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Is your paper here?
2,665 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.
24 matches for
Almgren P,
showing the first 4.
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
Perry JR,
Voight BF,
Yengo L,
Amin N,
Dupuis J,
Ganser M,
Grallert H,
Navarro P,
Li M,
Qi L,
Steinthorsdottir V,
Scott RA
and 63 more — show all
Almgren P,
Arking DE,
Aulchenko Y,
Balkau B,
Benediktsson R,
Bergman RN,
Boerwinkle E,
Bonnycastle L,
Burtt NP,
Campbell H,
Charpentier G,
Collins FS,
Gieger C,
Green T,
Hadjadj S,
Hattersley AT,
Herder C,
Hofman A,
Johnson AD,
Kottgen A,
Kraft P,
Labrune Y,
Langenberg C,
Manning AK,
Mohlke KL,
Morris AP,
Oostra B,
Pankow J,
Petersen AK,
Pramstaller PP,
Prokopenko I,
Rathmann W,
Rayner W,
Roden M,
Rudan I,
Rybin D,
Scott LJ,
Sigurdsson G,
Sladek R,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Uitterlinden AG,
Vivequin S,
Weedon MN,
Wright AF,
Hu FB,
Illig T,
Kao L,
Meigs JB,
Wilson JF,
Stefansson K,
van Duijn C,
Altschuler D,
Morris AD,
Boehnke M,
McCarthy MI,
Froguel P,
Palmer CN,
Wareham NJ,
Groop L,
Frayling TM,
Cauchi S
MAGIC · DIAGRAM Consortium and 1 more consortia
PLoS genetics · 2012 · PMID 22693455 · open access
1 page
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
and 163 more — show all
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
Steinbach G,
Wennauer R,
Eriksson JG,
Mӓnnistö S,
Peltonen L,
Tikkanen E,
Charpentier G,
Eury E,
Lobbens S,
Gigante B,
Leander K,
McLeod O,
Bottinger EP,
Gottesman O,
Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
Moebus S,
de Faire U,
Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
Pedersen O,
Barroso I,
Lannfelt L,
Ingelsson E,
Lind L,
Lindgren CM,
Cauchi S,
Froguel P,
Loos RJF,
Balkau B,
Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
Altshuler D,
Groop LC,
Langenberg C,
Wareham NJ,
Sijbrands E,
van Duijn CM,
Florez JC,
Meigs JB,
Boerwinkle E,
Gieger C,
Strauch K,
Metspalu A,
Morris AD,
Palmer CNA,
Hu FB,
Thorsteinsdottir U,
Stefansson K,
Dupuis J,
Morris AP,
Boehnke M,
McCarthy MI,
Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
Genetic determinants of circulating GIP and GLP-1 concentrations
Almgren P,
Lindqvist A,
Krus U,
Hakaste L,
Ottosson-Laakso E,
Asplund O,
Sonestedt E,
Prasad RB,
Laurila E,
Orho-Melander M,
Melander O,
Tuomi T
and 5 more — show all
JCI insight · 2017 · PMID 29093273
1 page
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
and 69 more — show all
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and 4 more consortia
Diabetes · 2018 · PMID 29703844
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.