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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.
7 matches for
Magnusson M.
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+
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Folkersen L,
Gustafsson S,
Wang Q,
Hansen DH,
Hedman ÅK,
Schork A,
Page K,
Zhernakova DV,
Wu Y,
Peters J,
Eriksson N,
Bergen SE
and 71 more — show all
Boutin TS,
Bretherick AD,
Enroth S,
Kalnapenkis A,
Gådin JR,
Suur BE,
Chen Y,
Matic L,
Gale JD,
Lee J,
Zhang W,
Quazi A,
Ala-Korpela M,
Choi SH,
Claringbould A,
Danesh J,
Davey Smith G,
de Masi F,
Elmståhl S,
Engström G,
Fauman E,
Fernandez C,
Franke L,
Franks PW,
Giedraitis V,
Haley C,
Hamsten A,
Ingason A,
Johansson Å,
Joshi PK,
Lind L,
Lindgren CM,
Lubitz S,
Palmer T,
Macdonald-Dunlop E,
Magnusson M,
Melander O,
Michaelsson K,
Morris AP,
Mägi R,
Nagle MW,
Nilsson PM,
Nilsson J,
Orho-Melander M,
Polasek O,
Prins B,
Pålsson E,
Qi T,
Sjögren M,
Sundström J,
Surendran P,
Võsa U,
Werge T,
Wernersson R,
Westra HJ,
Yang J,
Zhernakova A,
Ärnlöv J,
Fu J,
Smith JG,
Esko T,
Hayward C,
Gyllensten U,
Landen M,
Siegbahn A,
Wilson JF,
Wallentin L,
Butterworth AS,
Holmes MV,
Ingelsson E,
Mälarstig A
Nature metabolism · 2020 · PMID 33067605
12 pages+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
and 60 more — show all
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Stacey SN,
Zink F,
Halldorsson GH,
Stefansdottir L,
Gudjonsson SA,
Einarsson G,
Hjörleifsson G,
Eiriksdottir T,
Helgadottir A,
Björnsdottir G,
Thorgeirsson TE,
Olafsdottir TA
and 19 more — show all
Jonsdottir I,
Gretarsdottir S,
Tragante V,
Magnusson MK,
Jonsson H,
Gudmundsson J,
Olafsson S,
Holm H,
Gudbjartsson DF,
Sulem P,
Helgason A,
Thorsteinsdottir U,
Tryggvadottir L,
Rafnar T,
Melsted P,
Ulfarsson MÖ,
Vidarsson B,
Thorleifsson G,
Stefansson K
Nature genetics · 2023 · PMID 37932435 · open access
4 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 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
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Iglesias MJ,
Sanchez-Rivera L,
Ibrahim-Kosta M,
Naudin C,
Munsch G,
Goumidi L,
Farm M,
Smith PM,
Thibord F,
Kral-Pointner JB,
Hong MG,
Suchon P
and 31 more — show all
Germain M,
Schrottmaier W,
Dusart P,
Boland A,
Kotol D,
Edfors F,
Koprulu M,
Pietzner M,
Langenberg C,
Damrauer SM,
Johnson AD,
Klarin DM,
Smith NL,
Smadja DM,
Holmström M,
Magnusson M,
Silveira A,
Uhlén M,
Renné T,
Martinez-Perez A,
Emmerich J,
Deleuze JF,
Antovic J,
Soria Fernandez JM,
Assinger A,
Schwenk JM,
Souto Andres JC,
Morange PE,
Butler LM,
Trégouët DA,
Odeberg J
Nature communications · 2023 · PMID 37286573 · 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.