A.J.M. Janssen

3.6k citations

69 papers · 2.9k indexed · h-index 27

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Biochemistry top 2%
- Biochemical Acid Research Studies

Papers in

Clinical Biochemistry 38
- Metabolism and Genetic Disorders 38
Biochemistry 12
- Biochemical Acid Research Studies 9
- Amino Acid Enzymes and Metabolism 5

Co-authors: R. C. A. Sengers J. M. F. Trijbels W. Ruitenbeek Jan Smeıtınk Johan Fischer Richard J. Rodenburg Frans J.M. Trijbels Ad M. Stadhouders
Journals: Journal of Inherited Metabolic Disease (8 papers)European Journal of Pediatrics (7 papers)Clinica Chimica Acta (7 papers)Clinical Chemistry (4 papers)Pediatric Research (4 papers)
Partner nations: Netherlands Germany Belgium

In The Last Decade

A.J.M. Janssen

68 papers receiving 2.8k citations

Peers

Countries citing papers authored by A.J.M. Janssen

Since Specialization

Citations

This map shows the geographic impact of A.J.M. Janssen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A.J.M. Janssen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.J.M. Janssen more than expected).

Fields of papers citing papers by A.J.M. Janssen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.J.M. Janssen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A.J.M. Janssen. The network helps show where A.J.M. Janssen may publish in the future.

Co-authors

The 25 scholars most cited alongside A.J.M. Janssen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with A.J.M. Janssen Line = papers co-authored together A.J.M. Janssen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	APOE deficiency inhibits amyloid-facilitated (A) tau pathology (T) and neurodegeneration (N), halting progressive ATN pathology in a preclinical model Molecular Psychiatry ·Sanchez-Renedo Manuel, A.J.M. Janssen, Carla Sofia Gonçalves Ferreira, María Antonia Beltrán, Carly Densmore, 王璐玮 Wang Luwei, Sofie Kessels, M. Lo Cascio, Michael KittoI, Yanyan Wang, Ilie‐Cosmin Stancu, Andrei Segal, Markus Kleinewietfeld, Thomas Voets, Bert Brône, Suresh Poovathingal, Yeranddy A. Alpízar, Ilse Dewachter	2025	1
2	Mitochondrial enzymes discriminate between mitochondrial disorders and chronic fatigue syndrome Mitochondrion ·Lj. Simic, Lambert van den Heuvel, Hans Knoop, Benno Küsters, A.J.M. Janssen, George F. Borm, Gijs Bleijenberg, Richard J. Rodenburg, Baziel G.M. van Engelen	2011	60
3	Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy Acta Neurologica Scandinavica ·F.J.M. Gabreëls, M.J.J. Prick, J. M. F. Trijbels, W.O. Renier, H. H. J. Jaspar, A.J.M. Janssen, J.L. Slooff	2009	4
4	Muscle 3243A→G mutation load and capacity of the mitochondrial energy‐generating system Annals of Neurology ·A.J.M. Janssen, Markus Schuelke, Jan Smeıtınk, Frans J.M. Trijbels, R. C. A. Sengers, Barbara Lucke, Liesbeth T. Wintjes, Éva Morava, Baziel G.M. van Engelen, Lj. Simic, Frans A. Hol, Yayat Dimyati, H. ter Laak, Marjo S. van der Knaap, Francjan J. van Spronsen, Richard J. Rodenburg, Lambert P. van den Heuvel	2008	20
5	Decreased Intracellular ATP Content and Intact Mitochondrial Energy Generating Capacity in Human Cystinotic Fibroblasts Pediatric Research ·Elena Levtchenko, Martijn J. Wilmer, A.J.M. Janssen, Jan J. Koenderink, Henk-Jan Visch, Peter H.G.M. Willems, Adriana de Graaf-Hess, Henk J. Blom, Lambertus P. van den Heuvel, L.A.H. Monnens	2006	44
6	De novo double mutation in PAX6 and mtDNA tRNA Lys associated with atypical aniridia and mitochondrial disease Journal of Molecular Medicine ·Jørgen Ægidius, Klaus Rüther, Kathleen A. Williamson, Birgit Lorenz, Barbara Lucke, Peter Nürnberg, Frans J.M. Trijbels, A.J.M. Janssen, Markus Schuelke	2006	9
7	Metabolic capacity of the diaphragm in patients with COPD Respiratory Medicine ·Emanuely Alencar de Melo De Paula, A.J.M. Janssen, Toin H. Van Kuppevelt, Richard J. Rodenburg, P.N.R. Dekhuijzen	2005	34
8	Coenzyme Q– responsive Leigh's encephalopathy in two sisters Annals of Neurology ·Lionel Van Maldergem, Frans J.M. Trijbels, Salvatore DiMauro, Pavel Šindelář, Olimpia Musumeci, A.J.M. Janssen, Yueguey Lee, Jean‐Jacques Martin, Y. Gillerot	2002	105
9	Septo‐optic dysplasia associated with a new mitochondrial cytochrome b mutation Annals of Neurology ·Markus Schuelke, Heiko Krude, Barbara Finckh, Ertan Mayatepek, A.J.M. Janssen, M Polubiec, Friedrich K. Trefz, Frans J.M. Trijbels, Jan Smeıtınk	2002	66
10	Combined Enzymatic Complex I and III Deficiency Associated with Mutations in the Nuclear Encoded NDUFS4 Gene Biochemical and Biophysical Research Communications ·MH Seo, Lambert P.W.J. van den Heuvel, A.J.M. Janssen, Roel Smeets, Carin A. F. Buskens, Tatsushige Fukunaga, Rudy Van Coster, Martina Baethmann, Thomas Voit, J. M. F. Trijbels, Jan A. M. Smeitink	2000	165
11	The X‐chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: Tissue expression and mutation detection Journal of Inherited Metabolic Disease ·Jan Loeffen, Roel Smeets, Jan Smeıtınk, W. Ruitenbeek, A.J.M. Janssen, Ravi Kothuri, R. C. A. Sengers, F. Trijbels, Lambert van den Heuvel	1998	16
12	Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns–Sayre/MELAS overlap syndrome and A3243G mtDNA mutation Journal of the Neurological Sciences ·Ekkehard Wilichowski, Georg Christoph Korenke, W. Ruitenbeek, Linda De Meırleır, Макарова Татьяна Николаевна, A.J.M. Janssen, Willy Lissens, F. Hanefeld	1998	23
13	Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies Biochimica et Biophysica Acta (BBA) - Biomembranes ·Herman Bentlage, A.J.M. Janssen, Anne Chomyn, Giuseppe Attardi, John E. Walker, Hermann Schägger, 金赵, F. Trijbels	1995	17
14	Measurement of Totally Activated Pyruvate Dehydrogenase Complex Activity in Human Muscle: Evaluation of a Useful Assay PubMed ·Wolfgang Sperl, J.M.F. Trijbels, W. Ruitenbeek, W Zhang, A.J.M. Janssen, Yu-Peng Liu, R. C. A. Sengers	1993	25
15	Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies European Journal of Pediatrics ·J. M. F. Trijbels, H.R. Scholte, W. Ruitenbeek, R. C. A. Sengers, A.J.M. Janssen, H. F. M. Busch	1993	36
16	Postnatal Development of Pyruvate Oxidation in Quadriceps Muscle of the Rat Neonatology ·Wolfgang Sperl, 金赵, J. M. F. Trijbels, W. Ruitenbeek, Robin de Graaf, H. ter Laak, Muna Agnita, Dean A. Karalis, A.J.M. Janssen	1992	5
17	Pyruvate Metabolism in Lafora Disease Epilepsia ·Ana Paula Feitosa Santos, W.O. Renier, F.J.M. Gabreëls, J. M. F. Trijbels, A.J.M. Janssen, K.J.B. Lamers	1989	4
18	Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach European Journal of Pediatrics ·J. M. F. Trijbels, R. C. A. Sengers, W. Ruitenbeek, Johan Fischer, J. A. J. M. Bakkeren, A.J.M. Janssen	1988	51
19	Disturbed Oxidative Metabolism in Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome) Neuropediatrics ·Jeane Mantiri, W. Ruitenbeek, F.J.M. Gabreëls, W. O. Renier, Johan Fischer, A.J.M. Janssen	1986	19
20	In VivoInduced Malignant Hyperthermia in Pigs II. Metabolism of Skeletal Muscle Mitochondria Acta Anaesthesiologica Scandinavica ·W. Ruitenbeek, Qi Xin, A.J.M. Janssen, A. M. Stadhouders, R. C. A. Sengers	1984	8

About A.J.M. Janssen

A.J.M. Janssen is a scholar working on Clinical Biochemistry, Biochemistry, Molecular Biology, Physiology and Cell Biology, having authored 69 papers that have together received 2.9k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (41 papers), Metabolism and Genetic Disorders (38 papers), ATP Synthase and ATPases Research (16 papers), Biochemical Acid Research Studies (9 papers), Adipose Tissue and Metabolism (8 papers), Muscle metabolism and nutrition (6 papers), Amino Acid Enzymes and Metabolism (5 papers) and Analytical Chemistry and Chromatography (4 papers). The work is most often cited by research in Clinical Biochemistry (1.3k citations), Biochemistry (261 citations), Molecular Biology (2.2k citations), Biological Psychiatry (55 citations) and Physiology (404 citations). A.J.M. Janssen has collaborated with scholars based in Netherlands, Germany and Belgium. Frequent co-authors include R. C. A. Sengers, J. M. F. Trijbels, W. Ruitenbeek, Jan Smeıtınk, Johan Fischer, Richard J. Rodenburg, Frans J.M. Trijbels, Ad M. Stadhouders, Jacques H. Veerkamp and J.A. Berden. Their work appears in journals such as Journal of Inherited Metabolic Disease, European Journal of Pediatrics, Clinica Chimica Acta, Clinical Chemistry and Pediatric Research.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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