Dewi Astuti

29 papers receiving 3.3k citations

Dewi Astuti's Hit Papers

Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma 2001 · 937 citations
9370+8+16Years since publication250500750

Peers

Dewi Astuti
Comparison fields: 5 of 85
  • Cancer Research 1.5k
  • Endocrinology, Diabetes and Metabolism 573
  • Surgery 1.1k
  • Molecular Biology 1.7k
  • Pulmonary and Respiratory Medicine 581
Replace Silviu Sbiera with:
Silviu Sbiera Germany
Christoforos Giatzakis United States
Ludmila Matyakhina United States
Emily Gardner United Kingdom
Nathalie Baeza France
Janel L. Kopp United States
Fangwei Zhou China
Joan E. Willett-Brozick United States
Ann Bouché Belgium
Daniel Nyqvist Sweden
Dewi Astuti relative to Silviu Sbiera Germany Silviu Sbiera's profile →
Citations per field
00.5×2×2.6×
Silviu Sbiera · 1×
Citations per year

Countries citing papers authored by Dewi Astuti

Since Specialization
Citations

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

Fields of papers citing papers by Dewi Astuti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Dewi Astuti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dewi Astuti Line = papers co-authored together Dewi Astuti links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma
Hit paper breakdown →
2001937
2 2008282
3 2006237
4 2001208
5 2012186
6
Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma.
2001168
7 2009153
8 2001123
9 2001119
10 2005115
11 200393
12 200392
13 200389
14 200460
15 200555
16 201754
17 201452
18 201051
19 201251
20 200447

About Dewi Astuti

Dewi Astuti is a scholar working on Cancer Research, Cell Biology, Molecular Biology, Surgery and Neurology, having authored 30 papers that have together received 3.4k indexed citations. Recurring topics across this work include Cancer, Hypoxia, and Metabolism (9 papers), Epigenetics and DNA Methylation (8 papers), Adrenal and Paraganglionic Tumors (8 papers), Renal and related cancers (7 papers), Endoplasmic Reticulum Stress and Disease (6 papers), Renal cell carcinoma treatment (5 papers), RNA modifications and cancer (5 papers) and Neuroblastoma Research and Treatments (4 papers). The work is most often cited by research in Cancer Research (1.5k citations), Endocrinology, Diabetes and Metabolism (573 citations), Surgery (1.1k citations), Molecular Biology (1.7k citations) and Pulmonary and Respiratory Medicine (581 citations). Dewi Astuti has collaborated with scholars based in United Kingdom, United States and Sweden. Frequent co-authors include Farida Latif, Eamonn Richard Maher, Charis Eng, Fiona Douglas, Ashraf Dallol, Patricia L. M. Dahia, Eamonn R. Maher, Emad George, Mark R. Morris and Emma Roisin Woodward. Their work appears in journals such as British Journal of Cancer, Endocrine Related Cancer, Oncogene, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Human Molecular 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.

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