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성함이나 학술지명, PMID로 찾아보십시오.
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144건, 그중 20건 표시.
Heritability and genome-wide association study of diffusing capacity of the lung
Terzikhan N,
Sun F,
Verhamme FM,
Adams HHH,
Loth D,
Bracke KR,
Stricker BHC,
Lahousse L,
Dupuis J,
Brusselle GG,
O'Connor GT
The European respiratory journal · 2018 · PMID 30049742
페이지 1개
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines
Scepanovic P,
Alanio C,
Hammer C,
Hodel F,
Hodel F,
Bergstedt J,
Patin E,
Thorball CW,
Chaturvedi N,
Charbit B,
Abel L,
Quintana-Murci L
외 3명 — 모두 보기
Milieu Intérieur Consortium
Genome medicine · 2018 · PMID 30053915 · open access
페이지 1개
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia
Pasman JA,
Verweij KJH,
Gerring Z,
Stringer S,
Sanchez-Roige S,
Treur JL,
Abdellaoui A,
Nivard MG,
Baselmans BML,
Ong JS,
Ip HF,
van der Zee MD
외 36명 — 모두 보기
Bartels M,
Day FR,
Fontanillas P,
Elson SL,
de Wit H,
Davis LK,
MacKillop J,
Derringer JL,
Branje SJT,
Hartman CA,
Heath AC,
van Lier PAC,
Madden PAF,
Mägi R,
Meeus W,
Montgomery GW,
Oldehinkel AJ,
Pausova Z,
Ramos-Quiroga JA,
Paus T,
Ribases M,
Kaprio J,
Boks MPM,
Bell JT,
Spector TD,
Gelernter J,
Boomsma DI,
Martin NG,
MacGregor S,
Perry JRB,
Palmer AA,
Posthuma D,
Munafò MR,
Gillespie NA,
Derks EM,
Vink JM
23andMe Research Team · Substance Use Disorders Working Group of the Psychiatric Genomics Consortium 외 컨소시엄 1곳
Nature neuroscience · 2018 · PMID 30150663
페이지 1개
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Vojinovic D,
Adams HH,
Jian X,
Yang Q,
Smith AV,
Bis JC,
Teumer A,
Scholz M,
Armstrong NJ,
Hofer E,
Saba Y,
Luciano M
외 79명 — 모두 보기
Bernard M,
Trompet S,
Yang J,
Gillespie NA,
van der Lee SJ,
Neumann A,
Ahmad S,
Andreassen OA,
Ames D,
Amin N,
Arfanakis K,
Bastin ME,
Becker DM,
Beiser AS,
Beyer F,
Brodaty H,
Bryan RN,
Bülow R,
Dale AM,
De Jager PL,
Deary IJ,
DeCarli C,
Fleischman DA,
Gottesman RF,
van der Grond J,
Gudnason V,
Harris TB,
Homuth G,
Knopman DS,
Kwok JB,
Lewis CE,
Li S,
Loeffler M,
Lopez OL,
Maillard P,
El Marroun H,
Mather KA,
Mosley TH,
Muetzel RL,
Nauck M,
Nyquist PA,
Panizzon MS,
Pausova Z,
Psaty BM,
Rice K,
Rotter JI,
Royle N,
Satizabal CL,
Schmidt R,
Schofield PR,
Schreiner PJ,
Sidney S,
Stott DJ,
Thalamuthu A,
Uitterlinden AG,
Valdés Hernández MC,
Vernooij MW,
Wen W,
White T,
Witte AV,
Wittfeld K,
Wright MJ,
Yanek LR,
Tiemeier H,
Kremen WS,
Bennett DA,
Jukema JW,
Paus T,
Wardlaw JM,
Schmidt H,
Sachdev PS,
Villringer A,
Grabe HJ,
Longstreth WT,
van Duijn CM,
Launer LJ,
Seshadri S,
Ikram MA,
Fornage M
Nature communications · 2018 · PMID 30258056 · open access
페이지 1개
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
Oskarsson GR,
Kristjansson RP,
Lee AL,
Sveinbjornsson G,
Magnusson MK,
Ivarsdottir EV,
Benonisdottir S,
Oddsson A,
Davidsson OB,
Saemundsdottir J,
Halldorsson GH,
Arthur J
외 11명 — 모두 보기
Arnadottir GA,
Masson G,
Jensson BO,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2018 · PMID 30271932 · open access
페이지 1개
Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time
Pinar A,
Hawi Z,
Cummins T,
Johnson B,
Pauper M,
Tong J,
Tiego J,
Finlay A,
Klein M,
Franke B,
Fornito A,
Bellgrove MA
Translational psychiatry · 2018 · PMID 30287865 · open access
페이지 1개
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Chen J,
Loukola A,
Gillespie NA,
Peterson R,
Jia P,
Riley B,
Maes H,
Dick DM,
Kendler KS,
Damaj MI,
Miles MF,
Zhao Z
외 34명 — 모두 보기
Li MD,
Vink JM,
Minica CC,
Willemsen G,
Boomsma DI,
Qaiser B,
Madden PAF,
Korhonen T,
Jousilahti P,
Hällfors J,
Gelernter J,
Kranzler HR,
Sherva R,
Farrer L,
Maher B,
Vanyukov M,
Taylor M,
Ware JJ,
Munafò MR,
Lutz SM,
Hokanson JE,
Gu F,
Landi MT,
Caporaso NE,
Hancock DB,
Gaddis NC,
Baker TB,
Bierut LJ,
Johnson EO,
Chenoweth M,
Lerman C,
Tyndale R,
Kaprio J,
Chen X
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
페이지 1개
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response
Adeyemo AA,
Zaghloul NA,
Chen G,
Doumatey AP,
Leitch CC,
Hostelley TL,
Nesmith JE,
Zhou J,
Bentley AR,
Shriner D,
Fasanmade O,
Okafor G
외 14명 — 모두 보기
Eghan B Jr,
Agyenim-Boateng K,
Chandrasekharappa S,
Adeleye J,
Balogun W,
Owusu S,
Amoah A,
Acheampong J,
Johnson T,
Oli J,
Adebamowo C,
Collins F,
Dunston G,
Rotimi CN
South Africa Zulu Type 2 Diabetes Case-Control Study
Nature communications · 2019 · PMID 31324766 · open access
페이지 1개
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
Hobbs BD,
Putman RK,
Araki T,
Nishino M,
Gudmundsson G,
Gudnason V,
Eiriksdottir G,
Zilhao Nogueira NR,
Dupuis J,
Xu H,
O'Connor GT,
Manichaikul A
외 30명 — 모두 보기
Nguyen J,
Podolanczuk AJ,
Madahar P,
Rotter JI,
Lederer DJ,
Barr RG,
Rich SS,
Ampleford EJ,
Ortega VE,
Peters SP,
O'Neal WK,
Newell JD Jr,
Bleecker ER,
Meyers DA,
Allen RJ,
Oldham JM,
Ma SF,
Noth I,
Jenkins RG,
Maher TM,
Hubbard RB,
Wain LV,
Fingerlin TE,
Schwartz DA,
Washko GR,
Rosas IO,
Silverman EK,
Hatabu H,
Cho MH,
Hunninghake GM
American journal of respiratory and critical care medicine · 2019 · PMID 31339356
페이지 1개
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen J,
Evans DS,
Arking DE,
Tesi N,
Nygaard M,
Liu X,
Wojczynski MK,
Biggs ML,
van der Spek A,
Atzmon G,
Ware EB,
Sarnowski C
외 72명 — 모두 보기
Smith AV,
Seppälä I,
Cordell HJ,
Dose J,
Amin N,
Arnold AM,
Ayers KL,
Barzilai N,
Becker EJ,
Beekman M,
Blanché H,
Christensen K,
Christiansen L,
Collerton JC,
Cubaynes S,
Cummings SR,
Davies K,
Debrabant B,
Deleuze JF,
Duncan R,
Faul JD,
Franceschi C,
Galan P,
Gudnason V,
Harris TB,
Huisman M,
Hurme MA,
Jagger C,
Jansen I,
Jylhä M,
Kähönen M,
Karasik D,
Kardia SLR,
Kingston A,
Kirkwood TBL,
Launer LJ,
Lehtimäki T,
Lieb W,
Lyytikäinen LP,
Martin-Ruiz C,
Min J,
Nebel A,
Newman AB,
Nie C,
Nohr EA,
Orwoll ES,
Perls TT,
Province MA,
Psaty BM,
Raitakari OT,
Reinders MJT,
Robine JM,
Rotter JI,
Sebastiani P,
Smith J,
Sørensen TIA,
Taylor KD,
Uitterlinden AG,
van der Flier W,
van der Lee SJ,
van Duijn CM,
van Heemst D,
Vaupel JW,
Weir D,
Ye K,
Zeng Y,
Zheng W,
Holstege H,
Kiel DP,
Lunetta KL,
Slagboom PE,
Murabito JM
Nature communications · 2019 · PMID 31413261 · open access
페이지 1개
A Prospective Analysis of Genetic Variants Associated with Human Lifespan
Wright KM,
Rand KA,
Kermany A,
Noto K,
Curtis D,
Garrigan D,
Slinkov D,
Dorfman I,
Granka JM,
Byrnes J,
Myres N,
Ball CA
외 1명 — 모두 보기
G3 (Bethesda, Md.) · 2019 · PMID 31484785 · open access
페이지 1개
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Bandres-Ciga S,
Ahmed S,
Sabir MS,
Blauwendraat C,
Adarmes-Gómez AD,
Bernal-Bernal I,
Bonilla-Toribio M,
Buiza-Rueda D,
Carrillo F,
Carrión-Claro M,
Gómez-Garre P,
Jesús S
외 83명 — 모두 보기
Labrador-Espinosa MA,
Macias D,
Méndez-Del-Barrio C,
Periñán-Tocino T,
Tejera-Parrado C,
Vargas-González L,
Diez-Fairen M,
Alvarez I,
Tartari JP,
Buongiorno M,
Aguilar M,
Gorostidi A,
Bergareche JA,
Mondragon E,
Vinagre-Aragon A,
Croitoru I,
Ruiz-Martínez J,
Dols-Icardo O,
Kulisevsky J,
Marín-Lahoz J,
Pagonabarraga J,
Pascual-Sedano B,
Ezquerra M,
Cámara A,
Compta Y,
Fernández M,
Fernández-Santiago R,
Muñoz E,
Tolosa E,
Valldeoriola F,
Gonzalez-Aramburu I,
Sanchez Rodriguez A,
Sierra M,
Menéndez-González M,
Blazquez M,
Garcia C,
Suarez-San Martin E,
García-Ruiz P,
Martínez-Castrillo JC,
Vela-Desojo L,
Ruz C,
Barrero FJ,
Escamilla-Sevilla F,
Mínguez-Castellanos A,
Cerdan D,
Tabernero C,
Gomez Heredia MJ,
Perez Errazquin F,
Romero-Acebal M,
Feliz C,
Lopez-Sendon JL,
Mata M,
Martínez Torres I,
Kim JJ,
Dalgard CL,
Brooks J,
Saez-Atienzar S,
Gibbs JR,
Jorda R,
Botia JA,
Bonet-Ponce L,
Morrison KE,
Clarke C,
Tan M,
Morris H,
Edsall C,
Hernandez D,
Simon-Sanchez J,
Nalls MA,
Scholz SW,
Jimenez-Escrig A,
Duarte J,
Vives F,
Duran R,
Hoenicka J,
Alvarez V,
Infante J,
Marti MJ,
Clarimón J,
López de Munain A,
Pastor P,
Mir P,
Singleton A
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
페이지 1개
Systematic review and meta-analysis of the moderating effect of rs1799971 in OPRM1, the mu-opioid receptor gene, on response to naltrexone treatment of alcohol use disorder
Hartwell EE,
Feinn R,
Morris PE,
Gelernter J,
Krystal J,
Arias AJ,
Hoffman M,
Petrakis I,
Gueorguieva R,
Schacht JP,
Oslin D,
Anton RF
외 1명 — 모두 보기
Addiction (Abingdon, England) · 2020 · PMID 31961981
페이지 1개
Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium
Verma SS,
Bergmeijer TO,
Gong L,
Reny JL,
Lewis JP,
Mitchell BD,
Alexopoulos D,
Aradi D,
Altman RB,
Bliden K,
Bradford Y,
Campo G
외 36명 — 모두 보기
Chang K,
Cleator JH,
Déry JP,
Dridi NP,
Fernandez-Cadenas I,
Fontana P,
Gawaz M,
Geisler T,
Gensini GF,
Giusti B,
Gurbel PA,
Hochholzer W,
Holmvang L,
Kim EY,
Kim HS,
Marcucci R,
Montaner J,
Backman JD,
Pakyz RE,
Roden DM,
Schaeffeler E,
Schwab M,
Shin JG,
Siller-Matula JM,
Ten Berg JM,
Trenk D,
Valgimigli M,
Wallace J,
Wen MS,
Kubo M,
Lee MTM,
Whaley R,
Winter S,
Klein TE,
Shuldiner AR,
Ritchie MD
ICPC Investigators
Clinical pharmacology and therapeutics · 2020 · PMID 32472697
페이지 1개
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
Ellinghaus D,
Degenhardt F,
Bujanda L,
Buti M,
Albillos A,
Invernizzi P,
Fernández J,
Prati D,
Baselli G,
Asselta R,
Grimsrud MM,
Milani C
외 136명 — 모두 보기
Aziz F,
Kässens J,
May S,
Wendorff M,
Wienbrandt L,
Uellendahl-Werth F,
Zheng T,
Yi X,
de Pablo R,
Chercoles AG,
Palom A,
Garcia-Fernandez AE,
Rodriguez-Frias F,
Zanella A,
Bandera A,
Protti A,
Aghemo A,
Lleo A,
Biondi A,
Caballero-Garralda A,
Gori A,
Tanck A,
Carreras Nolla A,
Latiano A,
Fracanzani AL,
Peschuck A,
Julià A,
Pesenti A,
Voza A,
Jiménez D,
Mateos B,
Nafria Jimenez B,
Quereda C,
Paccapelo C,
Gassner C,
Angelini C,
Cea C,
Solier A,
Pestaña D,
Muñiz-Diaz E,
Sandoval E,
Paraboschi EM,
Navas E,
García Sánchez F,
Ceriotti F,
Martinelli-Boneschi F,
Peyvandi F,
Blasi F,
Téllez L,
Blanco-Grau A,
Hemmrich-Stanisak G,
Grasselli G,
Costantino G,
Cardamone G,
Foti G,
Aneli S,
Kurihara H,
ElAbd H,
My I,
Galván-Femenia I,
Martín J,
Erdmann J,
Erdmann J,
Ferrusquía-Acosta J,
Garcia-Etxebarria K,
Izquierdo-Sanchez L,
Bettini LR,
Sumoy L,
Terranova L,
Moreira L,
Santoro L,
Scudeller L,
Mesonero F,
Roade L,
Rühlemann MC,
Schaefer M,
Carrabba M,
Riveiro-Barciela M,
Figuera Basso ME,
Valsecchi MG,
Hernandez-Tejero M,
Acosta-Herrera M,
D'Angiò M,
Baldini M,
Cazzaniga M,
Schulzky M,
Cecconi M,
Wittig M,
Ciccarelli M,
Rodríguez-Gandía M,
Bocciolone M,
Miozzo M,
Montano N,
Braun N,
Sacchi N,
Martínez N,
Özer O,
Palmieri O,
Faverio P,
Preatoni P,
Bonfanti P,
Omodei P,
Tentorio P,
Castro P,
Rodrigues PM,
Blandino Ortiz A,
de Cid R,
Ferrer R,
Gualtierotti R,
Nieto R,
Goerg S,
Badalamenti S,
Marsal S,
Matullo G,
Pelusi S,
Juzenas S,
Aliberti S,
Monzani V,
Moreno V,
Wesse T,
Lenz TL,
Pumarola T,
Rimoldi V,
Bosari S,
Albrecht W,
Peter W,
Romero-Gómez M,
D'Amato M,
D'Amato M,
Duga S,
Banales JM,
Hov JR,
Folseraas T,
Valenti L,
Franke A,
Karlsen TH
Severe Covid-19 GWAS Group
The New England journal of medicine · 2020 · PMID 32558485 · open access
페이지 1개
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Maihofer AX,
Choi KW,
Coleman JRI,
Daskalakis NP,
Denckla CA,
Ketema E,
Morey RA,
Polimanti R,
Ratanatharathorn A,
Torres K,
Wingo AP,
Zai CC
외 169명 — 모두 보기
Aiello AE,
Almli LM,
Amstadter AB,
Andersen SB,
Andreassen OA,
Arbisi PA,
Ashley-Koch AE,
Austin SB,
Avdibegović E,
Borglum AD,
Babić D,
Bækvad-Hansen M,
Baker DG,
Beckham JC,
Bierut LJ,
Bisson JI,
Boks MP,
Bolger EA,
Bradley B,
Brashear M,
Breen G,
Bryant RA,
Bustamante AC,
Bybjerg-Grauholm J,
Calabrese JR,
Caldas-de-Almeida JM,
Chen CY,
Dale AM,
Dalvie S,
Deckert J,
Delahanty DL,
Dennis MF,
Disner SG,
Domschke K,
Duncan LE,
Džubur Kulenović A,
Erbes CR,
Evans A,
Farrer LA,
Feeny NC,
Flory JD,
Forbes D,
Franz CE,
Galea S,
Garrett ME,
Gautam A,
Gelaye B,
Gelernter J,
Geuze E,
Gillespie CF,
Goçi A,
Gordon SD,
Guffanti G,
Hammamieh R,
Hauser MA,
Heath AC,
Hemmings SMJ,
Hougaard DM,
Jakovljević M,
Jett M,
Johnson EO,
Jones I,
Jovanovic T,
Qin XJ,
Karstoft KI,
Kaufman ML,
Kessler RC,
Khan A,
Kimbrel NA,
King AP,
Koen N,
Kranzler HR,
Kremen WS,
Lawford BR,
Lebois LAM,
Lewis C,
Liberzon I,
Linnstaedt SD,
Logue MW,
Lori A,
Lugonja B,
Luykx JJ,
Lyons MJ,
Maples-Keller JL,
Marmar C,
Martin NG,
Maurer D,
Mavissakalian MR,
McFarlane A,
McGlinchey RE,
McLaughlin KA,
McLean SA,
Mehta D,
Mellor R,
Michopoulos V,
Milberg W,
Miller MW,
Morris CP,
Mors O,
Mortensen PB,
Nelson EC,
Nordentoft M,
Norman SB,
O'Donnell M,
Orcutt HK,
Panizzon MS,
Peters ES,
Peterson AL,
Peverill M,
Pietrzak RH,
Polusny MA,
Rice JP,
Risbrough VB,
Roberts AL,
Rothbaum AO,
Rothbaum BO,
Roy-Byrne P,
Ruggiero KJ,
Rung A,
Rutten BPF,
Saccone NL,
Sanchez SE,
Schijven D,
Seedat S,
Seligowski AV,
Seng JS,
Sheerin CM,
Silove D,
Smith AK,
Smoller JW,
Sponheim SR,
Stein DJ,
Stevens JS,
Teicher MH,
Thompson WK,
Trapido E,
Uddin M,
Ursano RJ,
van den Heuvel LL,
Van Hooff M,
Vermetten E,
Vinkers CH,
Voisey J,
Wang Y,
Wang Z,
Werge T,
Williams MA,
Williamson DE,
Winternitz S,
Wolf C,
Wolf EJ,
Yehuda R,
Young KA,
Young RM,
Zhao H,
Zoellner LA,
Haas M,
Lasseter H,
Provost AC,
Salem RM,
Sebat J,
Shaffer RA,
Wu T,
Ripke S,
Daly MJ,
Ressler KJ,
Koenen KC,
Stein MB,
Nievergelt CM
Biological psychiatry · 2022 · PMID 34865855 · open access
페이지 1개
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
Dubé MP,
Chazara O,
Lemaçon A,
Asselin G,
Provost S,
Barhdadi A,
Lemieux Perreault LP,
Mongrain I,
Wang Q,
Carss K,
Paul DS,
Cunningham JW
외 8명 — 모두 보기
ESC heart failure · 2022 · PMID 35736394 · open access
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.