Lúcia Inês Macedo‐Souza

708 citations

18 papers · 338 indexed · h-index 10

Co-authors: Fernando Kok Mayana Zatz Silvana Santos Karina Lezirovitz Diogo Meyer Regina Célia Mingroni‐Netto Jorge Rocha Angelina Maria Martins Lino
Topics: Neurogenetic and Muscular Disorders Research (6 papers)Hereditary Neurological Disorders (6 papers)Neurological diseases and metabolism (4 papers)
Cited by: Neurology Genetics Cellular and Molecular Neuroscience
Journals: Annals of Neurology Human Molecular Genetics EMBO Reports
Partner nations: Brazil United States United Kingdom

In The Last Decade

Lúcia Inês Macedo‐Souza

18 papers receiving 330 citations

Peers

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

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18 of 18 papers shown

#	Work	Indexed citations
1	Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia. 2022 ·Molecular Case Studies ·(unknown),(unknown),Paulo Ribeiro Nóbrega,Anderson Rodrigues Brandão de Paiva,(unknown),(unknown),Lúcia Inês Macedo‐Souza,Clarissa Bueno,David S. Lynch,Henry Houlden,Leandro Tavares Lucato,Fernando Kok	4
2	Apraxia of Eyelid Opening and Blepharospasm in Two Spinocerebellar Ataxia Type 3 Patients 2022 ·Tremor and Other Hyperkinetic Movements ·(unknown),(unknown),(unknown),Anderson Rodrigues Brandão de Paiva,Lúcia Inês Macedo‐Souza,Fernando Kok	2
3	MECP2-related conditions in males: A systematic literature review and 8 additional cases 2021 ·European Journal of Paediatric Neurology ·(unknown),(unknown),Lúcia Inês Macedo‐Souza,(unknown),Juliana Gurgel‐Giannetti,Fabíola Paoli Monteiro,(unknown),(unknown),(unknown),Charles Marques Lourenço,(unknown),Lucia Sukys-Claudino,(unknown),Sérgio Antônio Antoniuk,(unknown),(unknown),(unknown),Eliana Garzón,Fernando Kok	9
4	Additional observation of a de novo pathogenic variant in KCNT2 leading to epileptic encephalopathy with clinical features of frontal lobe epilepsy 2020 ·Brain and Development ·(unknown),Lúcia Inês Macedo‐Souza,(unknown),Fabíola Paoli Monteiro,(unknown),João Paulo Kitajima,Eliana Garzón,Fernando Kok	9
5	ATP6V1B2‐related epileptic encephalopathy 2020 ·Epileptic Disorders ·(unknown),Lúcia Inês Macedo‐Souza,(unknown),Fabíola Paoli Monteiro,(unknown),Luís Filipe de Souza Godoy,(unknown),(unknown),Eliana Garzón,Fernando Kok	10
6	Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: two new cases and review of the literature 2019 ·Brain and Development ·(unknown),Lúcia Inês Macedo‐Souza,(unknown),(unknown),Fabíola Paoli Monteiro,João Paulo Kitajima,Luís Filipe de Souza Godoy,(unknown),Fernando Kok,Eliana Garzón	15
7	PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy 2019 ·Neurology Genetics ·Anderson Rodrigues Brandão de Paiva,David S. Lynch,Uirá Souto Melo,Leandro Tavares Lucato,(unknown),(unknown),Isabella Peixoto de Barcelos,(unknown),(unknown),Lúcia Inês Macedo‐Souza,Henry Houlden,Fernando Kok	16
8	Typical clinical and neuroimaging features in Sjögren-Larsson syndrome 2018 ·Arquivos de Neuro-Psiquiatria ·Anderson Rodrigues Brandão de Paiva,Uirá Souto Melo,(unknown),Denise Dória,(unknown),Lúcia Inês Macedo‐Souza,Leandro Tavares Lucato,Fernando Kok	1
9	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 2017 ·Stem Cell Reviews and Reports ·(unknown),(unknown),Marcos Valadares,Juliana Gomes,(unknown),(unknown),Amanda F. Assoni,(unknown),Alexander Birbrair,Antonio Carlos Pedroso de Lima,Júlio M. Singer,(unknown),Giovani L. Silva,Mário Sérgio Mantovani,Lúcia Inês Macedo‐Souza,M Ferrari,Mayana Zatz	48
10	Inferring paternal history of rural African‐derived Brazilian populations from Y chromosomes 2016 ·American Journal of Human Biology ·(unknown),Kelly Nunes,Lúcia Inês Macedo‐Souza,Jorge Rocha,Diogo Meyer,Regina Célia Mingroni‐Netto	32
11	Overexpression ofKLC2due to a homozygous deletion in the non-coding region causes SPOAN syndrome 2015 ·Human Molecular Genetics ·Uirá Souto Melo,Lúcia Inês Macedo‐Souza,(unknown),Alysson R. Muotri,Joseph G. Gleeson,(unknown),Pablo Armas,Nora B. Calcaterra,João Paulo Kitajima,(unknown),(unknown),Karina Griesi‐Oliveira,(unknown),Clarissa Ribeiro Reily Rocha,(unknown),Carlos Frederico Martins Menck,Maha S. Zaki,Fernando Kok,Mayana Zatz,Silvana Santos	35
12	Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease 2015 ·Neurology Genetics ·José Luiz Pedroso,Clarissa Ribeiro Reily Rocha,Lúcia Inês Macedo‐Souza,(unknown),Wilson Marques,Orlando Graziani Póvoas Barsottini,(unknown),Carlos Frederico Martins Menck,Fernando Kok	21
13	Leukodystrophy with premature ovarian failure: think on vanishing white matter disease (VWMD) 2015 ·Arquivos de Neuro-Psiquiatria ·(unknown),(unknown),Denise Dória,Anderson Rodrigues Brandão de Paiva,Lúcia Inês Macedo‐Souza,Fernando Kok	1
14	Nerve conduction studies in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome 2013 ·Muscle & Nerve ·(unknown),Carlos Otto Heise,Silvana Santos,Lúcia Inês Macedo‐Souza,Mayana Zatz,Fernando Kok	6
15	Motor and functional evaluation of patients with spastic paraplegia, optic atrophy, and neuropathy (SPOAN) 2010 ·Arquivos de Neuro-Psiquiatria ·(unknown),Silvana Santos,Lúcia Inês Macedo‐Souza,Carlos Bandeira de Mello Monteiro,(unknown),(unknown),Mayana Zatz,Fernando Kok	7
16	Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes 2009 ·Annals of Human Genetics ·Lúcia Inês Macedo‐Souza,Fernando Kok,Silvana Santos,(unknown),Karina Lezirovitz,(unknown),Clarissa Bueno,(unknown),André Luiz Santos Pessoa,(unknown),(unknown),(unknown),(unknown),Paulo Alberto Otto,Mayana Zatz	27
17	Mutation in the Scyl1 gene encoding amino‐terminal kinase‐like protein causes a recessive form of spinocerebellar neurodegeneration 2007 ·EMBO Reports ·Wolfgang M. Schmidt,Cornelia Kraus,Harald Höger,Sonja Hochmeister,Felicitas Oberndorfer,(unknown),(unknown),Hans Lassmann,(unknown),Lúcia Inês Macedo‐Souza,Mariz Vainzof,Mayana Zatz,André Reis,Reginald E. Bittner	48
18	Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13 2005 ·Annals of Neurology ·Lúcia Inês Macedo‐Souza,Fernando Kok,Silvana Santos,(unknown),Alessandra Starling,Agnes L. Nishimura,Karina Lezirovitz,Angelina Maria Martins Lino,Mayana Zatz	47

About Lúcia Inês Macedo‐Souza

Lúcia Inês Macedo‐Souza is a scholar working on Genetics, Neurology and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 338 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (6 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Neurology (57 citations), Genetics (68 citations) and Cellular and Molecular Neuroscience (90 citations). Lúcia Inês Macedo‐Souza has collaborated with scholars based in Brazil, United States and United Kingdom. Frequent co-authors include Fernando Kok, Mayana Zatz, Silvana Santos, Karina Lezirovitz, Diogo Meyer, Regina Célia Mingroni‐Netto, Jorge Rocha, Angelina Maria Martins Lino, Agnes L. Nishimura and Alessandra Starling. Their work appears in journals such as Annals of Neurology, Human Molecular Genetics and EMBO Reports.

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