Melegh B - Search Results

1

Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area.

Bánfai Z, Melegh BI, Sümegi K, Hadzsiev K, Miseta A, Kásler M, Melegh B. Bánfai Z, et al. Among authors: melegh b, melegh bi. Front Genet. 2019 Jun 13;10:558. doi: 10.3389/fgene.2019.00558. eCollection 2019. Front Genet. 2019. PMID: 31263480 Free PMC article.

2

Refining the South Asian Origin of the Romani people.

Melegh BI, Banfai Z, Hadzsiev K, Miseta A, Melegh B. Melegh BI, et al. Among authors: melegh b. BMC Genet. 2017 Aug 31;18(1):82. doi: 10.1186/s12863-017-0547-x. BMC Genet. 2017. PMID: 28859608 Free PMC article.

3

Marked Differences of Haplotype Tagging SNP Distribution, Linkage, and Haplotype Profile of APOA5 Gene in Roma Population Samples.

Sumegi K, Duga B, Melegh BI, Banfai Z, Kovesdi E, Maasz A, Melegh B. Sumegi K, et al. Among authors: melegh b, melegh bi. Pathol Oncol Res. 2017 Oct;23(4):853-861. doi: 10.1007/s12253-017-0197-3. Epub 2017 Jan 19. Pathol Oncol Res. 2017. PMID: 28102463 Free article.

4

High prevalence of CYP2C19*2 allele in Roma samples: study on Roma and Hungarian population samples with review of the literature.

Sipeky C, Weber A, Szabo M, Melegh BI, Janicsek I, Tarlos G, Szabo I, Sumegi K, Melegh B. Sipeky C, et al. Among authors: melegh b, melegh bi. Mol Biol Rep. 2013 Aug;40(8):4727-35. doi: 10.1007/s11033-013-2569-4. Epub 2013 May 5. Mol Biol Rep. 2013. PMID: 23645039 Review.

5

Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.

Janicsek I, Sipeky C, Bene J, Duga B, Melegh BI, Sümegi K, Jaromi L, Magyari L, Melegh B. Janicsek I, et al. Among authors: melegh b, melegh bi. Mol Biol Rep. 2015 Jan;42(1):227-32. doi: 10.1007/s11033-014-3762-9. Epub 2014 Oct 9. Mol Biol Rep. 2015. PMID: 25297118

6

Intrafamilial variability of limb-girdle muscular dystrophy, LGMD1D type.

Zima J, Eaton A, Pál E, Till Á, Ito YA, Warman-Chardon J, Hartley T, Cagnone G, Melegh BI; Care4Rare Canada; Boycott KM, Melegh B, Hadzsiev K. Zima J, et al. Among authors: melegh b, melegh bi. Eur J Med Genet. 2020 Feb;63(2):103655. doi: 10.1016/j.ejmg.2019.04.012. Epub 2019 Apr 27. Eur J Med Genet. 2020. PMID: 31034989

7

Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.

Janicsek I, Sipeky C, Bene J, Duga B, Melegh BI, Sümegi K, Jaromi L, Magyari L, Melegh B. Janicsek I, et al. Among authors: melegh b, melegh bi. Mol Biol Rep. 2015 Jan;42(1):317. doi: 10.1007/s11033-014-3798-x. Mol Biol Rep. 2015. PMID: 25366175 No abstract available.

8

Hodgkin disease therapy induced second malignancy susceptibility 6q21 functional variants in roma and hungarian population samples.

Varszegi D, Duga B, Melegh BI, Sumegi K, Kisfali P, Maasz A, Melegh B. Varszegi D, et al. Among authors: melegh b, melegh bi. Pathol Oncol Res. 2014 Jul;20(3):529-33. doi: 10.1007/s12253-013-9724-z. Epub 2013 Dec 5. Pathol Oncol Res. 2014. PMID: 24306881 Free article.

9

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Melegh B, Ablonczy M, Németh K, Fekete G. Komlósi K, et al. Among authors: melegh b, melegh bi. JIMD Rep. 2013;9:105-111. doi: 10.1007/8904_2012_187. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23430555 Free PMC article.

10

Erratum to: Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Komlósi K, Maász A, Kisfali P, Hadzsiev K, Bene J, Melegh BI, Ablonczy M, Németh K, Fekete G, Melegh B. Komlósi K, et al. Among authors: melegh b, melegh bi. JIMD Rep. 2013;9:E1. doi: 10.1007/978-3-642-35518-9_195. Epub 2012 Nov 2. JIMD Rep. 2013. PMID: 23832234 Free PMC article. No abstract available.

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