Lubov Blumkin

1.0k total citations
31 papers, 502 citations indexed

About

Lubov Blumkin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lubov Blumkin has authored 31 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lubov Blumkin's work include Mitochondrial Function and Pathology (6 papers), RNA regulation and disease (6 papers) and Fetal and Pediatric Neurological Disorders (6 papers). Lubov Blumkin is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), RNA regulation and disease (6 papers) and Fetal and Pediatric Neurological Disorders (6 papers). Lubov Blumkin collaborates with scholars based in Israel, United States and United Kingdom. Lubov Blumkin's co-authors include Tally Lerman‐Sagie, Dorit Lev, Esther Leshinsky‐Silver, Sara Kivity, Keren Yosovich, Marina Michelson, Ayelet Zerem, Ilan Linder, Nathan Watemberg and Sarit Cohen and has published in prestigious journals such as PEDIATRICS, Epilepsia and Journal of the Neurological Sciences.

In The Last Decade

Lubov Blumkin

29 papers receiving 493 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lubov Blumkin Israel 14 214 161 101 90 87 31 502
Monika Jeub Germany 11 189 0.9× 217 1.3× 100 1.0× 145 1.6× 33 0.4× 16 463
Zucai Xu China 12 226 1.1× 146 0.9× 94 0.9× 80 0.9× 31 0.4× 64 491
Andrea Mountney United States 16 275 1.3× 146 0.9× 44 0.4× 231 2.6× 29 0.3× 21 636
Margherita Marchi Italy 14 175 0.8× 129 0.8× 58 0.6× 149 1.7× 20 0.2× 29 530
João Ramalheira Portugal 10 122 0.6× 64 0.4× 215 2.1× 35 0.4× 66 0.8× 23 386
Pamela Rosso Italy 13 191 0.9× 153 1.0× 21 0.2× 44 0.5× 36 0.4× 27 495
Tiina Keränen Finland 11 134 0.6× 206 1.3× 279 2.8× 211 2.3× 133 1.5× 12 681
Lisa Flint United States 8 199 0.9× 96 0.6× 22 0.2× 26 0.3× 41 0.5× 9 514
Janna Kenny United Kingdom 9 271 1.3× 43 0.3× 61 0.6× 52 0.6× 47 0.5× 17 502

Countries citing papers authored by Lubov Blumkin

Since Specialization
Citations

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

Fields of papers citing papers by Lubov Blumkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lubov Blumkin

This figure shows the co-authorship network connecting the top 25 collaborators of Lubov Blumkin. A scholar is included among the top collaborators of Lubov Blumkin 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 Lubov Blumkin. Lubov Blumkin 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.
Blumkin, Lubov, et al.. (2024). Home-video EEG monitoring in a pediatric setting. Heliyon. 10(15). e35108–e35108.
2.
Bassan, Haim, Bruria Ben‐Zeev, Michal Tzadok, et al.. (2022). “Virtual patch clamp analysis” for predicting the functional significance of pathogenic variants in sodium channels. Epilepsy Research. 186. 107002–107002. 2 indexed citations
3.
Michelson, Marina, Emanuela Argilli, Keren Yosovich, et al.. (2021). Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders. Journal of Human Genetics. 67(2). 95–101. 2 indexed citations
4.
Blumkin, Lubov, Z. Leibovitz, Ayala Arad, et al.. (2020). Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. European Journal of Paediatric Neurology. 26. 46–60. 12 indexed citations
5.
Saitsu, Hirotomo, Naomichi Matsumoto, Ronen Spiegel, et al.. (2020). Myoclonic tremor status as a presenting symptom of adenylosuccinate lyase deficiency. European Journal of Medical Genetics. 63(12). 104061–104061. 1 indexed citations
6.
Yosovich, Keren, Lubov Blumkin, Liat Ben‐Sira, et al.. (2020). Expanding the genotype-phenotype spectrum of ISCA2-related multiple mitochondrial dysfunction syndrome-cavitating leukoencephalopathy and prolonged survival. Neurogenetics. 21(4). 243–249. 4 indexed citations
7.
Michelson, Marina, et al.. (2019). Infantile onset progressive cerebellar atrophy and anterior horn cell Degeneration-A novel phenotype associated with mutations in the PLA2G6 gene. European Journal of Medical Genetics. 63(4). 103801–103801. 3 indexed citations
8.
Zerem, Ayelet, Keren Yosovich, Lubov Blumkin, et al.. (2019). Metabolic stroke in a patient with bi-allelic OPA1 mutations. Metabolic Brain Disease. 34(4). 1043–1048. 16 indexed citations
9.
Goldberg‐Stern, Hadassa, Iris Noyman, Lubov Blumkin, et al.. (2016). RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia. European Journal of Paediatric Neurology. 20(3). 412–417. 22 indexed citations
10.
Blumkin, Lubov, Teisha Y. Bradshaw, Marina Michelson, et al.. (2015). Molecular and functional studies of retinal degeneration as a clinical presentation of SACS-related disorder. European Journal of Paediatric Neurology. 19(4). 472–476. 10 indexed citations
11.
Blumkin, Lubov, Esther Leshinsky‐Silver, Marina Michelson, et al.. (2015). Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A. European Journal of Paediatric Neurology. 19(3). 292–297. 31 indexed citations
12.
Blumkin, Lubov, Ayelet Halevy, Sarit Cohen, et al.. (2014). Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene. Neurogenetics. 15(2). 107–13. 31 indexed citations
13.
Edvardson, Simon, Dorit Lev, Esther Leshinsky‐Silver, et al.. (2014). Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder. European Journal of Paediatric Neurology. 18(4). 495–501. 7 indexed citations
14.
Blumkin, Lubov, Esther Leshinsky‐Silver, Ayelet Zerem, et al.. (2013). Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability. JIMD Reports. 12. 103–107. 34 indexed citations
15.
Blumkin, Lubov, Sara Kivity, Dorit Lev, et al.. (2012). A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome. Journal of Neurology. 259(12). 2590–2598. 35 indexed citations
16.
Bauer, Peter, Esther Leshinsky‐Silver, Lubov Blumkin, et al.. (2012). Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47). Neurogenetics. 13(1). 73–76. 46 indexed citations
17.
Blumkin, Lubov & Michael R. Pranzatelli. (2011). Acquired ataxias, infectious and para-infectious. Handbook of clinical neurology. 103. 137–146. 11 indexed citations
18.
Blumkin, Lubov, Tally Lerman‐Sagie, Dorit Lev, Keren Yosovich, & Esther Leshinsky‐Silver. (2011). A new locus (SPG47) maps to 1p13.2–1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum. Journal of the Neurological Sciences. 305(1-2). 67–70. 25 indexed citations
19.
Watemberg, Nathan, Ilan Linder, Ron Dabby, Lubov Blumkin, & Tally Lerman‐Sagie. (2007). Clinical Correlates of Occipital Intermittent Rhythmic Delta Activity (OIRDA) in Children. Epilepsia. 48(2). 330–334. 23 indexed citations
20.
Lev, Dorit, et al.. (2007). Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration—A late onset variant of PCH-1?. European Journal of Paediatric Neurology. 12(2). 97–101. 5 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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