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Is your paper here?
2,661 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.
5 matches for
Bergen AA.
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
and 86 more — show all
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
and 96 more — show all
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
A genome-wide association study of optic disc parameters
Ramdas WD,
van Koolwijk LM,
Ikram MK,
Jansonius NM,
de Jong PT,
Bergen AA,
Isaacs A,
Amin N,
Aulchenko YS,
Wolfs RC,
Hofman A,
Rivadeneira F
and 8 more — show all
PLoS genetics · 2010 · PMID 20548946 · open access
5 pages
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Solouki AM,
Verhoeven VJ,
van Duijn CM,
Verkerk AJ,
Ikram MK,
Hysi PG,
Despriet DD,
van Koolwijk LM,
Ho L,
Ramdas WD,
Czudowska M,
Kuijpers RW
and 23 more — show all
Amin N,
Struchalin M,
Aulchenko YS,
van Rij G,
Riemslag FC,
Young TL,
Mackey DA,
Spector TD,
Gorgels TG,
Willemse-Assink JJ,
Isaacs A,
Kramer R,
Swagemakers SM,
Bergen AA,
van Oosterhout AA,
Oostra BA,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
de Jong PT,
Hammond CJ,
Vingerling JR,
Klaver CC
Nature genetics · 2010 · PMID 20835239
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 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.