Rita Bertalan

610 total citations
23 papers, 328 citations indexed

About

Rita Bertalan is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Rita Bertalan has authored 23 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Rita Bertalan's work include Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Urological Disorders and Treatments (4 papers). Rita Bertalan is often cited by papers focused on Sexual Differentiation and Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Urological Disorders and Treatments (4 papers). Rita Bertalan collaborates with scholars based in Hungary, United Kingdom and France. Rita Bertalan's co-authors include Kàroly Rácz, Attila Patócs, Andrea Luczay, Zita Halász, J. Sólyom, Ágnes Sallai, Ágnes Szappanos, Anu Bashamboo, Anne Jørgensen and József Szabó and has published in prestigious journals such as The American Journal of Human Genetics, Clinica Chimica Acta and British Journal of Ophthalmology.

In The Last Decade

Rita Bertalan

23 papers receiving 323 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rita Bertalan Hungary 10 187 141 110 42 40 23 328
Fernanda Caroline Soardi Brazil 13 324 1.7× 171 1.2× 140 1.3× 16 0.4× 40 1.0× 28 421
R Gracia Spain 7 234 1.3× 250 1.8× 129 1.2× 26 0.6× 26 0.7× 8 353
Sonia V. Bengolea Argentina 11 180 1.0× 181 1.3× 352 3.2× 30 0.7× 49 1.2× 17 462
Débora Braslavsky Argentina 12 239 1.3× 187 1.3× 168 1.5× 73 1.7× 86 2.1× 25 454
J. L. Chaussain France 7 212 1.1× 92 0.7× 123 1.1× 42 1.0× 16 0.4× 11 321
Hannah Mandel Israel 5 155 0.8× 128 0.9× 25 0.2× 25 0.6× 35 0.9× 6 252
Anna Casteràs Spain 8 144 0.8× 95 0.7× 219 2.0× 48 1.1× 10 0.3× 21 380
Nigel P. Groome United Kingdom 9 211 1.1× 134 1.0× 124 1.1× 44 1.0× 177 4.4× 9 470
Michelle Welsh United Kingdom 8 145 0.8× 132 0.9× 96 0.9× 41 1.0× 208 5.2× 12 373
Andreína Cattani Chile 8 163 0.9× 121 0.9× 106 1.0× 42 1.0× 30 0.8× 19 335

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-authorship network of co-authors of Rita Bertalan

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

All Works

20 of 20 papers shown
1.
Tenenbaum‐Rakover, Yardena, Osnat Admoni, Charles Sultan, et al.. (2021). The evolving role of whole-exome sequencing in the management of disorders of sex development. Endocrine Connections. 10(6). 620–629. 13 indexed citations
2.
Bertalan, Rita, et al.. (2019). Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers. Molecular Biology Reports. 46(4). 4599–4604. 6 indexed citations
3.
Bertalan, Rita, Éva Erhardt, Attila Patócs, et al.. (2019). 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. 46(5). 5595–5601. 6 indexed citations
4.
Bashamboo, Anu, Caroline Eozénou, Anne Jørgensen, et al.. (2018). 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. 102(3). 487–493. 65 indexed citations
5.
Bertalan, Rita, et al.. (2018). Evaluation of DSD training schools organized by cost action BM1303 “DSDnet”. Orphanet Journal of Rare Diseases. 13(1). 227–227. 5 indexed citations
6.
Bashamboo, Anu, Caroline Eozénou, Annemette Jørgensen, et al.. (2018). 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. 2 indexed citations
7.
David, Anna L., Henriett Butz, Zita Halász, et al.. (2017). A SHOX géndeletio előfordulása idiopáthiás alacsonynövésben. Multicentrikus tanulmány. Orvosi Hetilap. 158(34). 1351–1356. 4 indexed citations
8.
Bertok, Sara, Primož Kotnik, Hans‐Christoph Duba, et al.. (2015). New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations. Annals of Human Genetics. 80(1). 50–62. 23 indexed citations
9.
Szappanos, Ágnes, Attila Patócs, Péter Gergics, et al.. (2010). 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. 123(1-2). 79–84. 12 indexed citations
10.
Bertalan, Rita, Ágnes Sallai, J. Sólyom, et al.. (2010). Hyperthyroidism Caused by a Germline Activating Mutation of the Thyrotropin Receptor Gene: Difficulties in Diagnosis and Therapy. Thyroid. 20(3). 327–332. 9 indexed citations
11.
Bertalan, Rita, Attila Patócs, Bálint Nagy, et al.. (2009). Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome. Clinica Chimica Acta. 405(1-2). 148–152. 9 indexed citations
12.
Bertalan, Rita, et al.. (2009). The protective effect of the ER22/23EK polymorphism against an excessive weight gain during pregnancy. Gynecological Endocrinology. 25(6). 379–382. 6 indexed citations
13.
Sallai, Ágnes, J. Sólyom, M. Dobos, et al.. (2009). Y-chromosome markers in Turner syndrome: Screening of 130 patients. Journal of Endocrinological Investigation. 33(4). 222–227. 39 indexed citations
14.
Bertalan, Rita, Attila Patócs, Barna Vásárhelyi, et al.. (2008). Association between birth weight in preterm neonates and the BclI polymorphism of the glucocorticoid receptor gene. The Journal of Steroid Biochemistry and Molecular Biology. 111(1-2). 91–94. 15 indexed citations
15.
Halász, Zita, Rita Bertalan, Judit Tõke, et al.. (2008). Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency. Journal of Endocrinological Investigation. 31(1). 74–78. 4 indexed citations
16.
Korányi, Katalin, Attila Patócs, István Likó, et al.. (2007). Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy. British Journal of Ophthalmology. 92(1). 131–134. 20 indexed citations
17.
Bertalan, Rita, et al.. (2007). Maternal hyperandrogenism beginning from early pregnancy and progressing until delivery does not produce virilization of a female newborn. Gynecological Endocrinology. 23(10). 581–583. 9 indexed citations
18.
Luczay, Andrea, Rita Bertalan, & Kàroly Rácz. (2007). 10th European Congress of Endocrinology. Journal of Endocrinological Investigation. 30(11). 979–979. 32 indexed citations
19.
Halász, Zita, Judit Tõke, Attila Patócs, et al.. (2006). High prevalence of PROP1 gene mutations in hungarian patients with childhood-onset combined anterior pituitary hormone deficiency. Endocrine. 30(3). 255–260. 18 indexed citations
20.
Patócs, Attila, István Likó, Péter Gergics, et al.. (2005). 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. 97(3). 257–265. 27 indexed citations

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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