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

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

1 Dec 2020

Abstract excerpt

BACKGROUND: The RecQ Like Helicase (RECQL) gene has previously been shown to predispose to breast cancer mainly in European populations, in particular to estrogen receptor (ER) and/or progesterone receptor (PR) positive tumor. Here, we investigated the contribution of pathogenic RECQL germline variants to hereditary breast cancer in early-onset and familial breast cancer patients from Pakistan. METHODS:...

Read the complete abstract on PubMed

Topics

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

Share to BRCA gene mutations in cancer
Share to Cancer-related Molecular Pathways
Share to DNA Repair Mechanisms

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

Source

Identifiers

PMID: 33342430
DOI: 10.1186/s13053-020-00159-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 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

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patientsPMID 33342430Read ↗

Germline RECQL mutations in high risk Chinese breast cancer patients.Semantic proximity Read ↗

Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer.Semantic proximity Read ↗

Germline RECQL mutations are associated with breast cancer susceptibility.Semantic proximity Read ↗

RECQL: a new breast cancer susceptibility gene.Semantic proximity Read ↗

Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.Semantic proximity Read ↗

RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibilitySemantic proximity Read ↗

Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe.Semantic proximity Read ↗

RecQ Helicase Somatic Alterations in CancerSemantic proximity Read ↗

FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine.Semantic proximity Read ↗

Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.Semantic proximity Read ↗

The spectrum of mutations predisposing to familial breast cancer in PolandSemantic proximity Read ↗

Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer.Semantic proximity Read ↗

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