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7 matches for
Xie J.
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+
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Fan Q,
Pozarickij A,
Tan NYQ,
Guo X,
Verhoeven VJM,
Vitart V,
Guggenheim JA,
Miyake M,
Tideman JWL,
Khawaja AP,
Zhang L,
MacGregor S
and 46 more — show all
Höhn R,
Chen P,
Biino G,
Wedenoja J,
Saffari SE,
Tedja MS,
Xie J,
Lanca C,
Wang YX,
Sahebjada S,
Mazur J,
Mirshahi A,
Martin NG,
Yazar S,
Pennell CE,
Yap M,
Haarman AEG,
Enthoven CA,
Polling J,
Hewitt AW,
Jaddoe VWV,
van Duijn CM,
Hayward C,
Polasek O,
Tai ES,
Yoshikatsu H,
Hysi PG,
Young TL,
Tsujikawa A,
Wang JJ,
Mitchell P,
Pfeiffer N,
Pärssinen O,
Foster PJ,
Fossarello M,
Yip SP,
Williams C,
Hammond CJ,
Jonas JB,
He M,
Mackey DA,
Wong TY,
Klaver CCW,
Saw SM,
Baird PN,
Cheng CY
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · 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
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Kiryluk K,
Li Y,
Scolari F,
Sanna-Cherchi S,
Choi M,
Verbitsky M,
Fasel D,
Lata S,
Prakash S,
Shapiro S,
Fischman C,
Snyder HJ
and 80 more — show all
Appel G,
Izzi C,
Viola BF,
Dallera N,
Del Vecchio L,
Barlassina C,
Salvi E,
Bertinetto FE,
Amoroso A,
Savoldi S,
Rocchietti M,
Amore A,
Peruzzi L,
Coppo R,
Salvadori M,
Ravani P,
Magistroni R,
Ghiggeri GM,
Caridi G,
Bodria M,
Lugani F,
Allegri L,
Delsante M,
Maiorana M,
Magnano A,
Frasca G,
Boer E,
Boscutti G,
Ponticelli C,
Mignani R,
Marcantoni C,
Di Landro D,
Santoro D,
Pani A,
Polci R,
Feriozzi S,
Chicca S,
Galliani M,
Gigante M,
Gesualdo L,
Zamboli P,
Battaglia GG,
Garozzo M,
Maixnerová D,
Tesar V,
Eitner F,
Rauen T,
Floege J,
Kovacs T,
Nagy J,
Mucha K,
Pączek L,
Zaniew M,
Mizerska-Wasiak M,
Roszkowska-Blaim M,
Pawlaczyk K,
Gale D,
Barratt J,
Thibaudin L,
Berthoux F,
Canaud G,
Boland A,
Metzger M,
Panzer U,
Suzuki H,
Goto S,
Narita I,
Caliskan Y,
Xie J,
Hou P,
Chen N,
Zhang H,
Wyatt RJ,
Novak J,
Julian BA,
Feehally J,
Stengel B,
Cusi D,
Lifton RP,
Gharavi AG
Nature genetics · 2014 · PMID 25305756 · open access
4 pages
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Kiryluk K,
Sanchez-Rodriguez E,
Zhou XJ,
Zanoni F,
Liu L,
Mladkova N,
Khan A,
Marasa M,
Zhang JY,
Balderes O,
Sanna-Cherchi S,
Bomback AS
and 177 more — show all
Canetta PA,
Appel GB,
Radhakrishnan J,
Trimarchi H,
Sprangers B,
Cattran DC,
Reich H,
Pei Y,
Ravani P,
Galesic K,
Maixnerova D,
Tesar V,
Stengel B,
Metzger M,
Canaud G,
Maillard N,
Berthoux F,
Berthelot L,
Pillebout E,
Monteiro R,
Nelson R,
Wyatt RJ,
Smoyer W,
Mahan J,
Samhar AA,
Hidalgo G,
Quiroga A,
Weng P,
Sreedharan R,
Selewski D,
Davis K,
Kallash M,
Vasylyeva TL,
Rheault M,
Chishti A,
Ranch D,
Wenderfer SE,
Samsonov D,
Claes DJ,
Akchurin O,
Goumenos D,
Stangou M,
Nagy J,
Kovacs T,
Fiaccadori E,
Amoroso A,
Barlassina C,
Cusi D,
Del Vecchio L,
Battaglia GG,
Bodria M,
Boer E,
Bono L,
Boscutti G,
Caridi G,
Lugani F,
Ghiggeri G,
Coppo R,
Peruzzi L,
Esposito V,
Esposito C,
Feriozzi S,
Polci R,
Frasca G,
Galliani M,
Garozzo M,
Mitrotti A,
Gesualdo L,
Granata S,
Zaza G,
Londrino F,
Magistroni R,
Pisani I,
Magnano A,
Marcantoni C,
Messa P,
Mignani R,
Pani A,
Ponticelli C,
Roccatello D,
Salvadori M,
Salvi E,
Santoro D,
Gembillo G,
Savoldi S,
Spotti D,
Zamboli P,
Izzi C,
Alberici F,
Delbarba E,
Florczak M,
Krata N,
Mucha K,
Pączek L,
Niemczyk S,
Moszczuk B,
Pańczyk-Tomaszewska M,
Mizerska-Wasiak M,
Perkowska-Ptasińska A,
Bączkowska T,
Durlik M,
Pawlaczyk K,
Sikora P,
Zaniew M,
Kaminska D,
Krajewska M,
Kuzmiuk-Glembin I,
Heleniak Z,
Bullo-Piontecka B,
Liberek T,
Dębska-Slizien A,
Hryszko T,
Materna-Kiryluk A,
Miklaszewska M,
Szczepańska M,
Szczepańska M,
Dyga K,
Machura E,
Siniewicz-Luzeńczyk K,
Pawlak-Bratkowska M,
Tkaczyk M,
Runowski D,
Kwella N,
Drożdż D,
Habura I,
Kronenberg F,
Prikhodina L,
van Heel D,
Fontaine B,
Cotsapas C,
Wijmenga C,
Franke A,
Annese V,
Gregersen PK,
Parameswaran S,
Weirauch M,
Kottyan L,
Harley JB,
Suzuki H,
Narita I,
Goto S,
Lee H,
Kim DK,
Kim YS,
Park JH,
Cho B,
Choi M,
Van Wijk A,
Huerta A,
Ars E,
Ballarin J,
Lundberg S,
Vogt B,
Mani LY,
Caliskan Y,
Barratt J,
Abeygunaratne T,
Kalra PA,
Gale DP,
Panzer U,
Rauen T,
Floege J,
Schlosser P,
Ekici AB,
Eckardt KU,
Chen N,
Xie J,
Lifton RP,
Loos RJF,
Kenny EE,
Ionita-Laza I,
Köttgen A,
Julian BA,
Novak J,
Scolari F,
Zhang H,
Gharavi AG
Nature genetics · 2023 · PMID 37337107
3 pages
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · 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.