Konstantina Kosma

1.5k total citations
30 papers, 288 citations indexed

About

Konstantina Kosma is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Konstantina Kosma has authored 30 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 17 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Konstantina Kosma's work include Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (7 papers) and Congenital heart defects research (7 papers). Konstantina Kosma is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (7 papers) and Congenital heart defects research (7 papers). Konstantina Kosma collaborates with scholars based in Greece, Switzerland and United States. Konstantina Kosma's co-authors include Maria Tzetis, Helen Fryssira, Christalena Sofocleous, Κρινιώ Γιαννίκου, Sophia Kitsiou‐Tzeli, Sofia Kitsiou‐Tzeli, Periklis Makrythanasis, Emmanuel Kanavakis, Joanne Traeger‐Synodinos and Demosthenes B. Panagiotakos and has published in prestigious journals such as International Journal of Molecular Sciences, Gene and Journal of the Neurological Sciences.

In The Last Decade

Konstantina Kosma

26 papers receiving 281 citations

Peers

Countries citing papers authored by Konstantina Kosma

Since Specialization

Citations

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

Fields of papers citing papers by Konstantina Kosma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konstantina Kosma

This figure shows the co-authorship network connecting the top 25 collaborators of Konstantina Kosma. A scholar is included among the top collaborators of Konstantina Kosma 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 Konstantina Kosma. Konstantina Kosma 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	Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children 2024 ·Genes ·(unknown), Konstantina Kosma, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Andromachi Mitsioni, (unknown), Christina Kanaka‐Gantenbein, Periklis Makrythanasis, Maria Tzetis, Joanne Traeger‐Synodinos	2
2	Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifier 2024 ·Muscle & Nerve ·(unknown), (unknown), (unknown), Constantinos Papadopoulos, Elisabeth Chroni, Roser Pons, Evangelos Pavlou, (unknown), Konstantina Kosma, Paraskevi Apostolou, Christalena Sofocleous, Joanne Traeger‐Synodinos, Kyriaki Kekou	0
3	Estimating at-risk couple rates across 1000 exome sequencing data cohort for 176 genes and its importance relevance for health policies 2024 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), Christalena Sofocleous, Kyriaki Kekou, Konstantina Kosma, (unknown), (unknown), (unknown), Amalia Sertedaki, Christina Kanaka‐Gantenbein, Joanne Traeger‐Synodinos, Periklis Makrythanasis	1
4	Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases 2023 ·Genes ·(unknown), (unknown), (unknown), (unknown), Kyriaki Kekou, (unknown), Maria Tzetis, Konstantina Kosma, Periklis Makrythanasis, Joanne Traeger‐Synodinos, Christalena Sofocleous	16
5	Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield? 2023 ·Genes ·(unknown), Konstantina Kosma, Periklis Makrythanasis, Maria Tzetis	3
6	Identification of a Novel IQCE Large Deletion through Copy Number Variant Analysis from Whole-Exome Sequencing Data of a Patient with Postaxial Polydactyly Type A7 2023 ·Molecular Syndromology ·(unknown), (unknown), Konstantina Kosma, Florentia Fostira, Joanne Traeger‐Synodinos	1
7	Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients 2022 ·European Journal of Pediatrics ·George Papadopoulos, Anna Papadopoulou, Konstantina Kosma, Anastasios Papadimitriou, Vassiliki Papaevangelou, Christina Kanaka‐Gantenbein, (unknown), Sophia Kitsiou‐Tzeli	7
8	239-kb Microdeletion Spanning <b><i>KMT2E</i></b> in a Child with Developmental Delay: Further Delineation of the Phenotype 2021 ·Molecular Syndromology ·Konstantina Kosma, Konstantinos Varvagiannis, (unknown), (unknown), Joanne Traeger‐Synodinos, Maria Tzetis	0
9	Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA 2018 ·Journal of the Neurological Sciences ·(unknown), Myrto Poulou, (unknown), Konstantina Kosma, (unknown), (unknown), (unknown), Sofia Kitsiou‐Tzeli, Helen Fryssira, Maria Tzetis	29
10	Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases 2016 ·Meta Gene ·(unknown), Maria Tzetis, Konstantina Kosma, (unknown), Maria Braoudaki, Myrto Poulou, Emmanuel Kanavakis, Sofia Kitsiou‐Tzeli	4
11	A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion 2016 ·Child and Adolescent Psychiatry and Mental Health ·Gerasimos Kolaitis, Christian G. Bouwkamp, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Konstantina Kosma, Sophia Kitsiou‐Tzeli, Maria Tzetis	5
12	Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease 2013 ·Pediatric Research ·(unknown), Maria Tzetis, Helen Fryssira, Konstantina Kosma, (unknown), Κρινιώ Γιαννίκου, Periklis Makrythanasis, Sophia Kitsiou‐Tzeli, Emmanuel Kanavakis	31
13	Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype 2013 ·Journal of Genetics ·(unknown), Spyridon Megremis, Andromachi Mitsioni, Sofia Kitsiou‐Tzeli, Konstantina Kosma, María Bitsori, Constantinos J. Stefanidis, Emmanuel Kanavakis, Joanne Traeger‐Synodinos	1
14	Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation 2013 ·European Journal of Paediatric Neurology ·(unknown), Maria Tzetis, Κρινιώ Γιαννίκου, (unknown), (unknown), Konstantina Kosma, (unknown), Emmanuel Kanavakis, Helen Fryssira	3
15	Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies 2013 ·American Journal of Medical Genetics Part A ·(unknown), Sofia Kitsiou‐Tzeli, (unknown), Konstantina Kosma, Periklis Makrythanasis, (unknown), Emmanuel Kanavakis, Maria Tzetis	4
16	An unusual case of cat‐eye syndrome phenotype and extragonadal mature teratoma: Review of the literature 2012 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Maria Tzetis, Kalliopi Stefanaki, (unknown), Konstantina Kosma, (unknown), Krinio Giannikou, (unknown), Christalena Sofocleous, (unknown), Aggeliki Kοlialexi, Periklis Makrythanasis, (unknown)	2
17	Familial Pelizaeus–Merzbacher disease caused by a 320.6‐kb Xq22.2 duplication and the pathological findings of a male fetus 2012 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Sophia Kitsiou‐Tzeli, Anastasia Konstantinidou, Christalena Sofocleous, Konstantina Kosma, (unknown), Κρινιώ Γιαννίκου, Stavros Sifakis, Periklis Makrythanasis, Maria Tzetis	3
18	Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment 2011 ·European Journal of Pediatrics ·Anna Papadopoulou, (unknown), (unknown), Konstantina Kosma, Helen Fryssira, Andreas Fretzayas, Polyxeni Nicolaidou, Sophia Kitsiou‐Tzeli	15
19	Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH 2011 ·Gene ·Sophia Kitsiou‐Tzeli, (unknown), Κρινιώ Γιαννίκου, (unknown), Konstantina Kosma, Georgia Kakourou, (unknown), Christalena Sofocleous, Emmanuel Kanavakis, Maria Tzetis	18
20	Distribution of serum lipids and lipoproteins in patients with beta thalassaemia major; an epidemiological study in young adults from Greece. 2004 ·Lipids in Health and Disease ·Christina Chrysohoou, Demosthenes B. Panagiotakos, Christos Pitsavos, Konstantina Kosma, John Barbetseas, Markisia Karagiorga, (unknown), Christodoulos Stefanadis	42

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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