Melanie Leffler
Melanie Leffler publishes mostly in Genetics, Molecular Biology and Cellular and Molecular Neuroscience, on topics such as Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities and Genomics and Rare Diseases.
- World rank
- #2,213,311 of 7,710,434 ranked researchers
- Rank in Australia
- #63,787 of 140,210
- Works
- 18
- Citations
- 598
- Citations per work
- 33.2
What does Melanie Leffler research?
Melanie Leffler's work is mostly in Biochemistry, Genetics and Molecular Biology (57%), Neuroscience (9%), Medicine (6%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences1266.7%
- Everything else424.0%
- Health Sciences15.6%
- Medicine15.6%
- Social Sciences13.7%
- Psychology13.7%
- 1Genetics37% of their works
- 2Molecular Biology20% of their works
- 3Cellular and Molecular Neuroscience6% of their works
- 4Immunology and Allergy6% of their works
- 5Clinical Psychology4% of their works
- 6Cognitive Neuroscience4% of their works
Research topics
Which keywords describe Melanie Leffler's research?
The keywords of their largest research topics: Fragile X Syndrome, Neurodevelopmental Disorders, Rett Syndrome, Copy Number Variation, Genomic Rearrangements, Genetic Variants, Sequence Interpretation and Angiogenesis.
- Tissue Inhibitors of Metalloproteinases
- m6A-seq
- Personalisation
- Direct Payments
- Integrins
- Cancer Progression
- Angiogenesis
- Genetic Variants
- Copy Number Variation
- Neurodevelopmental Disorders
- Fragile X Syndrome
- Rett Syndrome
- Genomic Rearrangements
- Sequence Interpretation
- Extracellular Matrix
- Cell Adhesion
- Autism Spectrum Disorders
- Genetics
- RNA methylation
- Matrix Metalloproteinases
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most.
All 20 words, with their numbers
- Fragile X Syndrome81 topic
- Neurodevelopmental Disorders82 topics
- Rett Syndrome81 topic
- Copy Number Variation61 topic
- Genomic Rearrangements61 topic
- Genetic Variants51 topic
- Sequence Interpretation51 topic
- Angiogenesis42 topics
- Extracellular Matrix42 topics
- Cancer Progression32 topics
- Cell Adhesion31 topic
- Integrins31 topic
- Autism Spectrum Disorders21 topic
- Direct Payments21 topic
- Genetics21 topic
- Personalisation21 topic
- RNA methylation21 topic
- m6A-seq21 topic
- Matrix Metalloproteinases11 topic
- Tissue Inhibitors of Metalloproteinases11 topic
Where does Melanie Leffler work?
Melanie Leffler's main affiliation in the publication record is Hunter Genetics, Australia.
How many publications and citations does Melanie Leffler have?
OpenAlex counts 18 works and 598 citations for Melanie Leffler, an h-index of 11, ranking #2,213,311 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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