Human Genetics And Genomics Advances

SCIE

国际简称：HUM GENET GENOM ADV 参考译名：人类遗传学和基因组学进展

主要研究方向：GENETICS & HEREDITY 非预警期刊审稿周期：14 Weeks

《人类遗传学和基因组学进展》(Human Genetics And Genomics Advances)是一本由Elsevier出版的以GENETICS & HEREDITY为研究特色的国际期刊，发表该领域相关的原创研究文章、评论文章和综述文章，及时报道该领域相关理论、实践和应用学科的最新发现，旨在促进该学科领域科学信息的快速交流。该期刊是一本未开放期刊，近三年没有被列入预警名单。该期刊享有很高的科学声誉，影响因子不断增加，发行量也同样高。

2区中科院分区
Q2 JCR分区
133 年发文量
3.1 IF影响因子
未开放 是否OA
English 出版语言

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.

[ 查看全部 ]

投稿咨询加急咨询

Human Genetics And Genomics Advances期刊信息

ISSN：2666-2477
出版语言：English
是否OA：未开放
出版地区：United States
是否预警：否
出版商：Elsevier
Gold OA文章占比：100.00%
研究类文章占比：98.50%

Human Genetics And Genomics Advances CiteScore评价数据（2026年6月最新版）

CiteScore

SJR

SNIP

CiteScore 指数

6.1

1.761

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%

名词解释：CiteScore 是衡量期刊所发表文献的平均受引用次数，是在 Scopus 中衡量期刊影响力的另一个指标。当年CiteScore 的计算依据是期刊最近4年（含计算年度）的被引次数除以该期刊近四年发表的文献数。例如，2022年的 CiteScore 计算方法为：2022年的 CiteScore =2019-2022年收到的对2019-2022年发表的文件的引用数量÷2019-2022年发布的文献数量注：文献类型包括：文章、评论、会议论文、书籍章节和数据论文。

Human Genetics And Genomics Advances中科院评价数据

《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
否	否	生物学	2区	GENETICS & HEREDITY 遗传学	2区

Human Genetics And Genomics Advances JCR评价数据

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

Human Genetics And Genomics Advances历年数据统计

影响因子

中科院分区

Human Genetics And Genomics Advances中国学者发文选摘

1、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
2、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
3、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
4、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
5、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