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Peter C. M. Molenaar

Researcher at Queensland University of Technology

Publications -  559
Citations -  22056

Peter C. M. Molenaar is an academic researcher from Queensland University of Technology. The author has contributed to research in topics: Acetylcholine & Myasthenia gravis. The author has an hindex of 72, co-authored 548 publications receiving 20418 citations. Previous affiliations of Peter C. M. Molenaar include Baker IDI Heart and Diabetes Institute & Leiden University.

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Antibody effector mechanisms in myasthenia gravis-pathogenesis at the neuromuscular junction.

TL;DR: Findings suggest that MuSK-MG may be different in etiological and pathological mechanisms from AChR-MG, and the effector functions of IgG subclasses on synapse structure and function are discussed in this review.
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Dynamic factor analysis of nonstationary multivariate time series

TL;DR: In this article, a dynamic nonstationary factor model (DNFM) is proposed for the analysis of multivariate non-stationary time series in the time domain, where nonstationarity in the series is represented by a linear time dependent mean function.
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Problems with centrality measures in psychopathology symptom networks: Why network psychometrics cannot escape psychometric theory

TL;DR: It is argued that centrality measures do not provide solid ground for understanding the structure of psychopathology when latent confounding exists and it is essential for network psychometric approaches to examine the evidence for latent variables prior to analyzing or interpreting patterns at the symptom level.
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Organizing heterogeneous samples using community detection of GIMME-derived resting state functional networks

TL;DR: Empirical evidence presented here supports notions that heterogeneity exists in brain physiology within ADHD and control samples, and can assist in better characterizing patients in terms of outcomes, optimal treatment strategies, potential gene-environment interactions, and the use of biological phenomenon to assist with mental health.
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Characterization of β1- and β2-adrenoceptors in rat skeletal muscles

TL;DR: Autoradiographic studies supported the findings from binding studies with membrane homogenates, and the ICYP binding pattern was associated closely with the muscle fiber types identified by SDH staining, and Propranolol-resistant binding sites were observed.