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. Donner; Emiel 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

doi:10.1093/hmg/ddy269

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^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	3801-3812
Number of pages	12
Journal	Human Molecular Genetics
Volume	27
Issue number	21
DOIs	https://doi.org/10.1093/hmg/ddy269
Publication status	Published - 1 Nov 2018

Keywords

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

Access to Document

10.1093/hmg/ddy269

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

Qiao, Dandi ; Ameli, Asher ; Prokopenko, Dmitry ; Chen, Han ; Kho, Alvin T. ; Parker, Margaret M. ; Morrow, Jarrett ; Hobbs, Brian D. ; Liu, Yanhong ; Beaty, Terri H. ; Crapo, James D. ; Barnes, Kathleen C. ; Nickerson, Deborah A. ; Bamshad, Michael ; Hersh, Craig P. ; Lomas, David A. ; Agusti, Alvar ; Make, Barry J. ; Calverley, Peter M. A. ; Donner, Claudio F. ; Wouters, Emiel F. ; Vestbo, Jorgen ; Pare, Peter D. ; Levy, Robert D. ; Rennard, Stephen ; Tal-Singer, Ruth ; Spitz, Margaret R. ; Sharma, Amitabh ; Ruczinski, Ingo ; Lange, Christoph ; Silverman, Edwin K. ; Cho, Michael H. / Whole exome sequencing analysis in severe chronic obstructive pulmonary disease. In: Human Molecular Genetics. 2018 ; Vol. 27, No. 21. pp. 3801-3812.

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title = "Whole exome sequencing analysis in severe chronic obstructive pulmonary disease",

keywords = "GENOME-WIDE ASSOCIATION, GENETIC EPIDEMIOLOGY, IDENTIFIES RARE, LUNG-FUNCTION, LOW-FREQUENCY, II RECEPTOR, CUTIS LAXA, VARIANTS, EXPRESSION, MUTATIONS",

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

year = "2018",

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day = "1",

doi = "10.1093/hmg/ddy269",

language = "English",

volume = "27",

pages = "3801--3812",

journal = "Human Molecular Genetics",

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Qiao, D, Ameli, A, Prokopenko, D, Chen, H, Kho, AT, Parker, MM, Morrow, J, Hobbs, BD, Liu, Y, Beaty, TH, Crapo, JD, Barnes, KC, Nickerson, DA, Bamshad, M, Hersh, CP, Lomas, DA, Agusti, A, Make, BJ, Calverley, PMA, Donner, CF, Wouters, EF, Vestbo, J, Pare, PD, Levy, RD, Rennard, S, Tal-Singer, R, Spitz, MR, Sharma, A, Ruczinski, I, Lange, C, Silverman, EK & Cho, MH 2018, 'Whole exome sequencing analysis in severe chronic obstructive pulmonary disease', Human Molecular Genetics, vol. 27, no. 21, pp. 3801-3812. https://doi.org/10.1093/hmg/ddy269

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

In: Human Molecular Genetics, Vol. 27, No. 21, 01.11.2018, p. 3801-3812.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - Whole exome sequencing analysis in severe chronic obstructive pulmonary disease

AU - Qiao, Dandi

AU - Ameli, Asher

AU - Prokopenko, Dmitry

AU - Chen, Han

AU - Kho, Alvin T.

AU - Parker, Margaret M.

AU - Morrow, Jarrett

AU - Hobbs, Brian D.

AU - Liu, Yanhong

AU - Beaty, Terri H.

AU - Crapo, James D.

AU - Barnes, Kathleen C.

AU - Nickerson, Deborah A.

AU - Bamshad, Michael

AU - Hersh, Craig P.

AU - Lomas, David A.

AU - Agusti, Alvar

AU - Make, Barry J.

AU - Calverley, Peter M. A.

AU - Donner, Claudio F.

AU - Wouters, Emiel F.

AU - Vestbo, Jorgen

AU - Pare, Peter D.

AU - Levy, Robert D.

AU - Rennard, Stephen

AU - Tal-Singer, Ruth

AU - Spitz, Margaret R.

AU - Sharma, Amitabh

AU - Ruczinski, Ingo

AU - Lange, Christoph

AU - Silverman, Edwin K.

AU - Cho, Michael H.

PY - 2018/11/1

Y1 - 2018/11/1

KW - GENOME-WIDE ASSOCIATION

KW - GENETIC EPIDEMIOLOGY

KW - IDENTIFIES RARE

KW - LUNG-FUNCTION

KW - LOW-FREQUENCY

KW - II RECEPTOR

KW - CUTIS LAXA

KW - VARIANTS

KW - EXPRESSION

KW - MUTATIONS

U2 - 10.1093/hmg/ddy269

DO - 10.1093/hmg/ddy269

M3 - Article

C2 - 30060175

VL - 27

SP - 3801

EP - 3812

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 21

ER -