Whole exome sequencing analysis in severe chronic obstructive pulmonary disease

Dandi Qiao, Asher Ameli, Dmitry Prokopenko, Han Chen, Alvin T. Kho, Margaret M. Parker, Jarrett Morrow, Brian D. Hobbs, Yanhong Liu, Terri H. Beaty, James D. Crapo, Kathleen C. Barnes, Deborah A. Nickerson, Michael Bamshad, Craig P. Hersh, David A. Lomas, Alvar Agusti, Barry J. Make, Peter M. A. Calverley, Claudio F. DonnerEmiel F. Wouters, Jorgen Vestbo, Peter D. Pare, Robert D. Levy, Stephen Rennard, Ruth Tal-Singer, Margaret R. Spitz, Amitabh Sharma, Ingo Ruczinski, Christoph Lange, Edwin K. Silverman, Michael H. Cho

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)3801-3812
Number of pages12
JournalHuman Molecular Genetics
Volume27
Issue number21
DOIs
Publication statusPublished - 1 Nov 2018

Keywords

  • GENOME-WIDE ASSOCIATION
  • GENETIC EPIDEMIOLOGY
  • IDENTIFIES RARE
  • LUNG-FUNCTION
  • LOW-FREQUENCY
  • II RECEPTOR
  • CUTIS LAXA
  • VARIANTS
  • EXPRESSION
  • MUTATIONS

Cite this

Qiao, D., Ameli, A., Prokopenko, D., Chen, H., Kho, A. T., Parker, M. M., Morrow, J., Hobbs, B. D., Liu, Y., Beaty, T. H., Crapo, J. D., Barnes, K. C., Nickerson, D. A., Bamshad, M., Hersh, C. P., Lomas, D. A., Agusti, A., Make, B. J., Calverley, P. M. A., ... Cho, M. H. (2018). Whole exome sequencing analysis in severe chronic obstructive pulmonary disease. Human Molecular Genetics, 27(21), 3801-3812. https://doi.org/10.1093/hmg/ddy269