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.
6 matches for
Benediktsdottir KR.
New basal cell carcinoma susceptibility loci
Stacey SN,
Helgason H,
Gudjonsson SA,
Thorleifsson G,
Zink F,
Sigurdsson A,
Kehr B,
Gudmundsson J,
Sulem P,
Sigurgeirsson B,
Benediktsdottir KR,
Thorisdottir K
and 31 more — show all
Ragnarsson R,
Fuentelsaz V,
Corredera C,
Gilaberte Y,
Grasa M,
Planelles D,
Sanmartin O,
Rudnai P,
Gurzau E,
Koppova K,
Nexø BA,
Tjønneland A,
Overvad K,
Jonasson JG,
Tryggvadottir L,
Johannsdottir H,
Kristinsdottir AM,
Stefansson H,
Masson G,
Magnusson OT,
Halldorsson BV,
Kong A,
Rafnar T,
Thorsteinsdottir U,
Vogel U,
Kumar R,
Nagore E,
Mayordomo JI,
Gudbjartsson DF,
Olafsson JH,
Stefansson K
Nature communications · 2015 · PMID 25855136 · open access
7 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
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
Two newly identified genetic determinants of pigmentation in Europeans
Sulem P,
Gudbjartsson DF,
Stacey SN,
Helgason A,
Rafnar T,
Jakobsdottir M,
Steinberg S,
Gudjonsson SA,
Palsson A,
Thorleifsson G,
Pálsson S,
Sigurgeirsson B
and 13 more — show all
Thorisdottir K,
Ragnarsson R,
Benediktsdottir KR,
Aben KK,
Vermeulen SH,
Goldstein AM,
Tucker MA,
Kiemeney LA,
Olafsson JH,
Gulcher J,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18488028
1 page
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
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.