A. Maász

D. Molnár, B. Melegh, N. Polgar, 2011, International journal of pediatric obesity : IJPO : an official journal of the International Association for the Study of Obesity.

[Genetics of ischemic stroke: where are we now?].

B. Melegh, Z. Szolnoki, L. Balikó, 2011, Orvosi hetilap.

Hodgkin Disease Therapy Induced Second Malignancy Susceptibility 6q21 Functional Variants in Roma and Hungarian Population Samples

B. Melegh, P. Kisfali, D. Várszegi, 2014, Pathology & Oncology Research.

Apolipoprotein A5 T-1131C variant confers risk for metabolic syndrome

B. Melegh, L. Markó, C. Sipeky, 2008, Pathology & Oncology Research.

Triglyceride Level-Influencing Functional Variants of the ANGPTL3, CILP2, and TRIB1 Loci in Ischemic Stroke

B. Melegh, N. Polgar, C. Sipeky, 2011, NeuroMolecular Medicine.

Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis

L. Czirják, B. Melegh, C. Sipeky, 2007, Annals of the rheumatic diseases.

Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation

B. Melegh, R. Kellermayer, K. Hollódy, 2008, Pathology & Oncology Research.

Triglyceride level modifying functional variants of GALTN2 and MLXIPL in patients with ischaemic stroke

B. Melegh, N. Polgar, C. Sipeky, 2010, European journal of neurology.

A Polymorphism within the Fructosamine-3-kinase Gene is Associated with HbA1c Levels and the Onset of Type 2 Diabetes Mellitus

B. Melegh, I. Wittmann, P. Kisfali, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

The combination of homozygous MTHFR 677T and angiotensin II type-1 receptor 1166C variants confers the risk of small-vessel-associated ischemic stroke

A. Kondacs, M. Szabó, B. Melegh, 2007, Journal of Molecular Neuroscience.

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

B. Melegh, E. Kóvesdi, B. Duga, 2017, Pathology & Oncology Research.

Mitochondrial DNA 11777C>A Mutation Associated Leigh Syndrome: Case Report with a Review of the Previously Described Pedigrees

E. Berényi, B. Melegh, P. Kisfali, 2010, NeuroMolecular Medicine.

Prevalence of functional haplotypes of the peptidylarginine deiminase citrullinating enzyme gene in patients with rheumatoid arthritis: no influence of the presence of anti-citrullinated peptide antibodies.

L. Czirják, B. Melegh, P. Kisfali, 2007, Clinical and experimental rheumatology.

[Mitochondrial DNA and its mutations: new advances in a new field].

B. Melegh, C. Sipeky, E. Sáfrány, 2007, Orvosi hetilap.

Haplotype analysis of the apolipoprotein A5 gene in patients with the metabolic syndrome.

B. Melegh, L. Markó, B. Gasztonyi, 2010, Nutrition, metabolism, and cardiovascular diseases : NMCD.