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.
5 matches for
Szeszenia-Dabrowska N.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Scelo G,
Purdue MP,
Brown KM,
Johansson M,
Wang Z,
Eckel-Passow JE,
Ye Y,
Hofmann JN,
Choi J,
Foll M,
Gaborieau V,
Machiela MJ
and 111 more — show all
Colli LM,
Li P,
Sampson JN,
Abedi-Ardekani B,
Besse C,
Blanche H,
Boland A,
Burdette L,
Chabrier A,
Durand G,
Le Calvez-Kelm F,
Prokhortchouk E,
Robinot N,
Skryabin KG,
Wozniak MB,
Yeager M,
Basta-Jovanovic G,
Dzamic Z,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Mukeriya A,
Rascu S,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Szeszenia-Dabrowska N,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Baglietto L,
Boeing H,
Khaw KT,
Weiderpass E,
Ljungberg B,
Sitaram RT,
Bruinsma F,
Jordan SJ,
Severi G,
Winship I,
Hveem K,
Vatten LJ,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Freeman LEB,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Gapstur SM,
Stevens VL,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Buring J,
Lee IM,
Chow WH,
Moore LE,
Wood C,
Eisen T,
Henrion M,
Larkin J,
Barman P,
Leibovich BC,
Choueiri TK,
Mark Lathrop G,
Rothman N,
Deleuze JF,
McKay JD,
Parker AS,
Wu X,
Houlston RS,
Brennan P,
Chanock SJ
Nature communications · 2017 · PMID 28598434 · open access
6 pages
Genome-wide association study reveals two new risk loci for bipolar disorder
Mühleisen TW,
Leber M,
Schulze TG,
Strohmaier J,
Degenhardt F,
Treutlein J,
Mattheisen M,
Forstner AJ,
Schumacher J,
Breuer R,
Meier S,
Herms S
and 51 more — show all
Hoffmann P,
Lacour A,
Witt SH,
Reif A,
Müller-Myhsok B,
Lucae S,
Maier W,
Schwarz M,
Vedder H,
Kammerer-Ciernioch J,
Pfennig A,
Bauer M,
Hautzinger M,
Moebus S,
Priebe L,
Czerski PM,
Hauser J,
Lissowska J,
Szeszenia-Dabrowska N,
Brennan P,
McKay JD,
Wright A,
Mitchell PB,
Fullerton JM,
Schofield PR,
Montgomery GW,
Medland SE,
Gordon SD,
Martin NG,
Krasnow V,
Chuchalin A,
Babadjanova G,
Pantelejeva G,
Abramova LI,
Tiganov AS,
Polonikov A,
Khusnutdinova E,
Alda M,
Grof P,
Rouleau GA,
Turecki G,
Laprise C,
Rivas F,
Mayoral F,
Kogevinas M,
Grigoroiu-Serbanescu M,
Propping P,
Becker T,
Rietschel M,
Nöthen MM,
Cichon S
Nature communications · 2014 · PMID 24618891
4 pages
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Hung RJ,
McKay JD,
Gaborieau V,
Boffetta P,
Hashibe M,
Zaridze D,
Mukeria A,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D
and 53 more — show all
Bencko V,
Foretova L,
Janout V,
Chen C,
Goodman G,
Field JK,
Liloglou T,
Xinarianos G,
Cassidy A,
McLaughlin J,
Liu G,
Narod S,
Krokan HE,
Skorpen F,
Elvestad MB,
Hveem K,
Vatten L,
Linseisen J,
Clavel-Chapelon F,
Vineis P,
Bueno-de-Mesquita HB,
Lund E,
Martinez C,
Bingham S,
Rasmuson T,
Hainaut P,
Riboli E,
Ahrens W,
Benhamou S,
Lagiou P,
Trichopoulos D,
Holcátová I,
Merletti F,
Kjaerheim K,
Agudo A,
Macfarlane G,
Talamini R,
Simonato L,
Lowry R,
Conway DI,
Znaor A,
Healy C,
Zelenika D,
Boland A,
Delepine M,
Foglio M,
Lechner D,
Matsuda F,
Blanche H,
Gut I,
Heath S,
Lathrop M,
Brennan P
Nature · 2008 · PMID 18385738
2 pages
Genome-wide association study of HPV seropositivity
Chen D,
McKay JD,
Clifford G,
Gaborieau V,
Chabrier A,
Waterboer T,
Zaridze D,
Lissowska J,
Rudnai P,
Fabianova E,
Bencko V,
Janout V
and 16 more — show all
Foretova L,
Mates IN,
Szeszenia-Dabrowska N,
Curado MP,
Koifman S,
Menezes A,
Wünsch-Filho V,
Eluf-Neto J,
Fernández Garrote L,
Matos E,
Zelenika D,
Boland A,
Boffetta P,
Pawlita M,
Lathrop M,
Brennan P
Human molecular genetics · 2011 · PMID 21896673
1 page
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Wang Y,
McKay JD,
Rafnar T,
Wang Z,
Timofeeva MN,
Broderick P,
Zong X,
Laplana M,
Wei Y,
Han Y,
Lloyd A,
Delahaye-Sourdeix M
and 71 more — show all
Chubb D,
Gaborieau V,
Wheeler W,
Chatterjee N,
Thorleifsson G,
Sulem P,
Liu G,
Kaaks R,
Henrion M,
Kinnersley B,
Vallée M,
LeCalvez-Kelm F,
Stevens VL,
Gapstur SM,
Chen WV,
Zaridze D,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D,
Bencko V,
Foretova L,
Janout V,
Krokan HE,
Gabrielsen ME,
Skorpen F,
Vatten L,
Njølstad I,
Chen C,
Goodman G,
Benhamou S,
Vooder T,
Välk K,
Nelis M,
Metspalu A,
Lener M,
Lubiński J,
Johansson M,
Vineis P,
Agudo A,
Clavel-Chapelon F,
Bueno-de-Mesquita HB,
Trichopoulos D,
Khaw KT,
Johansson M,
Weiderpass E,
Tjønneland A,
Riboli E,
Lathrop M,
Scelo G,
Albanes D,
Caporaso NE,
Ye Y,
Gu J,
Wu X,
Spitz MR,
Dienemann H,
Rosenberger A,
Su L,
Matakidou A,
Eisen T,
Stefansson K,
Risch A,
Chanock SJ,
Christiani DC,
Hung RJ,
Brennan P,
Landi MT,
Houlston RS,
Amos CI
Nature genetics · 2014 · PMID 24880342 · open access
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.