K. Sümegi

发表

Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples

J. Bene, B. Melegh, C. Sipeky, 2014, Molecular Biology Reports.

Stepwise Positive Association Between APOA5 Minor Allele Frequencies and Increasing Plasma Triglyceride Quartiles in Random Patients with Hypertriglyceridemia of Unclarified Origin

B. Melegh, I. Wittmann, P. Kisfali, 2011, Pathology & Oncology Research.

Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples

J. Bene, B. Melegh, C. Sipeky, 2014, Molecular Biology Reports.

Characterization of Danube Swabian population samples on a high-resolution genome-wide basis

B. Melegh, A. Miseta, M. Kásler, 2023, BMC Genomics.

Investigating the genetic characteristics of the Csangos, a traditionally Hungarian speaking ethnic group residing in Romania

B. Melegh, A. Miseta, K. Sümegi, 2020, Journal of Human Genetics.

Investigating the genetic characteristics of the Csangos, a traditionally Hungarian speaking ethnic group residing in Romania

B. Melegh, A. Miseta, K. Sümegi, 2020, Journal of Human Genetics.

Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area

B. Melegh, A. Miseta, M. Kásler, 2019, Front. Genet..

Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty

J. Krause, C. Posth, B. Melegh, 2021, Scientific Reports.

Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians

B. Melegh, A. Miseta, M. Kásler, 2022, Frontiers in Genetics.

[Identifying rare genomic disorders with array comparative genomic hybridization in Hungary].

B. Melegh, P. Kisfali, K. Komlosi, 2014, Orvosi hetilap.

GCKR gene functional variants in type 2 diabetes and metabolic syndrome: do the rare variants associate with increased carotid intima-media thickness?

B. Melegh, N. Polgar, E. Fehér, 2010, Cardiovascular diabetology.

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

A. Need, C. Tregidgo, J. Clayton-Smith, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Mutations of the apolipoprotein A5 gene with inherited hypertriglyceridaemia: review of the current literature.

B. Melegh, S. Komoly, P. Kisfali, 2012, Current medicinal chemistry.

GCKR gene functional variants in type 2 diabetes and metabolic syndrome : do the rare variants associate with increased carotid intima-media thickness ?

B. Melegh, N. Polgar, E. Fehér, 2010 .

Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible Pathomechanisms

B. Melegh, A. Szabó, G. Ternák, 2023, Antibiotics.

[Attention deficit hyperactivity disorder analyzed with array comparative genome hybridization method. Case report].

B. Melegh, P. Kisfali, K. Komlosi, 2014, Orvosi hetilap.