For researchers
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.
27 matches for
Thorgeirsson T,
showing the first 7.
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Sulem P,
Gudbjartsson DF,
Geller F,
Prokopenko I,
Feenstra B,
Aben KK,
Franke B,
den Heijer M,
Kovacs P,
Stumvoll M,
Mägi R,
Yanek LR
and 18 more — show all
Becker LC,
Boyd HA,
Stacey SN,
Walters GB,
Jonasdottir A,
Thorleifsson G,
Holm H,
Gudjonsson SA,
Rafnar T,
Björnsdottir G,
Becker DM,
Melbye M,
Kong A,
Tönjes A,
Thorgeirsson T,
Thorsteinsdottir U,
Kiemeney LA,
Stefansson K
Human molecular genetics · 2011 · PMID 21357676
1 page
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Power RA,
Tansey KE,
Buttenschøn HN,
Cohen-Woods S,
Bigdeli T,
Hall LS,
Kutalik Z,
Lee SH,
Ripke S,
Steinberg S,
Teumer A,
Viktorin A
and 64 more — show all
Wray NR,
Arolt V,
Baune BT,
Boomsma DI,
Børglum AD,
Byrne EM,
Castelao E,
Craddock N,
Craig IW,
Dannlowski U,
Deary IJ,
Degenhardt F,
Forstner AJ,
Gordon SD,
Grabe HJ,
Grove J,
Hamilton SP,
Hayward C,
Heath AC,
Hocking LJ,
Homuth G,
Hottenga JJ,
Kloiber S,
Krogh J,
Landén M,
Lang M,
Levinson DF,
Lichtenstein P,
Lucae S,
MacIntyre DJ,
Madden P,
Magnusson PKE,
Martin NG,
McIntosh AM,
Middeldorp CM,
Milaneschi Y,
Montgomery GW,
Mors O,
Müller-Myhsok B,
Nyholt DR,
Oskarsson H,
Owen MJ,
Padmanabhan S,
Penninx BWJH,
Pergadia ML,
Porteous DJ,
Potash JB,
Preisig M,
Rivera M,
Shi J,
Shyn SI,
Sigurdsson E,
Smit JH,
Smith BH,
Stefansson H,
Stefansson K,
Strohmaier J,
Sullivan PF,
Thomson P,
Thorgeirsson TE,
Van der Auwera S,
Weissman MM,
Breen G,
Lewis CM
CONVERGE Consortium, CARDIoGRAM Consortium, GERAD1 Consortium
Biological psychiatry · 2017 · PMID 27519822 · open access
1 page
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Lo MT,
Hinds DA,
Tung JY,
Franz C,
Fan CC,
Wang Y,
Smeland OB,
Schork A,
Holland D,
Kauppi K,
Sanyal N,
Escott-Price V
and 10 more — show all
Nature genetics · 2017 · PMID 27918536
1 page
The nature of nurture: Effects of parental genotypes
Kong A,
Thorleifsson G,
Frigge ML,
Vilhjalmsson BJ,
Young AI,
Thorgeirsson TE,
Benonisdottir S,
Oddsson A,
Halldorsson BV,
Masson G,
Gudbjartsson DF,
Helgason A
and 3 more — show all
Science (New York, N.Y.) · 2018 · PMID 29371463
1 page
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
Bjornsdottir G,
Ivarsdottir EV,
Bjarnadottir K,
Benonisdottir S,
Gylfadottir SS,
Arnadottir GA,
Benediktsson R,
Halldorsson GH,
Helgadottir A,
Jonasdottir A,
Jonasdottir A,
Jonsdottir I
and 21 more — show all
Kristinsdottir AM,
Magnusson OT,
Masson G,
Melsted P,
Rafnar T,
Sigurdsson A,
Sigurdsson G,
Skuladottir A,
Steinthorsdottir V,
Styrkarsdottir U,
Thorgeirsson G,
Thorleifsson G,
Vikingsson A,
Gudbjartsson DF,
Holm H,
Stefansson H,
Thorsteinsdottir U,
Norddahl GL,
Sulem P,
Thorgeirsson TE,
Stefansson K
Nature communications · 2019 · PMID 30992453 · 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
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
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.