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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.
7 matches for
Saemundsdottir J.
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Oskarsson GR,
Oddsson A,
Magnusson MK,
Kristjansson RP,
Halldorsson GH,
Ferkingstad E,
Zink F,
Helgadottir A,
Ivarsdottir EV,
Arnadottir GA,
Jensson BO,
Katrinardottir H
and 26 more — show all
Sveinbjornsson G,
Kristinsdottir AM,
Lee AL,
Saemundsdottir J,
Stefansdottir L,
Sigurdsson JK,
Davidsson OB,
Benonisdottir S,
Jonasdottir A,
Jonasdottir A,
Jonsson S,
Gudmundsson RL,
Asselbergs FW,
Tragante V,
Gunnarsson B,
Masson G,
Thorleifsson G,
Rafnar T,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2020 · PMID 32327693 · open access
12 pages+
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
Multiple genetic loci for bone mineral density and fractures
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Center JR,
Nguyen TV,
Bagger Y,
Gulcher JR
and 6 more — show all
The New England journal of medicine · 2008 · PMID 18445777
2 pages
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir S,
Baas AF,
Thorleifsson G,
Holm H,
den Heijer M,
de Vries JP,
Kranendonk SE,
Zeebregts CJ,
van Sterkenburg SM,
Geelkerken RH,
van Rij AM,
Williams MJ
and 90 more — show all
Boll AP,
Kostic JP,
Jonasdottir A,
Jonasdottir A,
Walters GB,
Masson G,
Sulem P,
Saemundsdottir J,
Mouy M,
Magnusson KP,
Tromp G,
Elmore JR,
Sakalihasan N,
Limet R,
Defraigne JO,
Ferrell RE,
Ronkainen A,
Ruigrok YM,
Wijmenga C,
Grobbee DE,
Shah SH,
Granger CB,
Quyyumi AA,
Vaccarino V,
Patel RS,
Zafari AM,
Levey AI,
Austin H,
Girelli D,
Pignatti PF,
Olivieri O,
Martinelli N,
Malerba G,
Trabetti E,
Becker LC,
Becker DM,
Reilly MP,
Rader DJ,
Mueller T,
Dieplinger B,
Haltmayer M,
Urbonavicius S,
Lindblad B,
Gottsäter A,
Gaetani E,
Pola R,
Wells P,
Rodger M,
Forgie M,
Langlois N,
Corral J,
Vicente V,
Fontcuberta J,
España F,
Grarup N,
Jørgensen T,
Witte DR,
Hansen T,
Pedersen O,
Aben KK,
de Graaf J,
Holewijn S,
Folkersen L,
Franco-Cereceda A,
Eriksson P,
Collier DA,
Stefansson H,
Steinthorsdottir V,
Rafnar T,
Valdimarsson EM,
Magnadottir HB,
Sveinbjornsdottir S,
Olafsson I,
Magnusson MK,
Palmason R,
Haraldsdottir V,
Andersen K,
Onundarson PT,
Thorgeirsson G,
Kiemeney LA,
Powell JT,
Carey DJ,
Kuivaniemi H,
Lindholt JS,
Jones GT,
Kong A,
Blankensteijn JD,
Matthiasson SE,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20622881
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
New sequence variants associated with bone mineral density
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Snorradóttir S,
Center JR,
Nguyen TV,
Alexandersen P
and 7 more — show all
Nature genetics · 2009 · PMID 19079262
1 page
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
Oskarsson GR,
Kristjansson RP,
Lee AL,
Sveinbjornsson G,
Magnusson MK,
Ivarsdottir EV,
Benonisdottir S,
Oddsson A,
Davidsson OB,
Saemundsdottir J,
Halldorsson GH,
Arthur J
and 11 more — show all
Arnadottir GA,
Masson G,
Jensson BO,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2018 · PMID 30271932 · 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.