Eva Sujansky
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Developmental Biology top 5%
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 3
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- Hedgehog Signaling Pathway Studies 3
- Advanced biosensing and bioanalysis techniques 2
- Co-authors
- Ann C. M. Smith (6 shared papers)Vincent M. Riccardi (1 shared paper)Uta Francke (1 shared paper)Lorraine Dugoff (1 shared paper)Patricia A. Gabow (2 shared papers)William J. Kimberling (1 shared paper)David E. Goldgar (1 shared paper)Judith B. Kenyon (1 shared paper)
- Journals
- Neurology (2 papers)Human Genetics (2 papers)New England Journal of Medicine (2 papers)American Journal of Medical Genetics (10 papers)Genetics in Medicine (1 paper)
- Partner nations
- United StatesNetherlandsSouth Africa
In The Last Decade
Eva Sujansky
30 papers receiving 1.9k citations
Eva Sujansky's Hit Papers
Peers
Comparison fields: 5 of 81
- Genetics 781
- Developmental Biology 44
- Pediatrics, Perinatology and Child Health 342
- Neurology 256
- Pathology and Forensic Medicine 269
Countries citing papers authored by Eva Sujansky
This map shows the geographic impact of Eva Sujansky'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 Eva Sujansky with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Sujansky more than expected).
Fields of papers citing papers by Eva Sujansky
This network shows the impact of papers produced by Eva Sujansky. 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 Eva Sujansky. The network helps show where Eva Sujansky may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva Sujansky, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion Hit paper breakdown → | 1978 | 557 |
| 2 | 1995 | 206 | |
| 3 | 2002 | 174 | |
| 4 | 1988 | 162 | |
| 5 | 1995 | 149 | |
| 6 | 1996 | 113 | |
| 7 | 1986 | 97 | |
| 8 | 2000 | 61 | |
| 9 | 1990 | 50 | |
| 10 | 1983 | 45 | |
| 11 | 1992 | 44 | |
| 12 | 1999 | 44 | |
| 13 | 2000 | 36 | |
| 14 | 1991 | 32 | |
| 15 | 1993 | 28 | |
| 16 | 1993 | 25 | |
| 17 | 1981 | 24 | |
| 18 | Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States. | 1987 | 22 |
| 19 | Frontonasal dysplasia with coronal craniosynostosis in three sibs. | 1979 | 20 |
| 20 | The familial occurrence of Poland syndrome. | 1977 | 18 |
About Eva Sujansky
Eva Sujansky is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Neurology, having authored 30 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (5 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic Syndromes and Imprinting (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Soft tissue tumor case studies (2 papers). The work is most often cited by research in Genetics (781 citations), Developmental Biology (44 citations), Pediatrics, Perinatology and Child Health (342 citations), Neurology (256 citations) and Pathology and Forensic Medicine (269 citations). Eva Sujansky has collaborated with scholars based in United States, Netherlands and South Africa. Frequent co-authors include Ann C. M. Smith, Vincent M. Riccardi, Uta Francke, Lorraine Dugoff, Patricia A. Gabow, William J. Kimberling, David E. Goldgar, Judith B. Kenyon, Pamela R. Fain and David A. Wenger. Their work appears in journals such as Neurology, Human Genetics, New England Journal of Medicine, American Journal of Medical Genetics and Genetics in Medicine.
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.