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.
12 matches for
Luo Y.
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease
de Lange KM,
Moutsianas L,
Lee JC,
Lamb CA,
Luo Y,
Kennedy NA,
Jostins L,
Rice DL,
Gutierrez-Achury J,
Ji SG,
Heap G,
Nimmo ER
and 20 more — show all
Edwards C,
Henderson P,
Mowat C,
Sanderson J,
Satsangi J,
Simmons A,
Wilson DC,
Tremelling M,
Hart A,
Mathew CG,
Newman WG,
Parkes M,
Lees CW,
Uhlig H,
Hawkey C,
Prescott NJ,
Ahmad T,
Mansfield JC,
Anderson CA,
Barrett JC
Nature genetics · 2017 · PMID 28067908 · open access
12 pages+
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
Ishigaki K,
Sakaue S,
Terao C,
Luo Y,
Sonehara K,
Yamaguchi K,
Amariuta T,
Too CL,
Laufer VA,
Scott IC,
Viatte S,
Takahashi M
and 78 more — show all
Ohmura K,
Murasawa A,
Hashimoto M,
Ito H,
Hammoudeh M,
Emadi SA,
Masri BK,
Halabi H,
Badsha H,
Uthman IW,
Wu X,
Lin L,
Li T,
Plant D,
Barton A,
Orozco G,
Verstappen SMM,
Bowes J,
MacGregor AJ,
Honda S,
Koido M,
Tomizuka K,
Kamatani Y,
Tanaka H,
Tanaka E,
Suzuki A,
Maeda Y,
Yamamoto K,
Miyawaki S,
Xie G,
Zhang J,
Amos CI,
Keystone E,
Wolbink G,
van der Horst-Bruinsma I,
Cui J,
Liao KP,
Carroll RJ,
Lee HS,
Bang SY,
Siminovitch KA,
de Vries N,
Alfredsson L,
Rantapää-Dahlqvist S,
Karlson EW,
Bae SC,
Kimberly RP,
Edberg JC,
Mariette X,
Huizinga T,
Dieudé P,
Schneider M,
Kerick M,
Denny JC,
Matsuda K,
Matsuo K,
Mimori T,
Matsuda F,
Fujio K,
Tanaka Y,
Kumanogoh A,
Traylor M,
Lewis CM,
Eyre S,
Xu H,
Saxena R,
Arayssi T,
Kochi Y,
Ikari K,
Harigai M,
Gregersen PK,
Yamamoto K,
Louis Bridges S Jr,
Padyukov L,
Martin J,
Klareskog L,
Okada Y,
Raychaudhuri S
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Barry A,
McNulty MT,
Jia X,
Gupta Y,
Debiec H,
Luo Y,
Nagano C,
Horinouchi T,
Jung S,
Colucci M,
Ahram DF,
Mitrotti A
and 58 more — show all
Sinha A,
Teeninga N,
Jin G,
Shril S,
Caridi G,
Bodria M,
Lim TY,
Westland R,
Zanoni F,
Marasa M,
Turudic D,
Giordano M,
Gesualdo L,
Magistroni R,
Pisani I,
Fiaccadori E,
Reiterova J,
Maringhini S,
Morello W,
Montini G,
Weng PL,
Scolari F,
Saraga M,
Tasic V,
Santoro D,
van Wijk JAE,
Milošević D,
Kawai Y,
Kiryluk K,
Pollak MR,
Gharavi A,
Lin F,
Simœs E Silva AC,
Loos RJF,
Kenny EE,
Schreuder MF,
Zurowska A,
Dossier C,
Ariceta G,
Drozynska-Duklas M,
Hogan J,
Jankauskiene A,
Hildebrandt F,
Prikhodina L,
Song K,
Bagga A,
Cheong H 2nd,
Ghiggeri GM,
Vachvanichsanong P,
Nozu K,
Lee D,
Vivarelli M,
Raychaudhuri S,
Tokunaga K,
Sanna-Cherchi S,
Ronco P,
Iijima K,
Sampson MG
Nature communications · 2023 · PMID 37120605 · open access
12 pages+
Multi-ancestry meta-analysis of keloids uncovers novel susceptibility loci in diverse populations
Greene CA,
Hampton G,
Jaworski J,
Shuey MM,
Khan A,
Luo Y,
Jarvik GP,
Namjou-Khales B,
Edwards TL,
Velez Edwards DR,
Hellwege JN
Nature communications · 2025 · PMID 40835838 · open access
11 pages
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Levin MG,
Tsao NL,
Singhal P,
Liu C,
Vy HMT,
Paranjpe I,
Backman JD,
Bellomo TR,
Bone WP,
Biddinger KJ,
Hui Q,
Dikilitas O
and 31 more — show all
Satterfield BA,
Yang Y,
Morley MP,
Bradford Y,
Burke M,
Reza N,
Charest B,
Judy RL,
Puckelwartz MJ,
Hakonarson H,
Khan A,
Kottyan LC,
Kullo I,
Luo Y,
McNally EM,
Rasmussen-Torvik LJ,
Day SM,
Do R,
Phillips LS,
Ellinor PT,
Nadkarni GN,
Ritchie MD,
Arany Z,
Cappola TP,
Margulies KB,
Aragam KG,
Haggerty CM,
Joseph J,
Sun YV,
Voight BF,
Damrauer SM
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
Guo Y,
Tan LJ,
Lei SF,
Yang TL,
Chen XD,
Zhang F,
Chen Y,
Pan F,
Yan H,
Liu X,
Tian Q,
Zhang ZX
and 21 more — show all
Zhou Q,
Qiu C,
Dong SS,
Xu XH,
Guo YF,
Zhu XZ,
Liu SL,
Wang XL,
Li X,
Luo Y,
Zhang LS,
Li M,
Wang JT,
Wen T,
Drees B,
Hamilton J,
Papasian CJ,
Recker RR,
Song XP,
Cheng J,
Deng HW
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration
Curtis J,
Luo Y,
Zenner HL,
Cuchet-Lourenço D,
Wu C,
Lo K,
Maes M,
Alisaac A,
Stebbings E,
Liu JZ,
Kopanitsa L,
Ignatyeva O
and 11 more — show all
Balabanova Y,
Nikolayevskyy V,
Baessmann I,
Thye T,
Meyer CG,
Nürnberg P,
Horstmann RD,
Drobniewski F,
Plagnol V,
Barrett JC,
Nejentsev S
Nature genetics · 2015 · PMID 25774636 · open access
2 pages
A positively selected FBN1 missense variant reduces height in Peruvian individuals
Asgari S,
Luo Y,
Akbari A,
Belbin GM,
Li X,
Harris DN,
Selig M,
Bartell E,
Calderon R,
Slowikowski K,
Contreras C,
Yataco R
and 14 more — show all
Galea JT,
Jimenez J,
Coit JM,
Farroñay C,
Nazarian RM,
O'Connor TD,
Dietz HC,
Hirschhorn JN,
Guio H,
Lecca L,
Kenny EE,
Freeman EE,
Murray MB,
Raychaudhuri S
Nature · 2020 · PMID 32499652
1 page
Integrative exome sequencing and multi-omics analysis elucidates the regulatory role of rare variants in metabolic syndrome
Wu CX,
Sang J,
Xu Q,
Zhan Y,
Yuan SJ,
Ge YY,
Yu XJ,
Zheng X,
Wang XF,
He XM,
Liu CJ,
Luo Y
and 2 more — show all
Functional & integrative genomics · 2026 · PMID 42472903
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.