Lea Papić

570 total citations
7 papers, 209 citations indexed

About

Lea Papić is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Lea Papić has authored 7 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 4 papers in Cell Biology and 2 papers in Molecular Biology. Recurrent topics in Lea Papić's work include Hereditary Neurological Disorders (6 papers), Cellular Mechanics and Interactions (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Lea Papić is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Cellular Mechanics and Interactions (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Lea Papić collaborates with scholars based in Austria, United States and Germany. Lea Papić's co-authors include Michaela Auer‐Grumbach, Andreas Janecke, Thomas R. Pieber, Slave Trajanoski, Maria Schabhüttl, Lea Leonardis, Janez Zidar, Eleonore Fröhlich, Christian Guelly and Heimo Strohmaier and has published in prestigious journals such as Brain, The American Journal of Human Genetics and Journal of Neurology.

In The Last Decade

Lea Papić

7 papers receiving 208 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lea Papić Austria	7	133	76	69	66	25	7	209
Eduardo Calpena Spain	11	114 0.9×	153 2.0×	39 0.6×	29 0.4×	25 1.0×	21	272
Menelaos Pipis United Kingdom	7	214 1.6×	90 1.2×	41 0.6×	79 1.2×	74 3.0×	10	289
Tomasz Rusielewicz United States	6	63 0.5×	107 1.4×	32 0.5×	114 1.7×	17 0.7×	7	239
Alexander P. Drew Australia	10	148 1.1×	152 2.0×	45 0.7×	84 1.3×	35 1.4×	15	303
Jeff Goldy United States	5	144 1.1×	168 2.2×	43 0.6×	57 0.9×	52 2.1×	5	316
Anna Walczak Poland	11	79 0.6×	174 2.3×	50 0.7×	30 0.5×	22 0.9×	19	271
M. Zimoń Belgium	8	142 1.1×	134 1.8×	73 1.1×	62 0.9×	41 1.6×	10	301
Florian Harmuth Germany	8	117 0.9×	120 1.6×	19 0.3×	52 0.8×	58 2.3×	11	235
Burçak Özeş United States	8	107 0.8×	88 1.2×	30 0.4×	39 0.6×	39 1.6×	12	185
Benjamin J. Yungher United States	7	206 1.5×	170 2.2×	19 0.3×	51 0.8×	12 0.5×	9	326

Countries citing papers authored by Lea Papić

Since Specialization

Citations

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

Fields of papers citing papers by Lea Papić

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lea Papić

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

All Works

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7 of 7 papers shown

1.

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

2.

Auer‐Grumbach, Michaela, Martin Weger, Regina Fink‐Puches, et al.. (2011). Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin. Brain. 134(6). 1839–1852. 46 indexed citations

3.

Finsterer, Josef, Lea Papić, & Michaela Auer‐Grumbach. (2011). Motor neuron, nerve, and neuromuscular junction disease. Current Opinion in Neurology. 24(5). 469–474. 7 indexed citations

4.

Fischer, Carina, Slave Trajanoski, Lea Papić, et al.. (2011). SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease. Journal of Neurology. 259(3). 515–523. 19 indexed citations

5.

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

6.

Papić, Lea, Dirk Fischer, Slave Trajanoski, et al.. (2010). SNP-array based whole genome homozygosity mapping: A quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients. European Journal of Medical Genetics. 54(3). 214–219. 13 indexed citations

7.

Auer‐Grumbach, Michaela, Carina Fischer, Lea Papić, et al.. (2008). Two Novel Mutations in the GDAP1 and PRX Genes in Early Onset Charcot-Marie-Tooth Syndrome. Neuropediatrics. 39(1). 33–38. 18 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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