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

DNA variations in human and medical genetics: 25 years of my experience.

Journal of human genetics - 1 Jan 2009

Nakamura Yusuke

Abstract excerpt

DNA variations have contributed enormously to the fields of medical and forensic science, especially through their use in studies on genes responsible or susceptible to various diseases and those on screening of chromosomal abnormalities in tumors. The types of genetic variations used in these studies have changed in the past 25 years and can be classified into five major classes: RFLP (restriction fragment...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to DNA
Share to Genetic Variation

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

Share to Genetics, Medical

Share to Genome-Wide Association Study

Share to Pharmacogenetics

Source

Identifiers

PMID: 19158818
DOI: 10.1038/jhg.2008.6

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

DNA variations in human and medical genetics: 25 years of my experience.PMID 19158818Read ↗

Role of genetic variability in Mendelian and multifactorial diseases.Semantic proximity Read ↗

[DNA polymorphisms].Semantic proximity Read ↗

The discovery of human genetic variations and their use as disease markers: past, present and future.Semantic proximity Read ↗

Genetic variation analysis for biomedical researchers: a primer.Semantic proximity Read ↗

A brief history of human disease genetics.Semantic proximity Read ↗

Genetic variations in medical research in the past, at present and in the future.Semantic proximity Read ↗

[Clinical significance and strategies to analyze genetic polymorphisms].Semantic proximity Read ↗

A brief history of genetic variation analysis.Semantic proximity Read ↗

[Structural variation in the human genome].Semantic proximity Read ↗

Polymorphic sequence variants in medicine: a challenge and an opportunity.Semantic proximity Read ↗

Implications of gene copy-number variation in health and diseases.Semantic proximity Read ↗

Genetic polymorphisms and implications for human diseases.Semantic proximity Read ↗

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