Dimitris Avramopoulos

1.1k total citations
12 papers, 700 citations indexed

About

Dimitris Avramopoulos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Dimitris Avramopoulos has authored 12 papers receiving a total of 700 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Dimitris Avramopoulos's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic Syndromes and Imprinting (4 papers). Dimitris Avramopoulos is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic Syndromes and Imprinting (4 papers). Dimitris Avramopoulos collaborates with scholars based in Greece, Denmark and United States. Dimitris Avramopoulos's co-authors include Stylianos E. Antonarakis, Margareta Mikkelsen, Michael B. Petersen, J L Blouin, Dimitrios Vassilopoulos, Constantinos Pángalos, Dorothy Pettay, Sallie B. Freeman, Neil E. Lamb and Terry Hassold and has published in prestigious journals such as The Lancet, Nature Genetics and Journal of Medical Genetics.

In The Last Decade

Dimitris Avramopoulos

12 papers receiving 676 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Dimitris Avramopoulos Greece 12 399 345 283 113 109 12 700
O Raoul France 15 715 1.8× 286 0.8× 474 1.7× 163 1.4× 118 1.1× 30 1.1k
Nicholas R. Dennis United Kingdom 16 640 1.6× 353 1.0× 368 1.3× 167 1.5× 144 1.3× 23 1.0k
Cecilia Anichini Italy 14 398 1.0× 160 0.5× 324 1.1× 66 0.6× 43 0.4× 32 585
Nicole Créau France 16 335 0.8× 66 0.2× 397 1.4× 55 0.5× 370 3.4× 25 801
F Ballesta Spain 14 249 0.6× 83 0.2× 246 0.9× 78 0.7× 21 0.2× 28 547
Milen Velinov United States 19 476 1.2× 103 0.3× 413 1.5× 51 0.5× 86 0.8× 57 1.0k
Cíntia Barros Santos-Rebouças Brazil 17 311 0.8× 82 0.2× 378 1.3× 45 0.4× 35 0.3× 64 767
Elisabeth Gabau Spain 16 463 1.2× 128 0.4× 336 1.2× 42 0.4× 45 0.4× 36 675
A. C. Warren United States 9 222 0.6× 61 0.2× 286 1.0× 77 0.7× 201 1.8× 15 611

Countries citing papers authored by Dimitris Avramopoulos

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Dimitris Avramopoulos

This figure shows the co-authorship network connecting the top 25 collaborators of Dimitris Avramopoulos. A scholar is included among the top collaborators of Dimitris Avramopoulos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dimitris Avramopoulos. Dimitris Avramopoulos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Barbi, Gotthold, et al.. (2000). Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype. American Journal of Medical Genetics. 91(2). 116–122. 12 indexed citations
2.
Karadima, Georgia, et al.. (2000). Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome. American Journal of Medical Genetics. 93(5). 366–372. 21 indexed citations
3.
Dikeos, Dimitris, G.N. Papadimitriou, Dimitris Avramopoulos, et al.. (1999). Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder. Psychiatric Genetics. 9(4). 189–196. 45 indexed citations
4.
Economou-Petersen, E, et al.. (1997). Apolipoprotein E polymorphism in the Greek population. Clinical Genetics. 52(4). 216–218. 38 indexed citations
5.
Bartsch, Oliver, Georg Klaus Hinkel, Merete Bugge, et al.. (1997). A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region. Human Genetics. 100(5-6). 669–675. 19 indexed citations
6.
Sarri, Catherine, Jolanda Gyftodimou, Dimitris Avramopoulos, et al.. (1997). Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter. American Journal of Medical Genetics. 70(1). 87–94. 17 indexed citations
7.
Avramopoulos, Dimitris, et al.. (1997). A case of apparent trisomy 21 without the Down's syndrome phenotype.. Journal of Medical Genetics. 34(7). 597–600. 12 indexed citations
8.
Avramopoulos, Dimitris, et al.. (1996). Apolipoprotein E allele distribution in parents of Down's syndrome children. The Lancet. 347(9005). 862–865. 47 indexed citations
9.
Lamb, Neil E., Sallie B. Freeman, Dorothy Pettay, et al.. (1996). Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II. Nature Genetics. 14(4). 400–405. 290 indexed citations
10.
Pángalos, Constantinos, Dimitris Avramopoulos, Jean‐Louis Blouin, et al.. (1994). Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. PubMed. 54(3). 473–81. 58 indexed citations
11.
Antonarakis, Stylianos E., J L Blouin, Jacqueline Y. Maher, et al.. (1993). Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.. PubMed. 52(6). 1145–52. 85 indexed citations
12.
Blouin, J L, Dimitris Avramopoulos, Constantinos Pángalos, & Stylianos E. Antonarakis. (1993). Normal phenotype with paternal uniparental isodisomy for chromosome 21.. PubMed. 53(5). 1074–8. 56 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by O Raoul Breakdown of academic impact, for papers by Nicholas R. Dennis Breakdown of academic impact, for papers by Cecilia Anichini Breakdown of academic impact, for papers by Nicole Créau Breakdown of academic impact, for papers by F Ballesta Breakdown of academic impact, for papers by Milen Velinov Breakdown of academic impact, for papers by Cíntia Barros Santos-Rebouças Breakdown of academic impact, for papers by Elisabeth Gabau Breakdown of academic impact, for papers by A. C. Warren
Rankless by CCL
2026