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성함이나 학술지명, PMID로 찾아보십시오.
Larsson S에 대해
9건.
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
외 188명 — 모두 보기
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
페이지 12개+
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Fernandez-Rozadilla C,
Timofeeva M,
Chen Z,
Law P,
Thomas M,
Schmit S,
Díez-Obrero V,
Hsu L,
Fernandez-Tajes J,
Palles C,
Sherwood K,
Briggs S
외 198명 — 모두 보기
Svinti V,
Donnelly K,
Farrington S,
Blackmur J,
Vaughan-Shaw P,
Shu XO,
Long J,
Cai Q,
Guo X,
Lu Y,
Broderick P,
Studd J,
Huyghe J,
Harrison T,
Conti D,
Dampier C,
Devall M,
Schumacher F,
Melas M,
Rennert G,
Obón-Santacana M,
Martín-Sánchez V,
Moratalla-Navarro F,
Oh JH,
Kim J,
Jee SH,
Jung KJ,
Kweon SS,
Shin MH,
Shin A,
Ahn YO,
Kim DH,
Oze I,
Wen W,
Matsuo K,
Matsuda K,
Tanikawa C,
Ren Z,
Gao YT,
Jia WH,
Hopper J,
Jenkins M,
Win AK,
Pai R,
Figueiredo J,
Haile R,
Gallinger S,
Woods M,
Newcomb P,
Duggan D,
Cheadle J,
Kaplan R,
Maughan T,
Kerr R,
Kerr D,
Kirac I,
Böhm J,
Mecklin LP,
Jousilahti P,
Knekt P,
Aaltonen L,
Rissanen H,
Pukkala E,
Eriksson J,
Cajuso T,
Hänninen U,
Kondelin J,
Palin K,
Tanskanen T,
Renkonen-Sinisalo L,
Zanke B,
Männistö S,
Albanes D,
Weinstein S,
Ruiz-Narvaez E,
Palmer J,
Buchanan D,
Platz E,
Visvanathan K,
Ulrich C,
Siegel E,
Brezina S,
Gsur A,
Campbell P,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Slattery M,
Potter J,
Tsilidis K,
Schulze M,
Gunter M,
Murphy N,
Castells A,
Castellví-Bel S,
Moreira L,
Arndt V,
Shcherbina A,
Stern M,
Pardamean B,
Bishop T,
Giles G,
Southey M,
Idos G,
McDonnell K,
Abu-Ful Z,
Greenson J,
Shulman K,
Lejbkowicz F,
Offit K,
Su YR,
Steinfelder R,
Keku T,
van Guelpen B,
Hudson T,
Hampel H,
Pearlman R,
Berndt S,
Hayes R,
Martinez ME,
Thomas S,
Corley D,
Pharoah P,
Larsson S,
Yen Y,
Lenz HJ,
White E,
Li L,
Doheny K,
Pugh E,
Shelford T,
Chan A,
Cruz-Correa M,
Lindblom A,
Hunter D,
Joshi A,
Schafmayer C,
Scacheri P,
Kundaje A,
Nickerson D,
Schoen R,
Hampe J,
Stadler Z,
Vodicka P,
Vodickova L,
Vymetalkova V,
Papadopoulos N,
Edlund C,
Gauderman W,
Thomas D,
Shibata D,
Toland A,
Markowitz S,
Kim A,
Chanock S,
van Duijnhoven F,
Feskens E,
Sakoda L,
Gago-Dominguez M,
Wolk A,
Naccarati A,
Pardini B,
FitzGerald L,
Lee SC,
Ogino S,
Bien S,
Kooperberg C,
Li C,
Lin Y,
Prentice R,
Qu C,
Bézieau S,
Tangen C,
Mardis E,
Yamaji T,
Sawada N,
Iwasaki M,
Haiman C,
Le Marchand L,
Wu A,
Qu C,
McNeil C,
Coetzee G,
Hayward C,
Deary I,
Harris S,
Theodoratou E,
Reid S,
Walker M,
Ooi LY,
Moreno V,
Casey G,
Gruber S,
Tomlinson I,
Zheng W,
Dunlop M,
Houlston R,
Peters U
Nature genetics · 2023 · PMID 36539618
페이지 12개+
Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
Yuan S,
Chen J,
Ruan X,
Li Y,
Abramowitz SA,
Wang L,
Jiang F,
Xiong Y,
Levin MG,
Voight BF,
Gill D,
Burgess S
외 5명 — 모두 보기
Nature communications · 2025 · PMID 40645996 · 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+
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Yuan S,
Chen J,
Geng J,
Zhao SS,
Yarmolinsky J,
Arkema EV,
Abramowitz S,
Levin MG,
Tsilidis KK,
Burgess S,
Damrauer SM,
Larsson SC
Nature communications · 2025 · PMID 40075078 · open access
페이지 7개
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Scelo G,
Purdue MP,
Brown KM,
Johansson M,
Wang Z,
Eckel-Passow JE,
Ye Y,
Hofmann JN,
Choi J,
Foll M,
Gaborieau V,
Machiela MJ
외 111명 — 모두 보기
Colli LM,
Li P,
Sampson JN,
Abedi-Ardekani B,
Besse C,
Blanche H,
Boland A,
Burdette L,
Chabrier A,
Durand G,
Le Calvez-Kelm F,
Prokhortchouk E,
Robinot N,
Skryabin KG,
Wozniak MB,
Yeager M,
Basta-Jovanovic G,
Dzamic Z,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Mukeriya A,
Rascu S,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Szeszenia-Dabrowska N,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Baglietto L,
Boeing H,
Khaw KT,
Weiderpass E,
Ljungberg B,
Sitaram RT,
Bruinsma F,
Jordan SJ,
Severi G,
Winship I,
Hveem K,
Vatten LJ,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Freeman LEB,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Gapstur SM,
Stevens VL,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Buring J,
Lee IM,
Chow WH,
Moore LE,
Wood C,
Eisen T,
Henrion M,
Larkin J,
Barman P,
Leibovich BC,
Choueiri TK,
Mark Lathrop G,
Rothman N,
Deleuze JF,
McKay JD,
Parker AS,
Wu X,
Houlston RS,
Brennan P,
Chanock SJ
Nature communications · 2017 · PMID 28598434 · open access
페이지 6개
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
외 261명 — 모두 보기
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
Miller A,
Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
Papp J,
Park-Simon TW,
Parsons MT,
Peissel B,
Peixoto A,
Peshkin B,
Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators 외 컨소시엄 2곳
Nature genetics · 2020 · PMID 32424353 · open access
페이지 2개
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
외 96명 — 모두 보기
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Beane Freeman LE,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Chow WH,
Moore LE,
Choueiri TK,
Wood C,
Johansson M,
McKay JD,
Brown KM,
Rothman N,
Lathrop MG,
Deleuze JF,
Wu X,
Brennan P,
Chanock SJ,
Purdue MP,
Scelo G
European journal of human genetics : EJHG · 2019 · PMID 31231134
페이지 1개
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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.