Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort-Reference-Cited by-同舟云学术

Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort

Published:2017-06-12 Issue:4 Volume:5 Page:418-428
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Garton Fleur C.¹²^ORCID,Benyamin Beben¹²,Zhao Qiongyi¹,Liu Zhijun¹²,Gratten Jacob¹²,Henders Anjali K.¹²,Zhang Zong-Hong¹,Edson Janette¹,Furlong Sarah¹,Morgan Sarah³⁴,Heggie Susan⁵,Thorpe Kathryn⁵,Pfluger Casey⁵,Mather Karen A.⁶,Sachdev Perminder S.⁶⁷,McRae Allan F.¹²,Robinson Matthew R.¹²,Shah Sonia¹,Visscher Peter M.¹²⁸,Mangelsdorf Marie¹,Henderson Robert D.⁹,Wray Naomi R.¹²,McCombe Pamela A.⁵

Affiliation:

1. Queensland Brain Institute; The University of Queensland; St Lucia Queensland 4072 Australia

2. Institute for Molecular Bioscience; The University of Queensland; St Lucia Queensland 4072 Australia

3. Reta Lila Weston Institute; UCL Institute of Neurology; London UK

4. Department of Molecular Neuroscience; UCL Institute of Neurology; London UK

5. UQ Centre for Clinical Research; The University of Queensland; Royal Brisbane & Women's Hospital; Brisbane 4029 Australia

6. Centre for Healthy Brain Ageing; School of Psychiatry; Faculty of Medicine; The University of New South Wales; Sydney New South Wales 2052 Australia

7. Neuropsychiatric Institute; Prince of Wales Hospital; Randwick New South Wales Australia

8. University of Queensland Diamantina Institute; Translational Research Institute; Brisbane Queensland 4012 Australia

9. Department of Neurology; Royal Brisbane & Women's Hospital; Brisbane 4029 Australia

Funder

Motor Neurone Disease Research Institute of Australia

Ross Maclean Fellowship

National Health and Medical Research Council

Peter Goodenough Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference51 articles.

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2. Credibility analysis of putative disease-causing genes using bioinformatics;Abel;PLoS One,2013

3. Utility of whole exome sequencing in evaluation of juvenile motor neuron disease;Agarwal;Muscle Nerve,2016

4. Use of genetic testing in amyotrophic lateral sclerosis by neurologists;Arthur;JAMA Neurol.,2017

5. Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland;Bansagi;J. Neurol.,2015

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