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Institution

University of Alberta

EducationEdmonton, Alberta, Canada
About: University of Alberta is a education organization based out in Edmonton, Alberta, Canada. It is known for research contribution in the topics: Population & Health care. The organization has 65403 authors who have published 154847 publications receiving 5358338 citations. The organization is also known as: Ualberta & UAlberta.


Papers
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Journal ArticleDOI
TL;DR: This work considers the stabilization problem for a kind of networked control systems in discrete-time domain with random delays, and it is shown that the state-feedback gains are different with different modes.
Abstract: We consider the stabilization problem for a class of networked control systems in the discrete-time domain with random delays. The sensor-to-controller and controller-to-actuator delays are modeled as two Markov chains, and the resulting closed-loop systems are jump linear systems with two modes. The necessary and sufficient conditions on the existence of stabilizing controllers are established. It is shown that state-feedback gains are mode-dependent. An iterative linear matrix inequality (LMI) approach is employed to calculate the state-feedback gains.

838 citations

Journal ArticleDOI
TL;DR: This paper conducted an empirical study of small firms that are owned and managed by their founder and found significant support for all three aspects of the stew- ardship perspective of FOBs, and no support for any elements of the stagnation perspective.
Abstract: Two major perspectives can be construed in the literature concerning the nature of family owned businesses (FOBs). The first implies that these enterprises have unique charac- teristics of stewardship. FOB owners are said to care deeply about the long-term prospects of the business, in large part because their family's fortune, reputation and future are at stake. Their stewardship is said to be manifested by unusual devotion to the continuity of the company, by more assiduous nurturing of a community of employees, and by seeking out closer connections with customers to sustain the business. The second perspective is less flattering. It proposes that FOBs are unusually subject to stagnation: they are said to face unique resource restrictions, embrace conservative strategies, eschew growth, and be doomed to short lives. This paper develops and examines the merits of the two perspectives, neither of which has been systematically articulated or researched. It does so in an empirical study of only small firms that are owned and managed by their founder. Within this sample, it compares firms that are FOBs, that is, family owned and managed, with non-FOBs, that is, owned and managed by a founder with no other relative involved in the business. The findings show significant support for all three aspects of the stew- ardship perspective of FOBs, and no support for any elements of the stagnation perspective.

838 citations

Journal ArticleDOI
TL;DR: In this paper, various mathematical models derived to explain and predict solute diffusion in hydrogels are reviewed and tested against literature data, and it was determined that a scaling hydrodynamic model provided the best explanation for solutes diffusion.
Abstract: Solute diffusion in hydrogels is important in many biotechnology fields. Solute behavior in hydrogels has been explained in terms of reduction in hydrogel free volume, enhanced hydrodynamic drag on the solute, increased path length due to obstruction, and a combination of hydrodynamic drag and obstruction effects. In this article the various mathematical models derived to explain and predict solute diffusion in hydrogels are reviewed and tested against literature data. These models can be divided into those applicable to hydrogels composed of flexible polymer chains (i.e., homogeneous hydrogels) and those composed of rigid polymer chains (i.e., heterogeneous hydrogels). For homogeneous hydrogels it was determined that a scaling hydrodynamic model provided the best explanation for solute diffusion, while for heterogeneous hydrogels obstruction models were more consistent with the experimental data. Both the scaling hydrodynamic model and the most appropriate obstruction model contain undefined parameters w...

838 citations

Book
15 Apr 2013
TL;DR: In this paper, D. Jean Clandininin, one of the pioneers in using narrative as research, updates her classic formulation on narrative inquiry (with F. Michael Connelly), clarifying, extending and refining the method based on an additional decade of work.
Abstract: Narrative inquiry examines human lives through the lens of a narrative, honouring lived experience as a source of important knowledge and understanding. In this concise volume, D. Jean Clandinin, one of the pioneers in using narrative as research, updates her classic formulation on narrative inquiry (with F. Michael Connelly), clarifying, extending and refining the method based on an additional decade of work. A valuable feature is the inclusion of several exemplary cases with the author's critique and analysis of the work. The rise of interest in narrative inquiry in recent years makes this is an essential guide for researchers and an excellent text for graduate courses in qualitative inquiry.

834 citations

Journal ArticleDOI
Dalila Pinto1, Elsa Delaby2, Elsa Delaby3, Elsa Delaby4, Daniele Merico5, Mafalda Barbosa1, Alison K. Merikangas6, Lambertus Klei7, Bhooma Thiruvahindrapuram5, Xiao Xu1, Robert Ziman5, Zhuozhi Wang5, Jacob A. S. Vorstman8, Ann P. Thompson9, Regina Regan10, Regina Regan11, Marion Pilorge4, Marion Pilorge2, Marion Pilorge3, Giovanna Pellecchia5, Alistair T. Pagnamenta12, Bárbara Oliveira13, Bárbara Oliveira14, Christian R. Marshall5, Tiago R. Magalhaes10, Tiago R. Magalhaes11, Jennifer K. Lowe15, Jennifer L. Howe5, Anthony J. Griswold16, John R. Gilbert16, Eftichia Duketis17, Beth A. Dombroski18, Maretha de Jonge8, Michael L. Cuccaro16, Emily L. Crawford19, Catarina Correia13, Catarina Correia14, Judith Conroy20, Inȇs C. Conceição13, Inȇs C. Conceição14, Andreas G. Chiocchetti17, Jillian P. Casey11, Jillian P. Casey10, Guiqing Cai1, Christelle Cabrol4, Christelle Cabrol2, Christelle Cabrol3, Nadia Bolshakova6, Elena Bacchelli21, Richard Anney6, Steven Gallinger5, Michelle Cotterchio22, Graham Casey23, Lonnie Zwaigenbaum24, Kerstin Wittemeyer25, Kirsty Wing12, Simon Wallace12, Herman van Engeland8, Ana Tryfon26, Susanne Thomson19, Latha Soorya27, Bernadette Rogé, Wendy Roberts5, Fritz Poustka17, Susana Mouga28, Nancy J. Minshew7, L. Alison McInnes29, Susan G. McGrew19, Catherine Lord30, Marion Leboyer, Ann Le Couteur31, Alexander Kolevzon1, Patricia Jiménez González, Suma Jacob32, Suma Jacob33, Richard Holt12, Stephen J. Guter32, Jonathan Green, Andrew Green11, Andrew Green10, Christopher Gillberg34, Bridget A. Fernandez35, Frederico Duque28, Richard Delorme, Geraldine Dawson36, Pauline Chaste, Cátia Café, Sean Brennan6, Thomas Bourgeron37, Patrick Bolton38, Patrick Bolton39, Sven Bölte17, Raphael Bernier40, Gillian Baird39, Anthony J. Bailey12, Evdokia Anagnostou5, Joana Almeida, Ellen M. Wijsman40, Veronica J. Vieland41, Astrid M. Vicente13, Astrid M. Vicente14, Gerard D. Schellenberg18, Margaret A. Pericak-Vance16, Andrew D. Paterson5, Jeremy R. Parr31, Guiomar Oliveira28, John I. Nurnberger42, Anthony P. Monaco43, Anthony P. Monaco12, Elena Maestrini21, Sabine M. Klauck44, Hakon Hakonarson18, Jonathan L. Haines19, Daniel H. Geschwind15, Christine M. Freitag17, Susan E. Folstein16, Sean Ennis10, Sean Ennis11, Hilary Coon45, Agatino Battaglia, Peter Szatmari9, James S. Sutcliffe19, Joachim Hallmayer46, Michael Gill6, Edwin H. Cook32, Joseph D. Buxbaum1, Bernie Devlin7, Louise Gallagher6, Catalina Betancur2, Catalina Betancur4, Catalina Betancur3, Stephen W. Scherer5 
TL;DR: For example, the authors analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p = 1.0 × 10(-5)) and an increase in affected subjects carrying exonic pathogenic CNVs overlapping known loci associated with dominant or X-linked ASD and intellectual disability.
Abstract: Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus control groups (1.41-fold, p = 1.0 × 10(-5)) and an increase in affected subjects carrying exonic pathogenic CNVs overlapping known loci associated with dominant or X-linked ASD and intellectual disability (odds ratio = 12.62, p = 2.7 × 10(-15), ∼3% of ASD subjects). Pathogenic CNVs, often showing variable expressivity, included rare de novo and inherited events at 36 loci, implicating ASD-associated genes (CHD2, HDAC4, and GDI1) previously linked to other neurodevelopmental disorders, as well as other genes such as SETD5, MIR137, and HDAC9. Consistent with hypothesized gender-specific modulators, females with ASD were more likely to have highly penetrant CNVs (p = 0.017) and were also overrepresented among subjects with fragile X syndrome protein targets (p = 0.02). Genes affected by de novo CNVs and/or loss-of-function single-nucleotide variants converged on networks related to neuronal signaling and development, synapse function, and chromatin regulation.

833 citations


Authors

Showing all 66027 results

NameH-indexPapersCitations
Salim Yusuf2311439252912
Yi Chen2174342293080
Robert M. Califf1961561167961
Douglas R. Green182661145944
Russel J. Reiter1691646121010
Jiawei Han1681233143427
Jaakko Kaprio1631532126320
Tobin J. Marks1591621111604
Josef M. Penninger154700107295
Subir Sarkar1491542144614
Gerald M. Edelman14754569091
Rinaldo Bellomo1471714120052
P. Sinervo138151699215
David A. Jackson136109568352
Andreas Warburton135157897496
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
2023234
20221,084
20219,315
20208,831
20198,177