Countries citing scholars working at Victorian Clinical Genetics Services
Since Specialization
Citations
This map shows the geographic impact of research produced by authors working at Victorian Clinical Genetics Services. 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 papers produced at Victorian Clinical Genetics Services with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Victorian Clinical Genetics Services more than expected).
Fields of papers published by authors at Victorian Clinical Genetics Services
This network shows the impact of papers affiliated with Victorian Clinical Genetics Services at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with Victorian Clinical Genetics Services at the time of their publication.
About Victorian Clinical Genetics Services
In recent decades, authors affiliated with Victorian Clinical Genetics Services have published 1.5k papers, which have received a total of 45.9k indexed citations . Scholars at this organization have produced 123 papers in Clinical Biochemistry, 509 papers in Genetics, 215 papers in Pediatrics, Perinatology and Child Health, 467 papers in Molecular Biology and 62 papers in Genetics on the topics of Genomics and Rare Diseases (143 papers), Mitochondrial Function and Pathology (142 papers), Prenatal Screening and Diagnostics (134 papers), Metabolism and Genetic Disorders (123 papers), Genomic variations and chromosomal abnormalities (115 papers), BRCA gene mutations in cancer (104 papers), Genetics and Neurodevelopmental Disorders (101 papers) and Genetic Neurodegenerative Diseases (78 papers). Their work is cited by papers focused on Clinical Biochemistry (5.3k citations), Genetics (11.0k citations), Pediatrics, Perinatology and Child Health (5.0k citations), Molecular Biology (18.3k citations) and Rheumatology (2.2k citations). Authors at Victorian Clinical Genetics Services collaborate with scholars in Australia, United States and United Kingdom and have published in prestigious journals including European Journal of Human Genetics, Genetics in Medicine, Prenatal Diagnosis, Human Mutation and Journal of Medical Genetics. Some of Victorian Clinical Genetics Services's most productive authors include David R. Thorburn, Ravi Savarirayan, Martin B. Delatycki, Avihu Boneh, Zornitza Stark, David J. Amor, Michael T. Ryan, Matthew McKenzie, Alison G. Compton and Jane Halliday.
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.
Explore institutions with similar magnitude of impact