Loretta Thomaidis

726 total citations
40 papers, 452 citations indexed

About

Loretta Thomaidis is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Loretta Thomaidis has authored 40 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 12 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Loretta Thomaidis's work include Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (10 papers) and Prenatal Screening and Diagnostics (8 papers). Loretta Thomaidis is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (10 papers) and Prenatal Screening and Diagnostics (8 papers). Loretta Thomaidis collaborates with scholars based in Greece, Italy and Germany. Loretta Thomaidis's co-authors include Emmanouil Manolakos, Ioannis Papoulidis, Άρτεμις Τσίτσικα, Annalisa Vetro, Sandro Orrù, Eleni Panagouli, Thomas Liehr, Theodoros Ν. Sergentanis, Θεοδώρα Ψαλτοπούλου and Orsetta Zuffardi and has published in prestigious journals such as Journal of Affective Disorders, Pediatric Research and Journal of Developmental & Behavioral Pediatrics.

In The Last Decade

Loretta Thomaidis

39 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Loretta Thomaidis Greece	14	205	128	105	84	56	40	452
Cláudia Berlim de Mello Brazil	13	121 0.6×	65 0.5×	57 0.5×	109 1.3×	98 1.8×	51	384
Hélène De Leersnyder France	10	227 1.1×	108 0.8×	49 0.5×	202 2.4×	120 2.1×	22	579
Monique Gingold United States	9	271 1.3×	187 1.5×	295 2.8×	109 1.3×	131 2.3×	14	749
Alice Bonuccelli Italy	15	145 0.7×	80 0.6×	111 1.1×	41 0.5×	143 2.6×	49	526
Elizabeth C. R. Mickelson Canada	7	118 0.6×	52 0.4×	86 0.8×	212 2.5×	77 1.4×	8	405
LeeAnne Green Snyder United States	10	262 1.3×	166 1.3×	43 0.4×	138 1.6×	42 0.8×	19	379
Susan Howell United States	14	638 3.1×	350 2.7×	225 2.1×	169 2.0×	29 0.5×	34	1.1k
Aimee Anido United States	7	397 1.9×	271 2.1×	65 0.6×	250 3.0×	43 0.8×	8	566
Kyle J. Steinman United States	9	198 1.0×	130 1.0×	152 1.4×	97 1.2×	54 1.0×	14	423
Katy Berg United Kingdom	10	432 2.1×	205 1.6×	56 0.5×	412 4.9×	110 2.0×	13	717

Countries citing papers authored by Loretta Thomaidis

Since Specialization

Citations

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

Fields of papers citing papers by Loretta Thomaidis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Loretta Thomaidis

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

All Works

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20 of 20 papers shown

Mitropoulos, Konstantinos, Eleni Panagouli, Θεοδώρα Ψαλτοπούλου, et al.. (2022). Gut microbiome and attention deficit/hyperactivity disorder: a systematic review. Pediatric Research. 92(6). 1507–1519. 36 indexed citations

Panagouli, Eleni, et al.. (2022). Postpartum depression and ADHD in the offspring: Systematic review and meta-analysis. Journal of Affective Disorders. 318. 314–330. 16 indexed citations

Dagklis, Themistoklis, Ανδρέας Παμπάνος, Georgios Papaioannou, et al.. (2018). Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization. 2(3). 1–10. 1 indexed citations

Thomaidis, Loretta, et al.. (2017). Long-term follow-up of a child with Klinefelter syndrome and achondroplasia from infancy to 16 years. Journal of Pediatric Endocrinology and Metabolism. 30(7). 797–803. 2 indexed citations

Papadopoulou, Zoe, Ioannis Papoulidis, Stavros Sifakis, et al.. (2017). Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization. Molecular Medicine Reports. 16(6). 8808–8818. 2 indexed citations

Thomaidis, Loretta, et al.. (2017). Attention Deficit/Hyperactivity Disorder (ADHD) symptoms and cognitive skills of preschool children. Psychiatriki. 28(1). 28–36. 15 indexed citations

Papoulidis, Ioannis, Sandro Orrù, Stavros Sifakis, et al.. (2015). Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male. Molecular Cytogenetics. 8(1). 71–71. 4 indexed citations

Papoulidis, Ioannis, et al.. (2015). Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay. Cytogenetic and Genome Research. 145(1). 19–24. 1 indexed citations

Manolakos, Emmanouil, Annalisa Vetro, Antonios Garas, et al.. (2014). Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature. Experimental and Therapeutic Medicine. 7(4). 953–957. 16 indexed citations

10.

Thomaidis, Loretta, et al.. (2014). Predictors of severity and outcome of global developmental delay without definitive etiologic yield: a prospective observational study. BMC Pediatrics. 14(1). 40–40. 18 indexed citations

11.

Manolakos, Emmanouil, Γεώργιος Μαρκόπουλος, Thomas Liehr, et al.. (2014). An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review. Cytogenetic and Genome Research. 142(4). 227–238. 6 indexed citations

12.

Manolakos, Emmanouil, Annalisa Vetro, George Daskalakis, et al.. (2013). Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH. Molecular Cytogenetics. 6(1). 47–47. 12 indexed citations

13.

Manolakos, Emmanouil, Stavros Sifakis, Sotirios Sotiriou, et al.. (2011). Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. Clinical Dysmorphology. 21(2). 101–105. 1 indexed citations

14.

Manolakos, Emmanouil, Annalisa Vetro, Antonios Garas, et al.. (2010). The use of array-CGH in a cohort of Greek children with developmental delay. Molecular Cytogenetics. 3(1). 22–22. 20 indexed citations

15.

Papoulidis, Ioannis, Emmanouil Manolakos, Loretta Thomaidis, et al.. (2010). A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth. Prenatal Diagnosis. 30(6). 586–588. 7 indexed citations

16.

Manolakos, Emmanouil, Sandro Orrù, Ioannis Papoulidis, et al.. (2009). Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome). Molecular Cytogenetics. 2(1). 26–26. 10 indexed citations

17.

Παμπάνος, Ανδρέας, Emmanuel Kanavakis, Sotiris Youroukos, et al.. (2009). A Substitution Involving the NLGN4 Gene Associated with Autistic Behavior in the Greek Population. Genetic Testing and Molecular Biomarkers. 13(5). 611–615. 37 indexed citations

18.

Kanaka‐Gantenbein, Christina, Helen Fryssira, Evrydiki A. Bouzas, et al.. (2006). Two Years of Growth Hormone Treatment in the First Growth Hormone Deficient Patient with Cerebrofaciothoracic Dysplasia. Journal of Pediatric Endocrinology and Metabolism. 19(9). 1179–83. 2 indexed citations

19.

Sofocleous, Christalena, A Kolialexi, Loretta Thomaidis, et al.. (2005). Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population. Pediatric Research. 57(6). 789–795. 33 indexed citations

20.

Thomaidis, Loretta, et al.. (1999). Cohen syndrome: two new cases in siblings. European Journal of Pediatrics. 158(10). 838–841. 6 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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