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International Journal of Molecular Sciences|August 10, 2024
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous AnomaliesGergely Büki, Gréta Antal, Judit Bene
International Journal of Molecular Sciences|September 28, 2023
Copy Number Variations in Neuropsychiatric DisordersGergely Büki, Kinga Hadzsiev, Judit Bene
Orvosi Hetilap|December 18, 2022
[Neurofibromatosis-1 microdeletion syndrome.]Gergely Büki, Ágnes Till, Anna Zsigmond, et al.
Gene|August 19, 2023
Copper-transporting ATPases throughout the animal evolution - From clinics to basal neuron-less animalsIstván Fodor, Luis Alfonso Yañez-Guerra, Bence Kiss, et al.
Plos One|September 11, 2018
Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide dataZsolt Bánfai, Valerián Ádám, Etelka Pöstyéni, et al.
Orvosi Hetilap|May 21, 2019
[A rare form of ion channel gene mutation identified as underlying cause of generalized epilepsy]Ágnes Till, Renáta Szalai, Márta Hegyi, et al.
Antibiotics (Basel, Switzerland)|June 28, 2023
Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible PathomechanismsGábor Ternák, Gergely Márovics, Katalin Sümegi, et al.
Frontiers in Genetics|April 14, 2022
Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler HungariansValerián Ádám, Zsolt Bánfai, Katalin Sümegi, et al.
International Journal of Molecular Sciences|September 9, 2023
Identification of an <i>NF1</i> Microdeletion with Optical Genome MappingGergely Büki, Anna Bekő, Csaba Bödör, et al.
Pathology Oncology Research : POR|May 29, 2024
Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosisGréta Antal, Anna Zsigmond, Ágnes Till, et al.
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