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2,661 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.
8 matches for
Frigge ML.
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Rafnar T,
Gunnarsson B,
Stefansson OA,
Sulem P,
Ingason A,
Frigge ML,
Stefansdottir L,
Sigurdsson JK,
Tragante V,
Steinthorsdottir V,
Styrkarsdottir U,
Stacey SN
and 25 more — show all
Gudmundsson J,
Arnadottir GA,
Oddsson A,
Zink F,
Halldorsson G,
Sveinbjornsson G,
Kristjansson RP,
Davidsson OB,
Salvarsdottir A,
Thoroddsen A,
Helgadottir EA,
Kristjansdottir K,
Ingthorsson O,
Gudmundsson V,
Geirsson RT,
Arnadottir R,
Gudbjartsson DF,
Masson G,
Asselbergs FW,
Jonasson JG,
Olafsson K,
Thorsteinsdottir U,
Halldorsson BV,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30194396 · open access
12 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
Genetic insight into sick sinus syndrome
Thorolfsdottir RB,
Sveinbjornsson G,
Aegisdottir HM,
Benonisdottir S,
Stefansdottir L,
Ivarsdottir EV,
Halldorsson GH,
Sigurdsson JK,
Torp-Pedersen C,
Weeke PE,
Brunak S,
Westergaard D
and 32 more — show all
Pedersen OB,
Sorensen E,
Nielsen KR,
Burgdorf KS,
Banasik K,
Brumpton B,
Zhou W,
Oddsson A,
Tragante V,
Hjorleifsson KE,
Davidsson OB,
Rajamani S,
Jonsson S,
Torfason B,
Valgardsson AS,
Thorgeirsson G,
Frigge ML,
Thorleifsson G,
Norddahl GL,
Helgadottir A,
Gretarsdottir S,
Sulem P,
Jonsdottir I,
Willer CJ,
Hveem K,
Bundgaard H,
Ullum H,
Arnar DO,
Thorsteinsdottir U,
Gudbjartsson DF,
Holm H,
Stefansson K
DBDS Genomic Consortium
European heart journal · 2021 · PMID 33580673 · open access
5 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
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
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
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Steinthorsdottir V,
McGinnis R,
Williams NO,
Stefansdottir L,
Thorleifsson G,
Shooter S,
Fadista J,
Sigurdsson JK,
Auro KM,
Berezina G,
Borges MC,
Bumpstead S
and 63 more — show all
Bybjerg-Grauholm J,
Colgiu I,
Dolby VA,
Dudbridge F,
Engel SM,
Franklin CS,
Frigge ML,
Frisbaek Y,
Geirsson RT,
Geller F,
Gretarsdottir S,
Gudbjartsson DF,
Harmon Q,
Hougaard DM,
Hegay T,
Helgadottir A,
Hjartardottir S,
Jääskeläinen T,
Johannsdottir H,
Jonsdottir I,
Juliusdottir T,
Kalsheker N,
Kasimov A,
Kemp JP,
Kivinen K,
Klungsøyr K,
Lee WK,
Melbye M,
Miedzybrodska Z,
Moffett A,
Najmutdinova D,
Nishanova F,
Olafsdottir T,
Perola M,
Pipkin FB,
Poston L,
Prescott G,
Saevarsdottir S,
Salimbayeva D,
Scaife PJ,
Skotte L,
Staines-Urias E,
Stefansson OA,
Sørensen KM,
Thomsen LCV,
Tragante V,
Trogstad L,
Simpson NAB,
Aripova T,
Casas JP,
Dominiczak AF,
Walker JJ,
Thorsteinsdottir U,
Iversen AC,
Feenstra B,
Lawlor DA,
Boyd HA,
Magnus P,
Laivuori H,
Zakhidova N,
Svyatova G,
Stefansson K,
Morgan L
FINNPEC Consortium · GOPEC Consortium
Nature communications · 2020 · PMID 33239696 · 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.