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% Source: https://alzhub.org/research?atag=sequencing
% 4 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{raghavan2018-30009200,
  author  = {Raghavan, N. S. and Brickman, A. M. and Andrews, H. and Manly, J. J. and Schupf, N. and Lantigua, R. and Wolock, C. J. and Kamalakaran, S. and others},
  title   = {{Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease}},
  journal = {Annals of clinical and translational neurology},
  year    = {2018},
  doi     = {10.1002/acn3.582},
  pmid    = {30009200},
  url     = {https://doi.org/10.1002/acn3.582}
}

@article{naj2019-29857119,
  author  = {Naj, A. C. and Lin, H. and Vardarajan, B. N. and White, S. and Lancour, D. and Ma, Y. and Schmidt, M. and Sun, F. and others},
  title   = {{Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project}},
  journal = {Genomics},
  year    = {2019},
  doi     = {10.1016/j.ygeno.2018.05.004},
  pmid    = {29857119},
  url     = {https://doi.org/10.1016/j.ygeno.2018.05.004}
}

@article{jin2012-22906081,
  author  = {Jin, S. C. and Pastor, P. and Cooper, B. and Cervantes, S. and Benitez, B. A. and Razquin, C. and Goate, A. and {Ibero-American Alzheimer Disease Genetics Group Researchers} and others},
  title   = {{Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort}},
  journal = {Alzheimer's research \& therapy},
  year    = {2012},
  doi     = {10.1186/alzrt137},
  pmid    = {22906081},
  url     = {https://doi.org/10.1186/alzrt137}
}

@article{ebbert2018-30126445,
  author  = {Ebbert, M. T. W. and Farrugia, S. L. and Sens, J. P. and Jansen-West, K. and Gendron, T. F. and Prudencio, M. and McLaughlin, I. J. and Bowman, B. and others},
  title   = {{Long-read sequencing across the C9orf72 'GGGGCC' repeat expansion: implications for clinical use and genetic discovery efforts in human disease}},
  journal = {Molecular neurodegeneration},
  year    = {2018},
  doi     = {10.1186/s13024-018-0274-4},
  pmid    = {30126445},
  url     = {https://doi.org/10.1186/s13024-018-0274-4}
}