查看最新文献
订阅
分享
11939
影响因子：
3.6
ISSN：
print: 2666-2477
研究领域：
Biochemistry, Genetics and Molecular Biology-Molecular Medicine
自引率：
4.50%
Gold OA文章占比：
97.28%
原创研究文献占比：
95.40%
SCI收录类型：
Directory of Open Access Journals (DOAJ)
CiteScore：
| CiteScore | SJR | SNIP | CiteScore排名 |
|---|---|---|---|
| 4.3 | 1.713 | 1.067 | 学科 排名 百分位 大类：Medicine 小类：Genetics (clinical) 53 / 99 46% 大类：Biochemistry, Genetics and Molecular Biology 小类：Molecular Medicine 118 / 178 33% |
发文信息
中科院SCI期刊分区
2025年3月20日发布
| 大类 | 小类 | TOP期刊 | 综述期刊 |
|---|---|---|---|
| 2区 生物学 | 3区 遗传学 GENETICS & HEREDITY | 否 | 否 |
WOS期刊分区
| 学科分类 |
|---|
Q2GENETICS & HEREDITY |
历年影响因子
| 2022年 | 4.4000 |
|---|---|
| 2023年 | 3.3000 |
| 2024年 | 3.6000 |
历年发表
| 2020年 | 5 |
|---|---|
| 2021年 | 46 |
| 2022年 | 69 |
投稿信息
出版语言：
English
出版国家(地区)：
United States
接受率：
73%
初审时长：
6 weeks
审稿时长：
14 weeks
发表时长：
3 weeks
论文处理费：
$3300
出版商：
Elsevier
HGG Advances - 最新文献
Layers in the sand: The genetic imprint of migration, culture, and Indus craft in the Thar desert.
Pub Date : 2026-05-06 DOI: 10.1016/j.xhgg.2026.100623 Rishabh Jain, Sachin M Rathod, Pankaj Jha, Deepika Jangir, Mohammed Faruq, Ganga Nath Jha, Mitali MukerjiGenome Sequencing for the Diagnosis of Rare Disorders: The Brazilian Rare Genomes Project.
Pub Date : 2026-05-04 DOI: 10.1016/j.xhgg.2026.100624 Antonio Victor Campos Coelho, Rafael Sales de Albuquerque, Catarina Dos Santos Gomes, José Bandeira do Nascimento Junior, Gustavo Santos de Oliveira, Livia Maria Silva Moura, Luciana Souto Mofatto, Rafael Lucas Muniz Guedes, Rodrigo Araújo Sequeira Barreiro, Marcel Pinheiro Caraciolo, Ana Paula de Andrade Oliveira, Anne Caroline Barbosa Teixeira, Bruna Mascaro Cordeiro de Azevedo, Carolina Dias Carlos, Lucas Santos de Santana, Marina Cadena da Matta, Matheus Martinelli Lima, Nuria Bengala Zurro, Renata Yoshiko Yamada, Vivian Pedigone Cintra, Gabriela Pereira Campilongo, Gabriela Borges Cherulli Colichio, Renata Martins Ribeiro da Silva, Caio Robledo D'Angioli Costa Quaio, Carolina Araujo Moreno, Eduardo Perrone, Jéssica Grasiela Araújo Espolaor, Joana Rosa Marques Prota, José Ricardo Magliocco Ceroni, Kelin Chen, Luiza do Amaral Virmond, Marina de França Basto Silva, Michele Patricia Migliavacca, Renata Moldenhauer Minillo, Thiago Yoshinaga Tonholo Silva, Karla de Oliveira Pelegrino, Ana Luiza Garcia Cunha, Joziele de Souza Lima, Anete Sevciovic Grumach, Caio Parente Barbosa, Angelina Xavier Acosta, Paula Brito Corrêa, Denise Pontes Cavalcanti, Carlos Eduardo Steiner, Erlane Marques Ribeiro, Wallace William da Silva Meireles, Giselle Maria Araujo Felix Adjuto, Ida Vanessa Doederlein Schwartz, Têmis Maria Felix, Irma Cecilia Douglas Paes Barreto, Antonette Souto El Husny, Jussara Melo de Cerqueira Maia, Vera Maria Dantas, Lúcia Helena de Oliveira Cordeiro, Luiza Zagne Braz, Magda Maria Sales Carneiro Sampaio, Mara Lucia Schmitz Ferreira Santos, Marco Antonio Curiati, Maria Teresinha de Oliveira Cardoso, Maria Teresa Alves da Silva Rosa, Mariana Paes Leme Ferriani, Ester Silveira Ramos, Paula Teixeira Lyra, Raquel Tavares Boy da Silva, Anna Cândida Ximenes de Mendonça Sobreira, Tatiana Regia Suzana Amorim Boa Sorte, Melissa Rossi Calvão Dumas, Thaís Bomfim Teixeira, Vandré Cabral Gomes Carneiro, Patrícia Silva Mota, Tatiana Ferreira de Almeida, João Bosco OliveiraBiallelic loss-of-function variants in DSCAM cause a neurodevelopmental syndrome with nystagmus and retinal dysfunction.
Pub Date : 2026-04-29 DOI: 10.1016/j.xhgg.2026.100622 Sofia Douzgou Houge, Cecilie Bredrup, Ragnhild Wivestad Jansson, Ognjen Bojovic, Bayan M Aljamal, Maha Al-Otaibi, Astrid S Plomp, Mahdi M Motazacker, Maria M van Genderen, Anne Mellgren, Hisham Alkuraya, Omar Hikmat, Bjørn Ivar Haukanes, Fowzan S Alkuraya, Gunnar Douzgos Houge
免责声明：
本页显示期刊或杂志信息，仅供参考学习，不是任何期刊杂志官网，不涉及出版事务，特此申明。如需出版一切事务需要用户自己向出版商联系核实。若本页展示内容有任何问题，请联系我们，邮箱：info@booksci.cn，我们会认真核实处理。
本页显示期刊或杂志信息，仅供参考学习，不是任何期刊杂志官网，不涉及出版事务，特此申明。如需出版一切事务需要用户自己向出版商联系核实。若本页展示内容有任何问题，请联系我们，邮箱：info@booksci.cn，我们会认真核实处理。
京公网安备 11010802042870号
