Adam Bournazos

1.8k total citations
15 papers, 211 citations indexed

About

Adam Bournazos is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Adam Bournazos has authored 15 papers receiving a total of 211 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Cell Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Adam Bournazos's work include Muscle Physiology and Disorders (5 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Adam Bournazos is often cited by papers focused on Muscle Physiology and Disorders (5 papers), RNA modifications and cancer (4 papers) and RNA Research and Splicing (4 papers). Adam Bournazos collaborates with scholars based in Australia, United States and Canada. Adam Bournazos's co-authors include Sandra T. Cooper, Frances A. Lemckert, Kathryn N. North, Samantha J. Bryen, Ruebena Dawes, Himanshu Joshi, David S. Winlaw, Jonathan R. Egan, Tanya L. Butler and Mark R. Davis and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Frontiers in Microbiology.

In The Last Decade

Adam Bournazos

15 papers receiving 211 citations

Peers

Adam Bournazos
Pamela A. Long United States
T.C. Lee United States
Steven C. Chen United States
Gundula Povysil United States
Adam Bournazos
Citations per year, relative to Adam Bournazos Adam Bournazos (= 1×) peers Rémi Bellance

Countries citing papers authored by Adam Bournazos

Since Specialization
Citations

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

Fields of papers citing papers by Adam Bournazos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adam Bournazos

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

All Works

15 of 15 papers shown
1.
Bournazos, Adam, Vanessa Sarkozy, John A. Lawson, et al.. (2024). Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort. Molecular Genetics & Genomic Medicine. 12(10). e70017–e70017. 1 indexed citations
2.
Dawes, Ruebena, et al.. (2023). SpliceVault predicts the precise nature of variant-associated mis-splicing. Nature Genetics. 55(2). 324–332. 34 indexed citations
3.
Bournazos, Adam, Frances J. Evesson, Chi Nam Ignatius Pang, et al.. (2023). Minimal expression of dysferlin prevents development of dysferlinopathy in dysferlin exon 40a knockout mice. Acta Neuropathologica Communications. 11(1). 15–15. 3 indexed citations
4.
Bryen, Samantha J., Adam Bournazos, Frances A. Lemckert, et al.. (2022). A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centre. Neuromuscular Disorders. 32(9). 707–717. 1 indexed citations
5.
Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate. Human Mutation. 41(11). 1884–1891. 8 indexed citations
6.
Anderson, Neil, et al.. (2020). Two novel B9D1 variants causing Joubert syndrome: Utility of mRNA and splicing studies. European Journal of Medical Genetics. 63(9). 104000–104000. 2 indexed citations
7.
Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct rna studies confirm pathogenicity of a novel homozygous asns splicing variant in a critically ill neonate. Pathology. 52. S106–S106. 2 indexed citations
8.
Evesson, Frances J., Omar A. Saleh, Adam Bournazos, et al.. (2020). Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy. American Journal of Physiology-Cell Physiology. 318(6). C1226–C1237. 14 indexed citations
9.
Jones, Hannah, Samantha J. Bryen, Leigh B. Waddell, et al.. (2019). Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants. Neuromuscular Disorders. 29(12). 913–919. 11 indexed citations
10.
Blondelle, Jordan, Jane T. Seto, Majid Ghassemian, et al.. (2019). Cullin-3–dependent deregulation of ACTN1 represents a pathogenic mechanism in nemaline myopathy. JCI Insight. 4(10). 18 indexed citations
11.
Gardiner, Melissa, et al.. (2017). Exoproteome Analysis of the Seaweed Pathogen Nautella italica R11 Reveals Temperature-Dependent Regulation of RTX-Like Proteins. Frontiers in Microbiology. 8. 1203–1203. 8 indexed citations
12.
Redpath, Gregory, Frances A. Lemckert, Adam Bournazos, et al.. (2017). Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling. Cellular Signalling. 33. 30–40. 14 indexed citations
13.
Bournazos, Adam, et al.. (2017). Limited proteolysis as a tool to probe the tertiary conformation of dysferlin and structural consequences of patient missense variant L344P. Journal of Biological Chemistry. 292(45). 18577–18591. 5 indexed citations
14.
Sandaradura, Sarah A., Adam Bournazos, Amali Mallawaarachchi, et al.. (2017). Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant. Human Mutation. 39(3). 383–388. 46 indexed citations
15.
Lemckert, Frances A., Adam Bournazos, Tanya L. Butler, et al.. (2016). Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factor. Cardiovascular Research. 110(2). 178–187. 44 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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