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.
5 matches for
Schwinn M.
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
and 18 more — show all
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
12 pages+
Genome-wide association study and polygenic risk prediction of hypothyroidism
Rand SA,
Ahlberg G,
Tragante V,
Monfort LM,
Zheng C,
Feldt-Rasmussen U,
Klose MC,
Teder-Laving M,
Metspalu A,
Poulsen HE,
Ellervik C,
Nygaard B
and 18 more — show all
Erikstrup C,
Bruun MT,
A Jensen B,
Ullum H,
Brunak S,
Schwinn M,
Ostrowski SR,
Pedersen OB,
Sørensen E,
Jonsdottir I,
Gudbjartsson DF,
Thorleifsson G,
Holm H,
Saevarsdottir S,
Stefansson K,
Salling Olesen M,
Bundgaard H,
Ghouse J
DBDS Genomic Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2025 · PMID 41238958 · open access
12 pages+
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
Tyrmi JS,
Karjalainen J,
Venkatesh SS,
Benoit-Pilven C,
Lemmelä SM,
Brunak S,
Aagaard B,
Bruun MT,
Erikstrup C,
Ullum H,
Pedersen OB,
Banasik K
and 19 more — show all
Sørensen E,
Mikkelsen C,
Schwinn M,
Sturluson A,
Ostrowski SR,
Kettunen J,
Nielsen HS,
Nyegaard M,
Westergaard D,
Rafnar T,
Sulem P,
Stefansson K,
Palta P,
Laisk T,
Tukiainen T,
Lindgren CM,
Daly M,
Havulinna AS,
Laivuori HM
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Ghouse J,
Ahlberg G,
Andreasen L,
Banasik K,
Brunak S,
Schwinn M,
Larsen IH,
Petersen O,
Sørensen E,
Ullum H,
Rasmussen ER,
Eriksson N
and 4 more — show all
Journal of the American College of Cardiology · 2021 · PMID 34384552
1 page
Established risk loci for systemic lupus erythematosus at NCF2, STAT4, TNPO3, IRF5 and ITGAM associate with distinct clinical manifestations: A Danish genome-wide association study
Leffers HCB,
Westergaard D,
Saevarsdottir S,
Jonsdottir I,
Pedersen OB,
Troldborg A,
Voss A,
Kristensen S,
Lindhardsen J,
Kumar P,
Linauskas A,
Juul L
and 12 more — show all
Krogh NS,
Deleuran B,
Dreyer L,
Schwinn M,
Thørner LW,
Hindhede L,
Erikstrup C,
Ullum H,
Brunak S,
Stefansson K,
Banasik K,
Jacobsen S
DBDS genomic consortium
Joint bone spine · 2022 · PMID 35167971
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.