Kalmár Tibor (Tibor Kalmár)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 26

Top Topics

Major Depressive Disorder

Parkinson Disease

Genome Wide Association

Top Venues

International journal of molecular sciences

Ideggyogyaszati szemle

Scientific reports

Scientific data

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

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)
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)
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)
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)
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)
Kitti Maár, Istvan Gergely Varga, Bence Kovács, Oszkár Schütz, Zoltán Maróti, Kalmár Tibor, 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
Maternal Lineages from 10-11th Century Commoner Cemeteries of the Carpathian Basin. Genes 12 (3) (2021)
András Salamon, Dénes Zádori, Anikó Ujfalusi, László Szpisjak, Melinda Lukács, Brigitta Bihari, Noémi Szépfalusi, Viola Luca Németh, Zoltán Maróti, Emese Horváth, István Balogh, Csaba Bereczki, Péter Klivényi, Kalmár Tibor
Hereditary and non-hereditary etiologies associated with extensive brain calcification: case series. Metabolic brain disease 36 (7) (2021)
Katalin Havasi, Zoltán Maróti, Andrea Jakab, István Raskó, Kalmár Tibor, Csaba Bereczki
Reference values for resting and post exercise hemodynamic parameters in a 6-18 year old population. Scientific data 7 (1) (2020)
Endre Neparáczki, Zoltán Maróti, Kalmár Tibor, Kitti Maár, István Nagy, Dóra Latinovics, Ágnes Kustár, György Pálfi, Erika Molnár, Antónia Marcsik, Csilla Balogh, Gábor Lőrinczy, Szilárd Sándor Gál, Péter Tomka, Bernadett Kovacsóczy, László Kovács, István Raskó, Tibor Török
Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin. Scientific reports 9 (1) (2019)
Dóra Tombácz, Zoltán Maróti, Kalmár Tibor, Miklós Palkovits, Michael Paul Snyder, Zsolt Boldogkői
Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder. Scientific data 6 (2019)
Dénes Zádori, László Szpisjak, István Balázs Németh, Zita Reisz, Gabor G Kovacs, Noémi Szépfalusi, Viola Luca Németh, Zoltán Maróti, Edit Tóth-Molnár, Judit Oláh, László Vécsei, Péter Klivényi, Kalmár Tibor
Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene-case series. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (1) (2019)
Zoltán Maróti, Zsolt Boldogkői, Dóra Tombácz, Michael Snyder, Kalmár Tibor
Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis. BMC genomics 19 (1) (2018)
Melinda Zombor, Kalmár Tibor, Zoltán Maróti, Alíz Zimmermann, Adrienn Máté, Csaba Bereczki, László Sztriha
Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability. Journal of human genetics 63 (11) (2018)
Endre Neparáczki, Zoltán Maróti, Kalmár Tibor, Klaudia Kocsy, Kitti Maár, Péter Bihari, István Nagy, Erzsébet Fóthi, Ildikó Pap, Ágnes Kustár, György Pálfi, István Raskó, Albert Zink, Tibor Török
Mitogenomic data indicate admixture components of Central-Inner Asian and Srubnaya origin in the conquering Hungarians. PloS one 13 (10) (2018)
Dóra Tombácz, Zoltán Maróti, Kalmár Tibor, Zsolt Csabai, Zsolt Balázs, Shinichi Takahashi, Miklós Palkovits, Michael Snyder, Zsolt Boldogkői
High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder. Scientific reports 7 (1) (2017)