For researchers
Is your paper here?
2,660 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.
4 matches for
Hennies HC.
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease
Riesmeijer SA,
Kamali Z,
Ng M,
Drichel D,
Piersma B,
Becker K,
Layton TB,
Nanchahal J,
Nothnagel M,
Vaez A,
Hennies HC,
Werker PMN
and 2 more — show all
Nature communications · 2024 · PMID 38172110 · open access
12 pages+
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis
Ng M,
Thakkar D,
Southam L,
Werker P,
Ophoff R,
Becker K,
Nothnagel M,
Franke A,
Nürnberg P,
Espirito-Santo AI,
Izadi D,
Hennies HC
and 3 more — show all
American journal of human genetics · 2017 · PMID 28886342 · open access
7 pages
Wnt signaling and Dupuytren's disease
Dolmans GH,
Werker PM,
Hennies HC,
Furniss D,
Festen EA,
Franke L,
Becker K,
van der Vlies P,
Wolffenbuttel BH,
Tinschert S,
Toliat MR,
Nothnagel M
and 7 more — show all
Dutch Dupuytren Study Group · German Dupuytren Study Group and 2 more consortia
The New England journal of medicine · 2011 · PMID 21732829
2 pages
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
Hillmer AM,
Hanneken S,
Ritzmann S,
Becker T,
Freudenberg J,
Brockschmidt FF,
Flaquer A,
Freudenberg-Hua Y,
Jamra RA,
Metzen C,
Heyn U,
Schweiger N
and 13 more — show all
Betz RC,
Blaumeiser B,
Hampe J,
Schreiber S,
Schulze TG,
Hennies HC,
Schumacher J,
Propping P,
Ruzicka T,
Cichon S,
Wienker TF,
Kruse R,
Nothen MM
American journal of human genetics · 2005 · PMID 15902657
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.