Citations 236

C9ORF72 hexanucleotide repeat expansions in patients with ALS from the Coriell Cell Repository

Neurology | July 20, 2012 | Volume: 79 | Issue: 5 | Pages: 482-483

10.1212/wnl.0b013e31826170f1 | PMID 22815561

P4‐155: Longitudinal gray and white matter changes in progranulin mutation carriers at risk for FTD: A VBM study

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_19 | Pages: No page available

10.1016/j.jalz.2012.05.1859

O4‐04‐01: Differentiating clinicopathologic and genetic aspects of hippocampal sclerosis in Alzheimer's disease from limbic predominant Alzheimer's disease and “pure” hippocampal sclerosis

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_17 | Pages: No page available

10.1016/j.jalz.2012.05.1652

P1‐178: Anteromedial temporal lobe DTI and structural MRI changes in presymptomatic and symptomatic MAPT mutation carriers

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_5 | Pages: No page available

10.1016/j.jalz.2012.05.456

IC‐P‐134: Anteromedial temporal lobe diffusion tensor imaging and structural MRI changes in presymptomatic and symptomatic microtubule‐associated protein tau (MAPT) mutation carriers

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_2 | Pages: No page available

10.1016/j.jalz.2012.05.168

O1‐05‐06: Characterization of frontotemporal dementia +/‐ amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

Alzheimer's & Dementia | July 19, 2012 | Volume: 8 | Issue: 4S_Part_3 | Pages: No page available

10.1016/j.jalz.2012.05.2129

Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin

Neurology | April 5, 2012 | Volume: 78 | Issue: 16 | Pages: 1245-1249

10.1212/wnl.0b013e318251594c | PMID 22491866

A yeast functional screen predicts new candidate ALS disease genes

Proceedings of the National Academy of Sciences | November 8, 2011 | Volume: 108 | Issue: 52 | Pages: 20881-20890

10.1073/pnas.1109434108 | PMID 22065782

Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and FUS, that harbor prion-like domains, cause some forms of ALS. There are at least 213 human proteins harboring RNA recognition motifs, including FUS and TDP-43, raising the possibility that additional RNA-binding proteins might contribute to ALS pathogenesis. We performed a systematic survey of these proteins to find additional candidates similar to TDP-43 and FUS, followed by bioinformatics to predict prion-like domains in a subset of them. We sequenced one of these genes, TAF15 , in patients with ALS and identified missense variants, which were absent in a large number of healthy controls. These disease-associated variants of TAF15 caused formation of cytoplasmic foci when expressed in primary cultures of spinal cord neurons. Very similar to TDP-43 and FUS, TAF15 aggregated in vitro and conferred neurodegeneration in Drosophila , with the ALS-linked variants having a more severe effect than wild type. Immunohistochemistry of postmortem spinal cord tissue revealed mislocalization of TAF15 in motor neurons of patients with ALS. We propose that aggregation-prone RNA-binding proteins might contribute very broadly to ALS pathogenesis and the genes identified in our yeast functional screen, coupled with prion-like domain prediction analysis, now provide a powerful resource to facilitate ALS disease gene discovery.
Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

Neurology | September 1, 2011 | Volume: 77 | Issue: 11 | Pages: 1102-1103

10.1212/wnl.0b013e31822e563c | PMID 21880997

Altered functional connectivity in asymptomatic MAPT subjects

Neurology | August 22, 2011 | Volume: 77 | Issue: 9 | Pages: 866-874

10.1212/wnl.0b013e31822c61f2 | PMID 21849646