For researchers
Is your paper here?
2,673 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.
9 matches for
Jonsson T.
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Olafsson S,
Alexandersson KF,
Gizurarson JGK,
Hauksdottir K,
Gunnarsson O,
Olafsson K,
Gudmundsson J,
Stacey SN,
Sveinbjornsson G,
Saemundsdottir J,
Bjornsson ES,
Olafsson S
and 22 more — show all
Bjornsson S,
Orvar KB,
Vikingsson A,
Geirsson AJ,
Arinbjarnarson S,
Bjornsdottir G,
Thorgeirsson TE,
Sigurdsson S,
Halldorsson GH,
Magnusson OT,
Masson G,
Holm H,
Jonsdottir I,
Sigurdardottir O,
Eyjolfsson GI,
Olafsson I,
Sulem P,
Thorsteinsdottir U,
Jonsson T,
Rafnar T,
Gudbjartsson DF,
Stefansson K
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
11 pages
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Gudmundsson J,
Sigurdsson JK,
Stefansdottir L,
Agnarsson BA,
Isaksson HJ,
Stefansson OA,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Frigge ML,
Stacey SN,
Sulem P
and 16 more — show all
Halldorsson GH,
Tragante V,
Holm H,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Jonsson T,
Jonsson E,
Barkardottir RB,
Hilmarsson R,
Asselbergs FW,
Geirsson G,
Thorsteinsdottir U,
Rafnar T,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30410027 · open access
9 pages
Rare and Common Variants Conferring Risk of Tooth Agenesis
Jonsson L,
Magnusson TE,
Thordarson A,
Jonsson T,
Geller F,
Feenstra B,
Melbye M,
Nohr EA,
Vucic S,
Vucic S,
Dhamo B,
Rivadeneira F
and 25 more — show all
Ongkosuwito EM,
Wolvius EB,
Leslie EJ,
Marazita ML,
Howe BJ,
Moreno Uribe LM,
Alonso I,
Santos M,
Pinho T,
Jonsson R,
Audolfsson G,
Gudmundsson L,
Nawaz MS,
Olafsson S,
Gustafsson O,
Ingason A,
Unnsteinsdottir U,
Bjornsdottir G,
Walters GB,
Zervas M,
Oddsson A,
Gudbjartsson DF,
Steinberg S,
Stefansson H,
Stefansson K
Journal of dental research · 2018 · PMID 29364747
4 pages
Many sequence variants affecting diversity of adult human height
Gudbjartsson DF,
Walters GB,
Thorleifsson G,
Stefansson H,
Halldorsson BV,
Zusmanovich P,
Sulem P,
Thorlacius S,
Gylfason A,
Steinberg S,
Helgadottir A,
Ingason A
and 25 more — show all
Steinthorsdottir V,
Olafsdottir EJ,
Olafsdottir GH,
Jonsson T,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Pedersen O,
Aben KK,
Witjes JA,
Swinkels DW,
den Heijer M,
Franke B,
Verbeek AL,
Becker DM,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Gulcher J,
Kiemeney LA,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18391951
3 pages
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Masson G,
He H,
Jonasdottir A,
Sigurdsson A,
Stacey SN,
Johannsdottir H,
Helgadottir HT,
Li W
and 35 more — show all
Nagy R,
Ringel MD,
Kloos RT,
de Visser MC,
Plantinga TS,
den Heijer M,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Walters GB,
Bjarnason H,
Tryggvadottir L,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Olafsson I,
Kristjansson K,
Kristvinsson H,
Magnusson OT,
Thorleifsson G,
Gulcher JR,
Kong A,
Kiemeney LA,
Jonsson T,
Hjartarson H,
Mayordomo JI,
Netea-Maier RT,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Rafnar T,
Stefansson K
Nature genetics · 2012 · PMID 22267200
3 pages
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Thorleifsson G,
Walters GB,
Gudbjartsson DF,
Steinthorsdottir V,
Sulem P,
Helgadottir A,
Styrkarsdottir U,
Gretarsdottir S,
Thorlacius S,
Jonsdottir I,
Jonsdottir T,
Olafsdottir EJ
and 23 more — show all
Olafsdottir GH,
Jonsson T,
Jonsson F,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Lauritzen T,
Aben KK,
Verbeek AL,
Roeleveld N,
Kampman E,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Becker DM,
Gulcher J,
Kiemeney LA,
Pedersen O,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19079260
2 pages
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
Gudmundsson J,
Sulem P,
Gudbjartsson DF,
Jonasson JG,
Sigurdsson A,
Bergthorsson JT,
He H,
Blondal T,
Geller F,
Jakobsdottir M,
Magnusdottir DN,
Matthiasdottir S
and 26 more — show all
Stacey SN,
Skarphedinsson OB,
Helgadottir H,
Li W,
Nagy R,
Aguillo E,
Faure E,
Prats E,
Saez B,
Martinez M,
Eyjolfsson GI,
Bjornsdottir US,
Holm H,
Kristjansson K,
Frigge ML,
Kristvinsson H,
Gulcher JR,
Jonsson T,
Rafnar T,
Hjartarsson H,
Mayordomo JI,
de la Chapelle A,
Hrafnkelsson J,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature genetics · 2009 · PMID 19198613
2 pages
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeirsson TE,
Geller F,
Sulem P,
Rafnar T,
Wiste A,
Magnusson KP,
Manolescu A,
Thorleifsson G,
Stefansson H,
Ingason A,
Stacey SN,
Bergthorsson JT
and 45 more — show all
Thorlacius S,
Gudmundsson J,
Jonsson T,
Jakobsdottir M,
Saemundsdottir J,
Olafsdottir O,
Gudmundsson LJ,
Bjornsdottir G,
Kristjansson K,
Skuladottir H,
Isaksson HJ,
Gudbjartsson T,
Jones GT,
Mueller T,
Gottsäter A,
Flex A,
Aben KKH,
de Vegt F,
Mulders PFA,
Isla D,
Vidal MJ,
Asin L,
Saez B,
Murillo L,
Blondal T,
Kolbeinsson H,
Stefansson JG,
Hansdottir I,
Runarsdottir V,
Pola R,
Lindblad B,
van Rij AM,
Dieplinger B,
Haltmayer M,
Mayordomo JI,
Kiemeney LA,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Gudbjartsson DF,
Gulcher JR,
Jonsson S,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature · 2008 · PMID 18385739
1 page
A genome-wide association study yields five novel thyroid cancer risk loci
Gudmundsson J,
Thorleifsson G,
Sigurdsson JK,
Stefansdottir L,
Jonasson JG,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Johannsdottir H,
Halldorsson GH,
Stacey SN,
Helgason H
and 28 more — show all
Sulem P,
Senter L,
He H,
Liyanarachchi S,
Ringel MD,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Xu L,
Kiemeney LA,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Kristvinsson H,
Netea-Maier RT,
Jonsson T,
Mayordomo JI,
Plantinga TS,
Hjartarson H,
Hrafnkelsson J,
Sturgis EM,
Thorsteinsdottir U,
Rafnar T,
de la Chapelle A,
Stefansson K
Nature communications · 2017 · PMID 28195142 · 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.