For researchers
Is your paper here?
2,676 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.
4 matches for
Eyer F.
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Buch S,
Stickel F,
Trépo E,
Way M,
Herrmann A,
Nischalke HD,
Brosch M,
Rosendahl J,
Berg T,
Ridinger M,
Rietschel M,
McQuillin A
and 36 more — show all
Frank J,
Kiefer F,
Schreiber S,
Lieb W,
Soyka M,
Semmo N,
Aigner E,
Datz C,
Schmelz R,
Brückner S,
Zeissig S,
Stephan AM,
Wodarz N,
Devière J,
Clumeck N,
Sarrazin C,
Lammert F,
Gustot T,
Deltenre P,
Völzke H,
Lerch MM,
Mayerle J,
Eyer F,
Schafmayer C,
Cichon S,
Nöthen MM,
Nothnagel M,
Ellinghaus D,
Huse K,
Franke A,
Zopf S,
Hellerbrand C,
Moreno C,
Franchimont D,
Morgan MY,
Hampe J
Nature genetics · 2015 · PMID 26482880
2 pages
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
and 79 more — show all
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
1 page
Genetic dissection of serum pro-neurotensin suggests potential causal impact on brain structure
Breitfeld J,
Horn K,
Velluva A,
Beyer F,
Pott J,
Baber R,
Stumvoll M,
Le Duc D,
Witte V,
Giontella A,
Melander O,
Kovacs P
and 2 more — show all
EBioMedicine · 2026 · PMID 41520650 · 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.