Victorian Clinical Genetics Services
In research, Victorian Clinical Genetics Services stands highest in Medicine (#6,800 of 17,978 worldwide), Health Sciences (#8,925 of 20,462 worldwide) and Life Sciences (#7,269 of 14,347 worldwide), over all time. Relative to its size it is most specialised in Biochemistry, Genetics and Molecular Biology — Biochemistry, Genetics and Molecular Biology is 7.3× its share of world research.
- World rank, 2022–2025
- #12,775 of 28,054 · #15,362 all time
- Rank in Australia
- #218 of 391
- Research works
- 407 ▲ 8% vs 2013–17
- Citations
- 14k 34.3 per fractional work
- Top-10% rate
- 30.9% record average 16.5%
- Open access
- 46% world 28%
What is Victorian Clinical Genetics Services known for in research?
The fields where it stands highest, over all time, ranked among every institution above the floor in each field.
| Field | World rank | Where that sits | Top-10% rate | Works |
|---|---|---|---|---|
| MedicineField | #6,800 of 17,978 | 27.0% | 188 | |
| Health SciencesDomain | #8,925 of 20,462 | 27.1% | 199 | |
| Life SciencesDomain | #7,269 of 14,347 | 27.3% | 186 | |
| Biochemistry, Genetics and Molecular BiologyField | #4,385 of 7,814 | 27.3% | 159 |
Each strip is that field’s whole ranked pool, with the notch where Victorian Clinical Genetics Services sits in it, in the colour of the band that rank falls in. The track under the rate is the rate itself: it carries no world mark, because the world rate differs by field (from about 6% to 21% in this record).
What does Victorian Clinical Genetics Services specialise in?
Where its research is concentrated relative to its size: Biochemistry, Genetics and Molecular Biology takes 7.3× the share of its output that it takes of world research.
- Biochemistry, Genetics and Molecular BiologyField · 29.8 works7.3×
Location quotient, a volume reading rather than an impact one. It surfaces small, lopsided specialities.
Field profile
Location quotient across every field it publishes in: outside the ring is more than an institution of this size would be expected to publish, inside it is less.
Rings at 0.5×, 1× and 2×. Widest outward: Biochemistry, Genetics and Molecular Biology, 7.3×. Every wedge is a field page.
- Biochemistry, Genetics and Molecular Biology 7.3×
- Medicine 2.2×
- Neuroscience 1.8×
- Pharmacology, Toxicology and Pharmaceutics 1.5×
- Psychology 1.4×
- Health Professions 0.9×
- Nursing 0.7×
- Economics, Econometrics and Finance 0.6×
- Decision Sciences 0.5×
- Immunology and Microbiology 0.5×
- Energy 0.3×
- Mathematics 0.2×
- Agricultural and Biological Sciences 0.2×
- Chemistry 0.2×
- Social Sciences 0.2×
- Business, Management and Accounting 0.1×
- Environmental Science 0.1×
- Engineering 0.1×
- Materials Science 0.0×
- Physics and Astronomy 0.0×
Who are the top researchers at Victorian Clinical Genetics Services?
Ranked on the composite score, Gabriele Medley, Belinda Chong and David Francis lead among researchers whose main affiliation is Victorian Clinical Genetics Services.
- 1 Gabriele Medley Australia · #596,188 worldwide 54 citations · 19 works
- 2 Belinda Chong Australia · #1,018,208 worldwide 52 citations · 17 works
- 3 David Francis Australia · #1,429,512 worldwide 46 citations · 15 works
- 4 Ivan Macciocca Australia · #1,560,912 worldwide 16 citations · 18 works
Which keywords describe research at Victorian Clinical Genetics Services?
By fractional works in 2022–2025, weighted toward what it does more of than the world: Genetic Variants, Clinical Genomics, Sequence Interpretation, Prenatal Diagnosis, Cell-Free DNA, Genetic Testing, Aneuploidy Screening and Maternal Plasma DNA Sequencing.
- Microbiota
- Copy Number Variation
- Neurobiology
- Neurodevelopmental Disorders
- Mitochondrial Fission
- Mitochondria
- Cell Death
- Tandem Mass Spectrometry
- Biochemical Genetics
- Prevalence
- Genetic Mutations
- Metabolic Disorders
- BRCA2
- Ovarian Cancer
- Breast Cancer
- Precision Medicine
- Aneuploidy Screening
- Cell-Free DNA
- Epidemiology
- Clinical Genomics
- Genetic Variants
- Sequence Interpretation
- Prenatal Diagnosis
- Genetic Testing
- Maternal Plasma DNA Sequencing
- Mitochondrial Dysfunction
- Cancer Risk
- BRCA1
- Oxidative Stress
- Newborn Screening
- Mitochondrial Function
- Aging
- Carnitine
- Genetics
- Metabolic Regulation
- Reactive Oxygen Species
- Mitochondrial Fusion
- Neurodevelopmental Outcomes
- Comorbidity
- Genomic Rearrangements
Size is fractional works in 2022–2025 in the topics tagged with each word; colour is the word's share of this institution's work against its share of the world's. The 40 words are chosen for being large and distinctive. Each links to the topic it comes from most.
All 40 words, with their numbers
- Genetic Variants7▲ 56×5 topics
- Clinical Genomics6▲ 225×1 topic
- Sequence Interpretation6▲ 225×1 topic
- Epidemiology5▲ 1.66×35 topics
- Prenatal Diagnosis5▲ 43×5 topics
- Cell-Free DNA5▲ 61×2 topics
- Genetic Testing4▲ 44×3 topics
- Aneuploidy Screening4▲ 185×1 topic
- Maternal Plasma DNA Sequencing4▲ 185×1 topic
- Precision Medicine4▲ 10×4 topics
- Mitochondrial Dysfunction4▲ 16×5 topics
- Breast Cancer4▲ 19×3 topics
- Cancer Risk4▲ 21×3 topics
- Ovarian Cancer4▲ 51×2 topics
- BRCA13▲ 170×1 topic
- BRCA23▲ 170×1 topic
- Oxidative Stress3▲ 2.7×13 topics
- Metabolic Disorders3▲ 32×4 topics
- Newborn Screening3▲ 70×2 topics
- Genetic Mutations3▲ 8.5×16 topics
- Mitochondrial Function3▲ 38×3 topics
- Prevalence3▲ 9.1×9 topics
- Aging3▲ 6.4×6 topics
- Biochemical Genetics3▲ 100×1 topic
- Carnitine3▲ 100×1 topic
- Tandem Mass Spectrometry3▲ 69×2 topics
- Genetics3▲ 4.9×13 topics
- Cell Death2▲ 13×3 topics
- Metabolic Regulation2▲ 19×2 topics
- Mitochondria2▲ 23×2 topics
- Reactive Oxygen Species2▲ 7.6×4 topics
- Mitochondrial Fission2▲ 55×1 topic
- Mitochondrial Fusion2▲ 55×1 topic
- Neurodevelopmental Disorders2▲ 20×3 topics
- Neurodevelopmental Outcomes2▲ 14×6 topics
- Neurobiology2▲ 9.4×5 topics
- Comorbidity2▲ 20×2 topics
- Copy Number Variation2▲ 149×1 topic
- Genomic Rearrangements2▲ 134×1 topic
- Microbiota2▲ 9.8×2 topics
Which research topics does Victorian Clinical Genetics Services publish most on?
By volume in 2022–2025: Genomics and Rare Diseases, Prenatal Screening and Diagnostics, BRCA gene mutations in cancer and Metabolism and Genetic Disorders.
Area is fractional works; colour is the subfield each topic belongs to.
- 1 Genomics and Rare Diseases Genetics 6 works
- 2 Prenatal Screening and Diagnostics Pediatrics, Perinatology and Child Health 4 works
- 3 BRCA gene mutations in cancer Genetics 3 works
- 4 Metabolism and Genetic Disorders Clinical Biochemistry 3 works
- 5 Mitochondrial Function and Pathology Molecular Biology 2 works
- 6 Genomic variations and chromosomal abnormalities Genetics 2 works
- 7 Cystic Fibrosis Research Advances Pulmonary and Respiratory Medicine 2 works
- 8 Sexual Differentiation and Disorders Molecular Biology 1 works
- 9 Attention Deficit Hyperactivity Disorder Psychiatry and Mental health 1 works
- 10 Genetics and Neurodevelopmental Disorders Genetics 1 works
How open and international is its research?
Against the world’s own shares — the tick on each track. Both are shares of its output, so they sit on one scale and can be read against each other as well as against the world.
World: 28% of research is openly available.
World: 19% is written across borders.
How has Victorian Clinical Genetics Services's research output changed?
Output in 2018–2022 was 8% higher than in 2013–2017.
The same series as a ribbon — one cell per year, darker for more. The line above answers how much; this answers when.
Other research institutions in Flemington
Research measures only: rankings here say nothing about teaching, admissions or student experience. Comparable institutions and collaboration partners are in the interactive view on the map.