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Markus Färkkilä
Observed names:
Farkkila, M.,
M Farkkila,
M. Farkkila,
M. Färkkilä,
M. Färkkilä
Observed institutions:
University of Helsinki,
Helsinki University Hospital
OpenAlex ID:
A5110164701
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
2010
·
Verneri Anttila
, M Stella Calafato
, et al.
·
Nature Genetics
·
400
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
2004
·
M. A. Kaunisto
, H. Harno
, et al.
·
Neurogenetics
·
65
The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families
2018
·
Marjo Eveliina Hiekkala
, Pietari Vuola
, et al.
·
Cephalalgia
·
48
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity
2023
·
Mark K. Bakker
, Jos P. Kanning
, et al.
·
Stroke
·
31
PDF
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (vol 98, pg 743, 2018)
2018
·
Gormley, P.
, Kurki, M.I.
, et al.
·
Leiden Repository (Leiden University)
·
20
Survey of Guillain-Barré Syndrome in Southern Finland
1991
·
Markus Färkkilä
, Esko Kinnunen
, et al.
·
Neuroepidemiology
·
19
Decreased cerebellar total creatine in episodic ataxia type 2: A 1 H MRS study
2005
·
H. Harno
, S. Heikkinen
, et al.
·
Neurology
·
17
Health-related quality of life in secondary progressive multiple sclerosis
2007
·
A.G Beiske
, H Naess
, et al.
·
Multiple Sclerosis Journal
·
6
Short Communications
2006
·
Beiske, A. G.
, Naess, H.
, et al.
·
European Journal of Neurology
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Works count:
11
Citation count:
606
H-index:
7
I10-index:
7
Year
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