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Is your paper here?
2,665 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
Xue Y.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou I,
Süveges D,
Min JL,
Ritchie GRS,
Steinberg J,
Walter K,
Iotchkova V,
Schwartzentruber J,
Huang J,
Memari Y,
McCarthy S,
Crawford AA
and 91 more — show all
Bombieri C,
Cocca M,
Farmaki AE,
Gaunt TR,
Jousilahti P,
Kooijman MN,
Lehne B,
Malerba G,
Männistö S,
Matchan A,
Medina-Gomez C,
Metrustry SJ,
Nag A,
Ntalla I,
Paternoster L,
Rayner NW,
Sala C,
Scott WR,
Shihab HA,
Southam L,
St Pourcain B,
Traglia M,
Trajanoska K,
Zaza G,
Zhang W,
Artigas MS,
Bansal N,
Benn M,
Chen Z,
Danecek P,
Lin WY,
Locke A,
Luan J,
Manning AK,
Mulas A,
Sidore C,
Tybjaerg-Hansen A,
Varbo A,
Zoledziewska M,
Finan C,
Hatzikotoulas K,
Hendricks AE,
Kemp JP,
Moayyeri A,
Panoutsopoulou K,
Szpak M,
Wilson SG,
Boehnke M,
Cucca F,
Di Angelantonio E,
Langenberg C,
Lindgren C,
McCarthy MI,
Morris AP,
Nordestgaard BG,
Scott RA,
Tobin MD,
Wareham NJ,
Burton P,
Chambers JC,
Smith GD,
Dedoussis G,
Felix JF,
Franco OH,
Gambaro G,
Gasparini P,
Hammond CJ,
Hofman A,
Jaddoe VWV,
Kleber M,
Kooner JS,
Perola M,
Relton C,
Ring SM,
Rivadeneira F,
Salomaa V,
Spector TD,
Stegle O,
Toniolo D,
Uitterlinden AG,
Barroso I,
Greenwood CMT,
Perry JRB,
Walker BR,
Butterworth AS,
Xue Y,
Durbin R,
Small KS,
Soranzo N,
Timpson NJ,
Zeggini E
SpiroMeta Consortium · GoT2D Consortium and 3 more consortia
American journal of human genetics · 2017 · PMID 28552196 · open access
12 pages+
A genome-wide association study of neonatal metabolites
He Q,
Liu H,
Lu L,
Zhang Q,
Wang Q,
Wang B,
Wu X,
Guan L,
Mao J,
Xue Y,
Zhang C,
Cao X
and 9 more — show all
Cell genomics · 2024 · PMID 39389019 · open access
9 pages
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Soranzo N,
Spector TD,
Mangino M,
Kühnel B,
Rendon A,
Teumer A,
Willenborg C,
Wright B,
Chen L,
Li M,
Salo P,
Voight BF
and 68 more — show all
Burns P,
Laskowski RA,
Xue Y,
Menzel S,
Altshuler D,
Bradley JR,
Bumpstead S,
Burnett MS,
Devaney J,
Döring A,
Elosua R,
Epstein SE,
Erber W,
Falchi M,
Garner SF,
Ghori MJ,
Goodall AH,
Gwilliam R,
Hakonarson HH,
Hall AS,
Hammond N,
Hengstenberg C,
Illig T,
König IR,
Knouff CW,
McPherson R,
Melander O,
Mooser V,
Nauck M,
Nieminen MS,
O'Donnell CJ,
Peltonen L,
Potter SC,
Prokisch H,
Rader DJ,
Rice CM,
Roberts R,
Salomaa V,
Sambrook J,
Schreiber S,
Schunkert H,
Schwartz SM,
Serbanovic-Canic J,
Sinisalo J,
Siscovick DS,
Stark K,
Surakka I,
Stephens J,
Thompson JR,
Völker U,
Völzke H,
Watkins NA,
Wells GA,
Wichmann HE,
Van Heel DA,
Tyler-Smith C,
Thein SL,
Kathiresan S,
Perola M,
Reilly MP,
Stewart AF,
Erdmann J,
Samani NJ,
Meisinger C,
Greinacher A,
Deloukas P,
Ouwehand WH,
Gieger C
Nature genetics · 2009 · PMID 19820697
8 pages
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Gurdasani D,
Carstensen T,
Fatumo S,
Chen G,
Franklin CS,
Prado-Martinez J,
Bouman H,
Abascal F,
Haber M,
Tachmazidou I,
Mathieson I,
Ekoru K
and 45 more — show all
DeGorter MK,
Nsubuga RN,
Finan C,
Wheeler E,
Chen L,
Cooper DN,
Schiffels S,
Chen Y,
Ritchie GRS,
Pollard MO,
Fortune MD,
Mentzer AJ,
Garrison E,
Bergström A,
Hatzikotoulas K,
Adeyemo A,
Doumatey A,
Elding H,
Wain LV,
Ehret G,
Auer PL,
Kooperberg CL,
Reiner AP,
Franceschini N,
Maher D,
Montgomery SB,
Kadie C,
Widmer C,
Xue Y,
Seeley J,
Asiki G,
Kamali A,
Young EH,
Pomilla C,
Soranzo N,
Zeggini E,
Pirie F,
Morris AP,
Heckerman D,
Tyler-Smith C,
Motala AA,
Rotimi C,
Kaleebu P,
Barroso I,
Sandhu MS
Cell · 2019 · PMID 31675503
6 pages
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits
Southam L,
Gilly A,
Süveges D,
Farmaki AE,
Schwartzentruber J,
Tachmazidou I,
Matchan A,
Rayner NW,
Tsafantakis E,
Karaleftheri M,
Xue Y,
Dedoussis G
and 1 more — show all
Nature communications · 2017 · PMID 28548082 · open access
5 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.