For researchers
Is your paper here?
2,682 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.
26 matches for
St Pourcain B,
showing the first 6.
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
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
Medina-Gomez C,
Kemp JP,
Estrada K,
Eriksson J,
Liu J,
Reppe S,
Evans DM,
Heppe DH,
Vandenput L,
Herrera L,
Ring SM,
Kruithof CJ
and 16 more — show all
Timpson NJ,
Zillikens MC,
Olstad OK,
Zheng HF,
Richards JB,
St Pourcain B,
Hofman A,
Jaddoe VW,
Smith GD,
Lorentzon M,
Gautvik KM,
Uitterlinden AG,
Brommage R,
Ohlsson C,
Tobias JH,
Rivadeneira F
PLoS genetics · 2012 · PMID 22792070 · open access
1 page
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans
Guggenheim JA,
McMahon G,
Kemp JP,
Akhtar S,
St Pourcain B,
Northstone K,
Ring SM,
Evans DM,
Smith GD,
Timpson NJ,
Williams C
Molecular vision · 2013 · PMID 23401653 · open access
1 page
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence
St Pourcain B,
Skuse DH,
Mandy WP,
Wang K,
Hakonarson H,
Timpson NJ,
Evans DM,
Kemp JP,
Ring SM,
McArdle WL,
Golding J,
Smith GD
Molecular autism · 2014 · PMID 24564958 · open access
1 page
A genome-wide association study of body mass index across early life and childhood
Warrington NM,
Howe LD,
Paternoster L,
Kaakinen M,
Herrala S,
Huikari V,
Wu YY,
Kemp JP,
Timpson NJ,
St Pourcain B,
Davey Smith G,
Tilling K
and 6 more — show all
International journal of epidemiology · 2015 · PMID 25953783 · open access
1 page
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology
Howe LJ,
Lee MK,
Sharp GC,
Davey Smith G,
St Pourcain B,
Shaffer JR,
Ludwig KU,
Mangold E,
Marazita ML,
Feingold E,
Zhurov A,
Stergiakouli E
and 5 more — show all
PLoS genetics · 2018 · PMID 30067744 · 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.