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2,662 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
7 matches for
Yamashiro K.
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
and 86 more — show all
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Chen W,
Stambolian D,
Edwards AO,
Branham KE,
Othman M,
Jakobsdottir J,
Tosakulwong N,
Pericak-Vance MA,
Campochiaro PA,
Klein ML,
Tan PL,
Conley YP
and 54 more — show all
Kanda A,
Kopplin L,
Li Y,
Augustaitis KJ,
Karoukis AJ,
Scott WK,
Agarwal A,
Kovach JL,
Schwartz SG,
Postel EA,
Brooks M,
Baratz KH,
Brown WL,
Brucker AJ,
Orlin A,
Brown G,
Ho A,
Regillo C,
Donoso L,
Tian L,
Kaderli B,
Hadley D,
Hagstrom SA,
Peachey NS,
Klein R,
Klein BE,
Gotoh N,
Yamashiro K,
Ferris Iii F,
Fagerness JA,
Reynolds R,
Farrer LA,
Kim IK,
Miller JW,
Cortón M,
Carracedo A,
Sanchez-Salorio M,
Pugh EW,
Doheny KF,
Brion M,
Deangelis MM,
Weeks DE,
Zack DJ,
Chew EY,
Heckenlively JR,
Yoshimura N,
Iyengar SK,
Francis PJ,
Katsanis N,
Seddon JM,
Haines JL,
Gorin MB,
Abecasis GR,
Swaroop A
Complications of Age-Related Macular Degeneration Prevention Trial Research Group
Proceedings of the National Academy of Sciences of the United States of America · 2010 · PMID 20385819
3 pages
CMPK1 and RBP3 are associated with corneal curvature in Asian populations
Chen P,
Miyake M,
Fan Q,
Liao J,
Yamashiro K,
Ikram MK,
Chew M,
Vithana EN,
Khor CC,
Aung T,
Tai ES,
Wong TY
and 4 more — show all
Human molecular genetics · 2014 · PMID 24963161
2 pages
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Khor CC,
Miyake M,
Chen LJ,
Shi Y,
Barathi VA,
Qiao F,
Nakata I,
Yamashiro K,
Zhou X,
Tam PO,
Cheng CY,
Tai ES
and 14 more — show all
Vithana EN,
Aung T,
Teo YY,
Wong TY,
Moriyama M,
Ohno-Matsui K,
Mochizuki M,
Matsuda F,
Yong RY,
Yap EP,
Yang Z,
Pang CP,
Saw SM,
Yoshimura N
Nagahama Study Group
Human molecular genetics · 2013 · PMID 23933737
1 page
CCDC102B confers risk of low vision and blindness in high myopia
Hosoda Y,
Yoshikawa M,
Miyake M,
Tabara Y,
Shimada N,
Zhao W,
Oishi A,
Nakanishi H,
Hata M,
Akagi T,
Ooto S,
Nagaoka N
and 8 more — show all
Nagahama Study group
Nature communications · 2018 · PMID 29725004 · open access
1 page
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy
Hosoda Y,
Miyake M,
Schellevis RL,
Boon CJF,
Hoyng CB,
Miki A,
Meguro A,
Sakurada Y,
Yoneyama S,
Takasago Y,
Hata M,
Muraoka Y
and 22 more — show all
Nakanishi H,
Oishi A,
Ooto S,
Tamura H,
Uji A,
Miyata M,
Takahashi A,
Ueda-Arakawa N,
Tajima A,
Sato T,
Mizuki N,
Shiragami C,
Iida T,
Khor CC,
Wong TY,
Yamada R,
Honda S,
de Jong EK,
Hollander AID,
Matsuda F,
Yamashiro K,
Tsujikawa A
Communications biology · 2019 · PMID 31872073 · 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.