NEUROGENETICS

Abbr. NEUROGENETICS ·GERMANY ·Frequency Quarterly ·Avg. articles/yr 33 articles

1.2

Latest IF

1.80%

Self-citation

约95%

Submission difficulty

平均6月

Review cycle

About Journal

NEUROGENETICS是一本专注于神经遗传学领域的国际学术期刊，ISSN号为1364-6745，由Springer出版，出版地为德国，出版周期为季刊。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，中科院分区为医学大类3区或4区。其发文特点集中于神经退行性疾病、神经发育障碍、遗传性神经疾病等研究领域，涵盖分子遗传学、基因组学和临床神经遗传学等内容。杂志质量中等，审稿周期较长，但近年来发文量较少，可能存在投稿竞争激烈或审稿标准较高的风险，适合从事神经遗传学研究的学者投稿。

IF Trend

Recent Articles

A rare ATM variant in a Colombian family with chorea-ataxia syndrome: implications for an early diagnosis 2026-09-24

Expanding the adult spectrum of TUBB4A disease: a spasticity–tremor phenotype with network imaging correlates 2026-09-19

Clinical and genetic findings in Parkinson’s disease in a Turkish cohort: a retrospective exome sequencing study 2026-09-19

Further delineation of 2p13.2–p11.2 deletion syndrome by optical genome mapping 2026-09-19

Glutaric aciduria type 1 presenting with Parkinsonism with presynaptic dopaminergic dysfunction in an adult female: a case report 2026-09-15

Expansion of the allelic and phenotypic spectrum of MED25-related developmental disorder: novel compound heterozygous variants with structural domain implications 2026-09-09

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report 2026-09-06

Non-convulsive status epilepticus revealing acute deterioration in AARS2 mutation–associated progressive leukoencephalopathy 2026-09-04

High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approach 2026-09-02

Clinical characteristics of THAP1 related dystonia: a case report with phenotypic review 2026-09-02