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Institution

University of Kansas

EducationLawrence, Kansas, United States
About: University of Kansas is a education organization based out in Lawrence, Kansas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 38183 authors who have published 81381 publications receiving 2986312 citations. The organization is also known as: KU & Univ of Kansas.


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Journal ArticleDOI
TL;DR: In the most completely studied series to date, at 20 to 28 years follow-up both braced and operated patients had similar, significant, and clinically meaningful reduced function and increased pain compared to non-scoliotic controls, however, their function and pain scores were much closer to normal than patient groups with other, more serious conditions.
Abstract: Adolescent idiopathic scoliosis is a lifetime, probably systemic condition of unknown cause, resulting in a spinal curve or curves of ten degrees or more in about 2.5% of most populations. However, in only about 0.25% does the curve progress to the point that treatment is warranted. Untreated, adolescent idiopathic scoliosis does not increase mortality rate, even though on rare occasions it can progress to the >100° range and cause premature death. The rate of shortness of breath is not increased, although patients with 50° curves at maturity or 80° curves during adulthood are at increased risk of developing shortness of breath. Compared to non-scoliotic controls, most patients with untreated adolescent idiopathic scoliosis function at or near normal levels. They do have increased pain prevalence and may or may not have increased pain severity. Self-image is often decreased. Mental health is usually not affected. Social function, including marriage and childbearing may be affected, but only at the threshold of relatively larger curves. Non-operative treatment consists of bracing for curves of 25° to 35° or 40° in patients with one to two years or more of growth remaining. Curve progression of ≥ 6° is 20 to 40% more likely with observation than with bracing. Operative treatment consists of instrumentation and arthrodesis to realign and stabilize the most affected portion of the spine. Lasting curve improvement of approximately 40% is usually achieved. In the most completely studied series to date, at 20 to 28 years follow-up both braced and operated patients had similar, significant, and clinically meaningful reduced function and increased pain compared to non-scoliotic controls. However, their function and pain scores were much closer to normal than patient groups with other, more serious conditions. Risks associated with treatment include temporary decrease in self-image in braced patients. Operated patients face the usual risks of major surgery, a 6 to 29% chance of requiring reoperation, and the remote possibility of developing a pain management problem. Knowledge of adolescent idiopathic scoliosis natural history and long-term treatment effects is and will always remain somewhat incomplete. However, enough is know to provide patients and parents the information needed to make informed decisions about management options.

515 citations

Journal ArticleDOI
Nasim Mavaddat1, Daniel Barrowdale1, Irene L. Andrulis2, Susan M. Domchek3, Diana Eccles4, Heli Nevanlinna5, Susan J. Ramus6, Amanda B. Spurdle7, Mark E. Robson8, Mark E. Sherman9, Anna Marie Mulligan2, Fergus J. Couch10, Christoph Engel11, Lesley McGuffog1, Sue Healey7, Olga M. Sinilnikova12, Melissa C. Southey13, Mary Beth Terry8, David E. Goldgar14, Frances P. O'Malley2, Esther M. John15, Ramunas Janavicius16, Laima Tihomirova17, Thomas Hansen18, Finn Cilius Nielsen18, Ana Osorio, Alexandra V. Stavropoulou, Javier Benitez19, Siranoush Manoukian, Bernard Peissel, Monica Barile, Sara Volorio, Barbara Pasini20, Riccardo Dolcetti, Anna Laura Putignano21, Laura Ottini22, Paolo Radice, Ute Hamann23, Muhammad Usman Rashid24, Frans B. L. Hogervorst, Mieke Kriege25, Rob B. van der Luijt26, Susan Peock1, Debra Frost1, D. Gareth Evans, Carole Brewer27, Lisa Walker28, Mark T. Rogers29, Lucy Side30, C. E. Houghton, Jo Ellen Weaver31, Andrew K. Godwin32, Rita K. Schmutzler33, Barbara Wappenschmidt33, Alfons Meindl34, Karin Kast35, Norbert Arnold36, Dieter Niederacher37, Christian Sutter38, Helmut Deissler39, Doroteha Gadzicki40, Sabine Preisler-Adams41, Raymonda Varon-Mateeva42, Ines Schönbuchner43, Heidrun Gevensleben, Dominique Stoppa-Lyonnet44, Muriel Belotti, Laure Barjhoux12, Claudine Isaacs45, Beth N. Peshkin45, Trinidad Caldés19, Miguel De Al Hoya, Carmen Cañadas, Tuomas Heikkinen5, Päivi Heikkilä5, Kristiina Aittomäki5, Ignacio Blanco, Conxi Lázaro, Joan Brunet, Bjarni A. Agnarsson, Adalgeir Arason, Rosa B. Barkardottir, Martine Dumont46, Jacques Simard46, Marco Montagna, Simona Agata, Emma D'Andrea47, Max Yan, Stephen B. Fox48, Timothy R. Rebbeck, Wendy S. Rubinstein49, Nadine Tung, Judy Garber50, Xianshu Wang10, Zachary S. Fredericksen10, Vernon S. Pankratz10, Noralane M. Lindor10, Csilla Szabo51, Kenneth Offit8, Rita A. Sakr8, Mia M. Gaudet52, Christian F. Singer53, Muy Kheng Tea53, Christine Rappaport53, Phuong L. Mai9, Mark H. Greene9, Anna P. Sokolenko, Evgeny N. Imyanitov, Amanda E. Toland54, Leigha Senter54, Kevin Sweet54, Mads Thomassen55, Anne-Marie Gerdes18, Torben A Kruse55, Maria A. Caligo56, Paolo Aretini56, Johanna Rantala57, Anna Von Wachenfeld57, Karin M. Henriksson58, Linda Steele59, Susan L. Neuhausen59, Robert L. Nussbaum60, Mary S. Beattie60, Kunle Odunsi61, Lara Sucheston61, Simon A. Gayther6, Katherine L. Nathanson3, Jenny Gross62, Christine Walsh62, Beth Y. Karlan62, Georgia Chenevix-Trench7, Douglas F. Easton1, Antonis C. Antoniou1 
University of Cambridge1, University of Toronto2, University of Pennsylvania3, University of Southampton4, University of Helsinki5, University of Southern California6, QIMR Berghofer Medical Research Institute7, Columbia University8, National Institutes of Health9, Mayo Clinic10, Leipzig University11, Claude Bernard University Lyon 112, University of Melbourne13, University of Utah14, Cancer Prevention Institute of California15, Vilnius University16, University of Latvia17, University of Copenhagen18, Complutense University of Madrid19, University of Turin20, University of Florence21, Sapienza University of Rome22, German Cancer Research Center23, Memorial Hospital of South Bend24, Erasmus University Rotterdam25, Utrecht University26, Royal Devon and Exeter Hospital27, Churchill Hospital28, University Hospital of Wales29, University College London30, Fox Chase Cancer Center31, University of Kansas32, University of Cologne33, Technische Universität München34, Dresden University of Technology35, University of Kiel36, University of Düsseldorf37, Heidelberg University38, University of Ulm39, Hannover Medical School40, University of Münster41, Charité42, University of Würzburg43, University of Paris44, Georgetown University45, Laval University46, University of Padua47, Peter MacCallum Cancer Centre48, University of Chicago49, Harvard University50, University of Delaware51, American Cancer Society52, Medical University of Vienna53, Ohio State University54, University of Southern Denmark55, University of Pisa56, Karolinska Institutet57, Lund University58, City of Hope National Medical Center59, University of California, San Francisco60, Roswell Park Cancer Institute61, Cedars-Sinai Medical Center62
TL;DR: Pathologic characteristics of BRCA1 and BRCa2 tumors may be useful for improving risk-prediction algorithms and informing clinical strategies for screening and prophylaxis.
Abstract: BACKGROUND: Previously, small studies have found that BRCA1 and BRCA2 breast tumors differ in their pathology. Analysis of larger datasets of mutation carriers should allow further tumor characterization.METHODS: We used data from 4,325 BRCA1 and 2,568 BRCA2 mutation carriers to analyze the pathology of invasive breast, ovarian, and contralateral breast cancers.RESULTS: There was strong evidence that the proportion of estrogen receptor (ER)-negative breast tumors decreased with age at diagnosis among BRCA1 (P-trend = 1.2 × 10(-5)), but increased with age at diagnosis among BRCA2, carriers (P-trend = 6.8 × 10(-6)). The proportion of triple-negative tumors decreased with age at diagnosis in BRCA1 carriers but increased with age at diagnosis of BRCA2 carriers. In both BRCA1 and BRCA2 carriers, ER-negative tumors were of higher histologic grade than ER-positive tumors (grade 3 vs. grade 1; P = 1.2 × 10(-13) for BRCA1 and P = 0.001 for BRCA2). ER and progesterone receptor (PR) expression were independently associated with mutation carrier status [ER-positive odds ratio (OR) for BRCA2 = 9.4, 95% CI: 7.0-12.6 and PR-positive OR = 1.7, 95% CI: 1.3-2.3, under joint analysis]. Lobular tumors were more likely to be BRCA2-related (OR for BRCA2 = 3.3, 95% CI: 2.4-4.4; P = 4.4 × 10(-14)), and medullary tumors BRCA1-related (OR for BRCA2 = 0.25, 95% CI: 0.18-0.35; P = 2.3 × 10(-15)). ER-status of the first breast cancer was predictive of ER-status of asynchronous contralateral breast cancer (P = 0.0004 for BRCA1; P = 0.002 for BRCA2). There were no significant differences in ovarian cancer morphology between BRCA1 and BRCA2 carriers (serous: 67%; mucinous: 1%; endometrioid: 12%; clear-cell: 2%).Conclusions/Impact: Pathologic characteristics of BRCA1 and BRCA2 tumors may be useful for improving risk-prediction algorithms and informing clinical strategies for screening and prophylaxis. Cancer Epidemiol Biomarkers Prev; 1-14. ©2011 AACR.

514 citations

Journal ArticleDOI
TL;DR: Biologic therapy is associated with increased risk for skin cancers, but not for solid tumors or lymphoproliferative malignancies, and these associations were consistent across different biologic therapies.
Abstract: Objective Induction of malignancy is a major concern when rheumatoid arthritis (RA) is treated with biologic therapy. A meta-analysis of RA biologic clinical trials found a general increased risk of malignancy, but this risk was not found in a large observational study. We undertook this study to assess the risk of malignancy among biologic-treated patients in a large US observational database. Methods We studied incident cases of cancer among 13,001 patients during ∼49,000 patient-years of observation in the years 1998–2005. Cancer rates were compared with population rates using the US National Cancer Institute SEER (Surveillance, Epidemiology, and End-Results) database. Assessment of the risk of biologic therapy utilized conditional logistic regression to calculate odds ratios (ORs) as estimates of the relative risk, further adjusted for 6 confounders: age, sex, education level, smoking history, RA severity, and prednisone use. Results Biologic exposure was 49%. There were 623 incident cases of nonmelanotic skin cancer and 537 other cancers. The standardized incidence ratios and 95% confidence intervals (95% CIs) compared with SEER data were as follows: all cancers 1.0 (1.0–1.1), breast 0.8 (0.6–0.9), colon 0.5 (0.4–0.6), lung 1.2 (1.0–1.4), lymphoma 1.7 (1.3–2.2). Biologics were associated with an increased risk of nonmelanotic skin cancer (OR 1.5, 95% CI 1.2–1.8) and melanoma (OR 2.3, 95% CI 0.9–5.4). No other malignancy was associated with biologic use; the OR (overall risk) of any cancer was 1.0 (95% CI 0.8–1.2). Conclusion Biologic therapy is associated with increased risk for skin cancers, but not for solid tumors or lymphoproliferative malignancies. These associations were consistent across different biologic therapies.

514 citations

Journal ArticleDOI
TL;DR: A novel disintegrin metalloproteinase with thrombospondin motifs that possesses aggrecanase activity is identified and cloned, which has extensive homology to ADAMTS4 (aggrecanases-1) and the inflammation-associated gene ADAMts1, which is hypothesized to play a pivotal role in cartilage damage.

513 citations

Journal ArticleDOI
TL;DR: In this article, the authors investigated the effects of the gas and liquid water hydrodynamics on the performance of an air cathode of a PEM fuel cell employing an interdigitated gas distributor.
Abstract: When interdigitated gas distributors are used in a PEM fuel cell, fluids entering the fuel cell are forced to flow through the electrodes porous layers. This characteristic increases transport rates of the reactants and products to and from the catalyst layers and reduces the amount of liquid water entrapped in the porous electrodes thereby minimizing electrode flooding. To investigate the effects of the gas and liquid water hydrodynamics on the performance of an air cathode of a PEM fuel cell employing an interdigitated gas distributor, a 2-D, two-phase, multicomponent transport model was developed. Darcy's law was used to describe the transport of the gas phase. The transport of liquid water through the porous electrode is driven by the shear force of gas flow and capillary force. An equation accounting for both forces was derived for the liquid phase transport in the porous gas electrode. Higher differential pressures between inlet and outlet channels yield higher electrode performance, because the oxygen transport rates are higher and liquid water removal is more effective. The electrode thickness needs to be optimized to get optimal performance because thinner electrode may reduce gas-flow rate and thicker electrode may increase the diffusion layer thickness. For a fixed-size electrode, more channels and shorter shoulder widths are preferred.

512 citations


Authors

Showing all 38401 results

NameH-indexPapersCitations
Gordon H. Guyatt2311620228631
Krzysztof Matyjaszewski1691431128585
Wei Li1581855124748
David Tilman158340149473
Tomas Hökfelt158103395979
Pete Smith1562464138819
Daniel J. Rader1551026107408
Melody A. Swartz1481304103753
Kevin Murphy146728120475
Carlo Rovelli1461502103550
Stephen Sanders1451385105943
Marco Zanetti1451439104610
Andrei Gritsan1431531135398
Gunther Roland1411471100681
Joseph T. Hupp14173182647
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202391
2022358
20214,211
20204,204
20193,766
20183,485