Judit Bene

9.2k total citations
77 papers, 1.0k citations indexed

About

Judit Bene is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Judit Bene has authored 77 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 23 papers in Clinical Biochemistry and 20 papers in Genetics. Recurrent topics in Judit Bene's work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (9 papers) and Metabolomics and Mass Spectrometry Studies (7 papers). Judit Bene is often cited by papers focused on Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (9 papers) and Metabolomics and Mass Spectrometry Studies (7 papers). Judit Bene collaborates with scholars based in Hungary, Germany and United States. Judit Bene's co-authors include Béla Melegh, Kinga Hadzsiev, Katalin Komlósi, Viktória Havasi, Mihály Szabó, András Kondacs, Ferenc Somogyvári, Lajos Fodor, Zoltán Szolnoki and Beáta Gasztonyi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Judit Bene

71 papers receiving 1.0k citations

Peers

Countries citing papers authored by Judit Bene

Since Specialization

Citations

This map shows the geographic impact of Judit Bene'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 Judit Bene with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judit Bene more than expected).

Fields of papers citing papers by Judit Bene

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judit Bene. 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 Judit Bene. The network helps show where Judit Bene may publish in the future.

Co-authorship network of co-authors of Judit Bene

This figure shows the co-authorship network connecting the top 25 collaborators of Judit Bene. A scholar is included among the top collaborators of Judit Bene 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 Judit Bene. Judit Bene is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Increased Phenotype Severity Associated with Splice-Site Variants in a Hungarian Pediatric Neurofibromatosis 1 Cohort: A Retrospective Study 2025 ·Biomedicines ·(unknown), (unknown), (unknown), Judit Bene, Kinga Hadzsiev, Márta Medvecz, László Szabó, Zsuzsanna Szalai	0
2	Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods 2024 ·Pathology & Oncology Research ·(unknown), Anita Maász, Alexandra Mikó, (unknown), (unknown), Judit Bene, (unknown), László Mangel, Kinga Hadzsiev	0
3	Case report: Initial atypical skeletal symptoms and dental anomalies as first signs of Gardner syndrome: the importance of genetic analysis in the early diagnosis 2024 ·Pathology & Oncology Research ·(unknown), (unknown), (unknown), (unknown), Ildikó Szántó, (unknown), (unknown), (unknown), Kinga Hadzsiev, Judit Bene	5
4	Co-occurrence of neurofibromatosis type 1 and pseudoachondroplasia – a first case report 2023 ·BMC Pediatrics ·(unknown), (unknown), Klára Farkas, (unknown), (unknown), (unknown), Zsuzsanna Szalai, Judit Bene, Kinga Hadzsiev, Zoltán Maróti, (unknown), Márta Medvecz	3
5	Copy Number Variations in Neuropsychiatric Disorders 2023 ·International Journal of Molecular Sciences ·(unknown), Kinga Hadzsiev, Judit Bene	2
6	Superimposed Mosaicism in the Form of Extremely Extended Segmental Plexiform Neurofibroma Caused by a Novel Pathogenic Variant in the NF1 Gene 2023 ·International Journal of Molecular Sciences ·(unknown), Judit Bene, Kinga Hadzsiev, Miklós Garami, (unknown), Rudolf Happle, Márta Medvecz, Zsuzsanna Szalai	3
7	Identification of an NF1 Microdeletion with Optical Genome Mapping 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Csaba Bödör, Péter Urbán, (unknown), Kinga Hadzsiev, György Fekete, Hildegard Kehrer‐Sawatzki, Judit Bene	2
8	Three-Year Follow-Up after Intrauterine mTOR Inhibitor Administration for Fetus with TSC-Associated Rhabdomyoma 2023 ·International Journal of Molecular Sciences ·Anita Maász, (unknown), (unknown), Gábor Molnár, (unknown), (unknown), (unknown), Judit Bene, Kinga Hadzsiev	7
9	TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness 2022 ·European Journal of Medical Genetics ·Anita Maász, Kinga Hadzsiev, (unknown), (unknown), Erika Maka, (unknown), (unknown), Á. Németh, Judit Bene, Bence Gálik, Attila Gyenesei, Béla Melegh	8
10	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
11	Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma 2019 ·European Journal of Human Genetics ·Isabelle Schrauwen, Béla Melegh, Imen Chakchouk, Anushree Acharya, Abdul Nasır, (unknown), (unknown), Zsolt Szabó, Tamás Karosi, Judit Bene, Suzanne M. Leal	10
12	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
13	Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations 2010 ·Journal of Human Genetics ·Kinga Hadzsiev, Noémi Polgár, Judit Bene, Katalin Komlósi, (unknown), Katalin Hollódy, György Kosztolányi, Alessandra Renieri, Béla Melegh	15
14	Prevalence of SLC22A4 1672T and SLC22A5 −207C combination defined TC haplotype in Hungarian ulcerative colitis patients 2007 ·Pathology & Oncology Research ·Lili Magyari, Judit Bene, Katalin Komlósi, (unknown), Bernadett Faragó, Veronika Csöngei, Luca Járomi, Enikő Sáfrány, Csilla Sipeky, Lilla Lakner, Márta Varga, Beáta Gasztonyi, Béla Melegh	8
15	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
16	Detection of the Leu40Arg variant of the platelet glycoprotein IIb/IIIa receptor in subjects with thrombotic diseases 2005 ·Thrombosis Research ·(unknown), Judit Bene, Viktória Havasi, Katalin Komlósi, (unknown), (unknown), Előd Papp, Beáta Gasztonyi, Zoltán Szolnoki, (unknown), Gyula Mózsik, Kálmán Tóth, Béla Melegh, István Wittmann	2
17	Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine‐responsive cardiomyopathy in Roma families 2004 ·American Journal of Medical Genetics Part A ·Béla Melegh, Judit Bene, (unknown), Viktória Havasi, Katalin Komlósi, László Pajor, Éva Oláh, Gyula Kispál, Balázs Sümegi, K Méhes	24
18	Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosis 2004 ·Acta Neurologica Scandinavica ·Zoltán Szolnoki, Ferenc Somogyvári, András Kondacs, Mihály Szabó, Lajos Fodor, Judit Bene, Béla Melegh	35
19	Mapping of Possible Laminin Binding Sites of Y. pestis Plasminogen Activator (Pla) via Phage Display 2004 ·Advances in experimental medicine and biology ·(unknown), Judit Bene, Béla Melegh, Levente Emödy	4
20	Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke 2004 ·Acta Neurologica Scandinavica ·(unknown), (unknown), Judit Bene, Katalin Komlósi, Dominika Szőke, Ferenc Somogyvári, András Kondacs, Mihály Szabó, Lajos Fodor, A. Bodor, Itamar Gati, (unknown), Béla Melegh	58

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.

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