Marina Michelson

658 total citations
19 papers, 239 citations indexed

About

Marina Michelson is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marina Michelson has authored 19 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marina Michelson's work include Genomic variations and chromosomal abnormalities (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Marina Michelson is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Marina Michelson collaborates with scholars based in Israel, United Kingdom and United States. Marina Michelson's co-authors include Tally Lerman‐Sagie, Dorit Lev, Andreea Nissenkorn, Esther Leshinsky‐Silver, Bruria Ben‐Zeev, Lubov Blumkin, Sara Kivity, Chana Vinkler, Ayelet Zerem and V. Barash and has published in prestigious journals such as Neurology, Investigative Ophthalmology & Visual Science and Human Mutation.

In The Last Decade

Marina Michelson

17 papers receiving 237 citations

Peers

Countries citing papers authored by Marina Michelson

Since Specialization

Citations

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

Fields of papers citing papers by Marina Michelson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Michelson

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene 2024 ·Clinical Genetics ·Marina Michelson, Keren Yosovich, (unknown), Yuval Yogev, Ohad S. Birk, (unknown), Dorit Lev	0
2	Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy 2023 ·Investigative Ophthalmology & Visual Science ·(unknown), Idan Hecht, (unknown), Alina Kotlyar, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Marina Michelson, Nitza Goldenberg‐Cohen, Eran Pras	0
3	Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A 2022 ·Human Mutation ·Elena Pavlova, Dorit Lev, Marina Michelson, Keren Yosovich, (unknown), Nicholas A. Bright, Paul T. Manna, Veronica Kane Dickson, Karen Tylee, Heather J. Church, J. Paul Luzio, Timothy M. Cox	10
4	Microdeletion of 16q24.1–q24.2—A unique etiology of Lymphedema–Distichiasis syndrome and neurodevelopmental disorder 2022 ·American Journal of Medical Genetics Part A ·Marina Michelson, Gabriel Lidzbarsky, (unknown), (unknown), Rachel P. Berger, (unknown), Noam Shomron, Dorit Lev, Yael Goldberg	5
5	Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders 2021 ·Journal of Human Genetics ·(unknown), Marina Michelson, Emanuela Argilli, Keren Yosovich, Elliott H. Sherr, (unknown), Eleina England, (unknown), Z. Leibovitz, Dorit Lev, (unknown), Tally Lerman‐Sagie, Lubov Blumkin	2
6	Infantile onset progressive cerebellar atrophy and anterior horn cell Degeneration-A novel phenotype associated with mutations in the PLA2G6 gene 2019 ·European Journal of Medical Genetics ·(unknown), Marina Michelson, Keren Yosovich, Lubov Blumkin, Tally Lerman‐Sagie, Dorit Lev	3
7	Familial Intracranial Hypertension in 2 Brothers With PTEN Mutation: Expansion of the Phenotypic Spectrum 2019 ·Journal of Child Neurology ·(unknown), (unknown), Marina Michelson, Keren Yosovich, Dorit Lev, Shlomi Constantini, Hana Leiba, Tally Lerman‐Sagie, Lubov Blumkin	6
8	Molecular and functional studies of retinal degeneration as a clinical presentation of SACS-related disorder 2015 ·European Journal of Paediatric Neurology ·Lubov Blumkin, Teisha Y. Bradshaw, Marina Michelson, (unknown), (unknown), Tally Lerman‐Sagie, Dorit Lev, J. Paul Chapple, Esther Leshinsky‐Silver	10
9	Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A 2015 ·European Journal of Paediatric Neurology ·Lubov Blumkin, Esther Leshinsky‐Silver, Marina Michelson, Ayelet Zerem, Sara Kivity, Dorit Lev, Tally Lerman‐Sagie	31
10	A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features 2014 ·European Journal of Medical Genetics ·Chana Vinkler, Esther Leshinsky‐Silver, Marina Michelson, Dorothea Haas, Tally Lerman‐Sagie, Dorit Lev	2
11	Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region 2012 ·American Journal of Medical Genetics Part A ·Marina Michelson, (unknown), Chana Vinkler, Esther Leshinsky‐Silver, (unknown), Ayala Frumkin, Sara Kivity, Tally Lerman‐Sagie, Dorit Lev	16
12	Autistic regression in a child with Silver–Russell Syndrome and maternal UPD 7 2011 ·European Journal of Paediatric Neurology ·(unknown), Michael Davidovitch, Chana Vinkler, Marina Michelson, Tally Lerman‐Sagie, Dorit Lev	1
13	Mosaic marker chromosome 16 resulting in 16q11.2–q12.1 gain in a child with intellectual disability, microcephaly, and cerebellar cortical dysplasia 2011 ·American Journal of Medical Genetics Part A ·Ayelet Zerem, Chana Vinkler, Marina Michelson, Esther Leshinsky‐Silver, Tally Lerman‐Sagie, Dorit Lev	5
14	Genetic Counseling and Testing for FSHD (Facioscapulohumeral Muscular Dystrophy) in the Israeli Population 2011 ·Journal of Genetic Counseling ·(unknown), Esther Leshinsky‐Silver, Sarit Cohen, Chana Vinkler, Marina Michelson, Tally Lerman‐Sagie, (unknown), Menahem Sadeh, Dorit Lev	4
15	Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother 2010 ·European Journal of Paediatric Neurology ·Marina Michelson, (unknown), Chana Vinkler, Esther Leshinsky‐Silver, (unknown), Tally Lerman‐Sagie, Dorit Lev	15
16	Congenital Ataxia, Mental Retardation, and Dyskinesia Associated With a Novel CACNA1A Mutation 2010 ·Journal of Child Neurology ·Lubov Blumkin, Marina Michelson, Esther Leshinsky‐Silver, Sara Kivity, Dorit Lev, Tally Lerman‐Sagie	39
17	A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion 2008 ·European Journal of Paediatric Neurology ·Esther Leshinsky‐Silver, Marina Michelson, Sarit Cohen, (unknown), Menachem Sadeh, V. Barash, Tally Lerman‐Sagie, Dorit Lev	12
18	Inborn errors of metabolism 2001 ·Neurology ·Andreea Nissenkorn, Marina Michelson, Bruria Ben‐Zeev, Tally Lerman‐Sagie	77
19	Urinary organic acid screening in children with developmental language delay 1999 ·Journal of Inherited Metabolic Disease ·Marina Michelson, S Harel, Alisa Gutman, Tally Lerman‐Sagie	1

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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