Monize Lazar

787 total citations
14 papers, 464 citations indexed

About

Monize Lazar is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Monize Lazar has authored 14 papers receiving a total of 464 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Monize Lazar's work include Muscle Physiology and Disorders (5 papers), Autophagy in Disease and Therapy (2 papers) and Genomics and Rare Diseases (2 papers). Monize Lazar is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Autophagy in Disease and Therapy (2 papers) and Genomics and Rare Diseases (2 papers). Monize Lazar collaborates with scholars based in Brazil, United States and Australia. Monize Lazar's co-authors include Mayana Zatz, Guilherme Lopes Yamamoto, Helga Cristina Almeida da Silva, Marcela Câmara Machado‐Costa, Maria Rita Passos‐Bueno, Miguel Mitne‐Neto, Alysson R. Muotri, Claudio A.P. Joazeiro, Hugo J. Bellen and Hiroshi Tsuda and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Monize Lazar

14 papers receiving 460 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Monize Lazar Brazil	9	292	129	97	72	59	14	464
Alessandra Ruggieri Italy	13	370 1.3×	115 0.9×	49 0.5×	55 0.8×	70 1.2×	21	536
Reza Maroofian United Kingdom	15	307 1.1×	131 1.0×	44 0.5×	35 0.5×	53 0.9×	57	667
Zhijian Yang China	15	319 1.1×	129 1.0×	102 1.1×	21 0.3×	43 0.7×	52	585
Rachel Schot Netherlands	16	355 1.2×	260 2.0×	57 0.6×	28 0.4×	107 1.8×	35	686
Jacek Pilch Poland	12	275 0.9×	117 0.9×	39 0.4×	70 1.0×	44 0.7×	24	469
Carmen Paradas Spain	14	389 1.3×	70 0.5×	117 1.2×	100 1.4×	46 0.8×	52	613
Simon Holden United Kingdom	12	296 1.0×	219 1.7×	61 0.6×	28 0.4×	50 0.8×	35	585
Teodora Chamova Bulgaria	13	416 1.4×	115 0.9×	59 0.6×	130 1.8×	105 1.8×	41	598
Dominique J. Verlaan Canada	12	224 0.8×	122 0.9×	327 3.4×	28 0.4×	40 0.7×	13	655
Andrew G. L. Douglas United Kingdom	12	498 1.7×	145 1.1×	214 2.2×	163 2.3×	43 0.7×	31	739

Countries citing papers authored by Monize Lazar

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Monize Lazar

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

All Works

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14 of 14 papers shown

Gurgel‐Giannetti, Juliana, Guilherme Lopes Yamamoto, Monize Lazar, et al.. (2022). Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization. International Journal of Molecular Sciences. 23(19). 11995–11995. 4 indexed citations

Martins, Luciane, Monize Lazar, Chong Ae Kim, et al.. (2022). Childhood Hypophosphatasia Associated with a Novel Biallelic ALPL Variant at the TNSALP Dimer Interface. International Journal of Molecular Sciences. 24(1). 282–282. 4 indexed citations

Rocha, Kátia Bones, Monize Lazar, Suzana Ezquina, et al.. (2020). Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer. Breast Cancer. 28(2). 346–354. 8 indexed citations

Fernandes, Stephanie, Camila de Almeida, Monize Lazar, et al.. (2019). Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy. Disease Models & Mechanisms. 13(2). 9 indexed citations

Naslavsky, Michel Satya, Guilherme Lopes Yamamoto, Tatiana Ferreira de Almeida, et al.. (2017). Exomic variants of an elderly cohort of Brazilians in the ABraOM database. Human Mutation. 38(7). 751–763. 161 indexed citations

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

Wajchenberg, Marcelo, Délio Eulálio Martins, & Monize Lazar. (2015). What is the best way to determine the cause of adolescent idiopathic scoliosis?. PubMed. 3(4). 48–48. 3 indexed citations

Zatz, Mayana, Monize Lazar, Guilherme Lopes Yamamoto, et al.. (2014). Milder course in Duchenne patients with nonsense mutations and no muscle dystrophin. Neuromuscular Disorders. 24(11). 986–989. 28 indexed citations

Yamamoto, Guilherme Lopes, Wagner Antonio da Rosa Baratela, Tatiana Ferreira de Almeida, et al.. (2014). Mutations in PCYT1A Cause Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy. The American Journal of Human Genetics. 94(1). 113–119. 36 indexed citations

10.

Vainzof, Mariz, Monize Lazar, Guilherme Lopes Yamamoto, et al.. (2014). A.P.14. Neuromuscular Disorders. 24(9-10). 834–835. 1 indexed citations

11.

Zatz, Mayana, Rita de Cássia M. Pavanello, Naila Cristina Vilaça Lourenço, et al.. (2012). Assessing Pathogenicity for Novel Mutation/Sequence Variants: The Value of Healthy Older Individuals. NeuroMolecular Medicine. 14(4). 281–284. 8 indexed citations

12.

Mitne‐Neto, Miguel, Marcela Câmara Machado‐Costa, Maria C. Marchetto, et al.. (2011). Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients. Human Molecular Genetics. 20(18). 3642–3652. 173 indexed citations

13.

Wajchenberg, Marcelo, Monize Lazar, Délio Eulálio Martins, et al.. (2010). Genetic aspects of adolescent idiopathic scoliosis in a family with multiple affected members: a research article. SHILAP Revista de lepidopterología. 5(1). 7–7. 13 indexed citations

14.

Godel, Victor, et al.. (1981). Maxillary Meningioma Appearing as Exophthalmos. Archives of Otolaryngology - Head and Neck Surgery. 107(10). 626–628. 9 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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