PSYCHIATRIC GENETICS
ISSN:0955-8829

PSYCHIATRIC GENETICS

PSYCHIAT 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:>12周,或约稿
新锐分区:医学4区
年发文量:21
影响因子:1.4
JCR分区:Q4

基本信息

该杂志旨在发表论文,汇集临床观察,心理和行为异常和遗传数据。精神遗传学也是一个报告精神病学和神经病学遗传学研究新方法的论坛。《精神遗传学》出版了涉及精神和神经疾病的遗传因素的原始研究报告。这包括基因定位和染色体标记、与精神疾病相关的神经元基因表达的变化、连锁遗传学分析、家族、双胞胎和收养研究以及基于遗传学的神经精神疾病动物模型。该期刊涵盖与精神疾病相关的分子神经生物学和分子遗传学等领域。将考虑出版当前感兴趣领域的文献综述和评论。精神遗传学以外的领域,但对精神遗传学感兴趣和重要的评论和评论,也将被考虑。精神遗传学也出版书评,简报和会议报告。
0955-8829SCIE/Scopus收录
1.4
1.3
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4区
GENETICS & HEREDITY 遗传学
4区
NEUROSCIENCES 神经科学
4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:GENETICS & HEREDITY
SCIE
Q4
154/192
学科:NEUROSCIENCES
SCIE
Q4
277/314
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科:GENETICS & HEREDITY
SCIE
Q4
172/192
学科:NEUROSCIENCES
SCIE
Q4
293/314
56
21
19%较易>12周,或约稿-医学-神经科学
7.1%
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
95.24%15.07%-
CiteScore:2.50
SJR:0.468
SNIP:0.403
学科类别分区排名百分位
大类:Medicine
小类:Psychiatry and Mental Health
Q3
338 / 580
大类:Medicine
小类:Biological Psychiatry
Q3
37 / 54
大类:Medicine
小类:Genetics (clinical)
Q3
72 / 100
大类:Medicine
小类:Genetics
Q4
266 / 348

期刊高被引文献

Missing a beat: assessment of circadian rhythm abnormalities in bipolar disorder in the genomic era
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000215
Genetic risk factors and gene–environment interactions in adult and childhood attention-deficit/hyperactivity disorder
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000220
Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder: lessons from CNTNAP2, ADGRL3, and PARK2
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000211
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000216
Schizophrenia in a genomic era: a review from the pathogenesis, genetic and environmental etiology to diagnosis and treatment insights
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000245
Genomics of human aggression: current state of genome-wide studies and an automated systematic review tool.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000239
Offspring of parents with schizophrenia, bipolar disorder, and depression: a review of familial high-risk and molecular genetics studies.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000240
Familial association of attention-deficit hyperactivity disorder with autoimmune diseases in the population of Sweden
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000212
The emerging pattern of shared polygenic architecture of psychiatric disorders, conceptual and methodological challenges.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000234
Brain-derived neurotrophic factor and schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000237
Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000241
Anorexia nervosa is associated with Neuronatin variants.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000224
Zinc finger proteins in psychiatric disorders and response to psychotropic medications.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000231
Understanding the schizophrenia phenotype in the first patient with the full SCN2A phenotypic spectrum
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000219
The interaction between estradiol change and the serotonin transporter gene (5-HTTLPR) polymorphism is associated with postpartum depressive symptoms.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000222
Buspirone for the treatment of anxiety-related symptoms in Angelman syndrome: a case series
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000218
Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000208
New insights and perspectives on the genetics of obsessive-compulsive disorder.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000230
Common variants in SATB2 are associated with schizophrenia in Uygur Chinese population.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000229
A case of intellectual disability reveals a novel mutation in IQSEC2 gene by whole exome sequencing.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000232
Association of polymorphisms in HTR2A, TPH1, and TPH2 genes with attempted suicide in rural China
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000221
Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000227
Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000235
Decreased serum complement component 4 levels in patients with schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000226
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000217
Gene knockout animal models of depression, anxiety and obsessive compulsive disorders.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000238
Catechol-O-methyltransferase gene expression in stress-induced and non-stress induced schizophrenia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000243
Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia.
来源期刊:Psychiatric geneticsDOI:10.1097/ypg.0000000000000242
Schizophrenia in microcephalic osteodysplastic primordial dwarfism type II syndrome: supporting evidence for an association between the PCNT gene and schizophrenia.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000214
No association between CYP2C19 genetic polymorphism with treatment remission to antidepressant venlafaxine in Han Chinese population
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000246
Association study of the PDE4D gene and obsessive-compulsive disorder in a Chinese Han population.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000236
Corpus callosum metrics predict severity of visuospatial and neuromotor dysfuntions in ARID1B mutations with Coffin-Siris syndrome.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000225
A preliminary exome sequence in three patients with tardive dystonia
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000248
Modification of the association between paroxetine serum concentration and SERT-occupancy by ABCB1 (P-glycoprotein) polymorphisms in major depressive disorder
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000244
Clinical association to FKBP5 rs1360780 in patients with depression.
来源期刊:Psychiatric geneticsDOI:10.1097/YPG.0000000000000228
Does 5-HTTLPR moderate the effect of the quality of environmental context on maternal sensitivity? Testing the differential susceptibility hypothesis
来源期刊:Psychiatric GeneticsDOI:10.1097/YPG.0000000000000247

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