Dian Soewarto

1.9k total citations
25 papers, 939 citations indexed

About

Dian Soewarto is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Dian Soewarto has authored 25 papers receiving a total of 939 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Dian Soewarto's work include Connexins and lens biology (7 papers), Pluripotent Stem Cells Research (4 papers) and DNA Repair Mechanisms (3 papers). Dian Soewarto is often cited by papers focused on Connexins and lens biology (7 papers), Pluripotent Stem Cells Research (4 papers) and DNA Repair Mechanisms (3 papers). Dian Soewarto collaborates with scholars based in Germany, United States and Russia. Dian Soewarto's co-authors include Martin Hrabě de Angelis, Helmut Fuchs, H. Schmiady, Ursula Eichenlaub-Ritter, Eckhard Wolf, Jochen Graw, Rudi Balling, Jana Löster, André Reis and Heribert Kentenich and has published in prestigious journals such as Genetics, Endocrinology and Journal of Allergy and Clinical Immunology.

In The Last Decade

Dian Soewarto

25 papers receiving 913 citations

Peers

Countries citing papers authored by Dian Soewarto

Since Specialization

Citations

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

Fields of papers citing papers by Dian Soewarto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dian Soewarto

This figure shows the co-authorship network connecting the top 25 collaborators of Dian Soewarto. A scholar is included among the top collaborators of Dian Soewarto 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 Dian Soewarto. Dian Soewarto 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	Sex- and age-dependent effects of Gpr30 genetic deletion on the metabolic and cardiovascular profiles of diet-induced obese mice 2014 ·Gene ·Luca Meoli, Jörg Isensee, Valeria Zazzu, Christoph S. Nabzdyk, Dian Soewarto, Henning Witt, Anna Foryst‐Ludwig, Ulrich Kintscher, Patricia Ruíz	39
2	Features and Strategies of ENU Mouse Mutagenesis 2009 ·Current Pharmaceutical Biotechnology ·Dian Soewarto, Matthias Klaften, Isabel Rubio‐Aliaga	9
3	Mutation in a Novel Connexin-like Gene ( Gjf1 ) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype 2008 ·Investigative Ophthalmology & Visual Science ·Oliver Puk, (unknown), Claudia Dalke, Dian Soewarto, Helmut Fuchs, Birgit Budde, (unknown), Eckhard Wolf, Martin Hrabě de Angelis, Jochen Graw	23
4	Novel mouse mutants with primary cellular immunodeficiencies generated by genome-wide mutagenesis 2007 ·Journal of Allergy and Clinical Immunology ·Thilo Jakob, Gabriele Köllisch, (unknown), (unknown), Birgit Rathkolb, Marcel L. Müller, Nadja Sandholzer, Lars Nitschke, Matthias Schiemann, Martin Mempel, Markus Ollert, Antonie Neubauer, Dian Soewarto, Elisabeth Kremmer, Johannes Ring, Heidrun Behrendt, Heinrich Flaswinkel	20
5	Novel lymphocyte-independent mechanisms to initiate inflammatory arthritis via bone marrow-derived cells of Ali18 mutant mice 2007 ·Lara D. Veeken ·Koichiro Abe, (unknown), Svetoslav Kalaydjiev, Tobias Franz, Dirk H. Busch, Helmut Fuchs, Dian Soewarto, Heidrun Behrendt, Sören Wagner, Thilo Jakob, Martin Hrabě de Angelis	7
6	Three NovelPax6Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters 2005 ·Investigative Ophthalmology & Visual Science ·Jochen Graw, (unknown), Oliver Puk, (unknown), Nicole Haubst, Dian Soewarto, Helmut Fuchs, Birgit Meyer, (unknown), Walter Pretsch, Paul B. Selby, Jack Favor, Eckhard Wolf, Martin Hrabě de Angelis	36
7	Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice 2004 ·Investigative Ophthalmology & Visual Science ·Claudia Dalke, (unknown), Helmut Fuchs, Valérie Gailus‐Durner, Dian Soewarto, Jack Favor, (unknown), Walter Pretsch, Florian Gekeler, Kei Shinoda, Eberhart Zrenner, Thomas Meitinger, Martin Hrabě de Angelis, Jochen Graw	44
8	Random ENU Mutagenesis 2003 ·Humana Press eBooks ·Dian Soewarto, Véronique Blanquet, Martin Hrabě de Angelis	5
9	V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice 2002 ·Mammalian Genome ·Jochen Graw, Jana Löster, Dian Soewarto, Helmut Fuchs, André Reis, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	23
10	Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract 2001 ·Experimental Eye Research ·Jochen Graw, Jana Löster, Dian Soewarto, Helmut Fuchs, Birgit Meyer, André Reis, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	47
11	Ethylnitrosourea-Induced Mutation in Mice Leads to the Expression of a Novel Protein in the Eye and to Dominant Cataracts 2001 ·Genetics ·Jochen Graw, Norman Klopp, Jana Löster, Dian Soewarto, Helmut Fuchs, (unknown), André Reis, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	16
12	Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene. 2001 ·PubMed ·Jochen Graw, Jana Löster, Dian Soewarto, Helmut Fuchs, Birgit Meyer, André Reis, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	38
13	Comet assay as a tool to screen for mouse models with inherited radiation sensitivity 2000 ·Mammalian Genome ·(unknown), (unknown), (unknown), Maria Gomolka, Dian Soewarto, (unknown), Walter Pargent, Narendra P. Singh, Thomas Jung, Martin Hrabě de Angelis	20
14	The large-scale Munich ENU-mouse-mutagenesis screen 2000 ·Mammalian Genome ·Dian Soewarto, (unknown), Andreas Teubner, Birgit Rathkolb, Walter Pargent, (unknown), Susan Marschall, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	36
15	MouseNet© database: digital management of a large-scale mutagenesis project 2000 ·Mammalian Genome ·Walter Pargent, (unknown), Karlheinz F. Schäble, Dian Soewarto, Helmut Fuchs, Martin Hrabě de Angelis	12
16	Identification of immunological relevant phenotypes in ENU mutagenized mice 2000 ·Mammalian Genome ·Heinrich Flaswinkel, Francesca Alessandrini, Birgit Rathkolb, (unknown), Elisabeth Kremmer, (unknown), Thilo Jakob, Dian Soewarto, Susan Marschall, (unknown), Heidrun Behrendt, Johannes Ring, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis, Klaus Pfeffer	15
17	The clinical-chemical screen in the Munich ENU Mouse Mutagenesis Project: screening for clinically relevant phenotypes 2000 ·Mammalian Genome ·Birgit Rathkolb, (unknown), (unknown), Dian Soewarto, (unknown), (unknown), Walter Pargent, Rüdiger Wanke, Rudi Balling, Martin Hrabě de Angelis, Helmut J. Kolb, Eckhard Wolf	37
18	Mutation in the βA3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse 1999 ·Genomics ·Jochen Graw, Martin Jung, Jana Löster, (unknown), Dian Soewarto, (unknown), Helmut Fuchs, André Reis, Eckhard Wolf, Rudi Balling, Martin Hrabě de Angelis	39
19	Fertilization and early embryology: Consequences of non-extrusion of the first polar body and control of the sequential segregation of homologues and chromatids in mammalian oocytes 1995 ·Human Reproduction ·Dian Soewarto, H. Schmiady, Ursula Eichenlaub-Ritter	59
20	Fertilization and early embryology: Recurrent failure in polar body formation and premature chromosome condensation in oocytes from a human patient: indicators of asynchrony in nuclear and cytoplasmic maturation 1995 ·Human Reproduction ·Ursula Eichenlaub-Ritter, H. Schmiady, Heribert Kentenich, Dian Soewarto	75

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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