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성함이나 학술지명, PMID로 찾아보십시오.
Sim X에 대해
57건, 그중 17건 표시.
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
외 45명 — 모두 보기
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
Taylor KD,
Li X,
Iyengar SK,
Xi Q,
Sivakumaran TA,
Mackey DA,
Macgregor S,
Martin NG,
Young TL,
Bis JC,
Wiggins KL,
Heckbert SR,
Hammond CJ,
Andrew T,
Fahy S,
Attia J,
Holliday EG,
Scott RJ,
Islam FM,
Rotter JI,
McAuley AK,
Boerwinkle E,
Tai ES,
Gudnason V,
Siscovick DS,
Vingerling JR,
Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
페이지 2개
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
Khor CC,
Ramdas WD,
Vithana EN,
Cornes BK,
Sim X,
Tay WT,
Saw SM,
Zheng Y,
Lavanya R,
Wu R,
Wang JJ,
Mitchell P
외 13명 — 모두 보기
Uitterlinden AG,
Rivadeneira F,
Teo YY,
Chia KS,
Seielstad M,
Hibberd M,
Vingerling JR,
Klaver CC,
Jansonius NM,
Tai ES,
Wong TY,
van Duijn CM,
Aung T
Human molecular genetics · 2011 · PMID 21307088
페이지 2개
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore
Han S,
Chen P,
Fan Q,
Khor CC,
Sim X,
Tay WT,
Ong RT,
Suo C,
Goh LK,
Lavanya R,
Zheng Y,
Wu R
외 10명 — 모두 보기
Human molecular genetics · 2011 · PMID 21665993
페이지 2개
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
Meta-analysis identifies common variants associated with body mass index in east Asians
Wen W,
Cho YS,
Zheng W,
Zheng W,
Dorajoo R,
Kato N,
Qi L,
Chen CH,
Delahanty RJ,
Okada Y,
Tabara Y,
Gu D
외 52명 — 모두 보기
Zhu D,
Haiman CA,
Mo Z,
Gao YT,
Saw SM,
Go MJ,
Takeuchi F,
Chang LC,
Kokubo Y,
Liang J,
Hao M,
Le Marchand L,
Zhang Y,
Hu Y,
Wong TY,
Long J,
Han BG,
Kubo M,
Yamamoto K,
Su MH,
Miki T,
Henderson BE,
Song H,
Tan A,
He J,
Ng DP,
Cai Q,
Tsunoda T,
Tsai FJ,
Iwai N,
Chen GK,
Shi J,
Xu J,
Sim X,
Xiang YB,
Maeda S,
Ong RT,
Li C,
Nakamura Y,
Aung T,
Kamatani N,
Liu JJ,
Lu W,
Yokota M,
Seielstad M,
Fann CS,
Wu JY,
Lee JY,
Hu FB,
Tanaka T,
Tai ES,
Shu XO
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
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
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
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
외 137명 — 모두 보기
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
페이지 2개
Identification of new genetic risk variants for type 2 diabetes
Shu XO,
Long J,
Cai Q,
Qi L,
Xiang YB,
Cho YS,
Tai ES,
Li X,
Lin X,
Chow WH,
Go MJ,
Seielstad M
외 19명 — 모두 보기
Bao W,
Li H,
Cornelis MC,
Yu K,
Wen W,
Shi J,
Han BG,
Sim XL,
Liu L,
Qi Q,
Kim HL,
Ng DP,
Lee JY,
Kim YJ,
Li C,
Gao YT,
Zheng W,
Zheng W,
Hu FB
PLoS genetics · 2010 · PMID 20862305 · open access
페이지 1개
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia
Sim X,
Ong RT,
Suo C,
Tay WT,
Liu J,
Ng DP,
Boehnke M,
Chia KS,
Wong TY,
Seielstad M,
Teo YY,
Tai ES
PLoS genetics · 2011 · PMID 21490949 · open access
페이지 1개
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
Kooner JS,
Saleheen D,
Sim X,
Sehmi J,
Zhang W,
Frossard P,
Been LF,
Chia KS,
Dimas AS,
Hassanali N,
Jafar T,
Jowett JB
외 55명 — 모두 보기
Li X,
Radha V,
Rees SD,
Takeuchi F,
Young R,
Aung T,
Basit A,
Chidambaram M,
Das D,
Grundberg E,
Hedman AK,
Hydrie ZI,
Islam M,
Khor CC,
Kowlessur S,
Kristensen MM,
Liju S,
Lim WY,
Matthews DR,
Liu J,
Morris AP,
Nica AC,
Pinidiyapathirage JM,
Prokopenko I,
Rasheed A,
Samuel M,
Shah N,
Shera AS,
Small KS,
Suo C,
Wickremasinghe AR,
Wong TY,
Yang M,
Zhang F,
Abecasis GR,
Barnett AH,
Caulfield M,
Deloukas P,
Frayling TM,
Froguel P,
Kato N,
Katulanda P,
Kelly MA,
Liang J,
Mohan V,
Sanghera DK,
Scott J,
Seielstad M,
Zimmet PZ,
Elliott P,
Teo YY,
McCarthy MI,
Danesh J,
Tai ES,
Chambers JC
DIAGRAM · MuTHER
Nature genetics · 2011 · PMID 21874001
페이지 1개
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
외 56명 — 모두 보기
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
페이지 1개
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
Huyghe JR,
Jackson AU,
Fogarty MP,
Buchkovich ML,
Stančáková A,
Stringham HM,
Sim X,
Yang L,
Fuchsberger C,
Cederberg H,
Chines PS,
Teslovich TM
외 17명 — 모두 보기
Romm JM,
Ling H,
McMullen I,
Ingersoll R,
Pugh EW,
Doheny KF,
Neale BM,
Daly MJ,
Kuusisto J,
Scott LJ,
Kang HM,
Collins FS,
Abecasis GR,
Watanabe RM,
Boehnke M,
Laakso M,
Mohlke KL
Nature genetics · 2013 · PMID 23263489
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
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
외 69명 — 모두 보기
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group 외 컨소시엄 4곳
Diabetes · 2018 · PMID 29703844
페이지 1개
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
외 290명 — 모두 보기
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
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COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30926973 · open access
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