Refining the South Asian Origin of the Romani people by Bela I. Melegh, Zsolt Banfai, Kinga Hadzsiev, Attila Miseta, Bela Melegh

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Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area by Zsolt Bánfai, Zsolt Bánfai, Béla I. Melegh, Béla I. Melegh, Katalin Sümegi, Katalin Sümegi, Kinga Hadzsiev, Kinga Hadzsiev, Attila Miseta, Miklós Kásler, Béla Melegh, Béla Melegh

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Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation by Márta Czakó, Márta Czakó, Ágnes Till, Judith Zima, Anna Zsigmond, András Szabó, András Szabó, Anita Maász, Anita Maász, Béla Melegh, Béla Melegh, Kinga Hadzsiev, Kinga Hadzsiev

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Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions by Gergely Büki, Gergely Büki, Anna Zsigmond, Márta Czakó, Márta Czakó, Renáta Szalai, Renáta Szalai, Gréta Antal, Viktor Farkas, György Fekete, Dóra Nagy, Márta Széll, Marianna Tihanyi, Béla Melegh, Béla Melegh, Béla Melegh, Kinga Hadzsiev, Kinga Hadzsiev, Judit Bene, Judit Bene, Judit Bene

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Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians by Valerián Ádám, Zsolt Bánfai, Zsolt Bánfai, Katalin Sümegi, Katalin Sümegi, Gergely Büki, Gergely Büki, András Szabó, András Szabó, Lili Magyari, Lili Magyari, Attila Miseta, Miklós Kásler, Béla Melegh, Béla Melegh

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

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Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature by Gergely Buki, Renata Szalai, Adrienn Pinter, Kinga Hadzsiev, Bela Melegh, Tibor Rauch, Judit Bene

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Revealing the impact of the Caucasus region on the genetic legacy of Romani people from genome-wide data. by Zsolt Bánfai, Valerián Ádám, Etelka Pöstyéni, Gergely Büki, Márta Czakó, Attila Miseta, Béla Melegh

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Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect by Hatice Mutlu-Albayrak, Judit Bene, Mehmet Burhan Oflaz, Tijen Tanyalçın, Hüseyin Çaksen, Bela Melegh

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Down-Syndrome-Related Maternal Dysbiosis Might Be Triggered by Certain Classes of Antibiotics: A New Insight into the Possible Pathomechanisms by Gábor Ternák, Gergely Márovics, Katalin Sümegi, Zsolt Bánfai, Gergely Büki, Lili Magyari, András Szabó, Béla Melegh

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Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty by Chuan-Chao Wang, Cosimo Posth, Anja Furtwängler, Katalin Sümegi, Zsolt Bánfai, Miklós Kásler, Johannes Krause, Béla Melegh

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Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty by Chuan‑Chao Wang, Cosimo Posth, Anja Furtwängler, Katalin Sümegi, Zsolt Bánfai, Miklós Kásler, Johannes Krause, Béla Melegh

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Emergence of Serotype G12 Rotaviruses, Hungary by Krisztián Bányai, Ágnes Bogdán, Péter Kisfali, Péter Molnár, Ilona Mihály, Béla Melegh, Vito Martella, Jon R. Gentsch, György Szücs

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Characterization of Danube Swabian population samples on a high-resolution genome-wide basis by Zsolt Bánfai, Erzsébet Kövesdi, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Valerián Ádám, Ferenc Pálos, Attila Miseta, Miklós Kásler, Béla Melegh

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Analysis of Gyimes Csango population samples on a high-resolution genome-wide basis by Zsolt Bánfai, Gergely Büki, Valerián Ádám, Katalin Sümegi, András Szabó, Kinga Hadzsiev, Krisztián Erős, Ferenc Gallyas, Attila Miseta, Miklós Kásler, Béla Melegh

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Reconstructing Roma history from genome-wide data. by Priya Moorjani, Nick Patterson, Po-Ru Loh, Mark Lipson, Péter Kisfali, Bela I Melegh, Michael Bonin, Ludevít Kádaši, Olaf Rieß, Bonnie Berger, David Reich, Béla Melegh

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Rare disease education in Europe and beyond: time to act by Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth Baynam

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Evaluation of a partial genome screening of two asthma susceptibility regions using bayesian network based bayesian multilevel analysis of relevance. by Ildikó Ungvári, Gábor Hullám, Péter Antal, Petra Sz Kiszel, András Gézsi, Éva Hadadi, Viktor Virág, Gergely Hajós, András Millinghoffer, Adrienne Nagy, András Kiss, Ágnes F Semsei, Gergely Temesi, Béla Melegh, Péter Kisfali, Márta Széll, András Bikov, Gabriella Gálffy, Lilla Tamási, András Falus, Csaba Szalai

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Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International by Domenica Taruscio, Marco Salvatore, Aimè Lumaka, Aimè Lumaka, Claudio Carta, Laura L. Cellai, Gianluca Ferrari, Savino Sciascia, Stephen Groft, Yasemin Alanay, Maleeha Azam, Gareth Baynam, Helene Cederroth, Eva Maria Cutiongco-de la Paz, Vajira Harshadeva Weerabaddana Dissanayake, Roberto Giugliani, Claudia Gonzaga-Jauregui, Dineshani Hettiarachchi, Oleg Kvlividze, Guida Landoure, Prince Makay, Béla Melegh, Ugur Ozbek, Ratna Dua Puri, Vanessa Romero, Vinod Scaria, Saumya S. Jamuar, Saumya S. Jamuar, Vorasuk Shotelersuk, Dario Roccatello, William A. Gahl, Samuel A. Wiafe, Olaf Bodamer, Manuel Posada

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A global survey about undiagnosed rare diseases: perspectives, challenges, and solutions by Simone Baldovino, Savino Sciascia, Claudio Carta, Marco Salvatore, Laura L. Cellai, Gianluca Ferrari, Aimé Lumaka, Stephen Groft, Yasemin Alanay, Maleeha Azam, Gareth Baynam, Helene Cederroth, Eva Maria Cutiongco-de la Paz, Vajira Harshadeva Weerabaddana Dissanayake, Roberto Giugliani, Claudia Gonzaga-Jauregui, Dineshani Hettiarachchi, Oleg Kvlividze, Guida Landoure, Prince Makay, Béla Melegh, Ugur Ozbek, Karaman Pagava, Ratna Dua Puri, Vaness I. Romero, Vinod Scaria, Saumya S. Jamuar, Vorasuk Shotelersuk, Dario Roccatello, William A. Gahl, Samuel A. Wiafe, Olaf Bodamer, Manuel Posada, Domenica Taruscio

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