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.
6 matches for
Du X.
Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology
Chen VL,
Du X,
Chen Y,
Kuppa A,
Handelman SK,
Vohnoutka RB,
Peyser PA,
Palmer ND,
Bielak LF,
Halligan B,
Speliotes EK
Nature communications · 2021 · PMID 33547301 · open access
12 pages+
Comprehensive genetic study of the insulin resistance marker TG:HDL-C in the UK Biobank
Oliveri A,
Rebernick RJ,
Kuppa A,
Pant A,
Chen Y,
Du X,
Cushing KC,
Bell HN,
Raut C,
Prabhu P,
Chen VL,
Halligan BD
and 1 more — show all
Nature genetics · 2024 · PMID 38200128
12 pages+
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network
Palmer MR,
Kim DS,
Crosslin DR,
Stanaway IB,
Rosenthal EA,
Carrell DS,
Cronkite DJ,
Gordon A,
Du X,
Li YK,
Williams MS,
Weng C
and 12 more — show all
Feng Q,
Li R,
Pendergrass SA,
Hakonarson H,
Fasel D,
Sohn S,
Sleiman P,
Handelman SK,
Speliotes E,
Kullo IJ,
Larson EB,
Jarvik GP
eMERGE Consortium
Genetic epidemiology · 2021 · PMID 32964493 · open access
2 pages
Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease
Chen Y,
Du X,
Kuppa A,
Feitosa MF,
Bielak LF,
O'Connell JR,
Musani SK,
Guo X,
Kahali B,
Chen VL,
Smith AV,
Ryan KA
and 25 more — show all
Eirksdottir G,
Allison MA,
Bowden DW,
Budoff MJ,
Carr JJ,
Chen YI,
Taylor KD,
Oliveri A,
Correa A,
Crudup BF,
Kardia SLR,
Mosley TH Jr,
Norris JM,
Terry JG,
Rotter JI,
Wagenknecht LE,
Halligan BD,
Young KA,
Hokanson JE,
Washko GR,
Gudnason V,
Province MA,
Peyser PA,
Palmer ND,
Speliotes EK
Nature genetics · 2023 · PMID 37709864
1 page
Genetic determinants of IgG antibody response to COVID-19 vaccination
Bian S,
Guo X,
Yang X,
Wei Y,
Yang Z,
Cheng S,
Yan J,
Chen Y,
Chen GB,
Du X,
Francis SS,
Shu Y
and 1 more — show all
American journal of human genetics · 2024 · PMID 38181733 · 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.