Genetic variation in CXCR4 and risk of chronic lymphocytic leukemia.

doi:10.1182/blood-2009-07-235184

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

Genetic variation in CXCR4 and risk of chronic lymphocytic leukemia.

Blood - 26 Nov 2009

Crowther-Swanepoel Dalemari, Qureshi Mobshra, Dyer Martin J S, Matutes Estella, Dearden Claire, Catovsky Daniel, Houlston Richard S

Abstract excerpt

A genome-wide linkage scan has provided evidence for a chronic lymphocytic leukemia (CLL) susceptibility locus at 2q21 to which the chemokine receptor CXCR4 gene maps. Recent data provide some evidence for common variation in CXCR4 according to the polymorphic variant rs2228014 defining CLL risk. To examine the role of genetic variation in CXCR4 on CLL risk, we screened 188 familial CLL cases and 213 controls for...

Read the complete abstract on PubMed

Topics

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

Share to Codon, Nonsense

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Gene Frequency

Share to Germ-Line Mutation

Share to Leukemia, Lymphocytic, Chronic, B-Cell

Share to Mutation, Missense

Share to Receptors, CXCR4

Share to Risk

Source

Open in PubMed

Identifiers

PMID: 19812382
DOI: 10.1182/blood-2009-07-235184

Genes

CXCR4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Genetic variation in CXCR4 and risk of chronic lymphocytic leukemia.PMID 19812382Read ↗

Genetic susceptibility variants for chronic lymphocytic leukemia.Semantic proximity Read ↗

CXCR5 polymorphisms in non-Hodgkin lymphoma risk and prognosis.Semantic proximity Read ↗

Genetic variation and risk of chronic lymphocytic leukaemia.Semantic proximity Read ↗

Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.Semantic proximity Read ↗

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.Semantic proximity Read ↗

Candidate gene association studies and risk of chronic lymphocytic leukemia: a systematic review and meta-analysis.Semantic proximity Read ↗

Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk.Semantic proximity Read ↗

A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.Semantic proximity Read ↗

Genetic susceptibility to chronic lymphocytic leukemia.Semantic proximity Read ↗

Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia.Semantic proximity Read ↗

Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.Semantic proximity Read ↗

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.Semantic proximity Read ↗

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