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

Evidence of a genetic background predisposing to complex regional pain syndrome type 1.

Journal of medical genetics - 19 Jan 2024

Shaikh Samiha S, Goebel Andreas, Lee Michael C, Nahorski Michael S, Shenker Nicholas, Pamela Yunisa, Drissi Ichrak, Brown Christopher, Ison Gillian, Shaikh Maliha F, Kuttikat Anoop, Woods William A, Dixit Abhishek, Stouffer Kaitlin, Clarke Murray Ch, Menon David K, Woods C Geoffrey

Abstract excerpt

BACKGROUND: Complex regional pain syndrome type 1 (CRPS-1) is a rare, disabling and sometimes chronic disorder usually arising after a trauma. This exploratory study examined whether patients with chronic CRPS-1 have a different genetic profile compared with those who do not have the condition. METHODS: Exome sequencing was performed to seek altered non-synonymous SNP allele frequencies in a discovery cohort of...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Fibromyalgia and Chronic Fatigue Syndrome Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genetic Background

Share to Pain Mechanisms and Treatments

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 37816627
DOI: 10.1136/jmg-2023-109236
PMCID: PMC10850724

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evidence of a genetic background predisposing to complex regional pain syndrome type 1.PMID 37816627Read ↗

Genetic and epigenetic epidemiology of chronic widespread painSemantic proximity Read ↗

The phenotypic and genetic signatures of common musculoskeletal pain conditions.Semantic proximity Read ↗

Human pain and genetics: some basicsSemantic proximity Read ↗

Rare variant association studies: Significance, methods, and applications in chronic pain studies.Semantic proximity Read ↗

Rare variant associations of chronic pain conditions in the UK Biobank Whole Exome SequencingSemantic proximity Read ↗

Genetic predictors of human chronic pain conditions.Semantic proximity Read ↗

P2RX7 gene variants associate with altered inflammasome assembly and reduced pyroptosis in chronic nonbacterial osteomyelitis (CNO)Semantic proximity Read ↗

Rare variant analyses in large-scale cohorts identified SLC13A1 associated with chronic pain.Semantic proximity Read ↗

Investigating genotype–phenotype relationship of extreme neuropathic pain disorders in a UK national cohortSemantic proximity Read ↗

Analysis of Common Single Nucleotide Polymorphisms in Complex Regional Pain Syndrome: Genome Wide Association Study Approach and Pooled DNA Strategy.Semantic proximity Read ↗

Identification of Two Biological Subgroups of Complex Regional Pain Syndrome Type 1 by Transcriptomic Profiling of Skin and BloodSemantic proximity Read ↗

Genome-Wide Association Study Identifies Novel Genetic Variants Associated with Widespread Pain in the UK Biobank (N=172,230)Semantic proximity Read ↗

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