Zoltán Maróti (Maróti Zoltán)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 22

Top Venues

International journal of molecular sciences

Genome biology

Ideggyogyaszati szemle

European journal of human genetics : EJHG

Szegedi Tudományegyetem Általános Orvostudományi Kar

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

Affiliation History

Szegedi Tudományegyetem Általános Orvostudományi Kar

Hungary

senior research fellow :: Pediatrics

Publications

Kalmár Tibor, Dániel Jakab, Zoltán Maróti, Orsolya Lakatos, Tibor Vas, Csaba Bereczki, Béla Iványi
The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases. International journal of molecular sciences 25 (2) (2024)
Ildikó Császár, Kalmár Tibor, Zoltán Maróti, János Ávéd, Edit Szederkényi, János Zombori, Gabriella Pankotai-Bodó, Sándor Turkevi-Nagy, Béla Iványi
Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family. International journal of molecular sciences 25 (11) (2024)
Ildikó Császár, Kalmár Tibor, Zoltán Maróti, János Ávéd, Edit Szederkényi, János Zombori, Gabriella Pankotai-Bodó, Sándor Turkevi-Nagy, Béla Iványi
Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family. International journal of molecular sciences 25 (11) (2024)
Kalmár Tibor, Dániel Jakab, Zoltán Maróti, Orsolya Lakatos, Tibor Vas, Csaba Bereczki, Béla Iványi
The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases. International journal of molecular sciences 25 (2) (2024)
Ildikó Császár, Kalmár Tibor, Zoltán Maróti, János Ávéd, Edit Szederkényi, János Zombori, Gabriella Pankotai-Bodó, Sándor Turkevi-Nagy, Béla Iványi
Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family. International journal of molecular sciences 25 (11) (2024)
Kalmár Tibor, Dániel Jakab, Zoltán Maróti, Orsolya Lakatos, Tibor Vas, Csaba Bereczki, Béla Iványi
The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases. International journal of molecular sciences 25 (2) (2024)
Kalmár Tibor, Dániel Jakab, Zoltán Maróti, Orsolya Lakatos, Tibor Vas, Csaba Bereczki, Béla Iványi
The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases. International journal of molecular sciences 25 (2) (2024)
Emil Nyerki, Tibor Kalmár, Oszkár Schütz, Rui M Lima, Endre Neparáczki, Tibor Török, Zoltán Maróti
correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Genome biology 24 (1) (2023)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Emil Nyerki, Tibor Kalmár, Oszkár Schütz, Rui M Lima, Endre Neparáczki, Tibor Török, Zoltán Maróti
correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Genome biology 24 (1) (2023)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Emil Nyerki, Tibor Kalmár, Oszkár Schütz, Rui M Lima, Endre Neparáczki, Tibor Török, Zoltán Maróti
correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Genome biology 24 (1) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Kalmár Tibor, Sándor Turkevi-Nagy, László Bitó, László Kaiser, Zoltán Maróti, Dániel Jakab, Annamária Letoha, Péter Légrády, Béla Iványi
Phenotype-Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis. International journal of molecular sciences 24 (24) (2023)
Emil Nyerki, Tibor Kalmár, Oszkár Schütz, Rui M Lima, Endre Neparáczki, Tibor Török, Zoltán Maróti
correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes. Genome biology 24 (1) (2023)
Kalmár Tibor, Sándor Turkevi-Nagy, László Bitó, László Kaiser, Zoltán Maróti, Dániel Jakab, Annamária Letoha, Péter Légrády, Béla Iványi
Phenotype-Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis. International journal of molecular sciences 24 (24) (2023)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Alexandra Gînguță, Bence Kovács, Balázs Tihanyi, Kitti Maár, Oszkár Schütz, Zoltán Maróti, Istvan Gergely Varga, Attila P Kiss, Ioan Stanciu, Tibor Török, Endre Neparáczki
Maternal Lineages of Gepids from Transylvania. Genes 13 (4) (2022)
Péter L Nagy, Judit Olasz, Endre Neparáczki, Nicholas Rouse, Karan Kapuria, Samantha Cano, Huijie Chen, Julie Di Cristofaro, Goran Runfeldt, Natalia Ekomasova, Zoltán Maróti, János Jeney, Sergey Litvinov, Murat Dzhaubermezov, Lilya Gabidullina, Zoltán Szentirmay, György Szabados, Dragana Zgonjanin, Jacques Chiaroni, Doron M Behar, Elza K Khusnutdinova, Peter A Underhill, Miklós Kásler
Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third. European journal of human genetics : EJHG 29 (1) (2020)

Zoltán Maróti.css-eqlu8i{font-size:small;padding-left:4px;} (Maróti Zoltán)

Publication Activity (10 Years)

Top Topics

Top Venues

Zoltán Maróti (Maróti Zoltán)