For researchers
Is your paper here?
2,661 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.
3 matches for
Linet MS.
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
Skibola CF,
Berndt SI,
Vijai J,
Conde L,
Wang Z,
Yeager M,
de Bakker PI,
Birmann BM,
Vajdic CM,
Foo JN,
Bracci PM,
Vermeulen RC
and 100 more — show all
Slager SL,
de Sanjose S,
Wang SS,
Linet MS,
Salles G,
Lan Q,
Severi G,
Hjalgrim H,
Lightfoot T,
Melbye M,
Gu J,
Ghesquières H,
Link BK,
Morton LM,
Holly EA,
Smith A,
Tinker LF,
Teras LR,
Kricker A,
Becker N,
Purdue MP,
Spinelli JJ,
Zhang Y,
Giles GG,
Vineis P,
Monnereau A,
Bertrand KA,
Albanes D,
Zeleniuch-Jacquotte A,
Gabbas A,
Chung CC,
Burdett L,
Hutchinson A,
Lawrence C,
Montalvan R,
Liang L,
Huang J,
Ma B,
Liu J,
Adami HO,
Glimelius B,
Ye Y,
Nowakowski GS,
Dogan A,
Thompson CA,
Habermann TM,
Novak AJ,
Liebow M,
Witzig TE,
Weiner GJ,
Schenk M,
Hartge P,
De Roos AJ,
Cozen W,
Zhi D,
Akers NK,
Riby J,
Smith MT,
Lacher M,
Villano DJ,
Maria A,
Roman E,
Kane E,
Jackson RD,
North KE,
Diver WR,
Turner J,
Armstrong BK,
Benavente Y,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
Staines A,
McKay J,
Brooks-Wilson AR,
Zheng T,
Holford TR,
Chamosa S,
Kaaks R,
Kelly RS,
Ohlsson B,
Travis RC,
Weiderpass E,
Clavel J,
Giovannucci E,
Kraft P,
Virtamo J,
Mazza P,
Cocco P,
Ennas MG,
Chiu BC,
Fraumeni JF Jr,
Nieters A,
Offit K,
Wu X,
Cerhan JR,
Smedby KE,
Chanock SJ,
Rothman N
American journal of human genetics · 2014 · PMID 25279986
5 pages
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21
Ostrom QT,
Kinnersley B,
Wrensch MR,
Eckel-Passow JE,
Armstrong G,
Rice T,
Chen Y,
Wiencke JK,
McCoy LS,
Hansen HM,
Amos CI,
Bernstein JL
and 24 more — show all
Claus EB,
Il'yasova D,
Johansen C,
Lachance DH,
Lai RK,
Merrell RT,
Olson SH,
Sadetzki S,
Schildkraut JM,
Shete S,
Rubin JB,
Lathia JD,
Berens ME,
Andersson U,
Rajaraman P,
Chanock SJ,
Linet MS,
Wang Z,
Yeager M,
Houlston RS,
Jenkins RB,
Melin B,
Bondy ML,
Barnholtz-Sloan JS
GliomaScan consortium
Scientific reports · 2018 · PMID 29743610 · open access
4 pages
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Berndt SI,
Skibola CF,
Joseph V,
Camp NJ,
Nieters A,
Wang Z,
Cozen W,
Monnereau A,
Wang SS,
Kelly RS,
Lan Q,
Teras LR
and 118 more — show all
Chatterjee N,
Chung CC,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Armstrong BK,
Cocco P,
Zhang Y,
Severi G,
Zeleniuch-Jacquotte A,
Lawrence C,
Burdette L,
Yuenger J,
Hutchinson A,
Jacobs KB,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Wang AH,
Smedby KE,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Jones B,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Holly EA,
Smith MT,
Jackson RD,
Tinker LF,
Benavente Y,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Rabe KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Lanasa MC,
Spector LG,
Leis JF,
Cunningham JM,
Weinberg JB,
Morrison VA,
Caporaso NE,
Norman AD,
Linet MS,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Trichopoulos D,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RC,
Travis RC,
Giles GG,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Offit K,
Zelenetz A,
Klein RJ,
Spinelli JJ,
Bertrand KA,
Laden F,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Vajdic CM,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Sampson J,
Crouch S,
Park JH,
North KE,
Cox A,
Snowden JA,
Wright J,
Carracedo A,
Lopez-Otin C,
Bea S,
Salaverria I,
Martin-Garcia D,
Campo E,
Fraumeni JF Jr,
de Sanjose S,
Hjalgrim H,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature genetics · 2013 · PMID 23770605 · 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.