Dimitris Avramopoulos
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
-
- Prenatal Screening and Diagnostics 7
- Genetics 6
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 3
- Co-authors
- Michael B. Petersen (7 shared papers)Margareta Mikkelsen (4 shared papers)Stylianos E. Antonarakis (3 shared papers)J L Blouin (2 shared papers)Sallie B. Freeman (1 shared paper)Neil E. Lamb (1 shared paper)Terry Hassold (1 shared paper)Stephanie L. Sherman (1 shared paper)
- Journals
- Psychiatric Genetics (1 paper)The Lancet (1 paper)Nature Genetics (1 paper)Clinical Genetics (1 paper)Human Genetics (1 paper)
- Partner nations
- GreeceDenmarkUnited States
In The Last Decade
Dimitris Avramopoulos
11 papers receiving 653 citations
Peers
Comparison fields: 5 of 69
- Pediatrics, Perinatology and Child Health 300
- Genetics 347
- Molecular Biology 257
- Public Health, Environmental and Occupational Health 95
- Plant Science 107
Countries citing papers authored by Dimitris Avramopoulos
This map shows the geographic impact of Dimitris Avramopoulos'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 Dimitris Avramopoulos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dimitris Avramopoulos more than expected).
Fields of papers citing papers by Dimitris Avramopoulos
This network shows the impact of papers produced by Dimitris Avramopoulos. 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 Dimitris Avramopoulos. The network helps show where Dimitris Avramopoulos may publish in the future.
Co-authors
The 25 scholars most cited alongside Dimitris Avramopoulos, 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 | 1996 | 309 | |
| 2 | Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14. | 1993 | 86 |
| 3 | Normal phenotype with paternal uniparental isodisomy for chromosome 21. | 1993 | 59 |
| 4 | 1996 | 53 | |
| 5 | 1999 | 49 | |
| 6 | 1997 | 40 | |
| 7 | 2000 | 25 | |
| 8 | 1997 | 19 | |
| 9 | 1997 | 17 | |
| 10 | 1997 | 13 | |
| 11 | 2000 | 13 |
About Dimitris Avramopoulos
Dimitris Avramopoulos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Plant Science, Molecular Biology and Surgery, having authored 11 papers that have together received 683 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (4 papers), Genetic Syndromes and Imprinting (3 papers), Lipoproteins and Cardiovascular Health (1 paper), Natural Antidiabetic Agents Studies (1 paper), DNA Repair Mechanisms (1 paper) and Alzheimer's disease research and treatments (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (300 citations), Genetics (347 citations), Molecular Biology (257 citations), Public Health, Environmental and Occupational Health (95 citations) and Plant Science (107 citations). Dimitris Avramopoulos has collaborated with scholars based in Greece, Denmark and United States. Frequent co-authors include Michael B. Petersen, Margareta Mikkelsen, Stylianos E. Antonarakis, J L Blouin, Sallie B. Freeman, Neil E. Lamb, Terry Hassold, Stephanie L. Sherman, Dorothy Pettay and Lisa F. Taft. Their work appears in journals such as Psychiatric Genetics, The Lancet, Nature Genetics, Clinical Genetics and 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.