연구자에게
내 논문이 여기 있나요?
논문 2,671편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Engert JC에 대해
8건.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Mahajan A,
Spracklen CN,
Zhang W,
Ng MCY,
Petty LE,
Kitajima H,
Yu GZ,
Rüeger S,
Speidel L,
Kim YJ,
Horikoshi M,
Mercader JM
외 337명 — 모두 보기
Taliun D,
Moon S,
Kwak SH,
Robertson NR,
Rayner NW,
Loh M,
Kim BJ,
Chiou J,
Miguel-Escalada I,
Della Briotta Parolo P,
Lin K,
Bragg F,
Preuss MH,
Takeuchi F,
Nano J,
Guo X,
Lamri A,
Nakatochi M,
Scott RA,
Lee JJ,
Huerta-Chagoya A,
Graff M,
Chai JF,
Parra EJ,
Yao J,
Bielak LF,
Tabara Y,
Hai Y,
Steinthorsdottir V,
Cook JP,
Kals M,
Grarup N,
Schmidt EM,
Pan I,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Long J,
Sun M,
Tong L,
Chen WM,
Ahmad M,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Lecoeur C,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Jensen RA,
Tajuddin S,
Kabagambe EK,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Flanagan J,
Abaitua F,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Akiyama M,
Anand SS,
Bertoni A,
Bian Z,
Bork-Jensen J,
Brandslund I,
Brody JA,
Brummett CM,
Buchanan TA,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
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,
Fornage M,
Franco OH,
Frayling TM,
Freedman BI,
Fuchsberger C,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Goodarzi MO,
Gordon-Larsen P,
Gorkin D,
Gross M,
Guo Y,
Hackinger S,
Han S,
Hattersley AT,
Herder C,
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 ME,
Jørgensen T,
Kamatani Y,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kohara K,
Kriebel J,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lyssenko V,
Mamakou V,
Mani KR,
Meitinger T,
Metspalu A,
Morris AD,
Nadkarni GN,
Nadler JL,
Nalls MA,
Nayak U,
Nongmaithem SS,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Pereira MA,
Peters A,
Pirie FJ,
Porneala B,
Prasad G,
Preissl S,
Rasmussen-Torvik LJ,
Reiner AP,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sander M,
Sandow K,
Sattar N,
Schönherr S,
Schurmann C,
Shahriar M,
Shi J,
Shin DM,
Shriner D,
Smith JA,
So WY,
Stančáková A,
Stilp AM,
Strauch K,
Suzuki K,
Takahashi A,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tomlinson B,
Torres JM,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Vujkovic M,
Wacher-Rodarte N,
Wheeler E,
Whitsel EA,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamauchi T,
Yengo L,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Hanis CL,
Peyser PA,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Zeggini E,
Yokota M,
Rich SS,
Kooperberg C,
Pankow JS,
Engert JC,
Chen YI,
Froguel P,
Wilson JG,
Sheu WHH,
Kardia SLR,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Groop L,
Mook-Kanamori DO,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Bottinger EP,
Dehghan A,
Tai ES,
Dupuis J,
Kato N,
Laakso M,
Köttgen A,
Koh WP,
Palmer CNA,
Liu S,
Abecasis G,
Kooner JS,
Loos RJF,
North KE,
Haiman CA,
Florez JC,
Saleheen D,
Hansen T,
Pedersen O,
Mägi R,
Langenberg C,
Wareham NJ,
Maeda S,
Kadowaki T,
Lee J,
Millwood IY,
Walters RG,
Stefansson K,
Myers SR,
Ferrer J,
Gaulton KJ,
Meigs JB,
Mohlke KL,
Gloyn AL,
Bowden DW,
Below JE,
Chambers JC,
Sim X,
Boehnke M,
Rotter JI,
McCarthy MI,
Morris AP
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · 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,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
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,
Kim DH,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee KM,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lynch JA,
Lyssenko V,
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,
Roden M,
Rohde R,
Roll K,
Sabanayagam C,
Sandow K,
Sankareswaran A,
Sattar N,
Schönherr S,
Shahriar M,
Shen B,
Shi J,
Shin DM,
Shojima N,
Smith JA,
So WY,
Stančáková A,
Steinthorsdottir V,
Stilp AM,
Strauch K,
Taylor KD,
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,
Wheeler E,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamamoto K,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zawistowski M,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
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,
Ruff CT,
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+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
외 89명 — 모두 보기
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium 외 컨소시엄 2곳
Nature genetics · 2026 · PMID 41419686 · open access
페이지 12개+
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
외 155명 — 모두 보기
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
페이지 7개
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Kathiresan S,
Voight BF,
Purcell S,
Musunuru K,
Ardissino D,
Mannucci PM,
Anand S,
Engert JC,
Samani NJ,
Schunkert H,
Erdmann J,
Reilly MP
외 174명 — 모두 보기
Rader DJ,
Morgan T,
Spertus JA,
Stoll M,
Girelli D,
McKeown PP,
Patterson CC,
Siscovick DS,
O'Donnell CJ,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Melander O,
Altshuler D,
Ardissino D,
Merlini PA,
Berzuini C,
Bernardinelli L,
Peyvandi F,
Tubaro M,
Celli P,
Ferrario M,
Fetiveau R,
Marziliano N,
Casari G,
Galli M,
Ribichini F,
Rossi M,
Bernardi F,
Zonzin P,
Piazza A,
Mannucci PM,
Schwartz SM,
Siscovick DS,
Yee J,
Friedlander Y,
Elosua R,
Marrugat J,
Lucas G,
Subirana I,
Sala J,
Ramos R,
Kathiresan S,
Meigs JB,
Williams G,
Nathan DM,
MacRae CA,
O'Donnell CJ,
Salomaa V,
Havulinna AS,
Peltonen L,
Melander O,
Berglund G,
Voight BF,
Kathiresan S,
Hirschhorn JN,
Asselta R,
Duga S,
Spreafico M,
Musunuru K,
Daly MJ,
Purcell S,
Voight BF,
Purcell S,
Nemesh J,
Korn JM,
McCarroll SA,
Schwartz SM,
Yee J,
Kathiresan S,
Lucas G,
Subirana I,
Elosua R,
Surti A,
Guiducci C,
Gianniny L,
Mirel D,
Parkin M,
Burtt N,
Gabriel SB,
Samani NJ,
Thompson JR,
Braund PS,
Wright BJ,
Balmforth AJ,
Ball SG,
Hall A,
Schunkert H,
Erdmann J,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König I,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Schunkert H,
Samani NJ,
Erdmann J,
Ouwehand W,
Hengstenberg C,
Deloukas P,
Scholz M,
Cambien F,
Reilly MP,
Li M,
Chen Z,
Wilensky R,
Matthai W,
Qasim A,
Hakonarson HH,
Devaney J,
Burnett MS,
Pichard AD,
Kent KM,
Satler L,
Lindsay JM,
Waksman R,
Knouff CW,
Waterworth DM,
Walker MC,
Mooser V,
Epstein SE,
Rader DJ,
Scheffold T,
Berger K,
Stoll M,
Huge A,
Girelli D,
Martinelli N,
Olivieri O,
Corrocher R,
Morgan T,
Spertus JA,
McKeown P,
Patterson CC,
Schunkert H,
Erdmann E,
Linsel-Nitschke P,
Lieb W,
Ziegler A,
König IR,
Hengstenberg C,
Fischer M,
Stark K,
Grosshennig A,
Preuss M,
Wichmann HE,
Schreiber S,
Hólm H,
Thorleifsson G,
Thorsteinsdottir U,
Stefansson K,
Engert JC,
Do R,
Xie C,
Anand S,
Kathiresan S,
Ardissino D,
Mannucci PM,
Siscovick D,
O'Donnell CJ,
Samani NJ,
Melander O,
Elosua R,
Peltonen L,
Salomaa V,
Schwartz SM,
Altshuler D
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
페이지 4개
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease
Elliott P,
Chambers JC,
Zhang W,
Clarke R,
Hopewell JC,
Peden JF,
Erdmann J,
Braund P,
Engert JC,
Bennett D,
Coin L,
Ashby D
외 24명 — 모두 보기
Tzoulaki I,
Brown IJ,
Mt-Isa S,
McCarthy MI,
Peltonen L,
Freimer NB,
Farrall M,
Ruokonen A,
Hamsten A,
Lim N,
Froguel P,
Waterworth DM,
Vollenweider P,
Waeber G,
Jarvelin MR,
Mooser V,
Scott J,
Hall AS,
Schunkert H,
Anand SS,
Collins R,
Samani NJ,
Watkins H,
Kooner JS
JAMA · 2009 · PMID 19567438
페이지 2개
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Loh M,
Zhang W,
Ng HK,
Schmid K,
Lamri A,
Tong L,
Ahmad M,
Lee JJ,
Ng MCY,
Petty LE,
Spracklen CN,
Takeuchi F
외 35명 — 모두 보기
Islam MT,
Jasmine F,
Kasturiratne A,
Kibriya M,
Mohlke KL,
Paré G,
Prasad G,
Shahriar M,
Chee ML,
de Silva HJ,
Engert JC,
Gerstein HC,
Mani KR,
Sabanayagam C,
Vujkovic M,
Wickremasinghe AR,
Wong TY,
Yajnik CS,
Yusuf S,
Ahsan H,
Bharadwaj D,
Anand SS,
Below JE,
Boehnke M,
Bowden DW,
Chandak GR,
Cheng CY,
Kato N,
Mahajan A,
Sim X,
McCarthy MI,
Morris AP,
Kooner JS,
Saleheen D,
Chambers JC
Communications biology · 2022 · PMID 35393509 · open access
페이지 2개
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
Voight BF,
Peloso GM,
Orho-Melander M,
Frikke-Schmidt R,
Barbalic M,
Jensen MK,
Hindy G,
Hólm H,
Ding EL,
Johnson T,
Schunkert H,
Samani NJ
외 114명 — 모두 보기
Clarke R,
Hopewell JC,
Thompson JF,
Li M,
Thorleifsson G,
Newton-Cheh C,
Musunuru K,
Pirruccello JP,
Saleheen D,
Chen L,
Stewart A,
Schillert A,
Thorsteinsdottir U,
Thorgeirsson G,
Anand S,
Engert JC,
Morgan T,
Spertus J,
Stoll M,
Berger K,
Martinelli N,
Girelli D,
McKeown PP,
Patterson CC,
Epstein SE,
Devaney J,
Burnett MS,
Mooser V,
Ripatti S,
Surakka I,
Nieminen MS,
Sinisalo J,
Lokki ML,
Perola M,
Havulinna A,
de Faire U,
Gigante B,
Ingelsson E,
Zeller T,
Wild P,
de Bakker PI,
Klungel OH,
Maitland-van der Zee AH,
Peters BJ,
de Boer A,
Grobbee DE,
Kamphuisen PW,
Deneer VH,
Elbers CC,
Onland-Moret NC,
Hofker MH,
Wijmenga C,
Verschuren WM,
Boer JM,
van der Schouw YT,
Rasheed A,
Frossard P,
Demissie S,
Willer C,
Do R,
Ordovas JM,
Abecasis GR,
Boehnke M,
Mohlke KL,
Daly MJ,
Guiducci C,
Burtt NP,
Surti A,
Gonzalez E,
Purcell S,
Gabriel S,
Marrugat J,
Peden J,
Erdmann J,
Diemert P,
Willenborg C,
König IR,
Fischer M,
Hengstenberg C,
Ziegler A,
Buysschaert I,
Lambrechts D,
Van de Werf F,
Fox KA,
El Mokhtari NE,
Rubin D,
Schrezenmeir J,
Schreiber S,
Schäfer A,
Danesh J,
Blankenberg S,
Roberts R,
McPherson R,
Watkins H,
Hall AS,
Overvad K,
Rimm E,
Boerwinkle E,
Tybjaerg-Hansen A,
Cupples LA,
Reilly MP,
Melander O,
Mannucci PM,
Ardissino D,
Siscovick D,
Elosua R,
Stefansson K,
O'Donnell CJ,
Salomaa V,
Rader DJ,
Peltonen L,
Schwartz SM,
Altshuler D,
Kathiresan S
Lancet (London, England) · 2012 · PMID 22607825 · open access
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.