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성함이나 학술지명, PMID로 찾아보십시오.
Cook J에 대해
28건, 그중 8건 표시.
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
외 198명 — 모두 보기
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
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Deloukas P,
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Kathiresan S,
Melander O,
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Mohlke KL,
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Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
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Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
Nature genetics · 2016 · PMID 27618447 · open access
페이지 11개
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Liu C,
Kraja AT,
Smith JA,
Brody JA,
Franceschini N,
Bis JC,
Rice K,
Morrison AC,
Lu Y,
Weiss S,
Guo X,
Palmas W
외 83명 — 모두 보기
Martin LW,
Chen YD,
Surendran P,
Drenos F,
Cook JP,
Auer PL,
Chu AY,
Giri A,
Zhao W,
Jakobsdottir J,
Lin LA,
Stafford JM,
Amin N,
Mei H,
Yao J,
Voorman A,
Larson MG,
Grove ML,
Smith AV,
Hwang SJ,
Chen H,
Huan T,
Kosova G,
Stitziel NO,
Kathiresan S,
Samani N,
Schunkert H,
Deloukas P,
Li M,
Fuchsberger C,
Pattaro C,
Gorski M,
Kooperberg C,
Papanicolaou GJ,
Rossouw JE,
Faul JD,
Kardia SL,
Bouchard C,
Raffel LJ,
Uitterlinden AG,
Franco OH,
Vasan RS,
O'Donnell CJ,
Taylor KD,
Liu K,
Bottinger EP,
Gottesman O,
Daw EW,
Giulianini F,
Ganesh S,
Salfati E,
Harris TB,
Launer LJ,
Dörr M,
Felix SB,
Rettig R,
Völzke H,
Kim E,
Lee WJ,
Lee IT,
Sheu WH,
Tsosie KS,
Edwards DR,
Liu Y,
Correa A,
Weir DR,
Völker U,
Ridker PM,
Boerwinkle E,
Gudnason V,
Reiner AP,
van Duijn CM,
Borecki IB,
Edwards TL,
Chakravarti A,
Rotter JI,
Psaty BM,
Loos RJ,
Fornage M,
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Newton-Cheh C,
Levy D,
Chasman DI
CHD Exome+ Consortium · ExomeBP Consortium 외 컨소시엄 4곳
Nature genetics · 2016 · PMID 27618448
페이지 9개
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Phelan CM,
Kuchenbaecker KB,
Tyrer JP,
Kar SP,
Lawrenson K,
Winham SJ,
Dennis J,
Pirie A,
Riggan MJ,
Chornokur G,
Earp MA,
Lyra PC Jr
외 402명 — 모두 보기
Lee JM,
Coetzee S,
Beesley J,
McGuffog L,
Soucy P,
Dicks E,
Lee A,
Barrowdale D,
Lecarpentier J,
Leslie G,
Aalfs CM,
Aben KKH,
Adams M,
Adlard J,
Andrulis IL,
Anton-Culver H,
Antonenkova N,
Aravantinos G,
Arnold N,
Arun BK,
Arver B,
Azzollini J,
Balmaña J,
Banerjee SN,
Barjhoux L,
Barkardottir RB,
Bean Y,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bermisheva M,
Bernardini MQ,
Birrer MJ,
Bjorge L,
Black A,
Blankstein K,
Blok MJ,
Bodelon C,
Bogdanova N,
Bojesen A,
Bonanni B,
Borg Å,
Bradbury AR,
Brenton JD,
Brewer C,
Brinton L,
Broberg P,
Brooks-Wilson A,
Bruinsma F,
Brunet J,
Buecher B,
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Caldes T,
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Campbell I,
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Carney ME,
Cescon T,
Chan SB,
Chang-Claude J,
Chanock S,
Chen XQ,
Chiew YE,
Chiquette J,
Chung WK,
Claes KBM,
Conner T,
Cook LS,
Cook J,
Cramer DW,
Cunningham JM,
D'Aloisio AA,
Daly MB,
Damiola F,
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Dansonka-Mieszkowska A,
Dao F,
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Peissel B,
Peixoto A,
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Pelttari LM,
Permuth JB,
Peterlongo P,
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Phillips KA,
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Piskorz AM,
Poblete SR,
Pocza T,
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Poppe B,
Porteous ME,
Prieur F,
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Richardson A,
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Runnebaum IB,
Salvesen HB,
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Setiawan VW,
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Sharma P,
Shelford T,
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Sieh W,
Singer CF,
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Song H,
Southey MC,
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Stadler Z,
Steinemann D,
Stoppa-Lyonnet D,
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Sutphen R,
Sutter C,
Swerdlow AJ,
Szabo CI,
Szafron L,
Tan YY,
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Teixeira MR,
Teo SH,
Terry KL,
Thompson PJ,
Thomsen LCV,
Thull DL,
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Toland AE,
Tone A,
Trabert B,
Travis RC,
Trichopoulou A,
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Vanderstichele A,
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Vega A,
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Vergote I,
Vierkant RA,
Vijai J,
Vratimos A,
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Walsh C,
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Wappenschmidt B,
Webb PM,
Weinberg CR,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Wijnen JT,
Wilkens LR,
Wolk A,
Woo M,
Wu X,
Wu AH,
Yang H,
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Ziogas A,
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Narod SA,
Easton DF,
Amos CI,
Schildkraut JM,
Ramus SJ,
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Monteiro AN,
Couch FJ,
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Pharoah PDP
AOCS study group · EMBRACE Study 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28346442
페이지 9개
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
외 121명 — 모두 보기
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
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Campbell A,
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Cook J,
De Vivo I,
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Harkki P,
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Healey M,
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Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
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Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
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Lindgren CM,
MacGregor S,
Mangino M,
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Matalliotaki C,
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Siewierska-Górska A,
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Terry KL,
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Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Wain LV,
Shrine N,
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Jackson VE,
Ntalla I,
Soler Artigas M,
Billington CK,
Kheirallah AK,
Allen R,
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Probert K,
Obeidat M
외 27명 — 모두 보기
Bossé Y,
Hao K,
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Hubbard R,
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Hansell AL,
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Strachan DP,
Tobin MD,
Hall IP
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
페이지 6개
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Mahajan A,
Wessel J,
Willems SM,
Zhao W,
Robertson NR,
Chu AY,
Gan W,
Kitajima H,
Taliun D,
Rayner NW,
Guo X,
Lu Y
외 228명 — 모두 보기
Li M,
Jensen RA,
Hu Y,
Huo S,
Lohman KK,
Zhang W,
Cook JP,
Prins BP,
Flannick J,
Grarup N,
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Kim YJ,
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Chen YI,
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Eastwood SV,
Eckardt KU,
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