S Bort

503 total citations
8 papers, 282 citations indexed

About

S Bort is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, S Bort has authored 8 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 3 papers in Neurology and 2 papers in Neurology. Recurrent topics in S Bort's work include Hereditary Neurological Disorders (7 papers), Neurological diseases and metabolism (3 papers) and Genetic Neurodegenerative Diseases (3 papers). S Bort is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Neurological diseases and metabolism (3 papers) and Genetic Neurodegenerative Diseases (3 papers). S Bort collaborates with scholars based in Spain, Belgium and United States. S Bort's co-authors include Francesc Palau, Juan J. Vílchez, Teresa Sevilla, Félix Prieto, Eva Nelis, Christine Van Broeckhoven, Javier Arpa, A Cruz-Martı́nez, José M. Millán and Ann Löfgren and has published in prestigious journals such as Human Molecular Genetics, Genomics and Human Mutation.

In The Last Decade

S Bort

8 papers receiving 275 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S Bort Spain	6	217	91	89	85	44	8	282
Michel Gugenheim France	11	424 2.0×	143 1.6×	235 2.6×	158 1.9×	71 1.6×	18	555
Tomoya Nishimura Japan	8	111 0.5×	109 1.2×	62 0.7×	50 0.6×	33 0.8×	17	246
Eric J. Meershoek Netherlands	10	252 1.2×	160 1.8×	86 1.0×	100 1.2×	73 1.7×	11	434
Peter De Jonghe Belgium	7	232 1.1×	73 0.8×	77 0.9×	95 1.1×	54 1.2×	10	271
Dagmara Kabzińska Poland	13	329 1.5×	210 2.3×	104 1.2×	140 1.6×	73 1.7×	50	482
Rolf Schiff United States	12	143 0.7×	142 1.6×	41 0.5×	50 0.6×	45 1.0×	20	345
Estelle Arnaud Switzerland	7	194 0.9×	227 2.5×	58 0.7×	63 0.7×	73 1.7×	7	381
Simona Capponi Italy	12	222 1.0×	211 2.3×	92 1.0×	74 0.9×	76 1.7×	16	405
Anne Kjersti Erichsen Norway	8	222 1.0×	113 1.2×	58 0.7×	103 1.2×	16 0.4×	12	297
Jeff Goldy United States	5	144 0.7×	168 1.8×	52 0.6×	57 0.7×	43 1.0×	5	316

Countries citing papers authored by S Bort

Since Specialization

Citations

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

Fields of papers citing papers by S Bort

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Bort

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Kalikin, Linda M., Marcel P. Keller, S Bort, et al.. (1999). An Integrated Physical and Gene Map of Human Distal Chromosome 17q24–Proximal 17q25 Encompassing Multiple Disease Loci. Genomics. 57(1). 36–42. 24 indexed citations

2.

Bort, S, Teresa Sevilla, Javier Garcı́a-Planells, et al.. (1998). Déjérine-Sottas neuropathy associated with de novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene. Human Mutation. 11(S1). S95–S98. 8 indexed citations

3.

Bort, S, Eva Nelis, Vincent Timmerman, et al.. (1997). Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. Human Genetics. 99(6). 746–754. 114 indexed citations

4.

Cruz-Martı́nez, A, S Bort, Javier Arpa, & Francesc Palau. (1997). Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) Revealed after Weight Loss. European Neurology. 37(4). 257–260. 16 indexed citations

5.

Cruz-Martı́nez, A, S Bort, Javier Arpa, J. Duarte, & Francesc Palau. (1997). Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2. European Journal of Neurology. 4(3). 274–286. 15 indexed citations

6.

Bort, S, Teresa Sevilla, Juan J. Vílchez, F. Prieto, & Francesc Palau. (1995). [The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1].. PubMed. 104(17). 648–52. 1 indexed citations

7.

Bufill, Enric, Juan J. Vílchez, Teresa Sevilla, et al.. (1995). [Deletion of 17p11.2 chromosome in Spanish families with hereditary neuropathy and abnormal sensitivity to pressure].. PubMed. 10(9). 367–74. 2 indexed citations

8.

Palau, Francesc, Ann Löfgren, Peter De Jonghe, et al.. (1993). Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Human Molecular Genetics. 2(12). 2031–2035. 102 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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