HUMAN GENETICS 期刊简介
Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology.
Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted.
The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
人类遗传学是月刊,发表有关人类遗传学各个方面的原始和及时的文章。该杂志特别欢迎在行为遗传学,生物信息学,癌症遗传学和基因组学,细胞遗传学,发育遗传学,疾病关联研究,畸形学,ELSI (伦理,法律和社会问题),进化遗传学,基因表达,基因结构和组织,复杂疾病的遗传学和上位相互作用,遗传流行病学,基因组生物学,基因组结构和组织,基因型-表型关系,人类基因组学,免疫遗传学和基因组学,连锁分析和遗传作图,统计遗传学方法,分子诊断,突变检测和分析,神经遗传学,物理作图和群体遗传学。也欢迎报道与人类生物学或疾病相关的动物模型的文章。将优先考虑那些解决临床相关问题或提供人类生物学新见解的文章。
除非报告一个主题的完全新颖和不寻常的方面,临床病例报告,细胞遗传学病例报告,描述性群体遗传学论文,关于基因内多态性或额外突变频率的文章,其中许多损伤已经被描述,而报告先前发表的数据集的元分析的论文通常不会被接受。
该期刊通常不会考虑仅报告隔离的出版手稿,定位功能未知的基因的位置,结构和组织表达谱,除非该基因特别感兴趣或是涉及人类性状或疾病的候选基因。
期刊ISSN
|
0340-6717 |
影响指数
|
4.091 |
最新CiteScore值
|
9.50 查看CiteScore评价数据 |
最新自引率
|
3.50% |
官方指定润色网址
|
https://www.deeredit.com/?type=ss1 |
投稿语言要求
|
Improve the quality of the paper, eliminate grammar and spelling errors, increase readability, ensure accurate communication of viewpoints, enhance academic reputation, and increase the chances of the paper being accepted. 建议点击这个网址:https://www.deeredit.com/?type=ss2,资深审稿专家为您评估稿件质量,提供针对性改进建议,最终可助您极大提升目标期刊录用率 |
期刊官方网址
hot |
https://www.peipusci.com/?type=9 |
杂志社征稿网址
hot |
https://www.peipusci.com/?type=10 |
通讯地址
|
SPRINGER, 233 SPRING ST, NEW YORK, USA, NY, 10013 |
偏重的研究方向(学科)
|
生物-遗传学 |
出版周期
|
Monthly |
出版年份
|
1964 |
出版国家/地区
|
UNITED STATES |
是否OA
|
No |
SCI期刊coverage
|
Science Citation Index Expanded(科学引文索引扩展) |
NCBI查询
|
PubMed Central (PMC)链接 全文检索(pubmed central) |
最新中科院JCR分区
|
大类(学科)
小类(学科)
综述期刊
生物
GENETICS & HEREDITY(遗传学)2区
否
|
|||||
最新的影响因子
|
4.091 | |||||
最新公布的期刊年发文量 |
|
|||||
总被引频次 | 126 | |||||
影响因子趋势图 |
近年的影响因子趋势图(整体平稳趋势)
|
2022年预警名单预测最新
最新CiteScore值
|
9.50
|
||||||||||||||
年文章数 | 156 | ||||||||||||||
SJR
|
2.351 | ||||||||||||||
SNIP
|
1.869 | ||||||||||||||
CiteScore排名
|
|
||||||||||||||
CiteScore趋势图 |
CiteScore趋势图
|
本刊同领域相关期刊
|
|
期刊名称 | IF值 |
SILVAE GENETICA | 0.787 |
Biology of Sex Differences | 4.977 |
Circulation-Cardiovascular Genetics | 4.264 |
HUMAN MUTATION | 4.829 |
Human Genomics | 4.593 |
CLINICAL GENETICS | 4.394 |
BMC Medical Genetics | 2.082 |
BMC Medical Genomics | 3.032 |
CURRENT GENE THERAPY | 4.347 |
本刊同分区等级的相关期刊
|
|
期刊名称 | IF值 |
HUMAN MUTATION | 4.829 |
CLINICAL GENETICS | 4.394 |
JOURNAL OF MEDICAL GENETICS | 6.255 |
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS | 3.869 |
Epigenetics | 4.483 |
HUMAN MOLECULAR GENETICS | 6.089 |
MOLECULAR PHYLOGENETICS AND EVOLUTION | 4.243 |
GENOMICS | 5.679 |
GENETICS | 4.516 |
分享者 | 点评内容 |