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Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00558
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- Publication type:
- Article
Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data.
- Published in:
- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0202890
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- Publication type:
- Article
Acylcarnitine esters profiling of serum and follicular fluid in patients undergoing in vitro fertilization.
- Published in:
- Reproductive Biology & Endocrinology, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1477-7827-11-67
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- Publication type:
- Article
Detection and characterization of a divergent avian reovirus strain from a broiler chicken with central nervous system disease.
- Published in:
- 2013
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- Publication type:
- Report
Molecular analysis of the VP7 gene of pheasant rotaviruses identifies a new genotype, designated G23.
- Published in:
- Archives of Virology, 2009, v. 154, n. 8, p. 1365, doi. 10.1007/s00705-009-0439-0
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- Publication type:
- Article
Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible Pathomechanisms.
- Published in:
- Antibiotics (2079-6382), 2023, v. 12, n. 6, p. 1029, doi. 10.3390/antibiotics12061029
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- Publication type:
- Article
Emergence of Serotype G12 Rotaviruses, Hungary.
- Published in:
- Emerging Infectious Diseases, 2007, v. 13, n. 6, p. 916
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- Publication type:
- Article
Towards a European consensus for reporting incidental findings during clinical NGS testing.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1601, doi. 10.1038/ejhg.2015.111
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- Publication type:
- Article
Search for Factor V Arg[sup 306] Cambridge and Hong Kong Mutations in Mixed Hungarian Population Samples.
- Published in:
- Acta Haematologica, 2003, v. 110, n. 4, p. 220, doi. 10.1159/000074233
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- Publication type:
- Article
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
- Published in:
- 2022
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- Publication type:
- journal article
Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4935, doi. 10.3390/ijms20194935
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- Publication type:
- Article
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
- Published in:
- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0463-y
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- Publication type:
- Article
Interaction between CTLA4 gene and IBD5 locus in Hungarian Crohn's disease patients.
- Published in:
- International Journal of Colorectal Disease, 2011, v. 26, n. 9, p. 1119, doi. 10.1007/s00384-011-1202-z
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- Publication type:
- Article
IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn’s disease in Hungarian patients.
- Published in:
- International Journal of Colorectal Disease, 2009, v. 24, n. 5, p. 503, doi. 10.1007/s00384-009-0670-x
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- Publication type:
- Article
Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.673025
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- Publication type:
- Article
Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.635458
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- Publication type:
- Article
Urinary glycosaminoglycan excretion in healthy and stone-forming children.
- Published in:
- Pediatric Nephrology, 1996, v. 10, n. 5, p. 555, doi. 10.1007/s004670050159
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- Publication type:
- Article
DNA profiling of Hungarian King Béla III and other skeletal remains originating from the Royal Basilica of Székesfehérvár.
- Published in:
- Archaeological & Anthropological Sciences, 2019, v. 11, n. 4, p. 1345, doi. 10.1007/s12520-018-0609-7
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- Publication type:
- Article
Reconstructing Roma History from Genome-Wide Data.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058633
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- Publication type:
- Article
Evaluation of a Partial Genome Screening of Two Asthma Susceptibility Regions Using Bayesian Network Based Bayesian Multilevel Analysis of Relevance.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033573
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- Publication type:
- Article
Genetic Structure of Europeans: A View from the North-East.
- Published in:
- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005472
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- Publication type:
- Article
Súlyos epilepsziás encephalopathia hátterében azonosított MECP2-gén-mutáció fiúbetegben.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2019, v. 160, n. 51, p. 2036, doi. 10.1556/650.2019.31520
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- Publication type:
- Article
Generalizált epilepszia hátterében azonosított ioncsatorna-génmutáció ritka formája.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2019, v. 160, n. 21, p. 835, doi. 10.1556/650.2019.31404
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- Publication type:
- Article
Rhabdomyolysis – Mikor vessük fel metabolikus myopathia lehetőségét? Esetismertetés és diagnosztikus algoritmus: Rhabdomyolysis – may it be a metabolic myopathy? Case report and diagnostic algorithm.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2017, v. 158, n. 47, p. 1873, doi. 10.1556/650.2017.30923
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- Publication type:
- Article
Neuroacanthocytosis diagnózisa új generációs exom-szekvenálással Neuroacanthocytosis diagnosis with new generation whole exome sequencing.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2017, v. 158, n. 42, p. 1681, doi. 10.1556/650.2017.30880
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- Publication type:
- Article
A nagyobb méretű géndeletiók jelentősége a sclerosis tuberosa diagnosztikájában: az első magyar esetek bemutatása: Importance of gross deletions in the diagnosis of tuberous sclerosis complex: the first Hungarian cases
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2017, v. 158, n. 30, p. 1188, doi. 10.1556/650.2017.30789
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- Publication type:
- Article
Két generációban megfigyelhető mitokondriális DNS A8344G mutáció.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2017, v. 158, n. 12, p. 468, doi. 10.1556/650.2017.30634
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- Publication type:
- Article
Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.841769
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- Publication type:
- Article
Detection of mutations by flow cytometric melting point analysis of PCR products.
- Published in:
- Cytometry. Part A, 2011, v. 79A, n. 9, p. 720, doi. 10.1002/cyto.a.21104
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- Publication type:
- Article
Triglyceride Level-Influencing Functional Variants of the ANGPTL3, CILP2, and TRIB1 Loci in Ischemic Stroke.
- Published in:
- NeuroMolecular Medicine, 2011, v. 13, n. 3, p. 179, doi. 10.1007/s12017-011-8149-7
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- Publication type:
- Article
Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98796-x
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- Publication type:
- Article
Characterization of Danube Swabian population samples on a high-resolution genome-wide basis.
- Published in:
- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-022-09092-5
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- Publication type:
- Article
Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
- Published in:
- 2015
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- Publication type:
- Case Study
GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?
- Published in:
- Cardiovascular Diabetology, 2010, v. 9, p. 79, doi. 10.1186/1475-2840-9-79
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- Publication type:
- Article
Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 5, p. 649, doi. 10.1007/s00415-008-0768-z
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- Publication type:
- Article
Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke.
- Published in:
- Journal of Molecular Neuroscience, 2010, v. 41, n. 1, p. 121, doi. 10.1007/s12031-009-9301-9
- By:
- Publication type:
- Article
Apolipoprotein A5 gene promoter region T-1131C polymorphism associates with elevated circulating triglyceride levels and confers susceptibility for development of ischemic stroke.
- Published in:
- Journal of Molecular Neuroscience, 2006, v. 29, n. 2, p. 177, doi. 10.1385/JMN:29:2:177
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- Publication type:
- Article
Angiotensin II type-1 receptor A1166C polymorphism is associated with increased risk of ischemic stroke in hypertensive smokers.
- Published in:
- Journal of Molecular Neuroscience, 2006, v. 28, n. 3, p. 285, doi. 10.1385/JMN:28:3:285
- By:
- Publication type:
- Article
Lymphotoxin-α gene 252G allelic variant is a risk factor for large-vessel-associated ischemic stroke.
- Published in:
- Journal of Molecular Neuroscience, 2005, v. 27, n. 2, p. 205, doi. 10.1385/JMN:27:2:205
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- Publication type:
- Article
Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 2, p. 1949, doi. 10.1007/s11033-011-0942-8
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- Publication type:
- Article
Stepwise Positive Association Between APOA5 Minor Allele Frequencies and Increasing Plasma Triglyceride Quartiles in Random Patients with Hypertriglyceridemia of Unclarified Origin.
- Published in:
- Pathology & Oncology Research, 2011, v. 17, n. 1, p. 39, doi. 10.1007/s12253-010-9273-7
- By:
- Publication type:
- Article
Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome.
- Published in:
- Pathology & Oncology Research, 2007, v. 13, n. 3, p. 243, doi. 10.1007/BF02893505
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- Publication type:
- Article
Prevalence of SLC22A4 1672T and SLC22A5 −207C combination defined TC haplotype in Hungarian ulcerative colitis patients.
- Published in:
- Pathology & Oncology Research, 2007, v. 13, n. 1, p. 53, doi. 10.1007/BF02893441
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- Publication type:
- Article
Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation.
- Published in:
- Pathology & Oncology Research, 2005, v. 11, n. 2, p. 82, doi. 10.1007/BF02893371
- By:
- Publication type:
- Article
Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2005, v. 43, n. 8, p. 862, doi. 10.1515/CCLM.2005.145
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- Publication type:
- Article
Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the <italic>IGF1R</italic> gene.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 2, p. 443, doi. 10.1002/ajmg.a.38566
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- Publication type:
- Article
Partial Trisomy of the Pericentromeric Region of Chromosome 5 in a Girl with Binder Phenotype.
- Published in:
- Cytogenetic & Genome Research, 2015, v. 144, n. 3, p. 190, doi. 10.1159/000369653
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- Publication type:
- Article
One Year Survey of Human Rotavirus Strains Suggests the Emergence of Genotype G12 in Cameroon.
- Published in:
- Journal of Medical Virology, 2013, v. 85, n. 8, p. 1485, doi. 10.1002/jmv.23603
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- Publication type:
- Article
Genetic diversity and zoonotic potential of human rotavirus strains, 2003-2006, hungary.
- Published in:
- Journal of Medical Virology, 2009, v. 81, n. 2, p. 362, doi. 10.1002/jmv.21375
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- Publication type:
- Article