Frans A. Hol

2.4k citations

41 papers · 1.6k indexed · h-index 21

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Rheumatology top 5%
- Folate and B Vitamins Research

Papers in

Clinical Biochemistry 10
- Metabolism and Genetic Disorders 10
Genetics 13
- Genetics and Neurodevelopmental Disorders 5

Co-authors: Edwin C.M. Mariman Jan Smeıtınk Richard J. Rodenburg Ben C.J. Hamel Lambertus P. van den Heuvel M.P.A. Geurds Éva Morava Marije Hogeveen
Journals: Journal of Medical Genetics (5 papers)European Journal of Human Genetics (4 papers)Journal of Inherited Metabolic Disease (2 papers)Human Genetics (2 papers)Human Mutation (2 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Frans A. Hol

39 papers receiving 1.6k citations

Peers

Countries citing papers authored by Frans A. Hol

Since Specialization

Citations

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

Fields of papers citing papers by Frans A. Hol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frans A. Hol. 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 A. Hol. The network helps show where Frans A. Hol may publish in the future.

Co-authors

The 25 scholars most cited alongside Frans A. Hol, 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 A. Hol Line = papers co-authored together Frans A. Hol 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	Genotype-phenotype correlations in MYCN-related Feingold syndrome Human Mutation ·Carlo Marcelis, Frans A. Hol, Gail E. Graham, Paul N.M.A. Rieu, Richárd Kellermayer, Rowdy Meijer, Dorien Lugtenberg, Hans Scheffer, Hans van Bokhoven, Han G. Brunner, Arjan P.M. de Brouwer	2008	60
3	Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib‐pair collection American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Carolien G. F. de Kovel, Barbara Franke, Frans A. Hol, Jérémie Lebrec, Ben Maassen, Han G. Brunner, George W. Padberg, Jill Platko, David L. Pauls	2007	26
4	Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene Annals of Neurology ·Marcel M. Verbeek, Gerry C. H. Steenbergen‐Spanjers, Michèl A.A.P. Willemsen, Frans A. Hol, Jan Smeitink, Jürgen Seeger, Padraic J. Grattan‐Smith, Monique M. Ryan, Georg F. Hoffmann, Maria Alice Donati, Nenad Blau, Ron A. Wevers	2007	19
5	Resting muscle pain as the first clinical symptom in children carrying the MTTK A8344G mutation European Journal of Paediatric Neurology ·Hudson, Maaike de Vries, Richard J. Rodenburg, Frans A. Hol, Jan Smeıtınk, Éva Morava	2007	14
6	The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White European Journal of Human Genetics ·David Bacher, Yayat Dimyati, Christa van den Elzen, Baziel G.M. van Engelen, Jan Smeıtınk, Richard J. Rodenburg, Frans A. Hol	2006	48
7	Mitochondrial dysfunction in Stüve–Wiedemann syndrome in a patient carrying an ND1 gene mutation American Journal of Medical Genetics Part A ·Éva Morava, Ben C.J. Hamel, Frans A. Hol, Richard J. Rodenburg, Jan Smeıtınk	2006	9
8	Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family Journal of Medical Genetics ·Carolien G. F. de Kovel, Frans A. Hol, J. G. A. M. Heister, О. Л. Зимина, L. Sandkuijl, Barbara Franke, George W. Padberg	2004	57
9	Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis Nephrology Dialysis Transplantation ·Marije M. Löwik, Frans A. Hol, E. J. Steenbergen, Jack F.M. Wetzels, Lambertus P. van den Heuvel	2004	66
10	Genetic variants in ZIC1, ZIC2, and ZIC3 are not major risk factors for neural tube defects in humans American Journal of Medical Genetics Part A ·Riko Klootwijk, Alexánder Acosta Jurado, Mascha M.V.A.P. Schijvenaars, Frans A. Hol, Ben C.J. Hamel, Huub Straatman, Régine P.M. Steegers‐Theunissen, Edwin C.M. Mariman, Barbara Franke	2003	20
11	Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes Genomics ·Frans A. Hol, Marga Schepens, Sylvia E. C. van Beersum, S. J. Lowry, Maurizio Affer, Paolo Vezzoni, Ben C.J. Hamel, Pamela S. Karnes, Edwin C.M. Mariman, Ileana Zucchi	2000	53
12	Nail-Patella Syndrome Journal of the American Society of Nephrology ·Nine V.A.M. Knoers, Ernie M.H.F. Bongers, Sylvia E. C. van Beersum, 茂弥植松, Hans van Bokhoven, Frans A. Hol	2000	41
13	Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome European Journal of Human Genetics ·Asli Silahtaroglu, Frans A. Hol, Kyoshi Naruse, Martin Erdel, Hans‐Christoph Duba, M.P.A. Geurds, Nine V.A.M. Knoers, Edwin C.M. Mariman, Zeynep Tümer, Gerd Utermann, Jutta Wirth, Merete Bugge, Niels Tommerup	1999	16
14	Susceptibility to spina bifida; an association study of five candidate genes Annals of Human Genetics ·Katie Morrison, Charalambos Papapetrou, Frans A. Hol, Edwin C.M. Mariman, Sally Ann Lynch, John Burn, Yvonne H. Edwards	1998	95
15	Identification of two PAX3 mutations causing waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X) Human Mutation ·Frans A. Hol, M.P.A. Geurds, Cor W. R. J. Cremers, Ben C.J. Hamel, Edwin C.M. Mariman	1998	7
16	Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate‐dehydrogenase, methenyltetrahydrofolate‐cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects Clinical Genetics ·Frans A. Hol, Earl Edmondson, M.P.A. Geurds, Sandra G. Heil, Frans J.M. Trijbels, Ben C.J. Hamel, Edwin C.M. Mariman, Henk J. Blom	1998	127
17	Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family Human Genetics ·Frans A. Hol, Ben C.J. Hamel, M.P.A. Geurds, I. Hansmann, Sue McNally, Norihito NAKAMICHI, Edwin C.M. Mariman	1995	21
18	Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family Human Genetics ·Frans A. Hol, M.P.A. Geurds, O Jensson, Ben C.J. Hamel, Gudrun E. Moore, Robert Newton, Edwin C.M. Mariman	1994	9
19	Improving the polymorphism content of the 3′ UTR of the human IGF2R gene Human Molecular Genetics ·Frans A. Hol, M.P.A. Geurds, Ben C.J. Hamel, Edwin C.M. Mariman	1992	31
20	Presence of hybridizing DNA sequences homologous to bovine acidic and basicβ-crystallins in all classes of vertebrates Journal of Molecular Evolution ·Gül Köknel Talu, Frans A. Hol, Weixuan Yuan, H. Bloemendal	1991	3

About Frans A. Hol

Frans A. Hol is a scholar working on Clinical Biochemistry, Genetics, Developmental Biology, Molecular Biology and Rheumatology, having authored 41 papers that have together received 1.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (10 papers), ATP Synthase and ATPases Research (9 papers), RNA modifications and cancer (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Folate and B Vitamins Research (5 papers), Cancer-related gene regulation (3 papers) and Kruppel-like factors research (3 papers). The work is most often cited by research in Clinical Biochemistry (357 citations), Rheumatology (285 citations), Molecular Biology (1.0k citations), Genetics (407 citations) and Pediatrics, Perinatology and Child Health (216 citations). Frans A. Hol has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Edwin C.M. Mariman, Jan Smeıtınk, Richard J. Rodenburg, Ben C.J. Hamel, Lambertus P. van den Heuvel, M.P.A. Geurds, Éva Morava, Marije Hogeveen, Maaike C. de Vries and Ineke van der Burgt. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Human Genetics and Human Mutation.

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