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.
2 matches for
Daniell M.
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Hardcastle AJ,
Liskova P,
Bykhovskaya Y,
McComish BJ,
Davidson AE,
Inglehearn CF,
Li X,
Choquet H,
Habeeb M,
Lucas SEM,
Sahebjada S,
Pontikos N
and 50 more — show all
Lopez KER,
Khawaja AP,
Ali M,
Dudakova L,
Skalicka P,
Van Dooren BTH,
Geerards AJM,
Haudum CW,
Faro VL,
Tenen A,
Simcoe MJ,
Patasova K,
Yarrand D,
Yin J,
Siddiqui S,
Rice A,
Farraj LA,
Chen YI,
Rahi JS,
Krauss RM,
Theusch E,
Charlesworth JC,
Szczotka-Flynn L,
Toomes C,
Meester-Smoor MA,
Richardson AJ,
Mitchell PA,
Taylor KD,
Melles RB,
Aldave AJ,
Mills RA,
Cao K,
Chan E,
Daniell MD,
Wang JJ,
Rotter JI,
Hewitt AW,
MacGregor S,
Klaver CCW,
Ramdas WD,
Craig JE,
Iyengar SK,
O'Brart D,
Jorgenson E,
Baird PN,
Rabinowitz YS,
Burdon KP,
Hammond CJ,
Tuft SJ,
Hysi PG
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
Meng W,
Shah KP,
Pollack S,
Toppila I,
Hebert HL,
McCarthy MI,
Groop L,
Ahlqvist E,
Lyssenko V,
Agardh E,
Daniell M,
Kaidonis G
and 28 more — show all
Craig JE,
Mitchell P,
Liew G,
Kifley A,
Wang JJ,
Christiansen MW,
Jensen RA,
Penman A,
Hancock HA,
Chen CJ,
Correa A,
Kuo JZ,
Li X,
Chen YI,
Rotter JI,
Klein R,
Klein B,
Wong TY,
Morris AD,
Doney ASF,
Colhoun HM,
Price AL,
Burdon KP,
Groop PH,
Sandholm N,
Grassi MA,
Sobrin L,
Palmer CNA
Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Acta ophthalmologica · 2018 · PMID 30178632 · 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.