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
ENGAGE Consortium.
The impact of low-frequency and rare variants on lipid levels
Surakka I,
Horikoshi M,
Mägi R,
Sarin AP,
Mahajan A,
Lagou V,
Marullo L,
Ferreira T,
Miraglio B,
Timonen S,
Kettunen J,
Pirinen M
and 74 more — show all
Karjalainen J,
Thorleifsson G,
Hägg S,
Hottenga JJ,
Isaacs A,
Ladenvall C,
Beekman M,
Esko T,
Ried JS,
Nelson CP,
Willenborg C,
Gustafsson S,
Westra HJ,
Blades M,
de Craen AJ,
de Geus EJ,
Deelen J,
Grallert H,
Hamsten A,
Havulinna AS,
Hengstenberg C,
Houwing-Duistermaat JJ,
Hyppönen E,
Karssen LC,
Lehtimäki T,
Lyssenko V,
Magnusson PK,
Mihailov E,
Müller-Nurasyid M,
Mpindi JP,
Pedersen NL,
Penninx BW,
Perola M,
Pers TH,
Peters A,
Rung J,
Smit JH,
Steinthorsdottir V,
Tobin MD,
Tsernikova N,
van Leeuwen EM,
Viikari JS,
Willems SM,
Willemsen G,
Schunkert H,
Erdmann J,
Samani NJ,
Kaprio J,
Lind L,
Gieger C,
Metspalu A,
Slagboom PE,
Groop L,
van Duijn CM,
Eriksson JG,
Jula A,
Salomaa V,
Boomsma DI,
Power C,
Raitakari OT,
Ingelsson E,
Järvelin MR,
Thorsteinsdottir U,
Franke L,
Ikonen E,
Kallioniemi O,
Pietiäinen V,
Lindgren CM,
Stefansson K,
Palotie A,
McCarthy MI,
Morris AP,
Prokopenko I,
Ripatti S
ENGAGE Consortium
Nature genetics · 2015 · PMID 25961943
12 pages+
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Aulchenko YS,
Ripatti S,
Lindqvist I,
Boomsma D,
Heid IM,
Pramstaller PP,
Penninx BW,
Janssens AC,
Wilson JF,
Spector T,
Martin NG,
Pedersen NL
and 45 more — show all
Kyvik KO,
Kaprio J,
Hofman A,
Freimer NB,
Jarvelin MR,
Gyllensten U,
Campbell H,
Rudan I,
Johansson A,
Marroni F,
Hayward C,
Vitart V,
Jonasson I,
Pattaro C,
Wright A,
Hastie N,
Pichler I,
Hicks AA,
Falchi M,
Willemsen G,
Hottenga JJ,
de Geus EJ,
Montgomery GW,
Whitfield J,
Magnusson P,
Saharinen J,
Perola M,
Silander K,
Isaacs A,
Sijbrands EJ,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Elliott P,
Ruokonen A,
Sabatti C,
Gieger C,
Meitinger T,
Kronenberg F,
Döring A,
Wichmann HE,
Smit JH,
McCarthy MI,
van Duijn CM,
Peltonen L
ENGAGE Consortium
Nature genetics · 2009 · PMID 19060911
4 pages
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
Kolz M,
Johnson T,
Sanna S,
Teumer A,
Vitart V,
Perola M,
Mangino M,
Albrecht E,
Wallace C,
Farrall M,
Johansson A,
Nyholt DR
and 44 more — show all
Aulchenko Y,
Beckmann JS,
Bergmann S,
Bochud M,
Brown M,
Campbell H,
Connell J,
Dominiczak A,
Homuth G,
Lamina C,
McCarthy MI,
Meitinger T,
Mooser V,
Munroe P,
Nauck M,
Peden J,
Prokisch H,
Salo P,
Salomaa V,
Samani NJ,
Schlessinger D,
Uda M,
Völker U,
Waeber G,
Waterworth D,
Wang-Sattler R,
Wright AF,
Adamski J,
Whitfield JB,
Gyllensten U,
Wilson JF,
Rudan I,
Pramstaller P,
Watkins H,
Doering A,
Wichmann HE,
Spector TD,
Peltonen L,
Völzke H,
Nagaraja R,
Vollenweider P,
Caulfield M,
Illig T,
Gieger C
EUROSPAN Consortium · ENGAGE Consortium and 3 more consortia
PLoS genetics · 2009 · PMID 19503597 · open access
3 pages
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.