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.
4 matches for
Vacic V.
Genome-wide association study of schizophrenia in Ashkenazi Jews
Goes FS,
McGrath J,
Avramopoulos D,
Wolyniec P,
Pirooznia M,
Ruczinski I,
Nestadt G,
Kenny EE,
Vacic V,
Peters I,
Lencz T,
Darvasi A
and 3 more — show all
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2015 · PMID 26198764
12 pages+
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Jansen PR,
Watanabe K,
Stringer S,
Skene N,
Bryois J,
Hammerschlag AR,
de Leeuw CA,
Benjamins JS,
Muñoz-Manchado AB,
Nagel M,
Savage JE,
Tiemeier H
and 12 more — show all
White T,
Tung JY,
Hinds DA,
Vacic V,
Wang X,
Sullivan PF,
van der Sluis S,
Polderman TJC,
Smit AB,
Hjerling-Leffler J,
Van Someren EJW,
Posthuma D
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
and 73 more — show all
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 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.