For researchers
Is your paper here?
2,660 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.
2 matches for
de Sanjosé S.
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
Conde L,
Halperin E,
Akers NK,
Brown KM,
Smedby KE,
Rothman N,
Nieters A,
Slager SL,
Brooks-Wilson A,
Agana L,
Riby J,
Liu J
and 59 more — show all
Adami HO,
Darabi H,
Hjalgrim H,
Low HQ,
Humphreys K,
Melbye M,
Chang ET,
Glimelius B,
Cozen W,
Davis S,
Hartge P,
Morton LM,
Schenk M,
Wang SS,
Armstrong B,
Kricker A,
Milliken S,
Purdue MP,
Vajdic CM,
Boyle P,
Lan Q,
Zahm SH,
Zhang Y,
Zheng T,
Becker N,
Benavente Y,
Boffetta P,
Brennan P,
Butterbach K,
Cocco P,
Foretova L,
Maynadié M,
de Sanjosé S,
Staines A,
Spinelli JJ,
Achenbach SJ,
Call TG,
Camp NJ,
Glenn M,
Caporaso NE,
Cerhan JR,
Cunningham JM,
Goldin LR,
Hanson CA,
Kay NE,
Lanasa MC,
Leis JF,
Marti GE,
Rabe KG,
Rassenti LZ,
Spector LG,
Strom SS,
Vachon CM,
Weinberg JB,
Holly EA,
Chanock S,
Smith MT,
Bracci PM,
Skibola CF
Nature genetics · 2010 · PMID 20639881 · open access
2 pages
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Din L,
Sheikh M,
Kosaraju N,
Smedby KE,
Bernatsky S,
Berndt SI,
Skibola CF,
Nieters A,
Wang S,
McKay JD,
Cocco P,
Maynadié M
and 80 more — show all
Foretová L,
Staines A,
Mack TM,
de Sanjosé S,
Vyse TJ,
Padyukov L,
Monnereau A,
Arslan AA,
Moore A,
Brooks-Wilson AR,
Novak AJ,
Glimelius B,
Birmann BM,
Link BK,
Stewart C,
Vajdic CM,
Haioun C,
Magnani C,
Conti DV,
Cox DG,
Casabonne D,
Albanes D,
Kane E,
Roman E,
Muzi G,
Salles G,
Giles GG,
Adami HO,
Ghesquières H,
De Vivo I,
Clavel J,
Cerhan JR,
Spinelli JJ,
Hofmann J,
Vijai J,
Curtin K,
Costenbader KH,
Onel K,
Offit K,
Teras LR,
Morton L,
Conde L,
Miligi L,
Melbye M,
Ennas MG,
Liebow M,
Purdue MP,
Glenn M,
Southey MC,
Din M,
Rothman N,
Camp NJ,
Wong Doo N,
Becker N,
Pradhan N,
Bracci PM,
Boffetta P,
Vineis P,
Brennan P,
Kraft P,
Lan Q,
Severson RK,
Vermeulen RCH,
Milne RL,
Kaaks R,
Travis RC,
Weinstein SJ,
Chanock SJ,
Ansell SM,
Slager SL,
Zheng T,
Zhang Y,
Benavente Y,
Taub Z,
Madireddy L,
Gourraud PA,
Oksenberg JR,
Cozen W,
Hjalgrim H,
Khankhanian P
Genetic epidemiology · 2019 · PMID 31407831
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.