R. Ionasescu

1.1k total citations
31 papers, 808 citations indexed

About

R. Ionasescu is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, R. Ionasescu has authored 31 papers receiving a total of 808 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 16 papers in Molecular Biology and 8 papers in Cell Biology. Recurrent topics in R. Ionasescu's work include Hereditary Neurological Disorders (18 papers), Genetic Neurodegenerative Diseases (10 papers) and Muscle Physiology and Disorders (9 papers). R. Ionasescu is often cited by papers focused on Hereditary Neurological Disorders (18 papers), Genetic Neurodegenerative Diseases (10 papers) and Muscle Physiology and Disorders (9 papers). R. Ionasescu collaborates with scholars based in United States, Japan and Canada. R. Ionasescu's co-authors include Victor Ionâşescu, Charles Searby, James A. Trofatter, Isaac Neuhaus, Rudolf Werner, Jonathan L. Haines, Anne Summers, Lawrence Z. Stern, Trudy L. Burns and Sansnee Chatkupt and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

R. Ionasescu

31 papers receiving 782 citations

Peers

R. Ionasescu
H. Skre Norway
Andrzej Kochański Poland
María José Chumillas Spain
Sandra Gill United States
Dagmara Kabzińska Poland
Е. Л. Дадали Russia
J. Blake United Kingdom
Bart W. Nieuwenhuijsen United States
Colleen Callahan United States
Tine Deconinck Belgium
H. Skre Norway
R. Ionasescu
Citations per year, relative to R. Ionasescu R. Ionasescu (= 1×) peers H. Skre

Countries citing papers authored by R. Ionasescu

Since Specialization
Citations

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

Fields of papers citing papers by R. Ionasescu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. Ionasescu. 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 R. Ionasescu. The network helps show where R. Ionasescu may publish in the future.

Co-authorship network of co-authors of R. Ionasescu

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

All Works

20 of 20 papers shown
1.
Ionâşescu, Victor, et al.. (1997). Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene. Muscle & Nerve. 20(1). 97–99. 59 indexed citations
2.
Ionâşescu, Victor, et al.. (1997). Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene. Muscle & Nerve. 20(10). 1308–1310. 18 indexed citations
3.
Ionâşescu, Victor, Charles Searby, R. Ionasescu, Isaac Neuhaus, & Rudolf Werner. (1996). Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy. Neurology. 47(2). 541–544. 79 indexed citations
4.
Ionâşescu, Victor, R. Ionasescu, & Charles Searby. (1996). Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-tooth neuropathy. American Journal of Medical Genetics. 63(3). 486–491. 73 indexed citations
5.
Ionâşescu, Victor, Jun Kimura, Charles Searby, et al.. (1996). A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8. Muscle & Nerve. 19(3). 319–323. 16 indexed citations
6.
Ionâşescu, Victor, Jun Kimura, Charles Searby, et al.. (1996). A Dejerine‐Sottas neuropathy family with a gene mapped on chromosome 8. Muscle & Nerve. 19(3). 319–323. 2 indexed citations
7.
Ionâşescu, Victor, et al.. (1995). New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy. Neuromuscular Disorders. 5(4). 297–299. 28 indexed citations
8.
Ionâşescu, Victor, et al.. (1995). Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene. Neurology. 45(9). 1766–1767. 46 indexed citations
9.
Pericak‐Vance, Margaret A., JoAnn Bergoffen, Phillip F. Chance, et al.. (1995). Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1. Human Heredity. 45(3). 121–128. 8 indexed citations
10.
Ionâşescu, Victor, Charles Searby, & R. Ionasescu. (1994). Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot — Marie — Tooth neuropathy. Human Molecular Genetics. 3(2). 355–358. 99 indexed citations
11.
Ionâşescu, Victor, R. Ionasescu, & Charles Searby. (1993). Screening of dominantly inherited Charcot–Marie–Tooth neuropathies. Muscle & Nerve. 16(11). 1232–1238. 46 indexed citations
12.
Ionâşescu, Victor, James A. Trofatter, Jonathan L. Haines, et al.. (1992). X‐linked recessive Charcot–Marie‐Tooth neuropathy: Clinical and genetic study. Muscle & Nerve. 15(3). 368–373. 27 indexed citations
13.
Ionâşescu, Victor, James A. Trofatter, Jonathan L. Haines, R. Ionasescu, & Charles Searby. (1992). Charcot‐marie‐tooth neuropathy related to chromosome 1. American Journal of Medical Genetics. 42(5). 728–732. 9 indexed citations
14.
Ionâşescu, Victor, James A. Trofatter, J.L. Haines, R. Ionasescu, & Charles Searby. (1992). Mapping of the gene for X‐linked dominant Charcot‐Marie‐Tooth neuropathy. Neurology. 42(4). 903–903. 24 indexed citations
15.
Ionâşescu, Victor, et al.. (1989). Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies. Acta Neurologica Scandinavica. 79(6). 500–503. 1 indexed citations
16.
Ionâşescu, Victor, et al.. (1988). Linkage between the loci for autosomal dominant Charcot-Marie-Tooth neuropathy type 1 and human glucocerebrosidase. Cytogenetic and Genome Research. 47(3). 173–174. 1 indexed citations
17.
Ionâşescu, Victor, R. Ionasescu, Charles Searby, & Trudy L. Burns. (1988). Becker muscular dystrophy recombinant DNA studies in identical twins. Muscle & Nerve. 11(4). 287–290. 1 indexed citations
18.
Ionâşescu, Victor, et al.. (1988). Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2).. PubMed. 42(1). 74–6. 11 indexed citations
19.
Ionâşescu, Victor, Trudy L. Burns, Charles Searby, & R. Ionasescu. (1988). X‐linked dominant charcot–marie–tooth neuropathy with 15 cases in a family genetic linkage study. Muscle & Nerve. 11(11). 1154–1156. 27 indexed citations
20.
Ionâşescu, Victor, R. Ionasescu, S. Anuras, et al.. (1983). Inherited ophthalmoplegia with intestinal pseudo-obstruction. Journal of the Neurological Sciences. 59(2). 215–228. 30 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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