Refining the South Asian Origin of the Romani people

por Melegh, Bela I., Banfai, Zsolt, Hadzsiev, Kinga, Miseta, Attila, Melegh, Bela
Publicado 2017

Three periods of one and a half decade of ischemic stroke susceptibility gene research: lessons we have learned

por Maasz, Anita, Melegh, Bela
Publicado 2010

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

por Bánfai, Zsolt, Melegh, Béla I., Sümegi, Katalin, Hadzsiev, Kinga, Miseta, Attila, Kásler, Miklós, Melegh, Béla
Publicado 2019

Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations

por Nagy, Agnes, Sipeky, Csilla, Szalai, Renata, Melegh, Bela Imre, Matyas, Petra, Ganczer, Alma, Toth, Kalman, Melegh, Bela
Publicado 2015

Role of carnitine and its derivatives in the development and management of type 2 diabetes

por Bene, Judit, Hadzsiev, Kinga, Melegh, Bela
Publicado 2018

Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine Homeostasis

por Bene, Judit, Szabo, Andras, Komlósi, Katalin, Melegh, Bela
Publicado 2020

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(∗)G Alle...

por Farago, Bernadett, Kisfali, Peter, Magyari, Lili, Polgar, Noemi, Melegh, Bela
Publicado 2009

Reconstructing Roma History from Genome-Wide Data

por Moorjani, Priya, Patterson, Nick, Loh, Po-Ru, Lipson, Mark, Kisfali, Péter, Melegh, Bela I., Bonin, Michael, Kádaši, Ľudevít, Rieß, Olaf, Berger, Bonnie, Reich, David, Melegh, Béla
Publicado 2013

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

por Szalai, Renata, Till, Agnes, Szabo, Andras, Melegh, Bela, Hadzsiev, Kinga, Czako, Marta
Publicado 2023

Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype

por Szabo, Andras, Czako, Marta, Hadzsiev, Kinga, Duga, Balazs, Komlosi, Katalin, Melegh, Bela
Publicado 2015

Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients

por Czakó, Márta, Till, Ágnes, Szabó, András, Ripszám, Réka, Melegh, Béla, Hadzsiev, Kinga
Publicado 2019

Acylcarnitine esters profiling of serum and follicular fluid in patients undergoing in vitro fertilization

por Várnagy, Ákos, Bene, Judit, Sulyok, Endre, Kovács, Gábor L, Bódis, József, Melegh, Béla
Publicado 2013

Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature

por Buki, Gergely, Szalai, Renata, Pinter, Adrienn, Hadzsiev, Kinga, Melegh, Bela, Rauch, Tibor, Bene, Judit
Publicado 2023

Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome

por Komlósi, Katalin, Duga, Balázs, Hadzsiev, Kinga, Czakó, Márta, Kosztolányi, György, Fogarasi, András, Melegh, Béla
Publicado 2015

Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect

por Mutlu-Albayrak, Hatice, Bene, Judit, Oflaz, Mehmet Burhan, Tanyalçın, Tijen, Çaksen, Hüseyin, Melegh, Bela
Publicado 2015

Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

por Bánfai, Zsolt, Hadzsiev, Kinga, Pál, Endre, Komlósi, Katalin, Melegh, Márton, Balikó, László, Melegh, Béla
Publicado 2017

Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

por Bánfai, Zsolt, Hadzsiev, Kinga, Pál, Endre, Komlósi, Katalin, Melegh, Márton, Balikó, László, Melegh, Béla
Publicado 2017

Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data

por Bánfai, Zsolt, Ádám, Valerián, Pöstyéni, Etelka, Büki, Gergely, Czakó, Márta, Miseta, Attila, Melegh, Béla
Publicado 2018

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

por Ternák, Gábor, Márovics, Gergely, Sümegi, Katalin, Bánfai, Zsolt, Büki, Gergely, Magyari, Lili, Szabó, András, Melegh, Béla
Publicado 2023

IL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis

por Fischer, Sarah, Kövesdi, Erzsébet, Magyari, Lili, Csöngei, Veronika, Hadzsiev, Kinga, Melegh, Béla, Hegyi, Péter, Sarlós, Patrícia
Publicado 2017