Mutations in DEPDC5 cause familial focal epilepsy with variable foci von 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, Mulley, John C, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul Q, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele F, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn M J M, Pandolfo, Massimo, Berkovic, Samuel F, Scheffer, Ingrid E

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Outbreaks of mumps genotype G viruses in the Netherlands between October 2019 and March 2020: clusters associated with multiple introductions von Shah, Anita A., Bodewes, Rogier, Reijnen, Linda, Boelsums, Timo, Weller, Claudia M., Fanoy, Ewout B., Veldhuijzen, Irene K.

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Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis von 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 MJM, de Vries, Boukje

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Ensuring HLA‐matched platelet support requires an ethnic diverse donor population von Kreuger, Aukje L., Haasnoot, Geert W., Somers, Judith A.E., Tomson, Bert, Bon, Johanna G., Kraaij, Marian G.J., Weller, Claudia M.

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A metabolomic profile is associated with the risk of incident coronary heart disease von Vaarhorst, Anika A.M., MSc, Verhoeven, Aswin, PhD, Weller, Claudia M., MD, Böhringer, Stefan, MD, PhD, Göraler, Sibel, MSc, Meissner, Axel, PhD, Deelder, André M., PhD, Henneman, Peter, PhD, Gorgels, Anton P.M., MD, PhD, van den Brandt, Piet A., PhD, Schouten, Leo J., MD, PhD, van Greevenbroek, Marleen M., PhD, Merry, Audrey H.H., PhD, Verschuren, W.M. Monique, PhD, van den Maagdenberg, Arn M.J.M., PhD, van Dijk, Ko Willems, PhD, Isaacs, Aaron, PhD, Boomsma, Dorret, PhD, Oostra, Ben A., PhD, van Duijn, Cornelia M., PhD, Jukema, J. Wouter, MD, PhD, Boer, Jolanda M.A., PhD, Feskens, Edith, PhD, Heijmans, Bastiaan T., PhD, Slagboom, P. Eline, PhD

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HLA‐matched platelet transfusions are effective only in refractory patients with positive HLA antibody screening von Kreuger, Aukje L., Mäkelburg, Anja B.U., Somers, Judith A.E., Tomson, Bert, Watering, Leo M. G., Bom, Johanna G., Kraaij, Marian G.J., Weller, Claudia M.

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Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome von Koutsopoulos, Olga S, Kretz, Christine, Weller, Claudia M, Roux, Aurelien, Mojzisova, Halina, Böhm, Johann, Koch, Catherine, Toussaint, Anne, Heckel, Emilie, Stemkens, Daphne, Ter Horst, Simone A J, Thibault, Christelle, Koch, Muriel, Mehdi, Syed Q, Bijlsma, Emilia K, Mandel, Jean-Louis, Vermot, Julien, Laporte, Jocelyn

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Migraine is not associated with enhanced atherosclerosis von Stam, Anine H, Weller, Claudia M, Janssens, A Cecile JW, Aulchenko, Yurii S, Oostra, Ben A, Frants, Rune R, van den Maagdenberg, Arn MJM, Ferrari, Michel D, van Duijn, Cornelia M, Terwindt, Gisela M

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Stepwise web-based questionnaires for diagnosing cluster headache: LUCA and QATCH von Wilbrink, Leopoldine A, Weller, Claudia M, Cheung, Carlo, Stijnen, Theo, Haan, Joost, Ferrari, Michel D, Terwindt, Gisela M

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Cluster-Tic Syndrome: A Cross-Sectional Study of Cluster Headache Patients von Wilbrink, Leopoldine A., Weller, Claudia M., Cheung, Carlo, Haan, Joost, Ferrari, Michel D.

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

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A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood von Weller, Claudia M, Leen, Wilhelmina G, Neville, Brian GR, Duncan, John S, Vries, Boukje de, Geilenkirchen, Marije A, Haan, Joost, Kamsteeg, Erik-Jan, Ferrari, Michel D, Maagdenberg, Arn MJM van den, Willemsen, Michèl AAP, Scheffer, Hans, Terwindt, Gisela M

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PRRT2 MUTATION CAUSES BENIGN FAMILIAL INFANTILE CONVULSIONS von DE VRIES, Boukje, CALLENBACH, Petra M. C, KAMPHORST, Jessica T, WELLER, Claudia M, KOELEWIJN, Stephany C, TEN HOUTEN, Robert, DE COO, Irenaeus F. M, BROUWER, Oebo F, DEN MAAGDENBERG, Arn M. J. M. Van

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Genome-wide Gene Expression Profiling of Formalin-fixed Paraffin-Embedded Breast Cancer Core Biopsies Using Microarrays von Budczies, Jan, Weichert, Wilko, Noske, Aurelia, Müller, Berit Maria, Weller, Claudia, Wittenberger, Timo, Hofmann, Hans-Peter, Dietel, Manfred, Denkert, Carsten, Gekeler, Volker

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Genome-wide meta-analysis identifies new susceptibility loci for migraine von 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, Dunham, Ian, Neale, Benjamin M, Palta, Priit, Hamalainen, Eija, Schürks, Markus, Rose, Lynda M, Buring, Julie E, Ridker, Paul M, Steinberg, Stacy, Stefansson, Hreinn, Jakobsson, Finnbogi, Lawlor, Debbie A, Evans, David M, Ring, Susan M, Färkkilä, Markus, Artto, Ville, Kaunisto, Mari A, Freilinger, Tobias, Schoenen, Jean, Frants, Rune R, Pelzer, Nadine, Weller, Claudia M, Zielman, Ronald, Heath, Andrew C, Madden, Pamela A F, Montgomery, Grant W, Martin, Nicholas G, Borck, Guntram, Göbel, Hartmut, Heinze, Axel, Heinze-Kuhn, Katja, Williams, Frances M K, Hartikainen, Anna-Liisa, Pouta, Anneli, van den Ende, Joyce, Uitterlinden, Andre G, Hofman, Albert, Amin, Najaf, Hottenga, Jouke-Jan, Vink, Jacqueline M, Heikkilä, Kauko, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Wichmann, Heinz Erich, Aromaa, Arpo, Eriksson, Johan G, Traynor, Bryan J, Trabzuni, Daniah, Rossin, Elizabeth, Lage, Kasper, Jacobs, Suzanne B R, Gibbs, J Raphael, Birney, Ewan, Kaprio, Jaakko, Penninx, Brenda W, Boomsma, Dorret I, van Duijn, Cornelia, Raitakari, Olli, Jarvelin, Marjo-Riitta, Zwart, John-Anker, Cherkas, Lynn, Strachan, David P, Kubisch, Christian, Ferrari, Michel D, van den Maagdenberg, Arn M J M, Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Daly, Mark J

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Changes in Gene Expression Induced by Phosphorothioate Oligodeoxynucleotides (Including G3139) in PC3 Prostate Carcinoma Cells Are Recapitulated at Least in Part by Treatment with... von BENIMETSKAYA, Luba, WITTENBERGER, Timo, STEIN, C. A, HOFMANN, Hans-Peter, WELLER, Claudia, LAI, Johnathan C, MILLERS, Paul, GEKELER, Volker

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Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 von ANTTILA, Verneri, STEFANSSON, Hreinn, 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, KALLELA, Mikko, GOEBEL, Ingrid, BORCK, Guntram, GÖBEL, Hartmut, STEINBERG, Stacy, WOLF, Christiane, BJÖRNSSON, Asgeir, GUDMUNDSSON, Gretar, KIRCHMANN, Malene, HAUGE, Anne, WERGE, Thomas, TODT, Unda, SCHOENEN, Jean, ERIKSSON, Johan G, HAGEN, Knut, STOVNER, Lars, WICHMANN, H-Erich, MEITINGER, Thomas, ALEXANDER, Michael, MOEBUS, Susanne, SCHREIBER, Stefan, AULCHENKO, Yurii S, TERWINDT, Gisela M, BRETELER, Monique M. B, UITTERLINDEN, Andre G, HOFMAN, Albert, VAN DUIJN, Cornelia M, TIKKA-KLEEMOLA, Päivi, VEPSÄLÄINEN, Salli, LUCAE, Susanne, TOZZI, Federica, MUGLIA, Pierandrea, BARRETT, Jeffrey, STELLA CALAFATO, M, KAPRIO, Jaakko, FÄRKKILÄ, Markus, PELTONEN, Leena, STEFANSSON, Kari, ZWART, John-Anker, FERRARI, Michel D, OLESEN, Jes, DALY, Mark, WESSMAN, Maija, VAN DEN MAAGDENBERG, Arn M.j M, NYHOLT, Dale R, DIMAS, Antigone S, FREILINGER, Tobias, MÜLLER-MYHSOK, Bertram

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Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder von Jacobsen, Kaya K, Nievergelt, Caroline M, Zayats, Tetyana, Greenwood, Tiffany A, Anttila, Verneri, Akiskal, Hagop S, Haavik, Jan, Bernt Fasmer, Ole, Kelsoe, John R, Johansson, Stefan, Oedegaard, Ketil J

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Mutations in DEPDC5 cause Familial Focal Epilepsy with Variable Foci and are a common cause of familial non-lesional focal epilepsy von Pandolfo, Massimo, Dibbens, Leanne, de Vries, Boukje, Donatello, Simona, Heron, Sarah, Hodgson, Bree, Chintawar, Satyan, Crompton, Douglas, Hughes, James, Bellows, Susannah, Klein, Karl Martin, Callenbach, Petra, Corbett, Mark, Gardner, Alison, Kivity, Sarah, Iona, Xenia, Regan, Brigid, Weller, Claudia, Crimmins, Denis, O'Brien, Terence, Guerrero-Lopez, Rosa, Mulley, John, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn, Berkovic, Samuel, Scheffer, Ingrid

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Photovoltaik: Technik, Produkte, Details von Weller, Bernhard

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