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Familial analysis reveals rare risk variants for migraine in regulatory regions. / Techlo, Tanya Ramdal; Rasmussen, Andreas Høiberg; Moller, Peter L.; Bottcher, Morten; Winther, Simon; Davidsson, Olafur B.; Olofsson, Isa A.; Chalmer, Mona Ameri; Kogelman, Lisette J.A.; Nyegaard, Mette; Olesen, Jes; Hansen, Thomas Folkmann.
In:
Neurogenetics, Vol. 21, No. 3, 2020, p. 149-157.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Techlo, TR, Rasmussen, AH, Moller, PL, Bottcher, M, Winther, S, Davidsson, OB, Olofsson, IA, Chalmer, MA, Kogelman, LJA, Nyegaard, M
, Olesen, J & Hansen, TF 2020, '
Familial analysis reveals rare risk variants for migraine in regulatory regions',
Neurogenetics, vol. 21, no. 3, pp. 149-157.
https://doi.org/10.1007/s10048-020-00606-5APA
Techlo, T. R., Rasmussen, A. H., Moller, P. L., Bottcher, M., Winther, S., Davidsson, O. B., Olofsson, I. A., Chalmer, M. A., Kogelman, L. J. A., Nyegaard, M.
, Olesen, J., & Hansen, T. F. (2020).
Familial analysis reveals rare risk variants for migraine in regulatory regions.
Neurogenetics,
21(3), 149-157.
https://doi.org/10.1007/s10048-020-00606-5Vancouver
Techlo TR, Rasmussen AH, Moller PL, Bottcher M, Winther S, Davidsson OB et al.
Familial analysis reveals rare risk variants for migraine in regulatory regions.
Neurogenetics. 2020;21(3):149-157.
https://doi.org/10.1007/s10048-020-00606-5Author
Techlo, Tanya Ramdal ; Rasmussen, Andreas Høiberg ; Moller, Peter L. ; Bottcher, Morten ; Winther, Simon ; Davidsson, Olafur B. ; Olofsson, Isa A. ; Chalmer, Mona Ameri ; Kogelman, Lisette J.A. ; Nyegaard, Mette ; Olesen, Jes ; Hansen, Thomas Folkmann. / Familial analysis reveals rare risk variants for migraine in regulatory regions. In: Neurogenetics. 2020 ; Vol. 21, No. 3. pp. 149-157.
Bibtex
@article{fe58ab1749e44f60a70cb0468bca490a,
title = "Familial analysis reveals rare risk variants for migraine in regulatory regions",
keywords = "Genetics, Genome-wide, Rare-variant association analysis, Migraine, Gene regulation, Family study",
author = "Techlo, {Tanya Ramdal} and Rasmussen, {Andreas H{\o}iberg} and Moller, {Peter L.} and Morten Bottcher and Simon Winther and Davidsson, {Olafur B.} and Olofsson, {Isa A.} and Chalmer, {Mona Ameri} and Kogelman, {Lisette J.A.} and Mette Nyegaard and Jes Olesen and Hansen, {Thomas Folkmann}",
year = "2020",
doi = "10.1007/s10048-020-00606-5",
language = "English",
volume = "21",
pages = "149--157",
journal = "Neurogenetics",
issn = "1364-6745",
publisher = "Springer",
number = "3",
}
RIS
TY - JOUR
T1 - Familial analysis reveals rare risk variants for migraine in regulatory regions
AU - Techlo, Tanya Ramdal
AU - Rasmussen, Andreas Høiberg
AU - Moller, Peter L.
AU - Bottcher, Morten
AU - Winther, Simon
AU - Davidsson, Olafur B.
AU - Olofsson, Isa A.
AU - Chalmer, Mona Ameri
AU - Kogelman, Lisette J.A.
AU - Nyegaard, Mette
AU - Olesen, Jes
AU - Hansen, Thomas Folkmann
PY - 2020
Y1 - 2020
KW - Genetics
KW - Genome-wide
KW - Rare-variant association analysis
KW - Migraine
KW - Gene regulation
KW - Family study
U2 - 10.1007/s10048-020-00606-5
DO - 10.1007/s10048-020-00606-5
M3 - Journal article
C2 - 32076896
VL - 21
SP - 149
EP - 157
JO - Neurogenetics
JF - Neurogenetics
SN - 1364-6745
IS - 3
ER -
