A Special Structural Based Weighted Network Approach for the Analysis of Protein Complexes by Peter Juma Ochieng, József Dombi, Tibor Kalmár, Miklós Krész

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PAX2 Mutation-Related Oligomeganephronia in a Young Adult Patient by László Bitó, Tibor Kalmár, Zoltán Maróti, Sándor Turkevi-Nagy, Csaba Bereczki, Béla Iványi

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Adaptive Savitzky–Golay Filters for Analysis of Copy Number Variation Peaks from Whole-Exome Sequencing Data by Peter Juma Ochieng, Zoltán Maróti, József Dombi, Miklós Krész, József Békési, Tibor Kalmár

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

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

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Childhood Obesity: Does it Have Any Effect on Young Arteries? by Andrea Emese Jakab, Erzsébet Valéria Hidvégi, Miklós Illyés, Attila Cziráki, Tibor Kalmár, Zoltán Maróti, Csaba Bereczki

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Regulated fluctuations in nanog expression mediate cell fate decisions in embryonic stem cells. by Tibor Kalmar, Chea Lim, Penelope Hayward, Silvia Muñoz-Descalzo, Jennifer Nichols, Jordi Garcia-Ojalvo, Alfonso Martinez Arias

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Phenotype–Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis by Tibor Kalmár, Sándor Turkevi-Nagy, László Bitó, László Kaiser, Zoltán Maróti, Dániel Jakab, Annamária Letoha, Péter Légrády, Béla Iványi

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Myopia-26, the female-limited form of early-onset high myopia, occurring in a European family by Noémi Széll, Tamás Fehér, Zoltán Maróti, Tibor Kalmár, Dóra Latinovics, István Nagy, Zsuzsanna Z. Orosz, Márta Janáky, Andrea Facskó, Zoltán Sohajda

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Time-course transcriptome analysis of host cell response to poxvirus infection using a dual long-read sequencing approach by Zoltán Maróti, Dóra Tombácz, István Prazsák, Norbert Moldován, Zsolt Csabai, Gábor Torma, Zsolt Balázs, Tibor Kalmár, Béla Dénes, Michael Snyder, Zsolt Boldogkői

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Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia – a first case report by Sára Pálla, Pálma Anker, Klára Farkas, Dóra Plázár, Sándor Kiss, Péter Marschalkó, Zsuzsanna Szalai, Judit Bene, Kinga Hadzsiev, Zoltán Maróti, Tibor Kalmár, Márta Medvecz

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Time course profiling of host cell response to herpesvirus infection using nanopore and synthetic long-read transcriptome sequencing by Zoltán Maróti, Dóra Tombácz, Norbert Moldován, Gábor Torma, Victoria A. Jefferson, Zsolt Csabai, Gábor Gulyás, Ákos Dörmő, Miklós Boldogkői, Tibor Kalmár, Florencia Meyer, Zsolt Boldogkői

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Correction to: Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study by Laszlo Szpisjak, Gabor Szaraz, Andras Salamon, Viola L. Nemeth, Noemi Szepfalusi, Gabor Veres, Balint Kincses, Zoltan Maroti, Tibor Kalmar, Malgorzata Rydzanicz, Rafal Ploski, Peter Klivenyi, Denes Zadori

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Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients: a pilot study by Laszlo Szpisjak, Gabor Szaraz, Andras Salamon, Viola L. Nemeth, Noemi Szepfalusi, Gabor Veres, Balint Kincses, Zoltan Maroti, Tibor Kalmar, Malgorzata Rydzanicz, Rafal Ploski, Peter Klivenyi, Denes Zadori

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Mitogenomic data indicate admixture components of Central-Inner Asian and Srubnaya origin in the conquering Hungarians. by Endre Neparáczki, Zoltán Maróti, Tibor Kalmár, Klaudia Kocsy, Kitti Maár, Péter Bihari, István Nagy, Erzsébet Fóthi, Ildikó Pap, Ágnes Kustár, György Pálfi, István Raskó, Albert Zink, Tibor Török

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Correction: Mitogenomic data indicate admixture components of Central-Inner Asian and Srubnaya origin in the conquering Hungarians. by Endre Neparáczki, Zoltán Maróti, Tibor Kalmár, Klaudia Kocsy, Kitti Maár, Péter Bihari, István Nagy, Erzsébet Fóthi, Ildikó Pap, Ágnes Kustár, György Pálfi, István Raskó, Albert Zink, Tibor Török

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Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the <i>CCDC88C</i> Gene by Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Dénes Zádori, András Salamon, Judit Danis, Tibor Kalmár, Zoltán Maróti, Mária Judit Molnár, Péter Klivényi, Márta Széll, Éva Ádám

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DAAM is required for thin filament formation and Sarcomerogenesis during muscle development in Drosophila. by Imre Molnár, Ede Migh, Szilárd Szikora, Tibor Kalmár, Attila G Végh, Ferenc Deák, Szilvia Barkó, Beáta Bugyi, Zacharias Orfanos, János Kovács, Gábor Juhász, György Váró, Miklós Nyitrai, John Sparrow, József Mihály

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Maternal Lineages from 10–11th Century Commoner Cemeteries of the Carpathian Basin by Kitti Maár, Gergely I. B. Varga, Bence Kovács, Oszkár Schütz, Zoltán Maróti, Tibor Kalmár, Emil Nyerki, István Nagy, Dóra Latinovics, Balázs Tihanyi, Antónia Marcsik, György Pálfi, Zsolt Bernert, Zsolt Gallina, Sándor Varga, László Költő, István Raskó, Tibor Török, Endre Neparáczki

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Hemizygous nonsense variant in the moesin gene (MSN) leads to a new autoimmune phenotype of Immunodeficiency 50 by András L. Kovács, Judit Kárteszi, Zoltán Prohászka, Tibor Kalmár, Gábor Késmárky, Katalin Koltai, Zsuzsanna Nagy, Judit Sebők, Tibor Vas, Krisztián Molnár, Tímea Berki, Katalin Böröcz, Csaba Gyömörei, József Szalma, Miklós Egyed, Szabina Horváth, Péter Oláh, Péter Oláh, Dorottya Csuka, Viktória Németh, Rolland Gyulai

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