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.
6 matches for
Armstrong G.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Melin BS,
Barnholtz-Sloan JS,
Wrensch MR,
Johansen C,
Il'yasova D,
Kinnersley B,
Ostrom QT,
Labreche K,
Chen Y,
Armstrong G,
Liu Y,
Eckel-Passow JE
and 51 more — show all
Decker PA,
Labussière M,
Idbaih A,
Hoang-Xuan K,
Di Stefano AL,
Mokhtari K,
Delattre JY,
Broderick P,
Galan P,
Gousias K,
Schramm J,
Schoemaker MJ,
Fleming SJ,
Herms S,
Heilmann S,
Nöthen MM,
Wichmann HE,
Schreiber S,
Swerdlow A,
Lathrop M,
Simon M,
Sanson M,
Andersson U,
Rajaraman P,
Chanock S,
Linet M,
Wang Z,
Yeager M,
Wiencke JK,
Hansen H,
McCoy L,
Rice T,
Kosel ML,
Sicotte H,
Amos CI,
Bernstein JL,
Davis F,
Lachance D,
Lau C,
Merrell RT,
Shildkraut J,
Ali-Osman F,
Sadetzki S,
Scheurer M,
Shete S,
Lai RK,
Claus EB,
Olson SH,
Jenkins RB,
Houlston RS,
Bondy ML
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 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 five susceptibility loci for glioma
Shete S,
Hosking FJ,
Robertson LB,
Dobbins SE,
Sanson M,
Malmer B,
Simon M,
Marie Y,
Boisselier B,
Delattre JY,
Hoang-Xuan K,
El Hallani S
and 25 more — show all
Idbaih A,
Zelenika D,
Andersson U,
Henriksson R,
Bergenheim AT,
Feychting M,
Lönn S,
Ahlbom A,
Schramm J,
Linnebank M,
Hemminki K,
Kumar R,
Hepworth SJ,
Price A,
Armstrong G,
Liu Y,
Gu X,
Yu R,
Lau C,
Schoemaker M,
Muir K,
Swerdlow A,
Lathrop M,
Bondy M,
Houlston RS
Nature genetics · 2009 · PMID 19578367
2 pages
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma
Chen C,
Song N,
Dong Q,
Sun X,
Mulder HL,
Easton J,
Zhang J,
Yasui Y,
Bhatia S,
Armstrong GT,
Wang H,
Ness KK
and 3 more — show all
JAMA network open · 2022 · PMID 35939300 · open access
2 pages
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma
Lin SH,
Sampson JN,
Grünewald TGP,
Surdez D,
Reynaud S,
Mirabeau O,
Karlins E,
Rubio RA,
Zaidi S,
Grossetête-Lalami S,
Ballet S,
Lapouble E
and 44 more — show all
Laurence V,
Michon J,
Pierron G,
Kovar H,
Kontny U,
González-Neira A,
Alonso J,
Patino-Garcia A,
Corradini N,
Bérard PM,
Miller J,
Freedman ND,
Rothman N,
Carter BD,
Dagnall CL,
Burdett L,
Jones K,
Manning M,
Wyatt K,
Zhou W,
Yeager M,
Cox DG,
Hoover RN,
Khan J,
Armstrong GT,
Leisenring WM,
Bhatia S,
Robison LL,
Kulozik AE,
Kriebel J,
Meitinger T,
Metzler M,
Krumbholz M,
Hartmann W,
Strauch K,
Kirchner T,
Dirksen U,
Mirabello L,
Tucker MA,
Tirode F,
Morton LM,
Chanock SJ,
Delattre O,
Machiela MJ
PloS one · 2020 · PMID 32881892 · open access
1 page
Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort
Richard MA,
Brown AL,
Belmont JW,
Scheurer ME,
Arroyo VM,
Foster KL,
Kern KD,
Hudson MM,
Leisenring WM,
Okcu MF,
Sapkota Y,
Yasui Y
and 8 more — show all
Cancer · 2021 · PMID 33048379
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.