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2,663 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.
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6 matches for
Chandran V.
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Tsoi LC,
Spain SL,
Knight J,
Ellinghaus E,
Stuart PE,
Capon F,
Ding J,
Li Y,
Tejasvi T,
Gudjonsson JE,
Kang HM,
Allen MH
and 53 more — show all
McManus R,
Novelli G,
Samuelsson L,
Schalkwijk J,
Ståhle M,
Burden AD,
Smith CH,
Cork MJ,
Estivill X,
Bowcock AM,
Krueger GG,
Weger W,
Worthington J,
Tazi-Ahnini R,
Nestle FO,
Hayday A,
Hoffmann P,
Winkelmann J,
Wijmenga C,
Langford C,
Edkins S,
Andrews R,
Blackburn H,
Strange A,
Band G,
Pearson RD,
Vukcevic D,
Spencer CC,
Deloukas P,
Mrowietz U,
Schreiber S,
Weidinger S,
Koks S,
Kingo K,
Esko T,
Metspalu A,
Lim HW,
Voorhees JJ,
Weichenthal M,
Wichmann HE,
Chandran V,
Rosen CF,
Rahman P,
Gladman DD,
Griffiths CE,
Reis A,
Kere J,
Nair RP,
Franke A,
Barker JN,
Abecasis GR,
Elder JT,
Trembath RC
Collaborative Association Study of Psoriasis (CASP) · Genetic Analysis of Psoriasis Consortium and 2 more consortia
Nature genetics · 2012 · PMID 23143594 · open access
12 pages+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
and 269 more — show all
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
Dand N,
Stuart PE,
Bowes J,
Ellinghaus D,
Nititham J,
Saklatvala JR,
Teder-Laving M,
Thomas LF,
Traks T,
Uebe S,
Assmann G,
Baudry D
and 73 more — show all
Behrens F,
Billi AC,
Brown MA,
Burkhardt H,
Capon F,
Chung R,
Curtis CJ,
Duckworth M,
Ellinghaus E,
FitzGerald O,
Gerdes S,
Griffiths CEM,
Gulliver S,
Helliwell PS,
Ho P,
Hoffmann P,
Holmen OL,
Huang ZM,
Hveem K,
Jadon D,
Köhm M,
Kraus C,
Lamacchia C,
Lee SH,
Ma F,
Mahil SK,
McHugh N,
McManus R,
Modalsli EH,
Nissen MJ,
Nöthen M,
Oji V,
Oksenberg JR,
Patrick MT,
Perez White BE,
Ramming A,
Rech J,
Rosen C,
Sarkar MK,
Schett G,
Schmidt B,
Tejasvi T,
Traupe H,
Voorhees JJ,
Wacker EM,
Warren RB,
Wasikowski R,
Weidinger S,
Wen X,
Zhang Z,
Barton A,
Chandran V,
Esko T,
Foerster J,
Franke A,
Gladman DD,
Gudjonsson JE,
Gulliver W,
Hüffmeier U,
Kingo K,
Kõks S,
Liao W,
Løset M,
Mägi R,
Nair RP,
Rahman P,
Reis A,
Smith CH,
Di Meglio P,
Barker JN,
Tsoi LC,
Simpson MA,
Elder JT
BSTOP study group · Estonian Biobank research team
Nature communications · 2025 · PMID 40021644 · open access
9 pages
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
Tsoi LC,
Stuart PE,
Tian C,
Gudjonsson JE,
Das S,
Zawistowski M,
Ellinghaus E,
Barker JN,
Chandran V,
Dand N,
Duffin KC,
Enerbäck C
and 26 more — show all
Esko T,
Franke A,
Gladman DD,
Hoffmann P,
Kingo K,
Kõks S,
Krueger GG,
Lim HW,
Metspalu A,
Mrowietz U,
Mucha S,
Rahman P,
Reis A,
Reis A,
Tejasvi T,
Trembath R,
Voorhees JJ,
Weidinger S,
Weichenthal M,
Wen X,
Eriksson N,
Kang HM,
Hinds DA,
Nair RP,
Abecasis GR,
Elder JT
Nature communications · 2017 · PMID 28537254 · open access
8 pages
A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study
Tintle NL,
Pottala JV,
Lacey S,
Ramachandran V,
Westra J,
Rogers A,
Clark J,
Olthoff B,
Larson M,
Harris W,
Shearer GC
Prostaglandins, leukotrienes, and essential fatty acids · 2015 · PMID 25500335
2 pages
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Stuart PE,
Nair RP,
Tsoi LC,
Tejasvi T,
Das S,
Kang HM,
Ellinghaus E,
Chandran V,
Callis-Duffin K,
Ike R,
Li Y,
Wen X
and 28 more — show all
Enerbäck C,
Gudjonsson JE,
Kõks S,
Kingo K,
Esko T,
Mrowietz U,
Reis A,
Wichmann HE,
Gieger C,
Hoffmann P,
Nöthen MM,
Winkelmann J,
Kunz M,
Moreta EG,
Mease PJ,
Ritchlin CT,
Bowcock AM,
Krueger GG,
Lim HW,
Weidinger S,
Weichenthal M,
Voorhees JJ,
Rahman P,
Gregersen PK,
Franke A,
Gladman DD,
Abecasis GR,
Elder JT
American journal of human genetics · 2015 · PMID 26626624
1 page
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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.