I. E. M. Luyt‐Houwen

1.8k total citations · 1 hit paper
26 papers, 1.1k citations indexed

About

I. E. M. Luyt‐Houwen is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, I. E. M. Luyt‐Houwen has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Clinical Biochemistry, 21 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in I. E. M. Luyt‐Houwen's work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (20 papers) and Coenzyme Q10 studies and effects (4 papers). I. E. M. Luyt‐Houwen is often cited by papers focused on Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (20 papers) and Coenzyme Q10 studies and effects (4 papers). I. E. M. Luyt‐Houwen collaborates with scholars based in Netherlands, Belgium and United States. I. E. M. Luyt‐Houwen's co-authors include H.R. Scholte, J.A. Berden, M.A. Sobotka-Plojhar, J.J. van der Harten, J. M. van der Klei‐van Moorsel, P. G. Barth, H. F. M. Busch, H. R. Scholte, Hildegard Przyrembel and W.F.M. Arts and has published in prestigious journals such as Neurology, FEBS Letters and Annals of the New York Academy of Sciences.

In The Last Decade

I. E. M. Luyt‐Houwen

26 papers receiving 1.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1983 548 citations P. G. Barth, H.R. Scholte et al. Journal of the Neurological Sciences profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
I. E. M. Luyt‐Houwen Netherlands	14	866	564	120	120	83	26	1.1k
J. M. van der Klei‐van Moorsel Netherlands	9	586 0.7×	254 0.5×	102 0.8×	110 0.9×	50 0.6×	10	786
Marion Paturneau-Jouas France	14	550 0.6×	263 0.5×	46 0.4×	171 1.4×	72 0.9×	29	788
M. Rimoldi Italy	21	1.2k 1.3×	892 1.6×	117 1.0×	213 1.8×	183 2.2×	58	1.6k
C. Jakobs Netherlands	17	680 0.8×	621 1.1×	44 0.4×	223 1.9×	171 2.1×	39	1.1k
Y. Goto Japan	10	859 1.0×	431 0.8×	278 2.3×	126 1.1×	75 0.9×	23	1.2k
Shoji Yano United States	17	386 0.4×	269 0.5×	121 1.0×	166 1.4×	107 1.3×	57	858
Diane S. Roe United States	19	811 0.9×	913 1.6×	53 0.4×	365 3.0×	35 0.4×	27	1.2k
A. A. M. Morris United Kingdom	17	613 0.7×	529 0.9×	21 0.2×	254 2.1×	58 0.7×	27	1.0k
H. R. Scholte Netherlands	13	370 0.4×	293 0.5×	34 0.3×	66 0.6×	35 0.4×	17	495
S. Lane Rutledge United States	19	844 1.0×	519 0.9×	31 0.3×	104 0.9×	295 3.6×	31	1.3k

Countries citing papers authored by I. E. M. Luyt‐Houwen

Since Specialization

Citations

This map shows the geographic impact of I. E. M. Luyt‐Houwen'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 I. E. M. Luyt‐Houwen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. E. M. Luyt‐Houwen more than expected).

Fields of papers citing papers by I. E. M. Luyt‐Houwen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I. E. M. Luyt‐Houwen. 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 I. E. M. Luyt‐Houwen. The network helps show where I. E. M. Luyt‐Houwen may publish in the future.

Co-authorship network of co-authors of I. E. M. Luyt‐Houwen

This figure shows the co-authorship network connecting the top 25 collaborators of I. E. M. Luyt‐Houwen. A scholar is included among the top collaborators of I. E. M. Luyt‐Houwen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with I. E. M. Luyt‐Houwen. I. E. M. Luyt‐Houwen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Scholte, H. R., H. F. M. Busch, H. D. Bakker, et al.. (1995). Riboflavin-responsive complex I deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1271(1). 75–83. 71 indexed citations

2.

Scholte, H.R., John D. Ross, W. Blom, et al.. (1992). Assessment of deficiencies of fatty acyl‐CoA dehydrogenases in fibroblasts, muscle and liver. Journal of Inherited Metabolic Disease. 15(3). 347–352. 14 indexed citations

3.

Scholte, H.R., Etienne Agsteribbe, H. F. M. Busch, et al.. (1990). Oxidative phosporylation in human muscle in patients with ocular myopathy and after general anaesthesia. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1018(2-3). 211–216. 9 indexed citations

4.

Martin, Jean‐Jacques, et al.. (1988). Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia. Journal of the Neurological Sciences. 84(2-3). 189–200. 27 indexed citations

5.

Pereira, Rob Rodrigues, et al.. (1988). Cardiomyopathy associated with carnitine loss in kidneys and small intestine. European Journal of Pediatrics. 148(3). 193–197. 26 indexed citations

6.

Scholte, H.R., et al.. (1987). The role of the carnitine system in myocardial fatty acid oxidation: carnitine deficiency, failing mitochondria and cardiomyopathy. Steinkopff eBooks. 82 Suppl 1. 63–73. 22 indexed citations

7.

Bär, P.R., et al.. (1987). A striking correlation between muscle damage after exercise and mitochondrial dysfunction in patients with chronic external ophthalmoplegia. Journal of Inherited Metabolic Disease. 10(S2). 252–255. 12 indexed citations

8.

Arts, W.F.M., H.R. Scholte, Maarten J. J. E. Loonen, et al.. (1987). Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy. Journal of the Neurological Sciences. 77(1). 103–115. 48 indexed citations

9.

Scholte, H.R., et al.. (1986). Biochemical Criteria for NADH-CoQ Reductase Deficiency. Annals of the New York Academy of Sciences. 488(1 Membrane Path). 513–516. 1 indexed citations

10.

Visser, Marianne de, H. R. Scholte, R. B. H. Schutgens, et al.. (1986). Riboflavin‐responsive lipid‐storage myopathy and glutaric aciduria type II of early adult onset. Neurology. 36(3). 367–367. 44 indexed citations

11.

Scholte, H.R., I. E. M. Luyt‐Houwen, W. Blom, et al.. (1986). Defects in Mitochondrial Beta Oxidation. Annals of the New York Academy of Sciences. 488(1 Membrane Path). 511–512. 1 indexed citations

12.

Scholte, H.R., et al.. (1986). Biochemical Criteria for NADH-CoQ Reductase Deficiency. Annals of the New York Academy of Sciences. 488(1 Membrane Path). 513–516. 2 indexed citations

13.

Scholte, H.R., et al.. (1986). The source of malonyl‐CoA in rat heart. FEBS Letters. 198(1). 47–50. 23 indexed citations

14.

Scholte, H.R., I. E. M. Luyt‐Houwen, W. Blom, et al.. (1986). Defects in Mitochondrial Beta Oxidation. Annals of the New York Academy of Sciences. 488(1 Membrane Path). 511–512. 1 indexed citations

15.

Busch, H. F. M., H.R. Scholte, & I. E. M. Luyt‐Houwen. (1986). Mitochondrial Myopathy due to Complex I Deficiency:.. Annals of the New York Academy of Sciences. 488(1 Membrane Path). 523–524. 1 indexed citations

16.

Acker, K. Van, et al.. (1986). Benign Mitochondrial Myopathy with Deficiency of NADH-CoQ Reductase and Cytochrome c Oxidase. Neuropediatrics. 17(4). 221–226. 34 indexed citations

17.

Scholte, H.R., I. E. M. Luyt‐Houwen, & H. F. M. Busch. (1985). Difficulties in assessing biochemical properties of abnormal muscle mitochondria. Journal of Inherited Metabolic Disease. 8(S2). 149–150. 11 indexed citations

18.

Giesberts, M. A. H., H. H. van Gelderen, H.R. Scholte, et al.. (1984). Glutaric Aciduria Type II: Multiple Defects in Isolated Muscle Mitochondria and Deficient β-Oxidation in Fibroblasts. PubMed. 7 Suppl 2. 101–102. 14 indexed citations

19.

Barth, P. G., H.R. Scholte, J.A. Berden, et al.. (1983). An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. Journal of the Neurological Sciences. 62(1-3). 327–355. 548 indexed citations breakdown →

20.

Scholte, H. R., H. F. M. Busch, & I. E. M. Luyt‐Houwen. (1981). Familial AMP deaminase deficiency with skeletal muscle type I atrophy and fatal cardiomyopathy. Journal of Inherited Metabolic Disease. 4(1). 169–170. 19 indexed citations

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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