标准化量化依据，同时帮助科研人员筛选优质期刊、规避学术风险，适配国内本土化的科研评价需求。

期刊分区表

《新锐期刊分区表》（2026年3月发布）

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

期刊分区表（2025年3月升级版）

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

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

中国学者近期发文

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