Ágnes Sallai

590 total citations
18 papers, 147 citations indexed

About

Ágnes Sallai is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Ágnes Sallai has authored 18 papers receiving a total of 147 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Ágnes Sallai's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sexual Differentiation and Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Ágnes Sallai is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sexual Differentiation and Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Ágnes Sallai collaborates with scholars based in Hungary, Germany and United States. Ágnes Sallai's co-authors include G. Fekete, Rita Bertalan, Zita Halász, J. Sólyom, Kàroly Rácz, József Szabó, Péter Ugocsai, M. Dobos, F. Dicső and I. Orbán and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Thyroid and Journal of the American College of Nutrition.

In The Last Decade

Ágnes Sallai

14 papers receiving 143 citations

Peers

Ágnes Sallai

GENET

EDM

EPIDE

RHEUM

Rita Valdéz Argentina

Ana Paula Dias Rangel Montenegro Brazil

Mika Ishige Japan

Andrew J. Grant Australia

Irum Atta Pakistan

Bob McClellan United States

Ruken Yıldırım Türkiye

Maria Kareva Russia

Zita Halász Hungary

Zhen Ye China

Rita Valdéz Argentina

Ágnes Sallai

46 ×0.7

GENET

30 ×0.5

62 ×1.3

EDM

28 ×0.8

EPIDE

17 ×0.8

RHEUM

Citations per year, relative to Ágnes Sallai Ágnes Sallai (= 1×) peers Rita Valdéz

Countries citing papers authored by Ágnes Sallai

Since Specialization

Citations

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

Fields of papers citing papers by Ágnes Sallai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ágnes Sallai

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

All Works

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18 of 18 papers shown

Micsík, Tamás, et al.. (2022). Cushing-szindrómát okozó gyermekkori mellékvesekéreg-adenoma. Orvosi Hetilap. 163(10). 407–412. 2 indexed citations

Sallai, Ágnes, et al.. (2019). A Magyar Tudományos Akadémia Könyvtár és Információs Központ alapító állományának állatani témájú könyvei. Repository of the Academy's Library (Library of the Hungarian Academy of Sciences). 105(1-2). 3–28.

Péterfia, Bálint, Péter Hollósi, Irén Haltrich, et al.. (2018). Elsődleges genetikai vizsgálat Prader–Willi-szindróma igazolására. Orvosi Hetilap. 159(2). 64–69. 1 indexed citations

Lengyel, Anna, et al.. (2018). Nemi kromoszóma-rendellenességek vizsgálata gyermekkorban. Orvosi Hetilap. 159(27). 1121–1128.

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

David, Anna L., Henriett Butz, Zita Halász, et al.. (2017). A SHOX géndeletio előfordulása idiopáthiás alacsonynövésben. Multicentrikus tanulmány | The prevalence of SHOX gene deletion in children with idiopathic short stature.A multicentric study. 1 indexed citations

Tõke, Judit, et al.. (2014). Gradual Development of Brachydactyly in Pseudohypoparathyroidism. The Journal of Clinical Endocrinology & Metabolism. 99(6). 1945–1946. 5 indexed citations

Dušátková, Petra, Roland Pfäffle, Barbora Obermannová, et al.. (2013). Ancestral origin of two most prevalent mutations in the PROP1 gene causing combined pituitary hormone deficiency in selected European populations. Lithuanian University of Health Sciences.

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

10.

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

11.

Czinner, A, Tamás Szamosi, Ágnes Sallai, et al.. (2008). Effect of Diet and Physical Exercise Treatment on Insulin Resistance Syndrome of Schoolchildren. Journal of the American College of Nutrition. 27(1). 177–183. 19 indexed citations

12.

Sallai, Ágnes, Éva Hosszú, Péter Gergics, Kàroly Rácz, & György Fekete. (2007). Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases. European Journal of Pediatrics. 167(4). 441–446. 7 indexed citations

13.

Constantin, Tamás, Andrea Ponyi, T. Kálovics, et al.. (2007). Disease course, frequency of relapses and survival of patients with juvenile or adult dermatomyositis. Orvosi Hetilap. 148(42). 1989–1997.

14.

Constantin, T., A. Ponyi, I. Orbán, et al.. (2006). National registry of patients with juvenile idiopathic inflammatory myopathies in Hungary—Clinical characteristics and disease course of 44 patients with juvenile dermatomyositis. Autoimmunity. 39(3). 223–232. 36 indexed citations

15.

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

16.

Barta, Csaba, Zita Halász, Ágnes Sallai, et al.. (2003). Mutational Analysis of Hungarian Patients with Androgen Insensitivity Syndrome. Journal of Pediatric Endocrinology and Metabolism. 16(3). 367–73. 4 indexed citations

17.

Sallai, Ágnes, et al.. (1997). [Late onset type I tyrosinemia].. PubMed. 138(28). 1805–8. 1 indexed citations

18.

Sallai, Ágnes. (1992). On the soil-inhabiting macrofauna of Nagy-Szenas, with special reference to the isopods, diplopods and chilopods. Repository of the Academy's Library (Library of the Hungarian Academy of Sciences). 25. 95–102. 1 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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