Anné Proos
Impact in
-
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Lysosomal Storage Disorders Research
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
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- Epigenetics and DNA Methylation 1
- Ubiquitin and proteasome pathways 1
- Co-authors
- Leslie Burnett (10 shared papers)Martin Delatycki (1 shared paper)Martin B. Delatycki (2 shared papers)Viive M. Howell (3 shared papers)Agnes Bankier (2 shared papers)Katherine Tucker (1 shared paper)Michael Friedländer (1 shared paper)Michael F. Buckley (1 shared paper)
- Journals
- The Medical Journal of Australia (4 papers)The Application of Clinical Genetics (1 paper)European Journal of Medical Genetics (1 paper)Cancer (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- AustraliaUnited StatesEstonia
In The Last Decade
Anné Proos
14 papers receiving 256 citations
Peers
Comparison fields: 5 of 51
- Genetics 103
- Physiology 40
- Pediatrics, Perinatology and Child Health 27
- Pulmonary and Respiratory Medicine 30
- Cancer Research 14
Countries citing papers authored by Anné Proos
This map shows the geographic impact of Anné Proos'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 Anné Proos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anné Proos more than expected).
Fields of papers citing papers by Anné Proos
This network shows the impact of papers produced by Anné Proos. 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 Anné Proos. The network helps show where Anné Proos may publish in the future.
Co-authors
The 25 scholars most cited alongside Anné Proos, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 43 | |
| 2 | The "GeneTrustee": a universal identification system that ensures privacy and confidentiality for human genetic databases. | 2003 | 33 |
| 3 | 2012 | 32 | |
| 4 | 2015 | 29 | |
| 5 | 2001 | 24 | |
| 6 | 2014 | 23 | |
| 7 | 2005 | 18 | |
| 8 | 2012 | 16 | |
| 9 | 1995 | 16 | |
| 10 | 2009 | 9 | |
| 11 | 2020 | 5 | |
| 12 | 2011 | 5 | |
| 13 | 1993 | 5 | |
| 14 | 2004 | 3 |
About Anné Proos
Anné Proos is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 14 papers that have together received 261 indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (2 papers), Cystic Fibrosis Research Advances (2 papers), Lysosomal Storage Disorders Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Fetal and Pediatric Neurological Disorders (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Epigenetics and DNA Methylation (1 paper) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Genetics (103 citations), Physiology (40 citations), Pediatrics, Perinatology and Child Health (27 citations), Pulmonary and Respiratory Medicine (30 citations) and Cancer Research (14 citations). Anné Proos has collaborated with scholars based in Australia, United States and Estonia. Frequent co-authors include Leslie Burnett, Martin Delatycki, Martin B. Delatycki, Viive M. Howell, Agnes Bankier, Katherine Tucker, Michael Friedländer, Michael F. Buckley, Anita Y. Bahar and Peter J. Taylor. Their work appears in journals such as The Medical Journal of Australia, The Application of Clinical Genetics, European Journal of Medical Genetics, Cancer and Journal of Inherited Metabolic Disease.
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.