• 2056 Citations
  • 23 h-Index
1969 …2020

Research output per year

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Fingerprint Dive into the research topics where G. Fekete is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome

Eßinger, C., Karch, S., Moog, U., Fekete, G., Lengyel, A., Pinti, E., Eggermann, T. & Begemann, M., máj. 11 2020, In : Clinical Epigenetics. 12, 1, 63.

Research output: Article

Open Access
  • Similar Cause, Different Phenotype: SOX9 Enhancer Duplication in a Family

    Pinti, E., Piko, H., Lengyel, A., Luczay, A., Karcagi, V., Fekete, G. & Haltrich, I., ápr. 1 2020, In : Hormone Research in Paediatrics. 92, 5, p. 335-339 5 p.

    Research output: Article

  • FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies

    Madar, L., Szakszon, K., Pfliegler, G., Szabó, G. P., Brúgós, B., Ronen, N., Papp, J., Zahuczky, K., Szakos, E., Fekete, G., Oláh, E., Koczok, K. & Balogh, I., aug. 10 2019, In : Journal of Biotechnology. 301, p. 105-111 7 p.

    Research output: Article