☰

Attila Patocs, Ph.D. - Publications

Affiliations: 
2004 Semmelweis Egyetem, Hungary 
Area:
Oncology
Tree Info Similar researchers PubMed Report error

111 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Madar L, Majoros V, Szűcs Z, Nagy O, Babicz T, Butz H, Patócs A, Balogh I, Koczok K. Double Heterozygosity for Rare Deleterious Variants in the and Genes in a Hungarian Patient with Breast Cancer. International Journal of Molecular Sciences. 24. PMID 37895014 DOI: 10.3390/ijms242015334  0.624
2023 Pálla S, Tőke J, Bozsik A, Butz H, Papp J, Likó I, Kuroli E, Bánvölgyi A, Hamar M, Bertherat J, Medvecz M, Patócs A. Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma. Scientific Reports. 13: 16339. PMID 37770543 DOI: 10.1038/s41598-023-43188-6  0.553
2023 Butz H, Nagy P, Papp J, Bozsik A, Grolmusz VK, Pócza T, Oláh E, Patócs A. Variants Extend the Mutational Profile of Hungarian Patients with Breast and Ovarian Cancer. Cancers. 15. PMID 37686625 DOI: 10.3390/cancers15174350  0.608
2023 Pálla S, Tőke J, Bozsik A, Butz H, Papp J, Likó I, Kuroli E, Bánvölgyi A, Hamar M, Bertherat J, Medvecz M, Patócs A. Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma. Scientific Reports. 13: 14658. PMID 37670105 DOI: 10.1038/s41598-023-41878-9  0.642
2023 Butz H, Bozsik A, Grolmusz V, Szőcs E, Papp J, Patócs A. Challenging interpretation of germline TP53 variants based on the experience of a national comprehensive cancer centre. Scientific Reports. 13: 14259. PMID 37653074 DOI: 10.1038/s41598-023-41481-y  0.629
2023 Butz H, Saskői É, Krokker L, Vereczki V, Alpár A, Likó I, Tóth E, Szőcs E, Cserepes M, Nagy K, Kacskovics I, Patócs A. Context-Dependent Role of Glucocorticoid Receptor Alpha and Beta in Breast Cancer Cell Behaviour. Cells. 12. PMID 36899920 DOI: 10.3390/cells12050784  0.586
2023 Grolmusz VK, Nagy P, Likó I, Butz H, Pócza T, Bozsik A, Papp J, Oláh E, Patócs A. A common genetic variation in may associate with cancer risk in patients with Lynch syndrome. Frontiers in Oncology. 13: 1005066. PMID 36890824 DOI: 10.3389/fonc.2023.1005066  0.634
2023 Bozsik A, Butz H, Grolmusz VK, Polgár C, Patócs A, Papp J. Genome sequencing-based discovery of a novel deep intronic APC pathogenic variant causing exonization. European Journal of Human Genetics : Ejhg. PMID 36828923 DOI: 10.1038/s41431-023-01322-y  0.634
2022 Szabó B, Németh K, Mészáros K, Krokker L, Likó I, Saskői É, Németh K, Szabó PT, Szücs N, Czirják S, Szalóki G, Patócs A, Butz H. Aspirin mediates its antitumoral effect through inhibiting PTTG1 in pituitary adenoma. The Journal of Clinical Endocrinology and Metabolism. PMID 36059148 DOI: 10.1210/clinem/dgac496  0.753
2022 Butz H, Patócs A. Mechanisms behind context-dependent role of glucocorticoids in breast cancer progression. Cancer Metastasis Reviews. PMID 35761157 DOI: 10.1007/s10555-022-10047-1  0.583
2022 Butz H, Lövey J, Szentkereszty M, Bozsik A, Tóth E, Patócs A. Case Report: A Novel Pathomechanism in PEComa by the Loss of Heterozygosity of . Frontiers in Oncology. 12: 849004. PMID 35419288 DOI: 10.3389/fonc.2022.849004  0.651
2022 Turai PI, Herold Z, Nyirő G, Borka K, Micsik T, Tőke J, Szücs N, Tóth M, Patócs A, Igaz P. Tissue miRNA Combinations for the Differential Diagnosis of Adrenocortical Carcinoma and Adenoma Established by Artificial Intelligence. Cancers. 14. PMID 35205648 DOI: 10.3390/cancers14040895  0.701
2022 Bozsik A, Papp J, Grolmusz VK, Patócs A, Oláh E, Butz H. Reclassification of Five BRCA1/2 Variants with Unknown Significance Using Complex Functional Study. Cancer Research and Treatment. PMID 35167739 DOI: 10.4143/crt.2021.1078  0.621
2022 Sarkadi B, Saskoi E, Butz H, Patocs A. Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach. International Journal of Molecular Sciences. 23. PMID 35163370 DOI: 10.3390/ijms23031450  0.635
2021 Igaz P, Toth G, Nagy P, Dezső K, Turai PI, Medvecz M, Wikonkal N, Huszty G, Piros L, Toth E, Bozsik A, Likó I, Patócs A, Butz H. Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of in Gorlin-Goltz syndrome. Journal of Medical Genetics. PMID 34916233 DOI: 10.1136/jmedgenet-2021-108082  0.659
2021 Butz H, Mészáros K, Likó I, Patocs A. Wnt-Signaling Regulated by Glucocorticoid-Induced miRNAs. International Journal of Molecular Sciences. 22. PMID 34769207 DOI: 10.3390/ijms222111778  0.611
2021 Sarkadi B, Liko I, Nyiro G, Igaz P, Butz H, Patocs A. Analytical Performance of NGS-Based Molecular Genetic Tests Used in the Diagnostic Workflow of Pheochromocytoma/Paraganglioma. Cancers. 13. PMID 34439371 DOI: 10.3390/cancers13164219  0.657
2021 Krokker L, Szabó B, Németh K, Tóháti R, Sarkadi B, Mészáros K, Patócs A, Butz H. Three Dimensional Cell Culturing for Modeling Adrenal and Pituitary Tumors. Pathology Oncology Research : Por. 27: 640676. PMID 34257605 DOI: 10.3389/pore.2021.640676  0.583
2021 Krokker L, Patócs A, Butz H. Essential Role of the 14q32 Encoded miRNAs in Endocrine Tumors. Genes. 12. PMID 34066712 DOI: 10.3390/genes12050698  0.592
2021 Pócza T, Grolmusz VK, Papp J, Butz H, Patócs A, Bozsik A. Germline Structural Variations in Cancer Predisposition Genes. Frontiers in Genetics. 12: 634217. PMID 33936164 DOI: 10.3389/fgene.2021.634217  0.623
2021 Turai PI, Nyírő G, Butz H, Patócs A, Igaz P. MicroRNAs, Long Non-Coding RNAs, and Circular RNAs: Potential Biomarkers and Therapeutic Targets in Pheochromocytoma/Paraganglioma. Cancers. 13. PMID 33810219 DOI: 10.3390/cancers13071522  0.604
2021 Butz H, Papp J, Bozsik A, Krokker L, Pócza T, Oláh E, Patócs A. Application of Multilayer Evidence for Annotation of C-Terminal Variants. Cancers. 13. PMID 33672545 DOI: 10.3390/cancers13040881  0.593
2021 Butz H, Blair J, Patócs A. Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes. Endocrine. PMID 33570725 DOI: 10.1007/s12020-021-02636-x  0.615
2020 Kövesdi A, Kurucz PA, Nyírő G, Darvasi O, Patócs A, Butz H. Circulating miRNA Increases the Diagnostic Accuracy of Chromogranin A in Metastatic Pancreatic Neuroendocrine Tumors. Cancers. 12. PMID 32887459 DOI: 10.3390/Cancers12092488  0.648
2020 Saskői É, Hujber Z, Nyírő G, Likó I, Mátyási B, Petővári G, Mészáros K, Kovács AL, Patthy L, Supekar S, Fan H, Sváb G, Tretter L, Sarkar A, Nazir A, et al. The SDHB Arg230His mutation causing familial paraganglioma alters glycolysis in a new model. Disease Models & Mechanisms. PMID 32859697 DOI: 10.1242/Dmm.044925  0.316
2020 Bozsik A, Pócza T, Papp J, Vaszkó T, Butz H, Patócs A, Oláh E. Complex Characterization of Germline Large Genomic Rearrangements of the and Genes in High-Risk Breast Cancer Patients-Novel Variants from a Large National Center. International Journal of Molecular Sciences. 21. PMID 32629901 DOI: 10.3390/Ijms21134650  0.674
2020 Szabó B, Németh K, Mészáros K, Szücs N, Czirják S, Reiniger L, Rajnai H, Krencz I, Karászi K, Krokker L, Patócs A, Butz H. Demethylation status of somatic DNA extracted from pituitary neuroendocrine tumors indicates proliferative behavior. The Journal of Clinical Endocrinology and Metabolism. PMID 32232382 DOI: 10.1210/Clinem/Dgaa156  0.763
2020 Butz H, Nyírő G, Kurucz PA, Likó I, Patócs A. Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice. Human Genetics. PMID 32222824 DOI: 10.1007/S00439-020-02148-0  0.669
2020 Sarkadi B, Meszaros K, Krencz I, Canu L, Krokker L, Zakarias S, Barna G, Sebestyen A, Papay J, Hujber Z, Butz H, Darvasi O, Igaz P, Doczi J, Luconi M, ... ... Patocs A, et al. Glutaminases as a Novel Target for SDHB-Associated Pheochromocytomas/Paragangliomas. Cancers. 12. PMID 32150977 DOI: 10.3390/Cancers12030599  0.646
2019 Decmann A, Nyírö G, Darvasi O, Turai P, Bancos I, Kaur RJ, Pezzani R, Iacobone M, Kraljevic I, Kastelan D, Parasiliti-Caprino M, Maccario M, Nirschl N, Heinrich D, Reincke M, et al. Circulating miRNA Expression Profiling in Primary Aldosteronism. Frontiers in Endocrinology. 10: 739. PMID 31736877 DOI: 10.3389/Fendo.2019.00739  0.339
2019 Sarkadi B, Patócs A. Hereditary Diseases Predisposing to Pheochromocytoma (VHL, NF-1, Paraganglioma Syndromes, and Novel Genes). Experientia Supplementum (2012). 111: 129-147. PMID 31588531 DOI: 10.1007/978-3-030-25905-1_8  0.38
2019 Decmann A, Patócs A, Igaz P. Overview of Genetically Determined Diseases/Multiple Endocrine Neoplasia Syndromes Predisposing to Endocrine Tumors. Experientia Supplementum (2012). 111: 105-127. PMID 31588530 DOI: 10.1007/978-3-030-25905-1_7  0.354
2019 Butz H, Patócs A. Brief Summary of the Most Important Molecular Genetic Methods (PCR, qPCR, Microarray, Next-Generation Sequencing, etc.). Experientia Supplementum (2012). 111: 33-52. PMID 31588527 DOI: 10.1007/978-3-030-25905-1_4  0.647
2019 Kövesdi A, Patócs A. Brief Description of Inheritance Patterns. Experientia Supplementum (2012). 111: 21-27. PMID 31588525 DOI: 10.1007/978-3-030-25905-1_2  0.362
2019 Nagy O, Kárteszi J, Hartwig M, Bertalan R, Jávorszky E, Erhardt É, Patócs A, Tornóczky T, Balogh I, Ujfalusi A. 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. PMID 31338750 DOI: 10.1007/S11033-019-04980-8  0.765
2019 Bertalan R, Bencsik Z, Mezei P, Vajda Z, Butz H, Patócs A. Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers. Molecular Biology Reports. PMID 31280422 DOI: 10.1007/S11033-019-04688-9  0.791
2019 Sarkadi B, Baghy K, Sápi Z, Nyirő G, Likó I, Patócs A. Germline Mutation Detected in a Multiple Endocrine Neoplasia Type 2 Case With Codon 634 Mutation. Frontiers in Genetics. 10: 544. PMID 31263477 DOI: 10.3389/Fgene.2019.00544  0.399
2019 Butz H, Patócs A. MicroRNAs in endocrine tumors. Ejifcc. 30: 146-164. PMID 31263390  0.621
2019 Németh K, Darvasi O, Likó I, Szücs N, Czirják S, Reiniger L, Szabó B, Krokker L, Pállinger É, Igaz P, Patócs A, Butz H. Comprehensive analysis of circulating microRNAs in plasma of patients with pituitary adenomas. The Journal of Clinical Endocrinology and Metabolism. PMID 31112271 DOI: 10.1210/Jc.2018-02479  0.785
2019 Kövesdi A, Tóth M, Butz H, Szücs N, Sármán B, Pusztai P, Tőke J, Reismann P, Fáklya M, Tóth G, Somogyi A, Borka K, Erdei A, Nagy EV, Deák V, et al. True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome. Endocrine. PMID 31044390 DOI: 10.1007/S12020-019-01932-X  0.796
2019 Krokker L, Nyírő G, Reiniger L, Darvasi O, Szücs N, Czirják S, Tóth M, Igaz P, Patócs A, Butz H. Differentially Expressed miRNAs Influence Metabolic Processes in Pituitary Oncocytoma. Neurochemical Research. PMID 30945144 DOI: 10.1007/S11064-019-02789-2  0.782
2019 Bazsó A, Szappanos Á, Rásonyi R, Nagy E, Farkas A, Várnai B, Patócs A, Kiss E, Poór G. Polymorphisms of human glucocorticoid receptor gene in systemic lupus erythematosus: a single-centre result. Clinical Rheumatology. PMID 30850964 DOI: 10.1007/S10067-019-04478-5  0.321
2018 Németh K, Szücs N, Czirják S, Reiniger L, Szabó B, Barna G, Karászi K, Igaz P, Zivkovic V, Korbonits M, Patócs A, Butz H. Survivin as a potential therapeutic target of acetylsalicylic acid in pituitary adenomas. Oncotarget. 9: 29180-29192. PMID 30018744 DOI: 10.18632/Oncotarget.25650  0.764
2018 Grolmusz VK, Kövesdi A, Borka K, Igaz P, Patocs A. Prognostic relevance of proliferation-related miRNAs in pancreatic neuroendocrine neoplasms. European Journal of Endocrinology. PMID 30006373 DOI: 10.1530/Eje-18-0305  0.315
2018 Marczell I, Balogh P, Nyiro G, Kiss AL, Kovacs B, Bekesi G, Racz K, Patocs A. Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells. European Journal of Medical Research. 23: 31. PMID 29880033 DOI: 10.1186/S40001-018-0328-7  0.502
2018 Neumann HPH, Young W, Krauss T, Bayley JP, Schiavi F, Opocher G, Boedeker C, Tirosh A, Castinetti F, Ruf J, Beltsevich D, Walz MK, Groeben H, Von Dobschuetz E, Gimm O, ... ... Patocs A, et al. Genetics Informs Precision Practice in the Diagnosis and Management of Pheochromocytoma. Endocrine-Related Cancer. PMID 29794110 DOI: 10.1530/Erc-18-0085  0.394
2018 Molnár Á, Patócs A, Likó I, Nyírő G, Rácz K, Tóth M, Sármán B. An unexpected, mild phenotype of glucocorticoid resistance associated with glucocorticoid receptor gene mutation case report and review of the literature. Bmc Medical Genetics. 19: 37. PMID 29510671 DOI: 10.1186/S12881-018-0552-6  0.571
2018 Sarkadi B, Grolmusz VK, Butz H, Kövesdi A, Likó I, Nyirő G, Igaz P, Patócs A. [Evolution of molecular genetic methods in the clinical diagnosis of hereditary endocrine tumour syndromes]. Orvosi Hetilap. 159: 285-292. PMID 29429353 DOI: 10.1556/650.2018.31036  0.668
2018 Doleschall M, Török D, Mészáros K, Luczay A, Halász Z, Németh K, Szücs N, Kiss R, Tőke J, Sólyom J, Fekete G, Patócs A, Igaz P, Tóth M. [Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]. Orvosi Hetilap. 159: 269-277. PMID 29429350 DOI: 10.1556/650.2018.30986  0.79
2018 Perge P, Decmann Á, Pezzani R, Bancos I, Fassina A, Luconi M, Canu L, Tóth M, Boscaro M, Patócs A, Igaz P. Analysis of circulating extracellular vesicle-associated microRNAs in cortisol-producing adrenocortical tumors. Endocrine. PMID 29299796 DOI: 10.1007/S12020-017-1506-Z  0.351
2017 Darvasi O, Szabo PM, Nemeth K, Szabo K, Spisak S, Liko I, Czirjak S, Racz K, Igaz P, Patocs A, Butz H. Limitations of high throughput methods for miRNA expression profiles in non-functioning pituitary adenomas. Pathology Oncology Research : Por. PMID 29043608 DOI: 10.1007/S12253-017-0330-3  0.708
2017 Dávid A, Butz H, Halász Z, Török D, Nyirő G, Muzsnai Á, Csákváry V, Luczay A, Sallai Á, Hosszú É, Felszeghy E, Tar A, Szántó Z, Fekete GL, Kun I, et al. [The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]. Orvosi Hetilap. 158: 1351-1356. PMID 28823207 DOI: 10.1556/650.2017.30829  0.767
2017 Perge P, Butz H, Pezzani R, Bancos I, Nagy Z, Pálóczi K, Nyírő G, Decmann Á, Pap E, Luconi M, Mannelli M, Buzás EI, Tóth M, Boscaro M, Patócs A, et al. Evaluation and diagnostic potential of circulating extracellular vesicle-associated microRNAs in adrenocortical tumors. Scientific Reports. 7: 5474. PMID 28710381 DOI: 10.1038/S41598-017-05777-0  0.642
2017 Castinetti F, Maia AL, Peczkowska M, Barontini M, Hasse-Lazar K, Links TP, Toledo RA, Dvorakova S, Mian C, Bugalho MJ, Zovato S, Alevizaki M, Kvachenyuk A, Bausch B, Loli P, ... ... Patocs A, et al. THE PENETRANCE OF MEN2 PHEOCHROMOCYTOMA IS NOT ONLY DETERMINED BY RET MUTATIONS. Endocrine-Related Cancer. PMID 28649091 DOI: 10.1530/Erc-17-0189  0.353
2017 Grolmusz VK, Borka K, Kövesdi A, Németh K, Balogh K, Dékány C, Kiss A, Szentpéteri A, Sármán B, Somogyi A, Csajbók É, Valkusz Z, Tóth M, Igaz P, Rácz K, et al. MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism. Virchows Archiv : An International Journal of Pathology. PMID 28597079 DOI: 10.1007/S00428-017-2158-3  0.576
2017 Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt É, Szilágyi Á, Doleschall Z, Németh K, Török D, Prohászka Z, Gereben B, Fekete G, Gláz E, Igaz P, Korbonits M, et al. A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics. European Journal of Human Genetics : Ejhg. PMID 28401898 DOI: 10.1038/Ejhg.2017.38  0.519
2017 Bausch B, Schiavi F, Ni Y, Welander J, Patocs A, Ngeow J, Wellner U, Malinoc A, Taschin E, Barbon G, Lanza V, Söderkvist P, Stenman A, Larsson C, Svahn F, et al. Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. Jama Oncology. PMID 28384794 DOI: 10.1001/Jamaoncol.2017.0223  0.582
2017 Decmann Á, Perge P, Nagy Z, Butz H, Patócs A, Igaz P. [Circulating microRNAs in the diagnostics of endocrine neoplasms]. Orvosi Hetilap. 158: 483-490. PMID 28347154 DOI: 10.1556/650.2017.30708  0.67
2017 David A, Kun IZ, Nyírő G, Szántó Z, Patócs A. Heterozygous Deletion in Exons 4-5 of SHOX Gene in a Patient Diagnosed as Idiopathic Short Stature Acta Medica Marisiensis. 63: 155-158. DOI: 10.1515/Amma-2017-0028  0.372
2016 Butz H, Németh K, Czenke D, Likó I, Czirják S, Zivkovic V, Baghy K, Korbonits M, Kovalszky I, Igaz P, Rácz K, Patócs A. Systematic Investigation of Expression of G2/M Transition Genes Reveals CDC25 Alteration in Nonfunctioning Pituitary Adenomas. Pathology Oncology Research : Por. PMID 28004354 DOI: 10.1007/S12253-016-0163-5  0.719
2016 Grolmusz VK, Karászi K, Micsik T, Tóth EA, Mészáros K, Karvaly G, Barna G, Szabó PM, Baghy K, Matkó J, Kovalszky I, Tóth M, Rácz K, Igaz P, Patócs A. Cell cycle dependent RRM2 may serve as proliferation marker and pharmaceutical target in adrenocortical cancer. American Journal of Cancer Research. 6: 2041-2053. PMID 27725909  0.491
2016 Nagy Z, Marta A, Butz H, Liko I, Racz K, Patocs A. Modulation of the circadian clock by glucocorticoid receptor isoforms in the H295R cell line. Steroids. PMID 27725099 DOI: 10.1016/J.Steroids.2016.10.002  0.713
2016 Tóth G, Patócs A, Tóth M. [Hereditary phaeochromocytoma in twins]. Orvosi Hetilap. 157: 1326-1330. PMID 27523316 DOI: 10.1556/650.2016.30513  0.415
2016 Marczell I, Hrabak A, Nyiro G, Patocs A, Stark J, Dinya E, Kukor Z, Toth S, Tulassay ZS, Racz K, Bekesi G. 17-β-estradiol Decreases Neutrophil Superoxide Production through Rac1. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. PMID 27437916 DOI: 10.1055/s-0042-105556  0.436
2016 Grolmusz VK, Tóth EA, Baghy K, Likó I, Darvasi O, Kovalszky I, Matkó J, Rácz K, Patócs A. Fluorescence activated cell sorting followed by small RNA sequencing reveals stable microRNA expression during cell cycle progression. Bmc Genomics. 17: 412. PMID 27234232 DOI: 10.1186/S12864-016-2747-6  0.518
2016 Patócs A, Lendvai NK, Butz H, Liko I, Sapi Z, Szucs N, Toth G, Grolmusz VK, Igaz P, Toth M, Rácz K. Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome. Pathology Oncology Research : Por. PMID 26960314 DOI: 10.1007/S12253-016-0050-0  0.801
2016 Molnár Á, Kövesdi A, Szücs N, Tóth M, Igaz P, Rácz K, Patócs A. Polymorphisms of the GR and HSD11B1genes influence body mass index and weight gain during hormone replacement treatment in patients with Addison's disease. Clinical Endocrinology. PMID 26800219 DOI: 10.1111/Cen.13022  0.753
2015 Nagy Z, Baghy K, Hunyadi-Gulyás É, Micsik T, Nyírő G, Rácz G, Butz H, Perge P, Kovalszky I, Medzihradszky KF, Rácz K, Patócs A, Igaz P. Evaluation of 9-cis retinoic acid and mitotane as antitumoral agents in an adrenocortical xenograft model. American Journal of Cancer Research. 5: 3645-58. PMID 26885453  0.688
2015 Patócs A, Likó I, Butz H, Baghy K, Rácz K. [Novel methods and their applicability in the evaluation of the genetic background of endocrine system tumours]. Orvosi Hetilap. 156: 2063-9. PMID 26654542 DOI: 10.1556/650.2015.30316  0.735
2015 Butz H, Patócs A. Technical Aspects Related to the Analysis of Circulating microRNAs. Exs. 106: 55-71. PMID 26608199 DOI: 10.1007/978-3-0348-0955-9_3  0.64
2015 Nagy Z, Acs B, Butz H, Feldman K, Marta A, Szabo PM, Baghy K, Pazmany T, Racz K, Liko I, Patocs A. Overexpression of GRß in colonic mucosal cell line partly reflects altered gene expression in colonic mucosa of patients with inflammatory bowel disease. The Journal of Steroid Biochemistry and Molecular Biology. 155: 76-84. PMID 26480216 DOI: 10.1016/J.Jsbmb.2015.10.006  0.723
2015 Igaz I, Nyírő G, Nagy Z, Butz H, Nagy Z, Perge P, Sahin P, Tóth M, Rácz K, Igaz P, Patócs A. Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin. International Journal of Endocrinology. 2015: 589230. PMID 26161091 DOI: 10.1155/2015/589230  0.692
2015 Butz H, Kinga N, Racz K, Patocs A. Circulating miRNAs as biomarkers for endocrine disorders. Journal of Endocrinological Investigation. PMID 26015318 DOI: 10.1007/S40618-015-0316-5  0.696
2015 Butz H, Szabó PM, Khella HW, Nofech-Mozes R, Patocs A, Yousef GM. miRNA-target network reveals miR-124as a key miRNA contributing to clear cell renal cell carcinoma aggressive behaviour by targeting CAV1 and FLOT1. Oncotarget. 6: 12543-57. PMID 26002553 DOI: 10.18632/Oncotarget.3815  0.639
2015 Balog B, T?ke J, Róna K, Szücs N, Igaz P, Pusztai P, Sármán B, Gláz E, Kiss R, Patócs A, Rácz K, Tóth M. [Analysis of laboratory data of 155 patients with pheochromocytoma-paraganglioma syndrome diagnosed during the past 20 years]. Orvosi Hetilap. 156: 626-35. PMID 25864138 DOI: 10.1556/Oh.2015.30127  0.751
2015 Al-Aissa Z, Rosta K, Hadarits O, Harreiter J, Zóka A, Bancher-Todesca D, Patócs A, Kiss K, Sármán B, Pusztai P, Sziller I, Rigó J, Rácz K, Somogyi A, Kautzky-Willer A, et al. Cord serum dipeptidyl-peptidase 4 activity in gestational diabetes. European Journal of Clinical Investigation. 45: 196-203. PMID 25556541 DOI: 10.1111/Eci.12397  0.481
2015 Szappanos A, Nagy Z, Kovacs B, Poor G, Toth M, Racz K, Kiss E, Patocs A. Tissue-specific Glucocorticoid Signaling May Determine the Resistance Against Glucocorticoids in Autoimmune Diseases Current Medicinal Chemistry. 22: 1126-1135. DOI: 10.2174/0929867321666141216125012  0.532
2014 Szappanos A, Nagy Z, Kovács B, Poór G, Tóth M, Rácz K, Kiss E, Patócs A. Tissue-Specific Glucocorticoid Signaling May Determine The Resistance Against Glucocorticoids In Autoimmune Diseases. Current Medicinal Chemistry. PMID 25511778  0.475
2014 T?ke J, Czirják G, Tóth M, Rácz K, Patócs A. [Significance of biochemical markers in the diagnosis of neuroendocrine tumours and for the follow-up of patients]. Orvosi Hetilap. 155: 1775-82. PMID 25362640 DOI: 10.1556/Oh.2014.30035  0.529
2014 Doleschall M, Szabó JA, Pázmándi J, Szilágyi Á, Koncz K, Farkas H, Tóth M, Igaz P, Gláz E, Prohászka Z, Korbonits M, Rácz K, Füst G, Patócs A. Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels. Plos One. 9: e107244. PMID 25210767 DOI: 10.1371/Journal.Pone.0107244  0.554
2014 Butz H, Szabó PM, Nofech-Mozes R, Rotondo F, Kovacs K, Mirham L, Girgis H, Boles D, Patocs A, Yousef GM. Integrative bioinformatics analysis reveals new prognostic biomarkers of clear cell renal cell carcinoma. Clinical Chemistry. 60: 1314-26. PMID 25139457 DOI: 10.1373/Clinchem.2014.225854  0.602
2014 Grolmusz VK, Acs OD, Feldman-Kovács K, Szappanos Á, Stenczer B, Fekete T, Szendei G, Reismann P, Rácz K, Patócs A. Genetic variants of the HSD11B1 gene promoter may be protective against polycystic ovary syndrome. Molecular Biology Reports. 41: 5961-9. PMID 24969481 DOI: 10.1007/S11033-014-3473-2  0.542
2014 Castinetti F, Qi XP, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, ... ... Patocs A, et al. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet. Oncology. 15: 648-55. PMID 24745698 DOI: 10.1016/S1470-2045(14)70154-8  0.517
2014 Erdélyi LS, Balla A, Patócs A, Tóth M, Várnai P, Hunyady L. Altered agonist sensitivity of a mutant v2 receptor suggests a novel therapeutic strategy for nephrogenic diabetes insipidus. Molecular Endocrinology (Baltimore, Md.). 28: 634-43. PMID 24628417 DOI: 10.1210/Me.2013-1424  0.309
2014 Lendvai N, Pawlosky R, Bullova P, Eisenhofer G, Patocs A, Veech RL, Pacak K. Succinate-to-fumarate ratio as a new metabolic marker to detect the presence of SDHB/D-related paraganglioma: initial experimental and ex vivo findings. Endocrinology. 155: 27-32. PMID 24189137 DOI: 10.1210/En.2013-1549  0.343
2014 Bausch B, Wellner U, Bausch D, Schiavi F, Barontini M, Sanso G, Walz MK, Peczkowska M, Weryha G, Dall'igna P, Cecchetto G, Bisogno G, Moeller LC, Bockenhauer D, Patocs A, et al. Long-term prognosis of patients with pediatric pheochromocytoma. Endocrine-Related Cancer. 21: 17-25. PMID 24169644 DOI: 10.1530/Erc-13-0415  0.597
2013 Bekő G, Butz H, Berta K, Tislér A, Olajos F, Vásárhelyi B, Patócs A. Switching between parathormone (PTH) assays: the impact on the diagnosis of renal osteodystrophy. Clinical Chemistry and Laboratory Medicine. 51: 1251-6. PMID 23241601 DOI: 10.1515/Cclm-2012-0485  0.57
2012 Trivellin G, Butz H, Delhove J, Igreja S, Chahal HS, Zivkovic V, McKay T, Patócs A, Grossman AB, Korbonits M. MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro. American Journal of Physiology. Endocrinology and Metabolism. 303: E708-19. PMID 22811466 DOI: 10.1152/Ajpendo.00546.2011  0.645
2012 Offergeld C, Brase C, Yaremchuk S, Mader I, Rischke HC, Gläsker S, Schmid KW, Wiech T, Preuss SF, Suárez C, Kopeć T, Patocs A, Wohllk N, Malekpour M, Boedeker CC, et al. Head and neck paragangliomas: clinical and molecular genetic classification. Clinics (Sã£O Paulo, Brazil). 67: 19-28. PMID 22584701 DOI: 10.6061/Clinics/2012(Sup01)05  0.321
2012 Halászlaki C, Takács I, Butz H, Patócs A, Lakatos P. Novel genetic mutation in the background of Carney complex. Pathology Oncology Research : Por. 18: 149-52. PMID 22297707 DOI: 10.1007/S12253-012-9502-3  0.68
2011 Halászlaki C, Takács I, Patócs A, Lakatos P. [Novel mutation in a patient with Carney complex]. Orvosi Hetilap. 152: 802-4. PMID 21540154 DOI: 10.1556/Oh.2011.29117  0.397
2011 Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, ... ... Patocs A, et al. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human Mutation. 32: 51-8. PMID 20979234 DOI: 10.1002/Humu.21385  0.348
2010 Boyle B, Butz H, Liko I, Zalatnai A, Toth M, Feldman K, Horanyi J, Igaz P, Racz K, Patocs A. Expression of glucocorticoid receptor isoforms in human adrenocortical adenomas. Steroids. 75: 695-700. PMID 20438742 DOI: 10.1016/J.Steroids.2010.04.008  0.687
2010 Beko G, Varga I, Glaz E, Sereg M, Feldman K, Toth M, Racz K, Patocs A. Cutoff values of midnight salivary cortisol for the diagnosis of overt hypercortisolism are highly influenced by methods. Clinica Chimica Acta; International Journal of Clinical Chemistry. 411: 364-7. PMID 19968981 DOI: 10.1016/J.Cca.2009.11.033  0.506
2010 Butz H, Likó I, Czirják S, Igaz P, Khan MM, Zivkovic V, Bálint K, Korbonits M, Rácz K, Patócs A. Down-Regulation of Wee1 Kinase by a Specific Subset of microRNAs in Human Sporadic Pituitary Adenomas Molecular Endocrinology. 24: 1886-1886. DOI: 10.1210/mend.24.9.9995  0.673
2010 Pregun I, Herszényi L, Miheller P, Juhász M, Lakatos G, Patócs A, Rácz K, Tulassay Z. W1097 Serum Chromogranin a Level Decreases Rapidly After Cessation of ProtonPump Inhibitor Therapy Gastroenterology. 138: S-650. DOI: 10.1016/S0016-5085(10)62995-2  0.472
2009 Patocs A, Balogh K, Racz K. Adrenal tumors in MEN1 syndrome and the role of menin in adrenal tumorigenesis. Advances in Experimental Medicine and Biology. 668: 97-103. PMID 20175457 DOI: 10.1007/978-1-4419-1664-8_10  0.547
2009 Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, Fazakas F, Szabo I, Kovacs B, Glaz E, Racz K. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. European Journal of Endocrinology / European Federation of Endocrine Societies. 161: 495-502. PMID 19574279 DOI: 10.1530/Eje-09-0399  0.79
2009 Mondok A, Varga I, Glaz E, Szucs N, Tóth M, Patocs A, Beko G, Racz K. 11beta-hydroxysteroid dehydrogenase activity in acromegalic patients with normal or impaired carbohydrate metabolism. Steroids. 74: 725-9. PMID 19540999 DOI: 10.1016/J.Steroids.2009.03.003  0.739
2009 Bertalan R, Patocs A, Nagy B, Derzsy Z, Gullai N, Szappanos A, Rigo J, Racz K. Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome. Clinica Chimica Acta; International Journal of Clinical Chemistry. 405: 148-52. PMID 19336230 DOI: 10.1016/J.Cca.2009.03.046  0.767
2009 Locsei Z, Racz K, Patocs A, Kovacs GL, Toldy E. Influence of sampling and storage conditions on plasma renin activity and plasma renin concentration. Clinica Chimica Acta; International Journal of Clinical Chemistry. 402: 203-5. PMID 19263530 DOI: 10.1016/J.Cca.2009.01.013  0.482
2009 Szappanos A, Toke J, Lippai D, Patocs A, Igaz P, Futo L, Racz K, Toth M. Bone turnover in patients with endogenous Cushing's syndrome before and after successful treatment Bone. 44. DOI: 10.1016/J.Bone.2009.03.173  0.504
2008 Bertalan R, Patocs A, Vasarhelyi B, Treszl A, Varga I, Szabo E, Tamas J, Toke J, Boyle B, Nobilis A, Rigo J, Racz K. 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: 91-4. PMID 18595687 DOI: 10.1016/J.Jsbmb.2008.05.002  0.753
2008 Patocs A, Gergics P, Balogh K, Toth M, Fazakas F, Liko I, Racz K. Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family. Bmc Medical Genetics. 9: 29. PMID 18416845 DOI: 10.1186/1471-2350-9-29  0.601
2008 Boyle B, Korányi K, Patocs A, Liko I, Szappanos A, Bertalan R, Racz K, Balazs C. Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy. The British Journal of Ophthalmology. 92: 131-4. PMID 18156379 DOI: 10.1136/Bjo.2007.126789  0.755
2007 Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1. Clinical Endocrinology. 67: 727-34. PMID 17953629 DOI: 10.1111/J.1365-2265.2007.02953.X  0.567
2007 Tõke J, Czirják G, Patócs A, Enyedi B, Gergics P, Csákváry V, Enyedi P, Tóth M. Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene. Clinical Endocrinology. 67: 385-92. PMID 17555508 DOI: 10.1111/J.1365-2265.2007.02896.X  0.351
2006 Patocs A, Klein I, Szilvasi A, Gergics P, Toth M, Valkusz Z, Forizs E, Igaz P, Al-Farhat Y, Tordai A, Varadi A, Racz K, Esik O. Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancer. Wiener Klinische Wochenschrift. 118: 417-21. PMID 16865647 DOI: 10.1007/S00508-006-0635-9  0.585
2006 Gergics P, Patocs A, Majnik J, Balogh K, Szappanos A, Toth M, Racz K. Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction. The Journal of Steroid Biochemistry and Molecular Biology. 100: 161-6. PMID 16806906 DOI: 10.1016/J.Jsbmb.2006.04.004  0.55
2006 Majnik J, Patocs A, Balogh K, Toth M, Gergics P, Szappanos A, Mondok A, Borgulya G, Panczel P, Prohaszka Z, Racz K. Overrepresentation of the N363S variant of the glucocorticoid receptor gene in patients with bilateral adrenal incidentalomas. The Journal of Clinical Endocrinology and Metabolism. 91: 2796-9. PMID 16636127 DOI: 10.1210/Jc.2006-0066  0.562
2005 Patocs A, Liko I, Varga I, Gergics P, Boros A, Futo L, Kun I, Bertalan R, Toth S, Pazmany T, Toth M, Szücs N, Horanyi J, Glaz E, Racz K. Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-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: 257-65. PMID 16176874 DOI: 10.1016/J.Jsbmb.2005.06.035  0.785
Show low-probability matches.