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Year Number of Results
1979 1
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2002 2
2003 4
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2005 2
2006 1
2007 2
2008 4
2009 7
2010 9
2011 11
2012 6
2013 13
2014 11
2015 12
2016 12
2017 17
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2019 11
2020 12
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2022 15
2023 11
2024 2

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170 results

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Page 1
Genetic variability in sporadic amyotrophic lateral sclerosis.
Van Daele SH, Moisse M, van Vugt JJFA, Zwamborn RAJ, van der Spek R, van Rheenen W, Van Eijk K, Kenna K, Corcia P, Vourc'h P, Couratier P, Hardiman O, McLaughin R, Gotkine M, Drory V, Ticozzi N, Silani V, Ratti A, de Carvalho M, Mora Pardina JS, Povedano M, Andersen PM, Weber M, Başak NA, Shaw C, Shaw PJ, Morrison KE, Landers JE, Glass JD, van Es MA, van den Berg LH, Al-Chalabi A, Veldink J, Van Damme P. Van Daele SH, et al. Among authors: vourc h p. Brain. 2023 Sep 1;146(9):3760-3769. doi: 10.1093/brain/awad120. Brain. 2023. PMID: 37043475 Free PMC article.
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker AM, Gawor K, Westeneng HJ, Tazelaar GHP, van Eijk KR, Kooyman M, Byrne RP, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith BN, Gromicho M, Chandran S, Pal S, Morrison KE, Shaw PJ, Hardy J, Orrell RW, Sendtner M, Meyer T, Başak N, van der Kooi AJ, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chiò A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh RH, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora Pardina JS, Assialioui A, Rojas-García R, Dion PA, Ross JP, Ludolph AC, Weishaupt JH, Brenner D, Freischmidt A, Bensimon G, Brice A, Durr A, Payan CAM, Saker-Delye S, Wood NW, Topp S, Rademakers R, Tittmann L, Lieb W, Franke A, Ripke S, Braun A, Kraft J, Whiteman DC, Olsen CM, Uitterlinden AG, Hofman A, Rietschel … See abstract for full author list ➔ van Rheenen W, et al. Among authors: vourc h p. Nat Genet. 2021 Dec;53(12):1636-1648. doi: 10.1038/s41588-021-00973-1. Epub 2021 Dec 6. Nat Genet. 2021. PMID: 34873335 Free PMC article.
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.
Hop PJ, Zwamborn RAJ, Hannon E, Shireby GL, Nabais MF, Walker EM, van Rheenen W, van Vugt JJFA, Dekker AM, Westeneng HJ, Tazelaar GHP, van Eijk KR, Moisse M, Baird D, Al Khleifat A, Iacoangeli A, Ticozzi N, Ratti A, Cooper-Knock J, Morrison KE, Shaw PJ, Basak AN, Chiò A, Calvo A, Moglia C, Canosa A, Brunetti M, Grassano M, Gotkine M, Lerner Y, Zabari M, Vourc'h P, Corcia P, Couratier P, Mora Pardina JS, Salas T, Dion P, Ross JP, Henderson RD, Mathers S, McCombe PA, Needham M, Nicholson G, Rowe DB, Pamphlett R, Mather KA, Sachdev PS, Furlong S, Garton FC, Henders AK, Lin T, Ngo ST, Steyn FJ, Wallace L, Williams KL; BIOS Consortium; Brain MEND Consortium; Neto MM, Cauchi RJ, Blair IP, Kiernan MC, Drory V, Povedano M, de Carvalho M, Pinto S, Weber M, Rouleau GA, Silani V, Landers JE, Shaw CE, Andersen PM, McRae AF, van Es MA, Pasterkamp RJ, Wray NR, McLaughlin RL, Hardiman O, Kenna KP, Tsai E, Runz H, Al-Chalabi A, van den Berg LH, Van Damme P, Mill J, Veldink JH. Hop PJ, et al. Among authors: vourc h p. Sci Transl Med. 2022 Feb 23;14(633):eabj0264. doi: 10.1126/scitranslmed.abj0264. Epub 2022 Feb 23. Sci Transl Med. 2022. PMID: 35196023 Free PMC article.
Time for optimism in amyotrophic lateral sclerosis.
Corcia P, Lunetta C, Vourc'h P, Pradat PF, Blasco H. Corcia P, et al. Among authors: vourc h p. Eur J Neurol. 2023 May;30(5):1459-1464. doi: 10.1111/ene.15738. Epub 2023 Feb 23. Eur J Neurol. 2023. PMID: 36773012 Review.
Treatment of hereditary amyotrophic lateral sclerosis.
Corcia P, Blasco H, Beltran S, Piegay AS, Vourc'h P. Corcia P, et al. Among authors: vourc h p. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):54-60. doi: 10.1016/j.neurol.2022.09.001. Epub 2022 Nov 3. Rev Neurol (Paris). 2023. PMID: 36336493 Review.
Genetics of amyotrophic lateral sclerosis.
Corcia P, Couratier P, Blasco H, Andres CR, Beltran S, Meininger V, Vourc'h P. Corcia P, et al. Among authors: vourc h p. Rev Neurol (Paris). 2017 May;173(5):254-262. doi: 10.1016/j.neurol.2017.03.030. Epub 2017 Apr 25. Rev Neurol (Paris). 2017. PMID: 28449881 Review.
The future of ALS might move towards Genetic Therapy.
Corcia P, Couratier P, Vourc'h P. Corcia P, et al. Among authors: vourc h p. Rev Neurol (Paris). 2021 Jun;177(6):613-614. doi: 10.1016/j.neurol.2021.01.007. Epub 2021 Mar 26. Rev Neurol (Paris). 2021. PMID: 33775441 No abstract available.
Primary Lateral Sclerosis: Clinical, radiological and molecular features.
Bede P, Pradat PF, Lope J, Vourc'h P, Blasco H, Corcia P. Bede P, et al. Among authors: vourc h p. Rev Neurol (Paris). 2022 Mar;178(3):196-205. doi: 10.1016/j.neurol.2021.04.008. Epub 2021 Jul 6. Rev Neurol (Paris). 2022. PMID: 34243936 Free article. Review.
InFUSing antisense oligonucleotides for treating ALS.
Codron P, Cassereau J, Vourc'h P. Codron P, et al. Among authors: vourc h p. Trends Mol Med. 2022 Apr;28(4):253-254. doi: 10.1016/j.molmed.2022.02.006. Epub 2022 Mar 1. Trends Mol Med. 2022. PMID: 35246398
170 results