Kalmár T - Search Results

1

correctKin: an optimized method to infer relatedness up to the 4th degree from low-coverage ancient human genomes.

Nyerki E, Kalmár T, Schütz O, Lima RM, Neparáczki E, Török T, Maróti Z. Nyerki E, et al. Among authors: kalmar t. Genome Biol. 2023 Feb 28;24(1):38. doi: 10.1186/s13059-023-02882-4. Genome Biol. 2023. PMID: 36855115 Free PMC article.

2

Regulated fluctuations in nanog expression mediate cell fate decisions in embryonic stem cells.

Kalmar T, Lim C, Hayward P, Muñoz-Descalzo S, Nichols J, Garcia-Ojalvo J, Martinez Arias A. Kalmar T, et al. PLoS Biol. 2009 Jul;7(7):e1000149. doi: 10.1371/journal.pbio.1000149. Epub 2009 Jul 7. PLoS Biol. 2009. PMID: 19582141 Free PMC article.

3

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.

4

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.

5

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.

6

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.

7

High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder.

Tombácz D, Maróti Z, Kalmár T, Csabai Z, Balázs Z, Takahashi S, Palkovits M, Snyder M, Boldogkői Z. Tombácz D, et al. Among authors: kalmar t. Sci Rep. 2017 Aug 2;7(1):7106. doi: 10.1038/s41598-017-06522-3. Sci Rep. 2017. PMID: 28769055 Free PMC article.

8

Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.

Iványi B, Rácz GZ, Gál P, Brinyiczki K, Bódi I, Kalmár T, Maróti Z, Bereczki C. Iványi B, et al. Among authors: kalmar t. Pediatr Nephrol. 2018 Mar;33(3):439-446. doi: 10.1007/s00467-017-3814-1. Epub 2017 Oct 14. Pediatr Nephrol. 2018. PMID: 29032433

9

Partial RAG deficiency in a patient with varicella infection, autoimmune cytopenia, and anticytokine antibodies.

Goda V, Malik A, Kalmar T, Maroti Z, Patel B, Ujhazi B, Csomos K, Hale JE, Chen K, Bleesing J, Palma P, Cancrini C, Comeau AM, Krivan G, Walter JE. Goda V, et al. Among authors: kalmar t. J Allergy Clin Immunol Pract. 2018 Sep-Oct;6(5):1769-1771.e2. doi: 10.1016/j.jaip.2018.01.015. Epub 2018 Feb 2. J Allergy Clin Immunol Pract. 2018. PMID: 29410113 Free PMC article. No abstract available.

10

Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.

Szabó T, Orosz P, Balogh E, Jávorszky E, Máttyus I, Bereczki C, Maróti Z, Kalmár T, Szabó AJ, Reusz G, Várkonyi I, Marián E, Gombos É, Orosz O, Madar L, Balla G, Kappelmayer J, Tory K, Balogh I. Szabó T, et al. Among authors: kalmar t. Pediatr Nephrol. 2018 Oct;33(10):1713-1721. doi: 10.1007/s00467-018-3992-5. Epub 2018 Jun 28. Pediatr Nephrol. 2018. PMID: 29956005

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