Catherine Sarri

490 total citations
22 papers, 279 citations indexed

About

Catherine Sarri is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Catherine Sarri has authored 22 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Plant Science. Recurrent topics in Catherine Sarri's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Catherine Sarri is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Catherine Sarri collaborates with scholars based in Greece, United States and Denmark. Catherine Sarri's co-authors include Rosemary C. Sarri, Michael B. Petersen, Jolanda Gyftodimou, Yolanda Gyftodimou, Maria Grigoriadou, John Tsiantis, Karen Brøndum‐Nielsen, Carol W. Runyan, Κaterina Papanikolaou and M B Petersen and has published in prestigious journals such as Gene, Journal of Autism and Developmental Disorders and Journal of Medical Genetics.

In The Last Decade

Catherine Sarri

21 papers receiving 256 citations

Peers

Countries citing papers authored by Catherine Sarri

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Sarri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Sarri

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Sarri. A scholar is included among the top collaborators of Catherine Sarri 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 Catherine Sarri. Catherine Sarri 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

#	Work	Indexed citations
1	Effectiveness of a multimodal training programme to improve general practitioners’ burnout, job satisfaction and psychological well-being 2019 ·BMC Family Practice ·(unknown), (unknown), Catherine Sarri, (unknown), Oriol Cunillera, (unknown), (unknown), (unknown), Concepción Barrio, (unknown), (unknown), Rafael Torrúbia	6
2	35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome 2015 ·Cytogenetic and Genome Research ·Catherine Sarri, Sofia Douzgou, (unknown), Katherine K. Anagnostopoulou, Zeynep Tümer, Maria Grigoriadou, Michael B. Petersen, Haris Kokotas, (unknown), (unknown), Έλενα Γιουρούκου, Κaterina Papanikolaou, (unknown), Yolanda Gyftodimou	1
3	Estudio epidemiológico: Pacientes atendidos por psicología clínica en el marco de aplicación del “Programa de soporte de salud mental en atención primaria” (PSP) 2014 ·(unknown), (unknown), (unknown), Catherine Sarri, (unknown), (unknown)	1
4	Pure de novo partial trisomy 6p in a girl with craniosynostosis 2013 ·American Journal of Medical Genetics Part A ·Konstantinos Varvagiannis, (unknown), Yolanda Gyftodimou, Helen Lord, Louise Williams, Catherine Sarri, (unknown), (unknown), (unknown), Tracy Lester, Andrew O.M. Wilkie, Michael B. Petersen	28
5	Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non‐acrocentric satellited chromosomes 2011 ·American Journal of Medical Genetics Part A ·Catherine Sarri, Sofia Douzgou, Yolanda Gyftodimou, Zeynep Tümer, Kirstine Ravn, Angela Pasparaki, Theologia Sarafidou, (unknown), Haris Kokotas, Georgia Karadima, Maria Grigoriadou, (unknown), (unknown), Nicholas Κ. Moschonas, Michael B. Petersen	5
6	Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy 2011 ·Molecular Cytogenetics ·Emmanouil Manolakos, Catherine Sarri, Annalisa Vetro, (unknown), (unknown), (unknown), George Kitsos, (unknown), Haris Kokotas, Anna Papadopoulou, Achilleas Attilakos, Michael B. Petersen, Sofia Kitsiou‐Tzeli	4
7	Congenital hypothyroidism as the initial presentation that led to the diagnosis of Williams syndrome 2011 ·Gene ·Meropi Dimitriadou, Athanasios Christoforidis, Catherine Sarri, Yolanda Gyftodimou, Miranda Athanassiou‐Metaxa	7
8	Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face 2006 ·Cytogenetic and Genome Research ·Catherine Sarri, Yolanda Gyftodimou, Maria Grigoriadou, (unknown), (unknown), Haris Kokotas, Kristin Mrasek, Anja Weise, Michael B. Petersen	7
9	A report of pure 7p duplication syndrome and review of the literature 2006 ·American Journal of Medical Genetics Part A ·Eirini Papadopoulou, S. Sifakis, Catherine Sarri, Jolanda Gyftodimou, Thomas Liehr, Kristin Mrasek, Maria Kalmanti, Michael B. Petersen	19
10	A Case of Partial Trisomy of Chromosome 8p Associated with Autism 2006 ·Journal of Autism and Developmental Disorders ·Κaterina Papanikolaou, (unknown), Jolanda Gyftodimou, (unknown), (unknown), Catherine Sarri, John Tsiantis	22
11	A novel case of craniosynostosis caused by a 6p21 duplication that includes the entire RUNX2 gene 2005 ·Journal of Medical Genetics ·Louise Williams, Tracy Lester, H. Beaumont, Melissa K. Crocker, (unknown), (unknown), Catherine Sarri, (unknown), A Seller, M B Petersen, (unknown)	8
12	Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy 2002 ·American Journal of Medical Genetics Part A ·Mazin Β. Qumsiyeh, Syed K. Rafi, Catherine Sarri, Maria Grigoriadou, Jolanda Gyftodimou, (unknown), (unknown), Michael B. Petersen	17
13	Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene(s) on chromosome 18 1999 ·Journal of Medical Genetics ·Catherine Dacou‐Voutetakis, Amalia Sertedaki, (unknown), Catherine Sarri, Georgia Karadima, M B Petersen, Athina Xaidara, Maria Kanariou, Polyxeni Nicolaidou	19
14	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 1997 ·American Journal of Medical Genetics ·Catherine Sarri, Jolanda Gyftodimou, Dimitris Avramopoulos, Maria Grigoriadou, (unknown), (unknown), Constantinos Pángalos, (unknown), George Kitsos, Dimitrios Vassilopoulos, Karen Brøndum‐Nielsen, Michael B. Petersen	17
15	Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation 1996 ·European Journal of Human Genetics ·Merete Bugge, Elisabeth Blennow, (unknown), Michael B. Petersen, Florence Pédeutour, Aspasia Tsezou, (unknown), (unknown), Troels Lyngbye, Catherine Sarri, Dimitrios Avramopoulos, Sofìa Kitsiou, (unknown), (unknown), Niels Tommerup, Karen Brøndum‐Nielsen	33
16	Hyperbrachycephaly, short face, midface hypoplasia, fusion of cervical vertebrae, radiolucent bone defects, and severe destruction of periodontium--a new syndrome: craniofaciocervical osteoglyphic dysplasia. 1994 ·PubMed ·(unknown), Ioannis Vrotsos, Stephanos Kyrkanides, (unknown), Konstantinos I. Tosios, (unknown), (unknown), (unknown), Catherine Sarri, Maria Grigoriadou	1
17	Organizational and Community Change Through Participatory Action Research 1993 ·Administration in Social Work ·Rosemary C. Sarri, Catherine Sarri	45
18	Sister-chromatid exchange in highly purified human CD4+ and CD8+ lymphocytes 1992 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Catherine Sarri, Constantin N. Baxevanis, (unknown), George J. Reclos, (unknown), (unknown), (unknown), Maria Grigoriadou, Michael Papamichail	6
19	Injuries among Medical Laboratory Housekeeping Staff: Incidence and Worker Perceptions 1991 ·Journal of Occupational and Environmental Medicine ·Catherine Sarri, Eugenia Eng, Carol W. Runyan	10
20	Increased rate of sister chromatid exchanges in ?-thalassaemia 1982 ·Annals of Hematology ·(unknown), Catherine Sarri, (unknown), (unknown), (unknown), S Pantelakis	4

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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