|
🐜
|
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
231 auth.
R. McLendon,
A. Friedman,
D. Bigner,
Erwin G. Van Meir,
D. Brat,
Gena M Mastrogianakis,
J. Olson,
T. Mikkelsen,
N. Lehman,
K. Aldape,
W. Yung,
O. Bogler,
J. Weinstein,
S. Vandenberg,
M. Berger,
...
M. Prados,
D. Muzny,
M. Morgan,
S. Scherer,
A. Sabo,
L. Nazareth,
L. Lewis,
O. Hall,
Yiming Zhu,
Yanru Ren,
Omar Alvi,
Jiqiang Yao,
A. Hawes,
S. Jhangiani,
G. Fowler,
A. Lucas,
C. Kovar,
Andrew Cree,
H. Dinh,
J. Santibanez,
Vandita Joshi,
M. Gonzalez-Garay,
Christopher A. Miller,
A. Milosavljevic,
L. Donehower,
D. Wheeler,
R. Gibbs,
K. Cibulskis,
C. Sougnez,
T. Fennell,
Scott Mahan,
Jane Wilkinson,
L. Ziaugra,
R. Onofrio,
Toby Bloom,
R. Nicol,
K. Ardlie,
J. Baldwin,
S. Gabriel,
E. Lander,
L. Ding,
R. Fulton,
M. McLellan,
J. Wallis,
D. Larson,
Xiaoqi Shi,
R. Abbott,
L. Fulton,
Ken Chen,
D. Koboldt,
M. Wendl,
R. Meyer,
Yuzhu Tang,
Ling Lin,
John R. Osborne,
Brian H. Dunford-Shore,
T. Miner,
K. Delehaunty,
C. Markovic,
Gary W. Swift,
W. Courtney,
C. Pohl,
S. Abbott,
Amy E. Hawkins,
Shin Leong,
C. Haipek,
Heather K. Schmidt,
M. Wiechert,
T. Vickery,
S. Scott,
D. Dooling,
A. Chinwalla,
G. Weinstock,
E. Mardis,
R. Wilson,
G. Getz,
W. Winckler,
R. Verhaak,
M. Lawrence,
Michael J. T. O’Kelly,
James Robinson,
Gabriele Alexe,
R. Beroukhim,
S. Carter,
Derek Y. Chiang,
Josh Gould,
Supriya Gupta,
Joshua M. Korn,
C. Mermel,
J. Mesirov,
S. Monti,
Huy L. Nguyen,
Melissa Parkin,
Michael Reich,
Nicolas Stransky,
B. Weir,
L. Garraway,
T. Golub,
M. Meyerson,
L. Chin,
A. Protopopov,
Jianhua Zhang,
I. Perna,
S. Aronson,
N. Sathiamoorthy,
Georgi Ren,
Jun Yao,
W. Wiedemeyer,
Hyun Soo Kim,
Won Kong Sek,
Yonghong Xiao,
I. Kohane,
J. Seidman,
P. Park,
R. Kucherlapati,
P. Laird,
L. Cope,
J. Herman,
D. Weisenberger,
F. Pan,
D. V. Berg,
L. V. Neste,
Mingyu Joo,
Kornel E. Schuebel,
S. Baylin,
D. Absher,
Jun Z. Li,
Audrey M. Southwick,
Shannon T. Brady,
A. Aggarwal,
Tisha Chung,
G. Sherlock,
J. Brooks,
R. Myers,
P. Spellman,
E. Purdom,
L. Jakkula,
A. Lapuk,
H. Marr,
S. Dorton,
Gi Choi Yoon,
Ju Han,
A. Ray,
V. Wang,
S. Durinck,
M. Robinson,
Nicholas J. Wang,
K. Vranizan,
V. Peng,
E. V. Name,
G. Fontenay,
J. Ngai,
J. Conboy,
B. Parvin,
H. Feiler,
T. Speed,
J. Gray,
C. Brennan,
N. Socci,
A. Olshen,
B. Taylor,
A. Lash,
N. Schultz,
B. Reva,
Yevgeniy Antipin,
Alexey Stukalov,
Benjamin E. Gross,
E. Cerami,
Qingqing Wei,
L. Qin,
V. Seshan,
L. Villafania,
Magali Cavatore,
L. Borsu,
A. Viale,
W. Gerald,
C. Sander,
M. Ladanyi,
C. Perou,
D. Hayes,
M. D. Topal,
K. Hoadley,
Yuan Qi,
S. Balu,
Yan Shi,
Junyuan Wu,
R. Penny,
M. Bittner,
T. Shelton,
E. Lenkiewicz,
S. Morris,
D. Beasley,
Sheri Sanders,
A. Kahn,
R. Sfeir,
Jessica Chen,
D. Nassau,
Larry Feng,
E. Hickey,
A. Barker,
D. Gerhard,
J. Vockley,
C. Compton,
J. Vaught,
P. Fielding,
M. Ferguson,
C. Schaefer,
Jinghui Zhang,
Subha Madhavan,
K. Buetow,
F. Collins,
P. Good,
M. Guyer,
B. Ozenberger,
Jane L. Peterson,
E. Thomson
|
12 |
2008 |
12
🐜
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|
🐜
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Integrating common and rare genetic variation in diverse human populations
69 auth.
D. Altshuler,
R. Gibbs,
L. Peltonen,
E. Dermitzakis,
S. Schaffner,
F. Yu,
P. Bonnen,
P. D. de Bakker,
P. Deloukas,
S. Gabriel,
R. Gwilliam,
S. Hunt,
M. Inouye,
Xiaoming Jia,
A. Palotie,
...
Melissa Parkin,
P. Whittaker,
K. Chang,
A. Hawes,
L. Lewis,
Yanru Ren,
D. Wheeler,
D. Muzny,
Chris P. Barnes,
K. Darvishi,
M. Hurles,
Joshua M. Korn,
K. Kristiansson,
Charles Lee,
Steven A McCarrol,
J. Nemesh,
A. Keinan,
S. Montgomery,
Samuela J. Pollack,
A. Price,
N. Soranzo,
C. Gonzaga‐Jauregui,
V. Anttila,
W. Brodeur,
M. Daly,
S. Leslie,
G. McVean,
L. Moutsianas,
Huy L. Nguyen,
Qingrun Zhang,
Mohammed J. R. Ghori,
R. McGinnis,
W. McLaren,
F. Takeuchi,
S. Grossman,
I. Shlyakhter,
E. Hostetter,
Pardis C Sabeti,
C. Adebamowo,
M. W. Foster,
D. R. Gordon,
J. Licinio,
M. Manca,
P. Marshall,
I. Matsuda,
D. Ngare,
V. Wang,
Deepa S. Reddy,
C. Rotimi,
C. Royal,
R. Sharp,
Changqing Zeng,
L. Brooks,
J. Mcewen
|
11 |
2010 |
11
🐜
|
|
🐜
|
Next-generation characterization of the Cancer Cell Line Encyclopedia
68 auth.
M. Ghandi,
F. Huang,
Judit Jané-Valbuena,
G. Kryukov,
Christopher C. Lo,
E. McDonald,
J. Barretina,
Ellen T. Gelfand,
C. Bielski,
Haoxin Li,
K. Hu,
Alexander Y. Andreev-Drakhlin,
Jaegil Kim,
J. Hess,
B. Haas,
...
F. Aguet,
B. Weir,
M. Rothberg,
B. Paolella,
M. Lawrence,
Rehan Akbani,
Yiling Lu,
Hong L. Tiv,
P. Gokhale,
Antoine de Weck,
Ali Amin Mansour,
Coyin Oh,
J. Shih,
Kevin Hadi,
Yanay Rosen,
J. Bistline,
K. Venkatesan,
Anupama Reddy,
D. Sonkin,
Manway Liu,
J. Lehár,
Joshua M. Korn,
D. Porter,
Michael D. Jones,
J. Golji,
G. Caponigro,
Jordan E. Taylor,
C. Dunning,
Amanda L. Creech,
Allison C. Warren,
James M. McFarland,
Mahdi Zamanighomi,
A. Kauffmann,
Nicolas Stransky,
M. Imieliński,
Y. Maruvka,
A. Cherniack,
Aviad Tsherniak,
F. Vazquez,
Jacob D. Jaffe,
A. Lane,
D. Weinstock,
Cory M. Johannessen,
Michael P. Morrissey,
F. Stegmeier,
R. Schlegel,
W. Hahn,
G. Getz,
G. Mills,
J. Boehm,
T. Golub,
L. Garraway,
W. Sellers
|
11 |
2019 |
11
🐜
|
|
🐜
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Association between microdeletion and microduplication at 16p11.2 and autism.
22 auth.
L. Weiss,
Yiping Shen,
Joshua M. Korn,
D. Arking,
David T. Miller,
R. Fossdal,
E. Saemundsen,
H. Stefánsson,
M. Ferreira,
Todd Green,
...
O. Platt,
D. Ruderfer,
C. Walsh,
D. Altshuler,
A. Chakravarti,
R. Tanzi,
K. Stefánsson,
S. Santangelo,
J. Gusella,
P. Sklar,
Bai-Lin Wu,
M. Daly
|
10 |
2008 |
10
🐜
|
|
🐜
|
Mapping and sequencing of structural variation from eight human genomes
46 auth.
J. Kidd,
G. Cooper,
W. Donahue,
H. Hayden,
N. Sampas,
Tina Graves,
Nancy F. Hansen,
Brian Teague,
C. Alkan,
F. Antonacci,
E. Haugen,
Troy Zerr,
N. A. Yamada,
P. Tsang,
Tera L. Newman,
...
Eray Tüzün,
Ze Cheng,
H. Ebling,
N. Tusneem,
R. David,
W. Gillett,
K. Phelps,
M. Weaver,
David J Saranga,
A. Brand,
Wei Tao,
E. Gustafson,
K. McKernan,
Lin Chen,
Maika Malig,
Joshua D. Smith,
Joshua M. Korn,
S. Mccarroll,
D. Altshuler,
D. Peiffer,
M. Dorschner,
J. Stamatoyannopoulos,
D. Schwartz,
D. Nickerson,
J. Mullikin,
R. Wilson,
L. Bruhn,
M. Olson,
R. Kaul,
Douglas R. Smith,
E. Eichler
|
10 |
2008 |
10
🐜
|
|
🐜
|
High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response
64 auth.
Hui Gao,
Joshua M. Korn,
S. Ferretti,
John E Monahan,
Youzhen Wang,
Mallika Singh,
Chao Zhang,
C. Schnell,
Guizhi Yang,
Yun Zhang,
O Alejandro Balbin,
S. Barbe,
H. Cai,
F. Casey,
S. Chatterjee,
...
Derek Y Chiang,
S. Chuai,
Shawn Cogan,
Scott D Collins,
Ernesta Dammassa,
N. Ebel,
M. Embry,
J. Green,
A. Kauffmann,
C. Kowal,
Rebecca J Leary,
J. Lehár,
Ying Liang,
Alice T. Loo,
Edward G. Lorenzana,
E. Robert McDonald,
Margaret E McLaughlin,
J. Merkin,
R. Meyer,
Tara L Naylor,
M. Patawaran,
Anupama Reddy,
Claudia Röelli,
D. Ruddy,
Fernando Salangsang,
F. Santacroce,
Angad P Singh,
Yan Tang,
W. Tinetto,
Sonja Tobler,
Roberto Velazquez,
K. Venkatesan,
Fabian Von Arx,
Hui Qin Wang,
Zongyao Wang,
M. Wiesmann,
D. Wyss,
Fiona Xu,
H. Bitter,
P. Atadja,
E. Lees,
F. Hofmann,
E. Li,
N. Keen,
R. Cozens,
M. Jensen,
N. Pryer,
J. Williams,
W. Sellers
|
10 |
2015 |
10
🐜
|
|
🐜
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
126 auth.
S. Kathiresan,
B. Voight,
S. Purcell,
K. Musunuru,
D. Ardissino,
P. Mannucci,
Sonia S Anand,
J. Engert,
N. Samani,
H. Schunkert,
J. Erdmann,
M. Reilly,
D. Rader,
T. Morgan,
J. Spertus,
...
M. Stoll,
D. Girelli,
P. McKeown,
C. Patterson,
D. Siscovick,
C. O’Donnell,
R. Elosúa,
L. Peltonen,
V. Salomaa,
S. Schwartz,
O. Melander,
D. Altshuler,
P. Merlini,
C. Berzuini,
L. Bernardinelli,
F. Peyvandi,
M. Tubaro,
P. Celli,
M. Ferrario,
R. Fetiveau,
N. Marziliano,
G. Casari,
M. Galli,
F. Ribichini,
M. Rossi,
F. Bernardi,
P. Zonzin,
A. Piazza,
Jean Yee,
Y. Friedlander,
J. Marrugat,
G. Lucas,
I. Subirana,
J. Sala,
R. Ramos,
J. Meigs,
G. Williams,
D. Nathan,
C. Macrae,
A. Havulinna,
G. Berglund,
J. Hirschhorn,
R. Asselta,
S. Duga,
M. Spreafico,
M. Daly,
J. Nemesh,
Joshua M. Korn,
S. Mccarroll,
Aarti Surti,
C. Guiducci,
Lauren Gianniny,
D. Mirel,
Melissa Parkin,
N. Burtt,
S. Gabriel,
J. Thompson,
P. Braund,
Benjamin J. Wright,
A. Balmforth,
S. Ball,
A. Hall,
P. Linsel-Nitschke,
W. Lieb,
A. Ziegler,
I. König,
C. Hengstenberg,
M. Fischer,
K. Stark,
A. Grosshennig,
Michael H. Preuss,
H. Wichmann,
S. Schreiber,
W. Ouwehand,
P. Deloukas,
Michaela Scholz,
F. Cambien,
Mingyao Li,
Zhen Chen,
R. Wilensky,
W. Matthai,
A. Qasim,
H. Hakonarson,
J. Devaney,
M. Burnett,
A. Pichard,
K. Kent,
L. Satler,
J. Lindsay,
R. Waksman,
C. Knouff,
D. Waterworth,
M. Walker,
V. Mooser,
S. Epstein,
T. Scheffold,
K. Berger,
A. Huge,
N. Martinelli,
O. Olivieri,
R. Corrocher,
P. McKeown,
E. Erdmann,
I. König,
H. Hólm,
G. Thorleifsson,
U. Thorsteinsdóttir,
K. Stefánsson,
R. Do,
C. Xie,
D. Siscovick
|
10 |
2009 |
10
🐜
|
|
🐜
|
Mapping copy number variation by population scale genome sequencing
57 auth.
Ryan E. Mills,
Klaudia Walter,
C. Stewart,
R. Handsaker,
Ken Chen,
C. Alkan,
A. Abyzov,
Seungtai Yoon,
K. Ye,
R. K. Cheetham,
A. Chinwalla,
D. Conrad,
Yutao Fu,
Fabian Grubert,
I. Hajirasouliha,
...
F. Hormozdiari,
L. Iakoucheva,
Z. Iqbal,
Shuli Kang,
J. Kidd,
Miriam K. Konkel,
Joshua M. Korn,
Ekta Khurana,
Deniz Kura,
Hugo Y. K. Lam,
Jing Leng,
Ruiqiang Li,
Yingrui Li,
Chang-Yun Lin,
Ruibang Luo,
X. Mu,
J. Nemesh,
H. Peckham,
T. Rausch,
A. Scally,
Xinghua Shi,
Michael P. Stromberg,
A. Stütz,
A. Urban,
Jerilyn A. Walker,
Jiantao Wu,
Yujun Zhang,
Zhengdong D. Zhang,
M. Batzer,
L. Ding,
G. T. Marth,
G. McVean,
J. Sebat,
M. Snyder,
Jun Wang,
Kenny Q. Ye,
E. Eichler,
M. Gerstein,
M. Hurles,
Charles Lee,
S. Mccarroll,
J. Korbel
|
10 |
2010 |
10
🐜
|
|
🐜
|
Integrated detection and population-genetic analysis of SNPs and copy number variation
26 auth.
S. Mccarroll,
F. Kuruvilla,
Joshua M. Korn,
S. Cawley,
J. Nemesh,
Alec Wysoker,
M. Shapero,
P. D. Bakker,
J. Maller,
Andrew W. Kirby,
A. Elliott,
Melissa Parkin,
E. Hubbell,
Teresa A. Webster,
R. Mei,
...
Jim Veitch,
P. Collins,
R. Handsaker,
S. Lincoln,
Marcia M. Nizzari,
J. Blume,
K. W. Jones,
R. Rava,
M. Daly,
S. Gabriel,
D. Altshuler
|
9 |
2008 |
9
🐜
|
|
🦁
|
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
16 auth.
Joshua M. Korn,
F. Kuruvilla,
S. Mccarroll,
Alec Wysoker,
J. Nemesh,
S. Cawley,
E. Hubbell,
Jim Veitch,
P. Collins,
K. Darvishi,
...
Charles Lee,
Marcia M. Nizzari,
S. Gabriel,
S. Purcell,
M. Daly,
D. Altshuler
|
9 |
2008 |
9
🦁
|
|
🐜
|
The plasticity of dendritic cell responses to pathogens and their components.
8 auth.
Qian Huang,
Dongyu Liu,
Paul Majewski,
Leah C. Schulte,
Joshua M. Korn,
R. Young,
...
E. Lander,
N. Hacohen
|
9 |
2001 |
9
🐜
|
|
🐜
|
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
38 auth.
M. Rivas,
M. Beaudoin,
A. Gardet,
C. Stevens,
Y. Sharma,
Clarence K. Zhang,
G. Boucher,
S. Ripke,
D. Ellinghaus,
N. Burtt,
T. Fennell,
Andrew W. Kirby,
A. Latiano,
P. Goyette,
Todd Green,
...
J. Halfvarson,
T. Haritunians,
Joshua M. Korn,
F. Kuruvilla,
Caroline Lagacé,
B. Neale,
K. S. Lo,
P. Schumm,
L. Törkvist,
M. Dubinsky,
S. Brant,
M. Silverberg,
R. Duerr,
D. Altshuler,
S. Gabriel,
G. Lettre,
A. Franke,
M. D’Amato,
D. McGovern,
Judy H. Cho,
J. Rioux,
R. Xavier,
M. Daly
|
9 |
2011 |
9
🐜
|
|
🐜
|
Project DRIVE: A Compendium of Cancer Dependencies and Synthetic Lethal Relationships Uncovered by Large-Scale, Deep RNAi Screening
100 auth.
E. McDonald,
Antoine de Weck,
M. Schlabach,
E. Billy,
Konstantinos J. Mavrakis,
G. Hoffman,
Dhiren Belur,
D. Castelletti,
Elizabeth Frias,
Kalyani Gampa,
J. Golji,
Iris Kao,
Li Li,
P. Megel,
Thomas A. Perkins,
...
N. Ramadan,
D. Ruddy,
S. Silver,
S. Sovath,
M. Stump,
Odile Weber,
R. Widmer,
Jianjun Yu,
Kristine Yu,
Yingzi Yue,
D. Abramowski,
Elizabeth Ackley,
R. Barrett,
Joel E. Berger,
J. Bernard,
Rebecca Billig,
S. Brachmann,
F. Buxton,
R. Caothien,
J. Caushi,
Franklin Chung,
Marta Cortés-Cros,
Rosalie S. deBeaumont,
Clara Delaunay,
Aurore Desplat,
William Duong,
Donald A. Dwoske,
Richard Eldridge,
Ali Farsidjani,
Fei Feng,
Jiajia Feng,
D. Flemming,
W. Forrester,
G. Galli,
Zhenhai Gao,
François Gauter,
V. Gibaja,
K. Haas,
M. Hattenberger,
T. Hood,
Kristen E. Hurov,
Zainab Jagani,
M. Jenal,
Jennifer A. Johnson,
Michael D. Jones,
A. Kapoor,
Joshua M. Korn,
Jilin Liu,
Qiumei Liu,
Shumei Liu,
Yue Liu,
Alice T. Loo,
Kaitlin J Macchi,
Typhaine Martin,
Gregory McAllister,
Amandine Meyer,
S. Mollé,
R. Pagliarini,
Tanushree Phadke,
Brian Repko,
Tanja Schouwey,
F. Shanahan,
Qiong Shen,
C. Stamm,
C. Stephan,
V. Stucke,
R. Tiedt,
Malini Varadarajan,
K. Venkatesan,
Alberto C. Vitari,
M. Wallroth,
J. Weiler,
Jing Zhang,
C. Mickanin,
V. Myer,
J. A. Porter,
A. Lai,
H. Bitter,
E. Lees,
N. Keen,
A. Kauffmann,
F. Stegmeier,
F. Hofmann,
Tobias Schmelzle,
W. Sellers
|
9 |
2017 |
9
🐜
|
|
🐜
|
An F876L mutation in androgen receptor confers genetic and phenotypic resistance to MDV3100 (enzalutamide).
16 auth.
M. Korpal,
Joshua M. Korn,
Xueliang Gao,
Daniel P. Rakiec,
D. Ruddy,
Shivang Doshi,
Jing Yuan,
S. Kovats,
Sunkyu Kim,
V. Cooke,
...
J. Monahan,
F. Stegmeier,
T. Roberts,
W. Sellers,
Wenlai Zhou,
P. Zhu
|
8 |
2013 |
8
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