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Institution

University of Washington Medical Center

HealthcareSeattle, Washington, United States
About: University of Washington Medical Center is a healthcare organization based out in Seattle, Washington, United States. It is known for research contribution in the topics: Population & Transplantation. The organization has 4087 authors who have published 4636 publications receiving 190834 citations. The organization is also known as: UW Medical Center & UW Medical Center - Montlake.


Papers
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Journal ArticleDOI
Rameen Beroukhim, Craig H. Mermel1, Craig H. Mermel2, Dale Porter3, Guo Wei2, Soumya Raychaudhuri2, Soumya Raychaudhuri4, Jerry Donovan3, Jordi Barretina2, Jordi Barretina1, Jesse S. Boehm2, Jennifer Dobson1, Jennifer Dobson2, Mitsuyoshi Urashima5, Kevin T. Mc Henry3, Reid M. Pinchback2, Azra H. Ligon4, Yoon Jae Cho6, Leila Haery1, Leila Haery2, Heidi Greulich, Michael R. Reich2, Wendy Winckler2, Michael S. Lawrence2, Barbara A. Weir1, Barbara A. Weir2, Kumiko E. Tanaka1, Kumiko E. Tanaka2, Derek Y. Chiang7, Derek Y. Chiang2, Derek Y. Chiang1, Adam J. Bass1, Adam J. Bass4, Adam J. Bass2, Alice Loo3, Carter Hoffman1, Carter Hoffman2, John R. Prensner2, John R. Prensner1, Ted Liefeld2, Qing Gao2, Derek Yecies1, Sabina Signoretti4, Sabina Signoretti1, Elizabeth A. Maher8, Frederic J. Kaye, Hidefumi Sasaki9, Joel E. Tepper7, Jonathan A. Fletcher4, Josep Tabernero10, José Baselga10, Ming-Sound Tsao11, Francesca Demichelis12, Mark A. Rubin12, Pasi A. Jänne4, Pasi A. Jänne1, Mark J. Daly1, Mark J. Daly2, Carmelo Nucera13, Ross L. Levine14, Benjamin L. Ebert1, Benjamin L. Ebert4, Benjamin L. Ebert2, Stacey Gabriel2, Anil K. Rustgi15, Cristina R. Antonescu14, Marc Ladanyi14, Anthony Letai1, Levi A. Garraway2, Levi A. Garraway1, Massimo Loda4, Massimo Loda1, David G. Beer16, Lawrence D. True17, Aikou Okamoto5, Scott L. Pomeroy6, Samuel Singer14, Todd R. Golub18, Todd R. Golub1, Todd R. Golub2, Eric S. Lander19, Eric S. Lander1, Eric S. Lander2, Gad Getz2, William R. Sellers3, Matthew Meyerson1, Matthew Meyerson2 
18 Feb 2010-Nature
TL;DR: It is demonstrated that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival, and a large majority of SCNAs identified in individual cancer types are present in several cancer types.
Abstract: A powerful way to discover key genes with causal roles in oncogenesis is to identify genomic regions that undergo frequent alteration in human cancers. Here we present high-resolution analyses of somatic copy-number alterations (SCNAs) from 3,131 cancer specimens, belonging largely to 26 histological types. We identify 158 regions of focal SCNA that are altered at significant frequency across several cancer types, of which 122 cannot be explained by the presence of a known cancer target gene located within these regions. Several gene families are enriched among these regions of focal SCNA, including the BCL2 family of apoptosis regulators and the NF-kappaBeta pathway. We show that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival. Finally, we demonstrate that a large majority of SCNAs identified in individual cancer types are present in several cancer types.

3,375 citations

Journal ArticleDOI
Dan R. Robinson1, Eliezer M. Van Allen2, Eliezer M. Van Allen3, Yi-Mi Wu1, Nikolaus Schultz4, Robert J. Lonigro1, Juan Miguel Mosquera, Bruce Montgomery5, Mary-Ellen Taplin3, Colin C. Pritchard5, Gerhardt Attard6, Gerhardt Attard7, Himisha Beltran, Wassim Abida4, Robert K. Bradley5, Jake Vinson4, Xuhong Cao1, Pankaj Vats1, Lakshmi P. Kunju1, Maha Hussain1, Felix Y. Feng1, Scott A. Tomlins, Kathleen A. Cooney1, David Smith1, Christine Brennan1, Javed Siddiqui1, Rohit Mehra1, Yu Chen8, Yu Chen4, Dana E. Rathkopf8, Dana E. Rathkopf4, Michael J. Morris4, Michael J. Morris8, Stephen B. Solomon4, Jeremy C. Durack4, Victor E. Reuter4, Anuradha Gopalan4, Jianjiong Gao4, Massimo Loda, Rosina T. Lis3, Michaela Bowden9, Michaela Bowden3, Stephen P. Balk10, Glenn C. Gaviola9, Carrie Sougnez2, Manaswi Gupta2, Evan Y. Yu5, Elahe A. Mostaghel5, Heather H. Cheng5, Hyojeong Mulcahy5, Lawrence D. True11, Stephen R. Plymate5, Heidi Dvinge5, Roberta Ferraldeschi7, Roberta Ferraldeschi6, Penny Flohr6, Penny Flohr7, Susana Miranda7, Susana Miranda6, Zafeiris Zafeiriou6, Zafeiris Zafeiriou7, Nina Tunariu7, Nina Tunariu6, Joaquin Mateo6, Joaquin Mateo7, Raquel Perez-Lopez6, Raquel Perez-Lopez7, Francesca Demichelis12, Francesca Demichelis8, Brian D. Robinson, Marc H. Schiffman8, David M. Nanus, Scott T. Tagawa, Alexandros Sigaras8, Kenneth Eng8, Olivier Elemento8, Andrea Sboner8, Elisabeth I. Heath13, Howard I. Scher4, Howard I. Scher8, Kenneth J. Pienta14, Philip W. Kantoff3, Johann S. de Bono7, Johann S. de Bono6, Mark A. Rubin, Peter S. Nelson, Levi A. Garraway2, Levi A. Garraway3, Charles L. Sawyers4, Arul M. Chinnaiyan 
21 May 2015-Cell
TL;DR: This cohort study provides clinically actionable information that could impact treatment decisions for affected individuals and identified new genomic alterations in PIK3CA/B, R-spondin, BRAF/RAF1, APC, β-catenin, and ZBTB16/PLZF.

2,713 citations

Journal ArticleDOI
TL;DR: There are several risk subgroups for which the available data are insufficient to recommend for or against screening, including women with a personal history of breast cancer, carcinoma in situ, atypical hyperplasia, and extremely dense breasts on mammography.
Abstract: New evidence on breast Magnetic Resonance Imaging (MRI) screening has become available since the American Cancer Society (ACS) last issued guidelines for the early detection of breast cancer in 2003. A guideline panel has reviewed this evidence and developed new recommendations for women at different defined levels of risk. Screening MRI is recommended for women with an approximately 20-25% or greater lifetime risk of breast cancer, including women with a strong family history of breast or ovarian cancer and women who were treated for Hodgkin disease. There are several risk subgroups for which the available data are insufficient to recommend for or against screening, including women with a personal history of breast cancer, carcinoma in situ, atypical hyperplasia, and extremely dense breasts on mammography. Diagnostic uses of MRI were not considered to be within the scope of this review.

2,332 citations

Journal ArticleDOI
TL;DR: This guideline is intended to provide new and updated evidence-based recommendations for the prevention of SSI and should be incorporated into comprehensive surgical quality improvement programs to improve patient safety.
Abstract: Importance The human and financial costs of treating surgical site infections (SSIs) are increasing. The number of surgical procedures performed in the United States continues to rise, and surgical patients are initially seen with increasingly complex comorbidities. It is estimated that approximately half of SSIs are deemed preventable using evidence-based strategies. Objective To provide new and updated evidence-based recommendations for the prevention of SSI. Evidence Review A targeted systematic review of the literature was conducted in MEDLINE, EMBASE, CINAHL, and the Cochrane Library from 1998 through April 2014. A modified Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach was used to assess the quality of evidence and the strength of the resulting recommendation and to provide explicit links between them. Of 5759 titles and abstracts screened, 896 underwent full-text review by 2 independent reviewers. After exclusions, 170 studies were extracted into evidence tables, appraised, and synthesized. Findings Before surgery, patients should shower or bathe (full body) with soap (antimicrobial or nonantimicrobial) or an antiseptic agent on at least the night before the operative day. Antimicrobial prophylaxis should be administered only when indicated based on published clinical practice guidelines and timed such that a bactericidal concentration of the agents is established in the serum and tissues when the incision is made. In cesarean section procedures, antimicrobial prophylaxis should be administered before skin incision. Skin preparation in the operating room should be performed using an alcohol-based agent unless contraindicated. For clean and clean-contaminated procedures, additional prophylactic antimicrobial agent doses should not be administered after the surgical incision is closed in the operating room, even in the presence of a drain. Topical antimicrobial agents should not be applied to the surgical incision. During surgery, glycemic control should be implemented using blood glucose target levels less than 200 mg/dL, and normothermia should be maintained in all patients. Increased fraction of inspired oxygen should be administered during surgery and after extubation in the immediate postoperative period for patients with normal pulmonary function undergoing general anesthesia with endotracheal intubation. Transfusion of blood products should not be withheld from surgical patients as a means to prevent SSI. Conclusions and Relevance This guideline is intended to provide new and updated evidence-based recommendations for the prevention of SSI and should be incorporated into comprehensive surgical quality improvement programs to improve patient safety.

1,895 citations


Authors

Showing all 4112 results

NameH-indexPapersCitations
Lawrence Corey14677378105
Richard J. Johnson13788072201
John D. Scott13562583878
Frederick R. Appelbaum12767766632
Rainer Storb12390558780
Thomas J. Ryan11667567462
David A. Schwartz11095853533
Thomas D. Koepsell11041539406
Paul A. Anderson10756041797
Thomas J. Montine10650069103
Noel S. Weiss10563040550
Mark P. Jensen10367247194
Elihu H. Estey10366743416
Walter E. Stamm10235133161
Anne McTiernan10238942037
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20239
202225
2021285
2020273
2019226
2018180