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Is your paper here?
2,663 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.
29 matches for
Pedersen OB,
showing the first 9.
Genetic effects on the timing of parturition and links to fetal birth weight
Solé-Navais P,
Flatley C,
Steinthorsdottir V,
Vaudel M,
Juodakis J,
Chen J,
Laisk T,
LaBella AL,
Westergaard D,
Bacelis J,
Brumpton B,
Skotte L
and 73 more — show all
Borges MC,
Helgeland Ø,
Mahajan A,
Wielscher M,
Lin F,
Briggs C,
Wang CA,
Moen GH,
Beaumont RN,
Bradfield JP,
Abraham A,
Thorleifsson G,
Gabrielsen ME,
Ostrowski SR,
Modzelewska D,
Nohr EA,
Hypponen E,
Srivastava A,
Talbot O,
Allard C,
Williams SM,
Menon R,
Shields BM,
Sveinbjornsson G,
Xu H,
Melbye M,
Lowe W Jr,
Bouchard L,
Oken E,
Pedersen OB,
Gudbjartsson DF,
Erikstrup C,
Sørensen E,
Lie RT,
Teramo K,
Hallman M,
Juliusdottir T,
Hakonarson H,
Ullum H,
Hattersley AT,
Sletner L,
Merialdi M,
Rifas-Shiman SL,
Steingrimsdottir T,
Scholtens D,
Power C,
West J,
Nyegaard M,
Capra JA,
Skogholt AH,
Magnus P,
Andreassen OA,
Thorsteinsdottir U,
Grant SFA,
Qvigstad E,
Pennell CE,
Hivert MF,
Hayes GM,
Jarvelin MR,
McCarthy MI,
Lawlor DA,
Nielsen HS,
Mägi R,
Rokas A,
Hveem K,
Stefansson K,
Feenstra B,
Njolstad P,
Muglia LJ,
Freathy RM,
Johansson S,
Zhang G,
Jacobsson B
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
Genomics of chronic dry cough unravels neurological pathways
Coley K,
John C,
Ghouse J,
Shepherd DJ,
Shrine N,
Izquierdo AG,
Kanoni S,
Magavern EF,
Packer R,
McGarvey L,
Smith JA,
Bundgaard H
and 11 more — show all
Ostrowski SR,
Erikstrup C,
Pedersen OBV,
van Heel DA,
Hennah W,
Marttila M,
Free RC,
Hollox EJ,
Wain LV,
Tobin MD,
Batini C
Genes and Health Research Team
The European respiratory journal · 2025 · PMID 40675770 · open access
4 pages
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
and 41 more — show all
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
and 66 more — show all
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus
Mathey CM,
Maj C,
Eriksson N,
Krebs K,
Westmeier J,
David FS,
Koromina M,
Scheer AB,
Szabo N,
Wedi B,
Wieczorek D,
Amann PM
and 39 more — show all
Löffler H,
Koch L,
Schöffl C,
Dickel H,
Ganjuur N,
Hornung T,
Buhl T,
Greve J,
Wurpts G,
Aygören-Pürsün E,
Steffens M,
Herms S,
Heilmann-Heimbach S,
Hoffmann P,
Schmidt B,
Mavarani L,
Andresen T,
Sørensen SB,
Andersen V,
Vogel U,
Landén M,
Bulik CM,
Bygum A,
Magnusson PKE,
von Buchwald C,
Hallberg P,
Rye Ostrowski S,
Sørensen E,
Pedersen OB,
Ullum H,
Erikstrup C,
Bundgaard H,
Milani L,
Rasmussen ER,
Wadelius M,
Ghouse J,
Sachs B,
Nöthen MM,
Forstner AJ
Estonian Biobank Research Team · DBDS Genomic Consortium
The Journal of allergy and clinical immunology · 2024 · PMID 38300190
2 pages
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
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
Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement
Henkel C,
Styrkársdóttir U,
Thorleifsson G,
Stefánsdóttir L,
Björnsdóttir G,
Banasik K,
Brunak S,
Erikstrup C,
Dinh KM,
Hansen TF,
Nielsen KR,
Bruun MT
and 10 more — show all
DBDS Genomic Consortium
Annals of the rheumatic diseases · 2023 · PMID 36376028
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.