Similar articles for PMID: 22118904

Year	Number of Results
1993	1
1994	1
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2003	1
2004	1
2005	5
2006	5
2007	10
2008	12
2009	7
2010	7
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2013	9
2014	8
2015	7
2016	4
2017	7
2018	5
2019	7
2020	4
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2022	5
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2024	0

1

UNC13A is a modifier of survival in amyotrophic lateral sclerosis.

Diekstra FP, van Vught PW, van Rheenen W, Koppers M, Pasterkamp RJ, van Es MA, Schelhaas HJ, de Visser M, Robberecht W, Van Damme P, Andersen PM, van den Berg LH, Veldink JH. Diekstra FP, et al. Neurobiol Aging. 2012 Mar;33(3):630.e3-8. doi: 10.1016/j.neurobiolaging.2011.10.029. Epub 2011 Nov 25. Neurobiol Aging. 2012. PMID: 22118904

2

UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis.

Yang B, Jiang H, Wang F, Li S, Wu C, Bao J, Zhu Y, Xu Z, Liu B, Ren H, Yang X. Yang B, et al. Neurol Sci. 2019 Nov;40(11):2293-2302. doi: 10.1007/s10072-019-03951-y. Epub 2019 Jun 14. Neurol Sci. 2019. PMID: 31201598

3

UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort.

Vidal-Taboada JM, Lopez-Lopez A, Salvado M, Lorenzo L, Garcia C, Mahy N, Rodríguez MJ, Gamez J. Vidal-Taboada JM, et al. J Neurol. 2015 Oct;262(10):2285-92. doi: 10.1007/s00415-015-7843-z. Epub 2015 Jul 11. J Neurol. 2015. PMID: 26162714 Free article.

4

UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study.

Chiò A, Mora G, Restagno G, Brunetti M, Ossola I, Barberis M, Ferrucci L, Canosa A, Manera U, Moglia C, Fuda G, Traynor BJ, Calvo A. Chiò A, et al. Neurobiol Aging. 2013 Jan;34(1):357.e1-5. doi: 10.1016/j.neurobiolaging.2012.07.016. Epub 2012 Aug 22. Neurobiol Aging. 2013. PMID: 22921269 Free PMC article.

5

Progranulin genetic variability contributes to amyotrophic lateral sclerosis.

Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P, van Vught PW, van der Zee J, Serneels S, De Pooter T, Van den Broeck M, Cruts M, Schymkowitz J, De Jonghe P, Rousseau F, van den Berg LH, Robberecht W, Van Broeckhoven C. Sleegers K, et al. Neurology. 2008 Jul 22;71(4):253-9. doi: 10.1212/01.wnl.0000289191.54852.75. Epub 2008 Jan 9. Neurology. 2008. PMID: 18184915

6

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.

van Blitterswijk M, Blokhuis A, van Es MA, van Vught PW, Rowicka PA, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH. van Blitterswijk M, et al. Neurobiol Aging. 2012 Aug;33(8):1845.e1-3. doi: 10.1016/j.neurobiolaging.2012.01.007. Epub 2012 Feb 11. Neurobiol Aging. 2012. PMID: 22330174

7

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

Daoud H, Belzil V, Martins S, Sabbagh M, Provencher P, Lacomblez L, Meininger V, Camu W, Dupré N, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2011 Jun;68(6):739-42. doi: 10.1001/archneurol.2011.111. Arch Neurol. 2011. PMID: 21670397

8

Analysis of the UNC13A gene as a risk factor for sporadic amyotrophic lateral sclerosis.

Daoud H, Belzil V, Desjarlais A, Camu W, Dion PA, Rouleau GA. Daoud H, et al. Arch Neurol. 2010 Apr;67(4):516-7. doi: 10.1001/archneurol.2010.46. Arch Neurol. 2010. PMID: 20385924 No abstract available.

9

Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.

Koppers M, Groen EJ, van Vught PW, van Rheenen W, Witteveen E, van Es MA, Pasterkamp RJ, van den Berg LH, Veldink JH. Koppers M, et al. Neurobiol Aging. 2013 May;34(5):1518.e5-7. doi: 10.1016/j.neurobiolaging.2012.09.018. Epub 2012 Nov 8. Neurobiol Aging. 2013. PMID: 23141412

10

A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient.

Corrado L, Carlomagno Y, Falasco L, Mellone S, Godi M, Cova E, Cereda C, Testa L, Mazzini L, D'Alfonso S. Corrado L, et al. Neurobiol Aging. 2011 Mar;32(3):552.e1-6. doi: 10.1016/j.neurobiolaging.2010.02.011. Epub 2010 Apr 3. Neurobiol Aging. 2011. PMID: 20363051

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