Márta Czakó

432 total citations
40 papers, 245 citations indexed

About

Márta Czakó is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Márta Czakó has authored 40 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 23 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Márta Czakó's work include Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Márta Czakó is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Márta Czakó collaborates with scholars based in Hungary, Germany and United Kingdom. Márta Czakó's co-authors include György Kosztolányi, Béla Melegh, Éva Morava, Kinga Hadzsiev, Mariluce Riegel, Oliver Bartsch, Judit Bene, Katalin Komlósi, Éva Erhardt and András Szabó and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Gene.

In The Last Decade

Márta Czakó

36 papers receiving 218 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Márta Czakó Hungary	11	141	112	30	30	25	40	245
Konstantina Kosma Greece	10	137 1.0×	130 1.2×	37 1.2×	17 0.6×	18 0.7×	30	288
Nada Quercia Canada	8	95 0.7×	148 1.3×	28 0.9×	22 0.7×	39 1.6×	17	256
Mirta Gryngarten Argentina	10	163 1.2×	268 2.4×	17 0.6×	25 0.8×	7 0.3×	20	522
B. A. Bharucha India	9	106 0.8×	69 0.6×	58 1.9×	20 0.7×	13 0.5×	41	251
Jillene Kogan United States	9	94 0.7×	105 0.9×	34 1.1×	25 0.8×	20 0.8×	13	217
Katheryn Grand United States	8	92 0.7×	130 1.2×	31 1.0×	6 0.2×	18 0.7×	27	219
Chantal Gendrot France	11	91 0.6×	82 0.7×	23 0.8×	13 0.4×	13 0.5×	15	301
Ricardo Gracía Spain	11	241 1.7×	277 2.5×	64 2.1×	13 0.4×	15 0.6×	17	461
Haruka Hamanoue Japan	10	84 0.6×	118 1.1×	33 1.1×	7 0.2×	21 0.8×	23	220
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	124 0.9×	92 0.8×	61 2.0×	35 1.2×	30 1.2×	13	212

Countries citing papers authored by Márta Czakó

Since Specialization

Citations

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

Fields of papers citing papers by Márta Czakó

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Márta Czakó

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

Szabó, András, et al.. (2022). Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate. Molecular Syndromology. 14(2). 109–122.

Czakó, Márta, et al.. (2021). Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation. Frontiers in Genetics. 12. 635458–635458. 2 indexed citations

Czakó, Márta, Viktor Farkas, György Fekete, et al.. (2021). Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions. Frontiers in Genetics. 12. 673025–673025. 15 indexed citations

Bene, Judit, et al.. (2019). Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy. Seizure. 74. 8–13. 9 indexed citations

Bánfai, Zsolt, et al.. (2018). Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data. PLoS ONE. 13(9). e0202890–e0202890. 5 indexed citations

Szabó, András, et al.. (2015). Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype. Molecular Cytogenetics. 8(1). 41–41. 3 indexed citations

Komlósi, Katalin, Kinga Hadzsiev, Márta Czakó, et al.. (2015). Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome. Molecular Cytogenetics. 8(1). 16–16. 10 indexed citations

Hadzsiev, Kinga, D. David, Gyula Szabó, et al.. (2014). Partial Trisomy of the Pericentromeric Region of Chromosome 5 in a Girl with Binder Phenotype. Cytogenetic and Genome Research. 144(3). 190–195. 14 indexed citations

Czakó, Márta, Katalin Komlósi, Kinga Hadzsiev, et al.. (2014). Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension. Molecular Cytogenetics. 7(1). 36–36. 10 indexed citations

10.

Czakó, Márta, Kinga Hadzsiev, Béla Melegh, & György Kosztolányi. (2012). Jumping translocation of 15q24-qter resulting in partial trisomy: A case report. Gene. 503(1). 155–159. 3 indexed citations

11.

Csábí, Györgyi, et al.. (2009). Severe dystrophy in DiGeorge syndrome. World Journal of Gastroenterology. 15(11). 1391–1391. 1 indexed citations

12.

Møller, Rikke S., Richárd Kellermayer, Márta Czakó, et al.. (2008). A cryptic unbalanced translocation resulting in del 13q and dup 15q. American Journal of Medical Genetics Part A. 146A(19). 2570–2573. 2 indexed citations

13.

Gyürüs, P, et al.. (2007). Comparison of mtDNA haplogroups in Hungarians with four other European populations: A small incidence of descents with Asian origin. Acta Biologica Hungarica. 58(2). 245–256. 18 indexed citations

14.

Funke, Simone, et al.. (2006). Influence of Genetic Polymorphisms on Bone Disease of Preterm Infants. Pediatric Research. 60(5). 607–612. 9 indexed citations

15.

Erhardt, Éva, et al.. (2005). The frequency of Trp64Arg polymorphism of the β3-adrenergic receptor gene in healthy and obese Hungarian children and its association with cardiovascular risk factors. European Journal of Clinical Nutrition. 59(8). 955–959. 19 indexed citations

16.

Kosztolányi, György, et al.. (2005). Transient progeroid phenotype and lipodystrophy in mosaic polyploidy. Clinical Dysmorphology. 15(1). 29–31. 5 indexed citations

17.

Czakó, Márta, et al.. (2004). Opitz “C” trigonocephaly‐like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q. American Journal of Medical Genetics Part A. 131A(3). 310–312. 14 indexed citations

18.

Czakó, Márta, et al.. (2003). Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome. Clinical Dysmorphology. 12(3). 161–165. 2 indexed citations

19.

Czakó, Márta, Mariluce Riegel, Éva Morava, Albert Schinzel, & György Kosztolányi. (2002). Patient with rheumatoid arthritis and MCA/MR syndrome due to unbalanced der(18) transmission of a paternal translocation t(18;20)(p11.1;p11.1). American Journal of Medical Genetics. 108(3). 226–228. 21 indexed citations

20.

Morava, Éva, et al.. (2000). Velo‐cardio‐facial phenotype and deletion of 22q11.2 in Hungarian children. Clinical Genetics. 58(5). 403–405. 1 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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