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Bryois, Julien, Skene, Nathan G ORCID: 0000-0002-6807-3180, Hansen, Thomas Folkmann
ORCID: 0000-0001-6703-7762, Kogelman, Lisette JA, Watson, Hunna J
ORCID: 0000-0001-8405-381X, Liu, Zijing
ORCID: 0000-0002-0189-7409, Eating Disorders Working Group of the Psychiatric Genomics Conso, , International Headache Genetics Consortium, , 23andMe Research Team, , Brueggeman, Leo et al (show 5 more authors)
(2020)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease.
Nature genetics, 52 (5).
pp. 482-493.
Winsvold, Bendik S ORCID: 0000-0003-4171-8919, Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig
ORCID: 0000-0002-8908-6968, Kurth, Tobias
ORCID: 0000-0001-7169-2620, Terwindt, Gisela M, Freilinger, Tobias M, Frei, Oleksander, Shadrin, Alexey et al (show 9 more authors)
(2017)
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.
PloS one, 12 (9).
e0185663-.
Guo, Yanjun, Rist, Pamela M, Daghlas, Iyas, Giulianini, Franco, International Headache Genetics Consortium, , 23andMe Research Team, , Kurth, Tobias and Chasman, Daniel I
(2020)
A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.
Nature communications, 11 (1).
3368-.