Béla Melegh

42.1k total citations
260 papers, 4.4k citations indexed

About

Béla Melegh is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Béla Melegh has authored 260 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Molecular Biology, 68 papers in Clinical Biochemistry and 63 papers in Genetics. Recurrent topics in Béla Melegh's work include Metabolism and Genetic Disorders (65 papers), Mitochondrial Function and Pathology (35 papers) and Viral gastroenteritis research and epidemiology (20 papers). Béla Melegh is often cited by papers focused on Metabolism and Genetic Disorders (65 papers), Mitochondrial Function and Pathology (35 papers) and Viral gastroenteritis research and epidemiology (20 papers). Béla Melegh collaborates with scholars based in Hungary, Germany and United States. Béla Melegh's co-authors include Judit Bene, Péter Kisfali, Kinga Hadzsiev, Krisztián Bànyai, Anita Maász, Enikő Sáfrány, János Kerner, Zoltán Szolnoki, Vito Martella and Lili Magyari and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Gut.

In The Last Decade

Béla Melegh

251 papers receiving 4.3k citations

Peers

Countries citing papers authored by Béla Melegh

Since Specialization

Citations

This map shows the geographic impact of Béla Melegh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Béla Melegh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Béla Melegh more than expected).

Fields of papers citing papers by Béla Melegh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Béla Melegh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Béla Melegh. The network helps show where Béla Melegh may publish in the future.

Co-authorship network of co-authors of Béla Melegh

This figure shows the co-authorship network connecting the top 25 collaborators of Béla Melegh. A scholar is included among the top collaborators of Béla Melegh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Béla Melegh. Béla Melegh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Cascade counselling and testing. Recommendations of the European Society of Human Genetics 2025 ·European Journal of Human Genetics ·Guido de Wert, Carla van El, Angus Clarke, Christophe Cordier, Florence Fellmann, Maurizio Genuardi, Sabine Hentze, Hülya Kayserili, Milan Maçek, (unknown), Béla Melegh, Álvaro Mendes, Emmanuelle Rial‐Sebbag, Vigdís Stefánsdóttir, Lisbeth Tranebjærg, Fiona Ulph, Francesca Forzano	0
2	Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation 2021 ·Frontiers in Genetics ·Márta Czakó, (unknown), (unknown), (unknown), András Szabó, Anita Maász, Béla Melegh, Kinga Hadzsiev	2
3	Revealing the Genetic Impact of the Ottoman Occupation on Ethnic Groups of East-Central Europe and on the Roma Population of the Area 2019 ·Frontiers in Genetics ·Zsolt Bánfai, Béla Melegh, Katalin Sümegi, Kinga Hadzsiev, Attila Miseta, Miklós Kásler, (unknown)	10
4	Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy 2019 ·Seizure ·(unknown), (unknown), (unknown), Judit Bene, Márta Czakó, András Szabó, Béla Melegh, Kinga Hadzsiev	9
5	Marked differences in frequencies of statin therapy relevant SLCO1B1 variants and haplotypes between Roma and Hungarian populations 2015 ·BMC Genetics ·Ãgnes Nagy, Csilla Sipeky, (unknown), Béla Melegh, (unknown), (unknown), Kálmán Tóth	12
6	Interethnic variability of CYP4F2 (V433M) in admixed population of Roma and Hungarians 2015 ·Environmental Toxicology and Pharmacology ·Csilla Sipeky, (unknown), Béla Melegh, (unknown), (unknown), (unknown), István Szabó, Réka Várnai, (unknown), (unknown)	2
7	Towards a European consensus for reporting incidental findings during clinical NGS testing 2015 ·European Journal of Human Genetics ·Jayne Y. Hehir‐Kwa, Mireille Claustres, Ros Hastings, Conny M.A. van Ravenswaaij‐Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon‐Thomsen, Philippos C. Patsalis, Joris Vermeesch, Martina C. Cornel, Beverly Searle, Aarno Palotie, Ettore Capoluongo, Borut Peterlin, Xavier Estivill, Peter N. Robinson	56
8	MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin 2015 ·PLoS ONE ·(unknown), Andrea Šoltýsová, Lukáš Varga, (unknown), Andrej Ficek, Miloslava Hučková, (unknown), Dana Šafka Brožková, Saima Anwar, Judit Bene, (unknown), (unknown), Zubair M. Ahmed, Pavel Seeman, Béla Melegh, Milan Profant, I Klimeś, Saima Riazuddin, Ľudevít Kádaši, Daniela Gašperíková	16
9	Marked differences of haplotype tagging SNP distribution, linkage, and haplotype profile of IL23 receptor gene in Roma and Hungarian population samples 2013 ·Cytokine ·Lili Magyari, (unknown), Patrícia Sarlós, Luca Járomi, (unknown), (unknown), (unknown), Péter Kisfali, Erzsébet Kövesdi, (unknown), András Szabó, (unknown), Béla Melegh	5
10	Automated signal pattern evaluation of a bladder cancer specific multiprobe‐fish assay applying a user‐trainable workstation 2011 ·Microscopy Research and Technique ·(unknown), Donát Alpár, Béla Kajtár, Béla Melegh, László Somogyi, (unknown), (unknown), László Pajor, Norbert Süle	9
11	Genetic Variability and Haplotype Profile of MDR1 (ABCB1) in Roma and Hungarian Population Samples with a Review of the Literature 2010 ·Drug Metabolism and Pharmacokinetics ·Csilla Sipeky, Veronika Csöngei, Luca Járomi, Enikő Sáfrány, Anita Maász, István Takács, Judit Béres, Lajos Fodor, Melinda Zsuzsanna Szabó, Béla Melegh	31
12	Falls in Spinocerebellar Ataxias: Results of the EuroSCA Fall Study 2010 ·The Cerebellum ·(unknown), Tanja Schmitz‐Hübsch, (unknown), (unknown), (unknown), Sylvia Boesch, (unknown), (unknown), Alexandra Dürr, (unknown), Paola Giunti, Christoph Globas, Thomas Klockgether, Béla Melegh, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	4
13	Assessment of DNA methylation at the interferon regulatory factor 5 (IRF5) promoter region in inflammatory bowel diseases 2010 ·International Journal of Colorectal Disease ·Alfred Balasa, Grace Gathungu, Péter Kisfali, Eric Smith, Judy H. Cho, Béla Melegh, Richárd Kellermayer	18
14	Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients 2010 ·International Journal of Pediatric Obesity ·Katalin Horvatovich, Szilvia Bokor, Ákos Baráth, Anita Maász, Péter Kisfali, Luca Járomi, Noémi Polgár, Dénes Tóth, (unknown), Emõke Endreffy, Dénes Molnár, Béla Melegh	21
15	Apolipoprotein A5 gene APOA52 haplotype variant confers risk for the development of metabolic syndrome 2008 ·Repository of the Academy's Library (Library of the Hungarian Academy of Sciences)* ·Péter Kisfali, Márton Mohás, Anita Maász, (unknown), Lajos Markó, (unknown), Tamás Oroszlán, (unknown), (unknown), (unknown), (unknown), István Wittmann, Béla Melegh	0
16	[Search for mitochondrial DNA T4291C mutation in Hungarian patients with metabolic syndrome]. 2006 ·PubMed ·Anita Maász, Katalin Horvatovich, Lili Magyari, (unknown), Szilvia Bokor, Boglárka Laczy, (unknown), Dénes Molnár, István Wittmann, Béla Melegh	3
17	Histopathologic Abnormalities of the Lymphoreticular Tissues in Organic Cation Transporter 2 Deficiency: Evidence for Impaired B Cell Maturation 2006 ·The Journal of Pediatrics ·Katalin Komlósi, Viktória Havasi, Judit Bene, Norbert Süle, László Pajor, Raffaella Nicolai, Paola Benatti, Menotti Calvani, Béla Melegh	14
18	Bigenic connexin mutations in a patient with hidrotic ectodermal dysplasia. 2005 ·PubMed ·Richárd Kellermayer, Matthew Keller, Paulina Ratajczak, Elizabeth Richardson, (unknown), (unknown), Béla Melegh, György Kosztolányi, Gabriele Richard	20
19	Tel Hashomer camptodactyly syndrome: 12‐year follow‐up of a Hungarian patient and review 2005 ·American Journal of Medical Genetics Part A ·Béla Melegh, Katalin Hollódy, (unknown), K Méhes	3
20	[Incidence of factor V G1681A (Leiden) mutation in samplings from the Hungarian population]. 1998 ·PubMed ·(unknown), Béla Melegh, Ãgnes Nagy, András Kis, János Molnár, Hajna Losonczy, (unknown), (unknown)	5

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact