E. Vámos
Impact in
- Developmental Biology top 10%
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Prenatal Screening and Diagnostics 8
- Assisted Reproductive Technology and Twin Pregnancy 2
- Genetics 8
- Genomic variations and chromosomal abnormalities 4
- Neurogenetic and Muscular Disorders Research 3
- Connective tissue disorders research 2
- Congenital Ear and Nasal Anomalies 2
- Co-authors
- Winnie Courtens (5 shared papers)Nicole Van Regemorter (8 shared papers)J Flament-Durand (4 shared papers)F Rodesch (5 shared papers)Marc Abramowicz (3 shared papers)Willy Lissens (3 shared papers)Albert Schinzel (1 shared paper)Jasmine Parma (2 shared papers)
In The Last Decade
E. Vámos
23 papers receiving 416 citations
Peers
Comparison fields: 5 of 59
- Developmental Biology 22
- Genetics 206
- Pediatrics, Perinatology and Child Health 112
- Genetics 59
- Neurology 71
Countries citing papers authored by E. Vámos
This map shows the geographic impact of E. Vámos'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 E. Vámos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Vámos more than expected).
Fields of papers citing papers by E. Vámos
This network shows the impact of papers produced by E. Vámos. 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 E. Vámos. The network helps show where E. Vámos may publish in the future.
Co-authors
The 25 scholars most cited alongside E. Vámos, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 69 | |
| 2 | 2010 | 67 | |
| 3 | 1994 | 48 | |
| 4 | 1984 | 44 | |
| 5 | 1991 | 30 | |
| 6 | 1997 | 30 | |
| 7 | Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor. | 1992 | 29 |
| 8 | 1998 | 25 | |
| 9 | Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer. | 1995 | 20 |
| 10 | 1983 | 17 | |
| 11 | Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14. | 1988 | 12 |
| 12 | 1994 | 11 | |
| 13 | 1985 | 9 | |
| 14 | 2004 | 9 | |
| 15 | 1991 | 9 | |
| 16 | Unusual early manifestation of multiple sulfatase deficiency. | 1981 | 8 |
| 17 | 1986 | 5 | |
| 18 | 1983 | 5 | |
| 19 | 1966 | 4 | |
| 20 | CHARGE association in a neonate exposed in utero to carbon monoxide. | 1996 | 3 |
About E. Vámos
E. Vámos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Molecular Biology and Genetics, having authored 25 papers that have together received 458 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital Anomalies and Fetal Surgery (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Cancer Genomics and Diagnostics (2 papers), Connective tissue disorders research (2 papers), Congenital Ear and Nasal Anomalies (2 papers) and Assisted Reproductive Technology and Twin Pregnancy (2 papers). The work is most often cited by research in Developmental Biology (22 citations), Genetics (206 citations), Pediatrics, Perinatology and Child Health (112 citations), Genetics (59 citations) and Neurology (71 citations). E. Vámos has collaborated with scholars based in Belgium, France and Hong Kong. Frequent co-authors include Winnie Courtens, Nicole Van Regemorter, J Flament-Durand, F Rodesch, Marc Abramowicz, Willy Lissens, Albert Schinzel, Jasmine Parma, Catherine Christophe and Harry Dorchy. Their work appears in journals such as Journal of Inherited Metabolic Disease, Archives of Virology, Neuroscience, Pediatric Research and Journal of Clinical Investigation.
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.