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Ewa Juścińska
Observed name:
E. Juścińska
Institution:
Medical University of Lodz
Observed institution:
Medical University of Lodz
OpenAlex ID:
A5093058742
Identification of rare variants in candidate genes associated with monogenic diabetes in polish mody-x patients
2023
·
Paulina Jakiel
, K. Gadzalska
, et al.
·
Journal of Diabetes & Metabolic Disorders
·
5
PDF
Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant in the AAAS gene
2026
·
Ewa Juścińska
, Karolina Gadzalska
, et al.
·
Neurogenetics
·
3
PDF
Patients with a Wide Range of Disorders Related to WFS1 Gene Variants: Novel Mutations and Genotype–Phenotype Correlations
2024
·
Julia Grzybowska-Adamowicz
, Karolina Gadzalska
, et al.
·
Genes
·
3
PDF
Screening for Rare Mitochondrial Genome Variants Reveals a Potentially Novel Association between MT-CO1 and MT-TL2 Genes and Diabetes Phenotype
2024
·
Tomasz Płoszaj
, Sebastian Skoczylas
, et al.
·
International Journal of Molecular Sciences
·
3
PDF
Phenotype–genotype correlations in patients with Alport syndrome from the Polish population
2025
·
Maria Malarska
, Hanna Moczulska
, et al.
·
Journal of Nephrology
·
2
Mitochondrial DNA variants revealed by whole exome sequencing: from screening to diagnosis and follow-up
2025
·
Sebastian Skoczylas
, Tomasz Płoszaj
, et al.
·
Neurogenetics
·
2
Search for the most precise diagnosis of monogenic diabetes - the usefulness of short-read NGS method in molecular testing in Polish patients
2026
·
Tomasz Płoszaj
, Sebastian Skoczylas
, et al.
·
Acta Diabetologica
·
1
The Clinical Spectrum and Significance of ABCC8 Gene Variants in the Diagnosis of Monogenic Diabetes
2026
·
Natalia Kapelan
, Piotr Tust
, et al.
·
Diabetology
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Works count:
7
Citation count:
17
H-index:
3
I10-index:
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