Neurology-Genetics
ISSN:2376-7839

Neurology-Genetics

NEUROL-GENET
学科领域:医学
是否预警:不在预警名单内
是否OA:
录用周期:15 Weeks
新锐分区:医学3区
年发文量:86
影响因子:4.3
JCR分区:Q1

基本信息

《神经学:遗传学》是一本在线开放获取期刊,发表神经遗传学领域的同行评议报告。将发表神经遗传学所有领域的原创文章,包括罕见和常见的遗传变异、基因型-表型相关性、已知疾病基因突变导致的离群表型,以及与疾病相关的遗传变异。这将包括报告遗传疾病风险和药物基因组学的研究。此外,神经病学:Genetics将发布基于基因的临床试验结果(病毒、阿索等)。基因工程模型系统不是神经病学的主要重点:遗传学,但使用模型系统进行治疗试验的研究是受欢迎的,包括报告阴性结果的把握度良好的研究。
2376-7839SCIE/Scopus收录/DOAJ开放期刊
4.3
3
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学3区
GENETICS & HEREDITY 遗传学
3区
CLINICAL NEUROLOGY 临床神经病学
3区
N/A
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q1
47/286
学科:GENETICS & HEREDITY
SCIE
Q1
38/192
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:CLINICAL NEUROLOGY
SCIE
Q2
80/286
学科:GENETICS & HEREDITY
SCIE
Q2
52/192
暂无h-index数据
86
3%-15 WeeksUSD3300Medicine-Neurology (clinical)
4.7%
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
95.35%95.58%2.2%
CiteScore:4.60
SJR:1.105
SNIP:0.888
学科类别分区排名百分位
大类:Medicine
小类:Neurology (clinical)
Q2
168 / 400
大类:Medicine
小类:Genetics (clinical)
Q2
47 / 100

期刊高被引文献

Genetic risk of Parkinson disease and progression:
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000348
Antisense oligonucleotides
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000323
Psychometric properties of the Friedreich Ataxia Rating Scale
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000371
Impaired kidney structure and function in spinal muscular atrophy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000353
Genotype-structure-phenotype relationships diverge in paralogs ATP1A1, ATP1A2, and ATP1A3
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000303
New family with HSPB8-associated autosomal dominant rimmed vacuolar myopathy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000349
Migraine polygenic risk score associates with efficacy of migraine-specific drugs
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000364
Genomic variation in educational attainment modifies Alzheimer disease risk
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000310
DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000338
Congenital myopathies in the adult neuromuscular clinic
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000341
Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZ
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000320
Lithium chloride corrects weakness and myopathology in a preclinical model of LGMD1D
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000318
Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>G
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000315
Copy number variation of LINGO1 in familial dystonic tremor
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000307
HTT haplogroups in Finnish patients with Huntington disease
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000334
HACE1 deficiency leads to structural and functional neurodevelopmental defects
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000330
Oligogenic basis of sporadic ALS
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000335
Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000339
Next-generation sequencing approach to hyperCKemia
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000352
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000337
Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000332
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000386
Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000345
Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000365
Epilepsy with migrating focal seizures
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000363
Brain-derived neurotrophic factor, epigenetics in stroke skeletal muscle, and exercise training
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000331
A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an ELOVL4 mutation
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000357
Missense mutations in DYT-TOR1A dystonia
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000350
Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000374
Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000359
Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000328
GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000366
Yield of comparative genomic hybridization microarray in pediatric neurology practice
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000367
Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000382
Unraveling the genetic complexity of Alzheimer disease with Mendelian Randomization
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000313
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000378
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000346
2018: Year in Review and Message from the Editors to Our Reviewers
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000309
Genome-wide Brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000355
Myelopathy in a patient with leukodystrophy due to CSF1R mutation
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000376
Proceedings of the 24th International Stroke Genetics Consortium Workshop: Washington, DC, USA
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000325
Epidemiology of DYT1 dystonia
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000358
X-linked myotubular myopathy and recurrent spontaneous pneumothorax
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000327
Fatal TTR amyloidosis with neuropathy from domino liver p.Val71Ala transplant
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000351
Galloping tongue syndrome in a PRRT2 mutation carrier
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000377
Hemorrhagic cerebral small vessel disease caused by a novel mutation in 3′ UTR of collagen type IV alpha 1
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000383
Human GABRG2 generalized epilepsy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000340
Rating scales for rare neurological diseases
来源期刊:Neurology: GeneticsDOI:10.1212/nxg.0000000000000380
A novel noncoding FKRP mutation in early onset limb-girdle muscular dystrophy
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000388
Altered CSF levels of monoamines in hereditary spastic paraparesis 10
来源期刊:Neurology: GeneticsDOI:10.1212/NXG.0000000000000344

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