HUMAN GENETICS Q1区

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》是一份月刊，出版关于人类遗传学各个方面的原创和及时的文章。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，形态异常学，ELSI领域的文章（伦理、法律的和社会问题）、进化遗传学、基因表达、基因结构和组织、复杂疾病遗传学和上位性相互作用、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、分子诊断学、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。优先考虑那些解决临床相关问题或对人类生物学有新见解的文章，除非报道了某个主题的全新和不寻常的方面，临床病例报告、细胞遗传学病例报告、描述性群体遗传学的文章、涉及多态性频率或基因内额外突变的文章（其中已描述了许多病变）、报告对以前发表的数据集进行荟萃分析的论文通常不予接受。期刊一般不考虑发表仅报告未知功能基因的分离、图谱位置、结构和组织表达谱的稿件，除非该基因是特别感兴趣的基因或与人类特征或疾病有关的候选基因。

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