Galuh Astuti

1.8k total citations
23 papers, 423 citations indexed

About

Galuh Astuti is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Galuh Astuti has authored 23 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Ophthalmology and 6 papers in Genetics. Recurrent topics in Galuh Astuti's work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Prenatal Screening and Diagnostics (4 papers). Galuh Astuti is often cited by papers focused on Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (8 papers) and Prenatal Screening and Diagnostics (4 papers). Galuh Astuti collaborates with scholars based in Netherlands, Indonesia and United Kingdom. Galuh Astuti's co-authors include Rob W.J. Collin, Frans P.M. Cremers, Sultana MH Faradz, Erwin van Wijk, Knut Stieger, Martijn A. Huynen, Ralph Slijkerman, Anna M. Siemiatkowska, Christian Gilissen and Thomas Rosenberg and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Reproduction and Progress in Retinal and Eye Research.

In The Last Decade

Galuh Astuti

21 papers receiving 416 citations

Peers

Countries citing papers authored by Galuh Astuti

Since Specialization

Citations

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

Fields of papers citing papers by Galuh Astuti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Galuh Astuti

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Detection of human cytomegalovirus cell‐free DNA in pregnant women with symptomatically infected fetuses: proof‐of‐concept study 2025 ·Ultrasound in Obstetrics and Gynecology ·Brigitte H. W. Faas, (unknown), Galuh Astuti, A. Reuss, Kim Stol, Erik A. Sistermans, (unknown), Esther van Leeuwen, Janette Rahamat–Langendoen, Freke A. Wilmink	3
2	Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal Dystrophy 2025 ·Investigative Ophthalmology & Visual Science ·(unknown), (unknown), Martin McKibbin, Suzanne E. de Bruijn, (unknown), Andrea L. Vincent, (unknown), Jordi Corominas, Galuh Astuti, Christian Gilissen, Elfride De Baere, Chris F. Inglehearn, Susanne Roosing, (unknown), Frans P.M. Cremers	0
3	Pulmonary contusion volume and radiomics as predictors of early-onset pneumonia in trauma patients, a retrospective single-centre study 2025 ·European Journal of Trauma and Emergency Surgery ·Lorenzo Gamberini, Galuh Astuti, (unknown), (unknown), (unknown), (unknown), (unknown), Carlo Coniglio, A Bertini, Paolo Emilio Orlandi, Marco Tartaglione, (unknown), Antonio Bruno	0
4	Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testing 2024 ·EBioMedicine ·Brigitte H. W. Faas, Galuh Astuti, Willem J. G. Melchers, A. Reuss, Christian Gilissen, Merryn Macville, (unknown), (unknown), Malgorzata I. Srebniak, (unknown), Janette Rahamat–Langendoen, Erik A. Sistermans, (unknown)	10
5	Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases 2024 ·Human Genetics ·(unknown), Maryam Vaseghi‐Shanjani, (unknown), (unknown), Jaap Oostrik, (unknown), Galuh Astuti, Helger G. Yntema, Lies H. Hoefsloot, Cris Lanting, Martijn A. Huynen, Anna Lehman, Stuart E. Turvey, Ronald J. E. Pennings, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
6	Lipopeptide-mediated Cas9 RNP delivery: A promising broad therapeutic strategy for safely removing deep-intronic variants in ABCA4 2024 ·Molecular Therapy — Nucleic Acids ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Galuh Astuti, (unknown), (unknown), (unknown), (unknown), (unknown), Olivier G. de Jong, Rob W.J. Collin, Enrico Mastrobattista, Alejandro Garanto	1
7	Automatized detection of uniparental disomies in a large cohort 2024 ·Human Genetics ·(unknown), (unknown), Thomas Liehr, Thomas Eggermann, Christian Gilissen, Rolph Pfundt, Galuh Astuti, Julia Hentschel, (unknown)	4
8	CORONARY ARTERY ANEURYSM IN IGG4–RELATED DISEASE 2024 ·European Heart Journal Supplements ·(unknown), Galuh Astuti, E Orlando, (unknown), C Farina, Francesco D’Angelo, (unknown), Salvatore Evola, Giuseppina Novo, Egle Corrado, (unknown)	1
9	Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing 2023 ·SHILAP Revista de lepidopterología ·Annechien E. G. Haarman, Caroline C. W. Klaver, Milly S. Tedja, Susanne Roosing, Galuh Astuti, Christian Gilissen, Lies H. Hoefsloot, Marianne van Tienhoven, (unknown), (unknown), (unknown), Annelies de Klein, Erwin Brosens, Virginie J. M. Verhoeven	4
10	CRISPR-Cas9 correction of a nonsense mutation in LCA5 rescues lebercilin expression and localization in human retinal organoids 2023 ·Molecular Therapy — Methods & Clinical Development ·(unknown), Dimitra Athanasiou, (unknown), (unknown), Lonneke Duijkers, Galuh Astuti, Jean Bennett, Alejandro Garanto, Jacqueline van der Spuy, Ronald Roepman, Michael E. Cheetham, Rob W.J. Collin	16
11	Common and rare variants in patients with early onset drusen maculopathy 2022 ·Clinical Genetics ·Anita de Breuk, Yara Lechanteur, Galuh Astuti, Jordi Corominas Galbany, Caroline C. W. Klaver, Carel B. Hoyng, Anneke I. den Hollander	1
12	Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease 2022 ·Journal of Pediatric Surgery ·Gunadi Gunadi, (unknown), Kristy Iskandar, (unknown), (unknown), (unknown), Akhmad Makhmudi, Galuh Astuti	3
13	De novo mutations in children born after medical assisted reproduction 2022 ·Human Reproduction ·(unknown), Miguel J. Xavier, Manon S. Oud, Galuh Astuti, (unknown), Petra F. de Vries, (unknown), (unknown), (unknown), (unknown), Karolis Šablauskas, Lisenka E.L.M. Vissers, Christian Gilissen, Kathrin Fleischer, D.D.M. Braat, Liliana Ramos, Joris A. Veltman	11
14	Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases 2021 ·npj Genomic Medicine ·(unknown), Laura Whelan, Tamar Ben‐Yosef, Adrian Dockery, (unknown), Christian Gilissen, Lonneke Haer‐Wigman, Jordi Corominas, Galuh Astuti, Laura de Rooij, L. Ingeborgh van den Born, Caroline C. W. Klaver, Carel B. Hoyng, (unknown), Emma Duignan, Paul F. Kenna, Frans P.M. Cremers, G. Jane Farrar, Susanne Roosing	34
15	Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 Alleles 2019 ·Investigative Ophthalmology & Visual Science ·Esmee H. Runhart, (unknown), Stéphanie S. Cornelis, Mubeen Khan, Riccardo Sangermano, Sílvia Albert, Nathalie M. Bax, Galuh Astuti, Christian Gilissen, Jan-Willem R. Pott, Joanne Verheij, Ellen A.W. Blokland, Frans P.M. Cremers, L. Ingeborgh van den Born, Carel B. Hoyng	27
16	Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes 2018 ·Genes ·Galuh Astuti, (unknown), Muhammad Imran Khan, Christian Hamel, Béatrice Bocquet, Gaël Manès, Mathieu Quinodoz, Manir Ali, Carmel Toomes, Martin McKibbin, Mohammed E. El‐Asrag, Lonneke Haer‐Wigman, Chris F. Inglehearn, Graeme C. Black, Carel C B Hoyng, Frans P.M. Cremers, Susanne Roosing	19
17	Mutations in AGBL5, Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa 2016 ·Investigative Ophthalmology & Visual Science ·Galuh Astuti, Gavin Arno, Sarah Hull, (unknown), Hanka Venselaar, Keren Carss, F. Lucy Raymond, Rob W.J. Collin, Sultana MH Faradz, L. Ingeborgh van den Born, Andrew R. Webster, Frans P.M. Cremers	23
18	Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark 2015 ·European Journal of Human Genetics ·Galuh Astuti, Mette Bertelsen, Markus N. Preising, Muhammad Ajmal, Birgit Lorenz, Sultana MH Faradz, Raheel Qamar, Rob W.J. Collin, Thomas Rosenberg, Frans P.M. Cremers	62
19	The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies 2015 ·Progress in Retinal and Eye Research ·Ralph Slijkerman, (unknown), Galuh Astuti, Martijn A. Huynen, Erwin van Wijk, Knut Stieger, Rob W.J. Collin	81
20	Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family. 2012 ·PubMed ·Anna M. Siemiatkowska, Galuh Astuti, (unknown), (unknown), Sultana MH Faradz, Frans P.M. Cremers, Rob W.J. Collin	21

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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