Found: 106
Select item for more details and to access through your institution.
Reconstructing Roma History from Genome-Wide Data.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058633
- By:
- 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.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00558
- By:
- Publication type:
- Article
Refining the South Asian Origin of the Romani people.
- Published in:
- BMC Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12863-017-0547-x
- By:
- Publication type:
- Article
Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0262-4
- By:
- Publication type:
- Article
Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations.
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0262-4
- By:
- Publication type:
- Article
Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12.
- Published in:
- Molecular Biology & Evolution, 2007, v. 24, n. 6, p. 1300, doi. 10.1093/molbev/msm049
- By:
- Publication type:
- Article
Effect of hemodialysis session on the dynamics of carnitine ester profile changes in l-carnitine pretreated end-stage renal disease patients.
- Published in:
- International Urology & Nephrology, 2013, v. 45, n. 3, p. 847, doi. 10.1007/s11255-012-0209-x
- By:
- Publication type:
- Article
Depression comorbidity in spinocerebellar ataxia.
- Published in:
- Movement Disorders, 2011, v. 26, n. 5, p. 870, doi. 10.1002/mds.23698
- By:
- Publication type:
- Article
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.
- Published in:
- Movement Disorders, 2008, v. 23, n. 15, p. 2232, doi. 10.1002/mds.22288
- By:
- Publication type:
- Article
Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients.
- Published in:
- Movement Disorders, 2006, v. 21, n. 5, p. 699, doi. 10.1002/mds.20781
- By:
- Publication type:
- 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
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects.
- Published in:
- Rheumatology International, 2009, v. 29, n. 7, p. 793, doi. 10.1007/s00296-008-0771-9
- By:
- Publication type:
- Article
Detection and characterization of a divergent avian reovirus strain from a broiler chicken with central nervous system disease.
- Published in:
- 2013
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 183, doi. 10.1038/jhg.2010.156
- By:
- Publication type:
- Article
Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect.
- Published in:
- Case Reports in Genetics, 2015, v. 2015, p. 1, doi. 10.1155/2015/259627
- By:
- Publication type:
- Article
Emergence of Serotype G12 Rotaviruses, Hungary.
- Published in:
- Emerging Infectious Diseases, 2007, v. 13, n. 6, p. 916
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Polymorphisms of the IL23R Gene Are Associated with Psoriasis but not with Immunoglobulin A Nephropathy in a Hungarian Population.
- Published in:
- Inflammation, 2011, v. 34, n. 6, p. 603, doi. 10.1007/s10753-010-9268-2
- By:
- Publication type:
- Article
Erratum zu: Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa.
- Published in:
- 2022
- By:
- Publication type:
- Erratum
Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa.
- Published in:
- Medizinische Genetik, 2022, v. 34, n. 1, p. 81, doi. 10.1515/medgen-2022-2116
- By:
- Publication type:
- Article
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.
- Published in:
- 2022
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease.
- Published in:
- Neurogenetics, 2006, v. 7, n. 1, p. 27, doi. 10.1007/s10048-005-0023-z
- By:
- 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
- By:
- Publication type:
- Article
Assessment of DNA methylation at the interferon regulatory factor 5 ( IRF5) promoter region in inflammatory bowel diseases.
- Published in:
- International Journal of Colorectal Disease, 2010, v. 25, n. 5, p. 553, doi. 10.1007/s00384-010-0874-0
- By:
- 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
- By:
- Publication type:
- Article
Body Mass Index Decline Is Related to Spinocerebellar Ataxia Disease Progression.
- Published in:
- Movement Disorders Clinical Practice, 2017, v. 4, n. 5, p. 689, doi. 10.1002/mdc3.12522
- By:
- 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.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 2, p. 109, doi. 10.1159/000525976
- By:
- Publication type:
- Article
Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted TSC1/TSC2 Sequencing.
- Published in:
- Genes, 2021, v. 12, n. 9, p. 1401, doi. 10.3390/genes12091401
- By:
- Publication type:
- Article
Cytotoxic T lymphocyte-Associated Antigen +49G Variant Confers Risk for Anti-CCP- and Rheumatoid Factor-Positive Type of Rheumatoid Arthritis Only in Combination with CT60 GAllele.
- Published in:
- Autoimmune Diseases (2090-0422), 2010, p. 1, doi. 10.4061/2010/285974
- By:
- Publication type:
- Article
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice.
- Published in:
- EMBO Molecular Medicine, 2020, v. 12, n. 7, p. 1, doi. 10.15252/emmm.201911803
- By:
- Publication type:
- Article
Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 5, p. 375, doi. 10.1038/sj.ejhg.5200975
- By:
- Publication type:
- Article
The role of a bioresource research impact factor as an incentive to share human bioresources.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Polymorphisms in glutathione S-transferase are risk factors for perioperative acute myocardial infarction after cardiac surgery: a preliminary study.
- Published in:
- Molecular & Cellular Biochemistry, 2014, v. 389, n. 1/2, p. 79, doi. 10.1007/s11010-013-1929-7
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Similarities in Serum Acylcarnitine Patterns in Type 1 and Type 2 Diabetes Mellitus and in Metabolic Syndrome.
- Published in:
- Annals of Nutrition & Metabolism, 2013, v. 62, n. 1, p. 80, doi. 10.1159/000345759
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- Publication type:
- Article