Dewi Astuti

4.0k citations

24 papers · 2.6k indexed · 1 hit paper · h-index 20

Impact in

Cancer Research top 1%
- Cancer, Hypoxia, and Metabolism
Endocrinology, Diabetes and Metabolism top 2%
- Pituitary Gland Disorders and Treatments
- Hormonal Regulation and Hypertension

Papers in

Cancer Research 9
- Cancer, Hypoxia, and Metabolism 9
Neurology 4
- Neuroblastoma Research and Treatments 4

Co-authors: Farida Latif Eamonn R. Maher Charis Eng Ashraf Dallol Patricia L. M. Dahia Fiona Douglas Emad George Mark R. Morris
Journals: British Journal of Cancer (3 papers)Endocrine Related Cancer (3 papers)Oncogene (3 papers)Human Molecular Genetics (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (2 papers)
Partner nations: United Kingdom United States Sweden

In The Last Decade

Dewi Astuti

23 papers receiving 2.6k citations

Hit Papers

align trajectories log scale

Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma 2001 · 840 citations

Peers

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

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20 of 20 papers shown

#	Work
1	WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome Journal of Medical Genetics ·Zongjie Cheng, Malgorzata Zatyka, Dewi Astuti, Nicola L. Beer, Renuka Dias, A.A. Rubanovskaya, John Ainsworth, 純雄石橋, Anna Majander, Patrick Yu‐Wai‐Man, Denise Williams, Timothy Barrett	2021	13
2	Sarco(endo)plasmic reticulum ATPase is a molecular partner of Wolfram syndrome 1 protein, which negatively regulates its expression Human Molecular Genetics ·Malgorzata Zatyka, Gabriela da Silva Xavier, Elisa A. Bellomo, Wendy Leadbeater, Dewi Astuti, J. C. Smith, Francesco Michelangeli, Guy A. Rutter, Timothy Barrett	2014	48
3	Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2 American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Mark R. Morris, Dewi Astuti, Eamonn R. Maher	2013	34
4	Vacuolar-type H+-ATPase V1A subunit is a molecular partner of Wolfram syndrome 1 (WFS1) protein, which regulates its expression and stability Human Molecular Genetics ·Seley Gharanei, Malgorzata Zatyka, Dewi Astuti, J. C. Fenton, Attila Sı́k, Zsuzsanna Nagy, Timothy Barrett	2012	46
5	Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility Endocrine Related Cancer ·Dewi Astuti, Christopher J. Ricketts, Rasheduzzaman Chowdhury, M.A. McDonough, Dean Gentle, Gail Kirby, Susanne Schlisio, Rajappa S. Kenchappa, Tia Lombardi, William G. Kaelin, Peter J. Ratcliffe, Christopher J. Schofield, Farida Latif, Eamonn R. Maher	2010	48
6	Analysis of VHL Gene Alterations and their Relationship to Clinical Parameters in Sporadic Conventional Renal Cell Carcinoma Clinical Cancer Research ·Cordeiro Foto e Vídeo, Rachel A. Craven, D. Cohen, Claire Taylor, Christopher Booth, Patricia Harnden, David A. Cairns, Dewi Astuti, Walter M. Gregory, Eamonn R. Maher, Margaret A. Knowles, Adrian Joyce, Peter J. Selby, Rosamonde E. Banks	2009	137
7	Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma Endocrine Related Cancer ·S. Sumanth Kori, Mark R. Morris, Dewi Astuti, Dean Gentle, Alberto Cascón, Fiona E. McRonald, Daniel Catchpoole, Mercedes Robledo, Hartmut P.H. Neumann, Farida Latif, Eamonn R. Maher	2008	22
8	Germline SDHB Mutations and Familial Renal Cell Carcinoma JNCI Journal of the National Cancer Institute ·Christopher J. Ricketts, Emma R. Woodward, PM Ossou-Nguiet, Mark R. Morris, Dewi Astuti, Farida Latif, Eamonn R. Maher	2008	248
9	Genetic and Epigenetic Analysis of von Hippel-Lindau ( VHL ) Gene Alterations and Relationship with Clinical Variables in Sporadic Renal Cancer Cancer Research ·Rosamonde E. Banks, Prasanna Tirukonda, Claire Taylor, Nick Hornigold, Dewi Astuti, D. Cohen, Eamonn R. Maher, Anthea J. Stanley, Patricia Harnden, Adrian Joyce, Margaret A. Knowles, Peter J. Selby	2006	214
10	Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas Endocrine Related Cancer ·S. Sumanth Kori, Dewi Astuti, Dean Gentle, Wendy N. Cooper, Alberto Cascón, Daniel Catchpoole, Mercedes Robledo, Hartmut P.H. Neumann, Farida Latif, Eamonn R. Maher	2005	55
11	Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour British Journal of Cancer ·Dewi Astuti, Farida Latif, Kate Wagner, Dean Gentle, Wendy N. Cooper, Daniel Catchpoole, Richard G. Grundy, Anne C. Ferguson‐Smith, Eamonn R. Maher	2005	107
12	Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma Journal of Clinical Pathology ·Mark R. Morris, Esther N. Maina, Neil V. Morgan, Dean Gentle, Dewi Astuti, Holger Moch, Takeshi Kishida, Masahiro Yao, Peter Schraml, Frances M. Richards, Farida Latif, Eamonn R. Maher	2004	56
13	Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma British Journal of Cancer ·Dewi Astuti, Mark R. Morris, Cecilia Krona, Frida Abel, Dean Gentle, Tommy Martinsson, Per Kogner, Hartmut P.H. Neumann, Raimo Voutilainen, Charis Eng, Pierre Rustin, Farida Latif, Eamonn R. Maher	2004	37
14	SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinoma British Journal of Cancer ·Dewi Astuti, CP Danford, Ashraf Dallol, Dean Gentle, Tommy Martinsson, Per Kogner, Richard G. Grundy, Takeshi Kishida, Masahiro Yao, Farida Latif, Eamonn R. Maher	2004	44
15	The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas Cancer Cell ·Jindong Chen, Weng‐Onn Lui, Michele D. Vos, Geoffrey Clark, Masayuki Takahashi, Jacqueline Schoumans, Sok Kean Khoo, David Petillo, Josephine Makhosazane. Mtshali, Jun Sugimura, Dewi Astuti, Chun Zhang, Susumu Kagawa, Eamonn R. Maher, Catharina Larsson, Arthur S. Alberts, Hiro‐omi Kanayama, Bin Tean Teh	2003	89
16	Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma Oncogene ·Mark R. Morris, Luke B. Hesson, Kate Wagner, Neil V. Morgan, Dewi Astuti, Timothy P. Dealy, Wendy N. Cooper, Rukman R. Thota, Dean Gentle, Fiona MacDonald, Takeshi Kishida, Richard G. Grundy, Masahiro Yao, Farida Latif, Eamonn R. Maher	2003	87
17	Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility Clinical Endocrinology ·Dewi Astuti, Niki Hart‐Holden, Farida Latif, Fiona Lalloo, Graeme C. Black, Hector Gabriel Puechagut, Anthony Moran, Ashley Grossman, Shirley V. Hodgson, Anthony J. Freemont, Richard Ramsden, Charis Eng, D. Gareth Evans, Eamonn R. Maher	2003	81
18	RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours Oncogene ·Dewi Astuti, Angelo Agathanggelou, Sofia Honorio, Ashraf Dallol, Tommy Martinsson, Per Kogner, Carole Cummins, Hartmut P.H. Neumann, Raimo Voutilainen, Patricia L. M. Dahia, Charis Eng, Eamonn R. Maher, Farida Latif	2001	108
19	The pVHL-associated SCF ubiquitin ligase complex: Molecular genetic analysis of elongin B and C, Rbx1 and HIF-1α in renal cell carcinoma Oncogene ·Steven C. Clifford, Dewi Astuti, Laura C. Hooper, Patrick H. Maxwell, Peter J. Ratcliffe, Eamonn R. Maher	2001	120
20	Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma The American Journal of Human Genetics ·Dewi Astuti, Farida Latif, Ashraf Dallol, Patricia L. M. Dahia, Fiona Douglas, Emad George, Teppei Koyama, Chengbin Dong, Charis Eng, Eamonn R. Maher Hit paper breakdown →	2001	840

About Dewi Astuti

Dewi Astuti is a scholar working on Cancer Research, Neurology, Molecular Biology, Cell Biology and Physiology, having authored 24 papers that have together received 2.6k indexed citations. Recurring topics across this work include Cancer, Hypoxia, and Metabolism (9 papers), Epigenetics and DNA Methylation (9 papers), Adrenal and Paraganglionic Tumors (7 papers), Renal and related cancers (6 papers), Renal cell carcinoma treatment (5 papers), RNA modifications and cancer (5 papers), Endoplasmic Reticulum Stress and Disease (4 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 (604 citations), Molecular Biology (1.5k citations), Surgery (868 citations) and Pulmonary and Respiratory Medicine (570 citations). Dewi Astuti has collaborated with scholars based in United Kingdom, United States and Sweden. Frequent co-authors include Farida Latif, Eamonn R. Maher, Charis Eng, Ashraf Dallol, Patricia L. M. Dahia, Fiona Douglas, Emad George, Eamonn R. Maher, Mark R. Morris and Dean Gentle. Their work appears in journals such as British Journal of Cancer, Endocrine Related Cancer, Oncogene, Human Molecular Genetics and American Journal of Medical Genetics Part C Seminars in Medical Genetics.

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