For researchers
Is your paper here?
2,663 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
Grotzinger A.
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
Demange PA,
Malanchini M,
Mallard TT,
Biroli P,
Cox SR,
Grotzinger AD,
Tucker-Drob EM,
Abdellaoui A,
Arseneault L,
van Bergen E,
Boomsma DI,
Caspi A
and 15 more — show all
Corcoran DL,
Domingue BW,
Harris KM,
Ip HF,
Mitchell C,
Moffitt TE,
Poulton R,
Prinz JA,
Sugden K,
Wertz J,
Williams BS,
de Zeeuw EL,
Belsky DW,
Harden KP,
Nivard MG
Nature genetics · 2021 · PMID 33414549 · open access
12 pages+
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
Thorp JG,
Campos AI,
Grotzinger AD,
Gerring ZF,
An J,
Ong JS,
Wang W,
Shringarpure S,
Byrne EM,
MacGregor S,
Martin NG,
Medland SE
and 2 more — show all
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
12 pages+
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
Karlsson Linnér R,
Mallard TT,
Barr PB,
Sanchez-Roige S,
Madole JW,
Driver MN,
Poore HE,
de Vlaming R,
Grotzinger AD,
Tielbeek JJ,
Johnson EC,
Liu M
and 17 more — show all
Rosenthal SB,
Ideker T,
Zhou H,
Kember RL,
Pasman JA,
Verweij KJH,
Liu DJ,
Vrieze S,
Kranzler HR,
Gelernter J,
Harris KM,
Tucker-Drob EM,
Waldman ID,
Palmer AA,
Harden KP,
Koellinger PD,
Dick DM
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders
Hatoum AS,
Colbert SMC,
Johnson EC,
Huggett SB,
Deak JD,
Pathak G,
Jennings MV,
Paul SE,
Karcher NR,
Hansen I,
Baranger DAA,
Edwards A
and 10 more — show all
Substance Use Disorder Working Group of the Psychiatric Genomics Consortium
Nature. Mental health · 2023 · PMID 37250466
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.