CLINICAL GENETICS

简称 CLIN GENET ·DENMARK ·出版周期 Monthly ·年均收录 169 篇

2.3

最新影响因子

4.40%

自引率

较易

投稿难度

一般,3-8周

审稿周期

期刊简介

CLINICAL GENETICS是一本专注于临床遗传学领域的国际学术期刊，ISSN号为0009-9163，由Wiley-Blackwell出版，出版地为丹麦，出版周期为月刊。该期刊的影响因子根据最新数据在2-3之间，属于非开放获取（非OA）期刊，并被SCI收录，在中科院分区中通常位于医学或遗传学领域的3区或4区。杂志的发文特点集中于人类遗传疾病的临床研究、分子遗传学、基因组学及其在诊断和治疗中的应用，涵盖遗传咨询、罕见病研究和遗传流行病学等方向。其质量较高，审稿严格，但影响因子相对中等，可能存在投稿竞争激烈和发表周期较长的风险，适合从事临床遗传学研究的学者投稿。

影响因子趋势

近期发表

10.1111/cge.v110.4 2026-09-02

Pathogenicity of <scp> NUSAP1 </scp> Variants Is Defined by <scp>NMD</scp> ‐Escape: Evidence From Two Novel Cases and Systematic Population‐Based Variant Analysis 2026-09-08

Biallelic <scp> ABCA13 </scp> Loss‐of‐Function Variants in a Child With Neurodevelopmental Delay: A Case Report 2026-09-04

10.1111/cge.v110.3 2026-08-03

Variants in the Imprinted <scp> IGF2 </scp> Gene: A Review and Phasing of De Novo Variants Using Long‐Read Sequencing 2026-09-02

Issue Information 2026-09-02

Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in <scp>MECP2</scp> Duplication Syndrome 2026-08-28

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/ <scp>DFNB</scp> ‐Related Genes: An Impossible Challenge? 2026-08-28

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease 2026-08-28

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas–Mexico Border 2026-08-26