Maria Syrrou

3.4k total citations · 1 hit paper
70 papers, 2.1k citations indexed

About

Maria Syrrou is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maria Syrrou has authored 70 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 25 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maria Syrrou's work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Chromosomal and Genetic Variations (11 papers). Maria Syrrou is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Chromosomal and Genetic Variations (11 papers). Maria Syrrou collaborates with scholars based in Greece, Cyprus and Germany. Maria Syrrou's co-authors include Ioannis Georgiou, Martin Konrad, Martin Sassen, Siegfried Waldegger, Stefanie Weber, Karl P. Schlingmann, Aggeliki Dasoula, Dganit Dinour, Melanie Peters and Ellinor Ristoff and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Annals of the New York Academy of Sciences.

In The Last Decade

Maria Syrrou

68 papers receiving 2.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

2002 578 citations Karl P. Schlingmann, Stefanie Weber et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Syrrou Greece	20	768	597	563	380	331	70	2.1k
Maija Wessman Finland	32	742 1.0×	539 0.9×	187 0.3×	221 0.6×	22 0.1×	83	2.8k
Kersten M. Small United States	27	1.9k 2.5×	586 1.0×	56 0.1×	77 0.2×	102 0.3×	39	3.2k
Luis A. Pérez‐Jurado Spain	36	1.6k 2.1×	1.5k 2.4×	105 0.2×	182 0.5×	25 0.1×	105	3.5k
Cynthia Klein United States	16	1.4k 1.8×	337 0.6×	458 0.8×	30 0.1×	597 1.8×	19	3.0k
James S. Acierno United States	20	1.8k 2.4×	1.1k 1.9×	83 0.1×	86 0.2×	2.6k 8.0×	32	3.9k
Yuan‐Shan Zhu United States	35	1.8k 2.3×	638 1.1×	57 0.1×	34 0.1×	318 1.0×	98	3.2k
A. Kemal Topaloğlu Türkiye	22	1.1k 1.4×	851 1.4×	52 0.1×	42 0.1×	1.5k 4.6×	80	2.4k
Danielle Carmignac United Kingdom	27	743 1.0×	536 0.9×	105 0.2×	39 0.1×	187 0.6×	46	2.5k
Zachary Madaj United States	25	956 1.2×	115 0.2×	134 0.2×	47 0.1×	67 0.2×	54	2.4k
Yoshikatsu Uematsu Japan	9	622 0.8×	434 0.7×	112 0.2×	15 0.0×	379 1.1×	10	1.7k

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

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20 of 20 papers shown

Syrrou, Maria, et al.. (2022). Nasal eosinophilia as a preliminary discriminative biomarker of non-allergic rhinitis in every day clinical pediatric practice. European Archives of Oto-Rhino-Laryngology. 280(4). 1775–1784. 6 indexed citations

Vavilis, Theofanis, Zoe Papadopoulou, Anna‐Bettina Haidich, et al.. (2021). Influence of conception and delivery mode on stress response marker Oct4B1 and imprinted gene expression related to embryo development: A cohort study. International Journal of Reproductive BioMedicine (IJRM). 19(3). 217–226. 1 indexed citations

Syrrou, Maria, et al.. (2021). Developmental Dyslexia: Environment Matters. Brain Sciences. 11(6). 782–782. 18 indexed citations

Hyvönen, Marko, et al.. (2021). Supporting data on combined transcriptomic and phosphoproteomic analysis of BMP4 signaling in human embryonic stem cells. SHILAP Revista de lepidopterología. 35. 106844–106844. 1 indexed citations

Sismani, Carolina, Athina Theodosiou, Maria Syrrou, et al.. (2020). Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Journal of Human Genetics. 65(9). 783–795. 9 indexed citations

Batistatou, Anna, et al.. (2019). Eugenics between Darwin’s Εra and the Holocaust. SHILAP Revista de lepidopterología. 4(2). 171–171. 5 indexed citations

Stellas, Dimitris, et al.. (2016). Generation of human induced pluripotent stem cells in defined, feeder-free conditions. Stem Cell Research. 17(2). 458–460. 7 indexed citations

Papadopoulou, Eleni, et al.. (2015). Cytogenetic behavior of cryoprotectant DMSO. 42(1). 1–7. 1 indexed citations

Dimitriadou, Eftychia, Γεώργιος Μαρκόπουλος, Joanne Traeger‐Synodinos, et al.. (2013). AbnormalDLK1/MEG3imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis. Stress. 16(6). 689–697. 14 indexed citations

10.

Georgiou, Ioannis, Eftychia Dimitriadou, Γεώργιος Μαρκόπουλος, et al.. (2009). Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes. Human Molecular Genetics. 18(7). 1221–1228. 54 indexed citations

11.

Thienpont, Bernard, Eftychia Dimitriadou, Jeroen Breckpot, et al.. (2009). Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1. European Journal of Medical Genetics. 52(6). 393–397. 6 indexed citations

12.

Schlingmann, Karl P., Martin Sassen, Stefanie Weber, et al.. (2005). Novel TRPM6 Mutations in 21 Families with Primary Hypomagnesemia and Secondary Hypocalcemia. Journal of the American Society of Nephrology. 16(10). 3061–3069. 113 indexed citations

13.

Syrrou, Maria, et al.. (2003). The value of opthalmic examinations in familial adenomatous polyposis syndrome screening. Annals of Gastroenterology. 16(4). 1 indexed citations

14.

Esch, Hilde Van, Maria Syrrou, & Liesbet Lagae. (2003). Refractory Photosensitive Epilepsy Associated with a Complex Rearrangement of Chromosome 2. Neuropediatrics. 33(6). 320–323. 16 indexed citations

15.

Frints, Suzanna G.M., J P Fryns, Lieven Lagae, et al.. (2001). Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations. Annales de Génétique. 44(2). 71–76. 11 indexed citations

16.

Syrrou, Maria, et al.. (1999). Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression.. PubMed. 18(3). 357–61. 7 indexed citations

17.

Syrrou, Maria, Ioannis Georgiou, Philippos C. Patsalis, et al.. (1999). Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction. American Journal of Medical Genetics. 84(3). 306–308. 28 indexed citations

18.

Syrrou, Maria, et al.. (1998). Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic population.. PubMed. 70(3). 621–9. 3 indexed citations

19.

Patsalis, Philippos C., Voula Velissariou, Sophia Kitsiou‐Tzeli, et al.. (1997). Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome. Clinical Genetics. 51(3). 184–190. 18 indexed citations

20.

Syrrou, Maria, et al.. (1996). Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus. American Journal of Medical Genetics. 64(1). 234–238. 16 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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