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2,661 papers hold this site up. Every variant and condition page names
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3 matches for
Lee SC.
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
and 188 more — show all
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
12 pages+
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
and 198 more — show all
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
12 pages+
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
Kar SP,
Beesley J,
Amin Al Olama A,
Michailidou K,
Tyrer J,
Kote-Jarai Z,
Lawrenson K,
Lindstrom S,
Ramus SJ,
Thompson DJ,
Kibel AS,
Dansonka-Mieszkowska A
and 212 more — show all
Michael A,
Dieffenbach AK,
Gentry-Maharaj A,
Whittemore AS,
Wolk A,
Monteiro A,
Peixoto A,
Kierzek A,
Cox A,
Rudolph A,
Gonzalez-Neira A,
Wu AH,
Lindblom A,
Swerdlow A,
Ziogas A,
Ekici AB,
Burwinkel B,
Karlan BY,
Nordestgaard BG,
Blomqvist C,
Phelan C,
McLean C,
Pearce CL,
Vachon C,
Cybulski C,
Slavov C,
Stegmaier C,
Maier C,
Ambrosone CB,
Høgdall CK,
Teerlink CC,
Kang D,
Tessier DC,
Schaid DJ,
Stram DO,
Cramer DW,
Neal DE,
Eccles D,
Flesch-Janys D,
Edwards DR,
Wokozorczyk D,
Levine DA,
Yannoukakos D,
Sawyer EJ,
Bandera EV,
Poole EM,
Goode EL,
Khusnutdinova E,
Høgdall E,
Song F,
Bruinsma F,
Heitz F,
Modugno F,
Hamdy FC,
Wiklund F,
Giles GG,
Olsson H,
Wildiers H,
Ulmer HU,
Pandha H,
Risch HA,
Darabi H,
Salvesen HB,
Nevanlinna H,
Gronberg H,
Brenner H,
Brauch H,
Anton-Culver H,
Song H,
Lim HY,
McNeish I,
Campbell I,
Vergote I,
Gronwald J,
Lubiński J,
Stanford JL,
Benítez J,
Doherty JA,
Permuth JB,
Chang-Claude J,
Donovan JL,
Dennis J,
Schildkraut JM,
Schleutker J,
Hopper JL,
Kupryjanczyk J,
Park JY,
Figueroa J,
Clements JA,
Knight JA,
Peto J,
Cunningham JM,
Pow-Sang J,
Batra J,
Czene K,
Lu KH,
Herkommer K,
Khaw KT,
Matsuo K,
Muir K,
Offitt K,
Chen K,
Moysich KB,
Aittomäki K,
Odunsi K,
Kiemeney LA,
Massuger LF,
Fitzgerald LM,
Cook LS,
Cannon-Albright L,
Hooning MJ,
Pike MC,
Bolla MK,
Luedeke M,
Teixeira MR,
Goodman MT,
Schmidt MK,
Riggan M,
Aly M,
Rossing MA,
Beckmann MW,
Moisse M,
Sanderson M,
Southey MC,
Jones M,
Lush M,
Hildebrandt MA,
Hou MF,
Schoemaker MJ,
Garcia-Closas M,
Bogdanova N,
Rahman N,
Le ND,
Orr N,
Wentzensen N,
Pashayan N,
Peterlongo P,
Guénel P,
Brennan P,
Paulo P,
Webb PM,
Broberg P,
Fasching PA,
Devilee P,
Wang Q,
Cai Q,
Li Q,
Kaneva R,
Butzow R,
Kopperud RK,
Schmutzler RK,
Stephenson RA,
MacInnis RJ,
Hoover RN,
Winqvist R,
Ness R,
Milne RL,
Travis RC,
Benlloch S,
Olson SH,
McDonnell SK,
Tworoger SS,
Maia S,
Berndt S,
Lee SC,
Teo SH,
Thibodeau SN,
Bojesen SE,
Gapstur SM,
Kjær SK,
Pejovic T,
Tammela TL,
Dörk T,
Brüning T,
Wahlfors T,
Key TJ,
Edwards TL,
Menon U,
Hamann U,
Mitev V,
Kosma VM,
Setiawan VW,
Kristensen V,
Arndt V,
Vogel W,
Zheng W,
Zheng W,
Sieh W,
Blot WJ,
Kluzniak W,
Shu XO,
Gao YT,
Schumacher F,
Freedman ML,
Berchuck A,
Dunning AM,
Simard J,
Haiman CA,
Spurdle A,
Sellers TA,
Hunter DJ,
Henderson BE,
Kraft P,
Chanock SJ,
Couch FJ,
Hall P,
Gayther SA,
Easton DF,
Chenevix-Trench G,
Eeles R,
Pharoah PD,
Lambrechts D
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
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Because a study that needed 622 people is a different kind of study from one that
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away. Everyone is searchable, including the 187th name on a consortium paper —
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Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
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