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

The simplest explanation does not have to be preferred: co-occurrence of pathogenic variants in cancer-predisposing genes.

European journal of human genetics : EJHG - 1 Mar 2022

Castellví-Bel Sergi

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 Alleles
Share to BRCA2 Protein
Share to Germ-Line Mutation
Share to Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 34983941
DOI: 10.1038/s41431-021-01031-4
PMCID: PMC8904836

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The simplest explanation does not have to be preferred: co-occurrence of pathogenic variants in cancer-predisposing genes.PMID 34983941Read ↗

Gene-Specific Cancer Patterns Among Pathogenic Germline Variant CarriersSemantic proximity Read ↗

Common susceptibility genes for cancer: search for the end of the rainbow.Semantic proximity Read ↗

Expanding cancer predisposition genes with ultra-rare cancer-exclusive human variationsSemantic proximity Read ↗

Expanding cancer predisposition genes with ultra-rare cancer-exclusive human variations.Semantic proximity Read ↗

Cancer-predisposing germline variants and subsequent cancer risk.Semantic proximity Read ↗

CoMutDB: the landscape of somatic mutation co-occurrence in cancers.Semantic proximity Read ↗

eTumorRisk, an algorithm predicts cancer risk based on comutated gene networks in an individual’s germline genomeSemantic proximity Read ↗

Unbiased co-occurring mutational landscapes in tumorigenesisSemantic proximity Read ↗

Using common variants to indicate cancer genes.Semantic proximity Read ↗

The predominance of the environment over genes in cancer causation: implications for genetic epidemiology.Semantic proximity Read ↗

Comparative study and meta-analysis of meta-analysis studies for the correlation of genomic markers with early cancer detection.Semantic proximity Read ↗

A growing network of cancer-susceptibility genes.Semantic proximity Read ↗

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