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

Seven years since the launch of the Matchmaker Exchange: The evolution of genomic matchmaking.

Human mutation - 1 Jun 2022

Boycott Kym M, Azzariti Danielle R, Hamosh Ada, Rehm Heidi L

Abstract excerpt

The Matchmaker Exchange (MME) was launched in 2015 to provide a robust mechanism to discover novel disease-gene relationships. It operates as a federated network connecting databases holding relevant data using a common application programming interface, where two or more users are looking for a match for the same gene (two-sided matchmaking). Seven years from its launch, it is clear that the MME is making...

Read the complete abstract on PubMed

Topics

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

Share to Databases, Genetic
Share to Genetic Predisposition to Disease
Share to Genomics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Information Dissemination

Share to Phenotype

Share to Rare Diseases

Source

Open in PubMed Open full text

Identifiers

PMID: 35537081
DOI: 10.1002/humu.24373
PMCID: PMC9133175

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Seven years since the launch of the Matchmaker Exchange: The evolution of genomic matchmaking.PMID 35537081Read ↗

Seven years since the launch of the Matchmaker Exchange: the evolution of genomic matchmakingSemantic proximity Read ↗

Genomic Data Sharing for Novel Mendelian Disease Gene Discovery: The Matchmaker Exchange.Semantic proximity Read ↗

Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada.Semantic proximity Read ↗

The Matchmaker Exchange: a platform for rare disease gene discovery.Semantic proximity Read ↗

ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease researchSemantic proximity Read ↗

Matchmaker Exchange.Semantic proximity Read ↗

PhenomeCentral: 7 years of rare disease matchmakingSemantic proximity Read ↗

PhenomeCentral: 7 years of rare disease matchmaking.Semantic proximity Read ↗

Variant-level matching for diagnosis and discovery: Challenges and opportunities.Semantic proximity Read ↗

Variant-level Matching ToolsSemantic proximity Read ↗

The Matchmaker Exchange API: automating patient matching through the exchange of structured phenotypic and genotypic profiles.Semantic proximity Read ↗

One-Sided Matching Portal (OSMP): a tool to facilitate rare disease patient matchmakingSemantic proximity Read ↗

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