Mihailo Vujic
Impact in
- Ophthalmology top 2%
- Retinal Diseases and Treatments
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- Genetic Syndromes and Imprinting 2
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- Congenital heart defects research 2
- Ion channel regulation and function 1
- Co-authors
- Guochun Xie (1 shared paper)Wen Li (1 shared paper)Kristina Forsman (1 shared paper)Arthur A. Bergen (1 shared paper)Christopher P. Austin (1 shared paper)Claes Wadelius (1 shared paper)Michael L. Metzker (1 shared paper)Konstantin Petrukhin (1 shared paper)
- Journals
- European Child & Adolescent Psychiatry (2 papers)Nature Genetics (1 paper)Journal of the American Society of Nephrology (1 paper)Acta Obstetricia Et Gynecologica Scandinavica (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- SwedenUnited KingdomNetherlands
In The Last Decade
Mihailo Vujic
14 papers receiving 1.0k citations
Mihailo Vujic's Hit Papers
Peers
Comparison fields: 5 of 65
- Ophthalmology 304
- Genetics 466
- Molecular Biology 797
- Cellular and Molecular Neuroscience 159
- Cell Biology 89
Countries citing papers authored by Mihailo Vujic
This map shows the geographic impact of Mihailo Vujic'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 Mihailo Vujic with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mihailo Vujic more than expected).
Fields of papers citing papers by Mihailo Vujic
This network shows the impact of papers produced by Mihailo Vujic. 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 Mihailo Vujic. The network helps show where Mihailo Vujic may publish in the future.
Co-authors
The 25 scholars most cited alongside Mihailo Vujic, 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 | Identification of the gene responsible for Best macular dystrophy Hit paper breakdown → | 1998 | 541 |
| 2 | 2010 | 110 | |
| 3 | 2001 | 107 | |
| 4 | 1994 | 91 | |
| 5 | 2003 | 55 | |
| 6 | 2012 | 46 | |
| 7 | 1996 | 35 | |
| 8 | Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus. | 1995 | 18 |
| 9 | 2008 | 17 | |
| 10 | 1999 | 14 | |
| 11 | 2013 | 12 | |
| 12 | 2002 | 9 | |
| 13 | 2004 | 5 | |
| 14 | 1993 | 4 |
About Mihailo Vujic
Mihailo Vujic is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Surgery, having authored 14 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (3 papers), Chromosomal and Genetic Variations (3 papers), Congenital heart defects research (2 papers), Genetic Syndromes and Imprinting (2 papers), Pancreatic function and diabetes (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Ophthalmology (304 citations), Genetics (466 citations), Molecular Biology (797 citations), Cellular and Molecular Neuroscience (159 citations) and Cell Biology (89 citations). Mihailo Vujic has collaborated with scholars based in Sweden, United Kingdom and Netherlands. Frequent co-authors include Guochun Xie, Wen Li, Kristina Forsman, Arthur A. Bergen, Christopher P. Austin, Claes Wadelius, Michael L. Metzker, Konstantin Petrukhin, Sten Andréasson and Ola Sandgren. Their work appears in journals such as European Child & Adolescent Psychiatry, Nature Genetics, Journal of the American Society of Nephrology, Acta Obstetricia Et Gynecologica Scandinavica 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.