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Karolina Antosik · SciRah

Researcher profile · Semantic Scholar

Karolina Antosik

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Karolina Antosik — researcher profile on SciRah

h-index: 14
Works: 39
Citations: 425

Most-cited papers

Less but better: cardioprotective lipid profile of patients with GCK-MODY despite lower HDL cholesterol level
W. Fendler, M. Rizzo, M. Borowiec, Beata Małachowska +7 more
2014Acta Diabetologica37 citations Open access
Semantic Scholar
HDL cholesterol as a diagnostic tool for clinical differentiation of GCK‐MODY from HNF1A‐MODY and type 1 diabetes in children and young adults
W. Fendler, M. Borowiec, Karolina Antosik, A. Szadkowska +8 more
2011Clinical Endocrinology34 citations
Semantic Scholar
Genetic Factors of Diabetes
Karolina Antosik, M. Borowiec
2016Archivum Immunologiae et Therapiae Experimentalis30 citations
Semantic Scholar
Wolfram syndrome in the Polish population: novel mutations and genotype–phenotype correlation
A. Zmysłowska, M. Borowiec, Karolina Antosik, M. Szalecki +5 more
2011Clinical Endocrinology27 citations
Semantic Scholar
Retinal Thinning as a Marker of Disease Progression in Patients With Wolfram Syndrome
A. Zmysłowska, W. Fendler, A. Niwald, Malgorzata Ludwikowska-Pawlowska +4 more
2015Diabetes Care26 citations
Semantic Scholar
Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene
M. Borowiec, M. Myśliwiec, W. Fendler, Karolina Antosik +3 more
2011Acta Diabetologica24 citations Open access
Semantic Scholar
Monogenic diabetes prevalence among Polish children—Summary of 11 years‐long nationwide genetic screening program
Beata Małachowska, M. Borowiec, Karolina Antosik, A. Michalak +16 more
2018Pediatric Diabetes23 citations Open access
Semantic Scholar
Genetic evaluation of patients with Alström syndrome in the Polish population
A. Zmysłowska, M. Borowiec, Karolina Antosik, R. Płoski +8 more
2016Clinical Genetics22 citations
Semantic Scholar
Abnormal serum microRNA profiles in tuberous sclerosis are normalized during treatment with everolimus: possible clinical implications
J. Trelińska, W. Fendler, Iwona Dachowska, K. Kotulska +5 more
2016Orphanet Journal of Rare Diseases22 citations Open access
Semantic Scholar
A cross‐sectional study of patients referred for HNF1B‐MODY genetic testing due to cystic kidneys and diabetes
P. Sztromwasser, A. Michalak, Beata Małachowska, Paulina Młudzik +6 more
2019Pediatric Diabetes21 citations Open access
Semantic Scholar
Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
Krzysztof Jeziorny, Karolina Antosik, P. Jakiel, W. Młynarski +2 more
2020Genes19 citations Open access
Semantic Scholar
Novel glucokinase mutations in patients with monogenic diabetes – clinical outline of GCK‐MD and potential for founder effect in Slavic population
M. Borowiec, Karolina Antosik, W. Fendler, G. Deja +6 more
2012Clinical Genetics18 citations
Semantic Scholar
Serum Tumor Necrosis Factor-α and Interleukin-10 Levels as Markers to Predict Outcome of Patients with Chronic Lymphocytic Leukemia in Different Risk Groups Defined by the IGHV Mutation Status
E. Lech-Maranda, O. Grzybowska-Izydorczyk, K. Wyka, W. Młynarski +10 more
2012Archivum Immunologiae et Therapiae Experimentalis18 citations
Semantic Scholar
Serum Metabolic Fingerprinting Identified Putatively Annotated Sphinganine Isomer as a Biomarker of Wolfram Syndrome.
A. Zmysłowska, M. Ciborowski, M. Borowiec, W. Fendler +7 more
2017Journal of Proteome Research15 citations
Semantic Scholar
Central Nervous System PET-CT Imaging Reveals Regional Impairments in Pediatric Patients with Wolfram Syndrome
A. Zmysłowska, B. Małkowski, W. Fendler, M. Borowiec +4 more
2014PLoS ONE12 citations Open access
Semantic Scholar
Doubling the referral rate of monogenic diabetes through a nationwide information campaign – update on glucokinase gene mutations in a Polish cohort
M. Borowiec, W. Fendler, Karolina Antosik, A. Baranowska +4 more
2012Clinical Genetics11 citations
Semantic Scholar
Screening for extremely rare pathogenic variants of monogenic diabetes using targeted panel sequencing
T. Płoszaj, Karolina Antosik, P. Jakiel, A. Zmysłowska +1 more
2021Endocrine9 citations Open access
Semantic Scholar
Atypical phenotypic features among carriers of a novel Q248X nonsense mutation in the HNF1B gene.
Anna Hogendorf, Małgorzata Kosińska-Urbańska, M. Borowiec, Karolina Antosik +2 more
2015Endokrynologia Polska9 citations Open access
Semantic Scholar
[Optimization of monogenic diabetes screening programme--initial report on recruitment efficacy of the TEAM project].
M. Borowiec, W. Fendler, Karolina Antosik, A. Ciepiela +5 more
2010Pediatric Endocrinology Diabetes and Metabolism9 citations
Semantic Scholar
Ancestral mutations may cause a significant proportion of GCK‐MODY
P. Dusatkova, Š. Průhová, M. Borowiec, K. Veselá +4 more
2012Pediatric Diabetes6 citations Open access
Semantic Scholar
Paternally Inherited Proinsulin Mutations May Result in Earlier Onset of Monogenic Diabetes Mutation Identity Effect in Monogenic Diabetes
W. Fendler, M. Borowiec, Karolina Antosik, Beata Jaroszewska-Świątek +4 more
2011Diabetes Care6 citations Open access
Semantic Scholar
The influence of INS VNTR class III allele on auxological parameters, glucose, insulin, lipids, and adipocytokines secretion in prepubertal children born small for gestational age.
R. Stawerska, M. Szałapska, M. Borowiec, Karolina Antosik +2 more
2016Endokrynologia Polska4 citations Open access
Semantic Scholar
HbA1c‐based diabetes diagnosis among patients with glucokinase mutation (GCK‐MODY) is affected by a genetic variant of glucose‐6‐phosphatase (G6PC2)
M. Borowiec, W. Fendler, P. Dusatkova, Karolina Antosik +6 more
2012Diabetic Medicine4 citations
Semantic Scholar
Endothelial integrity may be regulated by a specific antigen via an IgE-mediated mechanism.
P. Gorzelak-Pabiś, E. Luczak, Katarzyna Wojdan, Karolina Antosik +3 more
2017Postępy Higieny i Medycyny Doświadczalnej3 citations Open access
Semantic Scholar
Alkaptonuria in a boy with type 1 diabetes mellitus, vitiligo, autoimmune thyroiditis and immunoglobulin A deficiency - a case report.
Anna Hogendorf, I. Pietrzak, Karolina Antosik, M. Borowiec +1 more
2016Pediatric Endocrinology Diabetes and Metabolism3 citations Open access
Semantic Scholar
Single patient in GCK-MODY family successfully re-diagnosed into GCK-PNDM through targeted next-generation sequencing technology
Karolina Antosik, Piotr Gnyś, E. De Franco, M. Borowiec +3 more
2015Acta Diabetologica3 citations Open access
Semantic Scholar
An analysis of the sequence of the BAD gene among patients with maturity-onset diabetes of the young (MODY)
Karolina Antosik, Piotr Gnyś, P. Jarosz-Chobot, M. Myśliwiec +4 more
2017Journal of Pediatric Endocrinology & Metabolism (JPEM)2 citations Open access
Semantic Scholar
Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
R. Stawerska, M. Szałapska, M. Borowiec, W. Młynarski +3 more
2013Journal of Pediatric Endocrinology & Metabolism (JPEM)2 citations
Semantic Scholar
Serum Tumor Necrosis Factor-α and Interleukin-10 Levels as Markers to Predict Outcome of Patients with Chronic Lymphocytic Leukemia in Different Risk Groups Defined by the IGHV Mutation Status
E. Lech-Maranda, O. Grzybowska-Izydorczyk, K. Wyka, W. Młynarski +10 more
2012Archivum Immunologiae et Therapiae Experimentalis2 citations
Semantic Scholar
[An evaluation of HLA class 2 alleles and anti-islet antibodies as evidence for non-autoimmune diabetes in Wolfram syndrome].
A. Zmysłowska, M. Borowiec, Karolina Antosik, K. Wyka +3 more
2010Pediatric Endocrinology Diabetes and Metabolism2 citations
Semantic Scholar
Clinical use of NGS data from the targeted gene panel for mitochondrial diseases screening
T. Płoszaj, Karolina Antosik, Paulina Młudzik, M. Traczyk-Borszynska +1 more
2020Comput. Methods Programs Biomed.1 citations Open access
Semantic Scholar
Occurrence of c.976 G>T (p.Val326Leu) and c.452 G>A (p.Trp151Ter) variants in DHCR7 gene in population of polish women with recurrent miscarriage.
Marta Chrzanowska-Steglińska, H. Moczulska, Beata Skoczylas, M. Pietrusiński +5 more
2020European Journal of Obstetrics, Gynecology, and Reproductive Biology1 citations
Semantic Scholar
Genetic Factors of Diabetes
Karolina Antosik, M. Borowiec
2016Archivum Immunologiae et Therapiae Experimentalis0 citations
Semantic Scholar
The Implementation of European Market Infrastructure Regulation and Its Influence on Derivatives Market in Poland in 2010-2014
Karolina Antosik
20160 citations
Semantic Scholar
Assessment of the effect of IL-4 on IgE antibody high-affinity (FceRI) and low-affinity (FceRII) receptor mRNA expression on primary human aortic endothelial cells
P. Gorzelak-Pabiś, Katarzyna Wojdan, E. Luczak, Karolina Antosik +3 more
20150 citations
Semantic Scholar
Permanent neonatal diabetes in Polish population
Karolina Antosik, Piotr Gnyś, I. Dróżdż, W. Fendler +7 more
20140 citations
Semantic Scholar
Recurrent fractures and low bone mass in a patient with new mutation of LRP5 gene
A. Rusińska, M. Borowiec, W. Młynarski, Karolina Antosik +3 more
20130 citations
Semantic Scholar
Ocena fenotypowa homo- i heterozygotycznych nosicieli mutacji w genie WFS1 w populacji polskiej
A. Zmysłowska, M. Borowiec, Karolina Antosik, Maciej Szalecki +5 more
20110 citations
Semantic Scholar
The TNF −308G>A Polymorphism Predicts Outcome of Patients with B-Cell Chronic Lymphocytic Leukemia In Relation to the IgVH Mutation Status
E. Lech-Maranda, W. Młynarski, O. Grzybowska-Izydorczyk, M. Borowiec +11 more
20100 citations
Semantic Scholar

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