Lrig2 Negatively Regulates Ectodomain Shedding of Axon Guidance Receptors by ADAM Proteases von van Erp, Susan, van den Heuvel, Dianne M.A., Fujita, Yuki, Robinson, Ross A., Hellemons, Anita J.C.G.M., Adolfs, Youri, Van Battum, Eljo Y., Blokhuis, Anna M., Kuijpers, Marijn, Demmers, Jeroen A.A., Hedman, Håkan, Hoogenraad, Casper C., Siebold, Christian, Yamashita, Toshihide, Pasterkamp, R. Jeroen

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ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN von Groen, Ewout J N, Fumoto, Katsumi, Blokhuis, Anna M, Engelen-Lee, Jooyeon, Zhou, Yeping, van den Heuvel, Dianne M A, Koppers, Max, van Diggelen, Femke, van Heest, Jessica, Demmers, Jeroen A A, Kirby, Janine, Shaw, Pamela J, Aronica, Eleonora, Spliet, Wim G M, Veldink, Jan H, van den Berg, Leonard H, Pasterkamp, R Jeroen

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Protein aggregation in amyotrophic lateral sclerosis von Blokhuis, Anna M., Groen, Ewout J. N., Koppers, Max, van den Berg, Leonard H., Pasterkamp, R. Jeroen

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C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits von Koppers, Max, Blokhuis, Anna M., Westeneng, Henk-Jan, Terpstra, Margo L., Zundel, Caroline A. C., Vieira de Sá, Renata, Schellevis, Raymond D., Waite, Adrian J., Blake, Derek J., Veldink, Jan H., van den Berg, Leonard H., Pasterkamp, R. Jeroen

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Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways von Blokhuis, Anna M., Koppers, Max, Groen, Ewout J. N., van den Heuvel, Dianne M. A., Dini Modigliani, Stefano, Anink, Jasper J., Fumoto, Katsumi, van Diggelen, Femke, Snelting, Anne, Sodaar, Peter, Verheijen, Bert M., Demmers, Jeroen A. A., Veldink, Jan H., Aronica, Eleonora, Bozzoni, Irene, den Hertog, Jeroen, van den Berg, Leonard H., Pasterkamp, R. Jeroen

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The Dutch registry for facioscapulohumeral muscular dystrophy: Cohort profile and longitudinal patient reported outcomes von Kools, Joost, Deenen, Johanna Cw, Blokhuis, Anna M, Verbeek, André Lm, Voermans, Nicol C, van Engelen, Baziel Gm

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The socioeconomic burden of facioscapulohumeral muscular dystrophy von Blokhuis, Anna M., Deenen, Johanna C. W., Voermans, Nicol C., van Engelen, Baziel G. M., Kievit, Wietske, Groothuis, Jan T.

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von Dekker, Annelot M., Diekstra, Frank P., van der Spek, Rick A. A., Võsa, Urmo, Yang, Jian, Vajda, Alice, Lin, Kuang, Vrabec, Katarina, Koritnik, Blaž, Zidar, Janez, de Visser, Marianne, Leonardis, Lea, Millecamps, Stéphanie, Meininger, Vincent, Mora, Jesus S., Colville, Shuna, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Pittman, Alan, Sidle, Katie, Malaspina, Andrea, Petri, Susanne, Drepper, Carsten, Meyer, Thomas, Ophoff, Roel A., Staats, Kim A., Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, A Nazli, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Smith, Bradley N., Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R., Maurel, Cindy, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safaa, Tittmann, Lukas, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Tzourio, Christophe, Dartigues, Jean-François, Cereda, Cristina, Uitterlinden, Andre G., Estrada, Karol, Hofman, Albert, Curtis, Charles, Comi, Giacomo P., D'Alfonso, Sandra, Fogh, Isabella, Bertolin, Cinzia, Sorarù, Gianni, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Brunetti, Maura, van Doormaal, Perry T. C., Arcuti, Simona, Capozzo, Rosa, Lunetta, Christian, Riva, Nilo, Filosto, Massimiliano, Muller, Bernard, Tazelaar, Gijs H. P., Zhang, Katharine, McCann, Emily P., Rowe, Dominic B., Grosskreutz, Julian, Ringer, Thomas, Prell, Tino, Stubendorff, Beatrice, Beghi, Ettore, Pupillo, Elisabetta, Blokhuis, Anna M., Tortelli, Rosanna, Powell, John, Ludolph, Albert C., Van Damme, Philip, Franke, Lude, Brown, Robert H., Sproviero, William, Andersen, Peter M., Silani, Vincenzo, Jones, Ashley R., Pasterkamp, R Jeroen, Breen, Gerome, Al-Chalabi, Ammar, Veldink, Jan H., Kenna, Kevin P., Harschnitz, Oliver, Schellevis, Raymond D., Brands, William J.

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C 9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits von Koppers, Max, Blokhuis, Anna M., Westeneng, Henk‐Jan, Terpstra, Margo L., Zundel, Caroline A. C., Vieira de Sá, Renata, Schellevis, Raymond D., Waite, Adrian J., Blake, Derek J., Veldink, Jan H., van den Berg, Leonard H., Pasterkamp, R. Jeroen

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Lrig2 Negatively Regulates Ectodomain Shedding of Axon Guidance Receptors by ADAM Proteases von van Erp, Susan, van den Heuvel, Dianne M A, Fujita, Yuki, Robinson, Ross A, Hellemons, Anita J C G M, Adolfs, Youri, Van Battum, Eljo Y, Blokhuis, Anna M, Kuijpers, Marijn, Demmers, Jeroen A A, Hedman, Håkan, Hoogenraad, Casper C, Siebold, Christian, Yamashita, Toshihide, Pasterkamp, R Jeroen

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Proteomic profiling of the spinal cord in ALS: decreased ATP5D levels suggest synaptic dysfunction in ALS pathogenesis von Engelen-Lee, Jooyeon, Blokhuis, Anna M, Spliet, Wim G.M, Pasterkamp, R. Jeroen, Aronica, Eleonora, Demmers, Jeroen A A, Broekhuizen, Roel, Nardo, Giovanni, Bovenschen, Niels, Van Den Berg, Leonard H

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Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways von Blokhuis, Anna M, Koppers, Max, Groen, Ewout J N, van Den Heuvel, Dianne M A, Dini Modigliani, Stefano, Anink, Jasper J, Fumoto, Katsumi, van Diggelen, Femke, Snelting, Anne, Sodaar, Peter, Verheijen, Bert M, Demmers, Jeroen A A, Veldink, Jan H, Aronica, Eleonora, Bozzoni, Irene, den Hertog, Jeroen, van Den Berg, Leonard H, Pasterkamp, R. Jeroen

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von van Rheenen, Wouter, Shatunov, Aleksey, Dekker, Annelot M, McLaughlin, Russell L, Diekstra, Frank P, Pulit, Sara L, van der Spek, Rick A.A, Võsa, Urmo, de Jong, Simone, Robinson, Matthew R, Yang, Jian, Fogh, Isabella, van Doormaal, Perry Tc, Tazelaar, Gijs H.P, Koppers, Max, Blokhuis, Anna M, Sproviero, William, Jones, Ashley R, Kenna, Kevin P, van Eijk, Kristel R, Harschnitz, Oliver, Schellevis, Raymond D, Brands, William J, Medic, Jelena, Menelaou, Androniki, Vajda, Alice, Ticozzi, Nicola, Lin, Kuang, Rogelj, Boris, Vrabec, Katarina, Ravnik-Glavač, Metka, Koritnik, Blaž, Zidar, Janez, Leonardis, Lea, Grošelj, Leja Dolenc, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S, Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Topp, Simon, Petri, Susanne, Abdulla, Susanne, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Ophoff, Roel A, Staats, Kim A, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M, Trojanowski, John Q, Elman, Lauren, McCluskey, Leo, Basak, A. Nazli, Tunca, Ceren, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R, Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A.M, Saker-Delye, Safaa, Dürr, Alexandra, Wood, Nicholas W, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M, Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean-François, Uitterlinden, Andre G, Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, Blauw, Hylke M, van der Kooi, Anneke J

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Lameness assessment with automatic monitoring of activity in commercial broiler flocks von Silvera, A M, Knowles, T G, Butterworth, A, Berckmans, D, Vranken, E, Blokhuis, H J

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Antigen-specific, antibody-coated, exosome-like nanovesicles deliver suppressor T-cell microRNA-150 to effector T cells to inhibit contact sensitivity von Bryniarski, Krzysztof, PhD, Ptak, Wlodzimierz, MD, Jayakumar, Asha, PhD, Püllmann, Kerstin, MD, Caplan, Michael J., MD, PhD, Chairoungdua, Arthit, PhD, Lu, Jun, MD, PhD, Adams, Brian D., PhD, Sikora, Emilia, PhD, Nazimek, Katarzyna, MS, Marquez, Susanna, MS, Kleinstein, Steven H., PhD, Sangwung, Panjamaporn, BS, Iwakiri, Yasuko, PhD, Delgato, Eric, BS, Redegeld, Frank, PhD, Blokhuis, Bart R., MS, Wojcikowski, Jacek, PhD, Daniel, Anna Wladyslawa, PhD, Groot Kormelink, Tom, PhD, Askenase, Philip W., MD

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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis von Paternoster, Lavinia, Standl, Marie, Chen, Chih-Mei, Ramasamy, Adaikalavan, Bønnelykke, Klaus, Duijts, Liesbeth, Ferreira, Manuel A, Alves, Alexessander Couto, Thyssen, Jacob P, Albrecht, Eva, Baurecht, Hansjörg, Feenstra, Bjarke, Sleiman, Patrick M A, Warrington, Nicole M, Curjuric, Ivan, Myhre, Ronny, Curtin, John A, Groen-Blokhuis, Maria M, Kerkhof, Marjan, Franke, Andre, Ellinghaus, David, Fölster-Holst, Regina, Dermitzakis, Emmanouil, Montgomery, Stephen B, Prokisch, Holger, Heim, Katharina, Hartikainen, Anna-Liisa, Pouta, Anneli, Pekkanen, Juha, Blakemore, Alexandra I F, Buxton, Jessica L, Duffy, David L, Madden, Pamela A, Montgomery, Grant W, Matheson, Melanie C, Le Souëf, Peter, Pourcain, Beate St, Smith, George Davey, Henderson, John, Timpson, Nicholas J, Deloukas, Panos, Ring, Susan M, Wichmann, H-Erich, Müller-Nurasyid, Martina, Novak, Natalija, Klopp, Norman, Rodríguez, Elke, McArdle, Wendy, Linneberg, Allan, Menné, Torkil, Nohr, Ellen A, Hofman, Albert, Uitterlinden, André G, van Duijn, Cornélia M, Rivadeneira, Fernando, de Jongste, Johan C, van der Valk, Ralf J P, Wjst, Matthias, Jogi, Rain, Geller, Frank, Boyd, Heather A, Murray, Jeffrey C, Mentch, Frank, March, Michael, Mangino, Massimo, Spector, Tim D, Bataille, Veronique, Pennell, Craig E, Holt, Patrick G, Sly, Peter, Tiesler, Carla M T, Thiering, Elisabeth, Illig, Thomas, Imboden, Medea, Nystad, Wenche, Simpson, Angela, Hottenga, Jouke-Jan, Postma, Dirkje, Koppelman, Gerard H, Smit, Henriette A, Söderhäll, Cilla, Chawes, Bo, Kreiner-Møller, Eskil, Bisgaard, Hans, Melén, Erik, Boomsma, Dorret I, Custovic, Adnan, Jacobsson, Bo, Palmer, Lyle J, Glass, Daniel, Hakonarson, Hakon, Melbye, Mads, Jarvis, Deborah L, Jaddoe, Vincent W V, Gieger, Christian, Strachan, David P, Martin, Nicholas G, Jarvelin, Marjo-Riitta, Heinrich, Joachim, Evans, David M

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A novel common variant in DCST2 is associated with length in early life and height in adulthood von van der Valk, Ralf J P, Kreiner-Møller, Eskil, Kooijman, Marjolein N, Guxens, Mònica, Stergiakouli, Evangelia, Sääf, Annika, Bradfield, Jonathan P, Geller, Frank, Hayes, M Geoffrey, Cousminer, Diana L, Körner, Antje, Thiering, Elisabeth, Curtin, John A, Myhre, Ronny, Huikari, Ville, Joro, Raimo, Kerkhof, Marjan, Warrington, Nicole M, Pitkänen, Niina, Ntalla, Ioanna, Horikoshi, Momoko, Veijola, Riitta, Freathy, Rachel M, Teo, Yik-Ying, Barton, Sheila J, Evans, David M, Kemp, John P, St Pourcain, Beate, Ring, Susan M, Davey Smith, George, Bergström, Anna, Kull, Inger, Hakonarson, Hakon, Mentch, Frank D, Bisgaard, Hans, Chawes, Bo, Stokholm, Jakob, Waage, Johannes, Eriksen, Patrick, Sevelsted, Astrid, Melbye, Mads, van Duijn, Cornelia M, Medina-Gomez, Carolina, Hofman, Albert, de Jongste, Johan C, Taal, H Rob, Uitterlinden, André G, Armstrong, Loren L, Eriksson, Johan, Palotie, Aarno, Bustamante, Mariona, Estivill, Xavier, Gonzalez, Juan R, Llop, Sabrina, Kiess, Wieland, Mahajan, Anubha, Flexeder, Claudia, Tiesler, Carla M T, Murray, Clare S, Simpson, Angela, Magnus, Per, Sengpiel, Verena, Hartikainen, Anna-Liisa, Keinanen-Kiukaanniemi, Sirkka, Lewin, Alexandra, Da Silva Couto Alves, Alexessander, Blakemore, Alexandra I, Buxton, Jessica L, Kaakinen, Marika, Rodriguez, Alina, Sebert, Sylvain, Vaarasmaki, Marja, Lakka, Timo, Lindi, Virpi, Gehring, Ulrike, Postma, Dirkje S, Ang, Wei, Newnham, John P, Lyytikäinen, Leo-Pekka, Pahkala, Katja, Raitakari, Olli T, Panoutsopoulou, Kalliope, Zeggini, Eleftheria, Boomsma, Dorret I, Groen-Blokhuis, Maria, Ilonen, Jorma, Franke, Lude, Hirschhorn, Joel N, Pers, Tune H, Liang, Liming, Huang, Jinyan, Hocher, Berthold, Knip, Mikael, Saw, Seang-Mei, Holloway, John W, Melén, Erik, Grant, Struan F A, Feenstra, Bjarke, Lowe, William L, Widén, Elisabeth

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Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index von Felix, Janine F, Bradfield, Jonathan P, Monnereau, Claire, van der Valk, Ralf J P, Stergiakouli, Evie, Chesi, Alessandra, Gaillard, Romy, Feenstra, Bjarke, Thiering, Elisabeth, Kreiner-Møller, Eskil, Mahajan, Anubha, Pitkänen, Niina, Joro, Raimo, Cavadino, Alana, Huikari, Ville, Franks, Steve, Groen-Blokhuis, Maria M, Cousminer, Diana L, Marsh, Julie A, Lehtimäki, Terho, Curtin, John A, Vioque, Jesus, Ahluwalia, Tarunveer S, Myhre, Ronny, Price, Thomas S, Vilor-Tejedor, Natalia, Yengo, Loïc, Grarup, Niels, Ntalla, Ioanna, Ang, Wei, Atalay, Mustafa, Bisgaard, Hans, Blakemore, Alexandra I, Bonnefond, Amelie, Carstensen, Lisbeth, Eriksson, Johan, Flexeder, Claudia, Franke, Lude, Geller, Frank, Geserick, Mandy, Hartikainen, Anna-Liisa, Haworth, Claire M A, Hirschhorn, Joel N, Hofman, Albert, Holm, Jens-Christian, Horikoshi, Momoko, Hottenga, Jouke Jan, Huang, Jinyan, Kadarmideen, Haja N, Kähönen, Mika, Kiess, Wieland, Lakka, Hanna-Maaria, Lakka, Timo A, Lewin, Alexandra M, Liang, Liming, Lyytikäinen, Leo-Pekka, Ma, Baoshan, Magnus, Per, McCormack, Shana E, McMahon, George, Mentch, Frank D, Middeldorp, Christel M, Murray, Clare S, Pahkala, Katja, Pers, Tune H, Pfäffle, Roland, Postma, Dirkje S, Power, Christine, Simpson, Angela, Sengpiel, Verena, Tiesler, Carla M T, Torrent, Maties, Uitterlinden, André G, van Meurs, Joyce B, Vinding, Rebecca, Waage, Johannes, Wardle, Jane, Zeggini, Eleftheria, Zemel, Babette S, Dedoussis, George V, Pedersen, Oluf, Froguel, Philippe, Sunyer, Jordi, Plomin, Robert, Jacobsson, Bo, Hansen, Torben, Gonzalez, Juan R, Custovic, Adnan, Raitakari, Olli T, Pennell, Craig E, Widén, Elisabeth, Boomsma, Dorret I, Koppelman, Gerard H, Sebert, Sylvain, Järvelin, Marjo-Riitta, Hyppönen, Elina, McCarthy, Mark I, Lindi, Virpi, Harri, Niinikoski, Körner, Antje

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Serum metabolomics analysis for quantification of muscle loss in critically ill patients: An explorative study von Ackermans, Leanne L.G.C., Bels, Julia L.M., Seethaler, Benjamin, van Dinter, Maarten, Schweinlin, Anna, van de Poll, Marcel C.G., Bischoff, Stephan C., Poeze, Martijn, Blokhuis, Taco J., Ten Bosch, Jan A.

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Common variants at 6q22 and 17q21 are associated with intracranial volume von ARFAN IKRAM, M, FORNAGE, Myriam, MOOK-KANAMORI, Dennis O, COKER, Laura H, LONGSTRETH, W. T, NIESSEN, Wiro J, DESTEFANO, Anita L, BEISER, Alexa, ZIJDENBOS, Alex P, STRUCHALIN, Maksim, JACK, Clifford R, RIVADENEIRA, Fernando, SMITH, Albert V, UITTERLINDEN, Andre G, KNOPMAN, David S, HARTIKAINEN, Anna-Liisa, PENNELL, Craig E, THIERING, Elisabeth, STEEGERS, Eric A. P, HAKONARSON, Hakon, HEINRICH, Joachim, PALMER, Lyle J, JARVELIN, Marjo-Riitta, SESHADRI, Sudha, MCCARTHY, Mark I, GRANT, Struan F. A, ST POURCAIN, Beate, TIMPSON, Nicholas J, SMITH, George Davey, SOVIO, Ulla, NALLS, Mike A, AU, Rhoda, HOFMAN, Albert, GUDNASON, Haukur, SCHMIDT, Reinhold, DER LUGT, Aad Van, HARRIS, Tamara B, MEEKS, William M, VERNOOIJ, Meike W, BUCHEM, Mark A.van, CATELLIER, Diane, JADDOE, Vincent W. V, GUDNASON, Vilmundur, WINDHAM, B. Gwen, WOLF, Philip A, DEBETTE, Stephanie, DUIJN, Cornelia M.van, MOSLEY, Thomas H, SCHMIDT, Helena, LAUNER, Lenore J, BRETELER, Monique M. B, DECARLI, Charles, VROOMAN, Henri A, SIGURDSSON, Sigurdur, ROPELE, Stefan, TAAL, H. Rob

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