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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.
6 matches for
Einarsson G.
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+
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Bjornsdottir G,
Stefansdottir L,
Thorleifsson G,
Sulem P,
Norland K,
Ferkingstad E,
Oddsson A,
Zink F,
Lund SH,
Nawaz MS,
Bragi Walters G,
Skuladottir AT
and 32 more — show all
Gudjonsson SA,
Einarsson G,
Halldorsson GH,
Bjarnadottir V,
Sveinbjornsson G,
Helgadottir A,
Styrkarsdottir U,
Gudmundsson LJ,
Pedersen OB,
Hansen TF,
Werge T,
Banasik K,
Troelsen A,
Skou ST,
Thørner LW,
Erikstrup C,
Nielsen KR,
Mikkelsen S,
Jonsdottir I,
Bjornsson A,
Olafsson IH,
Ulfarsson E,
Blondal J,
Vikingsson A,
Brunak S,
Ostrowski SR,
Ullum H,
Thorsteinsdottir U,
Stefansson H,
Gudbjartsson DF,
Thorgeirsson TE,
Stefansson K
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
8 pages
Genetic correction of PSA values using sequence variants associated with PSA levels
Gudmundsson J,
Besenbacher S,
Sulem P,
Gudbjartsson DF,
Olafsson I,
Arinbjarnarson S,
Agnarsson BA,
Benediktsdottir KR,
Isaksson HJ,
Kostic JP,
Gudjonsson SA,
Stacey SN
and 37 more — show all
Gylfason A,
Sigurdsson A,
Holm H,
Bjornsdottir US,
Eyjolfsson GI,
Navarrete S,
Fuertes F,
Garcia-Prats MD,
Polo E,
Checherita IA,
Jinga M,
Badea P,
Aben KK,
Schalken JA,
van Oort IM,
Sweep FC,
Helfand BT,
Davis M,
Donovan JL,
Hamdy FC,
Kristjansson K,
Gulcher JR,
Masson G,
Kong A,
Catalona WJ,
Mayordomo JI,
Geirsson G,
Einarsson GV,
Barkardottir RB,
Jonsson E,
Jinga V,
Mates D,
Kiemeney LA,
Neal DE,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Science translational medicine · 2010 · PMID 21160077
4 pages
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Stacey SN,
Zink F,
Halldorsson GH,
Stefansdottir L,
Gudjonsson SA,
Einarsson G,
Hjörleifsson G,
Eiriksdottir T,
Helgadottir A,
Björnsdottir G,
Thorgeirsson TE,
Olafsdottir TA
and 19 more — show all
Jonsdottir I,
Gretarsdottir S,
Tragante V,
Magnusson MK,
Jonsson H,
Gudmundsson J,
Olafsson S,
Holm H,
Gudbjartsson DF,
Sulem P,
Helgason A,
Thorsteinsdottir U,
Tryggvadottir L,
Rafnar T,
Melsted P,
Ulfarsson MÖ,
Vidarsson B,
Thorleifsson G,
Stefansson K
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Gudmundsson J,
Sulem P,
Rafnar T,
Bergthorsson JT,
Manolescu A,
Gudbjartsson D,
Agnarsson BA,
Sigurdsson A,
Benediktsdottir KR,
Blondal T,
Jakobsdottir M,
Stacey SN
and 59 more — show all
Kostic J,
Kristinsson KT,
Birgisdottir B,
Ghosh S,
Magnusdottir DN,
Thorlacius S,
Thorleifsson G,
Zheng SL,
Sun J,
Chang BL,
Elmore JB,
Breyer JP,
McReynolds KM,
Bradley KM,
Yaspan BL,
Wiklund F,
Stattin P,
Lindström S,
Adami HO,
McDonnell SK,
Schaid DJ,
Cunningham JM,
Wang L,
Cerhan JR,
St Sauver JL,
Isaacs SD,
Wiley KE,
Partin AW,
Walsh PC,
Polo S,
Ruiz-Echarri M,
Navarrete S,
Fuertes F,
Saez B,
Godino J,
Weijerman PC,
Swinkels DW,
Aben KK,
Witjes JA,
Suarez BK,
Helfand BT,
Frigge ML,
Kristjansson K,
Ober C,
Jonsson E,
Einarsson GV,
Xu J,
Gronberg H,
Smith JR,
Thibodeau SN,
Isaacs WB,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Barkardottir RB,
Gulcher JR,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2008 · PMID 18264098
3 pages
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Blondal T,
Gylfason A,
Agnarsson BA,
Benediktsdottir KR,
Magnusdottir DN,
Orlygsdottir G,
Jakobsdottir M,
Stacey SN,
Sigurdsson A
and 32 more — show all
Wahlfors T,
Tammela T,
Breyer JP,
McReynolds KM,
Bradley KM,
Saez B,
Godino J,
Navarrete S,
Fuertes F,
Murillo L,
Polo E,
Aben KK,
van Oort IM,
Suarez BK,
Helfand BT,
Kan D,
Zanon C,
Frigge ML,
Kristjansson K,
Gulcher JR,
Einarsson GV,
Jonsson E,
Catalona WJ,
Mayordomo JI,
Kiemeney LA,
Smith JR,
Schleutker J,
Barkardottir RB,
Kong A,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2009 · PMID 19767754
3 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.