For researchers
Is your paper here?
2,665 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.
11 matches for
Nagel M.
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
Heilmann-Heimbach S,
Herold C,
Hochfeld LM,
Hillmer AM,
Nyholt DR,
Hecker J,
Javed A,
Chew EG,
Pechlivanis S,
Drichel D,
Heng XT,
Del Rosario RC
and 24 more — show all
Fier HL,
Paus R,
Rueedi R,
Galesloot TE,
Moebus S,
Anhalt T,
Prabhakar S,
Li R,
Kanoni S,
Papanikolaou G,
Kutalik Z,
Deloukas P,
Philpott MP,
Waeber G,
Spector TD,
Vollenweider P,
Kiemeney LA,
Dedoussis G,
Richards JB,
Nothnagel M,
Martin NG,
Becker T,
Hinds DA,
Nöthen MM
Nature communications · 2017 · PMID 28272467 · open access
12 pages+
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Nagel M,
Jansen PR,
Stringer S,
Watanabe K,
de Leeuw CA,
Bryois J,
Savage JE,
Hammerschlag AR,
Skene NG,
Muñoz-Manchado AB,
White T,
Tiemeier H
and 6 more — show all
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Savage JE,
Jansen PR,
Stringer S,
Watanabe K,
Bryois J,
de Leeuw CA,
Nagel M,
Awasthi S,
Barr PB,
Coleman JRI,
Grasby KL,
Hammerschlag AR
and 105 more — show all
Kaminski JA,
Karlsson R,
Krapohl E,
Lam M,
Nygaard M,
Reynolds CA,
Trampush JW,
Young H,
Zabaneh D,
Hägg S,
Hansell NK,
Karlsson IK,
Linnarsson S,
Montgomery GW,
Muñoz-Manchado AB,
Quinlan EB,
Schumann G,
Skene NG,
Webb BT,
White T,
Arking DE,
Avramopoulos D,
Bilder RM,
Bitsios P,
Burdick KE,
Cannon TD,
Chiba-Falek O,
Christoforou A,
Cirulli ET,
Congdon E,
Corvin A,
Davies G,
Deary IJ,
DeRosse P,
Dickinson D,
Djurovic S,
Donohoe G,
Conley ED,
Eriksson JG,
Espeseth T,
Freimer NA,
Giakoumaki S,
Giegling I,
Gill M,
Glahn DC,
Hariri AR,
Hatzimanolis A,
Keller MC,
Knowles E,
Koltai D,
Konte B,
Lahti J,
Le Hellard S,
Lencz T,
Liewald DC,
London E,
Lundervold AJ,
Malhotra AK,
Melle I,
Morris D,
Need AC,
Ollier W,
Palotie A,
Payton A,
Pendleton N,
Poldrack RA,
Räikkönen K,
Reinvang I,
Roussos P,
Rujescu D,
Sabb FW,
Scult MA,
Smeland OB,
Smyrnis N,
Starr JM,
Steen VM,
Stefanis NC,
Straub RE,
Sundet K,
Tiemeier H,
Voineskos AN,
Weinberger DR,
Widen E,
Yu J,
Abecasis G,
Andreassen OA,
Breen G,
Christiansen L,
Debrabant B,
Dick DM,
Heinz A,
Hjerling-Leffler J,
Ikram MA,
Kendler KS,
Martin NG,
Medland SE,
Pedersen NL,
Plomin R,
Polderman TJC,
Ripke S,
van der Sluis S,
Sullivan PF,
Vrieze SI,
Wright MJ,
Posthuma D
Nature genetics · 2018 · PMID 29942086
12 pages+
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Jansen PR,
Watanabe K,
Stringer S,
Skene N,
Bryois J,
Hammerschlag AR,
de Leeuw CA,
Benjamins JS,
Muñoz-Manchado AB,
Nagel M,
Savage JE,
Tiemeier H
and 12 more — show all
White T,
Tung JY,
Hinds DA,
Vacic V,
Wang X,
Sullivan PF,
van der Sluis S,
Polderman TJC,
Smit AB,
Hjerling-Leffler J,
Van Someren EJW,
Posthuma D
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
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
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Buch S,
Stickel F,
Trépo E,
Way M,
Herrmann A,
Nischalke HD,
Brosch M,
Rosendahl J,
Berg T,
Ridinger M,
Rietschel M,
McQuillin A
and 36 more — show all
Frank J,
Kiefer F,
Schreiber S,
Lieb W,
Soyka M,
Semmo N,
Aigner E,
Datz C,
Schmelz R,
Brückner S,
Zeissig S,
Stephan AM,
Wodarz N,
Devière J,
Clumeck N,
Sarrazin C,
Lammert F,
Gustot T,
Deltenre P,
Völzke H,
Lerch MM,
Mayerle J,
Eyer F,
Schafmayer C,
Cichon S,
Nöthen MM,
Nothnagel M,
Ellinghaus D,
Huse K,
Franke A,
Zopf S,
Hellerbrand C,
Moreno C,
Franchimont D,
Morgan MY,
Hampe J
Nature genetics · 2015 · PMID 26482880
2 pages
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.