639 related articles for article (PubMed ID: 22645277)
1. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
van Blitterswijk M; van Es MA; Hennekam EA; Dooijes D; van Rheenen W; Medic J; Bourque PR; Schelhaas HJ; van der Kooi AJ; de Visser M; de Bakker PI; Veldink JH; van den Berg LH
Hum Mol Genet; 2012 Sep; 21(17):3776-84. PubMed ID: 22645277
[TBL] [Abstract][Full Text] [Related]
2. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
[TBL] [Abstract][Full Text] [Related]
3. VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient.
van Blitterswijk M; van Es MA; Koppers M; van Rheenen W; Medic J; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Dec; 33(12):2950.e1-4. PubMed ID: 22878164
[TBL] [Abstract][Full Text] [Related]
4. Novel missense and truncating mutations in FUS/TLS in familial ALS.
Waibel S; Neumann M; Rabe M; Meyer T; Ludolph AC
Neurology; 2010 Aug; 75(9):815-7. PubMed ID: 20660363
[TBL] [Abstract][Full Text] [Related]
5. Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.
Zou ZY; Zhou ZR; Che CH; Liu CY; He RL; Huang HP
J Neurol Neurosurg Psychiatry; 2017 Jul; 88(7):540-549. PubMed ID: 28057713
[TBL] [Abstract][Full Text] [Related]
6. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
7. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V
J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center.
Chadi G; Maximino JR; Jorge FMH; Borba FC; Gilio JM; Callegaro D; Lopes CG; Santos SND; Rebelo GNS
Amyotroph Lateral Scler Frontotemporal Degener; 2017 May; 18(3-4):249-255. PubMed ID: 27978769
[TBL] [Abstract][Full Text] [Related]
9. Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease.
Lattante S; Conte A; Zollino M; Luigetti M; Del Grande A; Marangi G; Romano A; Marcaccio A; Meleo E; Bisogni G; Rossini PM; Sabatelli M
Neurology; 2012 Jul; 79(1):66-72. PubMed ID: 22722621
[TBL] [Abstract][Full Text] [Related]
10. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
Tsai CP; Soong BW; Lin KP; Tu PH; Lin JL; Lee YC
Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325
[TBL] [Abstract][Full Text] [Related]
11. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
Kamada M; Maruyama H; Tanaka E; Morino H; Wate R; Ito H; Kusaka H; Kawano Y; Miki T; Nodera H; Izumi Y; Kaji R; Kawakami H
J Neurol Sci; 2009 Sep; 284(1-2):69-71. PubMed ID: 19411082
[TBL] [Abstract][Full Text] [Related]
12. SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience.
Brown JA; Min J; Staropoli JF; Collin E; Bi S; Feng X; Barone R; Cao Y; O'Malley L; Xin W; Mullen TE; Sims KB
Amyotroph Lateral Scler; 2012 Feb; 13(2):217-22. PubMed ID: 22292843
[TBL] [Abstract][Full Text] [Related]
13. FUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish population.
Syriani E; Morales M; Gamez J
Amyotroph Lateral Scler; 2011 Mar; 12(2):118-23. PubMed ID: 21128870
[TBL] [Abstract][Full Text] [Related]
14. Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.
Kwon MJ; Baek W; Ki CS; Kim HY; Koh SH; Kim JW; Kim SH
Neurobiol Aging; 2012 May; 33(5):1017.e17-23. PubMed ID: 22244934
[TBL] [Abstract][Full Text] [Related]
15. Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study.
Debray S; Race V; Crabbé V; Herdewyn S; Matthijs G; Goris A; Dubois B; Thijs V; Robberecht W; Van Damme P
Neurobiol Aging; 2013 Dec; 34(12):2890.e7-2890.e12. PubMed ID: 23870417
[TBL] [Abstract][Full Text] [Related]
16. FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.
Sproviero W; La Bella V; Mazzei R; Valentino P; Rodolico C; Simone IL; Logroscino G; Ungaro C; Magariello A; Patitucci A; Tedeschi G; Spataro R; Condino F; Bono F; Citrigno L; Monsurrò MR; Muglia M; Gambardella A; Quattrone A; Conforti FL
Neurobiol Aging; 2012 Apr; 33(4):837.e1-5. PubMed ID: 22055719
[TBL] [Abstract][Full Text] [Related]
17. C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.
Drepper C; Herrmann T; Wessig C; Beck M; Sendtner M
Neurobiol Aging; 2011 Mar; 32(3):548.e1-4. PubMed ID: 20018407
[TBL] [Abstract][Full Text] [Related]
18. Dissection of genetic factors associated with amyotrophic lateral sclerosis.
Leblond CS; Kaneb HM; Dion PA; Rouleau GA
Exp Neurol; 2014 Dec; 262 Pt B():91-101. PubMed ID: 24780888
[TBL] [Abstract][Full Text] [Related]
19. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
[TBL] [Abstract][Full Text] [Related]
20. Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
Belzil VV; St-Onge J; Daoud H; Desjarlais A; Bouchard JP; Dupré N; Camu W; Dion PA; Rouleau GA
J Hum Genet; 2011 Mar; 56(3):247-9. PubMed ID: 21160488
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
