Monize Lazar
Impact in
-
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurology top 10%
- Amyotrophic Lateral Sclerosis Research
Papers in
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- Muscle Physiology and Disorders 5
- Congenital heart defects research 2
- Mitochondrial Function and Pathology 2
- Genetics 6
- Connective tissue disorders research 2
- Genomics and Rare Diseases 2
- Co-authors
- Mayana Zatz (8 shared papers)Guilherme Lopes Yamamoto (7 shared papers)Marcela Câmara Machado‐Costa (2 shared papers)Helga Cristina Almeida da Silva (2 shared papers)Miguel Mitne‐Neto (1 shared paper)Hugo J. Bellen (1 shared paper)Maria Rita Passos‐Bueno (4 shared papers)Maria C. Marchetto (1 shared paper)
- Journals
- Neuromuscular Disorders (2 papers)International Journal of Molecular Sciences (2 papers)Human Mutation (1 paper)NeuroMolecular Medicine (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- BrazilUnited StatesAustralia
In The Last Decade
Monize Lazar
14 papers receiving 460 citations
Peers
Comparison fields: 5 of 69
- Genetics 72
- Neurology 97
- Aging 11
- Genetics 129
- Developmental Neuroscience 18
Countries citing papers authored by Monize Lazar
This map shows the geographic impact of Monize Lazar'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 Monize Lazar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Monize Lazar more than expected).
Fields of papers citing papers by Monize Lazar
This network shows the impact of papers produced by Monize Lazar. 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 Monize Lazar. The network helps show where Monize Lazar may publish in the future.
Co-authors
The 25 scholars most cited alongside Monize Lazar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 173 | |
| 2 | 2017 | 161 | |
| 3 | 2014 | 36 | |
| 4 | 2014 | 28 | |
| 5 | 2010 | 13 | |
| 6 | 2019 | 9 | |
| 7 | 1981 | 9 | |
| 8 | 2020 | 8 | |
| 9 | 2012 | 8 | |
| 10 | 2016 | 7 | |
| 11 | 2022 | 4 | |
| 12 | 2022 | 4 | |
| 13 | 2015 | 3 | |
| 14 | 2014 | 1 |
About Monize Lazar
Monize Lazar is a scholar working on Molecular Biology, Genetics, Surgery, Epidemiology and Genetics, having authored 14 papers that have together received 464 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (5 papers), Cancer Genomics and Diagnostics (2 papers), Connective tissue disorders research (2 papers), Congenital heart defects research (2 papers), Scoliosis diagnosis and treatment (2 papers), Genomics and Rare Diseases (2 papers), Mitochondrial Function and Pathology (2 papers) and Autophagy in Disease and Therapy (2 papers). The work is most often cited by research in Genetics (72 citations), Neurology (97 citations), Aging (11 citations), Genetics (129 citations) and Developmental Neuroscience (18 citations). Monize Lazar has collaborated with scholars based in Brazil, United States and Australia. Frequent co-authors include Mayana Zatz, Guilherme Lopes Yamamoto, Marcela Câmara Machado‐Costa, Helga Cristina Almeida da Silva, Miguel Mitne‐Neto, Hugo J. Bellen, Maria Rita Passos‐Bueno, Maria C. Marchetto, Alysson R. Muotri and Hiroshi Tsuda. Their work appears in journals such as Neuromuscular Disorders, International Journal of Molecular Sciences, Human Mutation, NeuroMolecular Medicine and The American Journal of Human Genetics.
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.