University of New South Wales

About: University of New South Wales is a education organization based out in Sydney, New South Wales, Australia. It is known for research contribution in the topics: Population & Poison control. The organization has 51197 authors who have published 153634 publications receiving 4880608 citations. The organization is also known as: UNSW & UNSW Australia.

Efficient similarity joins for near-duplicate detection

Abstract: With the increasing amount of data and the need to integrate data from multiple data sources, one of the challenging issues is to identify near-duplicate records efficiently. In this article, we focus on efficient algorithms to find a pair of records such that their similarities are no less than a given threshold. Several existing algorithms rely on the prefix filtering principle to avoid computing similarity values for all possible pairs of records. We propose new filtering techniques by exploiting the token ordering information; they are integrated into the existing methods and drastically reduce the candidate sizes and hence improve the efficiency. We have also studied the implementation of our proposed algorithm in stand-alone and RDBMS-based settings. Experimental results show our proposed algorithms can outperform previous algorithms on several real datasets.

Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes.

Abstract: Context: The identification of mutations in genes encoding peptides of succinate dehydrogenase (SDH) in pheochromocytoma/paraganglioma syndromes has necessitated clear elucidation of genotype-phenotype associations. Objective: Our objective was to determine genotype-phenotype associations in a cohort of patients with pheochromocytoma/paraganglioma syndromes and succinate dehydrogenase subunit B (SDHB) or subunit D (SDHD) mutations. Design, Setting, and Participants: The International SDH Consortium studied 116 individuals (83 affected and 33 clinically unaffected) from 62 families with pheochromocytoma/paraganglioma syndromes and SDHB or SDHD mutations. Clinical data were collected between August 2003 and September 2004 from tertiary referral centers in Australia, France, New Zealand, Germany, United States, Canada, and Scotland. Main Outcome Measures: Data were collected on patients with pheochromocytomas and/or paragangliomas with respect to onset of disease, diagnosis, genetic testing, surgery, patholo...