M. De Silva

1.6k total citations
24 papers, 661 citations indexed

About

M. De Silva is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, M. De Silva has authored 24 papers receiving a total of 661 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Sensory Systems and 7 papers in Genetics. Recurrent topics in M. De Silva's work include Hearing, Cochlea, Tinnitus, Genetics (11 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). M. De Silva is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (11 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). M. De Silva collaborates with scholars based in Australia, United States and Canada. M. De Silva's co-authors include Bryony Coleman, Robert K. Shepherd, Michael S. Hildebrand, Hans‐Henrik M. Dahl, Jennifer Hardman, Richard J. Smith, Jeremy M. Crook, Stephanie B. Epp, Anne Coco and James B. Fallon and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and British Journal of Cancer.

In The Last Decade

M. De Silva

22 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. De Silva Australia 13 337 274 146 121 103 24 661
Cyrille Sage United States 14 519 1.5× 448 1.6× 145 1.0× 79 0.7× 71 0.7× 14 857
Noel L. Wys United States 8 226 0.7× 167 0.6× 142 1.0× 125 1.0× 23 0.2× 8 564
Judith S. Kempfle United States 13 380 1.1× 178 0.6× 131 0.9× 74 0.6× 24 0.2× 26 653
Luo Guo China 18 521 1.5× 473 1.7× 118 0.8× 45 0.4× 61 0.6× 44 940
Yayoi S. Kikkawa Japan 16 230 0.7× 122 0.4× 96 0.7× 56 0.5× 25 0.2× 32 572
Anil Sharma Australia 13 162 0.5× 257 0.9× 135 0.9× 230 1.9× 23 0.2× 19 648
Heping Yu United States 19 518 1.5× 376 1.4× 123 0.8× 48 0.4× 82 0.8× 37 909
Jean-Pierre Hardelin France 7 431 1.3× 873 3.2× 100 0.7× 107 0.9× 396 3.8× 7 1.5k
Heiko Locher Netherlands 11 210 0.6× 188 0.7× 78 0.5× 60 0.5× 19 0.2× 22 511

Countries citing papers authored by M. De Silva

Since Specialization
Citations

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

Fields of papers citing papers by M. De Silva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. De Silva. 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 M. De Silva. The network helps show where M. De Silva may publish in the future.

Co-authorship network of co-authors of M. De Silva

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

All Works

20 of 20 papers shown
1.
Leventer, Richard J., et al.. (2024). Anything is better than nothing’: exploring attitudes towards novel therapies in leukodystrophy clinical trials. Orphanet Journal of Rare Diseases. 19(1). 322–322.
2.
Patel, Chirag, John Christodoulou, Belinda McClaren, et al.. (2024). A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability. Genetics in Medicine. 26(10). 101224–101224. 3 indexed citations
3.
Boggs, Kirsten, Fiona Lynch, Michelle C. Ward, et al.. (2024). Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101878–101878. 2 indexed citations
4.
Brown, Natasha J., M. De Silva, Mark F. Bennett, et al.. (2023). Improving genetic diagnostic yield in a large cohort of children with rare vascular anomalies or PIK3CA-related overgrowth spectrum. Genetics in Medicine Open. 2. 100837–100837.
5.
Best, Stephanie, et al.. (2021). Understanding genomic health information: how to meet the needs of the culturally and linguistically diverse community—a mixed methods study. Journal of Community Genetics. 12(4). 549–557. 9 indexed citations
6.
Akesson, Lauren, David Francis, M. De Silva, et al.. (2020). Microarray diagnosis of autoimmune polyendocrinopathy‐candidiasis‐ectodermal dystrophy caused by a novel homozygous intragenic AIRE deletion. Journal of Paediatrics and Child Health. 57(7). 1109–1112. 1 indexed citations
7.
Coleman, Bryony, et al.. (2008). A protocol for cryoembedding the adult guinea pig cochlea for fluorescence immunohistology. Journal of Neuroscience Methods. 176(2). 144–151. 35 indexed citations
8.
Hildebrand, Michael S., Samuel P. Gubbels, Amit Kochhar, et al.. (2008). Advances in Molecular and Cellular Therapies for Hearing Loss. Molecular Therapy. 16(2). 224–236. 61 indexed citations
9.
Hildebrand, Michael S., M. De Silva, Tiong Yang Tan, et al.. (2007). Molecular characterization of a novel X‐linked syndrome involving developmental delay and deafness. American Journal of Medical Genetics Part A. 143A(21). 2564–2575. 13 indexed citations
10.
Hildebrand, Michael S., M. De Silva, Tuomas Klockars, et al.. (2007). Gene expression profiling analysis of the inner ear. Hearing Research. 225(1-2). 1–10. 8 indexed citations
11.
Silva, M. De, Michael S. Hildebrand, Katrina M. Bell, et al.. (2006). Gene expression changes during step-wise differentiation of embryonic stem cells along the inner ear hair cell pathway. Acta Oto-Laryngologica. 126(11). 1148–1157. 11 indexed citations
12.
Coleman, Bryony, et al.. (2006). Auditory hair cell explant co-cultures promote the differentiation of stem cells into bipolar neurons. Experimental Cell Research. 313(2). 232–243. 52 indexed citations
13.
Hildebrand, Michael S., M. De Silva, R. J McKinlay Gardner, et al.. (2006). Cochlear Implants for DFNA17 Deafness. The Laryngoscope. 116(12). 2211–2215. 21 indexed citations
14.
Hildebrand, Michael S., Hans‐Henrik M. Dahl, Jennifer Hardman, et al.. (2005). Survival of Partially Differentiated Mouse Embryonic Stem Cells in the Scala Media of the Guinea Pig Cochlea. Journal of the Association for Research in Otolaryngology. 6(4). 341–354. 69 indexed citations
15.
Hildebrand, Michael S., M. De Silva, Tuomas Klockars, et al.. (2004). Expression of the carrier protein apolipoprotein D in the mouse inner ear. Hearing Research. 200(1-2). 102–114. 15 indexed citations
16.
Hildebrand, Michael S., M. De Silva, Tuomas Klockars, et al.. (2004). Characterisation of DRASIC in the mouse inner ear. Hearing Research. 190(1-2). 149–160. 62 indexed citations
17.
18.
Kantharidis, Phillip, Assam El‐Osta, M. De Silva, et al.. (2000). Regulation of MDR1 gene expression: emerging concepts. Drug Resistance Updates. 3(2). 99–108. 20 indexed citations
19.
Silva, M. De, Phillip Kantharidis, Stephen W. Scherer, et al.. (1999). Physical Mapping of a Tandem Duplication on the Long Arm of Chromosome 7 Associated with a Multidrug Resistant Phenotype. Cancer Genetics and Cytogenetics. 110(1). 28–33. 9 indexed citations
20.
Silva, M. De, et al.. (1996). Inheritance of chromosome 7 is associated with a drug-resistant phenotype in somatic cell hybrids. British Journal of Cancer. 73(2). 169–174. 6 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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