Minal Menezes

1.7k total citations
17 papers, 290 citations indexed

About

Minal Menezes is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Minal Menezes has authored 17 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in Minal Menezes's work include Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Minal Menezes is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (7 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Minal Menezes collaborates with scholars based in Australia, United States and China. Minal Menezes's co-authors include John Christodoulou, Lisa G. Riley, David R. Thorburn, Sandra T. Cooper, Håkon Håkonarson, Yiran Guo, Carolyn M. Sue, Brendan J. Keating, Carolyn Ellaway and Mark J. Cowley and has published in prestigious journals such as The Journal of Experimental Medicine, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Minal Menezes

17 papers receiving 286 citations

Peers

Minal Menezes

GENET

PHYSI

SURGE

Mathilde Nizon France

Mohammad Al-Owain Saudi Arabia

Urania Kotzaeridou Germany

Lisa Worgan Australia

Mary Willis United States

Kent E. Kruckeberg United States

Katalin Szakszon Hungary

Seema Kapoor India

Claudia Soler‐Alfonso United States

Kotaro Yuge Japan

Mathilde Nizon France

Minal Menezes

239 ×1.2

70 ×0.8

153 ×2.4

GENET

23 ×0.9

PHYSI

28 ×1.6

SURGE

Citations per year, relative to Minal Menezes Minal Menezes (= 1×) peers Mathilde Nizon

Countries citing papers authored by Minal Menezes

Since Specialization

Citations

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

Fields of papers citing papers by Minal Menezes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Minal Menezes. 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 Minal Menezes. The network helps show where Minal Menezes may publish in the future.

Co-authorship network of co-authors of Minal Menezes

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

All Works

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17 of 17 papers shown

Ovchinnikov, Dmitry A., et al.. (2024). Generation of two lymphoblastoid-derived induced pluripotent stem cell (iPSC) lines from patients with phenylketonuria. Stem Cell Research. 77. 103407–103407. 1 indexed citations

Ovchinnikov, Dmitry A., et al.. (2024). Generation of fibroblast-derived induced pluripotent stem cell (iPSC) lines from two paediatric patients with phenylketonuria. Stem Cell Research. 77. 103405–103405. 4 indexed citations

Riley, Lisa G., Minal Menezes, Andrew Williams, et al.. (2021). FGF21 outperforms GDF15 as a diagnostic biomarker of mitochondrial disease in children. Molecular Genetics and Metabolism. 135(1). 63–71. 15 indexed citations

Cooper, Michael, et al.. (2021). Intravenous Tranexamic Acid is Associated With a Clinically Significant Reduction in Blood Loss in Craniosynostosis Surgery. Journal of Craniofacial Surgery. 33(2). 636–641. 6 indexed citations

Bergen, Nicole J. Van, Syed Mukhtar Ahmed, Felicity Collins, et al.. (2020). Mutations in the exocyst component EXOC2 cause severe defects in human brain development. The Journal of Experimental Medicine. 217(10). 19 indexed citations

Riley, Lisa G., Mark J. Cowley, Velimir Gayevskiy, et al.. (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine. 22(7). 1254–1261. 45 indexed citations

Ahmadpour, Naseem, et al.. (2020). Synthesizing Multiple Stakeholder Perspectives on Using Virtual Reality to Improve the Periprocedural Experience in Children and Adolescents: Survey Study. Journal of Medical Internet Research. 22(7). e19752–e19752. 15 indexed citations

Davids, Mariska, Minal Menezes, Yiran Guo, et al.. (2020). Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency. Molecular Genetics and Metabolism. 130(1). 49–57. 14 indexed citations

Weatherall, Andrew, et al.. (2019). Learner and educator experiences and priorities in paediatric airway education: A qualitative study. Anaesthesia and Intensive Care. 47(3). 274–280. 2 indexed citations

10.

Yoo, Soojeong, Andrew Weatherall, Sarah Scott, et al.. (2019). Clinician perspective on VR Games for Managing Periprocedural Anxiety in Children. 280–284. 6 indexed citations

11.

Menezes, Minal, Wendy Gold, Lisa G. Riley, et al.. (2018). Tread carefully: A functional variant in the human NADPH oxidase 4 ( NOX4 ) is not disease causing. Molecular Genetics and Metabolism. 123(3). 382–387. 1 indexed citations

12.

Rius, Rocío, Lisa G. Riley, Yiran Guo, et al.. (2018). Cryptic intronic NBAS variant reveals the genetic basis of recurrent liver failure in a child. Molecular Genetics and Metabolism. 126(1). 77–82. 12 indexed citations

13.

Menezes, Minal, Yiran Guo, Jianguo Zhang, et al.. (2015). Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia. Human Molecular Genetics. 24(8). 2297–2307. 58 indexed citations

14.

Miller, David K., Minal Menezes, Cas Simons, et al.. (2014). Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient. PLoS ONE. 9(8). e104879–e104879. 9 indexed citations

15.

Guo, Yiran, Minal Menezes, Manoj P. Menezes, et al.. (2014). Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect. Neuromuscular Disorders. 25(3). 257–261. 15 indexed citations

16.

Menezes, Minal, Lisa G. Riley, & John Christodoulou. (2014). Mitochondrial respiratory chain disorders in childhood: Insights into diagnosis and management in the new era of genomic medicine. Biochimica et Biophysica Acta (BBA) - General Subjects. 1840(4). 1368–1379. 28 indexed citations

17.

Riley, Lisa G., Minal Menezes, Joëlle Rudinger‐Thirion, et al.. (2013). Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia. Orphanet Journal of Rare Diseases. 8(1). 193–193. 40 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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