For researchers
Is your paper here?
2,662 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.
1 match for
Gianfagna F.
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret GB,
Ferreira T,
Chasman DI,
Jackson AU,
Schmidt EM,
Johnson T,
Thorleifsson G,
Luan J,
Donnelly LA,
Kanoni S,
Petersen AK,
Pihur V
and 301 more — show all
Strawbridge RJ,
Shungin D,
Hughes MF,
Meirelles O,
Kaakinen M,
Bouatia-Naji N,
Kristiansson K,
Shah S,
Kleber ME,
Guo X,
Lyytikäinen LP,
Fava C,
Eriksson N,
Nolte IM,
Magnusson PK,
Salfati EL,
Rallidis LS,
Theusch E,
Smith AJP,
Folkersen L,
Witkowska K,
Pers TH,
Joehanes R,
Kim SK,
Lataniotis L,
Jansen R,
Johnson AD,
Warren H,
Kim YJ,
Zhao W,
Wu Y,
Tayo BO,
Bochud M,
Absher D,
Adair LS,
Amin N,
Arking DE,
Axelsson T,
Baldassarre D,
Balkau B,
Bandinelli S,
Barnes MR,
Barroso I,
Bevan S,
Bis JC,
Bjornsdottir G,
Boehnke M,
Boerwinkle E,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Brown MJ,
Burnier M,
Cabrera CP,
Chambers JC,
Chang IS,
Cheng CY,
Chines PS,
Chung RH,
Collins FS,
Connell JM,
Döring A,
Dallongeville J,
Danesh J,
de Faire U,
Delgado G,
Dominiczak AF,
Doney ASF,
Drenos F,
Edkins S,
Eicher JD,
Elosua R,
Enroth S,
Erdmann J,
Eriksson P,
Esko T,
Evangelou E,
Evans A,
Fall T,
Farrall M,
Felix JF,
Ferrières J,
Ferrucci L,
Fornage M,
Forrester T,
Franceschini N,
Duran OHF,
Franco-Cereceda A,
Fraser RM,
Ganesh SK,
Gao H,
Gertow K,
Gianfagna F,
Gigante B,
Giulianini F,
Goel A,
Goodall AH,
Goodarzi MO,
Gorski M,
Gräßler J,
Groves C,
Gudnason V,
Gyllensten U,
Hallmans G,
Hartikainen AL,
Hassinen M,
Havulinna AS,
Hayward C,
Hercberg S,
Herzig KH,
Hicks AA,
Hingorani AD,
Hirschhorn JN,
Hofman A,
Holmen J,
Holmen OL,
Hottenga JJ,
Howard P,
Hsiung CA,
Hunt SC,
Ikram MA,
Illig T,
Iribarren C,
Jensen RA,
Kähönen M,
Kang H,
Kathiresan S,
Keating BJ,
Khaw KT,
Kim YK,
Kim E,
Kivimaki M,
Klopp N,
Kolovou G,
Komulainen P,
Kooner JS,
Kosova G,
Krauss RM,
Kuh D,
Kutalik Z,
Kuusisto J,
Kvaløy K,
Lakka TA,
Lee NR,
Lee IT,
Lee WJ,
Levy D,
Li X,
Liang KW,
Lin H,
Lin L,
Lindström J,
Lobbens S,
Männistö S,
Müller G,
Müller-Nurasyid M,
Mach F,
Markus HS,
Marouli E,
McCarthy MI,
McKenzie CA,
Meneton P,
Menni C,
Metspalu A,
Mijatovic V,
Moilanen L,
Montasser ME,
Morris AD,
Morrison AC,
Mulas A,
Nagaraja R,
Narisu N,
Nikus K,
O'Donnell CJ,
O'Reilly PF,
Ong KK,
Paccaud F,
Palmer CD,
Parsa A,
Pedersen NL,
Penninx BW,
Perola M,
Peters A,
Poulter N,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rao DC,
Rasheed A,
Rayner NWNWR,
Renström F,
Rettig R,
Rice KM,
Roberts R,
Rose LM,
Rossouw J,
Samani NJ,
Sanna S,
Saramies J,
Schunkert H,
Sebert S,
Sheu WH,
Shin YA,
Sim X,
Smit JH,
Smith AV,
Sosa MX,
Spector TD,
Stančáková A,
Stanton A,
Stirrups KE,
Stringham HM,
Sundstrom J,
Swift AJ,
Syvänen AC,
Tai ES,
Tanaka T,
Tarasov KV,
Teumer A,
Thorsteinsdottir U,
Tobin MD,
Tremoli E,
Uitterlinden AG,
Uusitupa M,
Vaez A,
Vaidya D,
van Duijn CM,
van Iperen EPA,
Vasan RS,
Verwoert GC,
Virtamo J,
Vitart V,
Voight BF,
Vollenweider P,
Wagner A,
Wain LV,
Wareham NJ,
Watkins H,
Weder AB,
Westra HJ,
Wilks R,
Wilsgaard T,
Wilson JF,
Wong TY,
Yang TP,
Yao J,
Yengo L,
Zhang W,
Zhao JH,
Zhu X,
Bovet P,
Cooper RS,
Mohlke KL,
Saleheen D,
Lee JY,
Elliott P,
Gierman HJ,
Willer CJ,
Franke L,
Hovingh GK,
Taylor KD,
Dedoussis G,
Sever P,
Wong A,
Lind L,
Assimes TL,
Njølstad I,
Schwarz PE,
Langenberg C,
Snieder H,
Caulfield MJ,
Melander O,
Laakso M,
Saltevo J,
Rauramaa R,
Tuomilehto J,
Ingelsson E,
Lehtimäki T,
Hveem K,
Palmas W,
März W,
Kumari M,
Salomaa V,
Chen YI,
Rotter JI,
Froguel P,
Jarvelin MR,
Lakatta EG,
Kuulasmaa K,
Franks PW,
Hamsten A,
Wichmann HE,
Palmer CNA,
Stefansson K,
Ridker PM,
Loos RJF,
Chakravarti A,
Deloukas P,
Morris AP,
Newton-Cheh C,
Munroe PB
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 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.