For researchers
Is your paper here?
2,657 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.
3 matches for
de Juan A.
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
Mutations in BRIP1 confer high risk of ovarian cancer
Rafnar T,
Gudbjartsson DF,
Sulem P,
Jonasdottir A,
Sigurdsson A,
Jonasdottir A,
Besenbacher S,
Lundin P,
Stacey SN,
Gudmundsson J,
Magnusson OT,
le Roux L
and 33 more — show all
Orlygsdottir G,
Helgadottir HT,
Johannsdottir H,
Gylfason A,
Tryggvadottir L,
Jonasson JG,
de Juan A,
Ortega E,
Ramon-Cajal JM,
García-Prats MD,
Mayordomo C,
Panadero A,
Rivera F,
Aben KK,
van Altena AM,
Massuger LF,
Aavikko M,
Kujala PM,
Staff S,
Aaltonen LA,
Olafsdottir K,
Bjornsson J,
Kong A,
Salvarsdottir A,
Saemundsson H,
Olafsson K,
Benediktsdottir KR,
Gulcher J,
Masson G,
Kiemeney LA,
Mayordomo JI,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2011 · PMID 21964575
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.