Judit Bene

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 15

Top Topics

Bipolar Disorder

Bioinformatics Analysis

Top Venues

International journal of molecular sciences

Molecular genetics & genomic medicine

Disease markers

This page only lists publications with an associated author ORCID identifier.

Publications

Renata Szalai, Kinga Hadzsiev, Agnes Till, Andras Fogarasi, Timea Bodo, Gergely Buki, Zsolt Banfai, Judit Bene
NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy. International journal of molecular sciences 25 (11) (2024)
Anna Zsigmond, Ágnes Till, Judit Bene, Márta Czakó, Alexandra Mikó, Kinga Hadzsiev
Case Report of Suspected Gonadal Mosaicism in FOXP1 -Related Neurodevelopmental Disorder. International journal of molecular sciences 25 (11) (2024)
Renata Szalai, Kinga Hadzsiev, Agnes Till, Andras Fogarasi, Timea Bodo, Gergely Buki, Zsolt Banfai, Judit Bene
NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy. International journal of molecular sciences 25 (11) (2024)
Gergely Büki, Gréta Antal, Judit Bene
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies. International journal of molecular sciences 25 (15) (2024)
Anna Zsigmond, Ágnes Till, Judit Bene, Márta Czakó, Alexandra Mikó, Kinga Hadzsiev
Case Report of Suspected Gonadal Mosaicism in FOXP1 -Related Neurodevelopmental Disorder. International journal of molecular sciences 25 (11) (2024)
Gergely Büki, Gréta Antal, Judit Bene
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies. International journal of molecular sciences 25 (15) (2024)
Renata Szalai, Kinga Hadzsiev, Agnes Till, Andras Fogarasi, Timea Bodo, Gergely Buki, Zsolt Banfai, Judit Bene
NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy. International journal of molecular sciences 25 (11) (2024)
Gergely Büki, Gréta Antal, Judit Bene
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies. International journal of molecular sciences 25 (15) (2024)
Anna Zsigmond, Ágnes Till, Judit Bene, Márta Czakó, Alexandra Mikó, Kinga Hadzsiev
Case Report of Suspected Gonadal Mosaicism in FOXP1 -Related Neurodevelopmental Disorder. International journal of molecular sciences 25 (11) (2024)
Gergely Büki, Kinga Hadzsiev, Judit Bene
Copy Number Variations in Neuropsychiatric Disorders. International journal of molecular sciences 24 (18) (2023)
Klára Veres, Judit Bene, Kinga Hadzsiev, Miklós Garami, Sára Pálla, Rudolf Happle, Marta Medvecz, Zsuzsanna Zsófia Szalai
Superimposed Mosaicism in the Form of Extremely Extended Segmental Plexiform Neurofibroma Caused by a Novel Pathogenic Variant in the NF1 Gene. International journal of molecular sciences 24 (15) (2023)
Gergely Buki, Renata Szalai, Adrienn Pinter, Kinga Hadzsiev, Bela Melegh, Tibor Rauch, Judit Bene
Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature. Molecular genetics & genomic medicine (2023)
Anita Maász, Tímea Bodó, Ágnes Till, Gábor Molnár, György Masszi, Gusztáv Labossa, Zsuzsanna Herbert, Judit Bene, Kinga Hadzsiev
Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma. International journal of molecular sciences 24 (16) (2023)
Gergely Büki, Anna Bekő, Csaba Bödör, Peter Urban, Krisztina Németh, Kinga Hadzsiev, György Fekete, Hildegard Kehrer-Sawatzki, Judit Bene
Identification of an NF1 Microdeletion with Optical Genome Mapping. International journal of molecular sciences 24 (17) (2023)
Mohammad Ali Mokhtari, Ramin Saravani, Ramin Saravani, Milad Heidari Nia, Shekoufeh Mirinejad, Kinga Hadzsiev, Judit Bene, Mansour Shakiba
Genetic Polymorphisms in miR-137 and Its Target Genes, TCF4 and CACNA1C, Contribute to the Risk of Bipolar Disorder: A Preliminary Case-Control Study and Bioinformatics Analysis. Disease markers 2022 (2022)