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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.
12 matches for
Allen R.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Wain LV,
Shrine N,
Artigas MS,
Erzurumluoglu AM,
Noyvert B,
Bossini-Castillo L,
Obeidat M,
Henry AP,
Portelli MA,
Hall RJ,
Billington CK,
Rimington TL
and 94 more — show all
Fenech AG,
John C,
Blake T,
Jackson VE,
Allen RJ,
Prins BP,
Campbell A,
Porteous DJ,
Jarvelin MR,
Wielscher M,
James AL,
Hui J,
Wareham NJ,
Zhao JH,
Wilson JF,
Joshi PK,
Stubbe B,
Rawal R,
Schulz H,
Imboden M,
Probst-Hensch NM,
Karrasch S,
Gieger C,
Deary IJ,
Harris SE,
Marten J,
Rudan I,
Enroth S,
Gyllensten U,
Kerr SM,
Polasek O,
Kähönen M,
Surakka I,
Vitart V,
Hayward C,
Lehtimäki T,
Raitakari OT,
Evans DM,
Henderson AJ,
Pennell CE,
Wang CA,
Sly PD,
Wan ES,
Busch R,
Hobbs BD,
Litonjua AA,
Sparrow DW,
Gulsvik A,
Bakke PS,
Crapo JD,
Beaty TH,
Hansel NN,
Mathias RA,
Ruczinski I,
Barnes KC,
Bossé Y,
Joubert P,
van den Berge M,
Brandsma CA,
Paré PD,
Sin DD,
Nickle DC,
Hao K,
Gottesman O,
Dewey FE,
Bruse SE,
Carey DJ,
Kirchner HL,
Jonsson S,
Thorleifsson G,
Jonsdottir I,
Gislason T,
Stefansson K,
Schurmann C,
Nadkarni G,
Bottinger EP,
Loos RJ,
Walters RG,
Chen Z,
Millwood IY,
Vaucher J,
Kurmi OP,
Li L,
Hansell AL,
Brightling C,
Zeggini E,
Cho MH,
Silverman EK,
Sayers I,
Trynka G,
Morris AP,
Strachan DP,
Hall IP,
Tobin MD
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis
Kemp JP,
Morris JA,
Medina-Gomez C,
Forgetta V,
Warrington NM,
Youlten SE,
Zheng J,
Gregson CL,
Grundberg E,
Trajanoska K,
Logan JG,
Pollard AS
and 26 more — show all
Sparkes PC,
Ghirardello EJ,
Allen R,
Leitch VD,
Butterfield NC,
Komla-Ebri D,
Adoum AT,
Curry KF,
White JK,
Kussy F,
Greenlaw KM,
Xu C,
Harvey NC,
Cooper C,
Adams DJ,
Greenwood CMT,
Maurano MT,
Kaptoge S,
Rivadeneira F,
Tobias JH,
Croucher PI,
Ackert-Bicknell CL,
Bassett JHD,
Williams GR,
Richards JB,
Evans DM
Nature genetics · 2017 · PMID 28869591 · open access
12 pages+
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
and 99 more — show all
Reeve NF,
Obeidat M,
Zhao JH,
Wielscher M,
Weiss S,
Kentistou KA,
Kentistou KA,
Cook JP,
Sun BB,
Zhou J,
Hui J,
Karrasch S,
Imboden M,
Harris SE,
Marten J,
Enroth S,
Kerr SM,
Surakka I,
Vitart V,
Lehtimäki T,
Allen RJ,
Bakke PS,
Beaty TH,
Bleecker ER,
Bossé Y,
Brandsma CA,
Chen Z,
Crapo JD,
Danesh J,
DeMeo DL,
Dudbridge F,
Ewert R,
Gieger C,
Gulsvik A,
Hansell AL,
Hao K,
Hoffman JD,
Hokanson JE,
Homuth G,
Joshi PK,
Joubert P,
Langenberg C,
Li X,
Li L,
Lin K,
Lind L,
Locantore N,
Luan J,
Mahajan A,
Maranville JC,
Murray A,
Nickle DC,
Packer R,
Parker MM,
Paynton ML,
Porteous DJ,
Porteous DJ,
Prokopenko D,
Qiao D,
Rawal R,
Runz H,
Sayers I,
Sin DD,
Smith BH,
Soler Artigas M,
Sparrow D,
Tal-Singer R,
Timmers PRHJ,
Van den Berge M,
Whittaker JC,
Woodruff PG,
Yerges-Armstrong LM,
Troyanskaya OG,
Raitakari OT,
Kähönen M,
Polašek O,
Gyllensten U,
Rudan I,
Deary IJ,
Probst-Hensch NM,
Schulz H,
James AL,
Wilson JF,
Stubbe B,
Zeggini E,
Jarvelin MR,
Wareham N,
Silverman EK,
Hayward C,
Morris AP,
Butterworth AS,
Scott RA,
Walters RG,
Meyers DA,
Cho MH,
Strachan DP,
Hall IP,
Tobin MD,
Wain LV
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair B,
Zhao C,
Bell S,
Tilch E,
Salminen AV,
Pütz B,
Dauvilliers Y,
Stefani A,
Högl B,
Poewe W,
Kemlink D,
Sonka K
and 39 more — show all
Bachmann CG,
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek Z,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Allen RP,
Earley CJ,
Ondo WG,
Xiong L,
Montplaisir J,
Gan-Or Z,
Perola M,
Vodicka P,
Dina C,
Franke A,
Tittmann L,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rouleau GA,
Berger K,
Oexle K,
Di Angelantonio E,
Hinds DA,
Müller-Myhsok B,
Winkelmann J
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
10 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
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Wain LV,
Shrine N,
Miller S,
Jackson VE,
Ntalla I,
Soler Artigas M,
Billington CK,
Kheirallah AK,
Allen R,
Cook JP,
Probert K,
Obeidat M
and 27 more — show all
Bossé Y,
Hao K,
Postma DS,
Paré PD,
Ramasamy A,
Mägi R,
Mihailov E,
Reinmaa E,
Melén E,
O'Connell J,
Frangou E,
Delaneau O,
Freeman C,
Petkova D,
McCarthy M,
Sayers I,
Deloukas P,
Hubbard R,
Pavord I,
Hansell AL,
Thomson NC,
Zeggini E,
Morris AP,
Marchini J,
Strachan DP,
Tobin MD,
Hall IP
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
6 pages
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1
Winkelmann J,
Czamara D,
Schormair B,
Knauf F,
Schulte EC,
Trenkwalder C,
Dauvilliers Y,
Polo O,
Högl B,
Berger K,
Fuhs A,
Gross N
and 45 more — show all
Stiasny-Kolster K,
Oertel W,
Bachmann CG,
Paulus W,
Xiong L,
Montplaisir J,
Rouleau GA,
Fietze I,
Vávrová J,
Kemlink D,
Sonka K,
Nevsimalova S,
Lin SC,
Wszolek Z,
Vilariño-Güell C,
Farrer MJ,
Gschliesser V,
Frauscher B,
Falkenstetter T,
Poewe W,
Allen RP,
Earley CJ,
Ondo WG,
Le WD,
Spieler D,
Kaffe M,
Zimprich A,
Kettunen J,
Perola M,
Silander K,
Cournu-Rebeix I,
Francavilla M,
Fontenille C,
Fontaine B,
Vodicka P,
Prokisch H,
Lichtner P,
Peppard P,
Faraco J,
Mignot E,
Gieger C,
Illig T,
Wichmann HE,
Müller-Myhsok B,
Meitinger T
PLoS genetics · 2011 · PMID 21779176 · open access
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
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
Hobbs BD,
Putman RK,
Araki T,
Nishino M,
Gudmundsson G,
Gudnason V,
Eiriksdottir G,
Zilhao Nogueira NR,
Dupuis J,
Xu H,
O'Connor GT,
Manichaikul A
and 30 more — show all
Nguyen J,
Podolanczuk AJ,
Madahar P,
Rotter JI,
Lederer DJ,
Barr RG,
Rich SS,
Ampleford EJ,
Ortega VE,
Peters SP,
O'Neal WK,
Newell JD Jr,
Bleecker ER,
Meyers DA,
Allen RJ,
Oldham JM,
Ma SF,
Noth I,
Jenkins RG,
Maher TM,
Hubbard RB,
Wain LV,
Fingerlin TE,
Schwartz DA,
Washko GR,
Rosas IO,
Silverman EK,
Hatabu H,
Cho MH,
Hunninghake GM
American journal of respiratory and critical care medicine · 2019 · PMID 31339356
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
Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection
Packer RJ,
Shrine N,
Hall R,
Melbourne CA,
Thompson R,
Williams AT,
Paynton ML,
Guyatt AL,
Allen RJ,
Lee PH,
John C,
Campbell A
and 12 more — show all
Hayward C,
de Vries M,
Vonk JM,
Davitte J,
Hessel E,
Michalovich D,
Betts JC,
Sayers I,
Yeo A,
Hall IP,
Tobin MD,
Wain LV
The European respiratory journal · 2023 · PMID 37263751 · 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.