For researchers
Is your paper here?
2,649 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.
5 matches for
Lewis S.
Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective
Dack K,
Ludwig KU,
Stergiakouli E,
Sandy J,
Aryee S,
Davey Smith G,
Davies A,
Wren Y,
Sharp GC,
Humphries K,
Mangold E,
Goudswaard L
and 3 more — show all
Human molecular genetics · 2025 · PMID 41075272 · open access
12 pages+
Novel genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
Multiple newly identified loci associated with prostate cancer susceptibility
Eeles RA,
Kote-Jarai Z,
Giles GG,
Olama AA,
Guy M,
Jugurnauth SK,
Mulholland S,
Leongamornlert DA,
Edwards SM,
Morrison J,
Field HI,
Southey MC
and 34 more — show all
Severi G,
Donovan JL,
Hamdy FC,
Dearnaley DP,
Muir KR,
Smith C,
Bagnato M,
Ardern-Jones AT,
Hall AL,
O'Brien LT,
Gehr-Swain BN,
Wilkinson RA,
Cox A,
Lewis S,
Brown PM,
Jhavar SG,
Tymrakiewicz M,
Lophatananon A,
Bryant SL,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Woodhouse CJ,
Thompson A,
Christmas T,
Ogden C,
Fisher C,
Jamieson C,
Cooper CS,
English DR,
Hopper JL,
Neal DE,
Easton DF
UK Genetic Prostate Cancer Study Collaborators · British Association of Urological Surgeons' Section of Oncology and 1 more consortia
Nature genetics · 2008 · PMID 18264097
3 pages
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.