Frans J.M. Trijbels

8.6k citations

77 papers · 6.8k indexed · 3 hit papers · h-index 38

Rheumatology top 0.1%
- Folate and B Vitamins Research 24
Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders 28
Hematology top 1%
Obstetrics and Gynecology top 1%
Pediatrics, Perinatology and Child Health top 1%
Molecular Biology
- Mitochondrial Function and Pathology 31
- ATP Synthase and ATPases Research 18
- Biochemical and Molecular Research 10
Surgery
- Esophageal and GI Pathology 15
Public Health, Environmental and Occupational Health
- Acute Lymphoblastic Leukemia research 8
Epidemiology
- Cytomegalovirus and herpesvirus research 6

Co-authors: Henk J. Blom Jan Smeıtınk N.M.J. van der Put Lambert P. van den Heuvel T.K.A.B. Eskes Godfried H.J. Boers F. Gabreëls R. C. A. Sengers
Cited by: Rheumatology Clinical Biochemistry Hematology
Journals: Clinical Chemistry (7 papers)Annals of Neurology (6 papers)The American Journal of Human Genetics (5 papers)
Partner nations: Netherlands Germany United States

In The Last Decade

Frans J.M. Trijbels

76 papers receiving 6.6k citations

Hit Papers

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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.

1998 The American Journal of Human Genetics
1996 PubMed
1985 New England Journal of Medicine

Peers

Countries citing papers authored by Frans J.M. Trijbels

Since Specialization

Citations

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

Fields of papers citing papers by Frans J.M. Trijbels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frans J.M. Trijbels. 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 Frans J.M. Trijbels. The network helps show where Frans J.M. Trijbels may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Frans J.M. Trijbels, 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 Frans J.M. Trijbels Line = papers co-authored together Frans J.M. Trijbels links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	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
2	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
3	Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency New England Journal of Medicine ·Marieke J. H. Coenen,Hana Antonická,Cristina Ugalde,Florin Sasarman,William H. Andrews,J. G. A. M. Heister,Robert F. Newbold,Frans J.M. Trijbels,Lambert P. van den Heuvel,Eric A. Shoubridge,Jan Smeıtınk	2004	152
4	Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene Annals of Neurology ·Marieke J. H. Coenen,Lambert P. van den Heuvel,Cristina Ugalde,Bad Ems,Leo Nijtmans,Frans J.M. Trijbels,Skadi Beblo,Esther M. Maier,Ania C. Muntau,Jan Smeıtınk	2004	41
5	Cystathionine β-synthase polymorphisms and hyperhomocysteinaemia: an association study European Journal of Human Genetics ·Karin J.A Lievers,Leo A. J. Kluijtmans,Sandra G. Heil,Godfried H.J. Boers,Petra Verhoef,Martin den Heijer,Frans J.M. Trijbels,Henk J. Blom	2003	17
6	Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation European Journal of Pediatrics ·Olga Grafakou,Konrad Oexle,Lambert van den Heuvel,Roel Smeets,Frans J.M. Trijbels,Hans H. Goebel,N. U. Bosshard,Andrea Superti‐Furga,Beat Steinmann,Jan Smeitink	2003	44
7	6-Mercaptopurine: Efficacy and Bone Marrow Toxicity in Childhood Acute Lymphoblastic Leukemia Advances in experimental medicine and biology ·Ronney A. De Abreu,Lambert H.J. Lambooy,Candy Esmeralda Hernández Bravo,C. Brouwer,Milena Franco da Silva,Jos P.M. Bökkerink,Frans J.M. Trijbels	2002	3
8	Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C→T) on plasma homocysteine, folate and vitamin B12 levels and its relationship to cardiovascular disease risk Atherosclerosis ·Karin J.A Lievers,Leo A. J. Kluijtmans,Godfried H.J. Boers,Petra Verhoef,Martin den Heijer,Frans J.M. Trijbels,Henk J. Blom	2002	49
9	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
10	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
11	Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome Annals of Neurology ·Paul De Bryas Dexmiers D'archiacchiac,Luigi Palmieri,Marjan Huizing,Lambert P. van den Heuvel,R. C. A. Sengers,Andrea Dörner,W. Ruitenbeek,Frans J.M. Trijbels,Wenyan Hou,Gunnlaugur Sigfússon,Ferdinando Palmieri,Jan Smeıtınk	2002	70
12	Human NADH:Ubiquinone Oxidoreductase Journal of Bioenergetics and Biomembranes ·Jan Smeitink,R. C. A. Sengers,Frans J.M. Trijbels,Lambert van den Heuvel	2001	100
13	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
14	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
15	The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients Human Genetics ·Ralf Triepels,Lambert van den Heuvel,Jan Loeffen,Roel Smeets,Frans J.M. Trijbels,Jan Smeitink	1998	18
16	Rapid and Reliable Measurement of Highly Elevated Blood Ammonia Concentrations in Children Clinical Chemistry and Laboratory Medicine (CCLM) ·Marinus H. de Keijzer,Bernadette S. Jakobs,Agrawal Yo,Faiza,Frans J.M. Trijbels,Jan A. M. Smeitink	1997	5
17	Decreased methylene tetrahydrofolate reductase activity due to the 677C→T mutation in families with spina bifida offspring Journal of Molecular Medicine ·N.M.J. van der Put,Lambertus P. van den Heuvel,Régine P.M. Steegers‐Theunissen,Frans J.M. Trijbels,T.K.A.B. Eskes,Edwin C.M. Mariman,Michelle Heyer,Henk J. Blom	1996	120
18	Prevention of neural tube defects by and toxicity of L‐homocysteine in cultured postimplantation rat embryos Teratology ·C Tomlinson,Henk J. Blom,Ronney A. De Abreu,Frans J.M. Trijbels,T.K.A.B. Eskes,J.H.J. Copius Peereboom‐Stegeman,J. Noordhoek	1994	95
19	The importance of methylthio-IMP for methylmercaptopurine ribonucleoside (Me-MPR) cytotoxicity in Molt F4 human malignant T-lymphoblasts Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Cuadrado Mspas,Devrim Sönmez,Ronney A. De Abreu,Jos P.M. Bökkerink,Lambert H.J. Lambooy,Frans J.M. Trijbels	1993	57
20	Reference values for amino acids in cerebrospinal fluid of children determined using ion-exchange chromatography with fluorimetric detection Clinica Chimica Acta ·G. P. J. M. Gerrits,Frans J.M. Trijbels,L.A.H. Monnens,F.J.M. Gabreëls,Ronney A. De Abreu,Ad Theeuwes,土田定雄	1989	35

About Frans J.M. Trijbels

Frans J.M. Trijbels is a scholar working on Clinical Biochemistry, Rheumatology and Transplantation, having authored 77 papers that have together received 6.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (28 papers), Folate and B Vitamins Research (24 papers), ATP Synthase and ATPases Research (18 papers), Esophageal and GI Pathology (15 papers), Biochemical and Molecular Research (10 papers), Acute Lymphoblastic Leukemia research (8 papers) and Cytomegalovirus and herpesvirus research (6 papers). The work is most often cited by research in Rheumatology (3.6k citations), Clinical Biochemistry (1.5k citations) and Hematology (956 citations). Frans J.M. Trijbels has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Henk J. Blom, Jan Smeıtınk, N.M.J. van der Put, Lambert P. van den Heuvel, T.K.A.B. Eskes, Godfried H.J. Boers, F. Gabreëls, R. C. A. Sengers, Leo A. J. Kluijtmans and Lambert van den Heuvel. Their work appears in journals such as Clinical Chemistry, Annals of Neurology, The American Journal of Human Genetics, Human Genetics and Clinica Chimica Acta.

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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