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Is your paper here?
2,660 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.
4 matches for
Andersen V.
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson CA,
Boucher G,
Lees CW,
Franke A,
D'Amato M,
Taylor KD,
Lee JC,
Goyette P,
Imielinski M,
Latiano A,
Lagacé C,
Scott R
and 101 more — show all
Amininejad L,
Bumpstead S,
Baidoo L,
Baldassano RN,
Barclay M,
Bayless TM,
Brand S,
Büning C,
Colombel JF,
Denson LA,
De Vos M,
Dubinsky M,
Edwards C,
Ellinghaus D,
Fehrmann RS,
Floyd JA,
Florin T,
Franchimont D,
Franke L,
Georges M,
Glas J,
Glazer NL,
Guthery SL,
Haritunians T,
Hayward NK,
Hugot JP,
Jobin G,
Laukens D,
Lawrance I,
Lémann M,
Levine A,
Libioulle C,
Louis E,
McGovern DP,
Milla M,
Montgomery GW,
Morley KI,
Mowat C,
Ng A,
Newman W,
Ophoff RA,
Papi L,
Palmieri O,
Peyrin-Biroulet L,
Panés J,
Phillips A,
Prescott NJ,
Proctor DD,
Roberts R,
Russell R,
Rutgeerts P,
Sanderson J,
Sans M,
Schumm P,
Seibold F,
Sharma Y,
Simms LA,
Seielstad M,
Steinhart AH,
Targan SR,
van den Berg LH,
Vatn M,
Verspaget H,
Walters T,
Wijmenga C,
Wilson DC,
Westra HJ,
Xavier RJ,
Zhao ZZ,
Ponsioen CY,
Andersen V,
Torkvist L,
Gazouli M,
Anagnou NP,
Karlsen TH,
Kupcinskas L,
Sventoraityte J,
Mansfield JC,
Kugathasan S,
Silverberg MS,
Halfvarson J,
Rotter JI,
Mathew CG,
Griffiths AM,
Gearry R,
Ahmad T,
Brant SR,
Chamaillard M,
Satsangi J,
Cho JH,
Schreiber S,
Daly MJ,
Barrett JC,
Parkes M,
Annese V,
Hakonarson H,
Radford-Smith G,
Duerr RH,
Vermeire S,
Weersma RK,
Rioux JD
Nature genetics · 2011 · PMID 21297633 · open access
12 pages+
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Jostins L,
Ripke S,
Weersma RK,
Duerr RH,
McGovern DP,
Hui KY,
Lee JC,
Schumm LP,
Sharma Y,
Anderson CA,
Essers J,
Mitrovic M
and 94 more — show all
Ning K,
Cleynen I,
Theatre E,
Spain SL,
Raychaudhuri S,
Goyette P,
Wei Z,
Abraham C,
Achkar JP,
Ahmad T,
Amininejad L,
Ananthakrishnan AN,
Andersen V,
Andrews JM,
Baidoo L,
Balschun T,
Bampton PA,
Bitton A,
Boucher G,
Brand S,
Büning C,
Cohain A,
Cichon S,
D'Amato M,
De Jong D,
Devaney KL,
Dubinsky M,
Edwards C,
Ellinghaus D,
Ferguson LR,
Franchimont D,
Fransen K,
Gearry R,
Georges M,
Gieger C,
Glas J,
Haritunians T,
Hart A,
Hawkey C,
Hedl M,
Hu X,
Karlsen TH,
Kupcinskas L,
Kugathasan S,
Latiano A,
Laukens D,
Lawrance IC,
Lees CW,
Louis E,
Mahy G,
Mansfield J,
Morgan AR,
Mowat C,
Newman W,
Palmieri O,
Ponsioen CY,
Potocnik U,
Prescott NJ,
Regueiro M,
Rotter JI,
Russell RK,
Sanderson JD,
Sans M,
Satsangi J,
Schreiber S,
Simms LA,
Sventoraityte J,
Targan SR,
Taylor KD,
Tremelling M,
Verspaget HW,
De Vos M,
Wijmenga C,
Wilson DC,
Winkelmann J,
Xavier RJ,
Zeissig S,
Zhang B,
Zhang CK,
Zhao H,
Silverberg MS,
Annese V,
Hakonarson H,
Brant SR,
Radford-Smith G,
Mathew CG,
Rioux JD,
Schadt EE,
Daly MJ,
Franke A,
Parkes M,
Vermeire S,
Barrett JC,
Cho JH
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · open access
12 pages+
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Saevarsdottir S,
Stefansdottir L,
Sulem P,
Thorleifsson G,
Ferkingstad E,
Rutsdottir G,
Glintborg B,
Westerlind H,
Grondal G,
Loft IC,
Sorensen SB,
Lie BA
and 66 more — show all
Brink M,
Ärlestig L,
Arnthorsson AO,
Baecklund E,
Banasik K,
Bank S,
Bjorkman LI,
Ellingsen T,
Erikstrup C,
Frei O,
Gjertsson I,
Gudbjartsson DF,
Gudjonsson SA,
Halldorsson GH,
Hendricks O,
Hillert J,
Hogdall E,
Jacobsen S,
Jensen DV,
Jonsson H,
Kastbom A,
Kockum I,
Kristensen S,
Kristjansdottir H,
Larsen MH,
Linauskas A,
Hauge EM,
Loft AG,
Ludviksson BR,
Lund SH,
Markusson T,
Masson G,
Melsted P,
Moore KHS,
Munk H,
Nielsen KR,
Norddahl GL,
Oddsson A,
Olafsdottir TA,
Olason PI,
Olsson T,
Ostrowski SR,
Hørslev-Petersen K,
Rognvaldsson S,
Sanner H,
Silberberg GN,
Stefansson H,
Sørensen E,
Sørensen IJ,
Turesson C,
Bergman T,
Alfredsson L,
Kvien TK,
Brunak S,
Steinsson K,
Andersen V,
Andreassen OA,
Rantapää-Dahlqvist S,
Hetland ML,
Klareskog L,
Askling J,
Padyukov L,
Pedersen OB,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus
Mathey CM,
Maj C,
Eriksson N,
Krebs K,
Westmeier J,
David FS,
Koromina M,
Scheer AB,
Szabo N,
Wedi B,
Wieczorek D,
Amann PM
and 39 more — show all
Löffler H,
Koch L,
Schöffl C,
Dickel H,
Ganjuur N,
Hornung T,
Buhl T,
Greve J,
Wurpts G,
Aygören-Pürsün E,
Steffens M,
Herms S,
Heilmann-Heimbach S,
Hoffmann P,
Schmidt B,
Mavarani L,
Andresen T,
Sørensen SB,
Andersen V,
Vogel U,
Landén M,
Bulik CM,
Bygum A,
Magnusson PKE,
von Buchwald C,
Hallberg P,
Rye Ostrowski S,
Sørensen E,
Pedersen OB,
Ullum H,
Erikstrup C,
Bundgaard H,
Milani L,
Rasmussen ER,
Wadelius M,
Ghouse J,
Sachs B,
Nöthen MM,
Forstner AJ
Estonian Biobank Research Team · DBDS Genomic Consortium
The Journal of allergy and clinical immunology · 2024 · PMID 38300190
2 pages
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.