Eloísa S. Moreira

1.4k citations

18 papers · 816 indexed · h-index 13

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 5%
Cardiology and Cardiovascular Medicine top 10%
Cell Biology top 10%
Genetics top 10%

Co-authors: Maria Rita Passos‐Bueno Mariz Vainzof Mayana Zatz Suely Kazue Nagahashi Marie Georgine Faulkner Oscar Suzuki Dieter E. Jenne Roger H. Reeves
Topics: Muscle Physiology and Disorders (10 papers)Genetic Neurodegenerative Diseases (5 papers)Calpain Protease Function and Regulation (3 papers)
Cited by: Cellular and Molecular Neuroscience Cardiology and Cardiovascular Medicine Molecular Biology
Journals: Nature Genetics Blood PLoS ONE
Partner nations: Brazil United States United Kingdom

In The Last Decade

Eloísa S. Moreira

18 papers receiving 786 citations

Peers

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

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18 of 18 papers shown

#	Work	Indexed citations
1	Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus 2019 ·Advances in Rheumatology ·(unknown),Sandro Félix Perazzio,(unknown),Eloísa S. Moreira,(unknown),(unknown),Neusa Pereira da Silva,Luís Eduardo Coelho Andrade	10
2	Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) 2016 ·Research in autism spectrum disorders ·Eloísa S. Moreira,Isabela Mayá Wayhs Silva,Naila Cristina Vilaça Lourenço,(unknown),(unknown),(unknown),Karina Griesi‐Oliveira,Monize Lazar,Silvia Souza da Costa,Michel Satya Naslavsky,Kátia M. Rocha,Meire Aguena,Agnes Cristina Fett‐Conte,Mayana Zatz,Carla Rosenberg,Elaine Cristina Zachi,Débora Romeo Bertola,(unknown),Maria Rita Passos‐Bueno	7
3	Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy 2014 ·PLoS ONE ·(unknown),Karina Griesi‐Oliveira,(unknown),Naila Cristina Vilaça Lourenço,(unknown),Kátia M. Rocha,Eloísa S. Moreira,(unknown),(unknown),Débora Romeo Bertola,(unknown),Tiago R. Magalhães,Agnes Cristina Fett‐Conte,Maria Rita Passos‐Bueno	19
4	Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR 2008 ·Brazilian Journal of Medical and Biological Research ·(unknown),Eloísa S. Moreira,Paula Fontes Asprino,(unknown),Fernando Alberto	7
5	HTR1B and HTR2C in autism spectrum disorders in Brazilian families 2008 ·Brain Research ·(unknown),Karina Griesi‐Oliveira,(unknown),(unknown),(unknown),Eloísa S. Moreira,(unknown),(unknown),(unknown),Sérgio Russo Matioli,Paulo Alberto Otto,Maria Rita Passos‐Bueno	25
6	Acute Promyelocytic Leukemia with T(15;17): Frequency of Additional Clonal Chromosome Abnormalities and FLT3 2008 ·Blood ·(unknown),(unknown),(unknown),Eloísa S. Moreira,Fernando Alberto	1
7	Factors associated with the intensity of liver fibrosis in renal transplant patients with hepatitis B virus infection 2007 ·European Journal of Gastroenterology & Hepatology ·(unknown),Renata de Mello Perez,(unknown),José Osmar Medina Pestana,Valéria Pereira Lanzoni,Fernando Alberto,Eloísa S. Moreira,Antônio Eduardo B. Silva,Maria Lúcia Gomes Ferraz	9
8	Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies 2001 ·Journal of Molecular Neuroscience ·Mariz Vainzof,Louise V.B. Anderson,Elizabeth M. McNally,Dawn Belt Davis,Georgine Faulkner,(unknown),Eloísa S. Moreira,Rita C.M. Pavanello,Maria Rita Passos‐Bueno,Mayana Zatz	53
9	A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma. 2001 ·PubMed ·Paula Iughetti,Oscar Suzuki,Paulo H. Godoi,Venâncio Avancini Ferreira Alves,Andréa L. Sertié,Todd Zorick,Fernando Augusto Soares,Anamaria A. Camargo,Eloísa S. Moreira,(unknown),Carlos Alberto Moreira‐Filho,Andrew Simpson,Glaucius Oliva,Maria Rita Passos‐Bueno	62
10	Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin 2000 ·Nature Genetics ·Eloísa S. Moreira,Tim Wiltshire,Georgine Faulkner,(unknown),Mariz Vainzof,Oscar Suzuki,Giorgio Valle,Roger H. Reeves,Mayana Zatz,Maria Rita Passos‐Bueno,Dieter E. Jenne	238
11	Partial α‐sarcoglycan deficiency with retention of the dystrophin‐glycoprotein complex in a LGMD2D family 2000 ·Muscle & Nerve ·Mariz Vainzof,Eloísa S. Moreira,Manuel Cánovas,Louise V.B. Anderson,Rita C.M. Pavanello,Maria Rita Passos‐Bueno,Mayana Zatz	22
12	Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G 1999 ·American Journal of Medical Genetics ·Maria Rita Passos‐Bueno,Mariz Vainzof,Eloísa S. Moreira,Mayana Zatz	76
13	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. 1998 ·Journal of Medical Genetics ·Eloísa S. Moreira,Mariz Vainzof,Suely Kazue Nagahashi Marie,Vincenzo Nigro,Mayana Zatz,Maria Rita Passos‐Bueno	41
14	The Seventh Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy Is Mapped to 17q11-12 1997 ·The American Journal of Human Genetics ·Eloísa S. Moreira,Mariz Vainzof,Suely Kazue Nagahashi Marie,Andréa L. Sertié,Mayana Zatz,Maria Rita Passos‐Bueno	97
15	Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy 1997 ·Neuropediatrics ·Mariz Vainzof,Claudia Ismania Samogy Costa,Suely Kazue Nagahashi Marie,Eloísa S. Moreira,(unknown),Maria Rita Passos‐Bueno,Alan H. Beggs,M Zatz	23
16	Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families. 1996 ·Journal of Medical Genetics ·Maria Rita Passos‐Bueno,Eloísa S. Moreira,Suely Kazue Nagahashi Marie,R. Bashir,(unknown),Donald R. Love,Mariz Vainzof,Paula Iughetti,(unknown),Egbert Bakker,T Strachan,Kate Bushby,Mayana Zatz	38
17	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 1995 ·Human Molecular Genetics ·(unknown),Eloísa S. Moreira,Mariz Vainzof,Jeffrey S. Chamberlain,(unknown),Leandro de Mattos Pereira,Jennifer A. Akiyama,Steven L. Roberds,Kevin P. Campbell,Mayana Zatz	57
18	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 1995 ·Genomics ·Maria-Rita Passos-Bueno,(unknown),Eloísa S. Moreira,Mariz Vainzof,Suely Kazue Nagahashi Marie,(unknown),Paula Iughetti,Egbert Bakker,Sharon Keers,A. Stephenson,Tom Strachan,(unknown),Jean Weissenbach,K. Bushby,Mayana Zatz	31

About Eloísa S. Moreira

Eloísa S. Moreira is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology, having authored 18 papers that have together received 816 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (5 papers) and Calpain Protease Function and Regulation (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (300 citations), Cardiology and Cardiovascular Medicine (234 citations) and Molecular Biology (701 citations). Eloísa S. Moreira has collaborated with scholars based in Brazil, United States and United Kingdom. Frequent co-authors include Maria Rita Passos‐Bueno, Mariz Vainzof, Mayana Zatz, Suely Kazue Nagahashi Marie, Georgine Faulkner, Oscar Suzuki, Dieter E. Jenne, Roger H. Reeves, Tim Wiltshire and Giorgio Valle. Their work appears in journals such as Nature Genetics, Blood and PLoS ONE.

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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