Anné Proos
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 5
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
-
- Cystic Fibrosis Research Advances 2
- Cerebrovascular and Carotid Artery Diseases 1
- Co-authors
- Leslie Burnett (10 shared papers)Martin Delatycki (1 shared paper)Viive Maarika Howell (3 shared papers)Peter James Taylor (1 shared paper)Anita Y. Bahar (1 shared paper)Michael Leonard Friedlander (1 shared paper)Michael F. Buckley (1 shared paper)Katherine Tucker (1 shared paper)
- Journals
- The Medical Journal of Australia (4 papers)Pathology (1 paper)Genetics in Medicine (1 paper)Neoplasia (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesNew Zealand
In The Last Decade
Anné Proos
15 papers receiving 412 citations
Peers
Comparison fields: 5 of 58
- Genetics 202
- Molecular Biology 152
- Physiology 48
- Cell Biology 32
- Cognitive Neuroscience 35
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 | 2010 | 128 | |
| 2 | 2001 | 45 | |
| 3 | 2012 | 37 | |
| 4 | 2015 | 33 | |
| 5 | The "GeneTrustee": a universal identification system that ensures privacy and confidentiality for human genetic databases. | 2003 | 33 |
| 6 | 2001 | 28 | |
| 7 | 1995 | 26 | |
| 8 | 2014 | 25 | |
| 9 | 2005 | 18 | |
| 10 | 2012 | 16 | |
| 11 | 2009 | 10 | |
| 12 | 2004 | 6 | |
| 13 | 1993 | 6 | |
| 14 | 2020 | 5 | |
| 15 | 2011 | 5 |
About Anné Proos
Anné Proos is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Physiology, having authored 15 papers that have together received 421 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (2 papers), Cystic Fibrosis Research Advances (2 papers), Autism Spectrum Disorder Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Lysosomal Storage Disorders Research (2 papers), CRISPR and Genetic Engineering (1 paper), Cerebrovascular and Carotid Artery Diseases (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Genetics (202 citations), Molecular Biology (152 citations), Physiology (48 citations), Cell Biology (32 citations) and Cognitive Neuroscience (35 citations). Anné Proos has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Leslie Burnett, Martin Delatycki, Viive Maarika Howell, Peter James Taylor, Anita Y. Bahar, Michael Leonard Friedlander, Michael F. Buckley, Katherine Tucker, Reet Rein and Katrin Õunap. Their work appears in journals such as The Medical Journal of Australia, Pathology, Genetics in Medicine, Neoplasia and European Journal of Medical Genetics.
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.