Yazar Araması Sonucu :: UTM Library Massive Scholar Tracking

1

No association between gluten sensitivity and amyotrophic lateral sclerosis Yazar: Visser, A, Pazoki, R, Pulit, S, van Rheenen, W, Raaphorst, J, van der Kooi, A, Ricaño-Ponce, I, Wijmenga, C, Otten, H, Veldink, J, van den Berg, L

Baskı/Yayın Bilgisi 2017

Journal article
2

Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. Yazar: Es, V, Van Vught, P, Veldink, J, Andersen, P, Birve, A, Lemmens, R, Cronin, S, Van Der Kooi, A, Visser, MD, Schelhaas, H, Hardiman, O, Ragoussis, I, Lambrechts, D, Robberecht, W, Wokke, J, Ophoff, R, Van Den Berg, L

Baskı/Yayın Bilgisi 2009

Journal article
3

Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. Yazar: Es, V, Van Vught, P, Veldink, J, Andersen, P, Birve, A, Lemmens, R, Cronin, S, Van Der Kooi, A, De Visser, M, Schelhaas, H, Hardiman, O, Ragoussis, I, Lambrechts, D, Robberecht, W, Wokke, J, Ophoff, R, Van Den Berg, L

Baskı/Yayın Bilgisi 2009

Journal article
4

Controversies and priorities in amyotrophic lateral sclerosis. Yazar: Turner, M, Hardiman, O, Benatar, M, Brooks, B, Chio, A, de Carvalho, M, Ince, P, Lin, C, Miller, R, Mitsumoto, H, Nicholson, G, Ravits, J, Shaw, P, Swash, M, Talbot, K, Traynor, B, Van den Berg, L, Veldink, J, Vucic, S, Kiernan, M

Baskı/Yayın Bilgisi 2013

Journal article
5

Systematic identification of trans eQTLs as putative drivers of known disease associations. Yazar: Westra, H, Peters, M, Esko, T, Yaghootkar, H, Schurmann, C, Kettunen, J, Christiansen, M, Fairfax, B, Schramm, K, Powell, J, Zhernakova, A, Zhernakova, D, Veldink, J, Van den Berg, L, Karjalainen, J, Withoff, S, Uitterlinden, A, Hofman, A, Rivadeneira, F, 't Hoen, P, Reinmaa, E, Fischer, K, Nelis, M, Milani, L, Melzer, D

Baskı/Yayın Bilgisi 2013

Journal article
6

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. Yazar: Simpson, C, Lemmens, R, Miskiewicz, K, Broom, W, Hansen, V, van Vught, P, Landers, J, Sapp, P, Van Den Bosch, L, Knight, J, Neale, B, Turner, M, Veldink, J, Ophoff, R, Tripathi, V, Beleza, A, Shah, M, Proitsi, P, Van Hoecke, A, Carmeliet, P, Horvitz, H, Leigh, P, Shaw, C, van den Berg, L, Sham, P

Baskı/Yayın Bilgisi 2009

Journal article
7

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation Yazar: Luijk, R, Wu, H, Ward-Caviness, C, Hannon, E, Carnero-Montoro, E, Min, J, Mandaviya, P, Müller-Nurasyid, M, Mei, H, Van Der Maarel, S, BIOS Consortium, Relton, C, Mill, J, Waldenberger, M, Bell, J, Jansen, R, Zhernakova, A, Franke, L, 'T Hoen, P, Boomsma, D, Van Duijn, C, Van Greevenbroek, M, Veldink, J, Wijmenga, C, Van Meurs, J, Daxinger, L, Slagboom, P, Van Zwet, E, Heijmans, B

Baskı/Yayın Bilgisi 2018

Journal article
8

Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis Yazar: Lees, J, Ferwerda, B, Kremer, PHC, Wheeler, N, Serón, M, Croucher, N, Gladstone, R, Bootsma, H, Rots, N, Wijmega-Monsuur, A, Sanders, EAM, Trzciński, K, Wyllie, A, Zwinderman, A, Van Den Berg, L, Van Rheenen, W, Veldink, J, Harboe, Z, Lundbo, L, De Groot, LCPGM, Van Schoor, N, Van Der Velde, N, Ängquist, L, Sørensen, TIA, Nohr, E, Mentzer, A, Mills, T, Knight, JC, Du Plessis, M, Nzenze, S, Weiser, J, Parkhill, J, Madhi, S, Benfield, T, Von Gottberg, A, Van Der Ende, A, Brouwer, M, Barrett, J, Bentley, S, Van De Beek, D

Baskı/Yayın Bilgisi 2019

Journal article
9

Prediction of personalised prognosis in patients with amyotrophic lateral sclerosis: development and validation of a prediction model Yazar: Westeneng, H, Debray, T, Visser, A, van Eijk, R, Rooney, J, Calvo, A, Martin, S, McDermott, C, Thompson, A, Pinto, S, Koboleva, X, Rosenbohm, A, Stubendorff, B, Sommer, H, Middelkoop, B, Dekker, A, van Vugt, J, van Rheenen, W, Vajda, A, Heverin, M, Kazoka, M, Hollinger, H, Gromicho, M, Körner, S, Ringer, T, Rödiger, A, Gunkel, A, Shaw, C, Bredenoord, A, Es, v, Corcia, P, Couratier, P, Weber, M, Grosskreutz, J, Ludolph, A, Petri, S, de Carvalho, M, Van Damme, P, Talbot, K, Turner, M, Shaw, P, Al-Chalabi, A, Chiò, A, Hardiman, O, Moons, K, Veldink, J, van den Berg, L

Baskı/Yayın Bilgisi 2018

Journal article
10

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis Yazar: Fogh, I, Lin, K, Tiloca, C, Rooney, J, Gellera, C, Diekstra, F, Ratti, A, Shatunov, A, Es, V, Proitsi, P, Jones, A, Sproviero, W, Chiò, A, McLaughlin, R, Sorarù, G, Corrado, L, Stahl, D, Del Bo, R, Cereda, C, Castellotti, B, Glass, J, Newhouse, S, Dobson, R, Smith, B, Topp, S, Van Rheenen, W, Meininger, V, Melki, J, Morrison, K, Shaw, P, Leigh, P, Andersen, P, Comi, G, Ticozzi, N, Mazzini, L, D'Alfonso, S, Traynor, B, Van Damme, P, Robberecht, W, Brown, R, Landers, J, Hardiman, O, Lewis, C, Van Den Berg, L, Shaw, C, Veldink, J, Silani, V, Al-Chalabi, A, Powell, J

Baskı/Yayın Bilgisi 2016

Journal article
11

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis Yazar: Kenna, P, van Doormaal PTC, P, Dekker, A, Ticozzi, N, Kenna, B, Diekstra, F, van Rheenen, W, van Eijk, K, Jones, A, Keagle, P, Shatunov, A, Sproviero, W, Smith, B, van Es, M, Topp, S, Kenna, A, Miller, J, Fallini, C, Tiloca, C, McLaughlin, R, Vance, C, Troakes, C, Colombrita, C, Mora, G, Calvo, A, Verde, F, Al-Sarraj, S, King, A, Calini, D, de Belleroche, J, Baas, F, van der Kooi, A, de Visser, M, ten Asbroek, A, Sapp, P, McKenna-Yasek, D, Polak, M, Asress, S, Munoz-Blanco, J, SLAGEN Consortium, Lauria, G, Williams, K, Leigh, P, Nicholson, G, Blair, I, Leblond, C, Dion, P, Rouleau, G, Pall, H, Shaw, P, Turner, M, Talbot, K, Taroni, F, Boylan, K, Van Blitterswijk, M, Rademakers, R, Esteban-Perez, J, Garcia-Redondo, A, Van Damme, P, Robberecht, W, Chio, A, Gellera, C, Drepper, C, Sendtner, M, Ratti, A, Glass, J, Mora, J, Basak, A, Hardiman, O, Ludolph, A, Andersen, P, Wesihaupt, J, Brown, R, Al-Chalabi, A, Silani, V, Shaw, C, van den Berg, L, Veldink, J, Landers, J

Baskı/Yayın Bilgisi 2016

Journal article