P. A. Bolhuis

2.9k citations

60 papers · 2.1k indexed · 1 hit paper · h-index 24

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 15
Hematology top 2%
- Platelet Disorders and Treatments 8
Molecular Biology top 10%
- Mitochondrial Function and Pathology 13
- Muscle Physiology and Disorders 8
- ATP Synthase and ATPases Research 6
Genetics top 10%
Internal Medicine top 10%
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 9
Pulmonary and Respiratory Medicine
- Blood properties and coagulation 5
Cell Biology
- Muscle metabolism and nutrition 5

Co-authors: J J Sixma Kjell S. Sakaríassen Roelof‐Jan Oostra Bernard A. van Oost P. G. Barth E. M. Bleeker‐Wagemakers Frits A. Wijburg Anneke J. van der Kooi
Cited by: Clinical Biochemistry Hematology Molecular Biology
Journals: Nature (1 paper)The Lancet (1 paper)Nucleic Acids Research (1 paper)
Partner nations: Netherlands France United States

In The Last Decade

P. A. Bolhuis

59 papers receiving 1.9k citations

Hit Papers

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Peers

Countries citing papers authored by P. A. Bolhuis

Since Specialization

Citations

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

Fields of papers citing papers by P. A. Bolhuis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside P. A. Bolhuis, 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 P. A. Bolhuis Line = papers co-authored together P. A. Bolhuis links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic Neuropathy The American Journal of Human Genetics ·Neil Howell,Roelof‐Jan Oostra,P. A. Bolhuis,Liesbeth Spruijt,L. Clarke,David A. Mackey,Gwen Preston,Corinna Herrnstadt	2003	91
2	Effects of 2,5-hexanedione on calpain-mediated degradation of human neurofilaments in vitro Chemico-Biological Interactions ·Elisabeth Heijink,Sander W Scholten,P. A. Bolhuis,Frederik A. de Wolff	2000	14
3	Action of lovastatin, simvastatin, and pravastatin on sterol synthesis and their antiproliferative effect in cultured myoblasts from human striated muscle Biochemical Pharmacology ·Arlène K. van Vliet,Pascale Nègre‐Aminou,Gerald Thiel,P. A. Bolhuis,Louis Cohen	1996	34
4	The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands Brain ·Anneke J. van der Kooi,P. G. Barth,H. F. M. Busch,Rob de Haan,H.B. Ginjaar,A. J. van Essen,L. J. M. A. van Hooff,C Höweler,F.G.I. Jennekens,Peter Joseph Jongen,Harry Oosterhuis,G.W. Padberg,Frank Spaans,Axel R. Wintzen,John H. J. Wokke,Egbert Bakker,G.J.B. van Ommen,P. A. Bolhuis,Marianne de Visser	1996	67
5	CMT1B : Heterogeneous nerve morphology Aktuelle Neurologie ·A.A.W.M. Gabreëls‐Festen,Jessica E. Hoogendijk,Edwin C.M. Mariman,P. A. Bolhuis,Baziel G.M. van Engelen,P.H.S. Meijerink,F.J.M. Gabreëls	1995	1
6	The Mitochondrial DNA Mutation ND614,484C Associated with Leber Hereditary Optic Neuropathy, Leads to Deficiency of Complex I of the Respiratory Chain Biochemical and Biophysical Research Communications* ·Roelof‐Jan Oostra,M.J.M. Vangalen,P. A. Bolhuis,E. M. Bleeker‐Wagemakers,C. Vandenbogert	1995	35
7	Identification of a Two Base Pair Deletion in Five Unrelated Families with Adrenoleukodystrophy: A Possible Hot Spot for Mutations Biochemical and Biophysical Research Communications ·Stephan Kemp,M.J.L. Ligtenberg,B.M. Vangeel,P. G. Barth,Ruud A. Wolterman,F. Schoute,Claude‐Olivier Sarde,Jean‐Louis Mandel,B.A. Vanoost,P. A. Bolhuis	1994	68
8	Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome. Journal of Medical Genetics ·Roelof‐Jan Oostra,P. A. Bolhuis,Frits A. Wijburg,G Zorn-Ende,E. M. Bleeker‐Wagemakers	1994	100
9	Mitochondrial DNA Analysis as a Diagnostic Tool in Singleton Cases of Leber's Hereditary Optic Neuropathy Ophthalmic Paediatrics and Genetics ·Roelof‐Jan Oostra,P. A. Bolhuis,E. M. Bleeker‐Wagemakers	1993	5
10	Steady-state transcript levels of cytochrome c oxidase genes during human myogenesis indicate subunit switching of subunit VIa and co-expression of subunit VIIa isoforms Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jan‐Willem Taanman,Nicole H. Herzberg,H. de Vries,P. A. Bolhuis,Coby Van den Bogert	1992	42
11	Metallothionein in Menkes' disease: Induction in cultured muscle cells Journal of the Neurological Sciences ·Nicole H. Herzberg,Ruud A. Wolterman,G.J. van den Berg,P. G. Barth,P. A. Bolhuis	1990	9
12	An unusual variant of Becker muscular dystrophy Annals of Neurology ·Marjolein Visser,Egbert Bakker,Joep C. Defesche,P. A. Bolhuis,G J van Ommen	1990	16
13	Nucleotide sequence of cDNA encoding subunit VIb of human cytochromecoxidase Nucleic Acids Research ·Jan‐Willem Taanman,Cobi Schrage,Nico J. Ponne,P. A. Bolhuis,H. de Vries,Etienne Agsteribbe	1989	23
14	Regional localization of the gene for thyroid peroxidase to human chromosome 2pter→p12 Cytogenetic and Genome Research ·Jan J. M. de Vijlder,Christiane Dinsart,Frédérick Libert,Geurts van Kessel,Hennie Bikker,P. A. Bolhuis,Gilbert Vassart	1988	27
15	The spectral stability of several sunscreening agents on stratum corneum sheets International Journal of Cosmetic Science ·Arthur Kammeyer,W. Westerhof,P. A. Bolhuis,A. J. Ris,E A Hische	1987	18
16	Collagen synthesis in cultured myoblasts and myotubes from patients with Duchenne muscular dystrophy Journal of the Neurological Sciences ·Luitzen de Jong,Ruud A. Wolterman,Sicco Hillarius,P. A. Bolhuis	1987	7
17	Breakdown of lysosomal glycogen in cultured fibroblasts from glycogenosis type II patients after uptake of acid α-glucosidase Journal of the Neurological Sciences ·Ans T. van der Ploeg,Marian A. Kroos,J.M. van Dongen,W.J. Visser,P. A. Bolhuis,Maarten J. J. E. Loonen,Arnold Reuser	1987	25
18	Clinical Neurology and Neurosurgery ·P. A. Bolhuis	1986	2
19	The Relationship Between The Multimeric Structure Of F VIII-VWF And The Facilitation Of Platelet Adhesion To Human Subendothelium (Von Willebrand Factor Activity VWF-A) Thrombosis and Haemostasis ·Jan J. Sixma,Kjell S. Sakaríassen,P. A. Bolhuis	1981	2
20	Physicochemical Characteristics of the Human Factor VIII-Von Willebrand Factor Oligomers Thrombosis and Haemostasis ·P. A. Bolhuis,A. J. Seinen,I. A. Mochtar	1977	3

About P. A. Bolhuis

P. A. Bolhuis is a scholar working on Clinical Biochemistry, Hematology and Cellular and Molecular Neuroscience, having authored 60 papers that have together received 2.1k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (13 papers), Genetic Neurodegenerative Diseases (9 papers), Muscle Physiology and Disorders (8 papers), Platelet Disorders and Treatments (8 papers), ATP Synthase and ATPases Research (6 papers), Blood properties and coagulation (5 papers) and Muscle metabolism and nutrition (5 papers). The work is most often cited by research in Clinical Biochemistry (335 citations), Hematology (548 citations) and Molecular Biology (1.2k citations). P. A. Bolhuis has collaborated with scholars based in Netherlands, France and United States. Frequent co-authors include J J Sixma, Kjell S. Sakaríassen, Roelof‐Jan Oostra, Bernard A. van Oost, P. G. Barth, E. M. Bleeker‐Wagemakers, Frits A. Wijburg, Anneke J. van der Kooi, Marianne de Visser and G.W. Bruyn. Their work appears in journals such as Nature, The Lancet and Nucleic Acids 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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