For researchers
Is your paper here?
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.
3 matches for
Lavanya R.
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
Khor CC,
Ramdas WD,
Vithana EN,
Cornes BK,
Sim X,
Tay WT,
Saw SM,
Zheng Y,
Lavanya R,
Wu R,
Wang JJ,
Mitchell P
and 13 more — show all
Uitterlinden AG,
Rivadeneira F,
Teo YY,
Chia KS,
Seielstad M,
Hibberd M,
Vingerling JR,
Klaver CC,
Jansonius NM,
Tai ES,
Wong TY,
van Duijn CM,
Aung T
Human molecular genetics · 2011 · PMID 21307088
2 pages
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore
Han S,
Chen P,
Fan Q,
Khor CC,
Sim X,
Tay WT,
Ong RT,
Suo C,
Goh LK,
Lavanya R,
Zheng Y,
Wu R
and 10 more — show all
Human molecular genetics · 2011 · PMID 21665993
2 pages
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur ME,
Khor CC,
Jia H,
Cornes BK,
Chen LJ,
Qiao C,
Nair KS,
Cheng CY,
Xu L,
George R,
Tan D,
Abu-Amero K
and 61 more — show all
Perera SA,
Ozaki M,
Mizoguchi T,
Kurimoto Y,
Low S,
Tajudin LS,
Ho CL,
Tham CC,
Soto I,
Chew PT,
Wong HT,
Shantha B,
Kuroda M,
Osman EA,
Tang G,
Fan S,
Meng H,
Wang H,
Feng B,
Yong VH,
Ting SM,
Li Y,
Wang YX,
Li Z,
Lavanya R,
Wu RY,
Zheng YF,
Su DH,
Loon SC,
Yong VK,
Allingham RR,
Hauser MA,
Soumittra N,
Ramprasad VL,
Waseem N,
Yaakub A,
Chia KS,
Kumaramanickavel G,
Wong TT,
How AC,
Chau TN,
Simmons CP,
Bei JX,
Zeng YX,
Bhattacharya SS,
Zhang M,
Tan DT,
Teo YY,
Al-Obeidan SA,
Hon DN,
Tai ES,
Saw SM,
Foster PJ,
Vijaya L,
Jonas JB,
Wong TY,
John SW,
Pang CP,
Vithana EN,
Wang N,
Aung T
PLoS genetics · 2014 · PMID 24603532 · 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.