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 (933)

Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models.

Spatially resolved multi-omics of human metabolic dysfunction-associated steatotic liver disease

人类代谢功能障碍相关脂肪肝疾病的空间分辨多组学研究

Uniform dynamics of cohesin-mediated loop extrusion in living human cells

活体人类细胞中黏连蛋白介导的环挤出的均匀动力学

Characterization of induced cohesin loop extrusion trajectories in living cells

活细胞中诱导的内聚蛋白环挤出轨迹的表征

Targeting histone H2B acetylated enhanceosomes via p300/CBP degradation in prostate cancer

通过p300/CBP降解靶向组蛋白H2B乙酰化增强子在前列腺癌中的应用

Detecting and quantifying clonal selection in somatic stem cells

检测和量化体细胞干细胞中的克隆选择

The long-term effects of chemotherapy on normal blood cells

化疗对正常血细胞的长期影响

DNA methylation cooperates with genomic alterations during non-small cell lung cancer evolution

DNA甲基化与基因组改变在非小细胞肺癌的演变过程中协同作用

Tracing the evolution of single-cell 3D genomes in Kras-driven cancers

追踪Kras驱动癌症中单细胞3D基因组的演变

Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery

近乎完整的中东基因组有助于更精确地确定纯合性，并增强致病变异和人群特异性变异的发现。