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.
4 matches for
Su MH.
Genome-wide meta-analyses of cross substance use disorders in diverse populations
Lai D,
Zhang M,
Green N,
Abreu M,
Schwantes-An TH,
Parker CC,
Zhang S,
Jin F,
Sun A,
Zhang P,
Edenberg HJ,
Liu Y
and 1 more — show all
Molecular psychiatry · 2026 · PMID 41057643 · open access
12 pages+
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
Meta-analysis identifies common variants associated with body mass index in east Asians
Wen W,
Cho YS,
Zheng W,
Zheng W,
Dorajoo R,
Kato N,
Qi L,
Chen CH,
Delahanty RJ,
Okada Y,
Tabara Y,
Gu D
and 52 more — show all
Zhu D,
Haiman CA,
Mo Z,
Gao YT,
Saw SM,
Go MJ,
Takeuchi F,
Chang LC,
Kokubo Y,
Liang J,
Hao M,
Le Marchand L,
Zhang Y,
Hu Y,
Wong TY,
Long J,
Han BG,
Kubo M,
Yamamoto K,
Su MH,
Miki T,
Henderson BE,
Song H,
Tan A,
He J,
Ng DP,
Cai Q,
Tsunoda T,
Tsai FJ,
Iwai N,
Chen GK,
Shi J,
Xu J,
Sim X,
Xiang YB,
Maeda S,
Ong RT,
Li C,
Nakamura Y,
Aung T,
Kamatani N,
Liu JJ,
Lu W,
Yokota M,
Seielstad M,
Fann CS,
Wu JY,
Lee JY,
Hu FB,
Tanaka T,
Tai ES,
Shu XO
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
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.