B. de Vries

发表

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.

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.

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

David B. Goldstein, Bertrand Fontaine, Stephany C. Koelewijn, 2012, Nature Genetics.

From migraine genes to mechanisms

M. Ferrari, G. Terwindt, B. de Vries, 2015, Pain.

Shared genetic basis for migraine and ischemic stroke

C. Sudlow, M. Fornage, A. Reiner, 2015, Neurology.

Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine

Sjoerd M. H. Huisman, M. Ferrari, M. Reinders, 2016, Molecular Neurobiology.

PRRT2 mutation causes benign familial infantile convulsions

Stephany C. Koelewijn, B. de Vries, A. M. van den Maagdenberg, 2012, Neurology.

First Mutation in the Voltage-Gated Nav1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy

M. Ferrari, B. de Vries, C. Lemos, 2009, Cephalalgia : an international journal of headache.

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.

Two novel SCN1A mutations identified in families with familial hemiplegic migraine

Stephany C. Koelewijn, M. Ferrari, G. Terwindt, 2014, Cephalalgia : an international journal of headache.

A long-term follow-up study of 18 patients with sporadic hemiplegic migraine

M. Ferrari, R. Frants, G. Terwindt, 2011, Cephalalgia : an international journal of headache.

CACNA1A Mutation Linking Hemiplegic Migraine and Alternating Hemiplegia of Childhood

M. Ferrari, H. Lauffer, B. de Vries, 2008, Cephalalgia : an international journal of headache.

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

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

Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses

Harish Dharuri, Cornelia M. van Duijn, Aswin Verhoeven, 2015, PLoS genetics.

Genetic analysis for a shared biological basis between migraine and coronary artery disease

M. Jarvelin, T. Assimes, T. Lehtimäki, 2015, Neurology: Genetics.

Pearls and pitfalls in genetic studies of migraine

M. Ferrari, G. Terwindt, E. Eising, 2013, Cephalalgia : an international journal of headache.

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Thomas Meitinger, Dorret I. Boomsma, M. Arfan Ikram, 2013, Nature Genetics.

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

I. Scheffer, D. Goldstein, S. Sisodiya, 2015, Orphanet Journal of Rare Diseases.

Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation

Stephany C. Koelewijn, M. Ferrari, G. Terwindt, 2018, Neurology.

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

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

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.

δ-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy

Stephany C. Koelewijn, M. Tijssen, A. Groffen, 2017, Neurology.

Selected Confirmed, Probable, and Exploratory Migraine Biomarkers

E. Loder, M. Harrington, B. de Vries, 2006, Headache.

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set

A. Palotie, M. Dichgans, V. Anttila, 2016, Cephalalgia : an international journal of headache.

Genetic Biomarkers for Migraine

R. Frants, B. de Vries, A. M. van den Maagdenberg, 2006, Headache.

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.

R. Baloh, M. Ferrari, R. Frants, 2009, Archives of neurology.

PRRT2 and hemiplegic migraine: A complex association

M. Ferrari, G. Terwindt, L. Vijfhuizen, 2014, Neurology.

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

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

Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis

Stephany C. Koelewijn, J. Houwing-Duistermaat, M. Ferrari, 2015, Cephalalgia : an international journal of headache.

Shared genetic factors in migraine and depression

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

Migraine Genes and the Relation to Gender

B. de Vries, A. M. van den Maagdenberg, R. Shyti, 2011, Headache.

B. de Vries, P. Koehler, J. Haan, 2011, Cephalalgia : an international journal of headache.

Involvement of astrocyte and oligodendrocyte gene sets in migraine

M. Ferrari, A. Palotie, D. Posthuma, 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.

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

Martin Dichgans, Michael Pusch, Lisa Norris, 2007, Human mutation.