L. Mesa

698 total citations
13 papers, 293 citations indexed

About

L. Mesa is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, L. Mesa has authored 13 papers receiving a total of 293 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in L. Mesa's work include Neurogenetic and Muscular Disorders Research (6 papers), Muscle Physiology and Disorders (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). L. Mesa is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Muscle Physiology and Disorders (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). L. Mesa collaborates with scholars based in Argentina, United States and Italy. L. Mesa's co-authors include Alberto Dubrovsky, Eduardo Luis De Vito, José Corderí, Gabriela Ferreyra, Pascual Marco, Aquiles J. Roncoroni, C. Angelini, Elena Pegoraro, Domenico Marco Bonifati and Hans H. Goebel and has published in prestigious journals such as Journal of Neuropathology & Experimental Neurology, Journal of the Neurological Sciences and Frontiers in Pharmacology.

In The Last Decade

L. Mesa

10 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. Mesa Argentina	6	137	94	78	56	51	13	293
M. Wohlgemuth Netherlands	9	338 2.5×	70 0.7×	109 1.4×	65 1.2×	27 0.5×	9	450
Fortunato Mangiola Italy	9	282 2.1×	30 0.3×	139 1.8×	52 0.9×	87 1.7×	9	518
Federica Trucco Italy	13	213 1.6×	88 0.9×	48 0.6×	119 2.1×	11 0.2×	35	399
L. Wahlgren Sweden	6	92 0.7×	49 0.5×	77 1.0×	54 1.0×	31 0.6×	7	222
Claire Le Guillou France	8	229 1.7×	67 0.7×	46 0.6×	58 1.0×	35 0.7×	13	414
Y. Khan United Kingdom	3	72 0.5×	161 1.7×	50 0.6×	106 1.9×	29 0.6×	8	296
M. van den Hauwe Belgium	13	375 2.7×	26 0.3×	96 1.2×	47 0.8×	18 0.4×	26	514
Acary Bulle Oliveira Brazil	8	54 0.4×	13 0.1×	57 0.7×	26 0.5×	110 2.2×	25	278
Yasumitsu Ichikawa Japan	10	46 0.3×	40 0.4×	28 0.4×	50 0.9×	91 1.8×	25	279
Peter Kühnlein Germany	10	65 0.5×	64 0.7×	200 2.6×	63 1.1×	337 6.6×	13	536

Countries citing papers authored by L. Mesa

Since Specialization

Citations

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

Fields of papers citing papers by L. Mesa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Mesa

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

All Works

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13 of 13 papers shown

Chaves, Hernán, et al.. (2025). Whole-Body Skeletal Muscle MRI Patterns in Female Dystrophinopathy Carriers. Neurology Genetics. 11(5). e200301–e200301.

Mesa, L., et al.. (2022). The difficult path to diagnosis of the patient with spinal muscular atrophy. Archivos Argentinos de Pediatria. 121(2). e202102542–e202102542. 2 indexed citations

Mesa, L., et al.. (2022). El difícil camino al diagnóstico del paciente con atrofia muscular espinal. Archivos Argentinos de Pediatria.

Mazzanti, Chiara Maria, et al.. (2021). Theragnosis for Duchenne Muscular Dystrophy. Frontiers in Pharmacology. 12. 648390–648390. 6 indexed citations

Mesa, L., et al.. (2021). Diagnostic journey of patients with spinal muscular atrophy in Argentina. Journal of the Neurological Sciences. 429. 118427–118427.

Dubrovsky, Alberto, et al.. (2011). P1.15 Left ventricular torsion analysis in Duchenne Muscular Dystrophy. Neuromuscular Disorders. 21(9-10). 646–646. 1 indexed citations

Taratuto, A.L., Hasan O. Akman, M. Saccoliti, et al.. (2010). Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: Muscle biopsy and autopsy findings, biochemical and molecular genetic studies. Neuromuscular Disorders. 20(12). 783–790. 21 indexed citations

Mesa, L., et al.. (2003). Nutritional Assessment of Patients with Neuromuscular Diseases. American Journal of Physical Medicine & Rehabilitation. 82(3). 182–185. 34 indexed citations

Mesa, L., et al.. (2003). . American Journal of Physical Medicine & Rehabilitation. 82(3). 182–185. 1 indexed citations

10.

Ferreyra, Gabriela, et al.. (2002). Peak Flow and Peak Cough Flow in the Evaluation of Expiratory Muscle Weakness and Bulbar Impairment in Patients with Neuromuscular Disease. American Journal of Physical Medicine & Rehabilitation. 81(7). 506–511. 130 indexed citations

11.

Dubrovsky, Alberto, C. Angelini, Domenico Marco Bonifati, Elena Pegoraro, & L. Mesa. (1998). Steroids in muscular dystrophy: where do we stand?. Neuromuscular Disorders. 8(6). 380–384. 20 indexed citations

12.

Taratuto, A.L., Alberto Dubrovsky, L. Mesa, et al.. (1997). α SARCOGLYCAN DEFICIENCY, TWO NOVEL MUTATIONS. Journal of Neuropathology & Experimental Neurology. 56(5). 619–619. 1 indexed citations

13.

Mesa, L., et al.. (1991). Steroids in duchenne muscular dystrophy — Deflazacort trial. Neuromuscular Disorders. 1(4). 261–266. 77 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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