연구자에게
내 논문이 여기 있나요?
논문 2,681편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Taylor K에 대해
114건, 그중 20건 표시.
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Franceschini N,
Fox E,
Zhang Z,
Edwards TL,
Nalls MA,
Sung YJ,
Tayo BO,
Sun YV,
Gottesman O,
Adeyemo A,
Johnson AD,
Young JH
외 94명 — 모두 보기
Rice K,
Duan Q,
Chen F,
Li Y,
Tang H,
Fornage M,
Keene KL,
Andrews JS,
Smith JA,
Faul JD,
Guangfa Z,
Guo W,
Liu Y,
Murray SS,
Musani SK,
Srinivasan S,
Velez Edwards DR,
Wang H,
Becker LC,
Bovet P,
Bochud M,
Broeckel U,
Burnier M,
Carty C,
Chasman DI,
Ehret G,
Chen WM,
Chen G,
Chen W,
Ding J,
Dreisbach AW,
Evans MK,
Guo X,
Garcia ME,
Jensen R,
Keller MF,
Lettre G,
Lotay V,
Martin LW,
Moore JH,
Morrison AC,
Mosley TH,
Ogunniyi A,
Palmas W,
Papanicolaou G,
Penman A,
Polak JF,
Ridker PM,
Salako B,
Singleton AB,
Shriner D,
Taylor KD,
Vasan R,
Wiggins K,
Williams SM,
Yanek LR,
Zhao W,
Zonderman AB,
Becker DM,
Berenson G,
Boerwinkle E,
Bottinger E,
Cushman M,
Eaton C,
Nyberg F,
Heiss G,
Hirschhron JN,
Howard VJ,
Karczewsk KJ,
Lanktree MB,
Liu K,
Liu Y,
Loos R,
Margolis K,
Snyder M,
Psaty BM,
Schork NJ,
Weir DR,
Rotimi CN,
Sale MM,
Harris T,
Kardia SL,
Hunt SC,
Arnett D,
Redline S,
Cooper RS,
Risch NJ,
Rao DC,
Rotter JI,
Chakravarti A,
Reiner AP,
Levy D,
Keating BJ,
Zhu X
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
페이지 2개
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Huang J,
Huffman JE,
Yamakuchi M,
Trompet S,
Asselbergs FW,
Sabater-Lleal M,
Trégouët DA,
Chen WM,
Smith NL,
Kleber ME,
Shin SY,
Becker DM
외 81명 — 모두 보기
Tang W,
Dehghan A,
Johnson AD,
Truong V,
Folkersen L,
Yang Q,
Oudot-Mellkah T,
Buckley BM,
Moore JH,
Williams FM,
Campbell H,
Silbernagel G,
Vitart V,
Rudan I,
Tofler GH,
Navis GJ,
Destefano A,
Wright AF,
Chen MH,
de Craen AJ,
Worrall BB,
Rudnicka AR,
Rumley A,
Bookman EB,
Psaty BM,
Chen F,
Keene KL,
Franco OH,
Böhm BO,
Uitterlinden AG,
Carter AM,
Jukema JW,
Sattar N,
Bis JC,
Bis JC,
Ikram MA,
Sale MM,
McKnight B,
Fornage M,
Ford I,
Taylor K,
Slagboom PE,
McArdle WL,
Hsu FC,
Franco-Cereceda A,
Goodall AH,
Yanek LR,
Furie KL,
Cushman M,
Hofman A,
Witteman JC,
Folsom AR,
Basu S,
Matijevic N,
van Gilst WH,
Wilson JF,
Westendorp RG,
Kathiresan S,
Reilly MP,
Tracy RP,
Polasek O,
Winkelmann BR,
Grant PJ,
Hillege HL,
Cambien F,
Stott DJ,
Lowe GD,
Spector TD,
Meigs JB,
Marz W,
Eriksson P,
Becker LC,
Morange PE,
Soranzo N,
Williams SM,
Hayward C,
van der Harst P,
Hamsten A,
Lowenstein CJ,
Strachan DP,
O'Donnell CJ
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium 외 컨소시엄 1곳
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
페이지 2개
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
Dehghan A,
Bis JC,
White CC,
Smith AV,
Morrison AC,
Cupples LA,
Trompet S,
Chasman DI,
Lumley T,
Völker U,
Buckley BM,
Ding J
외 55명 — 모두 보기
Jensen MK,
Folsom AR,
Kritchevsky SB,
Girman CJ,
Ford I,
Dörr M,
Salomaa V,
Uitterlinden AG,
Eiriksdottir G,
Vasan RS,
Franceschini N,
Carty CL,
Virtamo J,
Demissie S,
Amouyel P,
Arveiler D,
Heckbert SR,
Ferrières J,
Ducimetière P,
Smith NL,
Wang YA,
Siscovick DS,
Rice KM,
Wiklund PG,
Taylor KD,
Evans A,
Kee F,
Rotter JI,
Karvanen J,
Kuulasmaa K,
Heiss G,
Kraft P,
Launer LJ,
Hofman A,
Markus MR,
Rose LM,
Silander K,
Wagner P,
Benjamin EJ,
Lohman K,
Stott DJ,
Rivadeneira F,
Harris TB,
Levy D,
Liu Y,
Rimm EB,
Jukema JW,
Völzke H,
Ridker PM,
Blankenberg S,
Franco OH,
Gudnason V,
Psaty BM,
Boerwinkle E,
O'Donnell CJ
PloS one · 2016 · PMID 26950853 · open access
페이지 2개
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
외 76명 — 모두 보기
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
페이지 2개
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
Wood AR,
Jonsson A,
Jackson AU,
Wang N,
van Leewen N,
Palmer ND,
Kobes S,
Deelen J,
Boquete-Vilarino L,
Paananen J,
Stančáková A,
Boomsma DI
외 40명 — 모두 보기
de Geus EJC,
Eekhoff EMW,
Fritsche A,
Kramer M,
Nijpels G,
Simonis-Bik A,
van Haeften TW,
Mahajan A,
Boehnke M,
Bergman RN,
Tuomilehto J,
Collins FS,
Mohlke KL,
Banasik K,
Groves CJ,
McCarthy MI,
Pearson ER,
Natali A,
Mari A,
Buchanan TA,
Taylor KD,
Xiang AH,
Xiang AH,
Gjesing AP,
Grarup N,
Eiberg H,
Pedersen O,
Chen YD,
Laakso M,
Norris JM,
Smith U,
Wagenknecht LE,
Baier L,
Bowden DW,
Hansen T,
Walker M,
Watanabe RM,
't Hart LM,
Hanson RL,
Frayling TM
Diabetes Research on Patient Stratification (DIRECT)
Diabetes · 2017 · PMID 28490609 · open access
페이지 2개
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23
Robinson-Cohen C,
Bartz TM,
Lai D,
Ikizler TA,
Peacock M,
Imel EA,
Michos ED,
Foroud TM,
Akesson K,
Taylor KD,
Malmgren L,
Matsushita K
외 15명 — 모두 보기
Nethander M,
Eriksson J,
Ohlsson C,
Mellström D,
Wolf M,
Ljunggren O,
McGuigan F,
Rotter JI,
Karlsson M,
Econs MJ,
Ix JH,
Lutsey PL,
Psaty BM,
de Boer IH,
Kestenbaum BR
Journal of the American Society of Nephrology : JASN · 2018 · PMID 30217807
페이지 2개
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Spracklen CN,
Karaderi T,
Yaghootkar H,
Schurmann C,
Fine RS,
Kutalik Z,
Preuss MH,
Lu Y,
Wittemans LBL,
Adair LS,
Allison M,
Amin N
외 92명 — 모두 보기
Auer PL,
Bartz TM,
Blüher M,
Boehnke M,
Borja JB,
Bork-Jensen J,
Broer L,
Chasman DI,
Chen YI,
Chirstofidou P,
Demirkan A,
van Duijn CM,
Feitosa MF,
Garcia ME,
Graff M,
Grallert H,
Grarup N,
Guo X,
Haesser J,
Hansen T,
Harris TB,
Highland HM,
Hong J,
Ikram MA,
Ingelsson E,
Jackson R,
Jousilahti P,
Kähönen M,
Kizer JR,
Kovacs P,
Kriebel J,
Laakso M,
Lange LA,
Lehtimäki T,
Li J,
Li-Gao R,
Lind L,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mackey DA,
Mahajan A,
Mangino M,
Männistö S,
McCarthy MI,
McKnight B,
Medina-Gomez C,
Meigs JB,
Molnos S,
Mook-Kanamori D,
Morris AP,
de Mutsert R,
Nalls MA,
Nedeljkovic I,
North KE,
Pennell CE,
Pradhan AD,
Province MA,
Raitakari OT,
Raulerson CK,
Reiner AP,
Ridker PM,
Ripatti S,
Roberston N,
Rotter JI,
Salomaa V,
Sandoval-Zárate AA,
Sitlani CM,
Spector TD,
Strauch K,
Stumvoll M,
Taylor KD,
Thuesen B,
Tönjes A,
Uitterlinden AG,
Venturini C,
Walker M,
Wang CA,
Wang S,
Wareham NJ,
Willems SM,
Willems van Dijk K,
Wilson JG,
Wu Y,
Yao J,
Young KL,
Langenberg C,
Frayling TM,
Kilpeläinen TO,
Lindgren CM,
Loos RJF,
Mohlke KL
American journal of human genetics · 2019 · PMID 31178129
페이지 2개
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Lindström S,
Wang L,
Smith EN,
Gordon W,
van Hylckama Vlieg A,
de Andrade M,
Brody JA,
Pattee JW,
Haessler J,
Brumpton BM,
Chasman DI,
Suchon P
외 45명 — 모두 보기
Chen MH,
Turman C,
Germain M,
Wiggins KL,
MacDonald J,
Braekkan SK,
Armasu SM,
Pankratz N,
Jackson RD,
Nielsen JB,
Giulianini F,
Puurunen MK,
Ibrahim M,
Heckbert SR,
Damrauer SM,
Natarajan P,
Klarin D,
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Bammler TK,
Frazer KA,
McCauley BM,
Taylor K,
Pankow JS,
Reiner AP,
Gabrielsen ME,
Deleuze JF,
O'Donnell CJ,
Kim J,
McKnight B,
Kraft P,
Hansen JB,
Rosendaal FR,
Heit JA,
Psaty BM,
Tang W,
Kooperberg C,
Hveem K,
Ridker PM,
Morange PE,
Johnson AD,
Kabrhel C,
Trégouët DA,
Smith NL
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
페이지 2개
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
외 119명 — 모두 보기
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
페이지 2개
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
외 77명 — 모두 보기
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
페이지 2개
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
외 113명 — 모두 보기
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · 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
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
Rioux JD,
Xavier RJ,
Taylor KD,
Silverberg MS,
Goyette P,
Huett A,
Green T,
Kuballa P,
Barmada MM,
Datta LW,
Shugart YY,
Griffiths AM
외 13명 — 모두 보기
Targan SR,
Ippoliti AF,
Bernard EJ,
Mei L,
Nicolae DL,
Regueiro M,
Schumm LP,
Steinhart AH,
Rotter JI,
Duerr RH,
Cho JH,
Daly MJ,
Brant SR
Nature genetics · 2007 · PMID 17435756
페이지 1개
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
Hom G,
Graham RR,
Modrek B,
Taylor KE,
Ortmann W,
Garnier S,
Lee AT,
Chung SA,
Ferreira RC,
Pant PV,
Ballinger DG,
Kosoy R
외 15명 — 모두 보기
Demirci FY,
Kamboh MI,
Kao AH,
Tian C,
Gunnarsson I,
Bengtsson AA,
Rantapää-Dahlqvist S,
Petri M,
Manzi S,
Seldin MF,
Rönnblom L,
Syvänen AC,
Criswell LA,
Gregersen PK,
Behrens TW
The New England journal of medicine · 2008 · PMID 18204098
페이지 1개
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
Silverberg MS,
Cho JH,
Rioux JD,
McGovern DP,
Wu J,
Annese V,
Achkar JP,
Goyette P,
Scott R,
Xu W,
Barmada MM,
Klei L
외 22명 — 모두 보기
Daly MJ,
Abraham C,
Bayless TM,
Bossa F,
Griffiths AM,
Ippoliti AF,
Lahaie RG,
Latiano A,
Paré P,
Proctor DD,
Regueiro MD,
Steinhart AH,
Targan SR,
Schumm LP,
Kistner EO,
Lee AT,
Gregersen PK,
Rotter JI,
Brant SR,
Taylor KD,
Roeder K,
Duerr RH
Nature genetics · 2009 · PMID 19122664 · open access
페이지 1개
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
Dehghan A,
Yang Q,
Peters A,
Basu S,
Bis JC,
Rudnicka AR,
Kavousi M,
Chen MH,
Baumert J,
Lowe GD,
McKnight B,
Tang W
외 29명 — 모두 보기
de Maat M,
Larson MG,
Eyhermendy S,
McArdle WL,
Lumley T,
Pankow JS,
Hofman A,
Massaro JM,
Rivadeneira F,
Kolz M,
Taylor KD,
van Duijn CM,
Kathiresan S,
Illig T,
Aulchenko YS,
Volcik KA,
Johnson AD,
Uitterlinden AG,
Tofler GH,
Gieger C,
Psaty BM,
Couper DJ,
Boerwinkle E,
Koenig W,
O'Donnell CJ,
Witteman JC,
Strachan DP,
Smith NL,
Folsom AR
Wellcome Trust Case Control Consortium
Circulation. Cardiovascular genetics · 2009 · PMID 20031576
페이지 1개
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Fornage M,
Debette S,
Bis JC,
Schmidt H,
Ikram MA,
Dufouil C,
Sigurdsson S,
Lumley T,
DeStefano AL,
Fazekas F,
Vrooman HA,
Shibata DK
외 51명 — 모두 보기
Maillard P,
Zijdenbos A,
Smith AV,
Gudnason H,
de Boer R,
Cushman M,
Mazoyer B,
Heiss G,
Vernooij MW,
Enzinger C,
Glazer NL,
Beiser A,
Knopman DS,
Cavalieri M,
Niessen WJ,
Harris TB,
Petrovic K,
Lopez OL,
Au R,
Lambert JC,
Hofman A,
Gottesman RF,
Garcia M,
Heckbert SR,
Atwood LD,
Catellier DJ,
Uitterlinden AG,
Yang Q,
Smith NL,
Aspelund T,
Romero JR,
Rice K,
Taylor KD,
Nalls MA,
Rotter JI,
Sharrett R,
van Duijn CM,
Amouyel P,
Wolf PA,
Gudnason V,
van der Lugt A,
Boerwinkle E,
Psaty BM,
Seshadri S,
Tzourio C,
Breteler MM,
Mosley TH,
Schmidt R,
Longstreth WT,
DeCarli C,
Launer LJ
Annals of neurology · 2011 · PMID 21681796
페이지 1개
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
외 68명 — 모두 보기
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
페이지 1개
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
Huertas-Vazquez A,
Nelson CP,
Guo X,
Reinier K,
Uy-Evanado A,
Teodorescu C,
Ayala J,
Jerger K,
Chugh H,
Braund PS,
Deloukas P,
Hall AS
외 11명 — 모두 보기
Balmforth AJ,
Jones M,
Taylor KD,
Pulit SL,
Newton-Cheh C,
Gunson K,
Jui J,
Rotter JI,
Albert CM,
Samani NJ,
Chugh SS
WTCCC+
PloS one · 2013 · PMID 23593153 · open access
페이지 1개
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Yang SK,
Hong M,
Choi H,
Zhao W,
Jung Y,
Haritunians T,
Ye BD,
Kim KJ,
Park SH,
Lee I,
Kim WH,
Cheon JH
외 15명 — 모두 보기
Kim YH,
Jang BI,
Kim HS,
Choi JH,
Koo JS,
Lee JH,
Jung SA,
Shin HD,
Kang D,
Youn HS,
Taylor KD,
Rotter JI,
Liu J,
McGovern DP,
Song K
Inflammatory bowel diseases · 2015 · PMID 25489960
페이지 1개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
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.