Nature Genetics

期刊全称

Nature Genetics

期刊缩写

Nat. Genet.

涉及主题

生物遗传学化学生物化学基因医学内科学计算生物学进化生物学细胞生物学病理

期刊介绍

Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution -Nature Genetics

Nature Genetics

JCR学科分类

JCI学科分类

期刊相关文献 (2682)

Multi-ancestry genome-wide association and integrated multi-omics analyses of endometriosis and its clinical manifestations

子宫内膜异位症及其临床表现的多族裔全基因组关联分析和整合多组学分析

Interpretable, flexible and spatially aware integration of multiple spatial transcriptomics datasets from diverse sources

可解释、灵活且具有空间感知能力的整合来自不同来源的多个空间转录组学数据集

Pangenomic analyses of rose uncover widespread structure variation and empower genomics-directed breeding

对玫瑰进行泛基因组分析揭示了广泛的结构变异，并为基因组指导的育种提供了支持。

Somatic mosaicism in ALS and FTD identifies focal mutations associated with widespread degeneration

肌萎缩侧索硬化症 (ALS) 和额颞叶痴呆 (FTD) 中的体细胞嵌合现象可识别与广泛退行性变相关的局灶性突变。

Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction

多祖源全基因组关联分析有助于发现屈光不正的遗传特征并进行多基因预测

Systematic design of combination therapy by targeting master regulators of coexisting diffuse midline glioma cell states

通过靶向共存的弥漫性中线胶质瘤细胞状态的主调控因子，系统地设计联合疗法

Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome

基因组分析表明，激素和代谢紊乱与多囊卵巢综合征有关。

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder

出版商更正：RNU2-2基因的双等位基因变异会导致最常见的已知隐性神经发育障碍

Genetic association and machine learning improve the prediction of type 1 diabetes risk

基因关联和机器学习提高了对1型糖尿病风险的预测能力。

Transposable elements shape stemness in normal and leukemic hematopoiesis

转座因子在正常和白血病造血过程中塑造干细胞特性