Anthony Raizis

1.1k total citations
18 papers, 550 citations indexed

About

Anthony Raizis is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Anthony Raizis has authored 18 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Oncology and 3 papers in Genetics. Recurrent topics in Anthony Raizis's work include Hedgehog Signaling Pathway Studies (4 papers), Epigenetics and DNA Methylation (4 papers) and Cancer-related Molecular Pathways (4 papers). Anthony Raizis is often cited by papers focused on Hedgehog Signaling Pathway Studies (4 papers), Epigenetics and DNA Methylation (4 papers) and Cancer-related Molecular Pathways (4 papers). Anthony Raizis collaborates with scholars based in New Zealand, United States and Australia. Anthony Raizis's co-authors include J P Jost, Frédéric Schmitt, Andrew P. Feinberg, A E Reeve, Anthony E. Reeve, Peter M. George, D. M. O. Becroft, Michael R. Eccles, M.M. Ferguson and Timothy G. Yandle and has published in prestigious journals such as Molecular and Cellular Biology, Analytical Biochemistry and Biochemical Journal.

In The Last Decade

Anthony Raizis

18 papers receiving 545 citations

Peers

Anthony Raizis

GENET

PPCH

ONCOL

PRM

Cecilia Surace Italy

P. de Pagter-Holthuizen Netherlands

Jana Paděrová Canada

Bartłomiej Budny Poland

Pietro Sirleto Italy

Anthony R. Dallosso United Kingdom

Luke St Heaps Australia

Nora Wasserman United States

Germaine Caldwell United Kingdom

Pauline A.M. Roest Netherlands

Cecilia Surace Italy

Anthony Raizis

328 ×0.8

201 ×1.5

GENET

34 ×0.4

PPCH

68 ×1.0

ONCOL

58 ×0.9

PRM

Citations per year, relative to Anthony Raizis Anthony Raizis (= 1×) peers Cecilia Surace

Countries citing papers authored by Anthony Raizis

Since Specialization

Citations

This map shows the geographic impact of Anthony Raizis'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 Anthony Raizis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anthony Raizis more than expected).

Fields of papers citing papers by Anthony Raizis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anthony Raizis. 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 Anthony Raizis. The network helps show where Anthony Raizis may publish in the future.

Co-authorship network of co-authors of Anthony Raizis

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony Raizis. A scholar is included among the top collaborators of Anthony Raizis 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 Anthony Raizis. Anthony Raizis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Stutterd, Chloe, Alexa Kidd, Chris Florkowski, et al.. (2021). Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations. American Journal of Medical Genetics Part A. 185(10). 2941–2950. 2 indexed citations

Florkowski, Chris, et al.. (2018). A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 55(5). 616–619. 6 indexed citations

Tacik, Paweł, Fabienne C. Fiesel, Shinsuke Fujioka, et al.. (2014). Three families with Perry syndrome from distinct parts of the world. Parkinsonism & Related Disorders. 20(8). 884–888. 22 indexed citations

Raizis, Anthony, et al.. (2014). Novel inactivating mutation of the calcium‐sensing receptor in a young woman with mild hypercalcaemia. Internal Medicine Journal. 44(4). 413–416. 1 indexed citations

Raizis, Anthony, David Van Mater, Lauri A. Aaltonen, et al.. (2013). Trilateral Retinoblastoma in a Patient With Peutz–Jeghers Syndrome. American Journal of Medical Genetics Part A. 161(5). 1096–1100. 4 indexed citations

Schouten, Belinda J., Anthony Raizis, Steven Soule, et al.. (2011). Four cases of autosomal dominant hypocalcaemia with hypercalciuria including two with novel mutations in the calcium-sensing receptor gene. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 48(3). 286–290. 6 indexed citations

Pradhan, Monika, et al.. (2010). Role of genetic testing in retinoblastoma management at a tertiary referral centre. Clinical and Experimental Ophthalmology. 38(3). 231–236. 13 indexed citations

Raizis, Anthony, et al.. (2009). Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.. PubMed. 122(1296). 21–8. 5 indexed citations

Raizis, Anthony, et al.. (2002). Improved clinical management of retinoblastoma through gene testing.. PubMed. 115(1154). 231–4. 8 indexed citations

10.

Raizis, Anthony, M.M. Ferguson, & Peter M. George. (2000). Effect of nonsense mutations on PTEN mRNA stability. Human Genetics. 107(1). 24–27. 6 indexed citations

11.

Raizis, Anthony, M.M. Ferguson, & Peter M. George. (2000). Effect of nonsense mutations on PTEN mRNA stability. Human Genetics. 107(1). 24–27. 1 indexed citations

12.

Raizis, Anthony, et al.. (1999). The characterization of ovine genes for atrial, brain, and C-type natriuretic peptides. Domestic Animal Endocrinology. 16(2). 115–121. 18 indexed citations

13.

Raizis, Anthony, et al.. (1998). Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome.. Molecular Pathology. 51(6). 339–341. 14 indexed citations

14.

Raizis, Anthony, Frédéric Schmitt, & J P Jost. (1995). A Bisulfite Method of 5-Methylcytosine Mapping That Minimizes Template Degradation. Analytical Biochemistry. 226(1). 161–166. 166 indexed citations

15.

Raizis, Anthony, Michael R. Eccles, & Anthony E. Reeve. (1993). Structural analysis of the human insulin-like growth factor-II P3 promoter. Biochemical Journal. 289(1). 133–139. 23 indexed citations

16.

Reeve, A E, et al.. (1989). Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.. Molecular and Cellular Biology. 9(4). 1799–1803. 173 indexed citations

17.

Reeve, Anthony E., et al.. (1989). Loss of Allelic Heterozygosity at a Second Locus on Chromosome 11 in Sporadic Wilms’ Tumor Cells. Molecular and Cellular Biology. 9(4). 1799–1803. 45 indexed citations

18.

Raizis, Anthony, et al.. (1985). A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13. Human Genetics. 70(4). 344–346. 37 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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