165 related articles for article (PubMed ID: 21392527)
1. Using case-parent trios to look for rare de novo genetic variants in adult-onset neurodegenerative diseases.
Pamphlett R; Morahan JM; Yu B
J Neurosci Methods; 2011 Apr; 197(2):297-301. PubMed ID: 21392527
[TBL] [Abstract][Full Text] [Related]
2. Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis.
Pamphlett R; Morahan JM; Luquin N; Yu B
Muscle Nerve; 2011 Oct; 44(4):492-8. PubMed ID: 21826678
[TBL] [Abstract][Full Text] [Related]
3. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
Blauw HM; Veldink JH; van Es MA; van Vught PW; Saris CG; van der Zwaag B; Franke L; Burbach JP; Wokke JH; Ophoff RA; van den Berg LH
Lancet Neurol; 2008 Apr; 7(4):319-26. PubMed ID: 18313986
[TBL] [Abstract][Full Text] [Related]
4. Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.
Steinberg KM; Yu B; Koboldt DC; Mardis ER; Pamphlett R
Sci Rep; 2015 Mar; 5():9124. PubMed ID: 25773295
[TBL] [Abstract][Full Text] [Related]
5. A genome-wide analysis of brain DNA methylation identifies new candidate genes for sporadic amyotrophic lateral sclerosis.
Morahan JM; Yu B; Trent RJ; Pamphlett R
Amyotroph Lateral Scler; 2009; 10(5-6):418-29. PubMed ID: 19922134
[TBL] [Abstract][Full Text] [Related]
6. Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.
Cronin S; Blauw HM; Veldink JH; van Es MA; Ophoff RA; Bradley DG; van den Berg LH; Hardiman O
Hum Mol Genet; 2008 Nov; 17(21):3392-8. PubMed ID: 18689356
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Priebe L; Degenhardt FA; Herms S; Haenisch B; Mattheisen M; Nieratschker V; Weingarten M; Witt S; Breuer R; Paul T; Alblas M; Moebus S; Lathrop M; Leboyer M; Schreiber S; Grigoroiu-Serbanescu M; Maier W; Propping P; Rietschel M; Nöthen MM; Cichon S; Mühleisen TW
Mol Psychiatry; 2012 Apr; 17(4):421-32. PubMed ID: 21358712
[TBL] [Abstract][Full Text] [Related]
8. Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.
Takahashi Y; Seki N; Ishiura H; Mitsui J; Matsukawa T; Kishino A; Onodera O; Aoki M; Shimozawa N; Murayama S; Itoyama Y; Suzuki Y; Sobue G; Nishizawa M; Goto J; Tsuji S
Arch Neurol; 2008 Oct; 65(10):1326-32. PubMed ID: 18852346
[TBL] [Abstract][Full Text] [Related]
9. Whole-genome association studies of sporadic amyotrophic lateral sclerosis: are retroelements involved?
Mougeot JL; Richardson-Milazi S; Brooks BR
Trends Mol Med; 2009 Apr; 15(4):148-58. PubMed ID: 19332388
[TBL] [Abstract][Full Text] [Related]
10. Transmission of C9orf72 hexanucleotide repeat expansions in sporadic amyotrophic lateral sclerosis: an Australian trio study.
Pamphlett R; Cheong PL; Trent RJ; Yu B
Neuroreport; 2012 Jun; 23(9):556-9. PubMed ID: 22564974
[TBL] [Abstract][Full Text] [Related]
11. 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
Neurology; 2008 Jul; 71(4):253-9. PubMed ID: 18184915
[TBL] [Abstract][Full Text] [Related]
12. Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
Ghezzi S; Del Bo R; Scarlato M; Nardini M; Carlesi C; Prelle A; Corti S; Mancuso M; Briani C; Siciliano G; Murri L; Bresolin N; Comi GP
Neurobiol Aging; 2009 May; 30(5):842-4. PubMed ID: 17888545
[TBL] [Abstract][Full Text] [Related]
13. A miRNA signature in leukocytes from sporadic amyotrophic lateral sclerosis.
De Felice B; Guida M; Guida M; Coppola C; De Mieri G; Cotrufo R
Gene; 2012 Oct; 508(1):35-40. PubMed ID: 22903028
[TBL] [Abstract][Full Text] [Related]
14. High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
Malhotra D; McCarthy S; Michaelson JJ; Vacic V; Burdick KE; Yoon S; Cichon S; Corvin A; Gary S; Gershon ES; Gill M; Karayiorgou M; Kelsoe JR; Krastoshevsky O; Krause V; Leibenluft E; Levy DL; Makarov V; Bhandari A; Malhotra AK; McMahon FJ; Nöthen MM; Potash JB; Rietschel M; Schulze TG; Sebat J
Neuron; 2011 Dec; 72(6):951-63. PubMed ID: 22196331
[TBL] [Abstract][Full Text] [Related]
15. Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Belzil VV; Daoud H; St-Onge J; Desjarlais A; Bouchard JP; Dupre N; Lacomblez L; Salachas F; Pradat PF; Meininger V; Camu W; Dion PA; Rouleau GA
Amyotroph Lateral Scler; 2011 Mar; 12(2):113-7. PubMed ID: 21261515
[TBL] [Abstract][Full Text] [Related]
16. Fast detection of de novo copy number variants from SNP arrays for case-parent trios.
Scharpf RB; Beaty TH; Schwender H; Younkin SG; Scott AF; Ruczinski I
BMC Bioinformatics; 2012 Dec; 13():330. PubMed ID: 23234608
[TBL] [Abstract][Full Text] [Related]
17. Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre study.
Sabatelli M; Lattante S; Conte A; Marangi G; Luigetti M; Del Grande A; Chiò A; Corbo M; Giannini F; Mandrioli J; Mora G; Calvo A; Restagno G; Lunetta C; Penco S; Battistini S; Zeppilli P; Bizzarro A; Capoluongo E; Neri G; Rossini PM; Zollino M
Amyotroph Lateral Scler; 2012 Oct; 13(6):580-4. PubMed ID: 22873564
[TBL] [Abstract][Full Text] [Related]
18. ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.
Gellera C; Ticozzi N; Pensato V; Nanetti L; Castucci A; Castellotti B; Lauria G; Taroni F; Silani V; Mariotti C
Neurobiol Aging; 2012 Aug; 33(8):1847.e15-21. PubMed ID: 22425256
[TBL] [Abstract][Full Text] [Related]
19. Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis.
McLaughlin RL; Kenna KP; Vajda A; Bede P; Elamin M; Cronin S; Donaghy CG; Bradley DG; Hardiman O
Neurobiol Aging; 2015 Feb; 36(2):1221.e7-13. PubMed ID: 25442119
[TBL] [Abstract][Full Text] [Related]
20. Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
van Blitterswijk M; van Vught PW; van Es MA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 May; 33(5):1016.e1-7. PubMed ID: 21802176
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
