I. Nanda
Impact in
- Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic diversity and population structure
- Animal Genetics and Reproduction
- Genetic Mapping and Diversity in Plants and Animals
- Physiology top 2%
- Reproductive biology and impacts on aquatic species
Papers in
- Genetics 45
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 20
- Genetic diversity and population structure 14
- Animal Genetics and Reproduction 14
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- Genomics and Chromatin Dynamics 10
- DNA Repair Mechanisms 7
- Genomics and Phylogenetic Studies 6
- Advanced biosensing and bioanalysis techniques 5
- Co-authors
- Michael Schmid (46 shared papers)Manfred Schartl (21 shared papers)Thomas Haaf (17 shared papers)Jörg T. Epplen (9 shared papers)Jean‐Nicolas Volff (1 shared paper)Martina Guttenbach (6 shared papers)Claus Steinlein (9 shared papers)Ingo Schlupp (5 shared papers)
- Journals
- Cytogenetic and Genome Research (26 papers)Genomics (2 papers)Chromosome Research (2 papers)Chromosoma (2 papers)Proceedings of the National Academy of Sciences (2 papers)
- Partner nations
- GermanyUnited KingdomPoland
In The Last Decade
I. Nanda
61 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 90
- Genetics 1.7k
- Physiology 150
- Plant Science 1.0k
- Reproductive Medicine 124
- Molecular Biology 991
Countries citing papers authored by I. Nanda
This map shows the geographic impact of I. Nanda'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 I. Nanda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. Nanda more than expected).
Fields of papers citing papers by I. Nanda
This network shows the impact of papers produced by I. Nanda. 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 I. Nanda. The network helps show where I. Nanda may publish in the future.
Co-authors
The 25 scholars most cited alongside I. Nanda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 303 | |
| 2 | 2007 | 161 | |
| 3 | 2000 | 155 | |
| 4 | 2005 | 130 | |
| 5 | 2003 | 102 | |
| 6 | 2000 | 90 | |
| 7 | 1995 | 82 | |
| 8 | 1991 | 82 | |
| 9 | 2013 | 77 | |
| 10 | 2000 | 72 | |
| 11 | 2000 | 71 | |
| 12 | 2013 | 60 | |
| 13 | 2015 | 59 | |
| 14 | 2007 | 58 | |
| 15 | 1998 | 54 | |
| 16 | 2010 | 51 | |
| 17 | 2009 | 45 | |
| 18 | 2006 | 43 | |
| 19 | 1991 | 41 | |
| 20 | 1994 | 39 |
About I. Nanda
I. Nanda is a scholar working on Genetics, Molecular Biology, Plant Science, Oncology and Reproductive Medicine, having authored 64 papers that have together received 2.5k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (29 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (20 papers), Genetic diversity and population structure (14 papers), Animal Genetics and Reproduction (14 papers), Genomics and Chromatin Dynamics (10 papers), DNA Repair Mechanisms (7 papers), Genomics and Phylogenetic Studies (6 papers) and Advanced biosensing and bioanalysis techniques (5 papers). The work is most often cited by research in Genetics (1.7k citations), Physiology (150 citations), Plant Science (1.0k citations), Reproductive Medicine (124 citations) and Molecular Biology (991 citations). I. Nanda has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Michael Schmid, Manfred Schartl, Thomas Haaf, Jörg T. Epplen, Jean‐Nicolas Volff, Martina Guttenbach, Claus Steinlein, Ingo Schlupp, W. Feichtinger and Jakob Parzefall. Their work appears in journals such as Cytogenetic and Genome Research, Genomics, Chromosome Research, Chromosoma and Proceedings of the National Academy of Sciences.
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.