Salmo Raskin

6.5k total citations
147 papers, 2.8k citations indexed

About

Salmo Raskin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Salmo Raskin has authored 147 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 56 papers in Cellular and Molecular Neuroscience and 32 papers in Genetics. Recurrent topics in Salmo Raskin's work include Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (39 papers) and Cystic Fibrosis Research Advances (19 papers). Salmo Raskin is often cited by papers focused on Genetic Neurodegenerative Diseases (53 papers), Mitochondrial Function and Pathology (39 papers) and Cystic Fibrosis Research Advances (19 papers). Salmo Raskin collaborates with scholars based in Brazil, United States and Canada. Salmo Raskin's co-authors include Hélio Afonso Ghizoni Teive, Tetsuo Ashizawa, Renato P. Munhoz, Hélio A.G. Teive, Lineu César Werneck, Walter O. Arruda, Walter Oleschko Arruda, Josiane Souza, Mariana Moscovich and Adriana Moro and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Salmo Raskin

141 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Salmo Raskin Brazil 28 1.5k 1.1k 670 578 332 147 2.8k
David W. Stockton United States 32 3.3k 2.3× 1.3k 1.2× 483 0.7× 1.3k 2.3× 268 0.8× 70 4.9k
Erik‐Jan Kamsteeg Netherlands 32 2.2k 1.5× 704 0.6× 258 0.4× 470 0.8× 634 1.9× 124 3.2k
Morten Dunø Denmark 35 2.6k 1.8× 745 0.7× 346 0.5× 650 1.1× 141 0.4× 184 3.8k
Annie Laquerrière France 32 1.4k 0.9× 502 0.5× 248 0.4× 584 1.0× 241 0.7× 109 3.3k
Alfredo Brusco Italy 32 2.2k 1.5× 859 0.8× 355 0.5× 799 1.4× 122 0.4× 141 3.3k
James M. Killian United States 27 1.0k 0.7× 1.6k 1.5× 1.0k 1.5× 522 0.9× 125 0.4× 39 3.6k
Patrick MacLeod Canada 29 1.3k 0.9× 644 0.6× 266 0.4× 910 1.6× 382 1.2× 74 3.1k
I. K. Hart United Kingdom 21 1.2k 0.8× 801 0.7× 1.5k 2.2× 193 0.3× 95 0.3× 38 3.5k
Gaëtan Lesca France 33 1.2k 0.8× 610 0.6× 382 0.6× 1.0k 1.8× 708 2.1× 160 3.4k
C. Harker Rhodes United States 32 746 0.5× 361 0.3× 402 0.6× 264 0.5× 334 1.0× 65 2.8k

Countries citing papers authored by Salmo Raskin

Since Specialization
Citations

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

Fields of papers citing papers by Salmo Raskin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Salmo Raskin

This figure shows the co-authorship network connecting the top 25 collaborators of Salmo Raskin. A scholar is included among the top collaborators of Salmo Raskin 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 Salmo Raskin. Salmo Raskin 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.
Pellerin, David, Marcus Vinícius Della Coletta, Mariana Spitz, et al.. (2024). Frequency of GAA-FGF14 ataxia in a large cohort of Brazilian patients with unsolved adult-onset cerebellar ataxia. Parkinsonism & Related Disorders. 122. 106157–106157. 3 indexed citations
2.
Dulski, Jarosław, Samantha A. Banks, Rose Bruffaerts, et al.. (2024). Global Presence and Penetrance of CSF1R -Related Disorder. Neurology Genetics. 10(5). e200187–e200187. 4 indexed citations
3.
Efthymiou, Stéphanie, Georgios Koutsis, Reza Maroofian, et al.. (2023). Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn. Annals of Clinical and Translational Neurology. 10(10). 1910–1916. 2 indexed citations
4.
Valle, David, et al.. (2023). A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2. Revista Paulista de Pediatria. 41. e2022057–e2022057. 2 indexed citations
5.
Pellerin, David, Pedro José Tomaselli, Mariana Spitz, et al.. (2023). Frequency of GAA- FGF14 Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia. Neurology Genetics. 9(5). e200094–e200094. 17 indexed citations
6.
Štingl, Katarína, Britta Baumann, Pietro De Angeli, et al.. (2022). Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International Journal of Molecular Sciences. 23(12). 6868–6868. 4 indexed citations
7.
Raskin, Salmo, et al.. (2020). A comprehensive analysis of AHRR gene as a candidate for cleft lip with or without cleft palate. Mutation Research/Reviews in Mutation Research. 785. 108319–108319. 7 indexed citations
8.
Nascimento, Fábio A., Fernando Castilho Pelloso, Carlos Henrique Ferreira Camargo, et al.. (2019). Spinocerebellar ataxias in Southern Brazil: Genotypic and phenotypic evaluation of 213 families. Clinical Neurology and Neurosurgery. 184. 105427–105427. 21 indexed citations
9.
Nascimento, Fábio A., et al.. (2018). BEYOND WHOLE-EXOME SEQUENCING: A PROPOS OF TWO NEURODEGENERATIVE DISEASES. (P5.080). Neurology. 90(15_supplement). 1 indexed citations
10.
Teive, Hélio A.G., Adriana Moro, Mariana Moscovich, et al.. (2015). Ataxia-telangiectasia — A historical review and a proposal for a new designation: ATM syndrome. Journal of the Neurological Sciences. 355(1-2). 3–6. 73 indexed citations
11.
12.
Zechi‐Ceide, Roseli Maria, et al.. (2009). Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: Exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics Part A. 149A(6). 1277–1279. 7 indexed citations
13.
Kurotaki, Naohiro, Joseph Shen, Tatsuro Kondoh, et al.. (2005). Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency. Genetics in Medicine. 7(7). 479–483. 33 indexed citations
14.
Polityko, A., et al.. (2005). Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenetic and Genome Research. 111(2). 171–174. 13 indexed citations
15.
Lange, Marcos Christiano, Viviane Flumignan Zétola, Hélio Afonso Ghizoni Teive, et al.. (2004). Cerebrotendinous xanthomatosis: report of two Brazilian brothers. Arquivos de Neuro-Psiquiatria. 62(4). 1085–1089. 8 indexed citations
16.
Raskin, Salmo, Francisco J.C. Reis, Nelson Augusto Rosário Filho, et al.. (2003). High Allelic Heterogeneity Between Afro-Brazilians and Euro-Brazilians Impacts Cystic Fibrosis Genetic Testing. Genetic Testing. 7(3). 213–218. 19 indexed citations
17.
Noronha, Lúcia de, et al.. (1999). Neurocutaneous melanosis. Jornal de Pediatria. 75(4). 277–80. 3 indexed citations
18.
Raskin, Salmo, et al.. (1998). Analysis of the DF508 mutation in a Brazilian cystic fibrosis population: comparison of pulmonary status of homozygotes with other patients. SHILAP Revista de lepidopterología. 3 indexed citations
19.
Raskin, Salmo, et al.. (1996). Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism. Human Genetics. 98(6). 703–705. 8 indexed citations
20.
Raskin, Salmo, et al.. (1992). Cystic fibrosis genotyping by direct PCR analysis of Guthrie blood spots.. Genome Research. 2(2). 154–156. 32 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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