Maria Syrrou

3.4k citations
70 papers · 2.1k indexed · 1 hit paper · h-index 20
Topics
Genomic variations and chromosomal abnormalities (20 papers)Genetics and Neurodevelopmental Disorders (14 papers)Chromosomal and Genetic Variations (11 papers)
Journals
Nature GeneticsSHILAP Revista de lepidopterologíaAnnals of the New York Academy of Sciences
Partner nations
GreeceCyprusGermany

In The Last Decade

Maria Syrrou

68 papers receiving 2.0k citations

Hit Papers

Hypomagnesemia with secondary hypocalcemia is caused by m...20022026201020182002100200300400500

Peers

Maria Syrrou
Comparison fields: 5 of 122
  • Molecular Biology 768
  • Genetics 597
  • Nutrition and Dietetics 563
  • Plant Science 380
  • Reproductive Medicine 331
Replace Zachary Madaj with:
Zachary Madaj United States
Yoshikatsu Uematsu Japan
Kersten M. Small United States
Duarte Pignatelli Portugal
Gwendolyn W. Louis United States
Yuan‐Shan Zhu United States
Vı́ctor M. Arce Spain
Reiko Hanada Japan
Iain C.A.F. Robinson United Kingdom
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Citations per field
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Citations per year

Countries citing papers authored by Maria Syrrou

Since Specialization
Citations

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

Fields of papers citing papers by Maria Syrrou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Syrrou

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 6
2 1
3 9
4 5
5 2
6
Cytogenetic behavior of cryoprotectant DMSO
1
7 14
8 49
9 6
10 11
11 124
12 80
13 7
14 32
15
The value of opthalmic examinations in familial adenomatous polyposis syndrome screening
1
16 6
17 14
18 11
19 21
20
Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression.
7

About Maria Syrrou

Maria Syrrou is a scholar working on Behavioral Neuroscience, Biological Psychiatry and Genetics, having authored 70 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Chromosomal and Genetic Variations (11 papers). The work is most often cited by research in Reproductive Medicine (331 citations), Nutrition and Dietetics (563 citations) and Sensory Systems (142 citations). Maria Syrrou has collaborated with scholars based in Greece, Cyprus and Germany. Frequent co-authors include Ioannis Georgiou, Karl P. Schlingmann, Martin Sassen, Martin Konrad, Stefanie Weber, Siegfried Waldegger, Aggeliki Dasoula, Hannsjörg W. Seyberth, Ellinor Ristoff and Helga Vitzthum. Their work appears in journals such as Nature Genetics, SHILAP Revista de lepidopterología and Annals of the New York Academy of Sciences.

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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