Spatial division of labour of Schoenoplectus americanus by Ikegami, Makihiko, van Hal, Sander, van Rheenen, Jan W. A, Whigham, Dennis F, Werger, Marinus J. A

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High levels of inter-ramet water translocation in two rhizomatous Carex species, as quantified by deuterium labelling by Kroon, H. de, Fransen, B, Rheenen, J.W.A. van, Dijk, A. van, Kreulen, R. (Utrecht Univ. (Netherlands). Dept. of Plant Ecology and Evolutionary Biology)

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interaction between water and nitrogen translocation in a rhizomatous sedge (Carex flacca) by Kroon, H. de, Zalm, E. van der, Rheenen, J.W.A, Dijk, A. van, Kreulen, R

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Canopy development and leaf nitrogen distribution in a stand of Carex acutiformis by Hirose, T. (Tohoku University, Sendai, Japan), Werger, M.J.A, Rheenen, J.W.A

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Poor perfusion of the microvasculature in peritoneal metastases of ovarian cancer by Kastelein, Arnoud W., Vos, Laura M. C., van Baal, Juliette O. A. M., Koning, Jasper J., Hira, Vashendriya V. V., Nieuwland, Rienk, van Driel, Willemien J., Uz, Zühre, van Gulik, Thomas M., van Rheenen, Jacco, Ince, Can, Roovers, Jan-Paul W. R., van Noorden, Cornelis J. F., Lok, Christianne A. R.

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Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study by van Rheenen, Wouter, Diekstra, Frank P, Harschnitz, Oliver, Westeneng, Henk-Jan, van Eijk, Kristel R, Saris, Christiaan G J, Groen, Ewout J N, van Es, Michael A, Blauw, Hylke M, van Vught, Paul W J, Veldink, Jan H, van den Berg, Leonard H

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Diagnosing primary lateral sclerosis: a clinico-pathological study by de Boer, Eva M. J., de Vries, Bálint S., Van Hecke, Wim, Mühlebner, Angelika, Vincken, Koen L., Mol, Christian P., van Rheenen, Wouter, Westeneng, Henk-Jan, Veldink, Jan H., Höglinger, Günter U., Morris, Huw R., Litvan, Irene, Raaphorst, Joost, Ticozzi, Nicola, Corcia, Philippe, Vandenberghe, Wim, Pijnenburg, Yolande A. L., Seelaar, Harro, Ingre, Caroline, Van Damme, Philip, van den Berg, Leonard H., van de Warrenburg, Bart P. C., van Es, Michael A.

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Evidence for an oligogenic basis of amyotrophic lateral sclerosis by BLITTERSWIJK, Marka Van, ES, Michael A. Van, DE BAKKER, Paul I. W, VELDINK, Jan H, DEN BERG, Leonard H. Van, HENNEKAM, Eric A. M, DOOIJES, Dennis, RHEENEN, Wouter Van, MEDIC, Jelena, BOURQUE, Pierre R, SCHELHAAS, Helenius J, DER KOOI, Anneke J. Van, DE VISSER, Marianne

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UNC13A is a modifier of survival in amyotrophic lateral sclerosis by Diekstra, Frank P, van Vught, Paul W.J, van Rheenen, Wouter, Koppers, Max, Pasterkamp, R. Jeroen, van Es, Michael A, Schelhaas, Helenius J, de Visser, Marianne, Robberecht, Wim, Van Damme, Philip, Andersen, Peter M, van den Berg, Leonard H, Veldink, Jan H

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Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS by Hop, Paul J., Zwamborn, Ramona A. J., Hannon, Eilis, Shireby, Gemma L., Nabais, Marta F., Walker, Emma M., van Rheenen, Wouter, Westeneng, Henk-Jan, Tazelaar, Gijs H. P., Deelen, Joris, van Heemst, Diana, van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Bert A., Isaacs, Aaron, Uitterlinden, Andre G., van Eijk, Kristel R., van Meurs, Joyce, Suchiman, H. Eka D., Verkerk, Marijn, van Rooij, Jeroen, Lakenberg, Nico, Mei, Hailiang, van Iterson, Maarten, Moisse, Matthieu, van Galen, Michiel, Bot, Jan, Zhernakova, Dasha V., Jansen, Rick, van ‘t Hof, Peter, Deelen, Patrick, Nooren, Irene, t Hoen, Peter A. C., Heijmans, Bastiaan T., Baird, Denis, Franke, Lude, Vermaat, Martijn, Luijk, Rene, Jan Bonder, Marc, van Dijk, Freerk, Arindrarto, Wibowo, Al Khleifat, Ahmad, Swertz, Morris A., van Zwet, Erik W., Al-Chalabi, Ammar, Wray, Naomi R., Bensimon, Gilbert, Hardiman, Orla, Iacoangeli, Alfredo, Chio, Adriano, Mill, Jonathan, Ticozzi, Nicola, Ratti, Antonia, Cooper-Knock, Jonathan, Morrison, Karen E., Shaw, Pamela J., Basak, A. Nazli, Chiò, Adriano, Moglia, Cristina, Brunetti, Maura, Grassano, Maurizio, Gotkine, Marc, Lerner, Yossef, Zabari, Michal, Corcia, Philippe, Couratier, Philippe, Henderson, Robert D., Mathers, Susan, Needham, Merrilee, Nicholson, Garth, Rowe, Dominic B., Pamphlett, Roger, Mather, Karen A., Sachdev, Perminder S., Furlong, Sarah, Henders, Anjali K., Ngo, Shyuan T., Steyn, Frederik J., Williams, Kelly L., Cauchi, Ruben J., Blair, Ian P., Pinto, Susana, Weber, Markus, Silani, Vincenzo, Landers, John E., Shaw, Christopher E., van Es, Michael A., Pasterkamp, R. Jeroen, McLaughlin, Russell L., Kenna, Kevin P., Tsai, Ellen, Runz, Heiko, Van Damme, Philip, Boomsma, Dorret I., Pool, Rene, van Dongen, Jenny, Hottenga, Joukje J., Stehouwer, Coen D.A., van der Kallen, Carla J.H., Tigchelaar, Ettje F.

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Evidence for an oligogenic basis of amyotrophic lateral sclerosis by van Blitterswijk, Marka, van Es, Michael A, Hennekam, Eric A M, Dooijes, Dennis, van Rheenen, Wouter, Medic, Jelena, Bourque, Pierre R, Schelhaas, Helenius J, van der Kooi, Anneke J, de Visser, Marianne, de Bakker, Paul I W, Veldink, Jan H, van den Berg, Leonard H

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways by Cirulli, Elizabeth T., Lasseigne, Brittany N., Petrovski, Slavé, Sapp, Peter C., Dion, Patrick A., Leblond, Claire S., Couthouis, Julien, Lu, Yi-Fan, Wang, Quanli, Krueger, Brian J., Ren, Zhong, Keebler, Jonathan, Han, Yujun, Levy, Shawn E., Boone, Braden E., Wimbish, Jack R., Waite, Lindsay L., Jones, Angela L., Carulli, John P., Day-Williams, Aaron G., Staropoli, John F., Xin, Winnie W., Chesi, Alessandra, Raphael, Alya R., McKenna-Yasek, Diane, Cady, Janet, de Jong, J. M. B. Vianney, Kenna, Kevin P., Smith, Bradley N., Topp, Simon, Miller, Jack, Gkazi, Athina, Al-Chalabi, Ammar, van den Berg, Leonard H., Veldink, Jan, Silani, Vincenzo, Ticozzi, Nicola, Shaw, Christopher E., Baloh, Robert H., Appel, Stanley, Simpson, Ericka, Lagier-Tourenne, Clotilde, Pulst, Stefan M., Gibson, Summer, Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Grossman, Murray, Shneider, Neil A., Chung, Wendy K., Ravits, John M., Glass, Jonathan D., Sims, Katherine B., Van Deerlin, Vivianna M., Maniatis, Tom, Hayes, Sebastian D., Ordureau, Alban, Swarup, Sharan, Landers, John, Baas, Frank, Allen, Andrew S., Bedlack, Richard S., Harper, J. Wade, Gitler, Aaron D., Rouleau, Guy A., Brown, Robert, Harms, Matthew B., Cooper, Gregory M., Harris, Tim, Myers, Richard M., Goldstein, David B.

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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS by Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.

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Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis by van Es, Michael A., Schelhaas, Helenius J., van Vught, Paul W. J., Ticozzi, Nicola, Andersen, Peter M., Groen, Ewout J. N., Schulte, Claudia, Blauw, Hylke M., Koppers, Max, Diekstra, Frank P., Fumoto, Katsumi, LeClerc, Ashley Lyn, Keagle, Pamela, Bloem, Bastiaan R., Scheffer, Hans, van Nuenen, Bart F. L., van Blitterswijk, Marka, van Rheenen, Wouter, Wills, Anne-Marie, Lowe, Patrick P., Hu, Guo-fu, Yu, Wenhao, Kishikawa, Hiroko, Wu, David, Folkerth, Rebecca D., Mariani, Claudio, Goldwurm, Stefano, Pezzoli, Gianni, Van Damme, Philip, Lemmens, Robin, Dahlberg, Caroline, Birve, Anna, Fernández-Santiago, Rubén, Waibel, Stefan, Klein, Christine, Weber, Markus, van der Kooi, Anneke J., de Visser, Marianne, Verbaan, Dagmar, van Hilten, Jacobus J., Heutink, Peter, Hennekam, Eric A. M., Cuppen, Edwin, Berg, Daniela, Brown Jr, Robert H., Silani, Vincenzo, Gasser, Thomas, Ludolph, Albert C., Robberecht, Wim, Ophoff, Roel A., Veldink, Jan H., Pasterkamp, R. Jeroen, de Bakker, Paul I. W., Landers, John E., van de Warrenburg, Bart P., van den Berg, Leonard H.

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Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis by Dewan, Ramita, Keagle, Pamela, Bacikova, Dagmar, Soltis, Anthony R., Kost, Jason, Colombrita, Claudia, Lewis, Elizabeth A., Pensato, Viviana, Castellotti, Barbara, McLaughlin, Russell L., Comi, Giacomo P., Ceroni, Mauro, Gagliardi, Stella, van Blitterswijk, Marka, Corrado, Lucia, Sorarù, Gianni, Williams, Kelly L., Morrison, Karen E., Veldink, Jan H., Brown, Robert H., Ambrose, John C., Brittain, H., Elgar, Greg, Halai, Dina, Holman, James E., Jackson, Rob, Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Riesgo-Ferreiro, Pablo, Rogers, Tim, Watters, Sarah A., Arepalli, Sampath, Chiò, Adriano, Dunckley, Travis L., Faghri, Faraz, Feldman, Eva, Floeter, Mary Kay, Gerhard, Glenn, Jansson, Lilja, Kirby, Janine, Mora, Gabriele, Nalls, Mike A., Pulst, Stefan M., Ravits, John M., Renton, Alan E., Robberecht, Wim, Robey, Ian, Dols-Icardo, Oriol, Illán-Gala, Ignacio, Lleó, Alberto, Khoshnood, Behzad, Sorbi, Sandro, Pastor, Pau, Bigio, Eileen H., Black, Sandra E., Brunetti, Maura, Canosa, Antonio, Gan-Or, Ziv, Goate, Alison, Hupalo, Daniel, Infante, Jon, Kaufmann, Horacio, Kim, Ronald C., Krüger, Rejko, Logroscino, Giancarlo, Love, Seth, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Reynolds, Regina H., Scherzer, Clemens R., Serrano, Geidy E., Xiromerisiou, Georgia, Phatnani, Hemali, Kwan, Justin, Broach, James R., Arcila-Londono, Ximena, Malaspina, Andrea, Thompson, Leslie M., Dardiotis, Efthimios, Chandran, Siddharthan, Butovsky, Oleg, Dubnau, Joshua, Harms, Matt, Poss, Mary, Phillips-Cremins, Jennifer, Altschuler, Steven, Hu, Michele T.M., Leigh, P. Nigel, Massey, Luke A., Pavese, Nicola, Vaughan, Jenny, Rowe, James B., Ghidoni, Roberta, Ryten, Mina, Tanaka, Toshiko, Ferrucci, Luigi, Vonsattel, Jean Paul, Landers, John E.

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Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders by Nabais, Marta F, Laws, Simon M, Lin, Tian, Vallerga, Costanza L, Armstrong, Nicola J, Blair, Ian P, Kwok, John B, Mather, Karen A, Mellick, George D, Sachdev, Perminder S, Wallace, Leanne, Henders, Anjali K, Zwamborn, Ramona A J, Hop, Paul J, Lunnon, Katie, Pishva, Ehsan, Roubroeks, Janou A Y, Soininen, Hilkka, Tsolaki, Magda, Mecocci, Patrizia, Lovestone, Simon, Kłoszewska, Iwona, Vellas, Bruno, Furlong, Sarah, Garton, Fleur C, Henderson, Robert D, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Ngo, Shyuan T, Nicholson, Garth, Pamphlett, Roger, Rowe, Dominic B, Steyn, Frederik J, Williams, Kelly L, Anderson, Tim J, Bentley, Steven R, Dalrymple-Alford, John, Fowder, Javed, Gratten, Jacob, Halliday, Glenda, Hickie, Ian B, Kennedy, Martin, Lewis, Simon J G, Montgomery, Grant W, Pearson, John, Pitcher, Toni L, Silburn, Peter, Zhang, Futao, Visscher, Peter M, Yang, Jian, Stevenson, Anna J, Hillary, Robert F, Marioni, Riccardo E, Harris, Sarah E, Deary, Ian J, Jones, Ashley R, Shatunov, Aleksey, Iacoangeli, Alfredo, van Rheenen, Wouter, van den Berg, Leonard H, Shaw, Pamela J, Shaw, Cristopher E, Morrison, Karen E, Al-Chalabi, Ammar, Veldink, Jan H, Hannon, Eilis, Mill, Jonathan, Wray, Naomi R, McRae, Allan F

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NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis by BLAUW, Hylke M, RHEENEN, Wouter Van, CUPPEN, Edwin, PASTERKAMP, R. Jeroen, ROBBERECHT, Wim, LUDOLPH, Albert C, VELDINK, Jan H, DEN BERG, Leonard H. Van, KOPPERS, Max, VAN DAMME, Philip, WAIBEL, Stefan, LEMMENS, Robin, VUGHT, Paul W. J. Van, MEYER, Thomas, SCHULTE, Claudia, GASSER, Thomas

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Responsiveness and Minimal Important Change of the IKDC of Middle-Aged and Older Patients With a Meniscal Tear by Noorduyn, Julia C.A., van de Graaf, Victor A., Mokkink, Lidwine B., Willigenburg, Nienke W., Poolman, Rudolf W., Scholtes, Vanessa A.B., Butter, Ise, Mutsaerts, Eduard L.A.R., Wolkenfelt, Julius, Krijnen, Matthijs R., van Deurzen, Derek F.P., Moojen, Dirk Jan F., Bloembergen, Coen H., Nijland, Olivier J.F., de Gast, Arthur, Snijders, Thom, Halma, Jelle J., Saris, Daniel B.F., Wolterbeek, Nienke, Neeter, Camille, Kerkhoffs, Gino M.M.J., Peters, Rolf W., van den Brand, Igor C.J.B., de Vos-Jakobs, Suzanne, Spoor, Andy B., Gosens, Taco, Rezaie, Wahid, Hofstee, Dirk Jan, Burger, Bart J., Haverkamp, Daniel, Vervest, Anton M.J.S., van Rheenen, Thijs A., Wijsbek, Anne E., van Arkel, Ewoud R.A., Thomassen, Bregje J.W., Sprague, Sheila, Mol, Ben Willem J., van Tulder, Maurits W.

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H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis by van Rheenen, Wouter, Diekstra, Frank P, van Doormaal, Perry T.C, Seelen, Meinie, Kenna, Kevin, McLaughlin, Russell, Shatunov, Aleksey, Czell, David, van Es, Michael A, van Vught, Paul W.J, van Damme, Philip, Smith, Bradley N, Waibel, Stefan, Schelhaas, H. Jurgen, van der Kooi, Anneke J, de Visser, Marianne, Weber, Markus, Robberecht, Wim, Hardiman, Orla, Shaw, Pamela J, Shaw, Christopher E, Morrison, Karen E, Al-Chalabi, Ammar, Andersen, Peter M, Ludolph, Albert C, Veldink, Jan H, van den Berg, Leonard H

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Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy by Schijven, Dick, Stevelink, Remi, McCormack, Mark, van Rheenen, Wouter, Luykx, Jurjen J., Koeleman, Bobby P.C., Veldink, Jan H.

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