Matt Baker

发表

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

Wen-Lang Lin, John Hardy, Peter Davies, 2000, Nature Genetics.

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Ronald C. Petersen, Frank Owen, Stanley Fahn, 1998, Nature.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

Richard J Caselli, John V Pearson, Irene Litvan, 2007, American journal of human genetics.

Detection of long repeat expansions from PCR-free whole-genome sequence data

Chris Shaw, Giuseppe Narzisi, Aleksey Shatunov, 2016, bioRxiv.

SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia

Owen A. Ross, Dennis W. Dickson, A. Jon Stoessl, 2013, neurogenetics.

Detection of long repeat expansions from PCR-free whole-genome sequence data

Aleksey Shatunov, Egor Dolzhenko, Joke J.F.A. van Vugt, 2016 .

TYROBP genetic variants in early-onset Alzheimer's disease

Ronald C. Petersen, Guojun Bu, Cyril Pottier, 2016, Neurobiology of Aging.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

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.

C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic.

Dennis W Dickson, D. Dickson, S. Younkin, 2012, American journal of neurodegenerative disease.

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.