For researchers
Is your paper here?
2,655 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.
1 match for
Zollner S.
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Hou L,
Bergen SE,
Akula N,
Song J,
Hultman CM,
Landén M,
Adli M,
Alda M,
Ardau R,
Arias B,
Aubry JM,
Backlund L
and 127 more — show all
Badner JA,
Barrett TB,
Bauer M,
Baune BT,
Bellivier F,
Benabarre A,
Bengesser S,
Berrettini WH,
Bhattacharjee AK,
Biernacka JM,
Birner A,
Bloss CS,
Brichant-Petitjean C,
Bui ET,
Byerley W,
Cervantes P,
Chillotti C,
Cichon S,
Colom F,
Coryell W,
Craig DW,
Cruceanu C,
Czerski PM,
Davis T,
Dayer A,
Degenhardt F,
Del Zompo M,
DePaulo JR,
Edenberg HJ,
Étain B,
Falkai P,
Foroud T,
Forstner AJ,
Frisén L,
Frye MA,
Fullerton JM,
Gard S,
Garnham JS,
Gershon ES,
Goes FS,
Greenwood TA,
Grigoroiu-Serbanescu M,
Hauser J,
Heilbronner U,
Heilmann-Heimbach S,
Herms S,
Hipolito M,
Hitturlingappa S,
Hoffmann P,
Hofmann A,
Jamain S,
Jiménez E,
Kahn JP,
Kassem L,
Kelsoe JR,
Kittel-Schneider S,
Kliwicki S,
Koller DL,
König B,
Lackner N,
Laje G,
Lang M,
Lavebratt C,
Lawson WB,
Leboyer M,
Leckband SG,
Liu C,
Maaser A,
Mahon PB,
Maier W,
Maj M,
Manchia M,
Martinsson L,
McCarthy MJ,
McElroy SL,
McInnis MG,
McKinney R,
Mitchell PB,
Mitjans M,
Mondimore FM,
Monteleone P,
Mühleisen TW,
Nievergelt CM,
Nöthen MM,
Novák T,
Nurnberger JI Jr,
Nwulia EA,
Ösby U,
Pfennig A,
Potash JB,
Propping P,
Reif A,
Reininghaus E,
Rice J,
Rietschel M,
Rouleau GA,
Rybakowski JK,
Schalling M,
Scheftner WA,
Schofield PR,
Schork NJ,
Schulze TG,
Schumacher J,
Schweizer BW,
Severino G,
Shekhtman T,
Shilling PD,
Simhandl C,
Slaney CM,
Smith EN,
Squassina A,
Stamm T,
Stopkova P,
Streit F,
Strohmaier J,
Szelinger S,
Tighe SK,
Tortorella A,
Turecki G,
Vieta E,
Volkert J,
Witt SH,
Wright A,
Zandi PP,
Zhang P,
Zollner S,
McMahon FJ
Human molecular genetics · 2016 · PMID 27329760
2 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.