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.
4 matches for
Qian D.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
McKay JD,
Hung RJ,
Han Y,
Zong X,
Carreras-Torres R,
Christiani DC,
Caporaso NE,
Johansson M,
Xiao X,
Li Y,
Byun J,
Dunning A
and 128 more — show all
Pooley KA,
Qian DC,
Ji X,
Liu G,
Timofeeva MN,
Bojesen SE,
Wu X,
Le Marchand L,
Albanes D,
Bickeböller H,
Aldrich MC,
Bush WS,
Tardon A,
Rennert G,
Teare MD,
Field JK,
Kiemeney LA,
Lazarus P,
Haugen A,
Lam S,
Schabath MB,
Andrew AS,
Shen H,
Hong YC,
Yuan JM,
Bertazzi PA,
Pesatori AC,
Ye Y,
Diao N,
Su L,
Zhang R,
Brhane Y,
Leighl N,
Johansen JS,
Mellemgaard A,
Saliba W,
Haiman CA,
Wilkens LR,
Fernandez-Somoano A,
Fernandez-Tardon G,
van der Heijden HFM,
Kim JH,
Dai J,
Hu Z,
Davies MPA,
Marcus MW,
Brunnström H,
Manjer J,
Melander O,
Muller DC,
Overvad K,
Trichopoulou A,
Tumino R,
Doherty JA,
Barnett MP,
Chen C,
Goodman GE,
Cox A,
Taylor F,
Woll P,
Brüske I,
Wichmann HE,
Manz J,
Muley TR,
Risch A,
Rosenberger A,
Grankvist K,
Johansson M,
Shepherd FA,
Tsao MS,
Arnold SM,
Haura EB,
Bolca C,
Holcatova I,
Janout V,
Kontic M,
Lissowska J,
Mukeria A,
Ognjanovic S,
Orlowski TM,
Scelo G,
Swiatkowska B,
Zaridze D,
Bakke P,
Skaug V,
Zienolddiny S,
Duell EJ,
Butler LM,
Koh WP,
Gao YT,
Houlston RS,
McLaughlin J,
Stevens VL,
Joubert P,
Lamontagne M,
Nickle DC,
Obeidat M,
Timens W,
Zhu B,
Song L,
Kachuri L,
Artigas MS,
Tobin MD,
Wain LV,
Rafnar T,
Thorgeirsson TE,
Reginsson GW,
Stefansson K,
Hancock DB,
Bierut LJ,
Spitz MR,
Gaddis NC,
Lutz SM,
Gu F,
Johnson EO,
Kamal A,
Pikielny C,
Zhu D,
Lindströem S,
Jiang X,
Tyndale RF,
Chenevix-Trench G,
Beesley J,
Bossé Y,
Chanock S,
Brennan P,
Landi MT,
Amos CI
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
He Y,
Lu W,
Jee YH,
Shih MY,
Wang Y,
Tsuo K,
Qian DC,
Diao JA,
Huang H,
Patel CJ,
Byun J,
Pasaniuc B
and 6 more — show all
Nature genetics · 2026 · PMID 41565855
12 pages+
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Merkel PA,
Xie G,
Monach PA,
Ji X,
Ciavatta DJ,
Byun J,
Pinder BD,
Zhao A,
Zhang J,
Tadesse Y,
Qian D,
Weirauch M
and 32 more — show all
Nair R,
Tsoi A,
Pagnoux C,
Carette S,
Chung S,
Cuthbertson D,
Davis JC Jr,
Dellaripa PF,
Forbess L,
Gewurz-Singer O,
Hoffman GS,
Khalidi N,
Koening C,
Langford CA,
Mahr AD,
McAlear C,
Moreland L,
Seo EP,
Specks U,
Spiera RF,
Sreih A,
St Clair EW,
Stone JH,
Ytterberg SR,
Elder JT,
Qu J,
Ochi T,
Hirano N,
Edberg JC,
Falk RJ,
Amos CI,
Siminovitch KA
Vasculitis Clinical Research Consortium
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28029757 · open access
4 pages
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Cordell HJ,
Han Y,
Mells GF,
Li Y,
Hirschfield GM,
Greene CS,
Xie G,
Juran BD,
Zhu D,
Qian DC,
Floyd JA,
Morley KI
and 11 more — show all
Prati D,
Lleo A,
Cusi D,
Gershwin ME,
Anderson CA,
Lazaridis KN,
Invernizzi P,
Seldin MF,
Sandford RN,
Amos CI,
Siminovitch KA
Canadian-US PBC Consortium · Italian PBC Genetics Study Group and 1 more consortia
Nature communications · 2015 · PMID 26394269 · open access
3 pages
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.