Lea Leonardis

1.6k total citations
27 papers, 462 citations indexed

About

Lea Leonardis is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Lea Leonardis has authored 27 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 10 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Lea Leonardis's work include Neurogenetic and Muscular Disorders Research (10 papers), Hereditary Neurological Disorders (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Lea Leonardis is often cited by papers focused on Neurogenetic and Muscular Disorders Research (10 papers), Hereditary Neurological Disorders (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Lea Leonardis collaborates with scholars based in Slovenia, United Kingdom and United States. Lea Leonardis's co-authors include Janez Zidar, Leja Dolenc Grošelj, Blaž Koritnik, Boris Rogelj, Leja Dolenc‐Grošelj, Mara Popović, Michaela Auer‐Grumbach, Anja Kovanda, Rok Blagus and Lea Papić and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Lea Leonardis

26 papers receiving 451 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lea Leonardis Slovenia 11 196 160 157 103 103 27 462
Jose A. Mazzitelli United States 6 106 0.5× 170 1.1× 161 1.0× 38 0.4× 329 3.2× 7 646
Andreas von Ameln-Mayerhofer Germany 10 96 0.5× 212 1.3× 268 1.7× 196 1.9× 97 0.9× 15 666
Francesco Giribaldi Italy 7 262 1.3× 146 0.9× 217 1.4× 107 1.0× 48 0.5× 7 484
Elena Giusto United Kingdom 10 74 0.4× 203 1.3× 94 0.6× 46 0.4× 102 1.0× 16 438
Jun‐Hui Yuan Japan 13 93 0.5× 210 1.3× 314 2.0× 28 0.3× 133 1.3× 48 522
Kiyotaka Nakamagoe Japan 13 166 0.8× 135 0.8× 156 1.0× 19 0.2× 185 1.8× 45 525
Stephan Klebe Germany 9 453 2.3× 90 0.6× 124 0.8× 21 0.2× 83 0.8× 11 562
Andrew Crane United States 16 102 0.5× 307 1.9× 239 1.5× 138 1.3× 75 0.7× 32 589
Carlos A. Ayala‐Grosso Venezuela 8 50 0.3× 118 0.7× 86 0.5× 39 0.4× 100 1.0× 17 691
Sachiyo Misumi Japan 11 88 0.4× 102 0.6× 91 0.6× 26 0.3× 65 0.6× 17 365

Countries citing papers authored by Lea Leonardis

Since Specialization
Citations

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

Fields of papers citing papers by Lea Leonardis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lea Leonardis

This figure shows the co-authorship network connecting the top 25 collaborators of Lea Leonardis. A scholar is included among the top collaborators of Lea Leonardis 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 Lea Leonardis. Lea Leonardis 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.
Koritnik, Blaž, et al.. (2024). Genetic Variability in Oxidative Stress, Inflammatory, and Neurodevelopmental Pathways: Impact on the Susceptibility and Course of Spinal Muscular Atrophy. Cellular and Molecular Neurobiology. 44(1). 71–71. 1 indexed citations
2.
Kovanda, Anja, Luca Lovrečić, Goražd Rudolf, et al.. (2023). Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy. Genes. 14(12). 2166–2166. 2 indexed citations
3.
Koritnik, Blaž, Lea Leonardis, Leja Dolenc‐Grošelj, et al.. (2022). Shaky hands are a part of motor neuron disease phenotype: clinical and electrophysiological study of 77 patients. Journal of Neurology. 269(8). 4498–4509. 4 indexed citations
4.
5.
Božović, Ivana Babič, Aleš Maver, Lea Leonardis, et al.. (2021). Diagnostic yield of exome sequencing in myopathies: Experience of a Slovenian tertiary centre. PLoS ONE. 16(6). e0252953–e0252953. 10 indexed citations
6.
Rogač, Mihael, David Neubauer, Lea Leonardis, et al.. (2021). Clinical Experience of Neurological Mitochondrial Diseases in Children and Adults: A Single-Center Study. SHILAP Revista de lepidopterología. 24(2). 5–14. 2 indexed citations
7.
Meznarič, Marija, Ksenija Fumić, & Lea Leonardis. (2019). Selective screening of late-onset Pompe disease (LOPD) in patients with non-diagnostic muscle biopsies. Journal of Clinical Pathology. 72(7). 468–472. 2 indexed citations
8.
Kovanda, Anja, Lea Leonardis, Janez Zidar, et al.. (2018). Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls. Scientific Reports. 8(1). 5609–5609. 59 indexed citations
9.
Boštjančič, Emanuela, Blaž Koritnik, Lea Leonardis, et al.. (2018). Differential Expression of Several miRNAs and the Host Genes AATK and DNM2 in Leukocytes of Sporadic ALS Patients. Frontiers in Molecular Neuroscience. 11. 106–106. 44 indexed citations
10.
11.
Leonardis, Lea & Simon Podnar. (2017). Template-operated MUP analysis is not accurate in the diagnosis of myopathic or neuropathic changes in the diaphragm. Neurophysiologie Clinique. 47(5-6). 405–412. 1 indexed citations
12.
Leonardis, Lea, et al.. (2016). Fatal recurrent dermatoneuro syndrome associated with systemic AL amyloidosis. Clinical Neuropathology. 35(3). 72–77. 2 indexed citations
13.
Koritnik, Blaž, Lea Leonardis, Leja Dolenc‐Grošelj, et al.. (2014). Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population. Neurobiology of Aging. 36(3). 1601.e17–1601.e20. 13 indexed citations
14.
Leonardis, Lea, Rok Blagus, & Leja Dolenc Grošelj. (2014). Sleep and breathing disorders in myotonic dystrophy type 2. Acta Neurologica Scandinavica. 132(1). 42–48. 15 indexed citations
15.
Leonardis, Lea, Michaela Auer‐Grumbach, Lea Papić, & Janez Zidar. (2012). The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features. European Journal of Neurology. 19(7). 992–998. 11 indexed citations
16.
Leonardis, Lea, et al.. (2011). Relapses and remissions of hypokalaemic periodic paralysis and multiple sclerosis in the same patient. Clinical Neurology and Neurosurgery. 113(8). 683–685.
17.
Guelly, Christian, Lea Leonardis, Lea Papić, et al.. (2010). Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I. The American Journal of Human Genetics. 88(1). 99–105. 95 indexed citations
18.
Leonardis, Lea, Janez Zidar, Mara Popović, et al.. (2000). Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family. Pflügers Archiv - European Journal of Physiology. 439(S1). r208–r210. 18 indexed citations
19.
Leonardis, Lea, Janez Zidar, Mara Popović, et al.. (2000). Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family. Pflügers Archiv - European Journal of Physiology. 439(7). R208–R210. 1 indexed citations
20.
Zidar, Janez, Lea Leonardis, Mara Popović, et al.. (1999). Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred. Annals of Neurology. 46(1). 36–44. 58 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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