J. Sólyom

1.2k total citations
56 papers, 888 citations indexed

About

J. Sólyom is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Urology. According to data from OpenAlex, J. Sólyom has authored 56 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Endocrinology, Diabetes and Metabolism, 34 papers in Molecular Biology and 7 papers in Urology. Recurrent topics in J. Sólyom's work include Sexual Differentiation and Disorders (32 papers), Hormonal and reproductive studies (21 papers) and Adrenal Hormones and Disorders (13 papers). J. Sólyom is often cited by papers focused on Sexual Differentiation and Disorders (32 papers), Hormonal and reproductive studies (21 papers) and Adrenal Hormones and Disorders (13 papers). J. Sólyom collaborates with scholars based in Hungary, Austria and Germany. J. Sólyom's co-authors include Franz Waldhauser, József Kovács, Jan Lebl, Tadej Battelino, Felix Votava, H Frisch, J. Homoki, R. Vihko, Dóra Török and Zita Halász and has published in prestigious journals such as The Lancet, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

J. Sólyom

51 papers receiving 842 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Sólyom Hungary 18 610 508 258 173 118 56 888
F Lorenzen Germany 12 791 1.3× 721 1.4× 179 0.7× 231 1.3× 106 0.9× 17 1.1k
Felix Votava Czechia 16 327 0.5× 145 0.3× 119 0.5× 157 0.9× 70 0.6× 30 582
Marian L. Rivas United States 13 187 0.3× 38 0.1× 100 0.4× 18 0.1× 103 0.9× 23 545
R J Santen United States 9 161 0.3× 291 0.6× 146 0.6× 5 0.0× 15 0.1× 10 614
Ioanna Bouba Greece 13 147 0.2× 83 0.2× 202 0.8× 10 0.1× 8 0.1× 31 561
M. Dreyer Germany 14 189 0.3× 267 0.5× 127 0.5× 22 0.1× 3 0.0× 60 569
Motasem Melhem Kuwait 14 190 0.3× 54 0.1× 113 0.4× 27 0.2× 3 0.0× 32 531
Ariadna González‐del Angel Mexico 13 182 0.3× 18 0.0× 169 0.7× 50 0.3× 7 0.1× 65 420
Jiasun Su China 13 221 0.4× 211 0.4× 202 0.8× 19 0.1× 2 0.0× 38 477
Hilmer Negrete United States 8 168 0.3× 34 0.1× 15 0.1× 25 0.1× 123 1.0× 13 436

Countries citing papers authored by J. Sólyom

Since Specialization
Citations

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

Fields of papers citing papers by J. Sólyom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Sólyom

This figure shows the co-authorship network connecting the top 25 collaborators of J. Sólyom. A scholar is included among the top collaborators of J. Sólyom 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 J. Sólyom. J. Sólyom 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.
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
2.
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
3.
Sólyom, J., et al.. (2009). Blood-Spot 17-Hydroxyprogesterone Daily Profiles in Infants with Congenital Adrenal Hyperplasia. Experimental and Clinical Endocrinology & Diabetes. 96(4). 52–56. 1 indexed citations
4.
Sólyom, J., et al.. (2007). Appropriate Sampling Times for Growth Hormone (GH) Measurement during Insulin Tolerance Testing (ITT) in Children. Hormone Research in Paediatrics. 68(5). 205–206. 3 indexed citations
5.
Luczay, Andrea, et al.. (2006). Potential advantage of N363S glucocorticoid receptor polymorphism in 21-hydroxylase deficiency. European Journal of Endocrinology. 154(6). 859–864. 18 indexed citations
6.
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
7.
Sólyom, J., G. Fekete, József Kovács, et al.. (2005). Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia. European Journal of Endocrinology. 153(1). 99–106. 78 indexed citations
8.
Votava, Felix, Dóra Török, József Kovács, et al.. (2005). Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia. European Journal of Endocrinology. 152(6). 869–874. 44 indexed citations
9.
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
10.
Török, Dóra, Zita Halász, Miklós Garami, et al.. (2003). Limited Value of Serum Steroid Measurements in Identification of Mild Form of 21-Hydroxylase Deficiency. Experimental and Clinical Endocrinology & Diabetes. 111(1). 27–32. 11 indexed citations
11.
Frisch, H, Franz Waldhauser, Jan Lebl, et al.. (2002). Congenital Adrenal Hyperplasia: Lessons from a Multinational Study. Hormone Research in Paediatrics. 57(Suppl. 2). 95–101. 26 indexed citations
12.
Theodoropoulou, Marily, Csaba Barta, András Guttman, et al.. (2001). Prenatal Diagnosis of Steroid 21-Hydroxylase Deficiency by Allele-Specific Amplification. Fetal Diagnosis and Therapy. 16(4). 237–240. 3 indexed citations
13.
Kovács, József, Felix Votava, Georg Heinze, et al.. (2001). Lessons From 30 Years of Clinical Diagnosis and Treatment of Congenital Adrenal Hyperplasia in Five Middle European Countries1. The Journal of Clinical Endocrinology & Metabolism. 86(7). 2958–2964. 61 indexed citations
14.
Erhardt, Éva, et al.. (2000). Correlation of Blood-Spot 17-Hydroxyprogesterone Daily Profiles and Urinary Steroid Profiles in Congenital Adrenal Hyperplasia. Journal of Pediatric Endocrinology and Metabolism. 13(2). 205–10. 15 indexed citations
15.
Hosszú, Éva, et al.. (1999). Serum Osteocalcin and Insulin-Like Growth Factor I Levels in Children with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics. 52(3). 131–139. 9 indexed citations
16.
Peter, Michael, et al.. (1998). Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II. European Journal of Pediatrics. 157(5). 378–381. 19 indexed citations
17.
Tar, Attila, Alexandra Ion, J. Sólyom, et al.. (1997). Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13. American Journal of Medical Genetics. 68(2). 231–235. 7 indexed citations
18.
Homoki, J., J. Sólyom, Ulrich Wachter, & W. Teller. (1992). Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. European Journal of Pediatrics. 151(1). 24–28. 14 indexed citations
19.
Hauffa, B. P., J. Sólyom, Edit Gláz, et al.. (1991). Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies. European Journal of Pediatrics. 150(3). 149–153. 15 indexed citations
20.
Sólyom, J., et al.. (1989). Does Hypoprolactinaemia Affect Adrenal Androgen Levels in Children with Hypopituitarism?. Hormone and Metabolic Research. 21(9). 529–530. 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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