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Amyotrophic Lateral Sclerosis Volume 10, 2009 - Issue 5-6
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Original Article

Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis

Michael A. Van Es Department of Neurology
,
Paul W. J. Van Vught Department of Neurology
,
Jan H. Veldink Department of Neurology
,
Peter M. Andersen Institute of Clinical Neuroscience, Umeå University Hospital, Umeå, Sweden
,
Anna Birve Institute of Clinical Neuroscience, Umeå University Hospital, Umeå, Sweden
,
Robin Lemmens Department of Neurology, University Hospital Gasthuisberg, Belgium
,
Simon Cronin Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin, Ireland
,
Anneke J. Van Der Kooi Department of Neurology, Academic Medical Centre, Amsterdam
,
Marianne De Visser Department of Neurology, Academic Medical Centre, Amsterdam
,
Helenius J. Schelhaas Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands
,
Orla Hardiman Department of Neurology, Beaumont Hospital, Dublin, Ireland; Trinity College Institute of Neurosciences, Trinity College, Dublin, Ireland
,
Ioannis Ragoussis The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
,
Diether Lambrechts VIB Vesalius Research Centre, K.U. Leuven, Leuven, Belgium
,
Wim Robberecht Department of Neurology, University Hospital Gasthuisberg, Belgium; VIB Vesalius Research Centre, K.U. Leuven, Leuven, Belgium
,
John H. J. Wokke Department of Neurology
,
Roel A. Ophoff Medical Genetics, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, The Netherlands; Centre for Neurobehavioural Genetics, University of California, Los Angeles, California, USA
&
Leonard H. Van Den Berg Department of NeurologyCorrespondence[email protected]
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Pages 441-447 | Received 15 Sep 2008, Published online: 18 Nov 2009

Citations (13)

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Terry D. Heiman-Patterson, Roger B. Sher, Elizabeth A. Blankenhorn, Guillermo Alexander, Jeffrey S. Deitch, Catherine B. Kunst, Nicholas Maragakis & Gregory Cox. (2011) Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: A window of opportunity in the search for genetic modifiers. Amyotrophic Lateral Sclerosis 12:2, pages 79-86.
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Articles from other publishers (12)

Zeguo Sun, Rui Zhang, Xiao Zhang, Yifei Sun, Pengpeng Liu, Nancy Francoeur, Lei Han, Wan Yee Lam, Zhengzi Yi, Robert Sebra, Martin Walsh, Jinpu Yu & Weijia Zhang. (2022) LINE-1 promotes tumorigenicity and exacerbates tumor progression via stimulating metabolism reprogramming in non-small cell lung cancer. Molecular Cancer 21:1.
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Kelly A. Rich, Jennifer Roggenbuck & Stephen J. Kolb. (2021) Searching Far and Genome-Wide: The Relevance of Association Studies in Amyotrophic Lateral Sclerosis. Frontiers in Neuroscience 14.
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Ruben P. A. van Eijk, Marinus J. C. Eijkemans, Stavros Nikolakopoulos, Marc D. Jansen, Henk-Jan Westeneng, Kristel R. van Eijk, Rick A. A. van der Spek, Joke J. F. A. van Vugt, Sanne Piepers, Geert-Jan Groeneveld, Jan H. Veldink, Leonard H. van den Berg & Michael A. van Es. (2019) Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?. The Pharmacogenomics Journal 20:2, pages 220-226.
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Lianping Xu, Jiao Li, Danyang Tian, Lu Chen, Lu Tang & Dongsheng Fan. (2018) The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population. Frontiers in Aging Neuroscience 10.
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Ruben P.A. van EijkAshley R. JonesWilliam SprovieroAleksey ShatunovPamela J. ShawP. Nigel LeighCarolyn A. YoungChristopher E. ShawGabriele MoraJessica MandrioliGiuseppe BorgheroPaolo VolantiFrank P. DiekstraWouter van RheenenEsther VerstraeteMarinus J.C. EijkemansJan H. VeldinkAdriano ChioAmmar Al-ChalabiLeonard H. van den BergMichael A. van EsC Allen, C Counsell, A Farrin, A Al-Chalabi, B Dickie, J Kelly, P N Leigh, C L Murphy, C Payan, G Reynolds, P Shaw, I N Steen, M Thornhill, J Waters, J Zajicek, P N Leigh, A Al-Chalabi, P J Shaw, C A Young, M Thornhill, I N Steen, C L Murphy, K E Morrison, S Dhariwal, R Hornabrook, L Savage, D J Burn, T K Khoo, J Kelly, C L Murphy, A Al-Chalabi, A Dougherty, P N Leigh, L Wijesekera, M Thornhill, C M Ellis, R Ali, K O'Hanlon, J Panicker, L Pate, P Ray, L Wyatt, C A Young, L Copeland, J Ealing, H Hamdalla, I Leroi, C Murphy, F O'Keeffe, E Oughton, L Partington, P Paterson, D Rog, A Sathish, D Sexton, J Smith, H Vanek, S Dodds, T L Williams, I N Steen, J Clarke, C Eziefula, R Howard, R Orrell, K Sidle, R Sylvester, W Barrett, C Merritt, K Talbot, M R Turner, C Whatley, C Williams, J Williams, C Cosby, C O Hanemann, I Imam, C Phillips, L Timings, S E Crawford, C Hewamadduma, R Hibberd, H Hollinger, C McDermott, G Mills, M Rafiq, P J Shaw, A Taylor, E Waines, T Walsh, R Addison-Jones, J Birt, M Hare, T Majid, R. Tortelli, E. D'Errico, I. Bartolomei, E. Barbarossa, B. Depau, E. Costantino, E. D'Amico, A. Uncini, C. Manzoli, R. Quatrale, E. Sette, E. Montanari, M. Merello, D. Zarcone, M. Mascolo, M. Vignolo, S. Messina, C. Morelli, K. Marinou, L. Papetti, C. Lunetta, K. Gorni, D. De Cicco, C. Pipia, P. Sola, E. Georgoulopoulou, A. Sagnelli, G. Tedeschi, G. Oggioni, N. Nasuelli, C. D'Ascenzo, V. Cima, M. Aiello, R. Rizzi, E. Rinaldi, M. Luigetti, A. Conte, A. Torzini, G. Greco, R. Mutani, G. Fuda & M.A. Tommasi. (2017) Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials. Neurology 89:18, pages 1915-1922.
Crossref
Lianping Xu, Danyang Tian, Jiao Li, Lu Chen, Lu Tang & Dongsheng Fan. (2017) The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis. Frontiers in Aging Neuroscience 9.
Crossref
Charandeep Singh, Enrico Glaab & Carole L. Linster. (2017) Molecular Identification of d-Ribulokinase in Budding Yeast and Mammals. Journal of Biological Chemistry 292:3, pages 1005-1028.
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Ji He, Marie Mangelsdorf, Dongsheng Fan, Perry Bartlett & Matthew A. Brown. (2014) Amyotrophic Lateral Sclerosis Genetic Studies. The Neuroscientist 21:6, pages 599-615.
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Marka van Blitterswijk, Paul W.J. van Vught, Michael A. van Es, Helenius J. Schelhaas, Anneke J. van der Kooi, Marianne de Visser, Jan H. Veldink & Leonard H. van den Berg. (2012) Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients. Neurobiology of Aging 33:5, pages 1016.e1-1016.e7.
Crossref
Frank P. Diekstra, Christiaan G. J. Saris, Wouter van Rheenen, Lude Franke, Ritsert C. Jansen, Michael A. van Es, Paul W. J. van Vught, Hylke M. Blauw, Ewout J. N. Groen, Steve Horvath, Karol Estrada, Fernando Rivadeneira, Albert Hofman, Andre G. Uitterlinden, Wim Robberecht, Peter M. Andersen, Judith Melki, Vincent Meininger, Orla Hardiman, John E. Landers, Robert H. Brown, Aleksey Shatunov, Christopher E. Shaw, P. Nigel Leigh, Ammar Al-Chalabi, Roel A. Ophoff, Leonard H. van den Berg & Jan H. Veldink. (2012) Mapping of Gene Expression Reveals CYP27A1 as a Susceptibility Gene for Sporadic ALS. PLoS ONE 7:4, pages e35333.
Crossref
Lydia Coulter Kwee, Yutao Liu, Carol Haynes, Jason R. Gibson, Annjanette Stone, Steven A. Schichman, Freya Kamel, Lorene M. Nelson, Barbara Topol, Stephen K. Van Den Eeden, Caroline M. Tanner, Merit E. Cudkowicz, Daniela L. Grasso, Robert Lawson, Sumitra Muralidhar, Eugene Z. Oddone, Silke Schmidt & Michael A. Hauser. (2012) A High-Density Genome-Wide Association Screen of Sporadic ALS in US Veterans. PLoS ONE 7:3, pages e32768.
Crossref
Jean-Luc C Mougeot, Zhen Li, Andrea E Price, Fred A Wright & Benjamin R Brooks. (2011) Microarray analysis of peripheral blood lymphocytes from ALS patients and the SAFE detection of the KEGG ALS pathway. BMC Medical Genomics 4:1.
Crossref

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