Lambert van den Heuvel

5.3k citations

62 papers · 3.6k indexed · 1 hit paper · h-index 29

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders 30
Molecular Biology top 2%
- Mitochondrial Function and Pathology 37
- ATP Synthase and ATPases Research 22
- RNA modifications and cancer 8
Biochemistry top 2%
- Amino Acid Enzymes and Metabolism 5
Aging top 10%
Nephrology top 5%
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 5
Pathology and Forensic Medicine
- Biomedical Research and Pathophysiology 5
Immunology
- Complement system in diseases 5

Co-authors: Jan Smeitink Jan Smeıtınk S. DiMauro Frans J.M. Trijbels Roel Smeets Jan Loeffen R. C. A. Sengers Elena Levtchenko
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: SHILAP Revista de lepidopterología (1 paper)Nature Reviews Genetics (1 paper)Brain (1 paper)
Partner nations: Netherlands Belgium Germany

In The Last Decade

Lambert van den Heuvel

59 papers receiving 3.5k citations

Hit Papers

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Peers

Countries citing papers authored by Lambert van den Heuvel

Since Specialization

Citations

This map shows the geographic impact of Lambert van den Heuvel'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 Lambert van den Heuvel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lambert van den Heuvel more than expected).

Fields of papers citing papers by Lambert van den Heuvel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lambert van den Heuvel. 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 Lambert van den Heuvel. The network helps show where Lambert van den Heuvel may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Lambert van den Heuvel, 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 Lambert van den Heuvel Line = papers co-authored together Lambert van den Heuvel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Plasma chitotriosidase enzyme activity as a novel therapeutic monitor for cysteamine treatment in nephropathic cystinosis: A retrospective validation study Molecular Genetics and Metabolism ·Koenraad Veys,Mohamed A. Elmonem,Lambert van den Heuvel,William A. Gahl,Elena Levtchenko	2024	2
2	Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies Clinical Journal of the American Society of Nephrology ·Alexis Wérion,Pauline Storms,Ysaline Zizi,Claire Beguin,J. A. Bernards,J Cambier,Karin Dahan,Daan Dierickx,Nathalie Godefroid,Pascale Hilbert,Catherine Lambert,Elena Levtchenko,Thomas Meyskens,Xavier Poiré,Lambert van den Heuvel,Kathleen Claes,Johann Morelle,(unknown)	2023	12
3	Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy—A Case Report Frontiers in Neurology ·Aziza Miriam Belkheir,Janine Reunert,Christiane Elpers,Lambert van den Heuvel,Richard J. Rodenburg,Anja Seelhöfer,Stephan Rust,Astrid Jeibmann,Michael Frosch,Thorsten Marquardt	2021	5
4	CTNS mRNA molecular analysis revealed a novel mutation in a child with infantile nephropathic cystinosis: a case report BMC Nephrology ·Svetlana Papizh,Victoria Serzhanova,Alexandra Filatova,Mikhail Skoblov,Vyacheslav Tabakov,Lambert van den Heuvel,Elena Levtchenko,Larisa Prikhodina	2019	3
5	Occurrence of atypical HUS associated with influenza B European Journal of Pediatrics ·Karen van Hoeve,Corinne Vandermeulen,Marc Van Ranst,Elena Levtchenko,Lambert van den Heuvel,Djalila Mekahli	2017	15
6	Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation eLife ·Bianca Hartmann,Timothy Wai,Hao Hu,Thomas MacVicar,Luciana Musante,Björn Fischer‐Zirnsak,Werner Stenzel,Ralph Gräf,Lambert van den Heuvel,Hans-Hilger Ropers,Thomas F Wienker,Christoph Hübner,Thomas Langer,Angela M. Kaindl	2016	96
7	Novel biomarker and easy to perform ELISA for monitoring complement inhibition in patients with atypical hemolytic uremic syndrome treated with eculizumab Journal of Immunological Methods ·Magdalena Riedl,Johannes Hofer,Thomas Giner,Alejandra Rosales,Karsten Häffner,Giacomo D. Simonetti,Ulrike Walden,Tanja Maier,Dorothea Heininger,Verena Jeller,Günter Weiß,Lambert van den Heuvel,Lothar Bernd Zimmerhackl,Reinhard Würzner,Therese Jungraithmayr	2016	8
8	B4GALT1-Congenital Disorders of Glycosylation Presents as a Non-Neurologic Glycosylation Disorder with Hepatointestinal Involvement The Journal of Pediatrics ·Maïlys Guillard,Éva Morava,Jorg C. de Ruijter,Tony Roscioli,Johann Penzien,Lambert van den Heuvel,Michèl A.A.P. Willemsen,Arjan de Brouwer,Olaf A. Bodamer,Ron A. Wevers,Dirk J. Lefeber	2011	15
9	Genetic basis of cystinosis in Turkish patients: a single-center experience Pediatric Nephrology ·Rezan Topaloğlu,Thierry Vilboux,Turgay Coşkun,Fatih Özaltın,Brad Tinloy,Meral Gunay‐Aygun,Ayşı̇n Bakkaloğlu,Nesrin Beşbaş,Lambert van den Heuvel,Robert Kleta,William A. Gahl	2011	39
10	Functional consequences of mitochondrial tRNATrp and tRNAArg mutations causing combined OXPHOS defects European Journal of Human Genetics ·P. Smits,Sandy Mattijssen,Éva Morava,Mariël van den Brand,Frans van den Brandt,Frits A. Wijburg,Ger J.M. Pruijn,Jan Smeıtınk,Leo Nijtmans,Richard J. Rodenburg,Lambert van den Heuvel	2009	29
11	Shiga-toxin-induced firm adhesion of human leukocytes to endothelium is in part mediated by heparan sulfate Nephrology Dialysis Transplantation ·Joyce Geelen,F Valsecchi,T. van der Velden,Lambert van den Heuvel,L.A.H. Monnens,Marina Morigi	2008	5
12	Encephalomyopathy and optic atrophy with tall stature and mitochondrial dysfunction: a new syndrome Clinical Dysmorphology ·Éva Morava,Ernie M.H.F. Bongers,Wolfram Kreß,L.T.L. Sie,Richard J. Rodenburg,Lambert van den Heuvel,Han G. Brunner	2007	1
13	Induction of Glomerular Heparanase Expression in Rats with Adriamycin Nephropathy Is Regulated by Reactive Oxygen Species and the Renin-Angiotensin System Journal of the American Society of Nephrology ·Andrea B. Kramer,Mabel van den Hoven,Angelique L. Rops,Tessa J.M. Wijnhoven,Lambert van den Heuvel,Joost F.M. Lensen,Toin van Kuppevelt,Harry van Goor,Johan van der Vlag,Gerjan Navis,Jo H. M. Berden	2006	72
14	Cell Biological Consequences of Mitochondrial NADH: Ubiquinone Oxidoreductase Deficiency Current Neurovascular Research ·Jan Smeıtınk,Lambert van den Heuvel,Werner J.H. Koopman,Leo Nijtmans,Cristina Ugalde,Peter H.G.M. Willems	2004	48
15	CIA30 complex I assembly factor: a candidate for human complex I deficiency? Human Genetics ·Rolf J. R. J. Janssen,Jan Smeıtınk,Roel Smeets,Lambert van den Heuvel	2002	57
16	The genetics and pathology of oxidative phosphorylationbreakdown → Nature Reviews Genetics ·Jan Smeitink,Lambert van den Heuvel,S. DiMauro	2001	545
17	Human Mitochondrial Complex I in Health and Disease The American Journal of Human Genetics ·Jan Smeıtınk,Lambert van den Heuvel	1999	119
18	Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit The American Journal of Human Genetics ·Lambert van den Heuvel,W. Ruitenbeek,Roel Smeets,Z Gelman-Kohan,Orly Elpeleg,Jan Loeffen,Frans J.M. Trijbels,Edwin C.M. Mariman,Diederik de Bruijn,Jan Smeıtınk	1998	224
19	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,Edwin M. Mariman,R. C. A. Sengers,F. Trijbels,Lambert van den Heuvel	1998	16
20	cDNA Sequence and Chromosomal Localization of the Remaining Three Human Nuclear Encoded Iron Sulphur Protein (IP) Subunits of Complex I: The Human IP Fraction Is Completed Biochemical and Biophysical Research Communications ·Jan Loeffen,Lambert van den Heuvel,Roel Smeets,Ralf Triepels,R. C. A. Sengers,Frans J.M. Trijbels,Jan Smeıtınk	1998	19

About Lambert van den Heuvel

Lambert van den Heuvel is a scholar working on Clinical Biochemistry, Biochemistry and Nephrology, having authored 62 papers that have together received 3.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (30 papers), ATP Synthase and ATPases Research (22 papers), RNA modifications and cancer (8 papers), Amino Acid Enzymes and Metabolism (5 papers), Neonatal Health and Biochemistry (5 papers), Biomedical Research and Pathophysiology (5 papers) and Complement system in diseases (5 papers). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Molecular Biology (2.9k citations) and Biochemistry (205 citations). Lambert van den Heuvel has collaborated with scholars based in Netherlands, Belgium and Germany. Frequent co-authors include Jan Smeitink, Jan Smeıtınk, S. DiMauro, Frans J.M. Trijbels, Roel Smeets, Jan Loeffen, R. C. A. Sengers, Elena Levtchenko, Richard J. Rodenburg and P. Smits. Their work appears in journals such as SHILAP Revista de lepidopterología, Nature Reviews Genetics and Brain.

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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