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

Complex traits, including migraine, often aggregate in families, but the underlying genetic architecture behind this is not well understood. The aggregation could be explained by rare, penetrant variants that segregate according to Mendelian inheritance or by the sufficient polygenic accumulation of common variants, each with an individually small effect, or a combination of the two hypotheses. In 8,319 individuals across 1,589 migraine families, we calculated migraine polygenic risk scores (PRS) and found a significantly higher common variant burden in familial cases (n = 5,317, OR = 1.76, 95... Mehr ...

Verfasser: Boomsma, D.I.
Ligthart, L.
Posthuma, Danielle
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Reihe/Periodikum: Boomsma , D I , Ligthart , L , Posthuma , D & 23Andme Research Team 2018 , ' Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families ' , Neuron , vol. 98 , no. 4 , pp. 743-753.e4 . https://doi.org/10.1016/j.neuron.2018.04.014
Schlagwörter: disease aggregation / familial aggregation / families / genome-wide association study / GWAS / hemiplegic migraine / migraine / migraine with aura / polygenic risk score / PRS / /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_ / name=Netherlands Twin Register (NTR) / /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being / name=SDG 3 - Good Health and Well-being
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27620927
Datenquelle: BASE; Originalkatalog
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Link(s) : https://research.vu.nl/en/publications/ae1b30d7-cd0b-4b89-aa58-926f90855e72