For researchers
Is your paper here?
2,657 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.
3 matches for
Van der Zee MD.
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+
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
McCartney DL,
Min JL,
Richmond RC,
Lu AT,
Sobczyk MK,
Davies G,
Broer L,
Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
and 97 more — show all
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
Pasman JA,
Verweij KJH,
Gerring Z,
Stringer S,
Sanchez-Roige S,
Treur JL,
Abdellaoui A,
Nivard MG,
Baselmans BML,
Ong JS,
Ip HF,
van der Zee MD
and 36 more — show all
Bartels M,
Day FR,
Fontanillas P,
Elson SL,
de Wit H,
Davis LK,
MacKillop J,
Derringer JL,
Branje SJT,
Hartman CA,
Heath AC,
van Lier PAC,
Madden PAF,
Mägi R,
Meeus W,
Montgomery GW,
Oldehinkel AJ,
Pausova Z,
Ramos-Quiroga JA,
Paus T,
Ribases M,
Kaprio J,
Boks MPM,
Bell JT,
Spector TD,
Gelernter J,
Boomsma DI,
Martin NG,
MacGregor S,
Perry JRB,
Palmer AA,
Posthuma D,
Munafò MR,
Gillespie NA,
Derks EM,
Vink JM
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium and 1 more consortia
Nature neuroscience · 2018 · PMID 30150663
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.