Kinga Hadzsiev

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 14

Top Topics

Bipolar Disorder

Dna Methylation

Top Venues

International journal of molecular sciences

Children (Basel, Switzerland)

Disease markers

International journal of genomics

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)
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)
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)
Petronella Orosz, Zita Kollák, Ákos Géza Pethő, András Fogarasi, György Reusz, Kinga Hadzsiev, Tamás Szabó
The Importance of Genetic Testing in the Differential Diagnosis of Atypical TSC2-PKD1 Contiguous Gene Syndrome-Case Series. Children (Basel, Switzerland) 10 (3) (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)
Petronella Orosz, Zita Kollák, Ákos Géza Pethő, András Fogarasi, György Reusz, Kinga Hadzsiev, Tamás Szabó
The Importance of Genetic Testing in the Differential Diagnosis of Atypical TSC2-PKD1 Contiguous Gene Syndrome-Case Series. Children (Basel, Switzerland) 10 (3) (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)
Elisa Frullanti, Filomena Tiziana Papa, Elisa Grillo, Angus Clarke, Bruria Ben-Zeev, Mercedes Pineda, Nadia Bahi-Buisson, Thierry Bienvenu, Judith Armstrong, Ana Roche Martinez, Francesca Mari, Andreea Nissenkorn, Caterina Lo Rizzo, Edvige Veneselli, Silvia Russo, Aglaia Vignoli, Giorgio Pini, Milena Djuric, Anne-Marie Bisgaard, Kirstine Ravn, Vlatka Mejaski Bosnjak, Joussef Hayek, Rajni Khajuria, Barbara Montomoli, Francesca Cogliati, Maria Pintaudi, Kinga Hadzsiev, Dana Craiu, Victoria Voinova, Aleksandra Djukic, Laurent Villard, Alessandra Renieri
Analysis of the Phenotypes in the Rett Networked Database. International journal of genomics 2019 (2019)