Publications by authors named "Zoltan Maroti"

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The genetic origin of Huns, Avars, and conquering Hungarians.
Zoltán Maróti, Endre Neparáczki, Oszkár Schütz, Kitti Maár, Gergely I B Varga, Bence Kovács, Tibor Kalmár, Emil Nyerki, István Nagy, Dóra Latinovics

Curr Biol· July 2022

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Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin.
Endre Neparáczki, Zoltán Maróti, Tibor Kalmár, Kitti Maár, István Nagy, Dóra Latinovics, Ágnes Kustár, György Pálfi, Erika Molnár, Antónia Marcsik

Sci Rep· November 2019

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Intellectual developmental disorder 56 associated with novel variants in the clathrin heavy chain encoding CLTC gene and brief review of the literature.
Tibor Kalmár, Viktor Vedelek, Zoltán Maróti, Marianna Csenki, László Sztriha

Neurol Sci· December 2025

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The Presence of Risk and Protective HLA-DQ Haplotype Combinations and PLA2R1 Risk SNP in Hungarian Patients with Membranous Nephropathy.
Dóra Bajcsi, Zoltán Maróti, Emőke Endreffy, Péter Légrády, György Ábrahám

Int J Mol Sci· September 2025

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Unveiling the origins and genetic makeup of the "forgotten people": A study of the Sarmatian-period population in the Carpathian Basin.
Oszkár Schütz, Zoltán Maróti, Balázs Tihanyi, Attila P Kiss, Emil Nyerki

Cell· July 2025

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Fibronectin Glomerulopathy Without Typical Renal Biopsy Features in a 4-Year-Old Girl with Incidentally Discovered Proteinuria and a G417V Gene Mutation.
Tibor Kalmár, Dániel Jakab, Zoltán Maróti, Gyula Pásztor, Sándor Turkevi-Nagy

Int J Mol Sci· January 2025

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Temporal transcriptional profiling of host cells infected by a veterinary alphaherpesvirus using nanopore sequencing.
Dóra Tombácz, Zoltán Maróti, Péter Oláh, Ákos Dörmő, Gábor Gulyás

Sci Rep· January 2025

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A Patient Diagnosed with Mosaic Trisomy 18 Presenting New Symptoms: Diaphragmatic Relaxation and Cyclic Vomiting Syndrome. Updated Review of Mosaic Trisomy 18 Cases.
Magdolna Kósa, Emese Horváth, Tibor Kalmár, Zoltán Maróti, Imre Földesi

J Pediatr Genet· December 2024

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Optimizing sequence data analysis using convolution neural network for the prediction of CNV bait positions.
Zoltán Maróti, Peter Juma Ochieng, József Dombi, Miklós Krész, Tibor Kalmár

BMC Bioinformatics· December 2024

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'But no living man am I': Bioarchaeological evaluation of the first-known female burial with weapon from the 10th-century-CE Carpathian Basin.
Balázs Tihanyi, Kitti Maár, Luca Kis, Alexandra Gînguță, Gergely I B Varga

PLoS One· November 2024

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Cone dysfunction in ARR3-mutation-associated early-onset high myopia: an electrophysiological study.
Tamás Fehér, Noémi Széll, István Nagy, Zoltán Maróti, Tibor Kalmár

Orphanet J Rare Dis· October 2024

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The ASAP study: association of atherosclerosis with pathobiology in a caucasian cohort-a study of 3400 autopsy reports.
Andrea Emese Jakab, Mátyás Bukva, Zoltán Maróti, Tibor Kalmár, István Raskó

Sci Rep· October 2024

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Archaeogenetic analysis revealed East Eurasian paternal origin to the Aba royal family of Hungary.
Gergely I B Varga, Zoltán Maróti, Oszkár Schütz, Kitti Maár, Emil Nyerki

iScience· October 2024

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Phenotypic and Genotypic Features of the Mutation-Related Disease in a Large Hungarian Family.
Ildikó Császár, Tibor Kalmár, Zoltán Maróti, János Ávéd, Edit Szederkényi

Int J Mol Sci· May 2024

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The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases.
Tibor Kalmár, Dániel Jakab, Zoltán Maróti, Orsolya Lakatos, Tibor Vas

Int J Mol Sci· January 2024

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Phenotype-Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis.
Tibor Kalmár, Sándor Turkevi-Nagy, László Bitó, László Kaiser, Zoltán Maróti

Int J Mol Sci· December 2023

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Genetic identification of members of the prominent Báthory aristocratic family.
Alexandra Gînguță, Bence Kovács, Oszkár Schütz, Balázs Tihanyi, Emil Nyerki

iScience· October 2023

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[A rare tubulopathy: Dent's disease in the background of focal segmental glomerular sclerosis].
Dániel Jakab, Zoltán Maróti, Béla Iványi, Csaba Bereczki, Tibor Kalmár

Orv Hetil· May 2023

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Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia - a first case report.
Sára Pálla, Pálma Anker, Klára Farkas, Dóra Plázár, Sándor Kiss

BMC Pediatr· March 2023

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correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes.
Emil Nyerki, Tibor Kalmár, Oszkár Schütz, Rui M Lima, Endre Neparáczki

Genome Biol· February 2023

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The archaeogenomic validation of Saint Ladislaus' relic provides insights into the Árpád dynasty's genealogy.
Gergely I B Varga, Lilla Alida Kristóf, Kitti Maár, Luca Kis, Oszkár Schütz

J Genet Genomics· January 2023

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Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the Gene.
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Dénes Zádori

Int J Mol Sci· January 2023

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Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient.
Péter Klivényi, László Szpisjak, András Salamon, Viola Luca Németh, Noémi Szépfalusi

Ideggyogy Sz· January 2023

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The genetic legacy of the Hunyadi descendants.
Endre Neparáczki, Luca Kis, Zoltán Maróti, Bence Kovács, Gergely I B Varga

Heliyon· November 2022

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Maternal Lineages of Gepids from Transylvania.
Alexandra Gînguță, Bence Kovács, Balázs Tihanyi, Kitti Maár, Oszkár Schütz

Genes (Basel)· March 2022

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Atypical presentation of late-onset Sandhoff disease: a case report.
András Salamon, László Szpisjak, Dénes Zádori, István Lénárt, Zoltán Maróti

Ideggyogy Sz· November 2021

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