Eva Sujansky
Impact in
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 3
-
- Prenatal Screening and Diagnostics 7
- Co-authors
- Susan H. Conradi (2 shared papers)Ann C. M. Smith (6 shared papers)Uta Francke (1 shared paper)Vincent Michael Riccardi (1 shared paper)Lorraine Dugoff (1 shared paper)Patricia A. Gabow (2 shared papers)David E. Goldgar (1 shared paper)Judith B. Kenyon (1 shared paper)
- Journals
- Human Genetics (2 papers)Neurology (2 papers)New England Journal of Medicine (2 papers)American Journal of Medical Genetics (11 papers)The American Journal of Human Genetics (1 paper)
- Partner nations
- United StatesSouth AfricaNetherlands
In The Last Decade
Eva Sujansky
32 papers receiving 2.2k citations
Eva Sujansky's Hit Papers
Peers
Comparison fields: 5 of 83
- Genetics 840
- Neurology 351
- Pediatrics, Perinatology and Child Health 354
- Developmental Biology 42
- Molecular Biology 1.1k
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 33 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 | 626 |
| 2 | 1995 | 243 | |
| 3 | 2002 | 193 | |
| 4 | 1988 | 185 | |
| 5 | 1995 | 182 | |
| 6 | 1996 | 133 | |
| 7 | 1986 | 111 | |
| 8 | 2000 | 106 | |
| 9 | 2000 | 77 | |
| 10 | 1990 | 60 | |
| 11 | 1983 | 56 | |
| 12 | 1999 | 51 | |
| 13 | 1992 | 49 | |
| 14 | 2000 | 39 | |
| 15 | 1991 | 35 | |
| 16 | 1993 | 32 | |
| 17 | 1981 | 28 | |
| 18 | 1993 | 27 | |
| 19 | Frontonasal dysplasia with coronal craniosynostosis in three sibs. | 1979 | 24 |
| 20 | Genetic risk for recombinant 8 syndrome and the transmission rate of balanced inversion 8 in the Hispanic population of the southwestern United States. | 1987 | 24 |
About Eva Sujansky
Eva Sujansky is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Neurology, Rheumatology and Surgery, having authored 33 papers that have together received 2.4k 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), Neurofibromatosis and Schwannoma Cases (4 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic Syndromes and Imprinting (3 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Soft tissue tumor case studies (2 papers). The work is most often cited by research in Genetics (840 citations), Neurology (351 citations), Pediatrics, Perinatology and Child Health (354 citations), Developmental Biology (42 citations) and Molecular Biology (1.1k citations). Eva Sujansky has collaborated with scholars based in United States, South Africa and Netherlands. Frequent co-authors include Susan H. Conradi, Ann C. M. Smith, Uta Francke, Vincent Michael Riccardi, Lorraine Dugoff, Patricia A. Gabow, David E. Goldgar, Judith B. Kenyon, William J. Kimberling and Pamela R. Fain. Their work appears in journals such as Human Genetics, Neurology, New England Journal of Medicine, American Journal of Medical Genetics and The American Journal of Human 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.