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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.
9 matches for
Flores C.
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Waage J,
Standl M,
Curtin JA,
Jessen LE,
Thorsen J,
Tian C,
Schoettler N,
Flores C,
Abdellaoui A,
Ahluwalia TS,
Alves AC,
Amaral AFS
and 76 more — show all
Antó JM,
Arnold A,
Barreto-Luis A,
Baurecht H,
van Beijsterveldt CEM,
Bleecker ER,
Bonàs-Guarch S,
Boomsma DI,
Brix S,
Bunyavanich S,
Burchard EG,
Chen Z,
Curjuric I,
Custovic A,
den Dekker HT,
Dharmage SC,
Dmitrieva J,
Duijts L,
Ege MJ,
Gauderman WJ,
Georges M,
Gieger C,
Gilliland F,
Granell R,
Gui H,
Hansen T,
Heinrich J,
Henderson J,
Hernandez-Pacheco N,
Holt P,
Imboden M,
Jaddoe VWV,
Jarvelin MR,
Jarvis DL,
Jensen KK,
Jónsdóttir I,
Kabesch M,
Kaprio J,
Kumar A,
Lee YA,
Levin AM,
Li X,
Lorenzo-Diaz F,
Melén E,
Mercader JM,
Meyers DA,
Myers R,
Nicolae DL,
Nohr EA,
Palviainen T,
Paternoster L,
Pennell CE,
Pershagen G,
Pino-Yanes M,
Probst-Hensch NM,
Rüschendorf F,
Simpson A,
Stefansson K,
Sunyer J,
Sveinbjornsson G,
Thiering E,
Thompson PJ,
Torrent M,
Torrents D,
Tung JY,
Wang CA,
Weidinger S,
Weiss S,
Willemsen G,
Williams LK,
Ober C,
Hinds DA,
Ferreira MA,
Bisgaard H,
Strachan DP,
Bønnelykke K
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Pairo-Castineira E,
Rawlik K,
Bretherick AD,
Qi T,
Wu Y,
Nassiri I,
McConkey GA,
Zechner M,
Klaric L,
Griffiths F,
Oosthuyzen W,
Kousathanas A
and 43 more — show all
Richmond A,
Millar J,
Russell CD,
Malinauskas T,
Thwaites R,
Morrice K,
Keating S,
Maslove D,
Nichol A,
Semple MG,
Knight J,
Shankar-Hari M,
Summers C,
Hinds C,
Horby P,
Ling L,
McAuley D,
Montgomery H,
Openshaw PJM,
Begg C,
Walsh T,
Tenesa A,
Flores C,
Riancho JA,
Rojas-Martinez A,
Lapunzina P,
Yang J,
Ponting CP,
Wilson JF,
Vitart V,
Abedalthagafi M,
Luchessi AD,
Parra EJ,
Cruz R,
Carracedo A,
Fawkes A,
Murphy L,
Rowan K,
Pereira AC,
Law A,
Fairfax B,
Hendry SC,
Baillie JK
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · 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+
Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis
Allen RJ,
Stockwell A,
Oldham JM,
Guillen-Guio B,
Schwartz DA,
Maher TM,
Flores C,
Noth I,
Yaspan BL,
Jenkins RG,
Wain LV
International IPF Genetics Consortium
Thorax · 2022 · PMID 35688625
7 pages
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
Noth I,
Zhang Y,
Ma SF,
Flores C,
Barber M,
Huang Y,
Broderick SM,
Wade MS,
Hysi P,
Scuirba J,
Richards TJ,
Juan-Guardela BM
and 9 more — show all
The Lancet. Respiratory medicine · 2013 · PMID 24429156
2 pages
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study
Allen RJ,
Porte J,
Braybrooke R,
Flores C,
Fingerlin TE,
Oldham JM,
Guillen-Guio B,
Ma SF,
Okamoto T,
John AE,
Obeidat M,
Yang IV
and 31 more — show all
Henry A,
Hubbard RB,
Navaratnam V,
Saini G,
Thompson N,
Booth HL,
Hart SP,
Hill MR,
Hirani N,
Maher TM,
McAnulty RJ,
Millar AB,
Molyneaux PL,
Parfrey H,
Rassl DM,
Whyte MKB,
Fahy WA,
Marshall RP,
Oballa E,
Bossé Y,
Nickle DC,
Sin DD,
Timens W,
Shrine N,
Sayers I,
Hall IP,
Noth I,
Schwartz DA,
Tobin MD,
Wain LV,
Jenkins RG
The Lancet. Respiratory medicine · 2017 · PMID 29066090 · open access
2 pages
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis
Allen RJ,
Guillen-Guio B,
Oldham JM,
Ma SF,
Dressen A,
Paynton ML,
Kraven LM,
Obeidat M,
Li X,
Ng M,
Braybrooke R,
Molina-Molina M
and 54 more — show all
Hobbs BD,
Putman RK,
Sakornsakolpat P,
Booth HL,
Fahy WA,
Hart SP,
Hill MR,
Hirani N,
Hubbard RB,
McAnulty RJ,
Millar AB,
Navaratnam V,
Oballa E,
Parfrey H,
Saini G,
Whyte MKB,
Zhang Y,
Kaminski N,
Adegunsoye A,
Strek ME,
Neighbors M,
Sheng XR,
Gudmundsson G,
Gudnason V,
Hatabu H,
Lederer DJ,
Manichaikul A,
Newell JD Jr,
O'Connor GT,
Ortega VE,
Xu H,
Fingerlin TE,
Bossé Y,
Hao K,
Joubert P,
Nickle DC,
Sin DD,
Timens W,
Furniss D,
Morris AP,
Zondervan KT,
Hall IP,
Sayers I,
Tobin MD,
Maher TM,
Cho MH,
Hunninghake GM,
Schwartz DA,
Yaspan BL,
Molyneaux PL,
Flores C,
Noth I,
Jenkins RG,
Wain LV
American journal of respiratory and critical care medicine · 2020 · PMID 31710517 · open access
2 pages
Identification of a novel locus associated with skin colour in African-admixed populations
Hernandez-Pacheco N,
Flores C,
Alonso S,
Eng C,
Mak AC,
Hunstman S,
Hu D,
White MJ,
Oh SS,
Meade K,
Farber HJ,
Avila PC
and 10 more — show all
Scientific reports · 2017 · PMID 28300201 · open access
1 page
Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study
Allen RJ,
Oldham JM,
Jenkins DA,
Leavy OC,
Guillen-Guio B,
Melbourne CA,
Ma SF,
Jou J,
Kim JS,
Fahy WA,
Oballa E,
Hubbard RB
and 19 more — show all
Navaratnam V,
Braybrooke R,
Saini G,
Roach KM,
Tobin MD,
Hirani N,
Whyte MKB,
Kaminski N,
Zhang Y,
Martinez FJ,
Linderholm AL,
Adegunsoye A,
Strek ME,
Maher TM,
Molyneaux PL,
Flores C,
Noth I,
Gisli Jenkins R,
Wain LV
CleanUP-IPF Investigators of the Pulmonary Trials Cooperative
The Lancet. Respiratory medicine · 2023 · PMID 35985358 · 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.