Detalhe da pesquisa
1.
Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblings.
Exp Mol Pathol
; 115: 104471, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32446860
2.
Refining the South Asian Origin of the Romani people.
BMC Genet
; 18(1): 82, 2017 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28859608
3.
Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.
Mol Biol Rep
; 42(1): 227-32, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25297118
4.
Marked differences of haplotype tagging SNP distribution, linkage, and haplotype profile of IL23 receptor gene in Roma and Hungarian population samples.
Cytokine
; 65(2): 148-52, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24332578
5.
Difference of interleukin-23 receptor gene haplotype variants in ulcerative colitis compared to Crohn's disease and psoriasis.
Inflamm Res
; 62(2): 195-200, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23093364
6.
Marked diversity of IL23R gene haplotype variants in rheumatoid arthritis comparing with Crohn's disease and ankylosing spondylitis.
Mol Biol Rep
; 40(1): 359-63, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23054009
7.
High prevalence of CYP2C19*2 allele in Roma samples: study on Roma and Hungarian population samples with review of the literature.
Mol Biol Rep
; 40(8): 4727-35, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23645039
8.
Differences in circulating carnitine status of preterm infants fed fortified human milk or preterm infant formula.
J Pediatr Gastroenterol Nutr
; 57(5): 673-6, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23783025
9.
Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.
Mol Biol Rep
; 42(1): 317, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25366175
10.
Intrafamilial variability of limb-girdle muscular dystrophy, LGMD1D type.
Eur J Med Genet
; 63(2): 103655, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31034989
11.
Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area.
Front Genet
; 10: 558, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31263480
12.
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma.
Eur J Hum Genet
; 27(6): 869-878, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30872814
13.
Marked Differences of Haplotype Tagging SNP Distribution, Linkage, and Haplotype Profile of APOA5 Gene in Roma Population Samples.
Pathol Oncol Res
; 23(4): 853-861, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28102463
14.
Interethnic variability of CYP4F2 (V433M) in admixed population of Roma and Hungarians.
Environ Toxicol Pharmacol
; 40(1): 280-3, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26176903
15.
Hodgkin disease therapy induced second malignancy susceptibility 6q21 functional variants in roma and hungarian population samples.
Pathol Oncol Res
; 20(3): 529-33, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24306881
16.
Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.
JIMD Rep
; 9: 105-111, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23430555
17.
Reconstructing Roma history from genome-wide data.
PLoS One
; 8(3): e58633, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23516520
18.
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.
JIMD Rep
; 9: E1, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23832234