Kalmár T - Search Results

1

Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin.

Neparáczki E, Maróti Z, Kalmár T, Maár K, Nagy I, Latinovics D, Kustár Á, Pálfi G, Molnár E, Marcsik A, Balogh C, Lőrinczy G, Gál SS, Tomka P, Kovacsóczy B, Kovács L, Raskó I, Török T. Neparáczki E, et al. Among authors: kalmar t. Sci Rep. 2019 Nov 12;9(1):16569. doi: 10.1038/s41598-019-53105-5. Sci Rep. 2019. PMID: 31719606 Free PMC article.

2

Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in a Hungarian population.

Jakab K, Gárdián G, Endreffy E, Kalmár T, Bachrati C, Vécsei L, Raskó I. Jakab K, et al. Among authors: kalmar t. Eur Neurol. 1999;41(2):107-10. doi: 10.1159/000008013. Eur Neurol. 1999. PMID: 10023115

3

Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families.

Bachrati CZ, Somodi Z, Endreffy E, Kalmár T, Raskó I. Bachrati CZ, et al. Among authors: kalmar t. Ann Hum Genet. 1998 Nov;62(Pt 6):511-20. doi: 10.1046/j.1469-1809.1998.6260511.x. Ann Hum Genet. 1998. PMID: 10363129

4

A simple and efficient method for PCR amplifiable DNA extraction from ancient bones.

Kalmár T, Bachrati CZ, Marcsik A, Raskó I. Kalmár T, et al. Nucleic Acids Res. 2000 Jun 15;28(12):E67. doi: 10.1093/nar/28.12.e67. Nucleic Acids Res. 2000. PMID: 10871390 Free PMC article.

5

Mitochondrial DNA of ancient Cumanians: culturally Asian steppe nomadic immigrants with substantially more western Eurasian mitochondrial DNA lineages.

Bogácsi-Szabó E, Kalmár T, Csányi B, Tömöry G, Czibula A, Priskin K, Horváth F, Downes CS, Raskó I. Bogácsi-Szabó E, et al. Among authors: kalmar t. Hum Biol. 2005 Oct;77(5):639-62. Hum Biol. 2005. PMID: 16596944

6

Comparison of maternal lineage and biogeographic analyses of ancient and modern Hungarian populations.

Tömöry G, Csányi B, Bogácsi-Szabó E, Kalmár T, Czibula A, Csosz A, Priskin K, Mende B, Langó P, Downes CS, Raskó I. Tömöry G, et al. Among authors: kalmar t. Am J Phys Anthropol. 2007 Nov;134(3):354-68. doi: 10.1002/ajpa.20677. Am J Phys Anthropol. 2007. PMID: 17632797 Free article.

7

Novel frameshift mutation in the CHD7 gene associated with CHARGE syndrome with preaxial polydactyly.

Surányi A, Maróti Z, Tálosi G, Kalmár T, Kaiser L, Bereczki C, Pál A, Keresztúri A. Surányi A, et al. Among authors: kalmar t. Clin Dysmorphol. 2016 Jul;25(3):98-100. doi: 10.1097/MCD.0000000000000120. Clin Dysmorphol. 2016. PMID: 26901670 No abstract available.

8

Efficient Targeted Next Generation Sequencing-Based Workflow for Differential Diagnosis of Alport-Related Disorders.

Kovács G, Kalmár T, Endreffy E, Ondrik Z, Iványi B, Rikker C, Haszon I, Túri S, Sinkó M, Bereczki C, Maróti Z. Kovács G, et al. Among authors: kalmar t. PLoS One. 2016 Mar 2;11(3):e0149241. doi: 10.1371/journal.pone.0149241. eCollection 2016. PLoS One. 2016. PMID: 26934356 Free PMC article.

9

Revising mtDNA haplotypes of the ancient Hungarian conquerors with next generation sequencing.

Neparáczki E, Kocsy K, Tóth GE, Maróti Z, Kalmár T, Bihari P, Nagy I, Pálfi G, Molnár E, Raskó I, Török T. Neparáczki E, et al. Among authors: kalmar t. PLoS One. 2017 Apr 19;12(4):e0174886. doi: 10.1371/journal.pone.0174886. eCollection 2017. PLoS One. 2017. PMID: 28422985 Free PMC article.

10

Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.

Szpisjak L, Nemeth VL, Szepfalusi N, Zadori D, Maroti Z, Kalmar T, Vecsei L, Klivenyi P. Szpisjak L, et al. Among authors: kalmar t. Cerebellum. 2017 Dec;16(5-6):979-985. doi: 10.1007/s12311-017-0870-9. Cerebellum. 2017. PMID: 28660440 No abstract available.

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