Biljana Ilkovski

1.8k total citations
20 papers, 776 citations indexed

About

Biljana Ilkovski is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Biljana Ilkovski has authored 20 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Cardiology and Cardiovascular Medicine and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Biljana Ilkovski's work include Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (16 papers) and Genetic Neurodegenerative Diseases (7 papers). Biljana Ilkovski is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (16 papers) and Genetic Neurodegenerative Diseases (7 papers). Biljana Ilkovski collaborates with scholars based in Australia, United States and United Kingdom. Biljana Ilkovski's co-authors include Kathryn N. North, Sandra T. Cooper, Nigel G. Laing, Peter W. Gunning, Edna C. Hardeman, Ana Domazetovska, Monique M. Ryan, Christina Schnell, Sophie Clément and Caroline A. Sewry and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Biljana Ilkovski

20 papers receiving 767 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Biljana Ilkovski Australia	15	622	511	191	183	124	20	776
Vilma‐Lotta Lehtokari Finland	16	780 1.3×	800 1.6×	321 1.7×	363 2.0×	98 0.8×	38	1.1k
Francesco Muntoni United Kingdom	5	1.1k 1.8×	216 0.4×	171 0.9×	89 0.5×	85 0.7×	8	1.2k
Laurence Suel France	16	652 1.0×	162 0.3×	258 1.4×	61 0.3×	166 1.3×	18	741
Yeliz Yuva United Kingdom	8	567 0.9×	149 0.3×	124 0.6×	90 0.5×	202 1.6×	9	653
Florence Niel France	17	879 1.4×	279 0.5×	94 0.5×	82 0.4×	125 1.0×	24	1.3k
Svetlana Gorokhova France	9	409 0.7×	200 0.4×	221 1.2×	59 0.3×	101 0.8×	25	553
Aiping Du United States	13	522 0.8×	281 0.5×	160 0.8×	21 0.1×	59 0.5×	15	829
Padmanabhan Vakeel United States	11	444 0.7×	235 0.5×	222 1.2×	19 0.1×	103 0.8×	12	659
Maegen A. Ackermann United States	18	570 0.9×	477 0.9×	144 0.8×	59 0.3×	102 0.8×	25	792
Marie‐Aline Ludosky France	12	521 0.8×	121 0.2×	163 0.9×	139 0.8×	106 0.9×	15	632

Countries citing papers authored by Biljana Ilkovski

Since Specialization

Citations

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

Fields of papers citing papers by Biljana Ilkovski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Biljana Ilkovski

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

All Works

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20 of 20 papers shown

Yuen, Michaela, Sandra T. Cooper, Steven B. Marston, et al.. (2015). Muscle weakness inTPM3-myopathy is due to reduced Ca²⁺-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres. Human Molecular Genetics. 24(22). 6278–6292. 37 indexed citations

O’Grady, Gina, Heather Best, Emily C. Oates, et al.. (2014). Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine. European Journal of Human Genetics. 23(6). 883–886. 16 indexed citations

Vandebrouck, Aurélie, Ana Domazetovska, Nancy Mokbel, et al.. (2010). In Vitro Analysis of Rod Composition and Actin Dynamics in Inherited Myopathies. Journal of Neuropathology & Experimental Neurology. 69(5). 429–441. 24 indexed citations

Sambuughin, Nyamkhishig, Rachael M. Duff, Munkhuu Bayarsaikhan, et al.. (2010). O.12 A new member of the BTB/Kelch family of proteins is mutated in nemaline myopathy type 6 (NEM6). Neuromuscular Disorders. 20(9-10). 638–638. 1 indexed citations

Ilkovski, Biljana. (2008). Investigations into the Pathobiology of Thin-Filament Myopathies. Advances in experimental medicine and biology. 642. 55–65. 8 indexed citations

Compton, Alison G., Douglas E. Albrecht, Jane T. Seto, et al.. (2008). Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy. The American Journal of Human Genetics. 83(6). 714–724. 61 indexed citations

Ilkovski, Biljana, Nancy Mokbel, R. Lewis, et al.. (2008). Disease Severity and Thin Filament Regulation in M9RTPM3Nemaline Myopathy. Journal of Neuropathology & Experimental Neurology. 67(9). 867–877. 20 indexed citations

Clarke, Nigel F., Biljana Ilkovski, Sandra T. Cooper, et al.. (2007). The pathogenesis of ACTA1‐related congenital fiber type disproportion. Annals of Neurology. 61(6). 552–561. 49 indexed citations

Domazetovska, Ana, Biljana Ilkovski, Sandra T. Cooper, et al.. (2007). Mechanisms underlying intranuclear rod formation. Brain. 130(12). 3275–3284. 51 indexed citations

10.

Koy, Anne, Biljana Ilkovski, Nigel G. Laing, et al.. (2007). Nemaline Myopathy with Exclusively Intranuclear Rods and a Novel Mutation in ACTA1 (Q139H). Neuropediatrics. 38(6). 282–286. 12 indexed citations

11.

Vlahovich, Nicole, Galina Schevzov, Visalini Nair‐Shalliker, et al.. (2007). Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscle. Cell Motility and the Cytoskeleton. 65(1). 73–85. 39 indexed citations

12.

Domazetovska, Ana, Biljana Ilkovski, Vikash Kumar, et al.. (2007). Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weakness. Annals of Neurology. 62(6). 597–608. 34 indexed citations

13.

Hutchinson, David, Amanda Charlton, Nigel G. Laing, Biljana Ilkovski, & Kathryn N. North. (2006). Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: Clinical and pathological variability within a kindred. Neuromuscular Disorders. 16(2). 113–121. 43 indexed citations

14.

Ilkovski, Biljana, Sophie Clément, Caroline A. Sewry, Kathryn N. North, & Sandra T. Cooper. (2005). Defining α-skeletal and α-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy. Neuromuscular Disorders. 15(12). 829–835. 61 indexed citations

15.

Ilkovski, Biljana, Kristen L. Nowak, Ana Domazetovska, et al.. (2004). Mutant actins that cause congenital myopathy affect sarcomeric protein expression in patient muscle and produce intranuclear and cytoplasmic aggregates in cultured myoblasts. Neuromuscular Disorders. 14. 562–562. 3 indexed citations

16.

Ilkovski, Biljana. (2004). Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms. Human Molecular Genetics. 13(16). 1727–1743. 75 indexed citations

17.

Ryan, Monique M., Biljana Ilkovski, Corinne D. Strickland, et al.. (2003). Clinical course correlates poorly with muscle pathology in nemaline myopathy. Neurology. 60(4). 665–673. 97 indexed citations

18.

Ilkovski, Biljana, Sandra T. Cooper, Kristen L. Nowak, et al.. (2001). Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene. The American Journal of Human Genetics. 68(6). 1333–1343. 119 indexed citations

19.

Gallery, Eileen D.M., Suzanne Campbell, Biljana Ilkovski, Michael J. Sinosich, & Chris Jackson. (2001). A novel in vitro co‐culture system for the study of maternal decidual endothelial cell–trophoblast interactions in human pregnancy. BJOG An International Journal of Obstetrics & Gynaecology. 108(6). 651–653. 14 indexed citations

20.

Gallery, Eileen D.M., Suzanne Campbell, Biljana Ilkovski, Michael J. Sinosich, & Chris Jackson. (2001). A novel in vitro co-culture system for the study of maternal decidual endothelial cell–trophoblast interactions in human pregnancy. British Journal of Obstetrics and Gynaecology. 108(6). 651–653. 12 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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