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Institution

Fred Hutchinson Cancer Research Center

NonprofitCape Town, South Africa
About: Fred Hutchinson Cancer Research Center is a nonprofit organization based out in Cape Town, South Africa. It is known for research contribution in the topics: Population & Transplantation. The organization has 12322 authors who have published 30954 publications receiving 2288772 citations. The organization is also known as: Fred Hutch & The Hutch.


Papers
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Journal ArticleDOI
Ayuko Hoshino1, Ayuko Hoshino2, Han Sang Kim1, Han Sang Kim3, Linda Bojmar1, Linda Bojmar4, Linda Bojmar5, Kofi Ennu Gyan1, Michele Cioffi1, Jonathan M. Hernandez6, Jonathan M. Hernandez7, Jonathan M. Hernandez1, Constantinos P. Zambirinis6, Constantinos P. Zambirinis1, Gonçalo Rodrigues1, Gonçalo Rodrigues8, Henrik Molina9, Søren Heissel9, Milica Tesic Mark9, Loïc Steiner1, Loïc Steiner10, Alberto Benito-Martin1, Serena Lucotti1, Angela Di Giannatale1, Katharine Offer1, Miho Nakajima1, Caitlin Williams1, Laura Nogués11, Laura Nogués1, Fanny A. Pelissier Vatter1, Ayako Hashimoto12, Ayako Hashimoto2, Ayako Hashimoto1, Alexander E. Davies13, Daniela Freitas8, Daniela Freitas1, Candia M. Kenific1, Yonathan Ararso1, Weston Buehring1, Pernille Lauritzen1, Yusuke Ogitani1, Kei Sugiura12, Kei Sugiura2, Naoko Takahashi2, Maša Alečković14, Kayleen A. Bailey1, Joshua S. Jolissant6, Joshua S. Jolissant1, Huajuan Wang1, Ashton Harris1, L. Miles Schaeffer1, Guillermo García-Santos1, Guillermo García-Santos15, Zoe Posner1, Vinod P. Balachandran6, Yasmin Khakoo6, G. Praveen Raju16, Avigdor Scherz17, Irit Sagi17, Ruth Scherz-Shouval17, Yosef Yarden17, Moshe Oren17, Mahathi Malladi6, Mary Petriccione6, Kevin C. De Braganca6, Maria Donzelli6, Cheryl Fischer6, Stephanie Vitolano6, Geraldine P. Wright6, Lee Ganshaw6, Mariel Marrano6, Amina Ahmed6, Joe DeStefano6, Enrico Danzer6, Michael H.A. Roehrl6, Norman J. Lacayo18, Theresa C. Vincent19, Theresa C. Vincent4, Martin R. Weiser6, Mary S. Brady6, Paul A. Meyers6, Leonard H. Wexler6, Srikanth R. Ambati6, Alexander J. Chou6, Emily K. Slotkin6, Shakeel Modak6, Stephen S. Roberts6, Ellen M. Basu6, Daniel Diolaiti19, Benjamin A. Krantz19, Benjamin A. Krantz6, Fatima Cardoso20, Amber L. Simpson6, Michael F. Berger6, Charles M. Rudin6, Diane M. Simeone19, Maneesh Jain21, Cyrus M. Ghajar22, Surinder K. Batra21, Ben Z. Stanger23, Jack D. Bui24, Kristy A. Brown1, Vinagolu K. Rajasekhar6, John H. Healey6, Maria de Sousa1, Maria de Sousa8, Kim Kramer6, Sujit Sheth1, Jeanine Baisch1, Virginia Pascual1, Todd E. Heaton6, Michael P. La Quaglia6, David J. Pisapia1, Robert E. Schwartz1, Haiying Zhang1, Yuan Liu6, Arti Shukla25, Laurence Blavier26, Yves A. DeClerck26, Mark A. LaBarge27, Mina J. Bissell28, Thomas C. Caffrey21, Paul M. Grandgenett21, Michael A. Hollingsworth21, Jacqueline Bromberg1, Jacqueline Bromberg6, Bruno Costa-Silva20, Héctor Peinado11, Yibin Kang14, Benjamin A. Garcia23, Eileen M. O'Reilly6, David P. Kelsen6, Tanya M. Trippett6, David R. Jones6, Irina Matei1, William R. Jarnagin6, David Lyden1 
20 Aug 2020-Cell
TL;DR: EVP proteins can serve as reliable biomarkers for cancer detection and determining cancer type, and a panel of tumor-type-specific EVP proteins in TEs and plasma are defined, which can classify tumors of unknown primary origin.

565 citations

Journal ArticleDOI
TL;DR: A new class of E26 transformation-specific (ETS)-fusion-negative tumors defined by mutations in epigenetic regulators, as well as alterations in pathways not previously implicated in prostate cancer, such as the spliceosome pathway are identified.
Abstract: Comprehensive genomic characterization of prostate cancer has identified recurrent alterations in genes involved in androgen signaling, DNA repair, and PI3K signaling, among others. However, larger and uniform genomic analysis may identify additional recurrently mutated genes at lower frequencies. Here we aggregate and uniformly analyze exome sequencing data from 1,013 prostate cancers. We identify and validate a new class of E26 transformation-specific (ETS)-fusion-negative tumors defined by mutations in epigenetic regulators, as well as alterations in pathways not previously implicated in prostate cancer, such as the spliceosome pathway. We find that the incidence of significantly mutated genes (SMGs) follows a long-tail distribution, with many genes mutated in less than 3% of cases. We identify a total of 97 SMGs, including 70 not previously implicated in prostate cancer, such as the ubiquitin ligase CUL3 and the transcription factor SPEN. Finally, comparing primary and metastatic prostate cancer identifies a set of genomic markers that may inform risk stratification.

564 citations

Journal ArticleDOI
TL;DR: Models for the specific assembly of the RNA polymerase II transcription machinery at a promoter, conformational changes that occur during initiation of transcription, and the mechanism of initiation are discussed in light of recent developments.
Abstract: Advances in structure determination of the bacterial and eukaryotic transcription machinery have led to a marked increase in the understanding of the mechanism of transcription. Models for the specific assembly of the RNA polymerase II transcription machinery at a promoter, conformational changes that occur during initiation of transcription, and the mechanism of initiation are discussed in light of recent developments.

563 citations

Journal ArticleDOI
TL;DR: Transient HPV DNA was associated with a failure to seroconvert following incident HPV infection; however, some women with persistent HPV DNA never seroconverted, and antibody responses to HPV-16 and -18 were significantly more likely to persist during follow-up than were antibodies to HPV -6.
Abstract: The relationship between human papillomavirus (HPV) DNA in the genital mucosa and serum IgG to HPV-16, -18, and -6 was studied in a cohort of 588 college women. Among women with incident HPV infections, 59.5%, 54.1%, and 68.8% seroconverted for HPV-16, -18, or -6, respectively, within 18 months of detecting the corresponding HPV DNA. Transient HPV DNA was associated with a failure to seroconvert following incident HPV infection; however, some women with persistent HPV DNA never seroconverted. Antibody responses to each type were heterogeneous, but several type-specific differences were found: seroconversion for HPV-16 occurred most frequently between 6 and 12 months of DNA detection, but seroconversion for HPV-6 coincided with DNA detection. Additionally, antibody responses to HPV-16 and -18 were significantly more likely to persist during follow-up than were antibodies to HPV-6.

563 citations


Authors

Showing all 12368 results

NameH-indexPapersCitations
Walter C. Willett3342399413322
Robert Langer2812324326306
Meir J. Stampfer2771414283776
JoAnn E. Manson2701819258509
David J. Hunter2131836207050
Peer Bork206697245427
Eric Boerwinkle1831321170971
Ruedi Aebersold182879141881
Bruce M. Psaty1811205138244
Aaron R. Folsom1811118134044
David Baker1731226109377
Frederick W. Alt17157795573
Lily Yeh Jan16246773655
Yuh Nung Jan16246074818
Charles N. Serhan15872884810
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20237
202275
20211,981
20201,995
20191,685
20181,571