Dimitri Avramopoulos

2.0k total citations
12 papers, 487 citations indexed

About

Dimitri Avramopoulos is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Dimitri Avramopoulos has authored 12 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Dimitri Avramopoulos's work include Genomic variations and chromosomal abnormalities (5 papers), Genetic Associations and Epidemiology (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Dimitri Avramopoulos is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetic Associations and Epidemiology (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Dimitri Avramopoulos collaborates with scholars based in United States, Canada and Sweden. Dimitri Avramopoulos's co-authors include Lauren L. Jantzie, Andrew S. McCallion, David Valle, Jef D. Boeke, Daniel Ardeljan, Lindsay M. Payer, Jared P. Steranka, Chunhong Liu, Kathleen H. Burns and Wan Rou Yang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

Dimitri Avramopoulos

12 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dimitri Avramopoulos United States	11	225	198	76	60	55	12	487
Nancy Monroy‐Jaramillo Mexico	15	225 1.0×	78 0.4×	101 1.3×	26 0.4×	109 2.0×	43	577
Carmen Martínez Spain	17	268 1.2×	82 0.4×	55 0.7×	33 0.6×	136 2.5×	34	879
Krishnadas Nandagopal India	9	137 0.6×	44 0.2×	109 1.4×	30 0.5×	45 0.8×	28	425
Kara R. Vogel United States	14	315 1.4×	91 0.5×	27 0.4×	38 0.6×	147 2.7×	27	579
Shabeesh Balan Japan	16	290 1.3×	131 0.7×	104 1.4×	7 0.1×	56 1.0×	35	577
Patrícia Natália Silva Brazil	14	315 1.4×	123 0.6×	80 1.1×	7 0.1×	124 2.3×	17	502
Susanna M. I. Goorden Netherlands	9	273 1.2×	152 0.8×	26 0.3×	14 0.2×	150 2.7×	11	516
T PATEL United States	10	216 1.0×	66 0.3×	22 0.3×	38 0.6×	44 0.8×	11	526
Céline Bellenguez France	11	200 0.9×	199 1.0×	28 0.4×	9 0.1×	139 2.5×	17	450
Carla Montecinos-Oliva Chile	9	241 1.1×	105 0.5×	14 0.2×	20 0.3×	161 2.9×	11	451

Countries citing papers authored by Dimitri Avramopoulos

Since Specialization

Citations

This map shows the geographic impact of Dimitri 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 Dimitri Avramopoulos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dimitri Avramopoulos more than expected).

Fields of papers citing papers by Dimitri Avramopoulos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dimitri 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 Dimitri Avramopoulos. The network helps show where Dimitri Avramopoulos may publish in the future.

Co-authorship network of co-authors of Dimitri Avramopoulos

This figure shows the co-authorship network connecting the top 25 collaborators of Dimitri Avramopoulos. A scholar is included among the top collaborators of Dimitri 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 Dimitri Avramopoulos. Dimitri Avramopoulos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Avramopoulos, Dimitri, et al.. (2022). Neuroinflammation represents a common theme amongst genetic and environmental risk factors for Alzheimer and Parkinson diseases. Journal of Neuroinflammation. 19(1). 223–223. 78 indexed citations

Ehrhardt, Stephan, Anton P. Porsteinsson, Cynthia A. Munro, et al.. (2019). Escitalopram for agitation in Alzheimer's disease (S‐CitAD): Methods and design of an investigator‐initiated, randomized, controlled, multicenter clinical trial. Alzheimer s & Dementia. 15(11). 1427–1436. 34 indexed citations

Payer, Lindsay M., Jared P. Steranka, Wan Rou Yang, et al.. (2017). Structural variants caused byAluinsertions are associated with risks for many human diseases. Proceedings of the National Academy of Sciences. 114(20). E3984–E3992. 86 indexed citations

Song, Guang, et al.. (2016). The DPYSL2 gene connects mTOR and schizophrenia. Translational Psychiatry. 6(11). e933–e933. 30 indexed citations

Jurgens, Julie A., Hua Ling, Kurt N. Hetrick, et al.. (2015). Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics. Genetics in Medicine. 17(10). 782–788. 35 indexed citations

Pirooznia, Mehdi, et al.. (2015). High-throughput sequencing of the synaptome in major depressive disorder. Molecular Psychiatry. 21(5). 650–655. 17 indexed citations

Peters, Matthew E., Lea T. Drye, Davangere P. Devanand, et al.. (2015). Citalopram for the Treatment of Agitation in Alzheimer Dementia. Journal of Geriatric Psychiatry and Neurology. 29(2). 59–64. 9 indexed citations

Avramopoulos, Dimitri, et al.. (2012). SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes. Journal of Neurology. 259(7). 1440–1447. 16 indexed citations

Cubells, Joseph F., Xiangqing Sun, Wenbiao Li, et al.. (2011). Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia. Human Genetics. 130(5). 635–643. 44 indexed citations

10.

Li, Qing, M. Daniele Fallin, Thomas A. Louis, et al.. (2010). Detection of SNP‐SNP interactions in trios of parents with schizophrenic children. Genetic Epidemiology. 34(5). 396–406. 19 indexed citations

11.

Balciuniene, Jorune, Ningping Feng, Betsy Hirsch, et al.. (2007). Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities. The American Journal of Human Genetics. 80(5). 938–947. 85 indexed citations

12.

Avramopoulos, Dimitri, Virginia L. Willour, Peter Zandi, et al.. (2004). Linkage of bipolar affective disorder on chromosome 8q24: follow-up and parametric analysis. Molecular Psychiatry. 9(2). 191–196. 34 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.

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