Sharon Aharoni

722 total citations
40 papers, 414 citations indexed

About

Sharon Aharoni is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Sharon Aharoni has authored 40 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Neurology and 8 papers in Surgery. Recurrent topics in Sharon Aharoni's work include Neurogenetic and Muscular Disorders Research (8 papers), Congenital Anomalies and Fetal Surgery (5 papers) and Muscle Physiology and Disorders (4 papers). Sharon Aharoni is often cited by papers focused on Neurogenetic and Muscular Disorders Research (8 papers), Congenital Anomalies and Fetal Surgery (5 papers) and Muscle Physiology and Disorders (4 papers). Sharon Aharoni collaborates with scholars based in Israel, United States and Canada. Sharon Aharoni's co-authors include Avinoam Shuper, Yoram Nevo, Rony Cohen, Rachel Straussberg, Aviva Fattal‐Valevski, Malcolm Rabie, Yoram Nevo, Yakov Fellig, Ayelet Halevy and Zamir Shorer and has published in prestigious journals such as Blood, PLoS ONE and IEEE Transactions on Biomedical Engineering.

In The Last Decade

Sharon Aharoni

32 papers receiving 409 citations

Peers

Sharon Aharoni

NEURO

IMMUN

CMN

GENET

Koutaro Takamatsu Japan

Hadar Kolb Israel

Anna Cho South Korea

Rabab Debs France

Peter Karachunski United States

G. Cole United Kingdom

Joy B. Redman United States

Michael C. Molleston United States

Yiming Zheng China

Carlos Casasnovas Spain

Koutaro Takamatsu Japan

Sharon Aharoni

229 ×1.7

166 ×1.8

NEURO

175 ×2.3

IMMUN

44 ×0.7

CMN

35 ×0.5

GENET

Citations per year, relative to Sharon Aharoni Sharon Aharoni (= 1×) peers Koutaro Takamatsu

Countries citing papers authored by Sharon Aharoni

Since Specialization

Citations

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

Fields of papers citing papers by Sharon Aharoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sharon Aharoni

This figure shows the co-authorship network connecting the top 25 collaborators of Sharon Aharoni. A scholar is included among the top collaborators of Sharon Aharoni 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 Sharon Aharoni. Sharon Aharoni 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

Batzir, Nurit Assia, Julián Nevado, Jair Tenorio, et al.. (2025). N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder. European Journal of Human Genetics. 34(3). 314–323.

Aharoni, Sharon, et al.. (2025). The Role of Ultrasound in the Evolving Landscape of Precision Imaging of Endometriosis. Current Obstetrics and Gynecology Reports. 14(1).

Aharoni, Sharon, et al.. (2025). Use of intraoperative ultrasound to aid in diagnosis and management of unusual “endometrioma". 10. 100116–100116.

Tizzano, Eduardo F., Susana Quijano-Roy, Laurent Servais, et al.. (2024). Outcomes for patients in the RESTORE registry with spinal muscular atrophy and four or more SMN2 gene copies treated with onasemnogene abeparvovec. European Journal of Paediatric Neurology. 53. 18–24.

Lavie, Moran, Keren Armoni Domany, Inbal Golan‐Tripto, et al.. (2024). Respiratory outcomes of onasemnogene abeparvovec treatment for spinal muscular atrophy: national real-world cohort study. European Journal of Pediatrics. 184(1). 58–58. 2 indexed citations

Nevo, Yoram, Huda Mussaffi, Gabriel Chodick, et al.. (2023). Evaluation of sputum cultures in children with spinal Muscular atrophy. Respiratory Medicine. 209. 107143–107143. 3 indexed citations

Shochat, Tzippy, et al.. (2023). Pulmonary function tests for evaluating the severity of Duchenne muscular dystrophy disease. Acta Paediatrica. 112(4). 854–860. 3 indexed citations

Konen, Osnat, Elhanan Nahum, Sharon Aharoni, et al.. (2022). Clinical improvement of a toddler with COVID-19 focal cerebral arteriopathy possibly due to intra-arterial nimodipine. European Journal of Paediatric Neurology. 40. 40–43. 1 indexed citations

Magen, Iddo, Sharon Aharoni, Itay Tokatly Latzer, et al.. (2022). Muscle microRNAs in the cerebrospinal fluid predict clinical response to nusinersen therapy in type II and type III spinal muscular atrophy patients. European Journal of Neurology. 29(8). 2420–2430. 20 indexed citations

10.

Aharoni, Sharon, et al.. (2022). Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec –routine care evidence. Gene Therapy. 30(1-2). 101–106. 8 indexed citations

11.

Prais, Dario, et al.. (2021). COVID-19 in advanced Duchenne/Becker muscular dystrophy patients. Neuromuscular Disorders. 31(7). 607–611. 11 indexed citations

12.

Aharoni, Sharon, Menachem Sadeh, Yehuda Shapira, et al.. (2016). Congenital myasthenic syndrome in Israel: Genetic and clinical characterization. Neuromuscular Disorders. 27(2). 136–140. 26 indexed citations

13.

Cohen, Rony, Ayelet Halevy, Sharon Aharoni, et al.. (2016). Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A. Neurogenetics. 17(4). 251–257. 5 indexed citations

14.

Aharoni, Sharon, Katy Barwick, Rachel Straussberg, et al.. (2016). Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel. BMC Medical Genetics. 17(1). 82–82. 14 indexed citations

15.

Cohen, Rony, Tamar Steinberg, Liora Kornreich, et al.. (2014). Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1. European Journal of Pediatrics. 174(2). 199–203. 8 indexed citations

16.

Aharoni, Sharon, Susan Treves, Michal Becker‐Cohen, et al.. (2013). Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation. PLoS ONE. 8(7). e69296–e69296. 10 indexed citations

17.

Nevo, Yoram, Bruria Ben‐Zeev, Adi Tabib, et al.. (2012). CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy. Blood. 121(1). 129–135. 111 indexed citations

18.

Aharoni, Sharon, Gaurav V. Harlalka, Amaka C Offiah, et al.. (2011). Striking phenotypic variability in familial TRPV4‐axonal neuropathy spectrum disorder. American Journal of Medical Genetics Part A. 155(12). 3153–3156. 6 indexed citations

19.

Aharoni, Sharon, et al.. (2010). MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions. Journal of the Neurological Sciences. 296(1-2). 101–103. 5 indexed citations

20.

Aharoni, Sharon & Abraham Weinberger. (2004). Inflammatory Arthritis of the Hands as Expressed by the Impressionists in the Orsay Museum. JCR Journal of Clinical Rheumatology. 10(2). 63–65. 1 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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