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Meno a priezvisko:
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doc. MUDr. Juraj Staník, PhD.
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Typ dokumentu:
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Vedecko/umelecko-pedagogická charakteristika osoby
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Názov vysokej školy:
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Univerzita Komenského v Bratislave
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Sídlo vysokej školy:
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Šafárikovo námestie 6, 818 06 Bratislava
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| III.a - Zamestnanie-pracovné zaradenie | III.b - Inštitúcia | III.c - Časové vymedzenie |
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| Odborný asistent | Univerzita Komenského v Bratislave, Lekárska fakulta | 2002-2016 |
| docent | Univerzita Komenského v Bratislave, Lekárska fakulta | 2016-doteraz |
| IV.a - Popis aktivity, názov kurzu (ak išlo o kurz), iné | IV.b - Názov inštitúcie | IV.c - Rok |
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| Atestácia z Pediatrie | Slovenská zdravotnícka univerzita, | 2008 |
| Atestácia z Endokrinológie a Diabetológie | Institut postgraduálního vzdelávání, Praha, ČR | 2011 |
| V.1.a - Názov profilového predmetu | V.1.b - Študijný program | V.1.c - Stupeň | V.1.d - Študijný odbor |
|---|---|---|---|
| Pediatria | Všeobecné lekárstvo | I+II | všeobecné lekárstvo |
| Pediatria | Zubné lekárstvo | I+II | Zubné lekárstvo |
Staník, Juraj [UKOLF1DK] - Gašperíková, Daniela - PaškoStaník, Juraj [UKOLF1DK] - Gašperíková, Daniela - Pašková, Magdaléna - Barák, Ľubomír [UKOLF1DK] - Javorková, Jana - Jančová, Emília - Kuricová, Miriam [UKOLJ] - Hlava, Peter - Michálek, Jozef - Flanagan, Sarah E. - Pearson, Ewan - Hattersley,Andrew T. - Ellard, Sian - Klimeš, Iwar: Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers. Journal of Clinical Endocrinology & Metabolism. - Vol. 92, No. 4 (2007), s. 1276-1282. - ISSN 0021-972X (IF=5,493)
Gašperíková, Daniela (10%) - Tribble, Nicolas (5%) - Staník, Juraj [UKOLF1DK] (10%) - Hučková, Miroslava (5%) - Mišovicová, Nadežda (5%) - van de Bunt, Martijn (5%) - Valentínová, Lucia [UKOPRBZF] (5%) - Barrow, Beryl (5%) - Barák, Ľubomír[UKOLF1DK] (5%) - Dobránsky, Radoslav (5%) - Bereczková, Eva (5%) - Michálek, Jozef (5%) - Wicks, Kate (5%) - Colclough, Kevin (5%) - Knight, Julian (5%) - Ellard, Sian (5%) - Klimeš, Iwar (5%) - Gloyn, A. L. (5%): Identification of a novel beta-cell glucokinase (GCK) promoter mutation (- 71G>C) that modulates GCK gene expression through loss of allele-specific Sp1 binding causing mild fasting hyperglycaemia in humans. Diabetes. - Vol. 58, No. 8 (2009), s. 1929-1935. - ISSN 0012-1797. (IF=8,505)
Suliman, Sara G.I. - Staník, Juraj [UKOLF1DK] (15%) - McCulloch, Laura J. - Wilson, Natalie - Edghill, Emma L. - Mišovičová, Nadežda - Gašperíková, Daniela - Sandriková, Vilja - Elliott, Katherine S. - Barák, Ľubomír [UKOLF1DK] (5%) - Ellard, Sian -Volpi, Emanuela V. - Klimeš, Iwar - Gloyn, Anna L.: Severe insulin resistance and intrauterine growth deficiency associated with haploinsufficiency for INSR and CHN2. New insights into synergistic pathways involved in growth and metabolism. Diabetes. - Vol. 58, No. 12 (2009), s. 2954-2961. - ISSN 0012-1797. (IF=8,505)
Thanabalasingham, Gaya - Huffman, Jennifer E. - Kattla, Jayesh J. - Novokmet, Mislav - Rudan, Igor - Gašperíková, Daniela - Staník, Juraj [UKOLF1DK] - Klimeš, Iwar: Mutations in HNF1A result in marked alterations of plasma glycan profile. Diabetes. - Vol. 62, No. 4 (2013), s. 1329-1337. - ISSN 0012-1797. (IF=8,471)
Staník, Juraj [UKOLF1DK] (28%) - Dušátková, Petra (25%) - Cinek, Ondrej (3%) - Valentínová, Lucia (3%) - Hučková, Miroslava (3%) - Škopková, Martina (3%) - Dušátková, Lenka (3%) - Staníková, Daniela [UKOLF1DK] (3%) - Pura, Mikuláš (3%) - Klimeš,Iwar (3%) - Lebl, Jan (3%) - Gašperíková, Daniela [KAUT] (10%) - Průhová, Štepánka (10%): De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed. Diabetologia. - Vol. 57, No. 3 (2014), s. 480-484. - ISSN 0012-186X. (IF=6,671)
Kempf E, Vogel M, Vogel T, Kratzsch J, Landgraf K, Kühnapfel A, Gausche R, Gräfe D, Sergeyev E, Pfäffle R,
Kiess W, Stanik J, Körner A. Dynamic alterations in linear growth and endocrine parameters in children with
obesity and height reference values.EClinicalMedicine. 2021 Jun 23;37:100977. doi:
10.1016/j.eclinm.2021.100977. (2021: 17,033 - IF, Q1 - JCR, 4,657 - SJR, Q1 - SJR). Citácie: 14
Hammel MC, Stein R, Kratzsch J, Vogel M, Eckert AJ, Triatin RD, Colombo M, Meigen C, Baber R, Stanik J,
Spielau U, Stoltze A, Wirkner K, Tönjes A, Snieder H, Holl RW, Stumvoll M, Blüher M, Kiess W, Körner A.:
Fasting indices of glucose-insulin-metabolism across life span and prediction of glycemic deterioration in children
with obesity from new diagnostic cut-offs Lancet Reg Health Eur. 2023 May 23;30:100652. doi:
10.1016/j.lanepe.2023.100652. (2023: 13,6 - IF, Q1 - JCR, Q1 - SJR). Citácie: 8
Podolakova K, Barak L, Jancova E, Tarnokova S, Podracka L, Dobiasova Z, Skopkova M, Gasperikova D,
Stanik J. Complete remission in children and adolescents with type 1 diabetes mellitus-prevalence and factors.
Sci Rep. 2023 Apr 26;13(1):6790. doi: 10.1038/s41598-023-34037-7. (2022: 4,6 - IF, Q2 - JCR, 0,973- SJR, Q1 -
SJR) Citácie: 3
Tijardović M, Štambuk T, Juszczak A, Keser T, Gasperikova D, Novokmet M, Tjora E, Pape Medvidović E,
Stanik J, Rasmus Njolstad P, Lauc G, Owen KR, Gornik O. Fucosylated AGP glycopeptides as biomarkers of
HNF1A-Maturity onset diabetes of the young. Diabetes Res Clin Pract. 2022 Mar;185:109226. doi:
10.1016/j.diabres.2022.109226. (2021: 8,180 - IF, Q1 - JCR, 1,677 - SJR, Q1 - SJR) Citácie: 3
Kickova T, Skopkova M, Dobiasova Z, Lackova G, Belicova Z, Schenkova K, Stanik J, Gasperikova D. Analternative approach using hs-CRP levels and age of onset in diagnostics of HNF1A-MODY. Diabet Med. 2024
May;41(5):e15265. doi: 10.1111/dme.15265. (2023: 3,2 - IF, Q2 - JCR, 1,303 - SJR, Q1 - SJR)
Thanabalasingham, Gaya ... Staník, Juraj... Owen, K. R.: A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes. Diabetologia. - Vol. 54, No. 11 (2011), s. 2801-2810.
Citation: 2019 Tam, V. - Patel, N. - Turcotte, M. - Bosse, Y. - Paré, G. - Meyre, D.: Nature Reviews Genetics, vol. 20, no. 8, 2019, s. 467-484
Škopková, Martina (17%) - Hennig, Friederike (8%) - Shin, Byung-Sik (2%) - Turner, Clesson E. (2%) - Staníková, Daniela [UKOLF1DK] (5%) - Brennerová, Katarína [UKOLF1DK] (2%) - Staník, Juraj [UKOLF1DK] (5%) - Fischer, Ute (2%) - Henden, Lyndal (2%)- Müller, Ulrich (2%) - Steinberger, Daniela (2%) - Lesinsky-Silver, Esther (2%) - Bottani, Armand (2%) - Kurdiová, Timea (2%) - Ukropec, Jozef (2%) - Nyitrayová, Oľga (2%) - Kolníková, Miriam [UKOLFKDN] (2%) - Klimeš, Iwar (2%) - Borck, Guntram (2%) - Blaho, Melanie (2%) - Haas, Stefan A. (2%) - Kim, Joo-Ran (2%) - Lotspeich-Cole, Leda E. (2%) - Gašperíková, Daniela [KAUT] (9%) - Dever, Thomas E. (9%) - Kalscheuer, Vera M. (9%): EIF2S3 mutations associated with severe X-linked intellectual disability syndrome MEHMO. Human Mutation. - Vol. 38, No. 4 (2017), s. 409-425. - ISSN 1059-7794. (IF=5,359). Citácia: 2018 Tahmasebi, S. - Khoutorsky, A. - Mathews, M.B. - Sonenberg, N.: Nature Reviews Molecular Cell Biology, vol. 19, no. 12, 2018, s. 791-807
Škopková, Martina (17%) - Hennig, Friederike (8%) - Shin, Byung-Sik (2%) - Turner, Clesson E. (2%) - Staníková, Daniela [UKOLF1DK] (5%) - Brennerová, Katarína [UKOLF1DK] (2%) - Staník, Juraj [UKOLF1DK] (5%) - Fischer, Ute (2%) - Henden, Lyndal (2%)- Müller, Ulrich (2%) - Steinberger, Daniela (2%) - Lesinsky-Silver, Esther (2%) - Bottani, Armand (2%) - Kurdiová, Timea (2%) - Ukropec, Jozef (2%) - Nyitrayová, Oľga (2%) - Kolníková, Miriam [UKOLFKDN] (2%) - Klimeš, Iwar (2%) - Borck, Guntram (2%) - Blaho, Melanie (2%) - Haas, Stefan A. (2%) - Kim, Joo-Ran (2%) - Lotspeich-Cole, Leda E. (2%) - Gašperíková, Daniela [KAUT] (9%) - Dever, Thomas E. (9%) - Kalscheuer, Vera M. (9%): EIF2S3 mutations associated with severe X-linked intellectual disability syndrome MEHMO. Human Mutation. - Vol. 38, No. 4 (2017), s. 409-425. - ISSN 1059-7794. (IF=5,359). Citácia: 2020 Eizirik, D.L. - Pasquali, L. - Cnop, M.: Nature Reviews Endocrinology, vol. 16, no. 7, 2020, s. 349-362
Bowman, Pamela (0.868%) - Sulen, Asta (0.751%) - Barbetti, Fabrizio (0.751%) - Beltrand, Jacques (0.751%) - Svalastoga, Pernille (0.751%) - Staník, Juraj [UKOLF1DK] (0.751%)...: Effectiveness and safety oflong-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study: Lancet Diabetes & Endocrinology. - Roč. 6, č. 8 (2018), s. 637-646. - ISSN (print) 2213-8587. Citácia: 2020 Pipatpolkai, T. - Usher, S. - Stansfeld, P.J. - Ashcroft, F.M.: Nature Reviews Endocrinology, vol. 16, no. 7, 2020, s. 378-393
Škopková, Martina (15%) - Kuricová, Miriam [KAUT] [UKOLJ] (15%) - Havlíčeková, Zuzana [UKOLJ270] (6%) - Vojtková, Jarmila [UKOLJ270] (6%) - Valentínová, Lucia (3%) - Daniš, Daniel [UKOLF] (4%) - Murgaš, Dalibor [UKOLJ271] (7%) - Szépeová, Renáta[UKOLJ] (6%) - Staník, Juraj [UKOLF1DK] (8%) - Bánovčin, Peter [KAUT] [UKOLJ270] (10%) - Klimeš, Iwar [KAUT] (10%) - Gašperíková, Daniela [KAUT] (10%): Two novel RFX6 variants in siblings with Mitchell-Riley syndrome with later diabetes onset andheterotopic gastric mucosa In: European Journal of Medical Genetics. - Roč. 59, č. 9 (2016), s. 429-435. Citácia: ] 2017 Patel, K. A. - Kettunen, J. - Laakso, M. - Stancakova, A. - Laver, T. W. - Colclough, K. - Johnson, M. B. - Abramowicz, M. - Groop, L. - Miettinen, P. J. - Shepherd, M. H. - Flanagan, S. E. - Ellard, S. - Inagaki, N. - Hattersley, A.T. - Tuomi, T. - Cnop, M. - Weedon, M. N.: Nature Communications, roč. 8, 2017, čl. č. 888
2021-2024 VEGA 2/0131/21 Genetika vzácnych foriem diabetu s dôrazom na funkčnú charakterizáciu nových variantov. Zástupca zospovedného riešiteľa
2018-2021 VEGA 1/0211/18 Diagnostické a farmakogenetické aspekty monogénového diabetes mellitus typu MODY. Zospovedný riešiteľ
2020-2022 KEGA 053UK-4/2020 Implementácia ultrasonografie štítnej žľazy do štúdia pediatrie a pediatrickej endokrinológie.Zodpovedný riešiteľ.
2022-2025 VEGA 1/0659/22 Výskum klinických a genetických aspektov ketotických hypoglykémií u detí. Zodpovedný riešiteľ.
2019-2022 MZSR MinZdrav 2019/20-LFUK-8. Komplexná inovatívna diagnostika a personalizovaná liečba diabetes mellitus u detí. Zodpovedný riešiteľ.
Annual Price of the Slovak Academy of Sciences for Research (2009)
Best Research team (member) in Slovakia (2018)
Guoth price, Young investigator award (2007)
13x Price of Slovak Diabetes Association for the „Best publication of the Year”
3x Price of Slovak Pediatric Association for the „Best publication of the Year”
The „Best Presentation Award” at the 14th Meeting of the Pediatric Research of Central European Countries (2005)