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성함이나 학술지명, PMID로 찾아보십시오.
Cheng CY에 대해
62건, 그중 20건 표시.
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
외 10명 — 모두 보기
PLoS genetics · 2011 · PMID 22144915 · open access
페이지 2개
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
외 96명 — 모두 보기
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group 외 컨소시엄 2곳
American journal of human genetics · 2013 · PMID 24144296
페이지 2개
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract
Liao J,
Su X,
Chen P,
Wang X,
Xu L,
Li X,
Thean L,
Tan C,
Tan AG,
Tay WT,
Jun G,
Zheng Y
외 17명 — 모두 보기
Chew M,
Wang YX,
Tan QS,
Barathi VA,
Klein BE,
Saw SM,
Vithana EN,
Tai ES,
Iyengar SK,
Mitchell P,
Khor CC,
Aung T,
Wang JJ,
Jonas JB,
Teo YY,
Wong TY,
Cheng CY
Human molecular genetics · 2014 · PMID 24951543
페이지 2개
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
외 4명 — 모두 보기
Human molecular genetics · 2014 · PMID 24963161
페이지 2개
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
외 66명 — 모두 보기
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium 외 컨소시엄 1곳
Nature communications · 2014 · PMID 25241763 · open access
페이지 2개
Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Li M,
Foo JN,
Wang JQ,
Low HQ,
Tang XQ,
Toh KY,
Yin PR,
Khor CC,
Goh YF,
Irwan ID,
Xu RC,
Andiappan AK
외 29명 — 모두 보기
Bei JX,
Rotzschke O,
Chen MH,
Cheng CY,
Sun LD,
Jiang GR,
Wong TY,
Lin HL,
Aung T,
Liao YH,
Saw SM,
Ye K,
Ebstein RP,
Chen QK,
Shi W,
Chew SH,
Chen J,
Zhang FR,
Li SP,
Xu G,
Shyong Tai E,
Wang L,
Chen N,
Zhang XJ,
Zeng YX,
Zhang H,
Liu ZH,
Yu XQ,
Liu JJ
Nature communications · 2015 · PMID 26028593 · open access
페이지 2개
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
외 233명 — 모두 보기
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD 외 컨소시엄 2곳
Nature genetics · 2015 · PMID 26390057
페이지 2개
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
외 152명 — 모두 보기
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration 외 컨소시엄 8곳
Nature · 2019 · PMID 31118516 · open access
페이지 2개
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
외 119명 — 모두 보기
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
페이지 2개
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies
Sun Q,
Graff M,
Rowland B,
Wen J,
Huang L,
Miller-Fleming TW,
Haessler J,
Preuss MH,
Chai JF,
Lee MP,
Avery CL,
Cheng CY
외 7명 — 모두 보기
Journal of human genetics · 2022 · PMID 34376796 · open access
페이지 2개
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Loh M,
Zhang W,
Ng HK,
Schmid K,
Lamri A,
Tong L,
Ahmad M,
Lee JJ,
Ng MCY,
Petty LE,
Spracklen CN,
Takeuchi F
외 35명 — 모두 보기
Islam MT,
Jasmine F,
Kasturiratne A,
Kibriya M,
Mohlke KL,
Paré G,
Prasad G,
Shahriar M,
Chee ML,
de Silva HJ,
Engert JC,
Gerstein HC,
Mani KR,
Sabanayagam C,
Vujkovic M,
Wickremasinghe AR,
Wong TY,
Yajnik CS,
Yusuf S,
Ahsan H,
Bharadwaj D,
Anand SS,
Below JE,
Boehnke M,
Bowden DW,
Chandak GR,
Cheng CY,
Kato N,
Mahajan A,
Sim X,
McCarthy MI,
Morris AP,
Kooner JS,
Saleheen D,
Chambers JC
Communications biology · 2022 · PMID 35393509 · open access
페이지 2개
A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
Jiang C,
Melles RB,
Yin J,
Fan Q,
Guo X,
Cheng CY,
He M,
Mackey DA,
Guggenheim JA,
Klaver C,
Nair KS,
Jorgenson E
외 1명 — 모두 보기
Consortium for Refractive Error and Myopia (CREAM)
Frontiers in genetics · 2023 · PMID 37351342 · open access
페이지 2개
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Fan Q,
Li H,
Wang X,
Tham YC,
Teo KYC,
Yasuda M,
Lim WK,
Kwan YP,
Teo JX,
Chen CJ,
Chen LJ,
Ahn J
외 10명 — 모두 보기
Nature communications · 2023 · PMID 37696869 · open access
페이지 2개
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
Reich D,
Nalls MA,
Kao WH,
Akylbekova EL,
Tandon A,
Patterson N,
Mullikin J,
Hsueh WC,
Cheng CY,
Coresh J,
Boerwinkle E,
Li M
외 12명 — 모두 보기
Waliszewska A,
Neubauer J,
Li R,
Leak TS,
Ekunwe L,
Files JC,
Hardy CL,
Zmuda JM,
Taylor HA,
Ziv E,
Harris TB,
Wilson JG
PLoS genetics · 2009 · PMID 19180233 · open access
페이지 1개
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
외 14명 — 모두 보기
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
페이지 1개
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry
Chen P,
Ong RT,
Tay WT,
Sim X,
Ali M,
Xu H,
Suo C,
Liu J,
Chia KS,
Vithana E,
Young TL,
Aung T
외 6명 — 모두 보기
PloS one · 2013 · PMID 24244560 · open access
페이지 1개
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur ME,
Khor CC,
Jia H,
Cornes BK,
Chen LJ,
Qiao C,
Nair KS,
Cheng CY,
Xu L,
George R,
Tan D,
Abu-Amero K
외 61명 — 모두 보기
Perera SA,
Ozaki M,
Mizoguchi T,
Kurimoto Y,
Low S,
Tajudin LS,
Ho CL,
Tham CC,
Soto I,
Chew PT,
Wong HT,
Shantha B,
Kuroda M,
Osman EA,
Tang G,
Fan S,
Meng H,
Wang H,
Feng B,
Yong VH,
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