V. D. Marković
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
Papers in
-
- Prenatal Screening and Diagnostics 6
- Genetics 6
- Genetic Syndromes and Imprinting 4
- Genomic variations and chromosomal abnormalities 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Ikuko Teshima (3 shared papers)Diane W. Cox (1 shared paper)R. G. Worton (2 shared papers)J. M. Berg (2 shared papers)Ch. Verellen-Dumoulin (1 shared paper)C Laterre (1 shared paper)Mathias Freund (1 shared paper)J Frédéric (1 shared paper)
- Journals
- Prenatal Diagnosis (2 papers)Human Genetics (2 papers)Journal of Cellular Biochemistry (1 paper)Nature (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- CanadaBelgiumUnited States
In The Last Decade
V. D. Marković
9 papers receiving 409 citations
Peers
Comparison fields: 5 of 62
- Genetics 193
- Pediatrics, Perinatology and Child Health 78
- Molecular Biology 265
- Genetics 36
- Hematology 29
Countries citing papers authored by V. D. Marković
This map shows the geographic impact of V. D. Marković'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 V. D. Marković with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. D. Marković more than expected).
Fields of papers citing papers by V. D. Marković
This network shows the impact of papers produced by V. D. Marković. 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 V. D. Marković. The network helps show where V. D. Marković may publish in the future.
Co-authors
The 25 scholars most cited alongside V. D. Marković, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1982 | 124 | |
| 2 | 1984 | 123 | |
| 3 | 1978 | 73 | |
| 4 | 1992 | 44 | |
| 5 | 1993 | 42 | |
| 6 | 1980 | 24 | |
| 7 | 1992 | 12 | |
| 8 | 1996 | 12 | |
| 9 | 1996 | 1 | |
| 10 | 1992 | 0 |
About V. D. Marković
V. D. Marković is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Oncology, having authored 10 papers that have together received 455 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA Research and Splicing (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Glycosylation and Glycoproteins Research (1 paper), Muscle Physiology and Disorders (1 paper) and DNA and Nucleic Acid Chemistry (1 paper). The work is most often cited by research in Genetics (193 citations), Pediatrics, Perinatology and Child Health (78 citations), Molecular Biology (265 citations), Genetics (36 citations) and Hematology (29 citations). V. D. Marković has collaborated with scholars based in Canada, Belgium and United States. Frequent co-authors include Ikuko Teshima, Diane W. Cox, R. G. Worton, J. M. Berg, Ch. Verellen-Dumoulin, C Laterre, Mathias Freund, J Frédéric, E.J.T. Winsor and Sandra A. Farrell. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Journal of Cellular Biochemistry, Nature and Journal of Medical Genetics.
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.