For researchers
Is your paper here?
2,671 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.
5 matches for
Revez JA.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Revez JA,
Lin T,
Qiao Z,
Xue A,
Holtz Y,
Zhu Z,
Zeng J,
Wang H,
Sidorenko J,
Kemper KE,
Vinkhuyzen AAE,
Frater J
and 9 more — show all
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira MA,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
van Dongen J,
Lu Y,
Rüschendorf F
and 54 more — show all
Esparza-Gordillo J,
Medway CW,
Mountjoy E,
Burrows K,
Hummel O,
Grosche S,
Brumpton BM,
Witte JS,
Hottenga JJ,
Willemsen G,
Zheng J,
Rodríguez E,
Hotze M,
Franke A,
Revez JA,
Beesley J,
Matheson MC,
Dharmage SC,
Bain LM,
Fritsche LG,
Gabrielsen ME,
Balliu B,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Arnold A,
Homuth G,
Schmidt CO,
Thompson PJ,
Martin NG,
Duffy DL,
Novak N,
Schulz H,
Karrasch S,
Gieger C,
Strauch K,
Melles RB,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PKE,
Jansen R,
Jorgenson E,
Lee YA,
Boomsma DI,
Almqvist C,
Karlsson R,
Koppelman GH,
Paternoster L
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
Minimal phenotyping yields genome-wide association signals of low specificity for major depression
Cai N,
Revez JA,
Adams MJ,
Andlauer TFM,
Breen G,
Byrne EM,
Clarke TK,
Forstner AJ,
Grabe HJ,
Hamilton SP,
Levinson DF,
Lewis CM
and 21 more — show all
Lewis G,
Martin NG,
Milaneschi Y,
Mors O,
Müller-Myhsok B,
Penninx BWJH,
Perlis RH,
Pistis G,
Potash JB,
Potash JB,
Preisig M,
Shi J,
Smoller JW,
Streit F,
Tiemeier H,
Uher R,
Van der Auwera S,
Viktorin A,
Weissman MM,
Kendler KS,
Flint J
MDD Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2020 · PMID 32231276
6 pages
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
and 114 more — show all
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · 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.