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Is your paper here?
2,662 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
Jansen PR.
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Nagel M,
Jansen PR,
Stringer S,
Watanabe K,
de Leeuw CA,
Bryois J,
Savage JE,
Hammerschlag AR,
Skene NG,
Muñoz-Manchado AB,
White T,
Tiemeier H
and 6 more — show all
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Savage JE,
Jansen PR,
Stringer S,
Watanabe K,
Bryois J,
de Leeuw CA,
Nagel M,
Awasthi S,
Barr PB,
Coleman JRI,
Grasby KL,
Hammerschlag AR
and 105 more — show all
Kaminski JA,
Karlsson R,
Krapohl E,
Lam M,
Nygaard M,
Reynolds CA,
Trampush JW,
Young H,
Zabaneh D,
Hägg S,
Hansell NK,
Karlsson IK,
Linnarsson S,
Montgomery GW,
Muñoz-Manchado AB,
Quinlan EB,
Schumann G,
Skene NG,
Webb BT,
White T,
Arking DE,
Avramopoulos D,
Bilder RM,
Bitsios P,
Burdick KE,
Cannon TD,
Chiba-Falek O,
Christoforou A,
Cirulli ET,
Congdon E,
Corvin A,
Davies G,
Deary IJ,
DeRosse P,
Dickinson D,
Djurovic S,
Donohoe G,
Conley ED,
Eriksson JG,
Espeseth T,
Freimer NA,
Giakoumaki S,
Giegling I,
Gill M,
Glahn DC,
Hariri AR,
Hatzimanolis A,
Keller MC,
Knowles E,
Koltai D,
Konte B,
Lahti J,
Le Hellard S,
Lencz T,
Liewald DC,
London E,
Lundervold AJ,
Malhotra AK,
Melle I,
Morris D,
Need AC,
Ollier W,
Palotie A,
Payton A,
Pendleton N,
Poldrack RA,
Räikkönen K,
Reinvang I,
Roussos P,
Rujescu D,
Sabb FW,
Scult MA,
Smeland OB,
Smyrnis N,
Starr JM,
Steen VM,
Stefanis NC,
Straub RE,
Sundet K,
Tiemeier H,
Voineskos AN,
Weinberger DR,
Widen E,
Yu J,
Abecasis G,
Andreassen OA,
Breen G,
Christiansen L,
Debrabant B,
Dick DM,
Heinz A,
Hjerling-Leffler J,
Ikram MA,
Kendler KS,
Martin NG,
Medland SE,
Pedersen NL,
Plomin R,
Polderman TJC,
Ripke S,
van der Sluis S,
Sullivan PF,
Vrieze SI,
Wright MJ,
Posthuma D
Nature genetics · 2018 · PMID 29942086
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
and 111 more — show all
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Jansen PR,
Watanabe K,
Stringer S,
Skene N,
Bryois J,
Hammerschlag AR,
de Leeuw CA,
Benjamins JS,
Muñoz-Manchado AB,
Nagel M,
Savage JE,
Tiemeier H
and 12 more — show all
White T,
Tung JY,
Hinds DA,
Vacic V,
Wang X,
Sullivan PF,
van der Sluis S,
Polderman TJC,
Smit AB,
Hjerling-Leffler J,
Van Someren EJW,
Posthuma D
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
Watanabe K,
Jansen PR,
Savage JE,
Nandakumar P,
Wang X,
Hinds DA,
Gelernter J,
Levey DF,
Polimanti R,
Stein MB,
Van Someren EJW,
Smit AB
and 1 more — show all
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
Sniekers S,
Stringer S,
Watanabe K,
Jansen PR,
Coleman JRI,
Krapohl E,
Taskesen E,
Hammerschlag AR,
Okbay A,
Zabaneh D,
Amin N,
Breen G
and 18 more — show all
Cesarini D,
Chabris CF,
Iacono WG,
Ikram MA,
Johannesson M,
Koellinger P,
Lee JJ,
Magnusson PKE,
McGue M,
Miller MB,
Ollier WER,
Payton A,
Pendleton N,
Plomin R,
Rietveld CA,
Tiemeier H,
van Duijn CM,
Posthuma D
Nature genetics · 2017 · PMID 28530673 · open access
5 pages
Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals
Coleman JRI,
Bryois J,
Gaspar HA,
Jansen PR,
Savage JE,
Skene N,
Plomin R,
Muñoz-Manchado AB,
Linnarsson S,
Crawford G,
Hjerling-Leffler J,
Sullivan PF
and 2 more — show all
Molecular psychiatry · 2019 · PMID 29520040
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.