HUMAN HEREDITY 期刊简介
Gathering original research reports and short communications from all over the world, 'Human Heredity' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all 'Human Heredity' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
“人类遗传” 收集了来自世界各地的原始研究报告和简短交流,致力于人类种群遗传学,关联和连锁分析,疾病遗传机制以及统计遗传学新方法的方法学和应用研究,例如,稀有变体的分析和下一代测序的结果。该杂志在从免疫学和血液学到流行病学和公共卫生规划等领域的引用次数表明了该信息对许多医学分支的价值,而且,至少有50% 的 “人类遗传” 论文在发表后超过8年仍被引用 (根据ISI期刊引文报告)。关于方法学主题的特殊问题 (例如 “血缘关系和基因组学” 2014年; “分析复杂疾病中的罕见变异” 2012年) 或对特定领域进展的评论 (“欧洲人口的遗传多样性: 进化证据和医学意义” 2014年; “肥胖中的基因和环境” 2013年) 每年出版。邀请该领域的著名专家为这些特殊问题做出贡献。
期刊ISSN
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0001-5652 |
影响指数
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0.44 |
最新CiteScore值
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1.70 查看CiteScore评价数据 |
最新自引率
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0.00% |
官方指定润色网址
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https://www.deeredit.com/?type=ss1 |
投稿语言要求
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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
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KARGER, ALLSCHWILERSTRASSE 10, BASEL, SWITZERLAND, CH-4009 |
偏重的研究方向(学科)
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生物-遗传学 |
出版周期
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Bimonthly |
出版年份
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1969 |
出版国家/地区
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SWITZERLAND |
是否OA
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No |
SCI期刊coverage
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Science Citation Index Expanded(科学引文索引扩展) |
NCBI查询
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PubMed Central (PMC)链接 全文检索(pubmed central) |
最新中科院JCR分区
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大类(学科)
小类(学科)
综述期刊
生物
GENETICS & HEREDITY(遗传学)4区
否
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最新的影响因子
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0.44 | |||||
最新公布的期刊年发文量 |
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总被引频次 | 58 | |||||
影响因子趋势图 |
近年的影响因子趋势图(整体平稳趋势)
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2022年预警名单预测最新
最新CiteScore值
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1.70
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年文章数 | 13 | ||||||||||||||
SJR
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0.423 | ||||||||||||||
SNIP
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0.407 | ||||||||||||||
CiteScore排名
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CiteScore趋势图 |
CiteScore趋势图
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本刊同领域相关期刊
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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
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期刊名称 | IF值 |
SILVAE GENETICA | 0.787 |
BMC Medical Genetics | 2.082 |
CURRENT GENE THERAPY | 4.347 |
CLINICAL DYSMORPHOLOGY | 0.808 |
Balkan Journal of Medical Genetics | 0.514 |
European Journal of Medical Genetics | 2.681 |
Genes & Genomics | 1.821 |
BIOCHEMICAL GENETICS | 1.871 |
GENES & GENETIC SYSTEMS | 1.502 |
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