Loretta Thomaidis

726 citations

40 papers · 452 indexed · h-index 14

Genetics top 10%
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 6
- Congenital Ear and Nasal Anomalies 4
Developmental Neuroscience
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics 8
Biological Psychiatry
Cognitive Neuroscience
- Autism Spectrum Disorder Research 4
Plant Science
- Chromosomal and Genetic Variations 10
Molecular Biology
- Congenital heart defects research 5
Psychiatry and Mental health
- Attention Deficit Hyperactivity Disorder 4

Co-authors: Emmanouil Manolakos Ioannis Papoulidis Άρτεμις Τσίτσικα Annalisa Vetro Sandro Orrù Eleni Panagouli Thomas Liehr Theodoros Ν. Sergentanis
Cited by: Genetics Developmental Neuroscience Pediatrics, Perinatology and Child Health
Partner nations: Greece Italy Germany

In The Last Decade

Loretta Thomaidis

39 papers receiving 416 citations

Peers

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

The 25 scholars most cited alongside Loretta Thomaidis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Loretta Thomaidis Line = papers co-authored together Loretta Thomaidis links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Gut microbiome and attention deficit/hyperactivity disorder: a systematic review D. Gkougka,Konstantinos Mitropoulos,Georgia Tzanakaki,Eleni Panagouli,Θεοδώρα Ψαλτοπούλου,Loretta Thomaidis,Μαρία Τσολιά,Theodoros Ν. Sergentanis,Άρτεμις Τσίτσικα	2022	36
2	Postpartum depression and ADHD in the offspring: Systematic review and meta-analysis Vasileia Christaki,Ioanna Ismirnioglou,Asimina Katrali,Eleni Panagouli,Efthalia Tzila,Loretta Thomaidis,Θεοδώρα Ψαλτοπούλου,Theodoros Ν. Sergentanis,Άρτεμις Τσίτσικα	2022	16
3	Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization Maria Kontodiou,Vassilis Paspaliaris,Themistoklis Dagklis,Elisavet Siomou,Ahmed H. Al-Rikabi,Kalliopi Tsita,Theano Stavroulaki,Ανδρέας Παμπάνος,Apostolos Zavlanos,Georgios Papaioannou,Ioannis Papoulidis,Loretta Thomaidis,Emmanouil Manolakos	2018	1
4	Long-term follow-up of a child with Klinefelter syndrome and achondroplasia from infancy to 16 years Jessica D. Arditi,Loretta Thomaidis,Helen Frysira,Artemis Doulgeraki,George P. Chrousos,Christina Kanaka‐Gantenbein	2017	2
5	Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization Zoe Papadopoulou,Ioannis Papoulidis,Stavros Sifakis,Γεώργιος Μαρκόπουλος,Annalisa Vetro,Angeliki‐Maria Vlaikou,M Ziegler,Thomas Liehr,Loretta Thomaidis,Orsetta Zuffardi,Maria Syrrou,George Kitsos,Emmanouil Manolakos	2017	2
6	Attention Deficit/Hyperactivity Disorder (ADHD) symptoms and cognitive skills of preschool children Loretta Thomaidis,Antigoni Choleva,Mari Janikian,Georgia Bertou,Άρτεμις Τσίτσικα,George Giannakopoulos,Dimitrios Anagnostopoulos	2017	15
7	Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male Ioannis Papoulidis,Vassilis Paspaliaris,Elisavet Siomou,Sandro Orrù,R. Murru,Stavros Sifakis,Petros Nikolaidis,Antonios Garas,Sotirios Sotiriou,Loretta Thomaidis,Emmanouil Manolakos	2015	4
8	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 Ioannis Papoulidis,Vassilis Paspaliaris,Elena Papageorgiou,Elissavet Siomou,Themistoklis Dagklis,Sotirios Sotiriou,Loretta Thomaidis,Emmanouil Manolakos	2015	1
9	Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature Emmanouil Manolakos,Annalisa Vetro,Antonios Garas,Loretta Thomaidis,Konstantinos Kefalas,George Kitsos,Monika Ziegler,Thomas Liehr,Orsetta Zuffardi,Ioannis Papoulidis	2014	16
10	Predictors of severity and outcome of global developmental delay without definitive etiologic yield: a prospective observational study Loretta Thomaidis,Georgios Zacharias Zantopoulos,Sotirios Fouzas,Lito Mantagou,Chryssa Bakoula,Andreas Konstantopoulos	2014	18
11	An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review Angeliki-Maria Vlaikou,Emmanouil Manolakos,Dimitrios Noutsopoulos,Γεώργιος Μαρκόπουλος,Thomas Liehr,Annalisa Vetro,Monika Ziegler,Anja Weise,Katharina Kreskowski,Ioannis Papoulidis,Loretta Thomaidis,Maria Syrrou	2014	6
12	Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH Emmanouil Manolakos,Konstantinos Kefalas,Annalisa Vetro,Eirini Oikonomidou,George Daskalakis,Natasa Psara,E. Siomou,Elena Papageorgiou,Eirini Sevastopoulou,Anastasia Konstantinidou,Nikolaos Vrachnis,Loretta Thomaidis,Orsetta Zuffardi,Ioannis Papoulidis	2013	12
13	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 Emmanouil Manolakos,Stavros Sifakis,Sotirios Sotiriou,Panagiotis Peitsidis,Makarios Eleftheriades,Vassilis Mersinias,Thomas Liehr,Loretta Thomaidis,George Kitsos,Ioannis Papoulidis,Michael B. Petersen,Sandro Orrù	2011	1
14	The use of array-CGH in a cohort of Greek children with developmental delay Emmanouil Manolakos,Annalisa Vetro,Konstantinos Kefalas,Stamatia-Maria Rapti,Eirini Louizou,Antonios Garas,George Kitsos,Lefteris Vasileiadis,Panagiota Tsoplou,Makarios Eleftheriades,Panagiotis Peitsidis,Sandro Orrù,Thomas Liehr,Michael B. Petersen,Loretta Thomaidis	2010	20
15	A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth Ioannis Papoulidis,Emmanouil Manolakos,Elisavet Siomou,Kostantinos Kefalas,Loretta Thomaidis,Thomas Liehr,Annalisa Vetro,Apostolos Athanasiadis,Orsetta Zuffardi,Michael B. Petersen	2010	7
16	Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome) Emmanouil Manolakos,Sandro Orrù,Rosita Neroutsou,Konstantinos Kefalas,Eirini Louizou,Ioannis Papoulidis,Loretta Thomaidis,Panagiotis Peitsidis,Sotirios Sotiriou,George Kitsos,Panagiota Tsoplou,Michael B. Petersen,Aikaterini Metaxotou	2009	10
17	A Substitution Involving the NLGN4 Gene Associated with Autistic Behavior in the Greek Population Ανδρέας Παμπάνος,Konstantina Volaki,Emmanuel Kanavakis,Ourania Papandreou,Sotiris Youroukos,Loretta Thomaidis,Savvas Karkelis,Maria Tzetis,Sophia Kitsiou‐Tzeli	2009	37
18	Two Years of Growth Hormone Treatment in the First Growth Hormone Deficient Patient with Cerebrofaciothoracic Dysplasia Christina Kanaka‐Gantenbein,Helen Fryssira,Konstantinos Kakavakis,Evrydiki A. Bouzas,Loretta Thomaidis,George P. Chrousos,George Mastorakos	2006	2
19	Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population Stella Amenta,Christalena Sofocleous,A Kolialexi,Loretta Thomaidis,Sotiris Giouroukos,Emmanuel Karavitakis,Ariadni Mavrou,Sophia Kitsiou,Emmanuel Kanavakis,Helen Fryssira	2005	33
20	Cohen syndrome: two new cases in siblings Loretta Thomaidis,Helen Fryssira,Eustathia Katsarou,Catherine Metaxotou	1999	6

About Loretta Thomaidis

Loretta Thomaidis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 40 papers that have together received 452 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (10 papers), Prenatal Screening and Diagnostics (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (5 papers), Attention Deficit Hyperactivity Disorder (4 papers), Autism Spectrum Disorder Research (4 papers) and Congenital Ear and Nasal Anomalies (4 papers). The work is most often cited by research in Genetics (205 citations), Developmental Neuroscience (23 citations) and Pediatrics, Perinatology and Child Health (105 citations). Loretta Thomaidis has collaborated with scholars based in Greece, Italy and Germany. Frequent 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.

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