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.
3 matches for
Krestyaninova M.
A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection
Nicholson G,
Rantalainen M,
Li JV,
Maher AD,
Malmodin D,
Ahmadi KR,
Faber JH,
Barrett A,
Min JL,
Rayner NW,
Toft H,
Krestyaninova M
and 17 more — show all
Viksna J,
Neogi SG,
Dumas ME,
Sarkans U,
Donnelly P,
Illig T,
Adamski J,
Suhre K,
Allen M,
Zondervan KT,
Spector TD,
Nicholson JK,
Lindon JC,
Baunsgaard D,
Holmes E,
McCarthy MI,
Holmes CC
MolPAGE Consortium
PLoS genetics · 2011 · PMID 21931564 · open access
2 pages
Variants in MTNR1B influence fasting glucose levels
Prokopenko I,
Langenberg C,
Florez JC,
Saxena R,
Soranzo N,
Thorleifsson G,
Loos RJ,
Manning AK,
Jackson AU,
Aulchenko Y,
Potter SC,
Erdos MR
and 96 more — show all
Sanna S,
Hottenga JJ,
Wheeler E,
Kaakinen M,
Lyssenko V,
Chen WM,
Ahmadi K,
Beckmann JS,
Bergman RN,
Bochud M,
Bonnycastle LL,
Buchanan TA,
Cao A,
Cervino A,
Coin L,
Collins FS,
Crisponi L,
de Geus EJ,
Dehghan A,
Deloukas P,
Doney AS,
Elliott P,
Freimer N,
Gateva V,
Herder C,
Hofman A,
Hughes TE,
Hunt S,
Illig T,
Inouye M,
Isomaa B,
Johnson T,
Kong A,
Krestyaninova M,
Kuusisto J,
Laakso M,
Lim N,
Lindblad U,
Lindgren CM,
McCann OT,
Mohlke KL,
Morris AD,
Naitza S,
Orrù M,
Palmer CN,
Pouta A,
Randall J,
Rathmann W,
Saramies J,
Scheet P,
Scott LJ,
Scuteri A,
Sharp S,
Sijbrands E,
Smit JH,
Song K,
Steinthorsdottir V,
Stringham HM,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Voight BF,
Waterworth D,
Wichmann HE,
Willemsen G,
Witteman JC,
Yuan X,
Zhao JH,
Zeggini E,
Schlessinger D,
Sandhu M,
Boomsma DI,
Uda M,
Spector TD,
Penninx BW,
Altshuler D,
Vollenweider P,
Jarvelin MR,
Lakatta E,
Waeber G,
Fox CS,
Peltonen L,
Groop LC,
Mooser V,
Cupples LA,
Thorsteinsdottir U,
Boehnke M,
Barroso I,
Van Duijn C,
Dupuis J,
Watanabe RM,
Stefansson K,
McCarthy MI,
Wareham NJ,
Meigs JB,
Abecasis GR
Nature genetics · 2009 · PMID 19060907
1 page
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
and 82 more — show all
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
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.