P.F. Ippel

1.1k total citations
25 papers, 659 citations indexed

About

P.F. Ippel is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, P.F. Ippel has authored 25 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in P.F. Ippel's work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Muscle Physiology and Disorders (5 papers). P.F. Ippel is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Muscle Physiology and Disorders (5 papers). P.F. Ippel collaborates with scholars based in Netherlands, United States and Germany. P.F. Ippel's co-authors include Richard J. Sinke, F. A. Beemer, G. Hageman, Egbert Bakker, Dick Lindhout, E. R. Brunt, H.P.H. Kremer, Bart P.C. van de Warrenburg, Corien C. Verschuuren‐Bemelmans and Dennis Dooijes and has published in prestigious journals such as Brain, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

P.F. Ippel

24 papers receiving 646 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P.F. Ippel Netherlands	12	486	329	148	121	100	25	659
Andoni Urtizberea France	15	555 1.1×	203 0.6×	72 0.5×	129 1.1×	108 1.1×	27	796
C Höweler Netherlands	13	613 1.3×	496 1.5×	213 1.4×	78 0.6×	161 1.6×	22	976
Claudia Castiglioni Chile	15	320 0.7×	111 0.3×	61 0.4×	99 0.8×	125 1.3×	47	566
D Fontan France	14	271 0.6×	149 0.5×	87 0.6×	67 0.6×	152 1.5×	43	719
T. Voit Germany	13	304 0.6×	109 0.3×	56 0.4×	77 0.6×	50 0.5×	32	547
Nicoletta Checcarelli Italy	14	531 1.1×	71 0.2×	90 0.6×	88 0.7×	96 1.0×	23	731
M Fardeau France	16	680 1.4×	255 0.8×	80 0.5×	179 1.5×	48 0.5×	46	994
G Danieli Italy	10	348 0.7×	137 0.4×	45 0.3×	166 1.4×	42 0.4×	20	487
Janet E. Sowden United States	12	298 0.6×	213 0.6×	184 1.2×	35 0.3×	61 0.6×	23	577
Soledad Monges Argentina	12	360 0.7×	110 0.3×	39 0.3×	135 1.1×	52 0.5×	28	509

Countries citing papers authored by P.F. Ippel

Since Specialization

Citations

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

Fields of papers citing papers by P.F. Ippel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P.F. Ippel

This figure shows the co-authorship network connecting the top 25 collaborators of P.F. Ippel. A scholar is included among the top collaborators of P.F. Ippel 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 P.F. Ippel. P.F. Ippel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Straathof, C.S.M., P.F. Ippel, Jan G. Post, et al.. (2015). Diagnosis of becker muscular dystrophy: Results of Re‐analysis of DNA samples. Muscle & Nerve. 53(1). 44–48. 2 indexed citations

Straathof, C.S.M., P.F. Ippel, Jan G. Post, et al.. (2014). G.P.1. Neuromuscular Disorders. 24(9-10). 794–794.

Gierga, K., Helenius J. Schelhaas, E. R. Brunt, et al.. (2009). Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites. Neuropathology and Applied Neurobiology. 35(5). 515–527. 36 indexed citations

Verbeek, Dineke S., Bart P.C. van de Warrenburg, Frederic A. M. Hennekam, et al.. (2005). Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population. Human Genetics. 117(1). 88–91. 29 indexed citations

Warrenburg, Bart P.C. van de, Richard J. Sinke, Corien C. Verschuuren‐Bemelmans, et al.. (2002). Spinocerebellar ataxias in the Netherlands. Neurology. 58(5). 702–708. 165 indexed citations

Schelhaas, Helenius J., et al.. (2001). Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia. Journal of Neurology. 248(2). 113–120. 46 indexed citations

Schelhaas, Helenius J., P.F. Ippel, F. A. Beemer, & Gregory S. Hageman. (2000). Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxias. European Journal of Neurology. 7(3). 309–314. 19 indexed citations

Valk, P. van der, I. Snoeck, Linda C. Meiners, et al.. (1999). Subcortical Laminar Heterotopia in Two Sisters and Their Mother: MRI, Clinical Findings and Pathogenesis. Neuropediatrics. 30(3). 155–160. 3 indexed citations

Hoogerwaard, Edo M, Poll A. van der Wouw, Arthur A.M. Wilde, et al.. (1999). Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy. Neuromuscular Disorders. 9(5). 347–351. 120 indexed citations

10.

Ippel, P.F., et al.. (1998). Atelencephalic microcephaly: a case report and review of the literature. European Journal of Pediatrics. 157(6). 493–497. 8 indexed citations

11.

Pater, Jennie M., P.F. Ippel, J. B. Bijlsma, & Onno van Nieuwenhuizen. (1997). Interstitial deletion 11q. Case report and review of the literature.. PubMed. 8(4). 335–9. 7 indexed citations

12.

Hageman, G., et al.. (1996). A Dutch family with benign hereditary chorea of early onset: differentiation from Huntington's disease. Clinical Neurology and Neurosurgery. 98(2). 165–170. 9 indexed citations

13.

Dijk, Gert W. van, et al.. (1995). A new variant of sensory ataxic neuropathy with autosomal dominant inheritance. Brain. 118(6). 1557–1563. 8 indexed citations

14.

Ippel, P.F., D. Wittebol‐Post, Bernadette P. M. van Nesselrooij, & J. B. Bijlsma. (1994). Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation a new autosomal recessive disorder?. Ophthalmic Genetics. 15(3-4). 121–127. 3 indexed citations

15.

Ausems, Margreet G.E.M., et al.. (1994). Greig cephalopolysyndactyly syndrome in a large family. Clinical Dysmorphology. 3(1). 21???30–21???30. 5 indexed citations

16.

Ippel, P.F., et al.. (1992). Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: Confirmation of the Gorlin–Chaudhry–Moss syndrome. American Journal of Medical Genetics. 44(4). 518–522. 22 indexed citations

17.

Hageman, G., et al.. (1992). Autosomal dominant congenital Horner's syndrome in a Dutch family.. Journal of Neurology Neurosurgery & Psychiatry. 55(1). 28–30. 8 indexed citations

18.

Hageman, G., et al.. (1990). Familial, Alternating Bell’s Palsy with Dominant Inheritance. European Neurology. 30(6). 310–313. 17 indexed citations

19.

Toonstra, Johan, et al.. (1987). Are Lisch Nodules an Ocular Marker of the Neurofibromatosis Gene in Otherwise Unaffected Family Members. Dermatology. 174(5). 232–235. 5 indexed citations

20.

Hageman, Gilbert R., Dick Lindhout, P. G. Barth, et al.. (1985). The Pena-Shokeir I syndrome: fetal akinesia?. Clinical Neurology and Neurosurgery. 87(3). 232–232. 1 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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