K. Madan
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 39
- Genomic variations and chromosomal abnormalities 23
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
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- Genomics and Chromatin Dynamics 7
- Sexual Differentiation and Disorders 6
- Co-authors
- Martin Bobrow (8 shared papers)P. Pearson (4 shared papers)Aggie Nieuwint (5 shared papers)Yolande van Bever (1 shared paper)F. H. Menko (2 shared papers)Martijn H. Breuning (2 shared papers)J. Schoemaker (3 shared papers)Kerstin Hansson (5 shared papers)
- Journals
- Human Genetics (14 papers)Clinical Genetics (4 papers)Cytogenetic and Genome Research (3 papers)European Journal of Human Genetics (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- NetherlandsUnited KingdomPoland
In The Last Decade
K. Madan
50 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 104
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 613
- Plant Science 693
- Reproductive Medicine 148
- Developmental Biology 34
Countries citing papers authored by K. Madan
This map shows the geographic impact of K. Madan'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 K. Madan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Madan more than expected).
Fields of papers citing papers by K. Madan
This network shows the impact of papers produced by K. Madan. 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 K. Madan. The network helps show where K. Madan may publish in the future.
Co-authors
The 25 scholars most cited alongside K. Madan, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1972 | 197 | |
| 2 | 1973 | 133 | |
| 3 | 1997 | 120 | |
| 4 | 2005 | 94 | |
| 5 | 1998 | 82 | |
| 6 | 1995 | 81 | |
| 7 | 2012 | 77 | |
| 8 | 1983 | 63 | |
| 9 | 1992 | 62 | |
| 10 | Structural variation in chromosome No 9. | 1974 | 62 |
| 11 | 1999 | 61 | |
| 12 | 1973 | 56 | |
| 13 | 2012 | 45 | |
| 14 | 1984 | 39 | |
| 15 | 2020 | 37 | |
| 16 | 2001 | 37 | |
| 17 | 1981 | 36 | |
| 18 | 2013 | 35 | |
| 19 | 1973 | 34 | |
| 20 | 1987 | 34 |
About K. Madan
K. Madan is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Developmental Biology, having authored 50 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (19 papers), Chromosomal and Genetic Variations (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Genomics and Chromatin Dynamics (7 papers), Sexual Differentiation and Disorders (6 papers), Assisted Reproductive Technology and Twin Pregnancy (4 papers) and Reproductive Biology and Fertility (3 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (613 citations), Plant Science (693 citations), Reproductive Medicine (148 citations) and Developmental Biology (34 citations). K. Madan has collaborated with scholars based in Netherlands, United Kingdom and Poland. Frequent co-authors include Martin Bobrow, P. Pearson, Aggie Nieuwint, Yolande van Bever, F. H. Menko, Martijn H. Breuning, J. Schoemaker, Kerstin Hansson, S. Walker and C. E. Ford. Their work appears in journals such as Human Genetics, Clinical Genetics, Cytogenetic and Genome Research, European Journal of Human Genetics and Prenatal Diagnosis.
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.