Rick Kamps
Overview
Explore the profile of Rick Kamps including associated specialties, affiliations and a list of published articles.
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21
Citations
499
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Recent Articles
1.
Kamps R, Robinson E
Noncoding RNA
. 2024 Nov;
10(6).
PMID: 39585049
Primary mitochondrial disease (MD) is a group of rare genetic diseases reported to have a prevalence of 1:5000 and is currently without a cure. This group of diseases includes mitochondrial...
2.
Vallbona-Garcia A, Lindsey P, Kamps R, Stassen A, Nguyen N, van Tienen F, et al.
Front Ophthalmol (Lausanne)
. 2024 Jul;
3:1309836.
PMID: 38983060
Introduction: Primary open-angle glaucoma (POAG) is a characteristic optic neuropathy, caused by degeneration of the optic nerve-forming neurons, the retinal ganglion cells (RGCs). High intraocular pressure (IOP) and aging have...
3.
Nazzari M, Romitti M, Kip A, Kamps R, Costagliola S, van de Beucken T, et al.
Environ Int
. 2024 May;
188:108748.
PMID: 38763096
Introduction: Endocrine disruptors are compounds of manmade origin able to interfere with the endocrine system and constitute an important environmental concern. Indeed, detrimental effects on thyroid physiology and functioning have...
4.
Otten A, Kamps R, Lindsey P, Gerards M, Pendeville-Samain H, Muller M, et al.
Front Cell Dev Biol
. 2020 Jun;
8:381.
PMID: 32596237
High mitochondrial DNA (mtDNA) copy numbers are essential for oogenesis and embryogenesis and correlate with fertility of oocytes and viability of embryos. To understand the pathology and mechanisms associated with...
5.
Azodi M, Kamps R, Heymans S, Robinson E
Noncoding RNA
. 2020 Jan;
6(1).
PMID: 31947625
Cardiovascular disease (CVD) is one of the biggest threats to public health worldwide. Identifying key genetic contributors to CVD enables clinicians to assess the most effective treatment course and prognosis,...
6.
Theunissen T, Nguyen M, Kamps R, Hendrickx A, Sallevelt S, Gottschalk R, et al.
Front Genet
. 2018 Oct;
9:400.
PMID: 30369941
Mitochondrial disorders, characterized by clinical symptoms and/or OXPHOS deficiencies, are caused by pathogenic variants in mitochondrial genes. However, pathogenic variants in some of these genes can lead to clinical manifestations...
7.
Kamps R, Szklarczyk R, Theunissen T, Hellebrekers D, Sallevelt S, Boesten I, et al.
Eur J Hum Genet
. 2018 Feb;
26(4):537-551.
PMID: 29440775
This study aims to identify gene defects in pediatric cardiomyopathy and early-onset brain disease with oxidative phosphorylation (OXPHOS) deficiencies. We applied whole-exome sequencing in three patients with pediatric cardiomyopathy and...
8.
Geraets I, Chanda D, van Tienen F, van den Wijngaard A, Kamps R, Neumann D, et al.
Biochim Biophys Acta Mol Basis Dis
. 2017 Dec;
1864(5 Pt B):1960-1967.
PMID: 29277329
Patients with type 2 diabetes (T2D) and/or insulin resistance (IR) have an increased risk for the development of heart failure (HF). Evidence indicates that this increased risk is linked to...
9.
Theunissen T, Gerards M, Hellebrekers D, van Tienen F, Kamps R, Sallevelt S, et al.
Front Mol Neurosci
. 2017 Nov;
10:336.
PMID: 29093663
Mitochondrial disorders are genetically and clinically heterogeneous, mainly affecting high energy-demanding organs due to impaired oxidative phosphorylation (OXPHOS). Currently, effective treatments for OXPHOS defects, with complex I deficiency being the...
10.
Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification
Kamps R, Brandao R, van den Bosch B, Paulussen A, Xanthoulea S, Blok M, et al.
Int J Mol Sci
. 2017 Feb;
18(2).
PMID: 28146134
Next-generation sequencing (NGS) technology has expanded in the last decades with significant improvements in the reliability, sequencing chemistry, pipeline analyses, data interpretation and costs. Such advances make the use of...