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

Familial analysis reveals rare risk variants for migraine in regulatory regions.

Neurogenetics - 1 Jul 2020

Techlo Tanya Ramdal, Rasmussen Andreas Høiberg, Møller Peter L, Bøttcher Morten, Winther Simon, Davidsson Olafur B, Olofsson Isa A, Chalmer Mona Ameri, Kogelman Lisette J A, Nyegaard Mette, Olesen Jes, Hansen Thomas Folkmann

Abstract excerpt

The most recent genome-wide association study of migraine increased the total number of known migraine risk loci to 38. Still, most of the heritability of migraine remains unexplained, and it has been suggested that rare gene dysregulatory variants play an important role in migraine etiology. Addressing the missing heritability of migraine, we aim to fine-map signals from the known migraine risk loci to...

Read the complete abstract on PubMed

Topics

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

Share to Cohort Studies
Share to CpG Islands

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Migraine Disorders

Share to Quantitative Trait Loci

Share to Regulatory Sequences, Nucleic Acid

Share to Whole Genome Sequencing

Source

Open in PubMed Open full text

Identifiers

PMID: 32076896
DOI: 10.1007/s10048-020-00606-5
PMCID: PMC7283211

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial analysis reveals rare risk variants for migraine in regulatory regions.PMID 32076896Read ↗

Rare risk variants associate with epigenetic dysregulation in migraineSemantic proximity Read ↗

Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine.Semantic proximity Read ↗

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.Semantic proximity Read ↗

Genetics of migraine.Semantic proximity Read ↗

Migraine genetics: Status and road forward.Semantic proximity Read ↗

A review of migraine genetics: gathering genomic and transcriptomic factors.Semantic proximity Read ↗

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraineSemantic proximity Read ↗

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.Semantic proximity Read ↗

Genome-wide association studies in migraine: current state and route to follow.Semantic proximity Read ↗

Cell-type-specific gene regulation in migraine and its subtypes links genetic risk to brain structure.Semantic proximity Read ↗

Unveiling migraine subtype heterogeneity and risk loci: integrated genome-wide association study and single-cell transcriptomics discoverySemantic proximity Read ↗

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.Semantic proximity Read ↗

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