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Institution

The Chinese University of Hong Kong

EducationHong Kong, China
About: The Chinese University of Hong Kong is a education organization based out in Hong Kong, China. It is known for research contribution in the topics: Population & Computer science. The organization has 43411 authors who have published 93672 publications receiving 3066651 citations.
Topics: Population, Computer science, Cancer, Medicine, China


Papers
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Journal ArticleDOI
TL;DR: This paper proposes a secret transmit beamforming approach using a quality-of-service (QoS)-based perspective, and proves that SDR can exactly solve the design problems for a practically representative class of problem instances; e.g., when the intended receiver's instantaneous CSI is known.
Abstract: Secure transmission techniques have been receiving growing attention in recent years, as a viable, powerful alternative to blocking eavesdropping attempts in an open wireless medium. This paper proposes a secret transmit beamforming approach using a quality-of-service (QoS)-based perspective. Specifically, we establish design formulations that: i) constrain the maximum allowable signal-to-interference-and-noise ratios (SINRs) of the eavesdroppers, and that ii) provide the intended receiver with a satisfactory SINR through either a guaranteed SINR constraint or SINR maximization. The proposed designs incorporate a relatively new idea called artificial noise (AN), where a suitable amount of AN is added in the transmitted signal to confuse the eavesdroppers. Our designs advocate joint optimization of the transmit weights and AN spatial distribution in accordance with the channel state information (CSI) of the intended receiver and eavesdroppers. Our formulated design problems are shown to be NP-hard in general. We deal with this difficulty by using semidefinite relaxation (SDR), an approximation technique based on convex optimization. Interestingly, we prove that SDR can exactly solve the design problems for a practically representative class of problem instances; e.g., when the intended receiver's instantaneous CSI is known. Extensions to the colluding-eavesdropper scenario and the multi-intended-receiver scenario are also examined. Extensive simulation results illustrate that the proposed AN-aided designs can yield significant power savings or SINR enhancement compared to some other methods.

405 citations

Journal ArticleDOI
Virginie J. M. Verhoeven1, Pirro G. Hysi2, Robert Wojciechowski3, Robert Wojciechowski4, Qiao Fan5, Jeremy A. Guggenheim6, René Höhn7, Stuart MacGregor8, Alex W. Hewitt9, Alex W. Hewitt10, Abhishek Nag2, Ching-Yu Cheng11, Ching-Yu Cheng5, Ekaterina Yonova-Doing2, Xin Zhou5, M. Kamran Ikram11, M. Kamran Ikram5, Gabriëlle H.S. Buitendijk1, George McMahon12, John P. Kemp12, Beate St Pourcain12, Claire L. Simpson4, Kari-Matti Mäkelä13, Terho Lehtimäki13, Mika Kähönen13, Andrew D. Paterson14, S. Mohsen Hosseini14, Hoi Suen Wong14, Liang Xu15, Jost B. Jonas16, Olavi Pärssinen17, Juho Wedenoja18, Shea Ping Yip6, Daniel W.H. Ho19, Daniel W.H. Ho6, Chi Pui Pang19, Li Jia Chen19, Kathryn P. Burdon20, Jamie E Craig20, Barbara E.K. Klein21, Ronald Klein21, Toomas Haller22, Andres Metspalu22, Chiea Chuen Khor5, Chiea Chuen Khor23, E-Shyong Tai5, Tin Aung5, Tin Aung11, Eranga N. Vithana11, Wan Ting Tay11, Veluchamy A. Barathi11, Veluchamy A. Barathi5, Myopia (Cream), Peng Chen5, Ruoying Li5, Jiemin Liao5, Yingfeng Zheng11, Rick Twee-Hee Ong5, Angela Döring, Complications Trial24, Complications (Dcct)25, David M. Evans12, Nicholas J. Timpson12, Annemieke J.M.H. Verkerk1, Thomas Meitinger24, Olli T. Raitakari26, Felicia Hawthorne25, Tim D. Spector2, Lennart C. Karssen1, Mario Pirastu27, Federico Murgia27, Wei Ang9, Aniket Mishra8, Grant W. Montgomery8, Craig E. Pennell9, Phillippa M. Cumberland28, Ioana Cotlarciuc29, Paul Mitchell30, Jie Jin Wang30, Jie Jin Wang10, Maria Schache10, Sarayut Janmahasatian31, Robert P. Igo31, Jonathan H. Lass31, Emily Y. Chew4, Sudha K. Iyengar31, Theo G. M. F. Gorgels32, Igor Rudan33, Caroline Hayward33, Alan F. Wright33, Ozren Polasek34, Zoran Vatavuk35, James F. Wilson33, Brian W Fleck36, Tanja Zeller, Alireza Mirshahi7, Christian P. Müller, André G. Uitterlinden1, Fernando Rivadeneira1, Johannes R. Vingerling1, Albert Hofman1, Ben A. Oostra1, Najaf Amin1, Arthur A.B. Bergen, Yik Ying Teo5, Jugnoo S Rahi28, Jugnoo S Rahi8, Jugnoo S Rahi37, Veronique Vitart33, Cathy Williams12, Paul N. Baird10, Tien Yin Wong11, Tien Yin Wong5, Konrad Oexle24, Norbert Pfeiffer7, David A. Mackey10, David A. Mackey9, Terri L. Young25, Cornelia M. van Duijn1, Seang-Mei Saw5, Seang-Mei Saw38, Seang-Mei Saw11, Joan E. Bailey-Wilson38, Joan E. Bailey-Wilson4, Dwight Stambolian38, Caroline C W Klaver38, Caroline C W Klaver1, Christopher J Hammond2, Christopher J Hammond38 
TL;DR: The CREAM consortium conducted genome-wide meta-analyses, which identified 16 new loci for refractive error in individuals of European ancestry and 8 were shared with Asians, and identified 8 additional associated loci.
Abstract: Refractive error is the most common eye disorder worldwide and is a prominent cause of blindness Myopia affects over 30% of Western populations and up to 80% of Asians The CREAM consortium conducted genome-wide meta-analyses, including 37,382 individuals from 27 studies of European ancestry and 8,376 from 5 Asian cohorts We identified 16 new loci for refractive error in individuals of European ancestry, of which 8 were shared with Asians Combined analysis identified 8 additional associated loci The new loci include candidate genes with functions in neurotransmission (GRIA4), ion transport (KCNQ5), retinoic acid metabolism (RDH5), extracellular matrix remodeling (LAMA2 and BMP2) and eye development (SIX6 and PRSS56) We also confirmed previously reported associations with GJD2 and RASGRF1 Risk score analysis using associated SNPs showed a tenfold increased risk of myopia for individuals carrying the highest genetic load Our results, based on a large meta-analysis across independent multiancestry studies, considerably advance understanding of the mechanisms involved in refractive error and myopia

404 citations

Book ChapterDOI
06 Sep 2014
TL;DR: Experimental results demonstrate the effectiveness of SFV, and the combination of the traditional FV and SFV outperforms state-of-the-art methods on these datasets with a large margin.
Abstract: Representation of video is a vital problem in action recognition. This paper proposes Stacked Fisher Vectors (SFV), a new representation with multi-layer nested Fisher vector encoding, for action recognition. In the first layer, we densely sample large subvolumes from input videos, extract local features, and encode them using Fisher vectors (FVs). The second layer compresses the FVs of subvolumes obtained in previous layer, and then encodes them again with Fisher vectors. Compared with standard FV, SFV allows refining the representation and abstracting semantic information in a hierarchical way. Compared with recent mid-level based action representations, SFV need not to mine discriminative action parts but can preserve mid-level information through Fisher vector encoding in higher layer. We evaluate the proposed methods on three challenging datasets, namely Youtube, J-HMDB, and HMDB51. Experimental results demonstrate the effectiveness of SFV, and the combination of the traditional FV and SFV outperforms state-of-the-art methods on these datasets with a large margin.

404 citations

Journal ArticleDOI
TL;DR: This article showed that adenosine-to-inosine (A→I) RNA editing of AZIN1 (encoding antizyme inhibitor 1) is increased in hepatocellular carcinoma (HCC) specimens.
Abstract: A better understanding of human hepatocellular carcinoma (HCC) pathogenesis at the molecular level will facilitate the discovery of tumor-initiating events. Transcriptome sequencing revealed that adenosine-to-inosine (A→I) RNA editing of AZIN1 (encoding antizyme inhibitor 1) is increased in HCC specimens. A→I editing of AZIN1 transcripts, specifically regulated by ADAR1 (encoding adenosine deaminase acting on RNA-1), results in a serine-to-glycine substitution at residue 367 of AZIN1, located in β-strand 15 (β15) and predicted to cause a conformational change, induced a cytoplasmic-to-nuclear translocation and conferred gain-of-function phenotypes that were manifested by augmented tumor-initiating potential and more aggressive behavior. Compared with wild-type AZIN1 protein, the edited form has a stronger affinity to antizyme, and the resultant higher AZIN1 protein stability promotes cell proliferation through the neutralization of antizyme-mediated degradation of ornithine decarboxylase (ODC) and cyclin D1 (CCND1). Collectively, A→I RNA editing of AZIN1 may be a potential driver in the pathogenesis of human cancers, particularly HCC.

404 citations

Journal ArticleDOI
Nafees Ahmad, Shama D. Ahuja1, Onno W. Akkerman2, Jan-Willem C. Alffenaar2, Laura F Anderson3, Parvaneh Baghaei4, Didi Bang5, Pennan M. Barry6, Mayara Lisboa Bastos7, Digamber Behera8, Andrea Benedetti9, Gregory P. Bisson10, Martin J. Boeree11, Maryline Bonnet12, Sarah K. Brode13, James C.M. Brust14, Ying Cai15, Eric Caumes, J. Peter Cegielski16, Rosella Centis3, Pei-Chun Chan16, Edward D. Chan17, Kwok-Chiu Chang18, Macarthur Charles16, Andra Cirule, Margareth Pretti Dalcolmo19, Lia D'Ambrosio3, Gerard de Vries, Keertan Dheda20, Aliasgar Esmail20, Jennifer Flood6, Gregory J. Fox21, Mathilde Fréchet-Jachym, Geisa Fregona, Regina Gayoso19, Medea Gegia3, Maria Tarcela Gler, Sue Gu17, Lorenzo Guglielmetti22, Timothy H. Holtz16, Jennifer Hughes23, Petros Isaakidis23, Leah G. Jarlsberg24, Russell R. Kempker25, Salmaan Keshavjee26, Faiz Ahmad Khan9, Maia Kipiani, Serena P. Koenig26, Won-Jung Koh27, Afranio Lineu Kritski28, Liga Kuksa, Charlotte Kvasnovsky29, Nakwon Kwak30, Zhiyi Lan9, Christoph Lange31, Rafael Laniado-Laborín, Myungsun Lee, Vaira Leimane, Chi-Chiu Leung18, Eric Chung Ching Leung18, Pei Zhi Li9, Phil Lowenthal6, Ethel Leonor Noia Maciel, Suzanne M. Marks16, Sundari Mase16, Lawrence Mbuagbaw32, Giovanni Battista Migliori3, Vladimir Milanov33, Ann C. Miller34, Carole D. Mitnick34, Chawangwa Modongo10, Erika Mohr23, Ignacio Monedero, Payam Nahid24, Norbert Ndjeka, Max R. O'Donnell35, Nesri Padayatchi, Domingo Palmero, Jean W. Pape36, Laura Jean Podewils16, Ian R Reynolds17, Vija Riekstina, Jérôme Robert22, Maria I. Rodriguez, Barbara Seaworth37, Kwonjune J. Seung38, Kathryn Schnippel20, Tae Sun Shim39, Rupak Singla, Sarah Smith16, Giovanni Sotgiu40, Ganzaya Sukhbaatar, Payam Tabarsi4, Simon Tiberi41, Anete Trajman28, Lisa Trieu1, Zarir F Udwadia, Tjip S. van der Werf2, Nicolas Veziris22, Piret Viiklepp15, Stalz Charles Vilbrun, Kathleen F. Walsh, Janice Westenhouse6, Wing Wai Yew42, Jae-Joon Yim30, Nicola M. Zetola10, Matteo Zignol3, Dick Menzies9 
TL;DR: Treatment outcomes were significantly better with use of linezolid, later generation fluoroquinolones, bedaquiline, clofazimine, and carbapenems for treatment of multidrug-resistant tuberculosis, and the need for trials to ascertain the optimal combination and duration of these drugs is emphasised.

404 citations


Authors

Showing all 43993 results

NameH-indexPapersCitations
Michael Marmot1931147170338
Jing Wang1844046202769
Jiaguo Yu178730113300
Yang Yang1712644153049
Mark Gerstein168751149578
Gang Chen1673372149819
Jun Wang1661093141621
Jean Louis Vincent1611667163721
Wei Zheng1511929120209
Rui Zhang1512625107917
Ben Zhong Tang1492007116294
Kypros H. Nicolaides147130287091
Thomas S. Huang1461299101564
Galen D. Stucky144958101796
Joseph J.Y. Sung142124092035
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023212
2022904
20217,888
20207,245
20195,968
20185,372