Lidia Haţegan

422 total citations
13 papers, 231 citations indexed

About

Lidia Haţegan is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Plant Science. According to data from OpenAlex, Lidia Haţegan has authored 13 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 3 papers in Plant Science. Recurrent topics in Lidia Haţegan's work include Ion channel regulation and function (5 papers), Cardiac electrophysiology and arrhythmias (5 papers) and Plant Molecular Biology Research (3 papers). Lidia Haţegan is often cited by papers focused on Ion channel regulation and function (5 papers), Cardiac electrophysiology and arrhythmias (5 papers) and Plant Molecular Biology Research (3 papers). Lidia Haţegan collaborates with scholars based in Hungary, Belgium and Germany. Lidia Haţegan's co-authors include Miklós Szekeres, Masaharu Mizutani, Bunta Watanabe, Takao Yokota, Toshiyuki Ohnishi, Shozo Fujioka, Róbert Sepp, Tamás Forster, Zoltán Hegedüs and István Nagy and has published in prestigious journals such as Journal of Biological Chemistry, Cardiovascular Research and Planta.

In The Last Decade

Lidia Haţegan

13 papers receiving 227 citations

Peers

Countries citing papers authored by Lidia Haţegan

Since Specialization

Citations

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

Fields of papers citing papers by Lidia Haţegan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lidia Haţegan

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Geno- and phenotypic characteristics and clinical outcomes of CACNA1C gene mutation associated Timothy syndrome, “cardiac only” Timothy syndrome and isolated long QT syndrome 8: A systematic review 2022 ·Frontiers in Cardiovascular Medicine ·(unknown), Máté Vámos, Lidia Haţegan, Lilla Hanák, Nelli Farkas, Zsolt Szakács, Dezső Csupor, (unknown), Péter Kupó, (unknown), (unknown), András Komócsi, Tamás Habon, Péter Hegyi, Róbert Sepp	5
2	Variant Transthyretin Amyloidosis (ATTRv) in Hungary: First Data on Epidemiology and Clinical Features 2021 ·Genes ·Zoltán Pozsonyi, (unknown), (unknown), Dorottya Csuka, (unknown), Ágnes Szilágyi, Lidia Haţegan, (unknown), (unknown), Noémi Nyolczas, Lívia Dézsi, Mária Judit Molnár, Anita Csillik, Katalin Révész, Béla Iványi, (unknown), (unknown), Tamás Masszi, Zsuzsanna Arányi, Róbert Sepp	8
3	Genetic diagnosis in hypertrophic cardiomyopathy: two steps forward, one step back 2021 ·SZTE Publicatio Repozitórium (University of Szeged) ·Lidia Haţegan, (unknown), (unknown), (unknown), (unknown), (unknown), Róbert Sepp	1
4	Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen–Tawil syndrome patient 2020 ·Cardiovascular Research ·(unknown), (unknown), (unknown), Lidia Haţegan, (unknown), (unknown), Tamara Madácsy, József Maléth, Zoltán Hegedüs, István Nagy, Rohit Arora, Alain J. Labro, László Környei, András Varró, Róbert Sepp, Balázs Ördög	1
5	Direct Anticoagulants and Risk of Myocardial Infarction, a Multiple Treatment Network Meta-Analysis 2019 ·Angiology ·Péter Kupó, Zsolt Szakács, Margit Solymár, Tamás Habon, László Czopf, Lidia Haţegan, (unknown), (unknown), (unknown), Gábor Varga, Márta Balaskó, Róbert Sepp, Péter Hegyi, (unknown), András Komócsi	16
6	A novel ‘splice site’ HCN4 Gene mutation, c.1737 + 1 G > T, causes familial bradycardia, reduced heart rate response, impaired chronotropic competence and increased short-term heart rate variability 2017 ·International Journal of Cardiology ·Lidia Haţegan, (unknown), Balázs Ördög, (unknown), (unknown), Orsolya Kiss, Andrea Orosz, László Sághy, István Nagy, Zoltán Hegedüs, László Rudas, Márta Széll, András Varró, Tamás Forster, Róbert Sepp	11
7	Timothy syndrome 1 genotype without syndactyly and major extracardiac manifestations 2017 ·American Journal of Medical Genetics Part A ·Róbert Sepp, Lidia Haţegan, Attila Bácsi, (unknown), László Környei, (unknown), Márta Széll, Tamás Forster, István Nagy, Zoltán Hegedüs	15
8	Identification of a Novel <i>GLA</i> Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac Phenotype 2017 ·International Heart Journal ·(unknown), Lidia Haţegan, (unknown), Izabella Obál, Edina Varga, (unknown), (unknown), Sabrina Eichler, Tamás Forster, Arndt Rolfs, Róbert Sepp	12
9	Identification of Two Novel LAMP2 Gene Mutations in Danon Disease 2016 ·Canadian Journal of Cardiology ·(unknown), (unknown), Lidia Haţegan, Zoltán Hegedüs, (unknown), (unknown), (unknown), László Sághy, Béla Iványi, Miklós Csanády, Tamás Forster, Róbert Sepp	12
10	Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen–Tawil syndrome 2015 ·Canadian Journal of Physiology and Pharmacology ·Balázs Ördög, Lidia Haţegan, Mária Kovács, György Seprényi, Zsófia Kohajda, István Nagy, Zoltán Hegedüs, László Környei, Norbert Jost, Márta Katona, Miklós Szekeres, Tamás Forster, Julius Gy. Papp, András Varró, Róbert Sepp	4
11	Differential expression of the brassinosteroid receptor-encoding BRI1 gene in Arabidopsis 2014 ·Planta ·Lidia Haţegan, (unknown), László Kozma‐Bognár, Gerard J. Bishop, Miklós Szekeres	15
12	CYP90A1/CPD, a Brassinosteroid Biosynthetic Cytochrome P450 of Arabidopsis, Catalyzes C-3 Oxidation 2012 ·Journal of Biological Chemistry ·Toshiyuki Ohnishi, (unknown), Bunta Watanabe, Shozo Fujioka, Lidia Haţegan, (unknown), (unknown), Takao Yokota, Miklós Szekeres, Masaharu Mizutani	130
13	Developmentally regulated expression of the BRI1 brassinosteroid receptor in Arabidopsis thaliana 2008 ·Acta Biologica Szegediensis ·Lidia Haţegan, János Bindics, Miklós Szekeres	1

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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