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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.
4 matches for
Ardlie KG.
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Lango Allen H,
Estrada K,
Lettre G,
Berndt SI,
Weedon MN,
Rivadeneira F,
Willer CJ,
Jackson AU,
Vedantam S,
Raychaudhuri S,
Ferreira T,
Wood AR
and 281 more — show all
Weyant RJ,
Segrè AV,
Speliotes EK,
Wheeler E,
Soranzo N,
Park JH,
Yang J,
Gudbjartsson D,
Heard-Costa NL,
Randall JC,
Qi L,
Vernon Smith A,
Mägi R,
Pastinen T,
Liang L,
Heid IM,
Luan J,
Thorleifsson G,
Winkler TW,
Goddard ME,
Sin Lo K,
Palmer C,
Workalemahu T,
Aulchenko YS,
Johansson A,
Zillikens MC,
Feitosa MF,
Esko T,
Johnson T,
Ketkar S,
Kraft P,
Mangino M,
Prokopenko I,
Absher D,
Albrecht E,
Ernst F,
Glazer NL,
Hayward C,
Hottenga JJ,
Jacobs KB,
Knowles JW,
Kutalik Z,
Monda KL,
Polasek O,
Preuss M,
Rayner NW,
Robertson NR,
Steinthorsdottir V,
Tyrer JP,
Voight BF,
Wiklund F,
Xu J,
Zhao JH,
Nyholt DR,
Pellikka N,
Perola M,
Perry JR,
Surakka I,
Tammesoo ML,
Altmaier EL,
Amin N,
Aspelund T,
Bhangale T,
Boucher G,
Chasman DI,
Chen C,
Coin L,
Cooper MN,
Dixon AL,
Gibson Q,
Grundberg E,
Hao K,
Juhani Junttila M,
Kaplan LM,
Kettunen J,
König IR,
Kwan T,
Lawrence RW,
Levinson DF,
Lorentzon M,
McKnight B,
Morris AP,
Müller M,
Suh Ngwa J,
Purcell S,
Rafelt S,
Salem RM,
Salvi E,
Sanna S,
Shi J,
Sovio U,
Thompson JR,
Turchin MC,
Vandenput L,
Verlaan DJ,
Vitart V,
White CC,
Ziegler A,
Almgren P,
Balmforth AJ,
Campbell H,
Citterio L,
De Grandi A,
Dominiczak A,
Duan J,
Elliott P,
Elosua R,
Eriksson JG,
Freimer NB,
Geus EJ,
Glorioso N,
Haiqing S,
Hartikainen AL,
Havulinna AS,
Hicks AA,
Hui J,
Igl W,
Illig T,
Jula A,
Kajantie E,
Kilpeläinen TO,
Koiranen M,
Kolcic I,
Koskinen S,
Kovacs P,
Laitinen J,
Liu J,
Lokki ML,
Marusic A,
Maschio A,
Meitinger T,
Mulas A,
Paré G,
Parker AN,
Peden JF,
Petersmann A,
Pichler I,
Pietiläinen KH,
Pouta A,
Ridderstråle M,
Rotter JI,
Sambrook JG,
Sanders AR,
Schmidt CO,
Sinisalo J,
Smit JH,
Stringham HM,
Bragi Walters G,
Widen E,
Wild SH,
Willemsen G,
Zagato L,
Zgaga L,
Zitting P,
Alavere H,
Farrall M,
McArdle WL,
Nelis M,
Peters MJ,
Ripatti S,
van Meurs JB,
Aben KK,
Ardlie KG,
Beckmann JS,
Beilby JP,
Bergman RN,
Bergmann S,
Collins FS,
Cusi D,
den Heijer M,
Eiriksdottir G,
Gejman PV,
Hall AS,
Hamsten A,
Huikuri HV,
Iribarren C,
Kähönen M,
Kaprio J,
Kathiresan S,
Kiemeney L,
Kocher T,
Launer LJ,
Lehtimäki T,
Melander O,
Mosley TH Jr,
Musk AW,
Nieminen MS,
O'Donnell CJ,
Ohlsson C,
Oostra B,
Palmer LJ,
Raitakari O,
Ridker PM,
Rioux JD,
Rissanen A,
Rivolta C,
Schunkert H,
Shuldiner AR,
Siscovick DS,
Stumvoll M,
Tönjes A,
Tuomilehto J,
van Ommen GJ,
Viikari J,
Heath AC,
Martin NG,
Montgomery GW,
Province MA,
Kayser M,
Arnold AM,
Atwood LD,
Boerwinkle E,
Chanock SJ,
Deloukas P,
Gieger C,
Grönberg H,
Hall P,
Hattersley AT,
Hengstenberg C,
Hoffman W,
Lathrop GM,
Salomaa V,
Schreiber S,
Uda M,
Waterworth D,
Wright AF,
Assimes TL,
Barroso I,
Hofman A,
Mohlke KL,
Boomsma DI,
Caulfield MJ,
Cupples LA,
Erdmann J,
Fox CS,
Gudnason V,
Gyllensten U,
Harris TB,
Hayes RB,
Jarvelin MR,
Mooser V,
Munroe PB,
Ouwehand WH,
Penninx BW,
Pramstaller PP,
Quertermous T,
Rudan I,
Samani NJ,
Spector TD,
Völzke H,
Watkins H,
Wilson JF,
Groop LC,
Haritunians T,
Hu FB,
Kaplan RC,
Metspalu A,
North KE,
Schlessinger D,
Wareham NJ,
Hunter DJ,
O'Connell JR,
Strachan DP,
Wichmann HE,
Borecki IB,
van Duijn CM,
Schadt EE,
Thorsteinsdottir U,
Peltonen L,
Uitterlinden AG,
Visscher PM,
Chatterjee N,
Loos RJ,
Boehnke M,
McCarthy MI,
Ingelsson E,
Lindgren CM,
Abecasis GR,
Stefansson K,
Frayling TM,
Hirschhorn JN
Nature · 2010 · PMID 20881960 · open access
12 pages+
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
Stahl EA,
Raychaudhuri S,
Remmers EF,
Xie G,
Eyre S,
Thomson BP,
Li Y,
Kurreeman FA,
Zhernakova A,
Hinks A,
Guiducci C,
Chen R
and 56 more — show all
Alfredsson L,
Amos CI,
Ardlie KG,
Barton A,
Bowes J,
Brouwer E,
Burtt NP,
Catanese JJ,
Coblyn J,
Coenen MJ,
Costenbader KH,
Criswell LA,
Crusius JB,
Cui J,
de Bakker PI,
De Jager PL,
Ding B,
Emery P,
Flynn E,
Harrison P,
Hocking LJ,
Huizinga TW,
Kastner DL,
Ke X,
Lee AT,
Liu X,
Martin P,
Morgan AW,
Padyukov L,
Posthumus MD,
Radstake TR,
Reid DM,
Seielstad M,
Seldin MF,
Shadick NA,
Steer S,
Tak PP,
Thomson W,
van der Helm-van Mil AH,
van der Horst-Bruinsma IE,
van der Schoot CE,
van Riel PL,
Weinblatt ME,
Wilson AG,
Wolbink GJ,
Wordsworth BP,
Wijmenga C,
Karlson EW,
Toes RE,
de Vries N,
Begovich AB,
Worthington J,
Siminovitch KA,
Gregersen PK,
Klareskog L,
Plenge RM
BIRAC Consortium · YEAR Consortium
Nature genetics · 2010 · PMID 20453842
2 pages
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Ferreira MA,
O'Donovan MC,
Meng YA,
Jones IR,
Ruderfer DM,
Jones L,
Fan J,
Kirov G,
Perlis RH,
Green EK,
Smoller JW,
Grozeva D
and 50 more — show all
Stone J,
Nikolov I,
Chambert K,
Hamshere ML,
Nimgaonkar VL,
Moskvina V,
Thase ME,
Caesar S,
Sachs GS,
Franklin J,
Gordon-Smith K,
Ardlie KG,
Gabriel SB,
Fraser C,
Blumenstiel B,
Defelice M,
Breen G,
Gill M,
Morris DW,
Elkin A,
Muir WJ,
McGhee KA,
Williamson R,
MacIntyre DJ,
MacLean AW,
St CD,
Robinson M,
Van Beck M,
Pereira AC,
Kandaswamy R,
McQuillin A,
Collier DA,
Bass NJ,
Young AH,
Lawrence J,
Ferrier IN,
Anjorin A,
Farmer A,
Curtis D,
Scolnick EM,
McGuffin P,
Daly MJ,
Corvin AP,
Holmans PA,
Blackwood DH,
Gurling HM,
Owen MJ,
Purcell SM,
Sklar P,
Craddock N
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18711365
1 page
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
Klarin D,
Zhu QM,
Emdin CA,
Chaffin M,
Horner S,
McMillan BJ,
Leed A,
Weale ME,
Spencer CCA,
Aguet F,
Segrè AV,
Ardlie KG
and 4 more — show all
CARDIoGRAMplusC4D Consortium
Nature genetics · 2017 · PMID 28714974 · 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.