B. Vries

发表

Molecular genetics of migraine

M. Ferrari, R. Frants, B. D. Vries, 2009, Human Genetics.

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

D. Strachan, H. Stefánsson, K. Stefánsson, 2015, Cephalalgia : an international journal of headache.

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Thomas Meitinger, Martin Dichgans, Bertram Müller-Myhsok, 2012, Nature Genetics.

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

Wolfgang Hoffmann, Henry Völzke, Boukje de Vries, 2011, Nature Genetics.

Genome-wide association study of migraine implicates a common susceptibility variant on 8 q 22 . 1

A. Hofman, A. Uitterlinden, M. Daly, 2010 .

A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood

M. Ferrari, J. Duncan, H. Scheffer, 2015, Cephalalgia : an international journal of headache.

First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine

M. Ferrari, R. Frants, G. Terwindt, 2007, European Journal of Human Genetics.

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

B. D. Vries, B. Vries, 2020 .

Genome-wide association study for migraine in a Dutch genetic isolate and meta-analysis with other population-based cohorts

A. Hofman, M. Ferrari, F. Zitman, 2011 .

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies

N. Ramadan, M. Ferrari, M. Dichgans, 2007, Human mutation.

Noradrenergic and Cholinergic Modulation of Belief Updating

Sander Nieuwenhuis, Peter R. Murphy, Marieke Jepma, 2018, Journal of Cognitive Neuroscience.

A high-density association screen of 155 ion transport genes for involvement with common migraine.

M. Daly, L. Peltonen, D. Cox, 2008, Human molecular genetics.

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

François Dubeau, Frederick Andermann, Samuel F. Berkovic, 2013, Nature Genetics.

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

M. Ferrari, M. Dichgans, R. Frants, 2007, Neurology.

Familial hemiplegic migraine treated by sodium valproate and lamotrigine

M. Ferrari, G. Terwindt, A. M. van den Maagdenberg, 2014, Cephalalgia : an international journal of headache.

RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice

Stephany C. Koelewijn, M. Ferrari, J. Boer, 2014, Cephalalgia : an international journal of headache.

Alternating Hemiplegia of Childhood: No Mutations in the Glutamate Transporter EAAT1

M. Ferrari, H. Stroink, B. de Vries, 2006, Neuropediatrics.

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Thomas Meitinger, Michael Inouye, Martin Dichgans, 2010, Nature Genetics.

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

H. Stefánsson, K. Stefánsson, D. Chasman, 2016, Cephalalgia : an international journal of headache.

HLA-DR 2 and IKBL + 738 ( C ) in Dutch Ulcerative Colitis Patients

B. D. Vries, B. Vries, 2003 .

Shared genetic factors in migraine and depression

M. Ferrari, A. Janssens, C. V. van Duijn, 2010, Neurology.

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

Stephany C. Koelewijn, A. Hofman, A. Uitterlinden, 2011, European Journal of Human Genetics.

Identifying a gene expression signature of cluster headache in blood

M. Ferrari, P. ’. ‘t Hoen, G. Terwindt, 2017, Scientific Reports.

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

I. Scheffer, J. Gécz, F. Dubeau, 2013, Nature Genetics.

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups

H. Stefánsson, K. Stefánsson, D. Chasman, 2016, Cephalalgia : an international journal of headache.

Candidate-gene association study searching for genetic factors involved in migraine chronification

A. Palotie, J. Montaner, J. Álvarez-Sabín, 2015, Cephalalgia : an international journal of headache.

RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice

Stephany C. Koelewijn, M. Ferrari, J. Boer, 2014, Cephalalgia.

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

Sjoerd M. H. Huisman, D. Strachan, K. Stefánsson, 2016, Human Genetics.

Heterozygous TREX1 mutations in early-onset cerebrovascular disease

M. Ferrari, G. Terwindt, N. Pelzer, 2013, Journal of Neurology.