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Hatzikotoulas K에 대해
9건.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou I,
Süveges D,
Min JL,
Ritchie GRS,
Steinberg J,
Walter K,
Iotchkova V,
Schwartzentruber J,
Huang J,
Memari Y,
McCarthy S,
Crawford AA
외 91명 — 모두 보기
Bombieri C,
Cocca M,
Farmaki AE,
Gaunt TR,
Jousilahti P,
Kooijman MN,
Lehne B,
Malerba G,
Männistö S,
Matchan A,
Medina-Gomez C,
Metrustry SJ,
Nag A,
Ntalla I,
Paternoster L,
Rayner NW,
Sala C,
Scott WR,
Shihab HA,
Southam L,
St Pourcain B,
Traglia M,
Trajanoska K,
Zaza G,
Zhang W,
Artigas MS,
Bansal N,
Benn M,
Chen Z,
Danecek P,
Lin WY,
Locke A,
Luan J,
Manning AK,
Mulas A,
Sidore C,
Tybjaerg-Hansen A,
Varbo A,
Zoledziewska M,
Finan C,
Hatzikotoulas K,
Hendricks AE,
Kemp JP,
Moayyeri A,
Panoutsopoulou K,
Szpak M,
Wilson SG,
Boehnke M,
Cucca F,
Di Angelantonio E,
Langenberg C,
Lindgren C,
McCarthy MI,
Morris AP,
Nordestgaard BG,
Scott RA,
Tobin MD,
Wareham NJ,
Burton P,
Chambers JC,
Smith GD,
Dedoussis G,
Felix JF,
Franco OH,
Gambaro G,
Gasparini P,
Hammond CJ,
Hofman A,
Jaddoe VWV,
Kleber M,
Kooner JS,
Perola M,
Relton C,
Ring SM,
Rivadeneira F,
Salomaa V,
Spector TD,
Stegle O,
Toniolo D,
Uitterlinden AG,
Barroso I,
Greenwood CMT,
Perry JRB,
Walker BR,
Butterworth AS,
Xue Y,
Durbin R,
Small KS,
Soranzo N,
Timpson NJ,
Zeggini E
SpiroMeta Consortium · GoT2D Consortium 외 컨소시엄 3곳
American journal of human genetics · 2017 · PMID 28552196 · open access
페이지 12개+
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
Tachmazidou I,
Hatzikotoulas K,
Southam L,
Esparza-Gordillo J,
Haberland V,
Zheng J,
Johnson T,
Koprulu M,
Zengini E,
Steinberg J,
Wilkinson JM,
Bhatnagar S
외 9명 — 모두 보기
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
페이지 12개+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
외 351명 — 모두 보기
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
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Williamson A,
Kamali Z,
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Thangam M,
Adair LS,
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Aguilar-Salinas CA,
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Anand SS,
Bertoni A,
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Brandslund I,
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Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
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Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
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Kronenberg F,
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Läll K,
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Lee KM,
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Ligthart S,
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Luan J,
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Luo X,
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Maeda S,
Mamakou V,
Mansuri SR,
Matsuda K,
Meitinger T,
Melander O,
Metspalu A,
Mo H,
Morris AD,
Moura FA,
Nadler JL,
Nalls MA,
Nayak U,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Patil S,
Pei P,
Pereira MA,
Peters A,
Pirie FJ,
Polikowsky HG,
Porneala B,
Prasad G,
Rasmussen-Torvik LJ,
Reiner AP,
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Sabanayagam C,
Sandow K,
Sankareswaran A,
Sattar N,
Schönherr S,
Shahriar M,
Shen B,
Shi J,
Shin DM,
Shojima N,
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So WY,
Stančáková A,
Steinthorsdottir V,
Stilp AM,
Strauch K,
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Thorand B,
Thorsteinsdottir U,
Tomlinson B,
Tran TC,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Wacher-Rodarte N,
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Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamamoto K,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zawistowski M,
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Zheng W,
Raffel LJ,
Igase M,
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Redline S,
Cho YS,
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Province MA,
Fornage M,
Hanis CL,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Yokota M,
Kardia SLR,
Peyser PA,
Pankow JS,
Engert JC,
Bonnefond A,
Froguel P,
Wilson JG,
Sheu WHH,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Mook-Kanamori DO,
Tuomi T,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
Chen YI,
Rich SS,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Ghanbari M,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Bowden DW,
Palmer CNA,
Kooner JS,
Kooperberg C,
Liu S,
North KE,
Saleheen D,
Hansen T,
Pedersen O,
Wareham NJ,
Lee J,
Kim BJ,
Millwood IY,
Walters RG,
Stefansson K,
Ahlqvist E,
Goodarzi MO,
Mohlke KL,
Langenberg C,
Haiman CA,
Loos RJF,
Florez JC,
Rader DJ,
Ritchie MD,
Zöllner S,
Mägi R,
Marston NA,
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van Heel DA,
Finer S,
Denny JC,
Yamauchi T,
Kadowaki T,
Chambers JC,
Ng MCY,
Sim X,
Below JE,
Tsao PS,
Chang KM,
McCarthy MI,
Meigs JB,
Mahajan A,
Spracklen CN,
Mercader JM,
Boehnke M,
Rotter JI,
Vujkovic M,
Voight BF,
Morris AP,
Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Translational genomics of osteoarthritis in 1,962,069 individuals
Hatzikotoulas K,
Southam L,
Stefansdottir L,
Boer CG,
McDonald ML,
Pett JP,
Park YC,
Tuerlings M,
Mulders R,
Barysenka A,
Arruda AL,
Tragante V
외 162명 — 모두 보기
Rocco A,
Bittner N,
Chen S,
Horn S,
Srinivasasainagendra V,
To K,
Katsoula G,
Kreitmaier P,
Tenghe AMM,
Gilly A,
Arbeeva L,
Chen LG,
de Pins AM,
Dochtermann D,
Henkel C,
Höijer J,
Ito S,
Lind PA,
Lukusa-Sawalena B,
Minn AKK,
Mola-Caminal M,
Narita A,
Nguyen C,
Reimann E,
Silberstein MD,
Skogholt AH,
Tiwari HK,
Yau MS,
Yue M,
Zhao W,
Zhao W,
Zhou JJ,
Alexiadis G,
Banasik K,
Brunak S,
Campbell A,
Cheung JTS,
Dowsett J,
Faquih T,
Faul JD,
Fei L,
Fenstad AM,
Funayama T,
Gabrielsen ME,
Gocho C,
Gromov K,
Hansen T,
Hudjashov G,
Ingvarsson T,
Johnson JS,
Jonsson H,
Kakehi S,
Karjalainen J,
Kasbohm E,
Lemmelä S,
Lin K,
Liu X,
Loef M,
Mangino M,
McCartney D,
Millwood IY,
Richman J,
Roberts MB,
Ryan KA,
Samartzis D,
Shivakumar M,
Skou ST,
Sugimoto S,
Suzuki K,
Takuwa H,
Teder-Laving M,
Thomas L,
Tomizuka K,
Turman C,
Weiss S,
Wu TT,
Zengini E,
Zhang Y,
Ferreira MAR,
Babis G,
Baras A,
Barker T,
Carey DJ,
Cheah KSE,
Chen Z,
Cheung JP,
Daly M,
de Mutsert R,
Eaton CB,
Erikstrup C,
Furnes ON,
Golightly YM,
Gudbjartsson DF,
Hailer NP,
Hayward C,
Hochberg MC,
Homuth G,
Huckins LM,
Hveem K,
Ikegawa S,
Ishijima M,
Isomura M,
Jones M,
Kang JH,
Kardia SLR,
Kloppenburg M,
Kraft P,
Kumahashi N,
Kuwata S,
Lee MTM,
Lee PH,
Lerner R,
Li L,
Lietman SA,
Lotta L,
Lupton MK,
Mägi R,
Martin NG,
McAlindon TE,
Medland SE,
Michaëlsson K,
Mitchell BD,
Mook-Kanamori DO,
Morris AP,
Nabika T,
Nagami F,
Nelson AE,
Ostrowski SR,
Palotie A,
Pedersen OB,
Rosendaal FR,
Sakurai-Yageta M,
Schmidt CO,
Sham PC,
Singh JA,
Smelser DT,
Smith JA,
Song YQ,
Sørensen E,
Tamiya G,
Tamura Y,
Terao C,
Thorleifsson G,
Troelsen A,
Tsezou A,
Uchio Y,
Uitterlinden AG,
Ullum H,
Valdes AM,
van Heel DA,
Walters RG,
Weir DR,
Wilkinson JM,
Winsvold BS,
Yamamoto M,
Zwart JA,
Stefansson K,
Meulenbelt I,
Teichmann SA,
van Meurs JBJ,
Styrkarsdottir U,
Zeggini E
arcOGEN Consortium · ARGO Consortium 외 컨소시엄 7곳
Nature · 2025 · PMID 40205036 · open access
페이지 12개+
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Boer CG,
Hatzikotoulas K,
Southam L,
Stefánsdóttir L,
Zhang Y,
Coutinho de Almeida R,
Wu TT,
Zheng J,
Hartley A,
Teder-Laving M,
Skogholt AH,
Terao C
외 50명 — 모두 보기
Zengini E,
Alexiadis G,
Barysenka A,
Bjornsdottir G,
Gabrielsen ME,
Gilly A,
Ingvarsson T,
Johnsen MB,
Jonsson H,
Kloppenburg M,
Luetge A,
Lund SH,
Mägi R,
Mangino M,
Nelissen RRGHH,
Shivakumar M,
Steinberg J,
Takuwa H,
Thomas LF,
Tuerlings M,
Babis GC,
Cheung JPY,
Kang JH,
Kraft P,
Lietman SA,
Samartzis D,
Slagboom PE,
Stefansson K,
Thorsteinsdottir U,
Tobias JH,
Uitterlinden AG,
Winsvold B,
Zwart JA,
Davey Smith G,
Sham PC,
Thorleifsson G,
Gaunt TR,
Morris AP,
Valdes AM,
Tsezou A,
Cheah KSE,
Ikegawa S,
Hveem K,
Esko T,
Wilkinson JM,
Meulenbelt I,
Lee MTM,
van Meurs JBJ,
Styrkársdóttir U,
Zeggini E
arcOGEN Consortium · HUNT All-In Pain 외 컨소시엄 2곳
Cell · 2021 · PMID 34450027 · open access
페이지 11개
Genetic study identifies novel genes in developmental dysplasia of the hip
Yoshino S,
Chen S,
Yamaguchi R,
Kurakazu T,
Hatzikotoulas K,
Koike Y,
Inoue D,
Kohno Y,
Sasaki K,
Choe H,
Baba S,
Hara T
외 31명 — 모두 보기
Ito J,
Okuzu Y,
Shiomoto K,
Nakamura T,
Koyano G,
Shimizu T,
Kinoshita K,
Takahashi E,
Utsunomiya T,
Hara D,
Sato T,
Kawahara S,
Kaneuji A,
Yamamoto T,
Takahashi D,
Jinno T,
Kawano T,
Goto K,
Takagi M,
Mawatari T,
Inaba Y,
Nakamura T,
Kabata T,
Hamai S,
Motomura G,
Southam L,
Wilkinson JM,
Zeggini E,
Ikegawa S,
Nakashima Y,
Terao C
Bone research · 2026 · PMID 41912496 · open access
페이지 9개
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Gurdasani D,
Carstensen T,
Fatumo S,
Chen G,
Franklin CS,
Prado-Martinez J,
Bouman H,
Abascal F,
Haber M,
Tachmazidou I,
Mathieson I,
Ekoru K
외 45명 — 모두 보기
DeGorter MK,
Nsubuga RN,
Finan C,
Wheeler E,
Chen L,
Cooper DN,
Schiffels S,
Chen Y,
Ritchie GRS,
Pollard MO,
Fortune MD,
Mentzer AJ,
Garrison E,
Bergström A,
Hatzikotoulas K,
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Doumatey A,
Elding H,
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Kooperberg CL,
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Kadie C,
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Kamali A,
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Tyler-Smith C,
Motala AA,
Rotimi C,
Kaleebu P,
Barroso I,
Sandhu MS
Cell · 2019 · PMID 31675503
페이지 6개
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
Mattheisen M,
Medland SE,
Ripke S
외 198명 — 모두 보기
Yao S,
Giusti-Rodríguez P,
Hanscombe KB,
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Mitchell JE,
Olsen CM,
Pearson JF,
Pedersen NL,
Strober M,
Werge T,
Whiteman DC,
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Stuber GD,
Gordon S,
Grove J,
Henders AK,
Juréus A,
Kirk KM,
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Wade TD,
Birgegård A,
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Mortensen PB,
Sullivan PF,
Breen G,
Bulik CM
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
페이지 1개
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인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
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.