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Results: 1 to 20 of 92

Similar articles for PubMed (Select 21826678)

1.

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. doi: 10.1002/mus.22095. Epub 2011 Aug 8.

PMID:
21826678
2.

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 Oct-Dec;10(5-6):418-29. doi: 10.3109/17482960802635397.

PMID:
19922134
3.

Copy number imbalances in blood and hair in monozygotic twins discordant for amyotrophic lateral sclerosis.

Pamphlett R, Morahan JM.

J Clin Neurosci. 2011 Sep;18(9):1231-4. doi: 10.1016/j.jocn.2010.12.049. Epub 2011 Jul 7.

PMID:
21741244
4.

An approach to finding brain-situated mutations in sporadic Parkinson's disease.

Pamphlett R, Morahan JM, Luquin N, Yu B.

Parkinsonism Relat Disord. 2012 Jan;18(1):82-5. doi: 10.1016/j.parkreldis.2011.08.024. Epub 2011 Sep 13.

PMID:
21917499
5.

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 30;197(2):297-301. doi: 10.1016/j.jneumeth.2011.02.028. Epub 2011 Mar 15.

PMID:
21392527
6.

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

Wain LV, Pedroso I, Landers JE, Breen G, Shaw CE, Leigh PN, Brown RH, Tobin MD, Al-Chalabi A.

PLoS One. 2009 Dec 4;4(12):e8175. doi: 10.1371/journal.pone.0008175.

7.

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. doi: 10.1016/S1474-4422(08)70048-6. Epub 2008 Mar 3.

PMID:
18313986
8.

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 1;17(21):3392-8. doi: 10.1093/hmg/ddn233. Epub 2008 Aug 7.

9.

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 15;508(1):35-40. doi: 10.1016/j.gene.2012.07.058. Epub 2012 Aug 8.

PMID:
22903028
10.

Germline copy number variations in BRCA1-associated ovarian cancer patients.

Yoshihara K, Tajima A, Adachi S, Quan J, Sekine M, Kase H, Yahata T, Inoue I, Tanaka K.

Genes Chromosomes Cancer. 2011 Mar;50(3):167-77. doi: 10.1002/gcc.20841. Epub 2010 Dec 7.

PMID:
21213370
11.

SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis.

Wang XB, Cui NH, Gao JJ, Qiu XP, Zheng F.

J Neurol Sci. 2014 May 15;340(1-2):63-8. doi: 10.1016/j.jns.2014.02.026. Epub 2014 Feb 28.

PMID:
24630593
12.

Integrative gene-tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis.

Kudo LC, Parfenova L, Vi N, Lau K, Pomakian J, Valdmanis P, Rouleau GA, Vinters HV, Wiedau-Pazos M, Karsten SL.

Hum Mol Genet. 2010 Aug 15;19(16):3233-53. doi: 10.1093/hmg/ddq232. Epub 2010 Jun 8.

13.

Copy number variation in schizophrenia in the Japanese population.

Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N.

Biol Psychiatry. 2010 Feb 1;67(3):283-6. doi: 10.1016/j.biopsych.2009.08.034. Epub 2009 Oct 31.

PMID:
19880096
14.

A large genome scan for rare CNVs in amyotrophic lateral sclerosis.

Blauw HM, Al-Chalabi A, Andersen PM, van Vught PW, Diekstra FP, van Es MA, Saris CG, Groen EJ, van Rheenen W, Koppers M, Van't Slot R, Strengman E, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Kiemeney LA, Vermeulen SH, Birve A, Waibel S, Meyer T, Cronin S, McLaughlin RL, Hardiman O, Sapp PC, Tobin MD, Wain LV, Tomik B, Slowik A, Lemmens R, Rujescu D, Schulte C, Gasser T, Brown RH Jr, Landers JE, Robberecht W, Ludolph AC, Ophoff RA, Veldink JH, van den Berg LH.

Hum Mol Genet. 2010 Oct 15;19(20):4091-9. doi: 10.1093/hmg/ddq323. Epub 2010 Aug 4.

15.

A genome wide association study between copy number variation (CNV) and human height in Chinese population.

Li X, Tan L, Liu X, Lei S, Yang T, Chen X, Zhang F, Fang Y, Guo Y, Zhang L, Yan H, Pan F, Zhang Z, Peng Y, Zhou Q, He L, Zhu X, Cheng J, Zhang L, Liu Y, Tian Q, Deng H.

J Genet Genomics. 2010 Dec;37(12):779-85. doi: 10.1016/S1673-8527(09)60095-3.

PMID:
21193156
16.

An analysis of the entire SOD1 gene in sporadic ALS.

Luquin N, Yu B, Trent RJ, Morahan JM, Pamphlett R.

Neuromuscul Disord. 2008 Jul;18(7):545-52. doi: 10.1016/j.nmd.2008.04.013. Epub 2008 May 27.

PMID:
18504130
17.

Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis.

Luquin N, Yu B, Saunderson RB, Trent RJ, Pamphlett R.

Neuromuscul Disord. 2009 Oct;19(10):696-700. doi: 10.1016/j.nmd.2009.07.005. Epub 2009 Aug 19.

PMID:
19695877
18.

Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.

Hochstenbach R, Buizer-Voskamp JE, Vorstman JA, Ophoff RA.

Cytogenet Genome Res. 2011;135(3-4):174-202. doi: 10.1159/000332928. Epub 2011 Nov 2. Review.

PMID:
22056632
19.

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. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1.

PMID:
21358712
20.

Rare copy number variants are a common cause of short stature.

Zahnleiter D, Uebe S, Ekici AB, Hoyer J, Wiesener A, Wieczorek D, Kunstmann E, Reis A, Doerr HG, Rauch A, Thiel CT.

PLoS Genet. 2013;9(3):e1003365. doi: 10.1371/journal.pgen.1003365. Epub 2013 Mar 14.

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