Paolo Missier

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 4

Top Topics

Machine Learning

Cross Sectional

Antiretroviral Therapy

Top Venues

Newcastle University

University of Manchester (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Newcastle University Jan 01 2011

United Kingdom

Lecturer :: School of Computing Science

University of Manchester School of Computer Science

United Kingdom

Research Associate :: School of Computer Science

Bell Communications Research Jan 01 1994

United States

Research Scientist :: Applied Research

Education History

University of Manchester Sep 01 2004 - Feb 08 2008

United Kingdom

PHD :: School of Computer Science

University of Houston

United States

MSC :: Dept. of Computer Science

Universita degli Studi di Udine

Italy

MSC :: Dip. di Informatica

Publications

Fabiola Eto, Miriam Samuel, Rafael Henkin, Meera Mahesh, Tahania Ahmad, Alisha Angdembe, R Hamish McAllister-Williams, Paolo Missier, Nick J Reynolds, Michael R Barnes, Sally A Hull, Sarah Finer, Rohini Mathur
Ethnic differences in early onset multimorbidity and associations with health service use, long-term prescribing, years of life lost, and mortality: A cross-sectional study using clustering in the UK Clinical Practice Research Datalink. PLoS medicine 20 (10) (2023)
Benjamin Lam, Michael Catt, Sophie Cassidy, Jaume Bacardit, Philip Darke, Sam Butterfield, Ossama Alshabrawy, Michael I Trenell, Paolo Missier
Using Wearable Activity Trackers to Predict Type 2 Diabetes: Machine Learning-Based Cross-sectional Study of the UK Biobank Accelerometer Cohort. JMIR diabetes 6 (1) (2021)
Flavio Primo, Alexander Romanovsky, Rafael de Mello, Alessandro Garcia, Paolo Missier
A customisable pipeline for the semi-automated discovery of online activists and social campaigns on Twitter. World wide web (2021)
Rachel Thompson, Anastasios Papakonstantinou Ntalis, Sergi Beltran, Ana Töpf, Eduardo de Paula Estephan, Kiran Polavarapu, Peter A C 't Hoen, Paolo Missier, Hanns Lochmüller
Increasing phenotypic annotation improves the diagnostic rate of exome sequencing in a rare neuromuscular disorder. Human mutation 40 (10) (2019)