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Juraj Staník

Observed names: J STANÍK, J Stanik, J Staník, J. STANIK, J. STANÍK, J. Stanik, Juraj Stanik, Juraj Staník, Stanik J, Stanik, J., Stanik, Juraj
Observed institutions: Slovak Medical University, Slovak Academy of Sciences, University Hospital Bratislava, Národný ústav detských chorôb, Institute of Experimental Endocrinology of the Slovak Academy of Sciences, Biomedical Research Center of the Slovak Academy of Sciences, University Hospital Leipzig, Comenius University Bratislava, Leipzig University
ORCID: 0000-0002-0538-1274
Observed ORCID: 0000-0002-0538-1274
OpenAlex ID: A5063380073
Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
2018 · Pamela Bowman, Åsta Sulen, et al. · The Lancet Diabetes & Endocrinology · 175
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De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed
2013 · Juraj Stanik, Petra Dusatkova, et al. · Diabetologia · 120
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes
2011 · G. Thanabalasingham, N. Shah, et al. · Diabetologia · 117
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Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers
2007 · Juraj Stanik, Daniela Gasperikova, et al. · The Journal of Clinical Endocrinology & Metabolism · 112
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Mutations in HNF1A Result in Marked Alterations of Plasma Glycan Profile
2012 · Gaya Thanabalasingham, Jennifer E. Huffman, et al. · Diabetes · 105
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EIF2S3Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO
2017 · Martina Skopkova, Friederike Hennig, et al. · Human Mutation · 86
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Novel insights into genetics and clinics of the HNF1A-MODY
2019 · Terezia Valkovicova, Martina Skopkova, et al. · Endocrine Regulations · 83
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Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes
2020 · Pamela Bowman, Frances Mathews, et al. · Diabetes Care · 58
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Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism
2016 · Dennis Löffler, Susanne Behrendt, et al. · Molecular Metabolism · 50
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Serum Uric Acid Levels as an Indicator for Metabolically Unhealthy Obesity in Children and Adolescents
2018 · Edrienny Patrícia Alves Accioly Rocha, Mandy Vogel, et al. · Hormone Research in Paediatrics · 49
Testosterone imbalance may link depression and increased body weight in premenopausal women
2019 · Daniela Stanikova, Rachel G. Zsido, et al. · Translational Psychiatry · 47
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Clinical implications of the glucokinase impaired function – GCK MODY today
2020 · J Hulín, M Škopková, et al. · Physiological Research · 45
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Identification of a Novel β-Cell Glucokinase (GCK) Promoter Mutation (−71G>C) That ModulatesGCKGene Expression Through Loss of Allele-Specific Sp1 Binding Causing Mild Fasting Hyperglycemia in Humans
2009 · Daniela Gašperíková, Nicolas D. Tribble, et al. · Diabetes · 42
Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values
2021 · Elena Kempf, Mandy Vogel, et al. · EClinicalMedicine · 40
Fasting indices of glucose-insulin-metabolism across life span and prediction of glycemic deterioration in children with obesity from new diagnostic cut-offs
2023 · Maximiliane Chiara Hammel, Robert Stein, et al. · The Lancet Regional Health - Europe · 35
The Bone Markers Sclerostin, Osteoprotegerin, and Bone-Specific Alkaline Phosphatase Are Related to Insulin Resistance in Children and Adolescents, Independent of Their Association with Growth and Obesity
2019 · Juraj Stanik, Jürgen Kratzsch, et al. · Hormone Research in Paediatrics · 33
Neonatal Hypoglycemia, Early-Onset Diabetes and Hypopituitarism Due to the Mutation in EIF2S3 Gene Causing MEHMO Syndrome
2018 · J. STANIK, M. SKOPKOVA, et al. · Physiological Research · 33
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Increased estrogen level can be associated with depression in males
2017 · Daniela Stanikova, Tobias Luck, et al. · Psychoneuroendocrinology · 32
Identification and Functional Characterisation of Novel Glucokinase Mutations Causing Maturity-Onset Diabetes of the Young in Slovakia
2012 · Lucia Valentínová, Nicola L. Beer, et al. · PLoS ONE · 31
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Associations Between Anxiety, Body Mass Index, and Sex Hormones in Women
2019 · Daniela Stanikova, Tobias Luck, et al. · Frontiers in Psychiatry · 27
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Severe Insulin Resistance and Intrauterine Growth Deficiency Associated With Haploinsufficiency for INSR and CHN2
2009 · Sara G.I. Suliman, Juraj Stanik, et al. · Diabetes · 27
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DNM1 encephalopathy − atypical phenotype with hypomyelination due to a novel de novo variant in the DNM1 gene
2018 · Miriam Kolnikova, Martina Skopkova, et al. · Seizure · 21
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Two novel RFX6 variants in siblings with Mitchell-Riley syndrome with later diabetes onset and heterotopic gastric mucosa
2016 · Martina Skopkova, Miriam Ciljakova, et al. · European Journal of Medical Genetics · 20
Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family – case report
2012 · J. Stanik, M. Kusekova, et al. · Endocrine Regulations · 17
Congenital hyperinsulinism and glycogenosis-like phenotype due to a novel HNF4A mutation
2017 · Juraj Stanik, Martina Skopkova, et al. · Diabetes Research and Clinical Practice · 15
Works count: 84
Citation count: 1,632
H-index: 21
I10-index: 34
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