Works matching AU Vries, Boukje de

Results: 34

Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.

Published in:

2009

By:

de Vries, Boukje;
Stam, Anine H.;
Kirkpatrick, Martin;
Vanmolkot, Kaate R.J.;
Koenderink, Jan B.;
van den Heuvel, Jeroen J.M.W.;
Stunnenberg, Bas;
Goudie, David;
Shetty, Jay;
Jain, Vivek;
van Vark, Judith;
Terwindt, Gisela M.;
Frants, Rune R.;
Haan, Joost;
van den Maagdenberg, Arn M.J.M.;
Ferrari, Michel D.

Publication type:

Letter

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

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 8, p. 901, doi. 10.1038/ejhg.2011.48

By:

Ligthart, Lannie;
de Vries, Boukje;
Smith, Albert V.;
Ikram, M. Arfan;
Amin, Najaf;
Hottenga, Jouke-Jan;
Koelewijn, Stephany C.;
Kattenberg, V. Mathijs;
de Moor, Marleen H. M.;
Janssens, A. Cecile J. W.;
Aulchenko, Yurii S.;
Oostra, Ben A.;
de Geus, Eco J. C.;
Smit, Johannes H.;
Zitman, Frans G.;
Uitterlinden, André G.;
Hofman, Albert;
Willemsen, Gonneke;
Nyholt, Dale R.;
Montgomery, Grant W.

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 8, p. 884, doi. 10.1038/sj.ejhg.5201841

By:

Vanmolkot, Kaate R. J.;
Stam, Anine H.;
Raman, Ashok;
Koenderink, Jan B.;
de Vries, Boukje;
van den Boogerd, Eelke H.;
van Vark, Judith;
van den Heuvel, Jeroen J. M. W.;
Bajaj, Nin;
Terwindt, Gisela M.;
Haan, Joost;
Frants, Rune R.;
Ferrari, Michel D.;
van den Maagdenberg, Arn M. J. M.

Publication type:

Article

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.

Published in:

Nature Genetics, 2012, v. 44, n. 9, p. 1030, doi. 10.1038/ng.2358

By:

Heinzen, Erin L;
Swoboda, Kathryn J;
Hitomi, Yuki;
Gurrieri, Fiorella;
Nicole, Sophie;
de Vries, Boukje;
Tiziano, F Danilo;
Fontaine, Bertrand;
Walley, Nicole M;
Heavin, Sinéad;
Panagiotakaki, Eleni;
Neri, Giovanni;
Koelewijn, Stephany;
Kamphorst, Jessica;
Geilenkirchen, Marije;
Pelzer, Nadine;
Laan, Laura;
Haan, Joost;
Ferrari, Michel;
van den Maagdenberg, Arn

Publication type:

Article

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

Published in:

Nature Genetics, 2012, v. 44, n. 7, p. 777, doi. 10.1038/ng.2307

By:

Freilinger, Tobias;
Anttila, Verneri;
de Vries, Boukje;
Malik, Rainer;
Kallela, Mikko;
Terwindt, Gisela M;
Pozo-Rosich, Patricia;
Winsvold, Bendik;
Nyholt, Dale R;
van Oosterhout, Willebrordus P J;
Artto, Ville;
Todt, Unda;
Hämäläinen, Eija;
Fernández-Morales, Jèssica;
Louter, Mark A;
Kaunisto, Mari A;
Schoenen, Jean;
Raitakari, Olli;
Lehtimäki, Terho;
Vila-Pueyo, Marta

Publication type:

Article

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

Published in:

Nature Genetics, 2011, v. 43, n. 7, p. 695, doi. 10.1038/ng.856

By:

Chasman, Daniel I.;
Schürks, Markus;
Anttila, Verneri;
de Vries, Boukje;
Schminke, Ulf;
Launer, Lenore J.;
Terwindt, Gisela M.;
van den Maagdenberg, Arn M. J. M.;
Fendrich, Konstanze;
Völzke, Henry;
Ernst, Florian;
Griffiths, Lyn R.;
Buring, Julie E.;
Kallela, Mikko;
Freilinger, Tobias;
Kubisch, Christian;
Ridker, Paul M.;
Palotie, Aarno;
Ferrari, Michel D.;
Hoffmann, Wolfgang

Publication type:

Article

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

Published in:

Nature Genetics, 2010, v. 42, n. 10, p. 869, doi. 10.1038/ng.652

By:

Anttila, Verneri;
Stefansson, Hreinn;
Kallela, Mikko;
Todt, Unda;
Terwindt, Gisela M.;
Calafato, M. Stella;
Nyholt, Dale R.;
Dimas, Antigone S.;
Freilinger, Tobias;
Müller-Myhsok, Bertram;
Artto, Ville;
Inouye, Michael;
Alakurtti, Kirsi;
Kaunisto, Mari A.;
Hämäläinen, Eija;
de Vries, Boukje;
Stam, Anine H.;
Weller, Claudia M.;
Heinze, Axel;
Heinze-Kuhn, Katja

Publication type:

Article

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1068, doi. 10.1038/ng2082

By:

Richards, Anna;
van den Maagdenberg, Arn M. J. M.;
Jen, Joanna C.;
Kavanagh, David;
Bertram, Paula;
Spitzer, Dirk;
Liszewski, M. Kathryn;
Barilla-LaBarca, Maria-Louise;
Terwindt, Gisela M.;
Kasai, Yumi;
McLellan, Mike;
Grand, Mark Gilbert;
Vanmolkot, Kaate R. J.;
de Vries, Boukje;
Jijun Wan;
Kane, Michael J.;
Mamsa, Hafsa;
Schäfer, Ruth;
Stam, Anine H.;
Haan, Joost

Publication type:

Article

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

Published in:

PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004835

By:

Demirkan, Ayşe;
Henneman, Peter;
Verhoeven, Aswin;
Dharuri, Harish;
Amin, Najaf;
van Klinken, Jan Bert;
Karssen, Lennart C.;
de Vries, Boukje;
Meissner, Axel;
Göraler, Sibel;
van den Maagdenberg, Arn M. J. M.;
Deelder, André M.;
C ’t Hoen, Peter A.;
van Duijn, Cornelia M.;
van Dijk, Ko Willems

Publication type:

Article

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

Published in:

Nature Genetics, 2013, v. 45, n. 8, p. 912, doi. 10.1038/ng.2676

By:

Anttila, Verneri;
Winsvold, Bendik S;
Gormley, Padhraig;
Kurth, Tobias;
Bettella, Francesco;
McMahon, George;
Kallela, Mikko;
Malik, Rainer;
de Vries, Boukje;
Terwindt, Gisela;
Medland, Sarah E;
Todt, Unda;
McArdle, Wendy L;
Quaye, Lydia;
Koiranen, Markku;
Ikram, M Arfan;
Lehtimäki, Terho;
Stam, Anine H;
Ligthart, Lannie;
Wedenoja, Juho

Publication type:

Article

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

Published in:

Nature Genetics, 2013, v. 45, n. 5, p. 546, doi. 10.1038/ng.2599

By:

Dibbens, Leanne M;
de Vries, Boukje;
Donatello, Simona;
Heron, Sarah E;
Hodgson, Bree L;
Chintawar, Satyan;
Crompton, Douglas E;
Hughes, James N;
Bellows, Susannah T;
Klein, Karl Martin;
Callenbach, Petra M C;
Corbett, Mark A;
Gardner, Alison E;
Kivity, Sara;
Iona, Xenia;
Regan, Brigid M;
Weller, Claudia M;
Crimmins, Denis;
O'Brien, Terence J;
Guerrero-López, Rosa

Publication type:

Article

Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

Published in:

2013

By:

de Vries, Boukje;
Freilinger, Tobias;
Anttila, Verneri;
Malik, Rainer;
Kallela, Mikko;
Terwindt, Gisela;
Pozo-Rosich, Patricia;
Winsvold, Bendik;
Nyholt, Dale;
van Oosterhout, Willebrordus;
Artto, Ville;
Todt, Unda;
Hämäläinen, Eija;
Fernández-Morales, Jèssica;
Louter, Mark;
Kaunisto, Mari;
Schoenen, Jean;
Raitakari, Olli;
Lehtimäki, Terho;
Vila-Pueyo, Marta

Publication type:

Abstract

Noradrenergic and Cholinergic Modulation of Belief Updating.

Published in:

Journal of Cognitive Neuroscience, 2018, v. 30, n. 12, p. 1803, doi. 10.1162/jocn_a_01317

By:

Jepma, Marieke;
Brown, Stephen B. R. E.;
Murphy, Peter R.;
Koelewijn, Stephany C.;
de Vries, Boukje;
van den Maagdenberg, Arn M.;
Nieuwenhuis, Sander

Publication type:

Article

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

Published in:

2015

By:

Panagiotakaki, Eleni;
De Grandis, Elisa;
Stagnaro, Michela;
Heinzen, Erin L.;
Fons, Carmen;
Sisodiya, Sanjay;
de Vries, Boukje;
Goubau, Christophe;
Weckhuysen, Sarah;
Kemlink, David;
Scheffer, Ingrid;
Lesca, Gaëtan;
Rabilloud, Muriel;
Klich, Amna;
Ramirez-Camacho, Alia;
Ulate-Campos, Adriana;
Campistol, Jaume;
Giannotta, Melania;
Moutard, Marie-Laure;
Doummar, Diane

Publication type:

journal article

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

Published in:

Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9486

By:

Vanmolkot, Kaate R.J.;
Babini, Elena;
de Vries, Boukje;
Stam, Anine H.;
Freilinger, Tobias;
Terwindt, Gisela M.;
Norris, Lisa;
Haan, Joost;
Frants, Rune R.;
Ramadan, Nabih M.;
Ferrari, Michel D.;
Pusch, Michael;
van den Maagdenberg, Arn M.J.M.;
Dichgans, Martin

Publication type:

Article

Molecular genetics of migraine.

Published in:

Human Genetics, 2009, v. 126, n. 1, p. 115, doi. 10.1007/s00439-009-0684-z

By:

de Vries, Boukje;
Frants, Rune R.;
Ferrari, Michel D.;
van den Maagdenberg, Arn M. J. M.

Publication type:

Article

Migraine Genes and the Relation to Gender.

Published in:

Headache: The Journal of Head & Face Pain, 2011, v. 51, n. 6, p. 880, doi. 10.1111/j.1526-4610.2011.01913.x

By:

Shyti, Reinald;
De Vries, Boukje;
Van den Maagdenberg, Arn

Publication type:

Article

Genetic Biomarkers for Migraine.

Published in:

Headache: The Journal of Head & Face Pain, 2006, v. 46, n. 7, p. 1059, doi. 10.1111/j.1526-4610.2006.00499.x

By:

De Vries, Boukje;
Haan, Joost;
Frants, Rune R.;
Van den Maagdenberg, Arn M. J. M.;
Ferrari, Michel D.

Publication type:

Article

Selected Confirmed, Probable, and Exploratory Migraine Biomarkers.

Published in:

Headache: The Journal of Head & Face Pain, 2006, v. 46, n. 7, p. 1108, doi. 10.1111/j.1526-4610.2006.00525.x

By:

Loder, Elizabeth;
Harrington, Michael G.;
Cutrer, Michael;
Sandor, Peter;
De Vries, Boukje

Publication type:

Article

Identifying a gene expression signature of cluster headache in blood.

Published in:

Scientific Reports, 2017, p. 40218, doi. 10.1038/srep40218

By:

Eising, Else;
Pelzer, Nadine;
Vijfhuizen, Lisanne S.;
Vries, Boukje de;
Ferrari, Michel D.;
't Hoen, Peter A. C.;
Terwindt, Gisela M.;
van den Maagdenberg, Arn M. J. M.

Publication type:

Article

Involvement of astrocyte and oligodendrocyte gene sets in migraine.

Published in:

2016

By:

Eising, Else;
de Leeuw, Christiaan;
Min, Josine L.;
Anttila, Verneri;
Verheijen, Mark H. G.;
Terwindt, Gisela M.;
Dichgans, Martin;
Freilinger, Tobias;
Kubisch, Christian;
Ferrari, Michel D.;
Smit, August B.;
de Vries, Boukje;
Palotie, Aarno;
van den Maagdenberg, Arn M. J. M.;
Posthuma, Danielle;
Verheijen, Mark Hg;
International Headache Genetics Consortium;
van den Maagdenberg, Arn Mjm

Publication type:

journal article

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

Published in:

2016

By:

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, Stefan;
Meitinger, Thomas;
Aromas, Arpo;
Eriksson, Johan G.

Publication type:

journal article

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

Published in:

2016

By:

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 M. J. M.;
van den Maagdenberg, Arn Mjm;
International Headache Genetics Consortium

Publication type:

journal article

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

Published in:

Cephalalgia, 2015, v. 35, n. 9, p. 741, doi. 10.1177/0333102414557839

By:

Weller, Claudia M.;
Wilbrink, Leopoldine A.;
Houwing-Duistermaat, Jeanine J.;
Koelewijn, Stephany C.;
Vijfhuizen, Lisanne S.;
Haan, Joost;
Ferrari, Michel D.;
Terwindt, Gisela M.;
van den Maagdenberg, Arn M. J. M.;
de Vries, Boukje

Publication type:

Article

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

Published in:

Cephalalgia, 2015, v. 35, n. 6, p. 489, doi. 10.1177/0333102414547784

By:

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;
Meitinger, Thomas;
Aromaa, Arpo;
Eriksson, Johan G;
Kaprio, Jaakko

Publication type:

Article

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

Published in:

Cephalalgia, 2015, v. 35, n. 1, p. 10, doi. 10.1177/0333102414532379

By:

Weller, Claudia M;
Vries, Boukje de;
Geilenkirchen, Marije A;
Terwindt, Gisela M;
Leen, Wilhelmina G;
Neville, Brian GR;
Duncan, John S;
Haan, Joost;
Kamsteeg, Erik-Jan;
Scheffer, Hans;
Ferrari, Michel D;
Maagdenberg, Arn MJM van den;
Willemsen, Michèl AAP

Publication type:

Article

Two novel SCN1A mutations identified in families with familial hemiplegic migraine.

Published in:

Cephalalgia, 2014, v. 34, n. 13, p. 1062, doi. 10.1177/0333102414529195

By:

Weller, Claudia M;
Pelzer, Nadine;
de Vries, Boukje;
López, Mercè Artigas;
De Fàbregues, Oriol;
Pascual, Julio;
Arroyo, María A Ramos;
Koelewijn, Stephany C;
Stam, Anine H;
Haan, Joost;
Ferrari, Michel D;
Terwindt, Gisela M;
van den Maagdenberg, Arn MJM

Publication type:

Article

Familial hemiplegic migraine treated by sodium valproate and lamotrigine.

Published in:

2014

By:

Pelzer, Nadine;
Stam, Anine H;
Carpay, Johannes A;
Vries, Boukje de;
van den Maagdenberg, Arn MJM;
Ferrari, Michel D;
Haan, Joost;
Terwindt, Gisela M

Publication type:

journal article

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

Published in:

Cephalalgia, 2014, v. 34, n. 3, p. 174, doi. 10.1177/0333102413502736

By:

Vries, Boukje de;
Eising, Else;
Broos, Ludo AM;
Koelewijn, Stephany C;
Todorov, Boyan;
Frants, Rune R;
Boer, Judith M;
Ferrari, Michel D;
Hoen, Peter AC ‘t;
Maagdenberg, Arn MJM van den

Publication type:

Article

Pearls and pitfalls in genetic studies of migraine.

Published in:

Cephalalgia, 2013, v. 33, n. 8, p. 614, doi. 10.1177/0333102413484988

By:

Eising, Else;
de Vries, Boukje;
Ferrari, Michel D;
Terwindt, Gisela M;
van den Maagdenberg, Arn MJM

Publication type:

Article

Head tremor related to CACNA1A mutations.

Published in:

Cephalalgia, 2011, v. 31, n. 12, p. 1315, doi. 10.1177/0333102411414442

By:

Geerlings, Rianne PJ;
Koehler, Peter J;
Haane, Danielle YP;
Stam, Anine H;
de Vries, Boukje;
Boon, Elles MJ;
Haan, Joost

Publication type:

Article

Head tremor related to CACNA1A mutations.

Published in:

Cephalalgia, 2011, v. 31, n. 12, p. 1315, doi. 10.1177/0333102411414442

By:

Geerlings, Rianne PJ;
Koehler, Peter J;
Haane, Danielle YP;
Stam, Anine H;
de Vries, Boukje;
Boon, Elles MJ;
Haan, Joost

Publication type:

Article

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

Published in:

Cephalalgia, 2011, v. 31, n. 2, p. 199, doi. 10.1177/0333102410375629

By:

Stam, Anine H;
Louter, Mark A;
Haan, Joost;
de Vries, Boukje;
van den Maagdenberg, Arn MJM;
Frants, Rune R;
Ferrari, Michel D;
Terwindt, Gisela M

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2008, v. 17, n. 21, p. 3318, doi. 10.1093/hmg/ddn227

By:

Nyholt, Dale R.;
LaForge, K. Steven;
Kallela, Mikko;
Alakurtti, Kirsi;
Anttila, Verneri;
Färkkilä, Markus;
Hämaläinen, Eija;
Kaprio, Jaakko;
Kaunisto, Mari A.;
Heath, Andrew C.;
Montgomery, Grant W.;
Göbel, Hartmut;
Todt, Unda;
Ferrari, Michel D.;
Launer, Lenore J.;
Frants, Rune R.;
Terwindt, Gisela M.;
de Vries, Boukje;
Verschuren, W.M. Monique;
Brand, Jan

Publication type:

Article