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Cuno Kuiperi · SciRah

Researcher profile · Semantic Scholar

Cuno Kuiperi

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Cuno Kuiperi — researcher profile on SciRah

h-index: 14
Works: 32
Citations: 2,343

Most-cited papers

Acute treatment with the PPARγ agonist pioglitazone and ibuprofen reduces glial inflammation and Aβ1–42 levels in APPV717I transgenic mice
M. Heneka, M. Sastre, Lucia Dumitrescu-Ozimek, A. Hanke +6 more
2005534 citations Open access
Semantic Scholar
Therapeutic effects of PKC activators in Alzheimer's disease transgenic mice.
R. Etcheberrigaray, M. Tan, I. Dewachter, Cuno Kuiperi +8 more
2004Proceedings of the National Academy of Sciences of the United States of America329 citations Open access
Semantic Scholar
Acute treatment with the PPARgamma agonist pioglitazone and ibuprofen reduces glial inflammation and Abeta1-42 levels in APPV717I transgenic mice.
M. Heneka, M. Sastre, Lucia Dumitrescu-Ozimek, A. Hanke +6 more
2005Brain : a journal of neurology267 citations
Semantic Scholar
Neuronal Deficiency of Presenilin 1 Inhibits Amyloid Plaque Formation and Corrects Hippocampal Long-Term Potentiation But Not a Cognitive Defect of Amyloid Precursor Protein [V717I] Transgenic Mice
I. Dewachter, D. Reversé, N. Caluwaerts, L. Ris +10 more
2002Journal of Neuroscience243 citations Open access
Semantic Scholar
Prominent cerebral amyloid angiopathy in transgenic mice overexpressing the london mutant of human APP in neurons.
J. Van Dorpe, Liesbet Smeijers, I. Dewachter, D. Nuyens +13 more
2000American Journal of Pathology230 citations Open access
Semantic Scholar
Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin
A. La Gerche, C. Robberecht, Cuno Kuiperi, D. Nuyens +4 more
2010Heart220 citations
Semantic Scholar
Mutant Presenilins Disturb Neuronal Calcium Homeostasis in the Brain of Transgenic Mice, Decreasing the Threshold for Excitotoxicity and Facilitating Long-term Potentiation*
Ilka Schneider, D. Reversé, I. Dewachter, L. Ris +9 more
2001Journal of Biological Chemistry136 citations Open access
Semantic Scholar
Aging Increased Amyloid Peptide and Caused Amyloid Plaques in Brain of Old APP/V717I Transgenic Mice by a Different Mechanism than Mutant Presenilin1
I. Dewachter, J. Van Dorpe, Liesbet Smeijers, Martine Gilis +7 more
2000Journal of Neuroscience116 citations Open access
Semantic Scholar
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death.
T. Rossenbacker, Sheila J Carroll, Huajun Liu, Cuno Kuiperi +5 more
2004Heart Rhythm82 citations
Semantic Scholar
Aggressive behaviour in transgenic mice expressing APP is alleviated by serotonergic drugs
D. Moechars, Martine Gilis, Cuno Kuiperi, I. Laenen +1 more
1998NeuroReport64 citations
Semantic Scholar
Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy
T. Rossenbacker, E. Schollen, Cuno Kuiperi, T. de Ravel +5 more
2005Journal of Medical Genetics29 citations Open access
Semantic Scholar
Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome.
T. Robyns, R. Willems, B. Vandenberk, J. Ector +7 more
2017Heart Rhythm20 citations
Semantic Scholar
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation.
A. Nijak, M. Alaerts, Cuno Kuiperi, A. Corveleyn +7 more
2018European Journal of Medical Genetics19 citations Open access
Semantic Scholar
Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy.
T. Robyns, J. Breckpot, D. Nuyens, B. Vandenberk +5 more
2020European Journal of Medical Genetics17 citations Open access
Semantic Scholar
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI
J. Jacobs, L. Van Aelst, J. Breckpot, A. Corveleyn +8 more
2023European Journal of Human Genetics14 citations Open access
Semantic Scholar
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy
T. Robyns, Cuno Kuiperi, J. Breckpot, K. Devriendt +6 more
2017European Journal of Human Genetics13 citations Open access
Semantic Scholar
Genotype–phenotype relationship and risk stratification in loss‐of‐function SCN5A mutation carriers
T. Robyns, D. Nuyens, B. Vandenberk, Cuno Kuiperi +5 more
2018Annals of Noninvasive Electrocardiology8 citations Open access
Semantic Scholar
Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout.
T. Robyns, Cuno Kuiperi, R. Willems, A. Corveleyn +1 more
2015Acta Cardiologica1 citations
Semantic Scholar
Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout
T. Robyns, Cuno Kuiperi, R. Willems, A. Corveleyn +1 more
20151 citations
Semantic Scholar
P1597QT rate dependence in risk stratification for sudden death in hypertrophic cardiomyopathy
T. Robyns, D. Nuyens, B. Vandenberk, Cuno Kuiperi +4 more
20170 citations Open access
Semantic Scholar
Non-compaction cardiomyopathy with Ebstein anomaly attributed to a TPM1 mutation
A. Nijak, M. Alaerts, Cuno Kuiperi, G. Matthijs +7 more
20170 citations
Semantic Scholar
96-71: Altered heart rate variability in long QT syndrome assessed by 24 hour holter recordings
T. Robyns, D. Nuyens, B. Vandenberk, J. Ector +4 more
20160 citations Open access
Semantic Scholar
Abstract 14451: High Agreement Between a Cardiology Specific Scoring System and the ACMG Criteria for Genetic Variant Interpretation and Classification
T. Robyns, Cuno Kuiperi, R. Willems, J. Van Cleemput +4 more
20160 citations
Semantic Scholar
Late potentials are more pronounced in SCN5A mutation carriers compared to SCN5A negative Brugada syndrome patients
T. Robyns, B. Vandenberk, J. Ector, C. Garweg +5 more
20160 citations
Semantic Scholar
Targeted massive parallel sequencing for arrhythmias and cardiomyopathies in a diagnostic setting
A. Corveleyn, Cuno Kuiperi, T. Robyns, J. Breckpot +4 more
20160 citations
Semantic Scholar
Targeted capture sequencing identifies mutations in a substantial proportion of prior genotype negative - phenotype positive patients with inherited primary arrhythmia syndrome or cardiomyopathy
T. Robyns, Cuno Kuiperi, T. de Ravel de l'Argentière, K. Devriendt +5 more
20150 citations
Semantic Scholar
QT Rate Dependence is Reduced in Brugada Syndrome Independent of Genotypic Status
T. Robyns, R. Willems, J. Ector, C. Garweg +3 more
20150 citations
Semantic Scholar
Genetic retesting with targeted capture sequencing of prior genotype negative – phenotype positive patients with inherited primary arrhythmia syndromes or cardiomyopathy
T. Robyns, Cuno Kuiperi, J. Breckpot, K. Devriendt +5 more
20150 citations
Semantic Scholar
Repeat genetic testing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed with DHPLC
T. Robyns, Cuno Kuiperi, T. de Ravel de l'Argentière, A. Corveleyn +5 more
20140 citations
Semantic Scholar
The Centre for Hereditary Heart disease: an interdisciplinary approach towards cardio genetics
E. Schollen, Cuno Kuiperi, T. Rossenbacker, G. Matthijs +2 more
20060 citations
Semantic Scholar
Unconventional splice site mutation in SCN5A as cause (and modifier?) of overlapping phenotypes of Brugada syndrome and isolated cardiac conduction defect
T. Rossenbacker, E. Schollen, Cuno Kuiperi, T. de Ravel +3 more
20040 citations
Semantic Scholar
Altered IP3-dependent intracellular Ca2+ pools of hippocampal neurons in presenilin-1 mutant transgenic mice
J. Herms, Ilka Schneider, D. Moechars, Martine Gilis +3 more
20000 citations
Semantic Scholar

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