Lubov Blumkin

1.0k citations

31 papers · 502 indexed · h-index 14

Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases 5
- Neuroscience and Neuropharmacology Research 3
Psychiatry and Mental health top 10%
- Epilepsy research and treatment 4
Neurology
- Neurological diseases and metabolism 5
- Autoimmune Neurological Disorders and Treatments 4
Neurology
- Neurological diseases and metabolism 5
- Autoimmune Neurological Disorders and Treatments 4
Pediatrics, Perinatology and Child Health
- Fetal and Pediatric Neurological Disorders 6
Molecular Biology
- Mitochondrial Function and Pathology 6
- RNA regulation and disease 6

Co-authors: Tally Lerman‐Sagie Dorit Lev Esther Leshinsky‐Silver Sara Kivity Keren Yosovich Marina Michelson Ayelet Zerem Ilan Linder
Cited by: Cellular and Molecular Neuroscience Psychiatry and Mental health Neurology
Journals: PEDIATRICS (1 paper)Epilepsia (1 paper)Journal of the Neurological Sciences (1 paper)
Partner nations: Israel United States United Kingdom

In The Last Decade

Lubov Blumkin

29 papers receiving 493 citations

Peers

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

The 25 scholars most cited alongside Lubov Blumkin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lubov Blumkin Line = papers co-authored together Lubov Blumkin links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Home-video EEG monitoring in a pediatric setting Heliyon ·Yael Michaeli,Lubov Blumkin,Mordekhay Medvedovsky,Ilan Dalal,Andreea Nissenkorn	2024	0
2	“Virtual patch clamp analysis” for predicting the functional significance of pathogenic variants in sodium channels Epilepsy Research ·N. Bielopolski,Eilon Heyman,Haim Bassan,Bruria Ben‐Zeev,Michal Tzadok,M. Ginsberg,Lubov Blumkin,Yael Michaeli,R. Sokol,N. Yosha-Orpaz,R. Hady-Cohen,E. Banne,D. Lev,T. Lerman‐Sagie,S. Wald-Altman,Andreea Nissenkorn	2022	2
3	Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders Journal of Human Genetics ·Michal Gafner,Marina Michelson,Emanuela Argilli,Keren Yosovich,Elliott H. Sherr,Kendall C. Parks,Eleina England,Ronen Hady-Cohen,Z. Leibovitz,Dorit Lev,Yael Michaeli-Yosef,Tally Lerman‐Sagie,Lubov Blumkin	2021	2
4	Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features European Journal of Paediatric Neurology ·Lubov Blumkin,Z. Leibovitz,Karina Krajden-Haratz,Ayala Arad,Keren Yosovich,L. Gindes,Ayelet Zerem,Liat Ben‐Sira,Dorit Lev,Andrea Nissenkorn,Dvora Kidron,William B. Dobyns,G. Malinger,Nadia Bahi‐Buisson,Richard J. Leventer,Tally Lerman‐Sagie	2020	12
5	Myoclonic tremor status as a presenting symptom of adenylosuccinate lyase deficiency European Journal of Medical Genetics ·Michal M. Andelman‐Gur,Hirotomo Saitsu,Naomichi Matsumoto,Ronen Spiegel,Keren Yosovich,Dorit Lev,Tally Lerman‐Sagie,Lubov Blumkin	2020	1
6	Expanding the genotype-phenotype spectrum of ISCA2-related multiple mitochondrial dysfunction syndrome-cavitating leukoencephalopathy and prolonged survival Neurogenetics ·Tamar Gur Hartman,Keren Yosovich,Hila Gur Michaeli,Lubov Blumkin,Liat Ben‐Sira,Dorit Lev,Tally Lerman‐Sagie,Ayelet Zerem	2020	4
7	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 ·Michal Gafner,Marina Michelson,Keren Yosovich,Lubov Blumkin,Tally Lerman‐Sagie,Dorit Lev	2019	3
8	Metabolic stroke in a patient with bi-allelic OPA1 mutations Metabolic Brain Disease ·Ayelet Zerem,Keren Yosovich,Yael Cohen Rappaport,Stéphanie Libzon,Lubov Blumkin,Liat Ben‐Sira,Dorit Lev,Tally Lerman‐Sagie	2019	16
9	RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia European Journal of Paediatric Neurology ·Daniella Nishri,Hadassa Goldberg‐Stern,Iris Noyman,Lubov Blumkin,Sara Kivity,Hirotomo Saitsu,Mitsuko Nakashima,Naomichi Matsumoto,Esther Leshinsky‐Silver,Tally Lerman‐Sagie,Dorit Lev	2016	22
10	Molecular and functional studies of retinal degeneration as a clinical presentation of SACS-related disorder European Journal of Paediatric Neurology ·Lubov Blumkin,Teisha Y. Bradshaw,Marina Michelson,Tal Kopler,Dvir Dahari,Tally Lerman‐Sagie,Dorit Lev,J. Paul Chapple,Esther Leshinsky‐Silver	2015	10
11	Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A European Journal of Paediatric Neurology ·Lubov Blumkin,Esther Leshinsky‐Silver,Marina Michelson,Ayelet Zerem,Sara Kivity,Dorit Lev,Tally Lerman‐Sagie	2015	31
12	Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder European Journal of Paediatric Neurology ·Daniella Nishri,Simon Edvardson,Dorit Lev,Esther Leshinsky‐Silver,Liat Ben‐Sira,Marco Henneke,Tally Lerman‐Sagie,Lubov Blumkin	2014	7
13	Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene Neurogenetics ·Lubov Blumkin,Ayelet Halevy,Dominique Ben-Ami-Raichman,Dvir Dahari,Ami Haviv,Sarit Cohen,Dorit Lev,Marjo S. van der Knaap,Tally Lerman‐Sagie,Esther Leshinsky‐Silver	2014	31
14	Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability JIMD Reports ·Lubov Blumkin,Esther Leshinsky‐Silver,Ayelet Zerem,Keren Yosovich,Tally Lerman‐Sagie,Dorit Lev	2013	34
15	A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome Journal of Neurology ·Lubov Blumkin,Sara Kivity,Dorit Lev,Sarit Cohen,Ruth Shomrat,Tally Lerman‐Sagie,Esther Leshinsky‐Silver	2012	35
16	Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Neurogenetics ·Peter Bauer,Esther Leshinsky‐Silver,Lubov Blumkin,Nina Schlipf,Christopher Schröder,Julia Schicks,Dorit Lev,Olaf Rieß,Tally Lerman‐Sagie,Lüdger Schöls	2012	46
17	Acquired ataxias, infectious and para-infectious Handbook of clinical neurology ·Lubov Blumkin,Michael R. Pranzatelli	2011	11
18	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 ·Lubov Blumkin,Tally Lerman‐Sagie,Dorit Lev,Keren Yosovich,Esther Leshinsky‐Silver	2011	25
19	Clinical Correlates of Occipital Intermittent Rhythmic Delta Activity (OIRDA) in Children Epilepsia ·Nathan Watemberg,Ilan Linder,Ron Dabby,Lubov Blumkin,Tally Lerman‐Sagie	2007	23
20	Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration—A late onset variant of PCH-1? European Journal of Paediatric Neurology ·Dorit Lev,Marina Michelson-Kerman,Chana Vinkler,Lubov Blumkin,Stavit A. Shalev,Tally Lerman‐Sagie	2007	5

About Lubov Blumkin

Lubov Blumkin is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 31 papers that have together received 502 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (6 papers), RNA regulation and disease (6 papers), Fetal and Pediatric Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers), Genetic Neurodegenerative Diseases (5 papers), Autoimmune Neurological Disorders and Treatments (4 papers), Epilepsy research and treatment (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (161 citations), Psychiatry and Mental health (101 citations) and Neurology (50 citations). Lubov Blumkin has collaborated with scholars based in Israel, United States and United Kingdom. Frequent 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. Their work appears in journals such as PEDIATRICS, Epilepsia and Journal of the Neurological Sciences.

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.

Explore authors with similar magnitude of impact