Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Research advances on medical genetics in China in 2015].

Yi chuan = Hereditas - 1 May 2016

Li Yuan-feng, Han Yubo, Cao Peng-bo, Meng Jin-feng, Li Hai-bei, Qin Geng, Zhang Feng, Jin Guang-fu, Yang Yong, Wu Ling-qian, Ping Jie, Zhou Gang-qiao

Abstract excerpt

Steady progress has been achieved in the medical genetics in China in 2015, as numerous original researches were published in the world's leading journals. Chinese scientists have made significant contributions to various fields of medical genetics, such as pathogenicity of rare diseases, predisposition of common diseases, somatic mutations of cancer, new technologies and methods, disease-related microRNAs...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA Methylation
Share to Evolution, Molecular

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genetics, Medical

Share to MicroRNAs

Share to Mutation

Share to Neoplasms

Share to Rare Diseases

Source

Identifiers

PMID: 27232486
DOI: 10.16288/j.yczz.16-174

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Research advances on medical genetics in China in 2015].PMID 27232486Read ↗

[The importance of establishing genotype and phenotype database of Chinese population for accurate diagnosis of genetic diseases].Semantic proximity Read ↗

Analysis of phenotype-genotype connection: the story of dissecting disease pathogenesis in genomic era in China, and beyond.Semantic proximity Read ↗

Chinese geneticists across the Pacific: a century of scientific legacies in genetics and genomicsSemantic proximity Read ↗

Genetic variations associated with long noncoding RNAs.Semantic proximity Read ↗

Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individualsSemantic proximity Read ↗

lncRNASNP v3: an updated database for functional variants in long non-coding RNAs.Semantic proximity Read ↗

[Important role of single nucleotide polymorphisms in the study of complex diseases].Semantic proximity Read ↗

Comprehensive expanded carrier screening using next-generation sequencing in Southern Chinese couplesSemantic proximity Read ↗

NCAD v1.0: a database for non-coding variant annotation and interpretation.Semantic proximity Read ↗

[Advance of the research for disease-responsible genes].Semantic proximity Read ↗

Pathogenic variation distribution of ACMG 3.2 list genes in 11 ethnic groups in southwest China.Semantic proximity Read ↗

Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.