1.
Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS
by Ash, Peter E.A
Neuron (Cambridge, Mass.), 2013-02-20, Vol.77 (4), p.639-646

2.
Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma
by Carrasquillo, Minerva M
American journal of human genetics, 2010, Vol.87 (6), p.890-897

3.
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion
by Khan, Baber K
Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.358-364

4.
Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked frontotemporal dementia and amyotrophic lateral sclerosis
by DeJesus-Hernandez, Mariely Mariely
Neuron (Cambridge, Mass.), 2011-09-21, Vol.72 (2), p.245-256

5.
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
by Akimoto, Chizuru
Journal of Medical Genetics, 2014-06, Vol.51 (6), p.419-424

6.
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions inC9orf72reveals marked differences in results among 14 laboratories
by Akimoto, Chizuru
Journal of medical genetics, 2014-06, Vol.51 (6), p.419-424

7.
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region ofC9ORF72Causes Chromosome 9p-Linked FTD and ALS
by Mariely DeJesus-Hernandez
Neuron (Cambridge, Mass.), 2011-10-20, Vol.72 (2), p.245

8.
Expanded van der GCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
by DeJesus-Hernandez, Mariely
Neuron (Cambridge, Mass.), 2011-10-20, Vol.72 (2), p.245-256

9.
Atypical, slowly progressive behavioural variant frontotemporal dementia associated withC9ORF72hexanucleotide expansion
by Khan, Baber K
Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.358-364

10.
Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C90RF72 hexanucleotide expansion
by KHAN, Baber K
Journal of neurology, neurosurgery and psychiatry, 2012, Vol.83 (4), p.358-364
