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Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma
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Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma

Schrauwen, Isabelle ; Melegh, Béla I ; Chakchouk, Imen ; Acharya, Anushree ; Nasir, Abdul ; Poston, Alexis ; Cornejo-Sanchez, Diana M ; Szabo, Zsolt ; Karosi, Tamás ; Bene, Judit ; Melegh, Béla ; Leal, Suzanne M

European journal of human genetics : EJHG, 2019-06, Vol.27 (6), p.869-878 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
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Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty

Wang, Chuan-Chao ; Posth, Cosimo ; Furtwängler, Anja ; Sümegi, Katalin ; Bánfai, Zsolt ; Kásler, Miklós ; Krause, Johannes ; Melegh, Béla

Scientific reports, 2021-09, Vol.11 (1), p.19210-19210, Article 19210 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
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Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty

Wang, Chuan-Chao ; Posth, Cosimo ; Furtwängler, Anja ; Sümegi, Katalin ; Bánfai, Zsolt ; Kásler, Miklós ; Krause, Johannes ; Melegh, Béla

Scientific reports, 2022-05, Vol.12 (1), p.7157-7157, Article 7157 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Role of carnitine and its derivatives in the development and management of type 2 diabetes
Role of carnitine and its derivatives in the development and management of type 2 diabetes
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Role of carnitine and its derivatives in the development and management of type 2 diabetes

Bene, Judit ; Hadzsiev, Kinga ; Melegh, Bela

Nutrition & diabetes, 2018-03, Vol.8 (1), p.8-10, Article 8 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Characterization of Danube Swabian population samples on a high-resolution genome-wide basis
Characterization of Danube Swabian population samples on a high-resolution genome-wide basis
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Characterization of Danube Swabian population samples on a high-resolution genome-wide basis

Bánfai, Zsolt ; Kövesdi, Erzsébet ; Sümegi, Katalin ; Büki, Gergely ; Szabó, András ; Magyari, Lili ; Ádám, Valerián ; Pálos, Ferenc ; Miseta, Attila ; Kásler, Miklós ; Melegh, Béla

BMC genomics, 2023-01, Vol.24 (1), p.9-9, Article 9 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
New Clinical Genetics - 3rd edition
New Clinical Genetics - 3rd edition
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New Clinical Genetics - 3rd edition

Melegh, Béla

European Journal of Human Genetics, 2016-12, Vol.24 (12), p.1832-1837 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
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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Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

Bánfai, Zsolt ; Hadzsiev, Kinga ; Pál, Endre ; Komlósi, Katalin ; Melegh, Márton ; Balikó, László ; Melegh, Béla

BMC medical genetics, 2017-09, Vol.18 (1), p.105-105, Article 105 [Periódico revisado por pares]

England: BioMed Central Ltd

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8
Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions
Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions
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Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions

Büki, Gergely ; Zsigmond, Anna ; Czakó, Márta ; Szalai, Renáta ; Antal, Gréta ; Farkas, Viktor ; Fekete, György ; Nagy, Dóra ; Széll, Márta ; Tihanyi, Marianna ; Melegh, Béla ; Hadzsiev, Kinga ; Bene, Judit

Frontiers in genetics, 2021-06, Vol.12, p.673025-673025 [Periódico revisado por pares]

Frontiers Media S.A

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9
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
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Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'

Forzano, Francesca ; Antonova, Olga ; Clarke, Angus ; de Wert, Guido ; Hentze, Sabine ; Jamshidi, Yalda ; Moreau, Yves ; Perola, Markus ; Prokopenko, Inga ; Read, Andrew ; Reymond, Alexandre ; Stefansdottir, Vigdis ; van El, Carla ; Genuardi, Maurizio

European journal of human genetics : EJHG, 2023-03, Vol.31 (3), p.279-281 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians
Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians
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Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians

Ádám, Valerián ; Bánfai, Zsolt ; Sümegi, Katalin ; Büki, Gergely ; Szabó, András ; Magyari, Lili ; Miseta, Attila ; Kásler, Miklós ; Melegh, Béla

Frontiers in genetics, 2022-03, Vol.13, p.841769-841769 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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