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성함이나 학술지명, PMID로 찾아보십시오.
Young T에 대해
33건, 그중 13건 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
Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA
Jin G,
Zheng SL,
Lilja H,
Kim ST,
Tao S,
Gao Z,
Young T,
Wiklund F,
Feng J,
Isaacs WB,
Rittmaster RS,
Gronberg H
외 3명 — 모두 보기
Neoplasia (New York, N.Y.) · 2013 · PMID 23359319
페이지 2개
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Monda KL,
Chen GK,
Taylor KC,
Palmer C,
Edwards TL,
Lange LA,
Ng MC,
Adeyemo AA,
Allison MA,
Bielak LF,
Chen G,
Graff M
외 196명 — 모두 보기
Irvin MR,
Rhie SK,
Li G,
Liu Y,
Liu Y,
Lu Y,
Nalls MA,
Sun YV,
Wojczynski MK,
Yanek LR,
Aldrich MC,
Ademola A,
Amos CI,
Bandera EV,
Bock CH,
Britton A,
Broeckel U,
Cai Q,
Caporaso NE,
Carlson CS,
Carpten J,
Casey G,
Chen WM,
Chen F,
Chen YD,
Chiang CW,
Coetzee GA,
Demerath E,
Deming-Halverson SL,
Driver RW,
Dubbert P,
Feitosa MF,
Feng Y,
Freedman BI,
Gillanders EM,
Gottesman O,
Guo X,
Haritunians T,
Harris T,
Harris CC,
Hennis AJ,
Hernandez DG,
McNeill LH,
Howard TD,
Howard BV,
Howard VJ,
Johnson KC,
Kang SJ,
Keating BJ,
Kolb S,
Kuller LH,
Kutlar A,
Langefeld CD,
Lettre G,
Lohman K,
Lotay V,
Lyon H,
Manson JE,
Maixner W,
Meng YA,
Monroe KR,
Morhason-Bello I,
Murphy AB,
Mychaleckyj JC,
Nadukuru R,
Nathanson KL,
Nayak U,
N'diaye A,
Nemesure B,
Wu SY,
Leske MC,
Neslund-Dudas C,
Neuhouser M,
Nyante S,
Ochs-Balcom H,
Ogunniyi A,
Ogundiran TO,
Ojengbede O,
Olopade OI,
Palmer JR,
Ruiz-Narvaez EA,
Palmer ND,
Press MF,
Rampersaud E,
Rasmussen-Torvik LJ,
Rodriguez-Gil JL,
Salako B,
Schadt EE,
Schwartz AG,
Shriner DA,
Siscovick D,
Smith SB,
Wassertheil-Smoller S,
Speliotes EK,
Spitz MR,
Sucheston L,
Taylor H,
Tayo BO,
Tucker MA,
Van Den Berg DJ,
Edwards DR,
Wang Z,
Wiencke JK,
Winkler TW,
Witte JS,
Wrensch M,
Wu X,
Yang JJ,
Levin AM,
Young TR,
Zakai NA,
Cushman M,
Zanetti KA,
Zhao JH,
Zhao W,
Zheng Y,
Zhou J,
Ziegler RG,
Zmuda JM,
Fernandes JK,
Gilkeson GS,
Kamen DL,
Hunt KJ,
Spruill IJ,
Ambrosone CB,
Ambs S,
Arnett DK,
Atwood L,
Becker DM,
Berndt SI,
Bernstein L,
Blot WJ,
Borecki IB,
Bottinger EP,
Bowden DW,
Burke G,
Chanock SJ,
Cooper RS,
Ding J,
Duggan D,
Evans MK,
Fox C,
Garvey WT,
Bradfield JP,
Hakonarson H,
Grant SF,
Hsing A,
Chu L,
Hu JJ,
Huo D,
Ingles SA,
John EM,
Jordan JM,
Kabagambe EK,
Kardia SL,
Kittles RA,
Goodman PJ,
Klein EA,
Kolonel LN,
Le Marchand L,
Liu S,
McKnight B,
Millikan RC,
Mosley TH,
Padhukasahasram B,
Williams LK,
Patel SR,
Peters U,
Pettaway CA,
Peyser PA,
Psaty BM,
Redline S,
Rotimi CN,
Rybicki BA,
Sale MM,
Schreiner PJ,
Signorello LB,
Singleton AB,
Stanford JL,
Strom SS,
Thun MJ,
Vitolins M,
Zheng W,
Moore JH,
Williams SM,
Ketkar S,
Zhu X,
Zonderman AB,
Kooperberg C,
Papanicolaou GJ,
Henderson BE,
Reiner AP,
Hirschhorn JN,
Loos RJ,
North KE,
Haiman CA
NABEC Consortium · UKBEC Consortium 외 컨소시엄 2곳
Nature genetics · 2013 · PMID 23583978 · open access
페이지 2개
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2
Wu Y,
Gao H,
Li H,
Tabara Y,
Nakatochi M,
Chiu YF,
Park EJ,
Wen W,
Adair LS,
Borja JB,
Cai Q,
Chang YC
외 39명 — 모두 보기
Chen P,
Croteau-Chonka DC,
Fogarty MP,
Gan W,
He CT,
Hsiung CA,
Hwu CM,
Ichihara S,
Igase M,
Jo J,
Kato N,
Kawamoto R,
Kuzawa CW,
Lee JJ,
Liu J,
Lu L,
McDade TW,
Osawa H,
Sheu WH,
Teo Y,
Vadlamudi S,
Van Dam RM,
Wang Y,
Xiang YB,
Yamamoto K,
Ye X,
Young TL,
Zheng W,
Zheng W,
Zhu J,
Shu XO,
Shin C,
Jee SH,
Chuang LM,
Miki T,
Yokota M,
Lin X,
Mohlke KL,
Tai ES
Human molecular genetics · 2014 · PMID 24105470
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 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
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
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
외 7명 — 모두 보기
PLoS genetics · 2010 · PMID 20485516 · open access
페이지 1개
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Thorleifsson G,
Walters GB,
Hewitt AW,
Masson G,
Helgason A,
DeWan A,
Sigurdsson A,
Jonasdottir A,
Gudjonsson SA,
Magnusson KP,
Stefansson H,
Lam DS
외 35명 — 모두 보기
Tam PO,
Gudmundsdottir GJ,
Southgate L,
Burdon KP,
Gottfredsdottir MS,
Aldred MA,
Mitchell P,
St Clair D,
Collier DA,
Tang N,
Sveinsson O,
Macgregor S,
Martin NG,
Cree AJ,
Gibson J,
Macleod A,
Jacob A,
Ennis S,
Young TL,
Chan JC,
Karwatowski WS,
Hammond CJ,
Thordarson K,
Zhang M,
Wadelius C,
Lotery AJ,
Trembath RC,
Pang CP,
Hoh J,
Craig JE,
Kong A,
Mackey DA,
Jonasson F,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20835238
페이지 1개
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
Lettre G,
Palmer CD,
Young T,
Ejebe KG,
Allayee H,
Benjamin EJ,
Bennett F,
Bowden DW,
Chakravarti A,
Dreisbach A,
Farlow DN,
Folsom AR
외 48명 — 모두 보기
Fornage M,
Forrester T,
Fox E,
Haiman CA,
Hartiala J,
Harris TB,
Hazen SL,
Heckbert SR,
Henderson BE,
Hirschhorn JN,
Keating BJ,
Kritchevsky SB,
Larkin E,
Li M,
Rudock ME,
McKenzie CA,
Meigs JB,
Meng YA,
Mosley TH,
Newman AB,
Newton-Cheh CH,
Paltoo DN,
Papanicolaou GJ,
Patterson N,
Post WS,
Psaty BM,
Qasim AN,
Qu L,
Rader DJ,
Redline S,
Reilly MP,
Reiner AP,
Rich SS,
Rotter JI,
Liu Y,
Shrader P,
Siscovick DS,
Tang WH,
Taylor HA,
Tracy RP,
Vasan RS,
Waters KM,
Wilks R,
Wilson JG,
Fabsitz RR,
Gabriel SB,
Kathiresan S,
Boerwinkle E
PLoS genetics · 2011 · PMID 21347282 · open access
페이지 1개
Impact of ancestry and common genetic variants on QT interval in African Americans
Smith JG,
Avery CL,
Evans DS,
Nalls MA,
Meng YA,
Smith EN,
Palmer C,
Tanaka T,
Mehra R,
Butler AM,
Young T,
Buxbaum SG
외 39명 — 모두 보기
Kerr KF,
Berenson GS,
Schnabel RB,
Li G,
Ellinor PT,
Magnani JW,
Chen W,
Bis JC,
Curb JD,
Hsueh WC,
Rotter JI,
Liu Y,
Newman AB,
Limacher MC,
North KE,
Reiner AP,
Quibrera PM,
Schork NJ,
Singleton AB,
Psaty BM,
Soliman EZ,
Solomon AJ,
Srinivasan SR,
Alonso A,
Wallace R,
Redline S,
Zhang ZM,
Post WS,
Zonderman AB,
Taylor HA,
Murray SS,
Ferrucci L,
Arking DE,
Evans MK,
Fox ER,
Sotoodehnia N,
Heckbert SR,
Whitsel EA,
Newton-Cheh C
CARe and COGENT consortia
Circulation. Cardiovascular genetics · 2012 · PMID 23166209
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
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study
Gottlieb DJ,
Hek K,
Chen TH,
Watson NF,
Eiriksdottir G,
Byrne EM,
Cornelis M,
Warby SC,
Bandinelli S,
Cherkas L,
Evans DS,
Grabe HJ
외 74명 — 모두 보기
Lahti J,
Li M,
Lehtimäki T,
Lumley T,
Marciante KD,
Pérusse L,
Psaty BM,
Robbins J,
Tranah GJ,
Vink JM,
Wilk JB,
Stafford JM,
Bellis C,
Biffar R,
Bouchard C,
Cade B,
Curhan GC,
Eriksson JG,
Ewert R,
Ferrucci L,
Fülöp T,
Gehrman PR,
Goodloe R,
Harris TB,
Heath AC,
Hernandez D,
Hofman A,
Hottenga JJ,
Hunter DJ,
Jensen MK,
Johnson AD,
Kähönen M,
Kao L,
Kraft P,
Larkin EK,
Lauderdale DS,
Luik AI,
Medici M,
Montgomery GW,
Palotie A,
Patel SR,
Pistis G,
Porcu E,
Quaye L,
Raitakari O,
Redline S,
Rimm EB,
Rotter JI,
Smith AV,
Spector TD,
Teumer A,
Uitterlinden AG,
Vohl MC,
Widen E,
Willemsen G,
Young T,
Zhang X,
Liu Y,
Blangero J,
Boomsma DI,
Gudnason V,
Hu F,
Mangino M,
Martin NG,
O'Connor GT,
Stone KL,
Tanaka T,
Viikari J,
Gharib SA,
Punjabi NM,
Räikkönen K,
Völzke H,
Mignot E,
Tiemeier H
Molecular psychiatry · 2015 · PMID 25469926 · open access
페이지 1개
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가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.