% alzhub.org library filter
% Source: https://alzhub.org/research?author=Baker+M&institution=I4210146710
% 13 entries, in the order the page lists them. Built from alzhub.org's own records.
% 0 entries have no readable author in the source record and carry no author field.

@article{rutherford2008-18802454,
  author  = {Rutherford, N. J. and Zhang, Y. J. and Baker, M. and Gass, J. M. and Finch, N. A. and Xu, Y. F. and Stewart, H. and Kelley, B. J. and others},
  title   = {{Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis}},
  journal = {PLoS genetics},
  year    = {2008},
  doi     = {10.1371/journal.pgen.1000193},
  pmid    = {18802454},
  url     = {https://doi.org/10.1371/journal.pgen.1000193}
}

@article{hutton1998-9641683,
  author  = {Hutton, M. and Lendon, C. L. and Rizzu, P. and Baker, M. and Froelich, S. and Houlden, H. and Pickering-Brown, S. and Chakraverty, S. and others},
  title   = {{Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17}},
  journal = {Nature},
  year    = {1998},
  doi     = {10.1038/31508},
  pmid    = {9641683},
  url     = {https://doi.org/10.1038/31508}
}

@article{rayaprolu2013-23800361,
  author  = {Rayaprolu, S. and Mullen, B. and Baker, M. and Lynch, T. and Finger, E. and Seeley, W. W. and Hatanpaa, K. J. and Lomen-Hoerth, C. and others},
  title   = {{TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease}},
  journal = {Molecular neurodegeneration},
  year    = {2013},
  doi     = {10.1186/1750-1326-8-19},
  pmid    = {23800361},
  url     = {https://doi.org/10.1186/1750-1326-8-19}
}

@article{dejesushernandez2011-21944778,
  author  = {DeJesus-Hernandez, M. and Mackenzie, I. R. and Boeve, B. F. and Boxer, A. L. and Baker, M. and Rutherford, N. J. and Nicholson, A. M. and Finch, N. A. and others},
  title   = {{Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS}},
  journal = {Neuron},
  year    = {2011},
  doi     = {10.1016/j.neuron.2011.09.011},
  pmid    = {21944778},
  url     = {https://doi.org/10.1016/j.neuron.2011.09.011}
}

@article{baker2006-16862116,
  author  = {Baker, M. and Mackenzie, I. R. and Pickering-Brown, S. M. and Gass, J. and Rademakers, R. and Lindholm, C. and Snowden, J. and Adamson, J. and others},
  title   = {{Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17}},
  journal = {Nature},
  year    = {2006},
  doi     = {10.1038/nature05016},
  pmid    = {16862116},
  url     = {https://doi.org/10.1038/nature05016}
}

@article{whitwell2012-22366795,
  author  = {Whitwell, J. L. and Weigand, S. D. and Boeve, B. F. and Senjem, M. L. and Gunter, J. L. and DeJesus-Hernandez, M. and Rutherford, N. J. and Baker, M. and others},
  title   = {{Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics}},
  journal = {Brain : a journal of neurology},
  year    = {2012},
  doi     = {10.1093/brain/aws001},
  pmid    = {22366795},
  url     = {https://doi.org/10.1093/brain/aws001}
}

@article{finch2009-19158106,
  author  = {Finch, N. and Baker, M. and Crook, R. and Swanson, K. and Kuntz, K. and Surtees, R. and Bisceglio, G. and Rovelet-Lecrux, A. and others},
  title   = {{Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members}},
  journal = {Brain : a journal of neurology},
  year    = {2009},
  doi     = {10.1093/brain/awn352},
  pmid    = {19158106},
  url     = {https://doi.org/10.1093/brain/awn352}
}

@article{gass2006-16950801,
  author  = {Gass, J. and Cannon, A. and Mackenzie, I. R. and Boeve, B. and Baker, M. and Adamson, J. and Crook, R. and Melquist, S. and others},
  title   = {{Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration}},
  journal = {Human molecular genetics},
  year    = {2006},
  doi     = {10.1093/hmg/ddl241},
  pmid    = {16950801},
  url     = {https://doi.org/10.1093/hmg/ddl241}
}

@article{mackenzie2017-28817800,
  author  = {Mackenzie, I. R. and Nicholson, A. M. and Sarkar, M. and Messing, J. and Purice, M. D. and Pottier, C. and Annu, K. and Baker, M. and others},
  title   = {{TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics}},
  journal = {Neuron},
  year    = {2017},
  doi     = {10.1016/j.neuron.2017.07.025},
  pmid    = {28817800},
  url     = {https://doi.org/10.1016/j.neuron.2017.07.025}
}

@article{neumann2009-19674978,
  author  = {Neumann, M. and Rademakers, R. and Roeber, S. and Baker, M. and Kretzschmar, H. A. and Mackenzie, I. R.},
  title   = {{A new subtype of frontotemporal lobar degeneration with FUS pathology}},
  journal = {Brain : a journal of neurology},
  year    = {2009},
  doi     = {10.1093/brain/awp214},
  pmid    = {19674978},
  url     = {https://doi.org/10.1093/brain/awp214}
}

@article{rademakers2008-18723524,
  author  = {Rademakers, R. and Eriksen, J. L. and Baker, M. and Robinson, T. and Ahmed, Z. and Lincoln, S. J. and Finch, N. and Rutherford, N. J. and others},
  title   = {{Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia}},
  journal = {Human molecular genetics},
  year    = {2008},
  doi     = {10.1093/hmg/ddn257},
  pmid    = {18723524},
  url     = {https://doi.org/10.1093/hmg/ddn257}
}

@article{murray2011-22083254,
  author  = {Murray, M. E. and DeJesus-Hernandez, M. and Rutherford, N. J. and Baker, M. and Duara, R. and Graff-Radford, N. R. and Wszolek, Z. K. and Ferman, T. J. and others},
  title   = {{Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72}},
  journal = {Acta neuropathologica},
  year    = {2011},
  doi     = {10.1007/s00401-011-0907-y},
  pmid    = {22083254},
  url     = {https://doi.org/10.1007/s00401-011-0907-y}
}

@article{pottier2016-27658901,
  author  = {Pottier, C. and Ravenscroft, T. A. and Brown, P. H. and Finch, N. A. and Baker, M. and Parsons, M. and Asmann, Y. W. and Ren, Y. and others},
  title   = {{TYROBP genetic variants in early-onset Alzheimer's disease}},
  journal = {Neurobiology of aging},
  year    = {2016},
  doi     = {10.1016/j.neurobiolaging.2016.07.028},
  pmid    = {27658901},
  url     = {https://doi.org/10.1016/j.neurobiolaging.2016.07.028}
}