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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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- Article
Refining the South Asian Origin of the Romani people.
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- BMC Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12863-017-0547-x
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- Publication type:
- Article
Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00558
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- Article
Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.
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- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0262-4
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- Publication type:
- Article
Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.
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- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0262-4
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- Publication type:
- Article
Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.
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- Movement Disorders Clinical Practice, 2017, v. 4, n. 5, p. 689, doi. 10.1002/mdc3.12522
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- Publication type:
- Article
Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty.
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- 2022
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- Publication type:
- Correction Notice
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
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.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.635458
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- Publication type:
- Article
Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate.
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- Molecular Syndromology, 2023, v. 14, n. 2, p. 109, doi. 10.1159/000525976
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- Publication type:
- Article
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice.
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- EMBO Molecular Medicine, 2020, v. 12, n. 7, p. 1, doi. 10.15252/emmm.201911803
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- Article
Polymorphisms of the IL23R Gene Are Associated with Psoriasis but not with Immunoglobulin A Nephropathy in a Hungarian Population.
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- Inflammation, 2011, v. 34, n. 6, p. 603, doi. 10.1007/s10753-010-9268-2
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- Article
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
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- 2022
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- Publication type:
- journal article
Epilepsy in Rett syndrome-Lessons from the Rett networked database.
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- Epilepsia (Series 4), 2015, v. 56, n. 4, p. 569, doi. 10.1111/epi.12941
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- Publication type:
- Article
Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 19, p. 4935, doi. 10.3390/ijms20194935
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- Publication type:
- Article
One Year Survey of Human Rotavirus Strains Suggests the Emergence of Genotype G12 in Cameroon.
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- Journal of Medical Virology, 2013, v. 85, n. 8, p. 1485, doi. 10.1002/jmv.23603
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- Article
Genetic diversity and zoonotic potential of human rotavirus strains, 2003-2006, hungary.
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- Journal of Medical Virology, 2009, v. 81, n. 2, p. 362, doi. 10.1002/jmv.21375
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- Publication type:
- Article
One‐year survey of astrovirus infection in children with gastroenteritis in a large hospital in Hungary: Occurrence and genetic analysis of astroviruses.
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- Journal of Medical Virology, 2004, v. 74, n. 1, p. 71
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- Publication type:
- Article
Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome.
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- 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.
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- 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.
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- Pathology & Oncology Research, 2005, v. 11, n. 2, p. 82, doi. 10.1007/BF02893371
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- Publication type:
- Article
Spinocerebellar Ataxia Type 2 (SCA2): Identification of Early Brain Degeneration in One Monozygous Twin in the Initial Disease Stage.
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- Cerebellum, 2011, v. 10, n. 2, p. 245, doi. 10.1007/s12311-010-0239-9
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- Publication type:
- Article
Falls in Spinocerebellar Ataxias: Results of the EuroSCA Fall Study.
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- Cerebellum, 2010, v. 9, n. 2, p. 232, doi. 10.1007/s12311-010-0155-z
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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.
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- Antibiotics (2079-6382), 2023, v. 12, n. 6, p. 1029, doi. 10.3390/antibiotics12061029
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- Publication type:
- Article
Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 7, p. 1, doi. 10.1002/mgg3.2166
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- Publication type:
- Article
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
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- Journal of Human Genetics, 2011, v. 56, n. 3, p. 183, doi. 10.1038/jhg.2010.156
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- Article
Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.
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- Case Reports in Genetics, 2015, v. 2015, p. 1, doi. 10.1155/2015/259627
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- Article
Emergence of Serotype G12 Rotaviruses, Hungary.
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- Emerging Infectious Diseases, 2007, v. 13, n. 6, p. 916
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- Publication type:
- Article
Reference materials (RMs) for analysis of the human factor II (prothrombin) gene G20210A mutation.
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- 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.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 2, p. 443, doi. 10.1002/ajmg.a.38566
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- Article
The role of a bioresource research impact factor as an incentive to share human bioresources.
- Published in:
- 2011
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- Publication type:
- Letter
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
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- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0463-y
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- Publication type:
- Article
Functional Variants of Glucokinase Regulatory Protein and Apolipoprotein A5 Genes in Ischemic Stroke.
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- Journal of Molecular Neuroscience, 2010, v. 41, n. 1, p. 121, doi. 10.1007/s12031-009-9301-9
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- Publication type:
- Article
The combination of homozygous MTHFR 677T and angiotensin II type-1 receptor 1166C variants confers the risk of small-vessel-associated ischemic stroke.
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- Journal of Molecular Neuroscience, 2007, v. 31, n. 3, p. 201, doi. 10.1385/JMN:31:03:201
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- 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.
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- 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.
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- Journal of Molecular Neuroscience, 2006, v. 28, n. 3, p. 285, doi. 10.1385/JMN:28:3:285
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- Publication type:
- Article
Lymphotoxin-α gene 252G allelic variant is a risk factor for large-vessel-associated ischemic stroke.
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- 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
Assessment of DNA methylation at the interferon regulatory factor 5 ( IRF5) promoter region in inflammatory bowel diseases.
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- International Journal of Colorectal Disease, 2010, v. 25, n. 5, p. 553, doi. 10.1007/s00384-010-0874-0
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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.
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- 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
MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin.
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- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0124232
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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.
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- 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.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005472
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- Publication type:
- Article
Apolipoprotein A5 gene C56G variant confers risk for the development of large-vessel associated ischemic stroke.
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- Journal of Neurology, 2008, v. 255, n. 5, p. 649, doi. 10.1007/s00415-008-0768-z
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- Publication type:
- Article
Changes of plasma free amino acids and renal clearances of carnitines in premature infants during L-carnitine-supplemented human milk feeding.
- Published in:
- 1988
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- Publication type:
- journal article
Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease.
- Published in:
- Human Genetics, 2006, v. 120, n. 2, p. 285, doi. 10.1007/s00439-006-0221-2
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- Publication type:
- Article
Detection of mutations by flow cytometric melting point analysis of PCR products.
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- Cytometry. Part A, 2011, v. 79A, n. 9, p. 720, doi. 10.1002/cyto.a.21104
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- Publication type:
- Article
Urovysion: Considerations on modifying current evaluation scheme, including immunophenotypic targeting and locally set, statistically derived diagnostic criteria.
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- Cytometry. Part A, 2011, v. 79A, n. 5, p. 375, doi. 10.1002/cyto.a.21065
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- Publication type:
- Article
Towards a European consensus for reporting incidental findings during clinical NGS testing.
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- 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
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.
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- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 375, doi. 10.1038/sj.ejhg.5200975
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- Publication type:
- Article