Anné Proos

503 total citations
14 papers, 260 citations indexed

About

Anné Proos is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Anné Proos has authored 14 papers receiving a total of 260 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Anné Proos's work include Lysosomal Storage Disorders Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cystic Fibrosis Research Advances (3 papers). Anné Proos is often cited by papers focused on Lysosomal Storage Disorders Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cystic Fibrosis Research Advances (3 papers). Anné Proos collaborates with scholars based in Australia, United States and Estonia. Anné Proos's co-authors include Leslie Burnett, Martin Delatycki, Katherine Tucker, Martin B. Delatycki, Michael F. Buckley, Michael Friedländer, Michael Fietz, Agnes Bankier, Viive M. Howell and Peter J. Taylor and has published in prestigious journals such as Cancer, The Medical Journal of Australia and Genetics in Medicine.

In The Last Decade

Anné Proos

14 papers receiving 254 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anné Proos Australia 10 116 82 43 38 32 14 260
ACMG Board of Directors 6 208 1.8× 60 0.7× 38 0.9× 46 1.2× 8 0.3× 10 299
Arne Schillert Germany 10 83 0.7× 223 2.7× 35 0.8× 13 0.3× 20 0.6× 22 433
Shruti Marwaha United States 6 123 1.1× 131 1.6× 12 0.3× 8 0.2× 11 0.3× 19 283
Jennyfer M. Garcí­a-Cárdenas Ecuador 12 73 0.6× 195 2.4× 64 1.5× 11 0.3× 39 1.2× 35 451
Brenda Hermsen Netherlands 7 130 1.1× 41 0.5× 17 0.4× 22 0.6× 17 0.5× 16 286
Joanna Zhuang United Kingdom 9 203 1.8× 452 5.5× 15 0.3× 40 1.1× 32 1.0× 9 600
Clesson Turner United States 12 243 2.1× 224 2.7× 14 0.3× 61 1.6× 54 1.7× 40 499
May Chan United Kingdom 12 55 0.5× 155 1.9× 25 0.6× 8 0.2× 11 0.3× 13 655
Ioanna Tachmazidou United Kingdom 7 165 1.4× 91 1.1× 30 0.7× 8 0.2× 7 0.2× 11 284
Phillip Gray United States 8 173 1.5× 123 1.5× 42 1.0× 16 0.4× 23 0.7× 11 357

Countries citing papers authored by Anné Proos

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Anné Proos

This figure shows the co-authorship network connecting the top 25 collaborators of Anné Proos. A scholar is included among the top collaborators of Anné Proos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anné Proos. Anné Proos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
2.
Burnett, Leslie, et al.. (2015). Tay-Sachs disease: current perspectives from Australia. The Application of Clinical Genetics. 8. 19–19. 29 indexed citations
3.
Burnett, Leslie, Anné Proos, Kristine Barlow‐Stewart, et al.. (2014). Ashkenazi Jewish population screening for Tay–Sachs disease: The International and Australian experience. Journal of Paediatrics and Child Health. 51(3). 271–279. 23 indexed citations
4.
Õunap, Katrin, Maire Peters, Ulvi Vaher, et al.. (2012). A novel c.2T > C mutation of the KDM5C/JARID1C gene in one large family with X-linked intellectual disability. European Journal of Medical Genetics. 55(3). 178–184. 31 indexed citations
5.
Proos, Anné, et al.. (2012). Tay Sachs disease in Australia: reduced disease incidence despite stable carrier frequency in Australian Jews. The Medical Journal of Australia. 197(11-12). 652–654. 16 indexed citations
6.
7.
Christie, Louise, et al.. (2009). Outcomes of a cystic fibrosis carrier testing clinic for couples. The Medical Journal of Australia. 191(9). 499–501. 9 indexed citations
8.
Warren, Emma, et al.. (2005). Cost-effectiveness of a school-based Tay-Sachs and cystic fibrosis genetic carrier screening program. Genetics in Medicine. 7(7). 484–494. 18 indexed citations
9.
Howell, Viive M., et al.. (2004). Carrier screening for Canavan disease in Australia. Journal of Inherited Metabolic Disease. 27(2). 289–290. 3 indexed citations
10.
Burnett, Leslie, et al.. (2003). The "GeneTrustee": a universal identification system that ensures privacy and confidentiality for human genetic databases.. PubMed. 10(4). 506–13. 33 indexed citations
11.
Marsh, Deborah J., Viive M. Howell, Diana E. Benn, et al.. (2001). Rapid Mutation Scanning of Genes Associated with Familial Cancer Syndromes Using Denaturing High-Performance Liquid Chromatography. Neoplasia. 3(3). 236–244. 24 indexed citations
12.
Bahar, Anita Y., Peter J. Taylor, Anné Proos, et al.. (2001). The frequency of founder mutations in theBRCA1,BRCA2, andAPC genes in australian Ashkenazi Jews. Cancer. 92(2). 440–445. 43 indexed citations
13.
Burnett, Leslie, et al.. (1995). The Tay‐Sachs disease prevention program in Australia: Sydney pilot study. The Medical Journal of Australia. 163(6). 298–300. 16 indexed citations
14.
Burnett, John R., Anné Proos, Jerry Koutts, & Leslie Burnett. (1993). Familial hypobetalipoproteinaemia: a rare presentation to the lipid clinic. The Medical Journal of Australia. 159(4). 272–274. 5 indexed citations

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.

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