Rita Bertalan

610 citations

23 papers · 328 indexed · h-index 10

Impact in

Endocrinology, Diabetes and Metabolism top 10%
- Hormonal Regulation and Hypertension
- Adrenal Hormones and Disorders
- Growth Hormone and Insulin-like Growth Factors
- Pituitary Gland Disorders and Treatments
Genetics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in ⓘ

Urology 4
- Urological Disorders and Treatments 4
Endocrinology, Diabetes and Metabolism 9
- Hormonal Regulation and Hypertension 3
- Adrenal Hormones and Disorders 3

Co-authors: Kàroly Rácz (8 shared papers)Attila Patócs (13 shared papers)Andrea Luczay (3 shared papers)Zita Halász (8 shared papers)J. Sólyom (5 shared papers)Ágnes Sallai (5 shared papers)Anu Bashamboo (4 shared papers)Ágnes Szappanos (3 shared papers)
Journals: The Journal of Steroid Biochemistry and Molecular Biology (3 papers)Molecular Biology Reports (2 papers)Annals of Human Genetics (1 paper)Orphanet Journal of Rare Diseases (1 paper)Endocrine Connections (1 paper)
Partner nations: Hungary United Kingdom France

In The Last Decade

Rita Bertalan

23 papers receiving 323 citations

Peers

Countries citing papers authored by Rita Bertalan

Since Specialization

Citations

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

Fields of papers citing papers by Rita Bertalan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Rita Bertalan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rita Bertalan Line = papers co-authored together Rita Bertalan links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children The American Journal of Human Genetics ·Anu Bashamboo, Caroline Eozénou, Anne Jørgensen, Joëlle Bignon‐Topalovic, Jean‐Pierre Siffroi, Capucine Hyon, Attila Tar, Péter Nagy, J. Sólyom, Zita Halász, Annnabel Paye-Jaouen, Sophie Lambert, David Rodriguez‐Buritica, Rita Bertalan, Laëtitia Martinerie, Ewa Rajpert‐De Meyts, John C. Achermann, Ken McElreavey	2018	65
2	Y-chromosome markers in Turner syndrome: Screening of 130 patients Journal of Endocrinological Investigation ·Ágnes Sallai, J. Sólyom, M. Dobos, József Szabó, Zita Halász, László Ságodi, Tamás Niederland, Adrienn Kozári, Rita Bertalan, Péter Ugocsai, G. Fekete	2009	39
3	10th European Congress of Endocrinology Journal of Endocrinological Investigation ·Andrea Luczay, Rita Bertalan, Kàroly Rácz	2007	32
4	Novel mutation of the CYP17 gene in two unrelated patients with combined 17α-hydroxylase/17,20-lyase deficiency: Demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling The Journal of Steroid Biochemistry and Molecular Biology ·Attila Patócs, István Likó, Ibolya Varga, Péter Gergics, András Mihály Boros, László Fütő, Imre Zoltán Kun, Rita Bertalan, Szilvia Tóth, Tamás Pázmány, Miklós Tóth, Nikolette Szücs, J Horányi, Edit Gláz, Kàroly Rácz	2005	27
5	New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations Annals of Human Genetics ·M. Čizmárová, Katarina Hlinkova, Sara Bertok, Primož Kotnik, Hans‐Christoph Duba, Rita Bertalan, K. Poločková, Ľudmila Košťálová, Z. Pribilincová, Anna Hlavatá, László Kovács, Denisa Ilenčíková	2015	23
6	Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy British Journal of Ophthalmology ·B Boyle, Katalin Korányi, Attila Patócs, István Likó, Ágnes Szappanos, Rita Bertalan, K. Rácz, C Balázs	2007	20
7	High prevalence of PROP1 gene mutations in hungarian patients with childhood-onset combined anterior pituitary hormone deficiency Endocrine ·Zita Halász, Judit Tõke, Attila Patócs, Rita Bertalan, Zsófia Tömböl, Ágnes Sallai, Éva Hosszú, Ágota Muzsnai, László Kovács, J. Sólyom, György Fekete, Kàroly Rácz	2006	18
8	Association between birth weight in preterm neonates and the BclI polymorphism of the glucocorticoid receptor gene The Journal of Steroid Biochemistry and Molecular Biology ·Rita Bertalan, Attila Patócs, Barna Vásárhelyi, András Treszl, Ibolya Varga, András Szabó, Judit Tamás, Judit Tõke, Belema Boyle, András Nobilis, János Rigó, Kàroly Rácz	2008	15
9	The evolving role of whole-exome sequencing in the management of disorders of sex development Endocrine Connections ·Yardena Tenenbaum‐Rakover, Osnat Admoni, Ghadir Elias-Assad, Shira London, Marie Noufi-Barhoum, Hanna Ludar, Tal Almagor, Yoav Zehavi, Charles Sultan, Rita Bertalan, Anu Bashamboo, Kenneth McElreavey	2021	13
10	The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome The Journal of Steroid Biochemistry and Molecular Biology ·Ágnes Szappanos, Attila Patócs, Péter Gergics, Rita Bertalan, Andrea Kerti, Bence Ács, Karolina Feldmann, Kàroly Rácz, Miklós Tóth	2010	12
11	Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome Clinica Chimica Acta ·Rita Bertalan, Attila Patócs, Bálint Nagy, Zoltán Derzsy, Nóra Gullai, Ágnes Szappanos, János Rigó, Kàroly Rácz	2009	9
12	Maternal hyperandrogenism beginning from early pregnancy and progressing until delivery does not produce virilization of a female newborn Gynecological Endocrinology ·Rita Bertalan, László Csabay, Anna Blázovics, J Rigó, Ibolya Varga, Zita Halász, Erzsébet Toldy, Belema Boyle, Károly Rácz	2007	9
13	Hyperthyroidism Caused by a Germline Activating Mutation of the Thyrotropin Receptor Gene: Difficulties in Diagnosis and Therapy Thyroid ·Rita Bertalan, Ágnes Sallai, J. Sólyom, Gábor Lotz, István Szabó, Balázs Kovács, Éva Szabó, Attila Patócs, Kàroly Rácz	2010	9
14	Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers Molecular Biology Reports ·Rita Bertalan, Zsuzsa Bencsik, Piroska Mezei, Zsolt Vajda, Henriett Butz, Attila Patócs	2019	6
15	The importance of the multiplex ligation-dependent probe amplification in the identification of a novel two-exon deletion of the NR5A1 gene in a patient with 46,XY differences of sex development Molecular Biology Reports ·Orsolya Nagy, Judit Kárteszi, Marianna Hartwig, Rita Bertalan, Eszter Jávorszky, Éva Erhardt, Attila Patócs, Tamás Tornóczky, István Balogh, Anikó Újfalusi	2019	6
16	The protective effect of the ER22/23EK polymorphism against an excessive weight gain during pregnancy Gynecological Endocrinology ·Rita Bertalan, Attila Patócs, Belema Boyle, János Rigó, Kàroly Rácz	2009	6
17	Evaluation of DSD training schools organized by cost action BM1303 “DSDnet” Orphanet Journal of Rare Diseases ·Rita Bertalan, Angela Lucas-Herald, Zofia Kolesińska, M. Berra, Martine Cools, Antonio Balsamo, Olaf Hiort	2018	5
18	Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency Journal of Endocrinological Investigation ·Zita Halász, Rita Bertalan, Judit Tõke, Attila Patócs, Miklós Tóth, G. Fekete, Edit Gláz, K. Rácz	2008	4
19	A SHOX géndeletio előfordulása idiopáthiás alacsonynövésben. Multicentrikus tanulmány Orvosi Hetilap ·Anna L. David, Henriett Butz, Zita Halász, Dóra Török, Gábor Nyírő, Ágota Muzsnai, Violetta Csákváry, Andrea Luczay, Ágnes Sallai, Éva Hosszú, Enikő Felszeghy, Attila Tar, Zsuzsanna Szántó, Gy. László Fekete, Imre Zoltán Kun, Attila Patócs, Rita Bertalan	2017	4
20	Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children Yearbook of pediatric endocrinology ·Anu Bashamboo, Caroline Eozénou, Annemette Jørgensen, Joëlle Bignon‐Topalovic, JP Siffroi, Capucine Hyon, Tar A, P Nagy, J. Sólyom, Zita Halász, Annnabel Paye-Jaouen, Sophie Lambert, David Rodriguez‐Buritica, Rita Bertalan, Laëtitia Martinerie, Rajpert-De Meyts E, Achermann JC, Ken McElreavey	2018	2

About Rita Bertalan

Rita Bertalan is a scholar working on Urology, Endocrinology, Diabetes and Metabolism, Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 23 papers that have together received 328 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Urological Disorders and Treatments (4 papers), Birth, Development, and Health (3 papers), Hormonal Regulation and Hypertension (3 papers), Adrenal Hormones and Disorders (3 papers), Intestinal Malrotation and Obstruction Disorders (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (110 citations), Genetics (141 citations), Reproductive Medicine (40 citations), Urology (29 citations) and Molecular Biology (187 citations). Rita Bertalan has collaborated with scholars based in Hungary, United Kingdom and France. Frequent co-authors include Kàroly Rácz, Attila Patócs, Andrea Luczay, Zita Halász, J. Sólyom, Ágnes Sallai, Anu Bashamboo, Ágnes Szappanos, David Rodriguez‐Buritica and M. Dobos. Their work appears in journals such as The Journal of Steroid Biochemistry and Molecular Biology, Molecular Biology Reports, Annals of Human Genetics, Orphanet Journal of Rare Diseases and Endocrine Connections.

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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