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Is your paper here?
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.
Search your name, your journal, or a PMID.
3 matches for
Brion M.
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Arking DE,
Pulit SL,
Crotti L,
van der Harst P,
Munroe PB,
Koopmann TT,
Sotoodehnia N,
Rossin EJ,
Morley M,
Wang X,
Johnson AD,
Lundby A
and 218 more — show all
Gudbjartsson DF,
Noseworthy PA,
Eijgelsheim M,
Bradford Y,
Tarasov KV,
Dörr M,
Müller-Nurasyid M,
Lahtinen AM,
Nolte IM,
Smith AV,
Bis JC,
Isaacs A,
Newhouse SJ,
Evans DS,
Post WS,
Waggott D,
Lyytikäinen LP,
Hicks AA,
Eisele L,
Ellinghaus D,
Hayward C,
Navarro P,
Ulivi S,
Tanaka T,
Tester DJ,
Chatel S,
Gustafsson S,
Kumari M,
Morris RW,
Naluai ÅT,
Padmanabhan S,
Kluttig A,
Strohmer B,
Panayiotou AG,
Torres M,
Knoflach M,
Hubacek JA,
Slowikowski K,
Raychaudhuri S,
Kumar RD,
Harris TB,
Launer LJ,
Shuldiner AR,
Alonso A,
Bader JS,
Ehret G,
Huang H,
Kao WH,
Strait JB,
Macfarlane PW,
Brown M,
Caulfield MJ,
Samani NJ,
Kronenberg F,
Willeit J,
Smith JG,
Greiser KH,
Meyer Zu Schwabedissen H,
Werdan K,
Carella M,
Zelante L,
Heckbert SR,
Psaty BM,
Rotter JI,
Kolcic I,
Polašek O,
Wright AF,
Griffin M,
Daly MJ,
Arnar DO,
Hólm H,
Thorsteinsdottir U,
Denny JC,
Roden DM,
Zuvich RL,
Emilsson V,
Plump AS,
Larson MG,
O'Donnell CJ,
Yin X,
Bobbo M,
D'Adamo AP,
Iorio A,
Sinagra G,
Carracedo A,
Cummings SR,
Nalls MA,
Jula A,
Kontula KK,
Marjamaa A,
Oikarinen L,
Perola M,
Porthan K,
Erbel R,
Hoffmann P,
Jöckel KH,
Kälsch H,
Nöthen MM,
den Hoed M,
Loos RJ,
Thelle DS,
Gieger C,
Meitinger T,
Perz S,
Peters A,
Prucha H,
Sinner MF,
Waldenberger M,
de Boer RA,
Franke L,
van der Vleuten PA,
Beckmann BM,
Martens E,
Bardai A,
Hofman N,
Wilde AA,
Behr ER,
Dalageorgou C,
Giudicessi JR,
Medeiros-Domingo A,
Barc J,
Kyndt F,
Probst V,
Ghidoni A,
Insolia R,
Hamilton RM,
Scherer SW,
Brandimarto J,
Margulies K,
Moravec CE,
del Greco M F,
Fuchsberger C,
O'Connell JR,
Lee WK,
Watt GC,
Campbell H,
Wild SH,
El Mokhtari NE,
Frey N,
Asselbergs FW,
Mateo Leach I,
Navis G,
van den Berg MP,
van Veldhuisen DJ,
Kellis M,
Krijthe BP,
Franco OH,
Hofman A,
Kors JA,
Uitterlinden AG,
Witteman JC,
Kedenko L,
Lamina C,
Oostra BA,
Abecasis GR,
Lakatta EG,
Mulas A,
Orrú M,
Schlessinger D,
Uda M,
Markus MR,
Völker U,
Snieder H,
Spector TD,
Ärnlöv J,
Lind L,
Sundström J,
Syvänen AC,
Kivimaki M,
Kähönen M,
Mononen N,
Raitakari OT,
Viikari JS,
Adamkova V,
Kiechl S,
Brion M,
Nicolaides AN,
Paulweber B,
Haerting J,
Dominiczak AF,
Nyberg F,
Whincup PH,
Hingorani AD,
Schott JJ,
Bezzina CR,
Ingelsson E,
Ferrucci L,
Gasparini P,
Wilson JF,
Rudan I,
Franke A,
Mühleisen TW,
Pramstaller PP,
Lehtimäki TJ,
Paterson AD,
Parsa A,
Liu Y,
van Duijn CM,
Siscovick DS,
Gudnason V,
Jamshidi Y,
Salomaa V,
Felix SB,
Sanna S,
Ritchie MD,
Stricker BH,
Stefansson K,
Boyer LA,
Cappola TP,
Olsen JV,
Lage K,
Schwartz PJ,
Kääb S,
Chakravarti A,
Ackerman MJ,
Pfeufer A,
de Bakker PI,
Newton-Cheh C
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
Novel risk loci for COVID-19 hospitalization among admixed American populations
Diz-de Almeida S,
Cruz R,
Luchessi AD,
Lorenzo-Salazar JM,
de Heredia ML,
Quintela I,
González-Montelongo R,
Nogueira Silbiger V,
Porras MS,
Tenorio Castaño JA,
Nevado J,
Aguado JM
and 109 more — show all
Aguilar C,
Aguilera-Albesa S,
Almadana V,
Almoguera B,
Alvarez N,
Andreu-Bernabeu Á,
Arana-Arri E,
Arango C,
Arranz MJ,
Artiga MJ,
Baptista-Rosas RC,
Barreda-Sánchez M,
Belhassen-Garcia M,
Bezerra JF,
Bezerra MAC,
Boix-Palop L,
Brion M,
Brugada R,
Bustos M,
Calderón EJ,
Carbonell C,
Castano L,
Castelao JE,
Conde-Vicente R,
Cordero-Lorenzana ML,
Cortes-Sanchez JL,
Corton M,
Darnaude MT,
De Martino-Rodríguez A,
Del Campo-Pérez V,
de Bustamante AD,
Domínguez-Garrido E,
Eirós R,
Fariñas MC,
Fernandez-Nestosa MJ,
Fernández-Robelo U,
Fernández-Rodríguez A,
Fernández-Villa T,
Gago-Dominguez M,
Gil-Fournier B,
Gómez-Arrue J,
Álvarez BG,
Bernaldo de Quirós FG,
González-Neira A,
González-Peñas J,
Gutiérrez-Bautista JF,
Herrero MJ,
Herrero-Gonzalez A,
Jimenez-Sousa MA,
Lattig MC,
Borja AL,
Lopez-Rodriguez R,
Mancebo E,
Martín-López C,
Martín V,
Martinez-Nieto O,
Martinez-Lopez I,
Martinez-Resendez MF,
Martinez-Perez A,
Mazzeu JF,
Macías EM,
Minguez P,
Cuerda VM,
Oliveira SF,
Ortega-Paino E,
Parellada M,
Paz-Artal E,
Santos NPC,
Pérez-Matute P,
Perez P,
Pérez-Tomás ME,
Perucho T,
Pinsach-Abuin M,
Pita G,
Pompa-Mera EN,
Porras-Hurtado GL,
Pujol A,
León SR,
Resino S,
Fernandes MR,
Rodríguez-Ruiz E,
Rodriguez-Artalejo F,
Rodriguez-Garcia JA,
Ruiz-Cabello F,
Ruiz-Hornillos J,
Ryan P,
Soria JM,
Souto JC,
Tamayo E,
Tamayo-Velasco A,
Taracido-Fernandez JC,
Teper A,
Torres-Tobar L,
Urioste M,
Valencia-Ramos J,
Yáñez Z,
Zarate R,
de Rojas I,
Ruiz A,
Sánchez P,
Real LM,
Guillen-Navarro E,
Ayuso C,
Parra E,
Riancho JA,
Rojas-Martinez A,
Flores C,
Lapunzina P,
Carracedo Á
SCOURGE Cohort Group
eLife · 2024 · PMID 39361370 · open access
12 pages+
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Chen W,
Stambolian D,
Edwards AO,
Branham KE,
Othman M,
Jakobsdottir J,
Tosakulwong N,
Pericak-Vance MA,
Campochiaro PA,
Klein ML,
Tan PL,
Conley YP
and 54 more — show all
Kanda A,
Kopplin L,
Li Y,
Augustaitis KJ,
Karoukis AJ,
Scott WK,
Agarwal A,
Kovach JL,
Schwartz SG,
Postel EA,
Brooks M,
Baratz KH,
Brown WL,
Brucker AJ,
Orlin A,
Brown G,
Ho A,
Regillo C,
Donoso L,
Tian L,
Kaderli B,
Hadley D,
Hagstrom SA,
Peachey NS,
Klein R,
Klein BE,
Gotoh N,
Yamashiro K,
Ferris Iii F,
Fagerness JA,
Reynolds R,
Farrer LA,
Kim IK,
Miller JW,
Cortón M,
Carracedo A,
Sanchez-Salorio M,
Pugh EW,
Doheny KF,
Brion M,
Deangelis MM,
Weeks DE,
Zack DJ,
Chew EY,
Heckenlively JR,
Yoshimura N,
Iyengar SK,
Francis PJ,
Katsanis N,
Seddon JM,
Haines JL,
Gorin MB,
Abecasis GR,
Swaroop A
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
3 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.