Lúcia Inês Macedo‐Souza

708 total citations
18 papers, 338 citations indexed

About

Lúcia Inês Macedo‐Souza is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Lúcia Inês Macedo‐Souza has authored 18 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 6 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Lúcia Inês Macedo‐Souza's work include Neurogenetic and Muscular Disorders Research (6 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (4 papers). Lúcia Inês Macedo‐Souza is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (4 papers). Lúcia Inês Macedo‐Souza collaborates with scholars based in Brazil, United States and United Kingdom. Lúcia Inês Macedo‐Souza's co-authors include Fernando Kok, Mayana Zatz, Silvana Santos, Karina Lezirovitz, Angelina Maria Martins Lino, Kelly Nunes, Diogo Meyer, Jorge Rocha, Regina Célia Mingroni‐Netto and Alessandra Starling and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and EMBO Reports.

In The Last Decade

Lúcia Inês Macedo‐Souza

18 papers receiving 330 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lúcia Inês Macedo‐Souza Brazil 10 143 90 68 57 56 18 338
Hatice Karasoy Türkiye 10 147 1.0× 88 1.0× 48 0.7× 52 0.9× 59 1.1× 26 332
Mariangela Lo Giudice Italy 8 117 0.8× 94 1.0× 29 0.4× 44 0.8× 100 1.8× 18 283
Stefania Bassanini Italy 10 139 1.0× 204 2.3× 75 1.1× 35 0.6× 44 0.8× 13 424
Marta Jurek Poland 9 193 1.3× 51 0.6× 118 1.7× 34 0.6× 67 1.2× 24 345
Maria Chiara Malaguti Italy 7 118 0.8× 42 0.5× 32 0.5× 39 0.7× 60 1.1× 18 303
Mihaela Bustuchina ̆ Vlaicu France 7 114 0.8× 59 0.7× 33 0.5× 44 0.8× 121 2.2× 10 394
Genni Desiato Italy 9 169 1.2× 78 0.9× 27 0.4× 141 2.5× 41 0.7× 12 449
Giorgia Piccini Italy 12 346 2.4× 84 0.9× 26 0.4× 32 0.6× 128 2.3× 15 451
Tomokatsu Yoshida Japan 12 342 2.4× 51 0.6× 63 0.9× 57 1.0× 17 0.3× 54 546
Amy Harper United States 8 109 0.8× 99 1.1× 36 0.5× 29 0.5× 32 0.6× 19 281

Countries citing papers authored by Lúcia Inês Macedo‐Souza

Since Specialization
Citations

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

Fields of papers citing papers by Lúcia Inês Macedo‐Souza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lúcia Inês Macedo‐Souza. 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 Lúcia Inês Macedo‐Souza. The network helps show where Lúcia Inês Macedo‐Souza may publish in the future.

Co-authorship network of co-authors of Lúcia Inês Macedo‐Souza

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

All Works

18 of 18 papers shown
1.
Nóbrega, Paulo Ribeiro, Anderson Rodrigues Brandão de Paiva, Lúcia Inês Macedo‐Souza, et al.. (2022). Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.. Molecular Case Studies. mcs.a006232–mcs.a006232. 4 indexed citations
2.
Paiva, Anderson Rodrigues Brandão de, et al.. (2022). Apraxia of Eyelid Opening and Blepharospasm in Two Spinocerebellar Ataxia Type 3 Patients. Tremor and Other Hyperkinetic Movements. 12(1). 1–1. 2 indexed citations
3.
Macedo‐Souza, Lúcia Inês, Juliana Gurgel‐Giannetti, Fabíola Paoli Monteiro, et al.. (2021). MECP2-related conditions in males: A systematic literature review and 8 additional cases. European Journal of Paediatric Neurology. 34. 7–13. 9 indexed citations
4.
Macedo‐Souza, Lúcia Inês, et al.. (2020). Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy. Brain and Development. 42(9). 691–695. 9 indexed citations
5.
Macedo‐Souza, Lúcia Inês, et al.. (2020). ATP6V1B2‐related epileptic encephalopathy. Epileptic Disorders. 22(3). 317–322. 10 indexed citations
6.
Paiva, Anderson Rodrigues Brandão de, David S. Lynch, Uirá Souto Melo, et al.. (2019). PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy. Neurology Genetics. 5(1). e306–e306. 16 indexed citations
7.
Macedo‐Souza, Lúcia Inês, Fabíola Paoli Monteiro, João Paulo Kitajima, et al.. (2019). Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literature. Brain and Development. 42(2). 211–216. 15 indexed citations
8.
Paiva, Anderson Rodrigues Brandão de, Uirá Souto Melo, Denise Dória, et al.. (2018). Typical clinical and neuroimaging features in Sjögren-Larsson syndrome. Arquivos de Neuro-Psiquiatria. 76(4). 283–283. 1 indexed citations
9.
Valadares, Marcos, Juliana Gomes, Amanda F. Assoni, et al.. (2017). Pericytes Extend Survival of ALS SOD1 Mice and Induce the Expression of Antioxidant Enzymes in the Murine Model and in IPSCs Derived Neuronal Cells from an ALS Patient. Stem Cell Reviews and Reports. 13(5). 686–698. 48 indexed citations
10.
Nunes, Kelly, et al.. (2016). Inferring paternal history of rural African‐derived Brazilian populations from Y chromosomes. American Journal of Human Biology. 29(2). 32 indexed citations
11.
Melo, Uirá Souto, Lúcia Inês Macedo‐Souza, Alysson R. Muotri, et al.. (2015). Overexpression ofKLC2due to a homozygous deletion in the non-coding region causes SPOAN syndrome. Human Molecular Genetics. 24(24). ddv388–ddv388. 35 indexed citations
12.
Dória, Denise, et al.. (2015). Leukodystrophy with premature ovarian failure: think on vanishing white matter disease (VWMD). Arquivos de Neuro-Psiquiatria. 73(1). 65–65. 1 indexed citations
13.
Pedroso, José Luiz, Clarissa Ribeiro Reily Rocha, Lúcia Inês Macedo‐Souza, et al.. (2015). Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease. Neurology Genetics. 1(4). e30–e30. 21 indexed citations
14.
Heise, Carlos Otto, et al.. (2013). Nerve conduction studies in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. Muscle & Nerve. 49(1). 131–133. 6 indexed citations
15.
Santos, Silvana, et al.. (2010). Motor and functional evaluation of patients with spastic paraplegia, optic atrophy, and neuropathy (SPOAN). Arquivos de Neuro-Psiquiatria. 68(1). 3–6. 7 indexed citations
16.
Macedo‐Souza, Lúcia Inês, Fernando Kok, Silvana Santos, et al.. (2009). Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes. Annals of Human Genetics. 73(3). 382–387. 27 indexed citations
17.
Schmidt, Wolfgang M., Cornelia Kraus, Harald Höger, et al.. (2007). Mutation in the Scyl1 gene encoding amino‐terminal kinase‐like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO Reports. 8(7). 691–697. 48 indexed citations
18.
Macedo‐Souza, Lúcia Inês, Fernando Kok, Silvana Santos, et al.. (2005). Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13. Annals of Neurology. 57(5). 730–737. 47 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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