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% 4 entries, in the order the page lists them. Built from alzhub.org's own records.
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@article{majounie2012-22406228,
  author  = {Majounie, E. and Renton, A. E. and Mok, K. and Dopper, E. G. and Waite, A. and Rollinson, S. and Chiò, A. and Restagno, G. and others},
  title   = {{Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study}},
  journal = {The Lancet. Neurology},
  year    = {2012},
  doi     = {10.1016/s1474-4422(12)70043-1},
  pmid    = {22406228},
  url     = {https://doi.org/10.1016/s1474-4422(12)70043-1}
}

@article{renton2011-21944779,
  author  = {Renton, A. E. and Majounie, E. and Waite, A. and Simón-Sánchez, J. and Rollinson, S. and Gibbs, JR. and Schymick, J. C. and Laaksovirta, H. and others},
  title   = {{A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD}},
  journal = {Neuron},
  year    = {2011},
  doi     = {10.1016/j.neuron.2011.09.010},
  pmid    = {21944779},
  url     = {https://doi.org/10.1016/j.neuron.2011.09.010}
}

@article{johnson2010-21145000,
  author  = {Johnson, J. O. and Mandrioli, J. and Benatar, M. and Abramzon, Y. and Van Deerlin, V. M. and Trojanowski, J. Q. and Gibbs, JR. and Brunetti, M. and others},
  title   = {{Exome sequencing reveals VCP mutations as a cause of familial ALS}},
  journal = {Neuron},
  year    = {2010},
  doi     = {10.1016/j.neuron.2010.11.036},
  pmid    = {21145000},
  url     = {https://doi.org/10.1016/j.neuron.2010.11.036}
}

@article{johnson2014-24686783,
  author  = {Johnson, J. O. and Pioro, E. P. and Boehringer, A. and Chia, R. and Feit, H. and Renton, A. E. and Pliner, H. A. and Abramzon, Y. and others},
  title   = {{Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis}},
  journal = {Nature neuroscience},
  year    = {2014},
  doi     = {10.1038/nn.3688},
  pmid    = {24686783},
  url     = {https://doi.org/10.1038/nn.3688}
}