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.
206 matches for
Stefansson K,
showing the first 6.
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Didriksen M,
Nawaz MS,
Dowsett J,
Bell S,
Erikstrup C,
Pedersen OB,
Sørensen E,
Jennum PJ,
Burgdorf KS,
Burchell B,
Butterworth AS,
Soranzo N
and 22 more — show all
Rye DB,
Trotti LM,
Saini P,
Stefansdottir L,
Magnusson SH,
Thorleifsson G,
Sigmundsson T,
Sigurdsson AP,
Van Den Hurk K,
Quee F,
Tanck MWT,
Ouwehand WH,
Roberts DJ,
Earley EJ,
Busch MP,
Mast AE,
Page GP,
Danesh J,
Di Angelantonio E,
Stefansson H,
Ullum H,
Stefansson K
Communications biology · 2020 · PMID 33239738 · open access
1 page
Germline variants at SOHLH2 influence multiple myeloma risk
Duran-Lozano L,
Thorleifsson G,
Lopez de Lapuente Portilla A,
Niroula A,
Went M,
Thodberg M,
Pertesi M,
Ajore R,
Cafaro C,
Olason PI,
Stefansdottir L,
Bragi Walters G
and 15 more — show all
Halldorsson GH,
Turesson I,
Kaiser MF,
Weinhold N,
Abildgaard N,
Andersen NF,
Mellqvist UH,
Waage A,
Juul-Vangsted A,
Thorsteinsdottir U,
Hansson M,
Houlston R,
Rafnar T,
Stefansson K,
Nilsson B
Blood cancer journal · 2021 · PMID 33875642 · open access
1 page
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
Skuladottir AT,
Bjornsdottir G,
Nawaz MS,
Petersen H,
Rognvaldsson S,
Moore KHS,
Olafsson PI,
Magnusson SH,
Bjornsdottir A,
Sveinsson OA,
Sigurdardottir GR,
Saevarsdottir S
and 19 more — show all
Ivarsdottir EV,
Stefansdottir L,
Gunnarsson B,
Muhlestein JB,
Knowlton KU,
Jones DA,
Nadauld LD,
Hartmann AM,
Rujescu D,
Strupp M,
Walters GB,
Thorgeirsson TE,
Jonsdottir I,
Holm H,
Thorleifsson G,
Gudbjartsson DF,
Sulem P,
Stefansson H,
Stefansson K
Communications biology · 2021 · PMID 34620984 · open access
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
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
Kristjansson RP,
Oskarsson GR,
Skuladottir A,
Oddsson A,
Rognvaldsson S,
Sveinbjornsson G,
Lund SH,
Jensson BO,
Styrmisdottir EL,
Halldorsson GH,
Ferkingstad E,
Eldjarn GH
and 25 more — show all
Beyter D,
Kristmundsdottir S,
Juliusson K,
Fridriksdottir R,
Arnadottir GA,
Katrinardottir H,
Snorradottir MH,
Tragante V,
Stefansdottir L,
Ivarsdottir EV,
Bjornsdottir G,
Halldorsson BV,
Thorleifsson G,
Ludviksson BR,
Onundarson PT,
Saevarsdottir S,
Melsted P,
Norddahl GL,
Bjornsdottir US,
Olafsdottir T,
Gudbjartsson DF,
Thorsteinsdottir U,
Jonsdottir I,
Sulem P,
Stefansson K
Communications biology · 2023 · PMID 37430141 · open access
1 page
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development
Ghouse J,
Gellert-Kristensen H,
O'Rourke CJ,
Seidelin AS,
Thorleifsson G,
Sveinbjörnsson G,
Tragante V,
Konkwo C,
Brancale J,
Vilarinho S,
Eyrich TM,
Ahlberg G
and 36 more — show all
Bundgaard JS,
Rand SA,
Lundegaard PR,
Sørensen E,
Mikkelsen C,
Træholt J,
Erikstrup C,
Dinh KM,
Bruun MT,
Jensen BA,
Bay JT,
Brunak S,
Banasik K,
Ullum H,
Laisk T,
Mägi R,
Nadauld LD,
Knowlton KU,
Knight S,
Gluud LL,
Vistisen K,
Björnsson ES,
Ulfarsson MO,
Sulem P,
Holm H,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Rafnar T,
Stefansson K,
Lassen U,
Pommergaard HC,
Hillingsø JG,
Andersen JB,
Bundgaard H,
Stender S
DBDS Genomic Consortium, Estonian Biobank Research Team
JHEP reports : innovation in hepatology · 2025 · PMID 40823170 · 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.