For researchers
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.
27 matches for
Klaver C,
showing the first 7.
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes
Sobrin L,
Ripke S,
Yu Y,
Fagerness J,
Bhangale TR,
Tan PL,
Souied EH,
Buitendijk GH,
Merriam JE,
Richardson AJ,
Raychaudhuri S,
Reynolds R
and 22 more — show all
Chin KA,
Lee AY,
Leveziel N,
Zack DJ,
Campochiaro P,
Smith RT,
Barile GR,
Hogg RE,
Chakravarthy U,
Behrens TW,
Uitterlinden AG,
van Duijn CM,
Vingerling JR,
Brantley MA Jr,
Baird PN,
Klaver CC,
Allikmets R,
Katsanis N,
Graham RR,
Ioannidis JP,
Daly MJ,
Seddon JM
Ophthalmology · 2012 · PMID 22705344
2 pages
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
and 96 more — show all
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
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
Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA,
Clark R,
Cui J,
Terry L,
Patasova K,
Haarman AEG,
Musolf AM,
Verhoeven VJM,
Klaver CCW,
Bailey-Wilson JE,
Hysi PG,
Williams C
CREAM Consortium · UK Biobank Eye Vision Consortium
Human molecular genetics · 2022 · PMID 35022715 · open access
2 pages
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
Jiang C,
Melles RB,
Yin J,
Fan Q,
Guo X,
Cheng CY,
He M,
Mackey DA,
Guggenheim JA,
Klaver C,
Nair KS,
Jorgenson E
and 1 more — show all
Consortium for Refractive Error and Myopia (CREAM)
Frontiers in genetics · 2023 · PMID 37351342 · open access
2 pages
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness
Hoehn R,
Zeller T,
Verhoeven VJ,
Grus F,
Adler M,
Wolfs RC,
Uitterlinden AG,
Castagne R,
Schillert A,
Klaver CC,
Pfeiffer N,
Mirshahi A
Human genetics · 2012 · PMID 22814818
1 page
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry
Hauser MA,
Allingham RR,
Aung T,
Van Der Heide CJ,
Taylor KD,
Rotter JI,
Wang SJ,
Bonnemaijer PWM,
Williams SE,
Abdullahi SM,
Abu-Amero KK,
Anderson MG
and 81 more — show all
Akafo S,
Alhassan MB,
Asimadu I,
Ayyagari R,
Bakayoko S,
Nyamsi PB,
Bowden DW,
Bromley WC,
Budenz DL,
Carmichael TR,
Challa P,
Chen YI,
Chuka-Okosa CM,
Cooke Bailey JN,
Costa VP,
Cruz DA,
DuBiner H,
Ervin JF,
Feldman RM,
Flamme-Wiese M,
Gaasterland DE,
Garnai SJ,
Girkin CA,
Guirou N,
Guo X,
Haines JL,
Hammond CJ,
Herndon L,
Hoffmann TJ,
Hulette CM,
Hydara A,
Igo RP Jr,
Jorgenson E,
Kabwe J,
Kilangalanga NJ,
Kizor-Akaraiwe N,
Kuchtey RW,
Lamari H,
Li Z,
Liebmann JM,
Liu Y,
Loos RJF,
Melo MB,
Moroi SE,
Msosa JM,
Mullins RF,
Nadkarni G,
Napo A,
Ng MCY,
Nunes HF,
Obeng-Nyarkoh E,
Okeke A,
Okeke S,
Olaniyi O,
Olawoye O,
Oliveira MB,
Pasquale LR,
Perez-Grossmann RA,
Pericak-Vance MA,
Qin X,
Ramsay M,
Resnikoff S,
Richards JE,
Schimiti RB,
Sim KS,
Sponsel WE,
Svidnicki PV,
Thiadens AAHJ,
Uche NJ,
van Duijn CM,
de Vasconcellos JPC,
Wiggs JL,
Zangwill LM,
Risch N,
Milea D,
Ashaye A,
Klaver CCW,
Weinreb RN,
Ashley Koch AE,
Fingert JH,
Khor CC
Genetics of Glaucoma in People of African Descent (GGLAD) Consortium
JAMA · 2019 · PMID 31688885
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.