CLINICAL GENETICS

Abbr. CLIN GENET ·DENMARK ·Frequency Monthly ·Avg. articles/yr 169 articles

2.3

Latest IF

4.40%

Self-citation

较易

Submission difficulty

一般,3 - 8周

Review cycle

About Journal

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。

IF Trend

Recent Articles

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

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy 2026-09-16

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next‐Generation Sequencing: Case Series of 70 Patients 2026-09-15

Childhood‐Onset <scp> Filamin c </scp> Related Cardiomyopathy: Genotype–Phenotype Correlation and Outcome 2026-09-14

A Homozygous Variant in DMRTB1 Is Associated With Non‐Obstructive Azoospermia in Humans 2026-09-14

Genetic Testing Unveils a Novel Thrombospondin‐1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79‐Year‐Old Woman 2026-09-09

A Novel De Novo STAG1 Variant at the <scp>RAD21</scp> Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies 2026-09-09

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