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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.
11 matches for
Albagha O.
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations
Thareja G,
Belkadi A,
Arnold M,
Albagha OME,
Graumann J,
Schmidt F,
Grallert H,
Peters A,
Gieger C,
Consortium TQGPR,
Suhre K
Human molecular genetics · 2023 · PMID 36168886 · open access
12 pages+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
and 170 more — show all
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
Albagha OM,
Wani SE,
Visconti MR,
Alonso N,
Goodman K,
Brandi ML,
Cundy T,
Chung PY,
Dargie R,
Devogelaer JP,
Falchetti A,
Fraser WD
and 17 more — show all
Gennari L,
Gianfrancesco F,
Hooper MJ,
Van Hul W,
Isaia G,
Nicholson GC,
Nuti R,
Papapoulos S,
Montes Jdel P,
Ratajczak T,
Rea SL,
Rendina D,
Gonzalez-Sarmiento R,
Di Stefano M,
Ward LC,
Walsh JP,
Ralston SH
Genetic Determinants of Paget's Disease (GDPD) Consortium
Nature genetics · 2011 · PMID 21623375
4 pages
A multi-ancestry genome-wide association study and evaluation of polygenic scores of LDL-C levels
Ismail Umlai UK,
Toor SM,
Al-Sarraj YA,
Mohammed S,
Al Hail MSH,
Ullah E,
Kunji K,
El-Menyar A,
Gomaa M,
Jayyousi A,
Saad M,
Qureshi N
and 2 more — show all
Journal of lipid research · 2025 · PMID 39909172 · open access
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.