A.J.M. Janssen

Uppsala University — Sweden

Biochemistry, Genetics and Molecular Biology · Life Sciences

31h-index3.6kcitations98works0.32yr avg
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Research Topics

Mitochondrial Function and Pathology(51), Metabolism and Genetic Disorders(48), ATP Synthase and ATPases Research(19), Enzyme Catalysis and Immobilization(9), Adipose Tissue and Metabolism(9)

Publications98 total

Cytoskeletal control in adult microglia is essential to restore neurodevelopmental synaptic and cognitive deficits
Science Advances·2025Open Access
Prognostic Value and Repeatability of LVEF Measurements Using ECG-Gated First-Pass Data and (15O)-water PET
Journal of Nuclear Cardiology·2025
APOE deficiency inhibits amyloid-facilitated (A) tau pathology (T) and neurodegeneration (N), halting progressive ATN pathology in a preclinical model
Molecular Psychiatry·2025· 1 citedOpen Access
Dataset for 'How brands highlight country of origin in magazine advertising: A content analysis'
DANS Data Station SSH·2020Open Access
The effectiveness of adapting advertising appeals to cultural values: an experimental and meta-analytical approach
2019
Motor performance of very preterm and dysmature infants in the multi-ethnic society of Suriname
Annals of Global Health·2016Open Access
Cue-shoe dans la maladie de Parkinson : un seul pas du freezing vers la liberté
Neurophysiologie Clinique·2015
Tissue specific metabolic consequences of isolated mitochondrial complex I deficiency in mice
Biochimica et Biophysica Acta (BBA) - Bioenergetics·2012
Prenatal exposure to moderate doses of X-rays induces cognitive dysfunction in adult mice
2012
Impaired ubiquitin‐proteasome‐mediated <scp>PGC</scp>‐1α protein turnover and induced mitochondrial biogenesis secondary to complex‐<scp>I</scp> deficiency
PROTEOMICS·2012· 8 cited
Mitochondrial enzymes discriminate between mitochondrial disorders and chronic fatigue syndrome
Mitochondrion·2011· 73 cited
47 Measurement of mitochondrial oxygen consumption using a fluorescence-based oxygen-sensitive probe: Application to mitochondrial medicine
Mitochondrion·2010
46 Functional characterization of energy deficient myoblasts and myotubes
Mitochondrion·2010
The Influence of Neocate in Paediatric Short Bowel Syndrome on PN Weaning
Journal of Nutrition and Metabolism·2010· 39 citedOpen Access
High-Throughput Assay to Measure Oxygen Consumption in Digitonin-Permeabilized Cells of Patients with Mitochondrial Disorders
Clinical Chemistry·2009· 28 citedOpen Access
Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver
Acta Neurologica Scandinavica·2009· 39 cited
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy
Acta Neurologica Scandinavica·2009· 31 cited
A novel mitochondrial <i>ATP8</i> gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy
BMJ Case Reports·2009· 21 citedOpen Access
In Reply
Clinical Chemistry·2008Open Access
Muscle 3243A→G mutation load and capacity of the mitochondrial energy‐generating system
Annals of Neurology·2008· 29 cited
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Frequent Co-authors

R. C. A. Sengers(23), J. M. F. Trijbels(21), W. Ruitenbeek(16), Jan Smeıtınk(14), Johan Fischer(9), Richard J. Rodenburg(9), Frans J.M. Trijbels(8), F.J.M. Gabreëls(6), A. M. Stadhouders(5), F. Trijbels(5), Lambert van den Heuvel(5), J. A. J. M. Bakkeren(5), Lambertus P. van den Heuvel(4), Frans A. Hol(4), Éva Morava(4), Markus Schuelke(4), C. M. C. Kerkhof(4), Ad M. Stadhouders(3), Lambert P. van den Heuvel(3), Liesbeth T. Wintjes(3)