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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.
2 matches for
Payne AJ.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Mahajan A,
Taliun D,
Thurner M,
Robertson NR,
Torres JM,
Rayner NW,
Payne AJ,
Steinthorsdottir V,
Scott RA,
Grarup N,
Cook JP,
Schmidt EM
and 103 more — show all
Wuttke M,
Sarnowski C,
Mägi R,
Nano J,
Gieger C,
Trompet S,
Lecoeur C,
Preuss MH,
Prins BP,
Guo X,
Bielak LF,
Below JE,
Bowden DW,
Chambers JC,
Kim YJ,
Ng MCY,
Petty LE,
Sim X,
Zhang W,
Bennett AJ,
Bork-Jensen J,
Brummett CM,
Canouil M,
Ec Kardt KU,
Fischer K,
Kardia SLR,
Kronenberg F,
Läll K,
Liu CT,
Locke AE,
Luan J,
Ntalla I,
Nylander V,
Schönherr S,
Schurmann C,
Yengo L,
Bottinger EP,
Brandslund I,
Christensen C,
Dedoussis G,
Florez JC,
Ford I,
Franco OH,
Frayling TM,
Giedraitis V,
Hackinger S,
Hattersley AT,
Herder C,
Ikram MA,
Ingelsson M,
Jørgensen ME,
Jørgensen T,
Kriebel J,
Kuusisto J,
Ligthart S,
Lindgren CM,
Linneberg A,
Lyssenko V,
Mamakou V,
Meitinger T,
Mohlke KL,
Morris AD,
Nadkarni G,
Pankow JS,
Peters A,
Sattar N,
Stančáková A,
Strauch K,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tuomilehto J,
Witte DR,
Dupuis J,
Peyser PA,
Zeggini E,
Loos RJF,
Froguel P,
Ingelsson E,
Lind L,
Groop L,
Laakso M,
Collins FS,
Jukema JW,
Palmer CNA,
Grallert H,
Metspalu A,
Dehghan A,
Köttgen A,
Abecasis GR,
Meigs JB,
Rotter JI,
Marchini J,
Pedersen O,
Hansen T,
Langenberg C,
Wareham NJ,
Stefansson K,
Gloyn AL,
Morris AP,
Boehnke M,
McCarthy MI
Nature genetics · 2018 · PMID 30297969
12 pages+
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
and 152 more — show all
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
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.