Mariely DeJesus-Hernandez

How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?

Rosa Rademakers, Marka van Blitterswijk, Mariely DeJesus-Hernandez, 2012, Current opinion in neurology.

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.

Olaf Ansorge, Christian Haass, H. Kretzschmar, 2011, Brain : a journal of neurology.

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.

Allissa Dillman, Ronald C Petersen, Mark R Cookson, 2010, American journal of human genetics.

Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

Bruce L. Miller, William W. Seeley, Adam L. Boxer, 2011, Neuron.