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Author/Creator Anttila, Verneri

1. Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. (May 2015)

Authors:
Nyholt, Dale R; Anttila, Verneri; Winsvold, Bendik S; Kurth, Tobias; Stefansson, Hreinn; Kallela, Mikko; Malik, Rainer; Vries, Boukje de; Terwindt, Gisela M; Ikram, M Arfan; Stam, Anine H; Ligthart, Lannie; Freilinger, Tobias; Alexander, Michael; Muller-Myhsok, Bertram; Schreiber, Stefan; Meiting...
Journal:
Cephalalgia
Issue:
Volume 35:Number 6(2015)
Page Start:
489
Record Type:
Journal Article
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4. Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. (June 2016)

Authors:
Zhao, Huiying; Eising, Else; de Vries, Boukje; Vijfhuizen, Lisanne S; Anttila, Verneri; Winsvold, Bendik S; Kurth, Tobias; Stefansson, Hreinn; Kallela, Mikko; Malik, Rainer; Stam, Anine H; Ikram, M Arfan; Ligthart, Lannie; Freilinger, Tobias; Alexander, Michael; Müller-Myhsok, Bertram; Schreiber,...
Journal:
Cephalalgia
Issue:
Volume 36:Number 7(2016)
Page Start:
648
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Genetic analysis for a shared biological basis between migraine and coronary artery disease. (June 2015)

Authors:
Winsvold, Bendik S.; Nelson, Christopher P.; Malik, Rainer; Gormley, Padhraig; Anttila, Verneri; Vander Heiden, Jason; Elliott, Katherine S.; Jacobsen, Line M.; Palta, Priit; Amin, Najaf; de Vries, Boukje; Hämäläinen, Eija; Freilinger, Tobias; Ikram, M. Arfan; Kessler, Thorsten; Koiranen, Markku;...
Journal:
Neurology
Issue:
Volume 1:Number 1(2015)
Page Start:
Record Type:
Journal Article
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6. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. Issue 9 (29th July 2017)

Authors:
Pérez-Palma, Eduardo; Helbig, Ingo; Klein, Karl Martin; Anttila, Verneri; Horn, Heiko; Reinthaler, Eva Maria; Gormley, Padhraig; Ganna, Andrea; Byrnes, Andrea; Pernhorst, Katharina; Toliat, Mohammad R; Saarentaus, Elmo; Howrigan, Daniel P; Hoffman, Per; Miquel, Juan Francisco; De Ferrari, Giancar...
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 9(2017)
Page Start:
598
Record Type:
Journal Article
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7. Involvement of astrocyte and oligodendrocyte gene sets in migraine. (June 2016)

Authors:
Eising, Else; de Leeuw, Christiaan; Min, Josine L; Anttila, Verneri; Verheijen, Mark HG; Terwindt, Gisela M; Dichgans, Martin; Freilinger, Tobias; Kubisch, Christian; Ferrari, Michel D; Smit, August B; de Vries, Boukje; Palotie, Aarno; van den Maagdenberg, Arn MJM; Posthuma, Danielle
Journal:
Cephalalgia
Issue:
Volume 36:Number 7(2016)
Page Start:
640
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. Issue 6 (12th June 2012)

Authors:
Kousi, Maria; Anttila, Verneri; Schulz, Angela; Calafato, Stella; Jakkula, Eveliina; Riesch, Erik; Myllykangas, Liisa; Kalimo, Hannu; Topçu, Meral; Gökben, Sarenur; Alehan, Fusun; Lemke, Johannes R; Alber, Michael; Palotie, Aarno; Kopra, Outi; Lehesjoki, Anna-Elina
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 6(2012)
Page Start:
391
Record Type:
Journal Article
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10. Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set. (June 2016)

Authors:
de Vries, Boukje; Anttila, Verneri; Freilinger, Tobias; Wessman, Maija; Kaunisto, Mari A; Kallela, Mikko; Artto, Ville; Vijfhuizen, Lisanne S; Göbel, Hartmut; Dichgans, Martin; Kubisch, Christian; Ferrari, Michel D; Palotie, Aarno; Terwindt, Gisela M; van den Maagdenberg, Arn MJM
Journal:
Cephalalgia
Issue:
Volume 36:Number 7(2016)
Page Start:
604
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗