Publications by authors named "Danielle Moreno"

22Publications

DNA methylation age acceleration is associated with ALS age of onset and survival.

Acta Neuropathol 2020 05 7;139(5):943-946. Epub 2020 Mar 7.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Ave., Toronto, ON, M5T 2S8, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00401-020-02131-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181538PMC
May 2020

Interaction of APOE4 alleles and PET tau imaging in former contact sport athletes.

Neuroimage Clin 2020 13;26:102212. Epub 2020 Feb 13.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard avenue, Toronto, ON M5T 0S8, Canada; Institute of Medical Science, University of Toronto, 1 King's College Circle, Toronto, ON, M5S 1A8, Canada; Division of Neurology, Toronto Western Hospital, University Health Network, 399 Bathurst St., Toronto, ON, M5T 2S8, Canada; Canadian Concussion Center, Toronto Western Hospital, Krembil Neuroscience Centre, University Health Network, 399 Bathurst St., Toronto, ON, M5T 2S8, Canada. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nicl.2020.102212DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037542PMC
February 2020

Unaffected mosaic case: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.

Neurology 2018 01 27;90(4):e323-e331. Epub 2017 Dec 27.

From the Tanz Centre for Research in Neurodegenerative Diseases (P.M., M.Z., C.S., D.M., S.X., A.B.Z., P.M.M., A.W., R.S., J.R., E.R.), Department of Medicine (L.Z., E.R.), Division of Neurology, and Department of Laboratory Medicine and Pathobiology (J.R.), University of Toronto, Ontario, Canada; Department of Neuroscience (M.v.B., L.P., R.R.), Mayo Clinic, Jacksonville, FL; and Sunnybrook Health Sciences Centre (J.K., L.Z.), Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000004865DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5798652PMC
January 2018

DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patients.

Acta Neuropathol 2017 08 24;134(2):271-279. Epub 2017 Apr 24.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Ave., Toronto, ON, M5T 2S8, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00401-017-1713-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508035PMC
August 2017

C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism.

Mov Disord 2017 01 7;32(1):158-162. Epub 2016 Nov 7.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.26841DOI Listing
January 2017

Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.

J Neurol Neurosurg Psychiatry 2016 11 6;87(11):1268-1270. Epub 2016 May 6.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1136/jnnp-2016-313592DOI Listing
November 2016

Novel GRN Mutations in Patients with Corticobasal Syndrome.

Sci Rep 2016 Mar 10;6:22913. Epub 2016 Mar 10.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard avenue, Toronto, ON M5T 2S8, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/srep22913DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785496PMC
March 2016

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.

Neurobiol Aging 2016 Feb 6;38:217.e7-217.e8. Epub 2015 Nov 6.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada; Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2015.10.038DOI Listing
February 2016

Mutation analysis of C9orf72 in patients with corticobasal syndrome.

Neurobiol Aging 2015 Oct 12;36(10):2905.e1-5. Epub 2015 Jun 12.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada; Division of Neurology, University Health Network Memory Clinic, Toronto, Ontario, Canada. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S01974580150031
Publisher Site
http://dx.doi.org/10.1016/j.neurobiolaging.2015.06.008DOI Listing
October 2015

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Brain 2015 Sep 31;138(Pt 9):e380. Epub 2015 Mar 31.

1 Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Street, Toronto, Ontario, Canada, M5T 2S8 8 Department of Medicine, Division of Neurology, University of Toronto, Toronto, Ontario, Canada M5S 1A8

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awv082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547051PMC
September 2015

Identical twins with the C9orf72 repeat expansion are discordant for ALS.

Neurology 2014 Oct 10;83(16):1476-8. Epub 2014 Sep 10.

From the Tanz Centre for Research in Neurodegenerative Diseases (Z.X., S.D., M.G., D.M., C.S., Y.L., J.R., E.R.) and Division of Neurology (L.Z., E.R.), University of Toronto (Y.Y.); Sunnybrook Health Sciences Centre (Y.Y., L.Z.), Toronto, Canada; Mayo Clinic (M.v.B., R.R.), Jacksonville, FL; and the Laboratory of Neurogenetics (A.S.), National Institute on Aging, Bethesda, MD.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000000886DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206161PMC
October 2014

Mutation analysis of patients with neurodegenerative disorders using NeuroX array.

Neurobiol Aging 2015 Jan 1;36(1):545.e9-14. Epub 2014 Aug 1.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada; Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S01974580140050
Publisher Site
http://dx.doi.org/10.1016/j.neurobiolaging.2014.07.038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268030PMC
January 2015

Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patients.

Hum Mol Genet 2014 Nov 6;23(21):5630-7. Epub 2014 Jun 6.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 60 Leonard Street, Toronto, Ontario, Canada M5T 2S8, Department of Medicine, Division of Neurology, University of Toronto, 1 King's College Circle, Toronto, Ontario, Canada M5S 1A8 and

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddu279DOI Listing
November 2014

Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity.

JAMA Neurol 2013 Oct;70(10):1261-7

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada4Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaneurol.2013.3545DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991012PMC
October 2013

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion.

Am J Hum Genet 2013 Jun 23;92(6):981-9. Epub 2013 May 23.

Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 6 Queen's Park Crescent West, Toronto, ON M5S 3H2, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2013.04.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675239PMC
June 2013

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.

Mov Disord 2008 Jan;23(2):290-4

Movement Disorders Unit, Neurology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, PR, Brazil.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.21832DOI Listing
January 2008