Anné Proos
Impact in
-
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Leslie Burnett (10 shared papers)Martin Delatycki (1 shared paper)Viive M. Howell (3 shared papers)Michael F. Buckley (1 shared paper)Michael Friedländer (1 shared paper)Anita Y. Bahar (1 shared paper)Peter J. Taylor (1 shared paper)Michael Fietz (2 shared papers)
- Journals
- The Medical Journal of Australia (4 papers)Cancer (1 paper)Neoplasia (1 paper)Journal of Inherited Metabolic Disease (1 paper)Genetics in Medicine (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Anné Proos
14 papers receiving 254 citations
Peers
Comparison fields: 5 of 55
- Genetics 116
- Pediatrics, Perinatology and Child Health 38
- Physiology 43
- Cancer Research 21
- Molecular Biology 82
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 | 31 | |
| 4 | 2015 | 29 | |
| 5 | 2001 | 24 | |
| 6 | 2014 | 23 | |
| 7 | 2005 | 18 | |
| 8 | 1995 | 16 | |
| 9 | 2012 | 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, Physiology and Cognitive Neuroscience, having authored 14 papers that have together received 260 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (4 papers), Cystic Fibrosis Research Advances (3 papers), Autism Spectrum Disorder Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Child Nutrition and Feeding Issues (2 papers), Ethics and Legal Issues in Pediatric Healthcare (1 paper), Cardiac Arrhythmias and Treatments (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (116 citations), Pediatrics, Perinatology and Child Health (38 citations), Physiology (43 citations), Cancer Research (21 citations) and Molecular Biology (82 citations). Anné Proos has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Leslie Burnett, Martin Delatycki, Viive M. Howell, Michael F. Buckley, Michael Friedländer, Anita Y. Bahar, Peter J. Taylor, Michael Fietz, Katherine Tucker and Martin B. Delatycki. Their work appears in journals such as The Medical Journal of Australia, Cancer, Neoplasia, Journal of Inherited Metabolic Disease and Genetics in Medicine.
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.