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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.
5 matches for
Sjögren M.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Folkersen L,
Gustafsson S,
Wang Q,
Hansen DH,
Hedman ÅK,
Schork A,
Page K,
Zhernakova DV,
Wu Y,
Peters J,
Eriksson N,
Bergen SE
and 71 more — show all
Boutin TS,
Bretherick AD,
Enroth S,
Kalnapenkis A,
Gådin JR,
Suur BE,
Chen Y,
Matic L,
Gale JD,
Lee J,
Zhang W,
Quazi A,
Ala-Korpela M,
Choi SH,
Claringbould A,
Danesh J,
Davey Smith G,
de Masi F,
Elmståhl S,
Engström G,
Fauman E,
Fernandez C,
Franke L,
Franks PW,
Giedraitis V,
Haley C,
Hamsten A,
Ingason A,
Johansson Å,
Joshi PK,
Lind L,
Lindgren CM,
Lubitz S,
Palmer T,
Macdonald-Dunlop E,
Magnusson M,
Melander O,
Michaelsson K,
Morris AP,
Mägi R,
Nagle MW,
Nilsson PM,
Nilsson J,
Orho-Melander M,
Polasek O,
Prins B,
Pålsson E,
Qi T,
Sjögren M,
Sundström J,
Surendran P,
Võsa U,
Werge T,
Wernersson R,
Westra HJ,
Yang J,
Zhernakova A,
Ärnlöv J,
Fu J,
Smith JG,
Esko T,
Hayward C,
Gyllensten U,
Landen M,
Siegbahn A,
Wilson JF,
Wallentin L,
Butterworth AS,
Holmes MV,
Ingelsson E,
Mälarstig A
Nature metabolism · 2020 · PMID 33067605
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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
Genetic loci influencing kidney function and chronic kidney disease
Chambers JC,
Zhang W,
Lord GM,
van der Harst P,
Lawlor DA,
Sehmi JS,
Gale DP,
Wass MN,
Ahmadi KR,
Bakker SJ,
Beckmann J,
Bilo HJ
and 82 more — show all
Bochud M,
Brown MJ,
Caulfield MJ,
Connell JM,
Cook HT,
Cotlarciuc I,
Davey Smith G,
de Silva R,
Deng G,
Devuyst O,
Dikkeschei LD,
Dimkovic N,
Dockrell M,
Dominiczak A,
Ebrahim S,
Eggermann T,
Farrall M,
Ferrucci L,
Floege J,
Forouhi NG,
Gansevoort RT,
Han X,
Hedblad B,
Homan van der Heide JJ,
Hepkema BG,
Hernandez-Fuentes M,
Hypponen E,
Johnson T,
de Jong PE,
Kleefstra N,
Lagou V,
Lapsley M,
Li Y,
Loos RJ,
Luan J,
Luttropp K,
Maréchal C,
Melander O,
Munroe PB,
Nordfors L,
Parsa A,
Peltonen L,
Penninx BW,
Perucha E,
Pouta A,
Prokopenko I,
Roderick PJ,
Ruokonen A,
Samani NJ,
Sanna S,
Schalling M,
Schlessinger D,
Schlieper G,
Seelen MA,
Shuldiner AR,
Sjögren M,
Smit JH,
Snieder H,
Soranzo N,
Spector TD,
Stenvinkel P,
Sternberg MJ,
Swaminathan R,
Tanaka T,
Ubink-Veltmaat LJ,
Uda M,
Vollenweider P,
Wallace C,
Waterworth D,
Zerres K,
Waeber G,
Wareham NJ,
Maxwell PH,
McCarthy MI,
Jarvelin MR,
Mooser V,
Abecasis GR,
Lightstone L,
Scott J,
Navis G,
Elliott P,
Kooner JS
Nature genetics · 2010 · PMID 20383145
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.