For researchers
Is your paper here?
2,657 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.
8 matches for
Campbell M.
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
and 66 more — show all
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease
Western D,
Yang C,
Timsina J,
Liu M,
Wang C,
Campbell MC,
Kotzbauer P,
Perlmutter JS,
Schindler SE,
Morris JC,
Holtzman DM,
Alvarez I
and 12 more — show all
Pastor P,
Wyss-Coray T,
Marquié M,
Cano A,
Sung YJ,
de Rojas I,
Ruiz A,
Budde J,
Fernandez MV,
Tarawneh R,
Ibanez L,
Cruchaga C
Science translational medicine · 2026 · PMID 42054495
12 pages+
GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association
Rentería ME,
Coolen MW,
Statham AL,
Choi RS,
Qu W,
Campbell MJ,
Smith S,
Henders AK,
Montgomery GW,
Clark SJ,
Martin NG,
Medland SE
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2013 · PMID 23725790
4 pages
Sequence variants in three loci influence monocyte counts and erythrocyte volume
Ferreira MA,
Hottenga JJ,
Warrington NM,
Medland SE,
Willemsen G,
Lawrence RW,
Gordon S,
de Geus EJ,
Henders AK,
Smit JH,
Campbell MJ,
Wallace L
and 11 more — show all
Evans DM,
Wright MJ,
Nyholt DR,
James AL,
Beilby JP,
Penninx BW,
Palmer LJ,
Frazer IH,
Montgomery GW,
Martin NG,
Boomsma DI
American journal of human genetics · 2009 · PMID 19853236
1 page
Common variants in the trichohyalin gene are associated with straight hair in Europeans
Medland SE,
Nyholt DR,
Painter JN,
McEvoy BP,
McRae AF,
Zhu G,
Gordon SD,
Ferreira MA,
Wright MJ,
Henders AK,
Campbell MJ,
Duffy DL
and 6 more — show all
American journal of human genetics · 2009 · PMID 19896111
1 page
Multiethnic genome-wide and HLA association study of total serum IgE level
Daya M,
Cox C,
Acevedo N,
Boorgula MP,
Campbell M,
Chavan S,
Cho MH,
David GL,
Kachroo P,
Lasky-Su J,
Li X,
McHugh CP
and 35 more — show all
Qiao D,
Rafaels N,
Beck LA,
Bleecker ER,
Caraballo L,
Cupples AL,
Figueiredo CA,
Gallo RL,
Hanifin J,
Hansel NN,
Hata TR,
Hersh CP,
Knight-Madden J,
Leung DYM,
Guttman-Yassky E,
Meyers DA,
O'Connor G,
Ober C,
Ong PY,
Ortega VE,
Paller AS,
Putcha N,
Reed RM,
Schneider LC,
Silverman EK,
Slifka MK,
Spergel JM,
Vasan RS,
Viaud-Martinez KA,
Watson H,
Weiss ST,
Ruczinski I,
Beaty TH,
Mathias RA,
Barnes KC
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
The Journal of allergy and clinical immunology · 2021 · PMID 34536413
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.