For researchers
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.
5 matches for
Rajagopal VM.
Genetic analyses identify widespread sex-differential participation bias
Pirastu N,
Cordioli M,
Nandakumar P,
Mignogna G,
Abdellaoui A,
Hollis B,
Kanai M,
Rajagopal VM,
Parolo PDB,
Baya N,
Carey CE,
Karjalainen J
and 17 more — show all
Als TD,
Van der Zee MD,
Day FR,
Ong KK,
Morisaki T,
de Geus E,
Bellocco R,
Okada Y,
Børglum AD,
Joshi P,
Auton A,
Hinds D,
Neale BM,
Walters RK,
Nivard MG,
Perry JRB,
Ganna A
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Als TD,
Kurki MI,
Grove J,
Voloudakis G,
Therrien K,
Tasanko E,
Nielsen TT,
Naamanka J,
Veerapen K,
Levey DF,
Bendl J,
Bybjerg-Grauholm J
and 31 more — show all
Zeng B,
Demontis D,
Rosengren A,
Athanasiadis G,
Bækved-Hansen M,
Qvist P,
Bragi Walters G,
Thorgeirsson T,
Stefánsson H,
Musliner KL,
Rajagopal VM,
Farajzadeh L,
Thirstrup J,
Vilhjálmsson BJ,
McGrath JJ,
Mattheisen M,
Meier S,
Agerbo E,
Stefánsson K,
Nordentoft M,
Werge T,
Hougaard DM,
Mortensen PB,
Stein MB,
Gelernter J,
Hovatta I,
Roussos P,
Daly MJ,
Mors O,
Palotie A,
Børglum AD
Nature medicine · 2023 · PMID 37464041
12 pages+
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Demontis D,
Walters GB,
Athanasiadis G,
Walters R,
Therrien K,
Nielsen TT,
Farajzadeh L,
Voloudakis G,
Bendl J,
Zeng B,
Zhang W,
Grove J
and 35 more — show all
Als TD,
Duan J,
Satterstrom FK,
Bybjerg-Grauholm J,
Bækved-Hansen M,
Gudmundsson OO,
Magnusson SH,
Baldursson G,
Davidsdottir K,
Haraldsdottir GS,
Agerbo E,
Hoffman GE,
Dalsgaard S,
Martin J,
Ribasés M,
Boomsma DI,
Soler Artigas M,
Roth Mota N,
Howrigan D,
Medland SE,
Zayats T,
Rajagopal VM,
Nordentoft M,
Mors O,
Hougaard DM,
Mortensen PB,
Daly MJ,
Faraone SV,
Stefansson H,
Roussos P,
Franke B,
Werge T,
Neale BM,
Stefansson K,
Børglum AD
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Levey DF,
Galimberti M,
Deak JD,
Wendt FR,
Bhattacharya A,
Koller D,
Harrington KM,
Quaden R,
Johnson EC,
Gupta P,
Biradar M,
Lam M
and 18 more — show all
Cooke M,
Rajagopal VM,
Empke SLL,
Zhou H,
Nunez YZ,
Kranzler HR,
Edenberg HJ,
Agrawal A,
Smoller JW,
Lencz T,
Hougaard DM,
Børglum AD,
Demontis D,
Gaziano JM,
Gandal MJ,
Polimanti R,
Stein MB,
Gelernter J
Veterans Affairs Million Veteran Program
Nature genetics · 2023 · PMID 37985822 · open access
3 pages
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
Demontis D,
Walters RK,
Rajagopal VM,
Waldman ID,
Grove J,
Als TD,
Dalsgaard S,
Ribasés M,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Werge T,
Nordentoft M
and 8 more — show all
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature communications · 2021 · PMID 33495439 · 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.