Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

11 citing papers in PubMed.

1. Astrocytic Glutamate Transporters and Migraine.Neurochemical research · 2023
   Review
2. Migraine and major depression: localizing shared genetic susceptibility in different cell types of the nervous systems.Frontiers in neurology · 2023
   Article
3. An accurate prediction model of digenic interaction for estimating pathogenic gene pairs of human diseases.Computational and structural biotechnology journal · 2022
   Article
4. Evidence that blood-CSF barrier transport, but not inflammatory biomarkers, change in migraine, while CSF sVCAM1 associates with migraine frequency and CSF fibrinogen.Headache · 2021
   Article
5. Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia.iScience · 2020
   Article
6. Functional gene networks reveal distinct mechanisms segregating in migraine families.Brain : a journal of neurology · 2020
   Article
7. Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.Journal of medical genetics · 2020
   Article
8. Discovery and validation of biomarkers to aid the development of safe and effective pain therapeutics: challenges and opportunities.Nature reviews. Neurology · 2020
   Review
9. Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies.PLoS genetics · 2019
   Article
10. Animal models of migraine and experimental techniques used to examine trigeminal sensory processing.The journal of headache and pain · 2019
    Review
11. Family Clustering of Autoimmune Vitiligo Results Principally from Polygenic Inheritance of Common Risk Alleles.American journal of human genetics · 2019
    Article

Corrections and comments

• Erratum for
  Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.2018

Authors and funding

41 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.