For researchers
Is your paper here?
2,660 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
Kwan P.
ELF1 is associated with systemic lupus erythematosus in Asian populations
Yang J,
Yang W,
Hirankarn N,
Ye DQ,
Zhang Y,
Pan HF,
Pan HF,
Mok CC,
Chan TM,
Wong RW,
Mok MY,
Lee KW
and 24 more — show all
Wong SN,
Leung AM,
Li XP,
Avihingsanon Y,
Rianthavorn P,
Deekajorndej T,
Suphapeetiporn K,
Shotelersuk V,
Baum L,
Kwan P,
Lee TL,
Ho MH,
Lee PP,
Wong WH,
Zeng S,
Zhang J,
Wong CM,
Ng IO,
Garcia-Barceló MM,
Cherny SS,
Tam PK,
Sham PC,
Lau CS,
Lau YL
Human molecular genetics · 2011 · PMID 21044949
2 pages
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 variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
McCormack M,
Gui H,
Ingason A,
Speed D,
Wright GEB,
Zhang EJ,
Secolin R,
Yasuda C,
Kwok M,
Wolking S,
Becker F,
Rau S
and 37 more — show all
Avbersek A,
Heggeli K,
Leu C,
Depondt C,
Sills GJ,
Marson AG,
Auce P,
Brodie MJ,
Francis B,
Johnson MR,
Koeleman BPC,
Striano P,
Coppola A,
Zara F,
Kunz WS,
Sander JW,
Lerche H,
Klein KM,
Weckhuysen S,
Krenn M,
Gudmundsson LJ,
Stefánsson K,
Krause R,
Shear N,
Ross CJD,
Delanty N,
Pirmohamed M,
Carleton BC,
Cendes F,
Lopes-Cendes I,
Liao WP,
O'Brien TJ,
Sisodiya SM,
Cherny S,
Kwan P,
Baum L,
Cavalleri GL
EPIGEN Consortium; · Canadian Pharmacogenomics Network for Drug Safety; and 2 more consortia
Neurology · 2018 · PMID 29288229 · open access
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.