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Items: 29

1.

Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.

Czyz W, Morahan JM, Ebers GC, Ramagopalan SV.

BMC Med. 2012 Aug 17;10:93. doi: 10.1186/1741-7015-10-93. Review.

2.

Epstein-Barr virus, latitude and multiple sclerosis.

Disanto G, Pakpoor J, Morahan JM, Hall C, Meier UC, Giovannoni G, Ramagopalan SV.

Mult Scler. 2013 Mar;19(3):362-5. doi: 10.1177/1352458512451942. Epub 2012 Jul 5.

PMID:
22767435
3.

Month of birth, vitamin D and risk of immune-mediated disease: a case control study.

Disanto G, Chaplin G, Morahan JM, Giovannoni G, Hyppönen E, Ebers GC, Ramagopalan SV.

BMC Med. 2012 Jul 6;10:69. doi: 10.1186/1741-7015-10-69.

4.

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.

Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV.

Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27.

5.

Vitamin D receptor binding, chromatin states and association with multiple sclerosis.

Disanto G, Sandve GK, Berlanga-Taylor AJ, Ragnedda G, Morahan JM, Watson CT, Giovannoni G, Ebers GC, Ramagopalan SV.

Hum Mol Genet. 2012 Aug 15;21(16):3575-86. doi: 10.1093/hmg/dds189. Epub 2012 May 16.

6.

Multiple sclerosis: risk factors and their interactions.

Disanto G, Morahan JM, Ramagopalan SV.

CNS Neurol Disord Drug Targets. 2012 Aug;11(5):545-55. Review.

PMID:
22583442
7.

Seasonal distribution of psychiatric births in England.

Disanto G, Morahan JM, Lacey MV, DeLuca GC, Giovannoni G, Ebers GC, Ramagopalan SV.

PLoS One. 2012;7(4):e34866. doi: 10.1371/journal.pone.0034866. Epub 2012 Apr 4.

8.

The evidence for a role of B cells in multiple sclerosis.

Disanto G, Morahan JM, Barnett MH, Giovannoni G, Ramagopalan SV.

Neurology. 2012 Mar 13;78(11):823-32. doi: 10.1212/WNL.0b013e318249f6f0. Review.

9.

Genomic regions associated with multiple sclerosis are active in B cells.

Disanto G, Sandve GK, Berlanga-Taylor AJ, Morahan JM, Dobson R, Giovannoni G, Ramagopalan SV.

PLoS One. 2012;7(3):e32281. doi: 10.1371/journal.pone.0032281. Epub 2012 Mar 2.

10.

Functional analysis of missense variants in the TRESK (KCNK18) K channel.

Andres-Enguix I, Shang L, Stansfeld PJ, Morahan JM, Sansom MS, Lafrenière RG, Roy B, Griffiths LR, Rouleau GA, Ebers GC, Cader ZM, Tucker SJ.

Sci Rep. 2012;2:237. doi: 10.1038/srep00237. Epub 2012 Jan 27.

11.

Rare variants in the CYP27B1 gene are associated with multiple sclerosis.

Ramagopalan SV, Dyment DA, Cader MZ, Morrison KM, Disanto G, Morahan JM, Berlanga-Taylor AJ, Handel A, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC.

Ann Neurol. 2011 Dec;70(6):881-6. doi: 10.1002/ana.22678.

PMID:
22190362
12.

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
13.

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
14.

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
15.

Vitamin D and multiple sclerosis hospital admissions in Scotland.

Disanto G, Handel AE, Morahan JM, Deluca GC, Kimball SM, Hypponen E, Giovannoni G, Ebers GC, Ramagopalan SV.

QJM. 2011 Nov;104(11):1001-3. doi: 10.1093/qjmed/hcr101. Epub 2011 Jun 29. No abstract available.

16.

Epigenetic mechanisms in multiple sclerosis and the major histocompatibility complex (MHC).

Burrell AM, Handel AE, Ramagopalan SV, Ebers GC, Morahan JM.

Discov Med. 2011 Mar;11(58):187-96. Review.

17.

Comment on "Epigenetic reduction in invariant NKT cells following in utero vitamin D deficiency in mice".

Disanto G, Handel AE, Morahan JM, Ramagopalan SV.

J Immunol. 2011 Apr 1;186(7):3803-4. doi: 10.4049/jimmunol.1190005. No abstract available.

18.

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
19.

Heterogeneity in multiple sclerosis: scratching the surface of a complex disease.

Disanto G, Berlanga AJ, Handel AE, Para AE, Burrell AM, Fries A, Handunnetthi L, De Luca GC, Morahan JM.

Autoimmune Dis. 2010 Dec 9;2011:932351. doi: 10.4061/2011/932351.

20.

A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution.

Ramagopalan SV, Heger A, Berlanga AJ, Maugeri NJ, Lincoln MR, Burrell A, Handunnetthi L, Handel AE, Disanto G, Orton SM, Watson CT, Morahan JM, Giovannoni G, Ponting CP, Ebers GC, Knight JC.

Genome Res. 2010 Oct;20(10):1352-60. doi: 10.1101/gr.107920.110. Epub 2010 Aug 24.

21.

The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

Handel AE, Handunnetthi L, Berlanga AJ, Watson CT, Morahan JM, Ramagopalan SV.

PLoS One. 2010 Apr 13;5(4):e10142. doi: 10.1371/journal.pone.0010142.

22.

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
23.

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.

Wills AM, Cronin S, Slowik A, Kasperaviciute D, Van Es MA, Morahan JM, Valdmanis PN, Meininger V, Melki J, Shaw CE, Rouleau GA, Fisher EM, Shaw PJ, Morrison KE, Pamphlett R, Van den Berg LH, Figlewicz DA, Andersen PM, Al-Chalabi A, Hardiman O, Purcell S, Landers JE, Brown RH Jr.

Neurology. 2009 Jul 7;73(1):16-24. doi: 10.1212/WNL.0b013e3181a18674. Epub 2009 Mar 25.

24.

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
25.

Genetic susceptibility to environmental toxicants in ALS.

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

Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):885-90.

PMID:
17503480
26.

A gene-environment study of the paraoxonase 1 gene and pesticides in amyotrophic lateral sclerosis.

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

Neurotoxicology. 2007 May;28(3):532-40. Epub 2006 Nov 26.

PMID:
17204329
27.

Are metallothionein genes silenced in ALS?

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

Toxicol Lett. 2007 Jan 10;168(1):83-7. Epub 2006 Nov 15.

PMID:
17156946
28.

Amyotrophic lateral sclerosis and exposure to environmental toxins: an Australian case-control study.

Morahan JM, Pamphlett R.

Neuroepidemiology. 2006;27(3):130-5. Epub 2006 Aug 1.

PMID:
16946624
29.

Screening the metallothionein III gene in sporadic amyotrophic lateral sclerosis.

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

Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Jun;6(2):115-7.

PMID:
16036436

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