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.
5 matches for
Andersen G.
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants
Jin Y,
Andersen G,
Yorgov D,
Ferrara TM,
Ben S,
Brownson KM,
Holland PJ,
Birlea SA,
Siebert J,
Hartmann A,
Lienert A,
van Geel N
and 32 more — show all
Lambert J,
Luiten RM,
Wolkerstorfer A,
Wietze van der Veen JP,
Bennett DC,
Taïeb A,
Ezzedine K,
Kemp EH,
Gawkrodger DJ,
Weetman AP,
Kõks S,
Prans E,
Kingo K,
Karelson M,
Wallace MR,
McCormack WT,
Overbeck A,
Moretti S,
Colucci R,
Picardo M,
Silverberg NB,
Olsson M,
Valle Y,
Korobko I,
Böhm M,
Lim HW,
Hamzavi I,
Zhou L,
Mi QS,
Fain PR,
Santorico SA,
Spritz RA
Nature genetics · 2016 · PMID 27723757 · open access
12 pages+
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Zeggini E,
Scott LJ,
Saxena R,
Voight BF,
Marchini JL,
Hu T,
de Bakker PI,
Abecasis GR,
Almgren P,
Andersen G,
Ardlie K,
Boström KB
and 86 more — show all
Bergman RN,
Bonnycastle LL,
Borch-Johnsen K,
Burtt NP,
Chen H,
Chines PS,
Daly MJ,
Deodhar P,
Ding CJ,
Doney AS,
Duren WL,
Elliott KS,
Erdos MR,
Frayling TM,
Freathy RM,
Gianniny L,
Grallert H,
Grarup N,
Groves CJ,
Guiducci C,
Hansen T,
Herder C,
Hitman GA,
Hughes TE,
Isomaa B,
Jackson AU,
Jørgensen T,
Kong A,
Kubalanza K,
Kuruvilla FG,
Kuusisto J,
Langenberg C,
Lango H,
Lauritzen T,
Li Y,
Lindgren CM,
Lyssenko V,
Marvelle AF,
Meisinger C,
Midthjell K,
Mohlke KL,
Morken MA,
Morris AD,
Narisu N,
Nilsson P,
Owen KR,
Palmer CN,
Payne F,
Perry JR,
Pettersen E,
Platou C,
Prokopenko I,
Qi L,
Qin L,
Rayner NW,
Rees M,
Roix JJ,
Sandbaek A,
Shields B,
Sjögren M,
Steinthorsdottir V,
Stringham HM,
Swift AJ,
Thorleifsson G,
Thorsteinsdottir U,
Timpson NJ,
Tuomi T,
Tuomilehto J,
Walker M,
Watanabe RM,
Weedon MN,
Willer CJ,
Illig T,
Hveem K,
Hu FB,
Laakso M,
Stefansson K,
Pedersen O,
Wareham NJ,
Barroso I,
Hattersley AT,
Collins FS,
Groop L,
McCarthy MI,
Boehnke M,
Altshuler D
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18372903
5 pages
Many sequence variants affecting diversity of adult human height
Gudbjartsson DF,
Walters GB,
Thorleifsson G,
Stefansson H,
Halldorsson BV,
Zusmanovich P,
Sulem P,
Thorlacius S,
Gylfason A,
Steinberg S,
Helgadottir A,
Ingason A
and 25 more — show all
Steinthorsdottir V,
Olafsdottir EJ,
Olafsdottir GH,
Jonsson T,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Pedersen O,
Aben KK,
Witjes JA,
Swinkels DW,
den Heijer M,
Franke B,
Verbeek AL,
Becker DM,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Gulcher J,
Kiemeney LA,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18391951
3 pages
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
Unoki H,
Takahashi A,
Kawaguchi T,
Hara K,
Horikoshi M,
Andersen G,
Ng DP,
Holmkvist J,
Borch-Johnsen K,
Jørgensen T,
Sandbaek A,
Lauritzen T
and 18 more — show all
Hansen T,
Nurbaya S,
Tsunoda T,
Kubo M,
Babazono T,
Hirose H,
Hayashi M,
Iwamoto Y,
Kashiwagi A,
Kaku K,
Kawamori R,
Tai ES,
Pedersen O,
Kamatani N,
Kadowaki T,
Kikkawa R,
Nakamura Y,
Maeda S
Nature genetics · 2008 · PMID 18711366
3 pages
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Thorleifsson G,
Walters GB,
Gudbjartsson DF,
Steinthorsdottir V,
Sulem P,
Helgadottir A,
Styrkarsdottir U,
Gretarsdottir S,
Thorlacius S,
Jonsdottir I,
Jonsdottir T,
Olafsdottir EJ
and 23 more — show all
Olafsdottir GH,
Jonsson T,
Jonsson F,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Lauritzen T,
Aben KK,
Verbeek AL,
Roeleveld N,
Kampman E,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Becker DM,
Gulcher J,
Kiemeney LA,
Pedersen O,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19079260
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.