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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.
8 matches for
Li YJ.
Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women
Fan W,
Kan H,
Liu HY,
Wang TL,
He YN,
Zhang M,
Li YX,
Li YJ,
Meng W,
Li Q,
Hu AQ,
Zheng YJ
mSystems · 2021 · PMID 34282934 · open access
10 pages
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
Gorman BR,
Francis M,
Nealon CL,
Halladay CW,
Duro N,
Markianos K,
Genovese G,
Hysi PG,
Choquet H,
Afshari NA,
Li YJ,
Gaziano JM
and 7 more — show all
VA Million Veteran Program
Communications biology · 2024 · PMID 38582945 · open access
7 pages
Genome-wide association identifies ATOH7 as a major gene determining human optic disc size
Macgregor S,
Hewitt AW,
Hysi PG,
Ruddle JB,
Medland SE,
Henders AK,
Gordon SD,
Andrew T,
McEvoy B,
Sanfilippo PG,
Carbonaro F,
Tah V
and 11 more — show all
Li YJ,
Bennett SL,
Craig JE,
Montgomery GW,
Tran-Viet KN,
Brown NL,
Spector TD,
Martin NG,
Young TL,
Hammond CJ,
Mackey DA
Human molecular genetics · 2010 · PMID 20395239 · open access
2 pages
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Hysi PG,
Young TL,
Mackey DA,
Andrew T,
Fernández-Medarde A,
Solouki AM,
Hewitt AW,
Macgregor S,
Vingerling JR,
Li YJ,
Ikram MK,
Fai LY
and 13 more — show all
Sham PC,
Manyes L,
Porteros A,
Lopes MC,
Carbonaro F,
Fahy SJ,
Martin NG,
van Duijn CM,
Spector TD,
Rahi JS,
Santos E,
Klaver CC,
Hammond CJ
Nature genetics · 2010 · PMID 20835236
2 pages
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism
Fan Q,
Zhou X,
Khor CC,
Cheng CY,
Goh LK,
Sim X,
Tay WT,
Li YJ,
Ong RT,
Suo C,
Cornes B,
Ikram MK
and 10 more — show all
PLoS genetics · 2011 · PMID 22144915 · open access
2 pages
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Lan Q,
Hsiung CA,
Matsuo K,
Hong YC,
Seow A,
Wang Z,
Hosgood HD 3rd,
Chen K,
Wang JC,
Chatterjee N,
Hu W,
Wong MP
and 119 more — show all
Zheng W,
Caporaso N,
Park JY,
Chen CJ,
Kim YH,
Kim YT,
Landi MT,
Shen H,
Lawrence C,
Burdett L,
Yeager M,
Yuenger J,
Jacobs KB,
Chang IS,
Mitsudomi T,
Kim HN,
Chang GC,
Bassig BA,
Tucker M,
Wei F,
Yin Z,
Wu C,
An SJ,
Qian B,
Lee VH,
Lu D,
Liu J,
Jeon HS,
Hsiao CF,
Sung JS,
Kim JH,
Gao YT,
Tsai YH,
Jung YJ,
Guo H,
Hu Z,
Hutchinson A,
Wang WC,
Klein R,
Chung CC,
Oh IJ,
Chen KY,
Berndt SI,
He X,
Wu W,
Chang J,
Zhang XC,
Huang MS,
Zheng H,
Wang J,
Zhao X,
Li Y,
Choi JE,
Su WC,
Park KH,
Sung SW,
Shu XO,
Chen YM,
Liu L,
Kang CH,
Hu L,
Chen CH,
Pao W,
Kim YC,
Yang TY,
Xu J,
Guan P,
Tan W,
Su J,
Wang CL,
Li H,
Sihoe AD,
Zhao Z,
Chen Y,
Choi YY,
Hung JY,
Kim JS,
Yoon HI,
Cai Q,
Lin CC,
Park IK,
Xu P,
Dong J,
Kim C,
He Q,
Perng RP,
Kohno T,
Kweon SS,
Chen CY,
Vermeulen R,
Wu J,
Lim WY,
Chen KC,
Chow WH,
Ji BT,
Chan JK,
Chu M,
Li YJ,
Yokota J,
Li J,
Chen H,
Xiang YB,
Yu CJ,
Kunitoh H,
Wu G,
Jin L,
Lo YL,
Shiraishi K,
Chen YH,
Lin HC,
Wu T,
Wu YL,
Yang PC,
Zhou B,
Shin MH,
Fraumeni JF Jr,
Lin D,
Chanock SJ,
Rothman N
Nature genetics · 2012 · PMID 23143601
2 pages
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
Lu Y,
Dimasi DP,
Hysi PG,
Hewitt AW,
Burdon KP,
Toh T,
Ruddle JB,
Li YJ,
Mitchell P,
Healey PR,
Montgomery GW,
Hansell N
and 7 more — show all
PLoS genetics · 2010 · PMID 20485516 · open access
1 page
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
and 138 more — show all
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
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.