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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.
5 matches for
Wan E.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Wain LV,
Shrine N,
Artigas MS,
Erzurumluoglu AM,
Noyvert B,
Bossini-Castillo L,
Obeidat M,
Henry AP,
Portelli MA,
Hall RJ,
Billington CK,
Rimington TL
and 94 more — show all
Fenech AG,
John C,
Blake T,
Jackson VE,
Allen RJ,
Prins BP,
Campbell A,
Porteous DJ,
Jarvelin MR,
Wielscher M,
James AL,
Hui J,
Wareham NJ,
Zhao JH,
Wilson JF,
Joshi PK,
Stubbe B,
Rawal R,
Schulz H,
Imboden M,
Probst-Hensch NM,
Karrasch S,
Gieger C,
Deary IJ,
Harris SE,
Marten J,
Rudan I,
Enroth S,
Gyllensten U,
Kerr SM,
Polasek O,
Kähönen M,
Surakka I,
Vitart V,
Hayward C,
Lehtimäki T,
Raitakari OT,
Evans DM,
Henderson AJ,
Pennell CE,
Wang CA,
Sly PD,
Wan ES,
Busch R,
Hobbs BD,
Litonjua AA,
Sparrow DW,
Gulsvik A,
Bakke PS,
Crapo JD,
Beaty TH,
Hansel NN,
Mathias RA,
Ruczinski I,
Barnes KC,
Bossé Y,
Joubert P,
van den Berge M,
Brandsma CA,
Paré PD,
Sin DD,
Nickle DC,
Hao K,
Gottesman O,
Dewey FE,
Bruse SE,
Carey DJ,
Kirchner HL,
Jonsson S,
Thorleifsson G,
Jonsdottir I,
Gislason T,
Stefansson K,
Schurmann C,
Nadkarni G,
Bottinger EP,
Loos RJ,
Walters RG,
Chen Z,
Millwood IY,
Vaucher J,
Kurmi OP,
Li L,
Hansell AL,
Brightling C,
Zeggini E,
Cho MH,
Silverman EK,
Sayers I,
Trynka G,
Morris AP,
Strachan DP,
Hall IP,
Tobin MD
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 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
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
Higbee DH,
Lirio A,
Hamilton F,
Granell R,
Wyss AB,
London SJ,
Bartz TM,
Gharib SA,
Cho MH,
Wan E,
Silverman E,
Crapo JD
and 33 more — show all
Lominchar JVT,
Hansen T,
Grarup N,
Dantoft T,
Kårhus L,
Linneberg A,
O'Connor GT,
Dupuis J,
Xu H,
De Vries MM,
Hu X,
Rich SS,
Barr RG,
Manichaikul A,
Wijnant SRA,
Brusselle GG,
Lahousse L,
Li X,
Hernández Cordero AI,
Obeidat M,
Sin DD,
Harris SE,
Redmond P,
Taylor AM,
Cox SR,
Williams AT,
Shrine N,
John C,
Guyatt AL,
Hall IP,
Davey Smith G,
Tobin MD,
Dodd JW
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
New susceptibility loci associated with kidney disease in type 1 diabetes
Sandholm N,
Salem RM,
McKnight AJ,
Brennan EP,
Forsblom C,
Isakova T,
McKay GJ,
Williams WW,
Sadlier DM,
Mäkinen VP,
Swan EJ,
Palmer C
and 80 more — show all
Boright AP,
Ahlqvist E,
Deshmukh HA,
Keller BJ,
Huang H,
Ahola AJ,
Fagerholm E,
Gordin D,
Harjutsalo V,
He B,
Heikkilä O,
Hietala K,
Kytö J,
Lahermo P,
Lehto M,
Lithovius R,
Osterholm AM,
Parkkonen M,
Pitkäniemi J,
Rosengård-Bärlund M,
Saraheimo M,
Sarti C,
Söderlund J,
Soro-Paavonen A,
Syreeni A,
Thorn LM,
Tikkanen H,
Tolonen N,
Tryggvason K,
Tuomilehto J,
Wadén J,
Gill GV,
Prior S,
Guiducci C,
Mirel DB,
Taylor A,
Hosseini SM,
Parving HH,
Rossing P,
Tarnow L,
Ladenvall C,
Alhenc-Gelas F,
Lefebvre P,
Rigalleau V,
Roussel R,
Tregouet DA,
Maestroni A,
Maestroni S,
Falhammar H,
Gu T,
Möllsten A,
Cimponeriu D,
Ioana M,
Mota M,
Mota E,
Serafinceanu C,
Stavarachi M,
Hanson RL,
Nelson RG,
Kretzler M,
Colhoun HM,
Panduru NM,
Gu HF,
Brismar K,
Zerbini G,
Hadjadj S,
Marre M,
Groop L,
Lajer M,
Bull SB,
Waggott D,
Paterson AD,
Savage DA,
Bain SC,
Martin F,
Hirschhorn JN,
Godson C,
Florez JC,
Groop PH,
Maxwell AP
DCCT/EDIC Research Group
PLoS genetics · 2012 · PMID 23028342 · open access
2 pages
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
Emami NC,
Cavazos TB,
Rashkin SR,
Cario CL,
Graff RE,
Tai CG,
Mefford JA,
Kachuri L,
Wan E,
Wong S,
Aaronson D,
Presti J
and 14 more — show all
Habel LA,
Shan J,
Ranatunga DK,
Chao CR,
Ghai NR,
Jorgenson E,
Sakoda LC,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Hoffmann TJ,
Van Den Eeden SK,
Witte JS
Cancer research · 2021 · PMID 33293427
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.