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Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
International Journal of Molecular Sciences|September 27, 2025
Uncovering Rare Structural Chromosomal Rearrangements: Insights from Molecular CytogeneticsMárta Czakó, András Szabó, Ágnes Till, et al.
International Journal of Molecular Sciences|June 19, 2024
Case Report of Suspected Gonadal Mosaicism in <i>FOXP1</i>-Related Neurodevelopmental DisorderAnna Zsigmond, Ágnes Till, Judit Bene, et al.
International Journal of Molecular Sciences|December 11, 2025
Heterogeneity of Orodental Features in a Family with Noonan SyndromeGréta Antal, Laura Csabai, Anna Zsigmond, et al.
Orvosi Hetilap|December 28, 2020
Gene testing in Treacher Collins syndromeAnna Zsigmond, Ágnes Till, Adrienn Lilla Pintér, et al.
International Journal of Molecular Sciences|November 9, 2024
Molecular and Clinical Heterogeneity in Hungarian Patients with Treacher Collins Syndrome-Identification of Two Novel Mutations by Next-Generation SequencingGréta Antal, Anna Zsigmond, Ágnes Till, et al.
Frontiers in Genetics|May 3, 2021
Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number VariationMárta Czakó, Ágnes Till, Judith Zima, et al.
European Journal of Pharmacology|June 7, 2024
Nimodipine inhibits spreading depolarization, ischemic injury, and neuroinflammation in mouse live brain slice preparationsRita Frank, Péter Archibald Szarvas, István Pesti, et al.
Neuropediatrics|June 1, 2023
Observation of a Possible Successful Treatment of DEPDC5-Related Epilepsy with mTOR InhibitorKinga Hadzsiev, Márta Hegyi, András Fogarasi, et al.
Frontiers in Psychology|March 17, 2023
Cognitive functioning and clinical characteristics of children with non-syndromic orofacial clefts: A case-control studyKinga Amália Sándor-Bajusz, Tímea Dergez, Edit Molnár, et al.
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