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성함이나 학술지명, PMID로 찾아보십시오.
Williams A에 대해
14건.
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
외 136명 — 모두 보기
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
페이지 12개+
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
Williams AT,
Chen J,
Coley K,
Batini C,
Izquierdo A,
Packer R,
Abner E,
Kanoni S,
Shepherd DJ,
Free RC,
Hollox EJ,
Brunskill NJ
외 20명 — 모두 보기
Ntalla I,
Reeve N,
Brightling CE,
Venn L,
Adams E,
Bee C,
Wallace SE,
Pareek M,
Hansell AL,
Esko T,
Stow D,
Jacobs BM,
van Heel DA,
Hennah W,
Rao BS,
Dudbridge F,
Wain LV,
Shrine N,
Tobin MD,
John C
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · open access
페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
외 135명 — 모두 보기
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Kim J,
Williams A,
Noh H,
Jasper EA,
Jones SH,
Jaworski JA,
Shuey MM,
Ruiz-Narváez EA,
Wise LA,
Palmer JR,
Connolly J,
Keaton JM
외 11명 — 모두 보기
Denny JC,
Khan A,
Abbass MA,
Rasmussen-Torvik LJ,
Kottyan LC,
Madhivanan P,
Krupp K,
Wei WQ,
Edwards TL,
Velez Edwards DR,
Hellwege JN
Nature communications · 2025 · PMID 40050615 · open access
페이지 12개+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
외 73명 — 모두 보기
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium 외 컨소시엄 4곳
Nature genetics · 2026 · PMID 41644669 · open access
페이지 12개+
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Di Lorenzo B,
Camargo Tavares L,
Díaz-Muñoz C,
Heredia-Fernández F,
Bozzarelli I,
Esteban Blanco C,
Wang Z,
Smit RAJ,
Loos RJF,
Hirbo J,
Cox NJ,
Straub P
외 57명 — 모두 보기
Favé MJ,
Awadalla P,
Pozdeyev N,
Gignoux CR,
Gudbjartsson DF,
Thorleifsson G,
Jonsdottir I,
Stefansson K,
Abner E,
Palta P,
Williams AT,
Coley K,
Sze G,
John C,
Richmond A,
McCartney D,
Hayward C,
Mulford AJ,
Sanders AR,
Peculis R,
Rovite V,
Dombrovska MS,
Capasso M,
Lo Faro V,
Sinha T,
Lopera Maya EA,
Zhernakova A,
Wang Y,
Martin A,
Vanderwerff B,
Zöllner S,
Ferolito BR,
Pereira AC,
Gaziano JM,
Cho K,
Caruth L,
Guare L,
Kripke CM,
Rader DJ,
Verma SS,
Verma A,
Saad C,
Mbarek H,
Chao PY,
Chen TT,
Lin YF,
Feng YA,
Challa PK,
Khalili H,
Andries A,
Ness-Jensen E,
Brumpton BM,
Grover M,
Lemmelä S,
Sanna S,
Bonfiglio F,
D'Amato M
Colorado Center for Personalized Medicine · Estonian Biobank Research Team 외 컨소시엄 3곳
Gut · 2026 · PMID 42425734
페이지 6개
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
Harley JB,
Alarcón-Riquelme ME,
Criswell LA,
Jacob CO,
Kimberly RP,
Moser KL,
Tsao BP,
Vyse TJ,
Langefeld CD,
Nath SK,
Guthridge JM,
Cobb BL
외 29명 — 모두 보기
Mirel DB,
Marion MC,
Williams AH,
Divers J,
Wang W,
Frank SG,
Namjou B,
Gabriel SB,
Lee AT,
Gregersen PK,
Behrens TW,
Taylor KE,
Fernando M,
Zidovetzki R,
Gaffney PM,
Edberg JC,
Rioux JD,
Ojwang JO,
James JA,
Merrill JT,
Gilkeson GS,
Seldin MF,
Yin H,
Baechler EC,
Li QZ,
Wakeland EK,
Bruner GR,
Kaufman KM,
Kelly JA
International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN)
Nature genetics · 2008 · PMID 18204446
페이지 3개
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
Evangelou E,
Kerkhof HJ,
Styrkarsdottir U,
Ntzani EE,
Bos SD,
Esko T,
Evans DS,
Metrustry S,
Panoutsopoulou K,
Ramos YF,
Thorleifsson G,
Tsilidis KK
외 54명 — 모두 보기
Arden N,
Aslam N,
Bellamy N,
Birrell F,
Blanco FJ,
Carr A,
Chapman K,
Day-Williams AG,
Deloukas P,
Doherty M,
Engström G,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Keurentjes JC,
Kloppenburg M,
Lind PA,
McCaskie A,
Martin NG,
Milani L,
Montgomery GW,
Nelissen RG,
Nevitt MC,
Nilsson PM,
Ollier WE,
Parimi N,
Rai A,
Ralston SH,
Reed MR,
Riancho JA,
Rivadeneira F,
Rodriguez-Fontenla C,
Southam L,
Thorsteinsdottir U,
Tsezou A,
Wallis GA,
Wilkinson JM,
Gonzalez A,
Lane NE,
Lohmander LS,
Loughlin J,
Metspalu A,
Uitterlinden AG,
Jonsdottir I,
Stefansson K,
Slagboom PE,
Zeggini E,
Meulenbelt I,
Ioannidis JP,
Spector TD,
van Meurs JB,
Valdes AM
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
페이지 3개
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
Higbee DH,
Lirio A,
Hamilton F,
Granell R,
Wyss AB,
London SJ,
Bartz TM,
Gharib SA,
Cho MH,
Wan E,
Silverman E,
Crapo JD
외 33명 — 모두 보기
Lominchar JVT,
Hansen T,
Grarup N,
Dantoft T,
Kårhus L,
Linneberg A,
O'Connor GT,
Dupuis J,
Xu H,
De Vries MM,
Hu X,
Rich SS,
Barr RG,
Manichaikul A,
Wijnant SRA,
Brusselle GG,
Lahousse L,
Li X,
Hernández Cordero AI,
Obeidat M,
Sin DD,
Harris SE,
Redmond P,
Taylor AM,
Cox SR,
Williams AT,
Shrine N,
John C,
Guyatt AL,
Hall IP,
Davey Smith G,
Tobin MD,
Dodd JW
The European respiratory journal · 2024 · PMID 38097206 · open access
페이지 3개
A variant in MCF2L is associated with osteoarthritis
Day-Williams AG,
Southam L,
Panoutsopoulou K,
Rayner NW,
Esko T,
Estrada K,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Kerkhof HJ
외 33명 — 모두 보기
Thorleifsson G,
Arden NK,
Carr A,
Chapman K,
Deloukas P,
Loughlin J,
McCaskie A,
Ollier WE,
Ralston SH,
Spector TD,
Wallis GA,
Wilkinson JM,
Aslam N,
Birell F,
Carluke I,
Joseph J,
Rai A,
Reed M,
Walker K,
Doherty SA,
Jonsdottir I,
Maciewicz RA,
Muir KR,
Metspalu A,
Rivadeneira F,
Stefansson K,
Styrkarsdottir U,
Uitterlinden AG,
van Meurs JB,
Zhang W,
Valdes AM,
Doherty M,
Zeggini E
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
페이지 1개
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Zeggini E,
Panoutsopoulou K,
Southam L,
Rayner NW,
Day-Williams AG,
Lopes MC,
Boraska V,
Esko T,
Evangelou E,
Hoffman A,
Houwing-Duistermaat JJ,
Ingvarsson T
외 64명 — 모두 보기
Jonsdottir I,
Jonnson H,
Kerkhof HJ,
Kloppenburg M,
Bos SD,
Mangino M,
Metrustry S,
Slagboom PE,
Thorleifsson G,
Raine EV,
Ratnayake M,
Ricketts M,
Beazley C,
Blackburn H,
Bumpstead S,
Elliott KS,
Hunt SE,
Potter SC,
Shin SY,
Yadav VK,
Zhai G,
Sherburn K,
Dixon K,
Arden E,
Aslam N,
Battley PK,
Carluke I,
Doherty S,
Gordon A,
Joseph J,
Keen R,
Koller NC,
Mitchell S,
O'Neill F,
Paling E,
Reed MR,
Rivadeneira F,
Swift D,
Walker K,
Watkins B,
Wheeler M,
Birrell F,
Ioannidis JP,
Meulenbelt I,
Metspalu A,
Rai A,
Salter D,
Stefansson K,
Stykarsdottir U,
Uitterlinden AG,
van Meurs JB,
Chapman K,
Deloukas P,
Ollier WE,
Wallis GA,
Arden N,
Carr A,
Doherty M,
McCaskie A,
Willkinson JM,
Ralston SH,
Valdes AM,
Spector TD,
Loughlin J
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
페이지 1개
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes
Mercader JM,
Liao RG,
Bell AD,
Dymek Z,
Estrada K,
Tukiainen T,
Huerta-Chagoya A,
Moreno-Macías H,
Jablonski KA,
Hanson RL,
Walford GA,
Moran I
외 66명 — 모두 보기
Chen L,
Agarwala V,
Ordoñez-Sánchez ML,
Rodríguez-Guillen R,
Rodríguez-Torres M,
Segura-Kato Y,
García-Ortiz H,
Centeno-Cruz F,
Barajas-Olmos F,
Caulkins L,
Puppala S,
Fontanillas P,
Williams AL,
Bonàs-Guarch S,
Hartl C,
Ripke S,
Tooley K,
Lane J,
Zerrweck C,
Martínez-Hernández A,
Córdova EJ,
Mendoza-Caamal E,
Contreras-Cubas C,
González-Villalpando ME,
Cruz-Bautista I,
Muñoz-Hernández L,
Gómez-Velasco D,
Alvirde U,
Henderson BE,
Wilkens LR,
Le Marchand L,
Arellano-Campos O,
Riba L,
Harden M,
Gabriel S,
Abboud HE,
Cortes ML,
Revilla-Monsalve C,
Islas-Andrade S,
Soberon X,
Curran JE,
Jenkinson CP,
DeFronzo RA,
Lehman DM,
Hanis CL,
Bell GI,
Boehnke M,
Blangero J,
Duggirala R,
Saxena R,
MacArthur D,
Ferrer J,
McCarroll SA,
Torrents D,
Knowler WC,
Baier LJ,
Burtt N,
González-Villalpando C,
Haiman CA,
Aguilar-Salinas CA,
Tusié-Luna T,
Flannick J,
Jacobs SBR,
Orozco L,
Altshuler D,
Florez JC
Diabetes Prevention Program Research Group · Broad Genomics Platform 외 컨소시엄 2곳
Diabetes · 2017 · PMID 28838971 · open access
페이지 1개
Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection
Packer RJ,
Shrine N,
Hall R,
Melbourne CA,
Thompson R,
Williams AT,
Paynton ML,
Guyatt AL,
Allen RJ,
Lee PH,
John C,
Campbell A
외 12명 — 모두 보기
Hayward C,
de Vries M,
Vonk JM,
Davitte J,
Hessel E,
Michalovich D,
Betts JC,
Sayers I,
Yeo A,
Hall IP,
Tobin MD,
Wain LV
The European respiratory journal · 2023 · PMID 37263751 · open access
페이지 1개
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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.