For researchers
Is your paper here?
2,657 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
Catellier D.
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Fornage M,
Debette S,
Bis JC,
Schmidt H,
Ikram MA,
Dufouil C,
Sigurdsson S,
Lumley T,
DeStefano AL,
Fazekas F,
Vrooman HA,
Shibata DK
and 51 more — show all
Maillard P,
Zijdenbos A,
Smith AV,
Gudnason H,
de Boer R,
Cushman M,
Mazoyer B,
Heiss G,
Vernooij MW,
Enzinger C,
Glazer NL,
Beiser A,
Knopman DS,
Cavalieri M,
Niessen WJ,
Harris TB,
Petrovic K,
Lopez OL,
Au R,
Lambert JC,
Hofman A,
Gottesman RF,
Garcia M,
Heckbert SR,
Atwood LD,
Catellier DJ,
Uitterlinden AG,
Yang Q,
Smith NL,
Aspelund T,
Romero JR,
Rice K,
Taylor KD,
Nalls MA,
Rotter JI,
Sharrett R,
van Duijn CM,
Amouyel P,
Wolf PA,
Gudnason V,
van der Lugt A,
Boerwinkle E,
Psaty BM,
Seshadri S,
Tzourio C,
Breteler MM,
Mosley TH,
Schmidt R,
Longstreth WT,
DeCarli C,
Launer LJ
Annals of neurology · 2011 · PMID 21681796
1 page
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram MA,
Fornage M,
Smith AV,
Seshadri S,
Schmidt R,
Debette S,
Vrooman HA,
Sigurdsson S,
Ropele S,
Taal HR,
Mook-Kanamori DO,
Coker LH
and 44 more — show all
Longstreth WT Jr,
Niessen WJ,
DeStefano AL,
Beiser A,
Zijdenbos AP,
Struchalin M,
Jack CR Jr,
Rivadeneira F,
Uitterlinden AG,
Knopman DS,
Hartikainen AL,
Pennell CE,
Thiering E,
Steegers EA,
Hakonarson H,
Heinrich J,
Palmer LJ,
Jarvelin MR,
McCarthy MI,
Grant SF,
St Pourcain B,
Timpson NJ,
Smith GD,
Sovio U,
Nalls MA,
Au R,
Hofman A,
Gudnason H,
van der Lugt A,
Harris TB,
Meeks WM,
Vernooij MW,
van Buchem MA,
Catellier D,
Jaddoe VW,
Gudnason V,
Windham BG,
Wolf PA,
van Duijn CM,
Mosley TH Jr,
Schmidt H,
Launer LJ,
Breteler MM,
DeCarli C
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
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.