Eloísa S. Moreira

1.4k total citations
18 papers, 816 citations indexed

About

Eloísa S. Moreira is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Eloísa S. Moreira has authored 18 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Eloísa S. Moreira's work include Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (5 papers) and Calpain Protease Function and Regulation (3 papers). Eloísa S. Moreira is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (5 papers) and Calpain Protease Function and Regulation (3 papers). Eloísa S. Moreira collaborates with scholars based in Brazil, United States and United Kingdom. Eloísa S. Moreira's co-authors include Maria Rita Passos‐Bueno, Mariz Vainzof, Mayana Zatz, Suely Kazue Nagahashi Marie, Georgine Faulkner, Oscar Suzuki, Roger H. Reeves, Giorgio Valle, Dieter E. Jenne and Tim Wiltshire and has published in prestigious journals such as Nature Genetics, Blood and PLoS ONE.

In The Last Decade

Eloísa S. Moreira

18 papers receiving 786 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eloísa S. Moreira Brazil 13 701 300 234 161 106 18 816
Leta S. Steffen United States 11 714 1.0× 117 0.4× 97 0.4× 176 1.1× 73 0.7× 12 946
Paula Scotland United States 10 548 0.8× 218 0.7× 71 0.3× 212 1.3× 88 0.8× 15 817
Pietro Spitali Netherlands 20 1.0k 1.4× 132 0.4× 191 0.8× 145 0.9× 115 1.1× 55 1.1k
Marry Markman Netherlands 8 524 0.7× 107 0.4× 220 0.9× 31 0.2× 28 0.3× 11 815
Mayana Zatz Brazil 10 1.0k 1.5× 407 1.4× 268 1.1× 534 3.3× 116 1.1× 19 1.2k
Hernán Gonorazky Canada 12 532 0.8× 76 0.3× 122 0.5× 95 0.6× 208 2.0× 43 710
Malika Chaouch Algeria 10 691 1.0× 275 0.9× 83 0.4× 203 1.3× 70 0.7× 14 910
Christina L. Liquori United States 8 922 1.3× 750 2.5× 136 0.6× 53 0.3× 97 0.9× 8 1.5k
Loreto Martorell Spain 22 1.0k 1.4× 735 2.5× 59 0.3× 92 0.6× 65 0.6× 73 1.4k
Irène Marics France 12 721 1.0× 89 0.3× 157 0.7× 127 0.8× 18 0.2× 16 897

Countries citing papers authored by Eloísa S. Moreira

Since Specialization
Citations

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

Fields of papers citing papers by Eloísa S. Moreira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eloísa S. Moreira. 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 Eloísa S. Moreira. The network helps show where Eloísa S. Moreira may publish in the future.

Co-authorship network of co-authors of Eloísa S. Moreira

This figure shows the co-authorship network connecting the top 25 collaborators of Eloísa S. Moreira. A scholar is included among the top collaborators of Eloísa S. Moreira 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 Eloísa S. Moreira. Eloísa S. Moreira 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.
Perazzio, Sandro Félix, et al.. (2019). Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus. Advances in Rheumatology. 59(1). 36–36. 10 indexed citations
2.
Moreira, Eloísa S., Isabela Mayá Wayhs Silva, Naila Cristina Vilaça Lourenço, et al.. (2016). Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in autism spectrum disorders. 23. 145–151. 7 indexed citations
3.
Griesi‐Oliveira, Karina, Naila Cristina Vilaça Lourenço, Kátia M. Rocha, et al.. (2014). Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy. PLoS ONE. 9(9). e107705–e107705. 19 indexed citations
4.
Moreira, Eloísa S., et al.. (2008). Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR. Brazilian Journal of Medical and Biological Research. 41(10). 833–838. 7 indexed citations
5.
Griesi‐Oliveira, Karina, et al.. (2008). HTR1B and HTR2C in autism spectrum disorders in Brazilian families. Brain Research. 1250. 14–19. 25 indexed citations
6.
Moreira, Eloísa S., et al.. (2008). Acute Promyelocytic Leukemia with T(15;17): Frequency of Additional Clonal Chromosome Abnormalities and FLT3. Blood. 112(11). 4857–4857. 1 indexed citations
7.
Perez, Renata de Mello, José Osmar Medina Pestana, Valéria Pereira Lanzoni, et al.. (2007). Factors associated with the intensity of liver fibrosis in renal transplant patients with hepatitis B virus infection. European Journal of Gastroenterology & Hepatology. 19(8). 653–657. 9 indexed citations
8.
Vainzof, Mariz, Louise V.B. Anderson, Elizabeth M. McNally, et al.. (2001). Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience. 17(1). 71–80. 53 indexed citations
9.
Iughetti, Paula, Oscar Suzuki, Paulo H. Godoi, et al.. (2001). A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma.. PubMed. 61(20). 7375–8. 62 indexed citations
10.
Moreira, Eloísa S., Tim Wiltshire, Georgine Faulkner, et al.. (2000). Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin. Nature Genetics. 24(2). 163–166. 238 indexed citations
11.
Vainzof, Mariz, Eloísa S. Moreira, Manuel Cánovas, et al.. (2000). Partial α‐sarcoglycan deficiency with retention of the dystrophin‐glycoprotein complex in a LGMD2D family. Muscle & Nerve. 23(6). 984–988. 22 indexed citations
12.
Passos‐Bueno, Maria Rita, Mariz Vainzof, Eloísa S. Moreira, & Mayana Zatz. (1999). Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics. 82(5). 392–398. 76 indexed citations
13.
Moreira, Eloísa S., Mariz Vainzof, Suely Kazue Nagahashi Marie, et al.. (1998). A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.. Journal of Medical Genetics. 35(11). 951–953. 41 indexed citations
14.
Moreira, Eloísa S., Mariz Vainzof, Suely Kazue Nagahashi Marie, et al.. (1997). The Seventh Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy Is Mapped to 17q11-12. The American Journal of Human Genetics. 61(1). 151–159. 97 indexed citations
15.
Vainzof, Mariz, Claudia Ismania Samogy Costa, Suely Kazue Nagahashi Marie, et al.. (1997). Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy. Neuropediatrics. 28(4). 223–228. 23 indexed citations
16.
Passos‐Bueno, Maria Rita, Eloísa S. Moreira, Suely Kazue Nagahashi Marie, et al.. (1996). Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.. Journal of Medical Genetics. 33(2). 97–102. 38 indexed citations
17.
Moreira, Eloísa S., Mariz Vainzof, Jeffrey S. Chamberlain, et al.. (1995). A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Human Molecular Genetics. 4(7). 1163–1167. 57 indexed citations
18.
Passos-Bueno, Maria-Rita, Eloísa S. Moreira, Mariz Vainzof, et al.. (1995). Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region. Genomics. 27(1). 192–195. 31 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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