Sergiu C. Blumen

1.7k total citations
37 papers, 898 citations indexed

About

Sergiu C. Blumen is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Sergiu C. Blumen has authored 37 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 15 papers in Neurology. Recurrent topics in Sergiu C. Blumen's work include Genetic Neurodegenerative Diseases (11 papers), Muscle Physiology and Disorders (10 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Sergiu C. Blumen is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Muscle Physiology and Disorders (10 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Sergiu C. Blumen collaborates with scholars based in Israel, Canada and France. Sergiu C. Blumen's co-authors include Amos D. Korczyn, Puiu Nisipeanu, R Carasso, A. Asherov, Bernard Brais, Menachem Sadeh, Miriam Y. Neufeld, Rivka Inzelberg, Yisrael Parmet and Guy A. Rouleau and has published in prestigious journals such as Nature Communications, The EMBO Journal and Neurology.

In The Last Decade

Sergiu C. Blumen

37 papers receiving 873 citations

Peers

Sergiu C. Blumen

MB

CMN

NEURO

GENET

NEURO

Joachim Schessl Germany

Maria Vittoria De Angelis Italy

Yasuo Aihara Japan

Guilherme Lepski Brazil

Jun Namiki Japan

Peter Van den Bergh Belgium

Anna Modoni Italy

Kensuke Shiga Japan

Byoung Joon Kim South Korea

Koji Kakishita Japan

Joachim Schessl Germany

Sergiu C. Blumen

622 ×1.5

MB

386 ×1.0

CMN

310 ×1.0

NEURO

165 ×1.0

GENET

76 ×0.6

NEURO

Citations per year, relative to Sergiu C. Blumen Sergiu C. Blumen (= 1×) peers Joachim Schessl

Countries citing papers authored by Sergiu C. Blumen

Since Specialization

Citations

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

Fields of papers citing papers by Sergiu C. Blumen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sergiu C. Blumen. 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 Sergiu C. Blumen. The network helps show where Sergiu C. Blumen may publish in the future.

Co-authorship network of co-authors of Sergiu C. Blumen

This figure shows the co-authorship network connecting the top 25 collaborators of Sergiu C. Blumen. A scholar is included among the top collaborators of Sergiu C. Blumen 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 Sergiu C. Blumen. Sergiu C. Blumen 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

1.

Berdichevsky, Yevgeny, Itzhak Braverman, Sergiu C. Blumen, et al.. (2024). Disease-associated polyalanine expansion mutations impair UBA6-dependent ubiquitination. The EMBO Journal. 43(2). 250–276. 3 indexed citations

2.

Berdichevsky, Yevgeny, et al.. (2023). Oculopharyngeal muscular dystrophy mutations link the RNA‐binding protein HNRNPQ to autophagosome biogenesis. Aging Cell. 22(10). e13949–e13949. 4 indexed citations

3.

Braverman, Itzhak, Sergiu C. Blumen, Hadas Newman, et al.. (2017). Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL Genes. Genetic Testing and Molecular Biomarkers. 21(7). 450–453. 2 indexed citations

4.

Malerba, Alberto, Pierre Klein, Susan Jarmin, et al.. (2017). PABPN1 gene therapy for oculopharyngeal muscular dystrophy. Nature Communications. 8(1). 14848–14848. 57 indexed citations

5.

Ben‐Yosef, Tamar, Hadas Newman, Itzhak Braverman, et al.. (2016). A combination of oculopharyngeal muscular dystrophy and a variant of enhanced S-cone syndrome in Bukharan Jews due to linked mutations in PABPN1 and NRL. Investigative Ophthalmology & Visual Science. 57(12). 3165–3165. 1 indexed citations

6.

Gotkine, Marc, Alon Abraham, Vivian E. Drory, et al.. (2014). Dynamic MRI testing of the cervical spine has prognostic significance in patients with progressive upper-limb distal weakness and atrophy. Journal of the Neurological Sciences. 345(1-2). 168–171. 8 indexed citations

7.

Blumen, Sergiu C., Anat Kesler, Ron Dabby, et al.. (2013). Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?. PubMed. 15(12). 748–52. 7 indexed citations

8.

Abraham, Alon, Marc Gotkine, Vivian E. Drory, & Sergiu C. Blumen. (2013). Effect of neck flexion on somatosensory and motor evoked potentials in Hirayama disease. Journal of the Neurological Sciences. 334(1-2). 102–105. 14 indexed citations

9.

Blumen, Sergiu C., Stéphanie Astord, Valérie Robin, et al.. (2011). A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation. Annals of Neurology. 71(4). 509–519. 55 indexed citations

10.

Blumen, Sergiu C., Vivian E. Drory, Menachem Sadeh, et al.. (2010). Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease. Amyotrophic Lateral Sclerosis. 11(1-2). 237–239. 8 indexed citations

11.

Blumen, Sergiu C., Rivka Inzelberg, Puiu Nisipeanu, et al.. (2010). Aggressive familial ALS with unusual brain MRI and a SOD1 gene mutation. Amyotrophic Lateral Sclerosis. 11(1-2). 228–231. 5 indexed citations

12.

Blumen, Sergiu C., Saif Abu‐Mouch, David Negus, et al.. (2003). A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24‐q32. Annals of Neurology. 54(6). 796–803. 31 indexed citations

13.

Blumen, Sergiu C., Bernard Brais, Amos D. Korczyn, et al.. (1999). Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease. Annals of Neurology. 46(1). 115–118. 68 indexed citations

14.

Blumen, Sergiu C., Bernard Brais, Amos D. Korczyn, et al.. (1999). Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease. Annals of Neurology. 46(1). 115–118. 2 indexed citations

15.

Blumen, Sergiu C., et al.. (1998). Cyclosporine-induced optic neuropathy, ophthalmoplegia, and nystagmus in a patient with Crohn disease. American Journal of Ophthalmology. 126(4). 607–609. 22 indexed citations

16.

Blumen, Sergiu C., Puiu Nisipeanu, Menachem Sadeh, et al.. (1997). Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel. Neuromuscular Disorders. 7. S38–S40. 34 indexed citations

17.

Treves, T. A., Natan Gadoth, Sergiu C. Blumen, & Amos D. Korczyn. (1995). Intravascular Malignant Lymphomatosis: A Cause of Subacute Dementia. Dementia and Geriatric Cognitive Disorders. 6(5). 286–293. 38 indexed citations

18.

Neufeld, Miriam Y., et al.. (1994). EEG Frequency Analysis in Demented and Nondemented Parkinsonian Patients. Dementia and Geriatric Cognitive Disorders. 5(1). 23–28. 88 indexed citations

19.

Blumen, Sergiu C., et al.. (1990). Does the pupillary sparing oculomotor nerve palsy really spare the pupil?. Electroencephalography and Clinical Neurophysiology. 75(2). S12–S12. 3 indexed citations

20.

Neufeld, Miriam Y., Sergiu C. Blumen, Puiu Nisipeanu, & Amos D. Korczyn. (1988). Lingual Seizures¹. Epilepsia. 29(1). 30–33. 7 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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