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.
3 matches for
Aviv A.
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Lu AT,
Xue L,
Salfati EL,
Chen BH,
Ferrucci L,
Levy D,
Joehanes R,
Murabito JM,
Kiel DP,
Tsai PC,
Yet I,
Bell JT
and 27 more — show all
Mangino M,
Tanaka T,
McRae AF,
Marioni RE,
Visscher PM,
Wray NR,
Deary IJ,
Levine ME,
Quach A,
Assimes T,
Tsao PS,
Absher D,
Stewart JD,
Li Y,
Reiner AP,
Hou L,
Baccarelli AA,
Whitsel EA,
Aviv A,
Cardona A,
Day FR,
Wareham NJ,
Perry JRB,
Ong KK,
Raj K,
Lunetta KL,
Horvath S
Nature communications · 2018 · PMID 29374233 · open access
6 pages
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans
Mangino M,
Hwang SJ,
Spector TD,
Hunt SC,
Kimura M,
Fitzpatrick AL,
Christiansen L,
Petersen I,
Elbers CC,
Harris T,
Chen W,
Srinivasan SR
and 27 more — show all
Kark JD,
Benetos A,
El Shamieh S,
Visvikis-Siest S,
Christensen K,
Berenson GS,
Valdes AM,
Viñuela A,
Garcia M,
Arnett DK,
Broeckel U,
Province MA,
Pankow JS,
Kammerer C,
Liu Y,
Nalls M,
Tishkoff S,
Thomas F,
Ziv E,
Psaty BM,
Bis JC,
Rotter JI,
Taylor KD,
Smith E,
Schork NJ,
Levy D,
Aviv A
Human molecular genetics · 2012 · PMID 23001564 · open access
4 pages
Common variants near TERC are associated with mean telomere length
Codd V,
Mangino M,
van der Harst P,
Braund PS,
Kaiser M,
Beveridge AJ,
Rafelt S,
Moore J,
Nelson C,
Soranzo N,
Zhai G,
Valdes AM
and 16 more — show all
Blackburn H,
Mateo Leach I,
de Boer RA,
Kimura M,
Aviv A,
Goodall AH,
Ouwehand W,
van Veldhuisen DJ,
van Gilst WH,
Navis G,
Burton PR,
Tobin MD,
Hall AS,
Thompson JR,
Spector T,
Samani NJ
Wellcome Trust Case Control Consortium
Nature genetics · 2010 · PMID 20139977
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.