Bringing monogenic disease screening to the clinic.

doi:10.1038/s41591-020-1017-y

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

Community

Back to search

Article

Bringing monogenic disease screening to the clinic.

Nature medicine - 1 Aug 2020

Murray Michael F, Giovanni Monica A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to Genetic Diseases, Inborn
Share to Genetic Testing
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Risk Factors

Source

Open in PubMed

Identifiers

PMID: 32733075
DOI: 10.1038/s41591-020-1017-y

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bringing monogenic disease screening to the clinic.PMID 32733075Read ↗

Lessons from studying monogenic disease for common disease.Semantic proximity Read ↗

The Future of Genetics and Genomics: Closing the Phenotype Gap in Precision Medicine.Semantic proximity Read ↗

Genetics: An integrated genetic analysis of disease.Semantic proximity Read ↗

Prevention of genetic disorders.Semantic proximity Read ↗

Genetic studies: look no further than your own backyard.Semantic proximity Read ↗

Molecular genetics as the route to understanding, prevention, and treatment.Semantic proximity Read ↗

Realising the benefits of genetics for health.Semantic proximity Read ↗

Beyond genetic screening-functionality-based precision medicine in monogenic obesity.Semantic proximity Read ↗

Molecular approaches for screening of genetic diseases.Semantic proximity Read ↗

RETIRED: Use of preimplantation genetic testing for monogenic defects (PGT-M) for adult-onset conditions: an Ethics Committee opinionSemantic proximity Read ↗

Global burden of genetic disease and the role of genetic screeningSemantic proximity Read ↗

Prospects for genetic screening.Semantic proximity Read ↗

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