For researchers
Is your paper here?
2,663 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
8 matches for
COPDGene Investigators.
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry
Lutz SM,
Cho MH,
Young K,
Hersh CP,
Castaldi PJ,
McDonald ML,
Regan E,
Mattheisen M,
DeMeo DL,
Parker M,
Foreman M,
Make BJ
and 12 more — show all
Jensen RL,
Casaburi R,
Lomas DA,
Bhatt SP,
Bakke P,
Gulsvik A,
Crapo JD,
Beaty TH,
Laird NM,
Lange C,
Hokanson JE,
Silverman EK
ECLIPSE Investigators · COPDGene Investigators
BMC genetics · 2015 · PMID 26634245 · open access
12 pages+
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis
Cho MH,
McDonald ML,
Zhou X,
Mattheisen M,
Castaldi PJ,
Hersh CP,
Demeo DL,
Sylvia JS,
Ziniti J,
Laird NM,
Lange C,
Litonjua AA
and 17 more — show all
Sparrow D,
Casaburi R,
Barr RG,
Regan EA,
Make BJ,
Hokanson JE,
Lutz S,
Dudenkov TM,
Farzadegan H,
Hetmanski JB,
Tal-Singer R,
Lomas DA,
Bakke P,
Gulsvik A,
Crapo JD,
Silverman EK,
Beaty TH
NETT Genetics, ICGN, ECLIPSE and COPDGene Investigators
The Lancet. Respiratory medicine · 2014 · PMID 24621683
3 pages
A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes
Cho MH,
Castaldi PJ,
Hersh CP,
Hobbs BD,
Barr RG,
Tal-Singer R,
Bakke P,
Gulsvik A,
San José Estépar R,
Van Beek EJ,
Coxson HO,
Lynch DA
and 5 more — show all
NETT Genetics, ECLIPSE, and COPDGene Investigators
American journal of respiratory and critical care medicine · 2015 · PMID 26030696
3 pages
A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease
Hardin M,
Cho MH,
McDonald ML,
Wan E,
Lomas DA,
Coxson HO,
MacNee W,
Vestbo J,
Yates JC,
Agusti A,
Calverley PM,
Celli B
and 13 more — show all
Crim C,
Rennard S,
Wouters E,
Bakke P,
Bhatt SP,
Kim V,
Ramsdell J,
Regan EA,
Make BJ,
Hokanson JE,
Crapo JD,
Beaty TH,
Hersh CP
ECLIPSE and COPDGene Investigators · COPDGene Investigators—clinical centers
The pharmacogenomics journal · 2016 · PMID 26503814 · open access
3 pages
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis
Hobbs BD,
de Jong K,
Lamontagne M,
Bossé Y,
Shrine N,
Artigas MS,
Wain LV,
Hall IP,
Jackson VE,
Wyss AB,
London SJ,
North KE
and 64 more — show all
Franceschini N,
Strachan DP,
Beaty TH,
Hokanson JE,
Crapo JD,
Castaldi PJ,
Chase RP,
Bartz TM,
Heckbert SR,
Psaty BM,
Gharib SA,
Zanen P,
Lammers JW,
Oudkerk M,
Groen HJ,
Locantore N,
Tal-Singer R,
Rennard SI,
Vestbo J,
Timens W,
Paré PD,
Latourelle JC,
Dupuis J,
O'Connor GT,
Wilk JB,
Kim WJ,
Lee MK,
Oh YM,
Vonk JM,
de Koning HJ,
Leng S,
Belinsky SA,
Tesfaigzi Y,
Manichaikul A,
Wang XQ,
Rich SS,
Barr RG,
Sparrow D,
Litonjua AA,
Bakke P,
Gulsvik A,
Lahousse L,
Brusselle GG,
Stricker BH,
Uitterlinden AG,
Ampleford EJ,
Bleecker ER,
Woodruff PG,
Meyers DA,
Qiao D,
Lomas DA,
Yim JJ,
Kim DK,
Hawrylkiewicz I,
Sliwinski P,
Hardin M,
Fingerlin TE,
Schwartz DA,
Postma DS,
MacNee W,
Tobin MD,
Silverman EK,
Boezen HM,
Cho MH
COPDGene Investigators · ECLIPSE Investigators and 5 more consortia
Nature genetics · 2017 · PMID 28166215
2 pages
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease
McDonald ML,
Cho MH,
Sørheim IC,
Lutz SM,
Castaldi PJ,
Lomas DA,
Coxson HO,
Edwards LD,
MacNee W,
Vestbo J,
Yates JC,
Agusti A
and 19 more — show all
Calverley PM,
Celli B,
Crim C,
Rennard SI,
Wouters EF,
Bakke P,
Tal-Singer R,
Miller BE,
Gulsvik A,
Casaburi R,
Wells JM,
Regan EA,
Make BJ,
Hokanson JE,
Lange C,
Crapo JD,
Beaty TH,
Silverman EK,
Hersh CP
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators
American journal of respiratory cell and molecular biology · 2014 · PMID 24825563
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.