Avi Fellner

703 total citations
20 papers, 326 citations indexed

About

Avi Fellner is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Avi Fellner has authored 20 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Neurology. Recurrent topics in Avi Fellner's work include Genomics and Rare Diseases (5 papers), RNA regulation and disease (5 papers) and Neurological diseases and metabolism (4 papers). Avi Fellner is often cited by papers focused on Genomics and Rare Diseases (5 papers), RNA regulation and disease (5 papers) and Neurological diseases and metabolism (4 papers). Avi Fellner collaborates with scholars based in Israel, United States and Australia. Avi Fellner's co-authors include Kishore R. Kumar, Fangzhi Jia, Israel Steiner, Shlomit Yust‐Katz, Shai Rosenberg, Alexander Lossos, Chen Makranz, Tali Siegal, Michal Lotem and Felix Bokstein and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Avi Fellner

20 papers receiving 322 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Avi Fellner Israel 7 135 87 80 63 51 20 326
Joshua Menke United States 7 320 2.4× 79 0.9× 63 0.8× 49 0.8× 87 1.7× 20 504
Céline Ruegsegger Switzerland 7 136 1.0× 114 1.3× 173 2.2× 48 0.8× 108 2.1× 8 430
Bercin Kutluk Cenik United States 4 161 1.2× 68 0.8× 127 1.6× 27 0.4× 18 0.4× 6 318
Yugong Feng China 12 119 0.9× 24 0.3× 116 1.4× 45 0.7× 29 0.6× 69 316
Sravanthi Koduri United States 11 205 1.5× 28 0.3× 131 1.6× 66 1.0× 57 1.1× 37 425
Huanyu Meng China 10 125 0.9× 38 0.4× 88 1.1× 19 0.3× 22 0.4× 28 280
Suyue Zheng China 13 61 0.5× 39 0.4× 156 1.9× 27 0.4× 31 0.6× 23 329
Antonio Guerrero Spain 11 241 1.8× 30 0.3× 92 1.1× 33 0.5× 107 2.1× 19 435
Huan Du China 8 106 0.8× 33 0.4× 92 1.1× 17 0.3× 17 0.3× 14 349
Kiichiro Beppu Japan 8 58 0.4× 76 0.9× 159 2.0× 39 0.6× 57 1.1× 16 360

Countries citing papers authored by Avi Fellner

Since Specialization
Citations

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

Fields of papers citing papers by Avi Fellner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avi Fellner

This figure shows the co-authorship network connecting the top 25 collaborators of Avi Fellner. A scholar is included among the top collaborators of Avi Fellner 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 Avi Fellner. Avi Fellner 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.
Fellner, Avi, Matthew Hobbs, Ira W. Deveson, et al.. (2024). An Inversion Affecting the GCH1 Gene as a Novel Finding in Dopa‐Responsive Dystonia. Movement Disorders Clinical Practice. 11(5). 582–585. 2 indexed citations
2.
Basel‐Salmon, Lina, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2023). Clinically actionable incidental and secondary parental genomic findings after proband exome sequencing: Yield and dilemmas. SHILAP Revista de lepidopterología. 1(1). 100813–100813. 1 indexed citations
3.
Williams, Laura, Ira W. Deveson, Igor Stevanovski, et al.. (2023). NOTCH2NLC GGC Repeat Expansion Presenting as Adult‐Onset Cervical Dystonia. Movement Disorders Clinical Practice. 10(4). 704–706. 1 indexed citations
4.
Davis, Mark R., G. Michael Hálmagyi, Avi Fellner, et al.. (2023). Two New Families and a Literature Review of ELOVL4-Associated Spinocerebellar Ataxia Type 34. The Cerebellum. 23(1). 268–277. 5 indexed citations
5.
Fellner, Avi, Yael Goldberg, & Lina Basel‐Salmon. (2023). Ordering genetic testing by neurologists: points to consider. Journal of Neurology. 270(8). 3714–3722. 2 indexed citations
6.
Fellner, Avi, et al.. (2022). Elevated lumbar puncture opening pressure in aseptic meningitis. Journal of Clinical Neuroscience. 106. 55–60. 1 indexed citations
7.
Fellner, Avi, Yael Goldberg, Dorit Lev, et al.. (2022). In-silico phenotype prediction by normal mode variant analysis in TUBB4A-related disease. Scientific Reports. 12(1). 58–58. 1 indexed citations
8.
Jia, Fangzhi, Avi Fellner, & Kishore R. Kumar. (2022). Monogenic Parkinson’s Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing. Genes. 13(3). 471–471. 95 indexed citations
9.
Tisch, Stephen, Michel Tchan, Victor S.C. Fung, et al.. (2022). A novel synonymous KMT2B variant in a patient with dystonia causes aberrant splicing. Molecular Genetics & Genomic Medicine. 10(5). e1923–e1923. 4 indexed citations
10.
Fellner, Avi, Noa Ruhrman‐Shahar, Naama Orenstein, et al.. (2021). The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disorders. Genetics in Medicine. 23(6). 1095–1100. 4 indexed citations
11.
Morales‐Briceño, Hugo, Laura Williams, Shekeeb S. Mohammad, et al.. (2021). Possible EIF2AK2‐Associated Stress‐Related Neurological Decompensation with Combined Dystonia and Striatal Lesions. Movement Disorders Clinical Practice. 9(2). 240–244. 11 indexed citations
12.
Stern, Tomer, Naama Orenstein, Avi Fellner, et al.. (2021). Epilepsy and electroencephalogram evolution in YWHAG gene mutation: A new phenotype and review of the literature. American Journal of Medical Genetics Part A. 185(3). 901–908. 6 indexed citations
13.
Wilf‐Yarkoni, Adi, Oded Shor, Avi Fellner, et al.. (2021). Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin. Neurology Genetics. 7(2). e578–e578. 12 indexed citations
14.
Fellner, Avi, Alexander Lossos, Е А Коган, et al.. (2021). Two intronic cis‐acting variants in both alleles of the POLR3A gene cause progressive spastic ataxia with hypodontia. Clinical Genetics. 99(5). 713–718. 1 indexed citations
15.
Fellner, Avi, Naama Orenstein, Lily Bazak, et al.. (2021). Biallelic truncating variants in the muscular A‐type lamin‐interacting protein (MLIP) gene cause myopathy with hyperCKemia. European Journal of Neurology. 29(4). 1174–1180. 4 indexed citations
16.
Fellner, Avi, et al.. (2019). Meningitis without meningeal irritation signs: What are the alerting clinical markers?. Journal of the Neurological Sciences. 410. 116663–116663. 5 indexed citations
17.
Fellner, Avi, Chen Makranz, Michal Lotem, et al.. (2018). Neurologic complications of immune checkpoint inhibitors. Journal of Neuro-Oncology. 137(3). 601–609. 109 indexed citations
18.
Fellner, Avi, Yael Barhum, Ariel Angel, et al.. (2017). Toll-Like Receptor-4 Inhibitor TAK-242 Attenuates Motor Dysfunction and Spinal Cord Pathology in an Amyotrophic Lateral Sclerosis Mouse Model. International Journal of Molecular Sciences. 18(8). 1666–1666. 43 indexed citations
19.
Fellner, Avi, Felix Benninger, & Ruth Djaldetti. (2015). Synthetic cannabinoids revealing adrenoleukodystrophy. Journal of Clinical Neuroscience. 24. 155–156. 2 indexed citations
20.
Fellner, Avi, et al.. (2014). Multiple sclerosis is associated with psoriasis. A case–control study. Journal of the Neurological Sciences. 338(1-2). 226–228. 17 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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