Ewa Gutmajster

Silesian University of Technology — Poland

Neuroscience · Life Sciences

8h-index170citations18works1.02yr avg
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Research Topics

Autism Spectrum Disorder Research(3), Aortic aneurysm repair treatments(3), Congenital heart defects research(3), Genetics and Neurodevelopmental Disorders(3), Aortic Disease and Treatment Approaches(2)

Publications18 total

The EMT status in the primary tumor of adamantinomatous craniopharyngioma predict postoperative recurrence in children
Child s Nervous System·2024
The CD44s Isoform is a Potential Biomarker for Predicting Craniopharyngioma Recurrence in Children
NeuroMolecular Medicine·2024· 2 citedOpen Access
Gene-repaired iPS cells as novel approach for patient with osteogenesis imperfecta
Frontiers in Bioengineering and Biotechnology·2023· 9 citedOpen Access
Characteristic of cells isolated from human Abdominal Aortic Aneurysm samples cultured in vitro
Acta Angiologica·2022· 2 citedOpen Access
Clinics and genetic background of hereditary gingival fibromatosis
Orphanet Journal of Rare Diseases·2021· 21 citedOpen Access
mRNA Expression of thrombospondin 1, 2 and 3 from proximal to distal in human abdominal aortic aneurysm – preliminary report
Acta Biochimica Polonica·2021· 6 citedOpen Access
Expression gradient of metalloproteinases and their inhibitors from proximal to distal segments of abdominal aortic aneurysm
Journal of Applied Genetics·2021· 11 citedOpen Access
Fibroblast and keratinocyte crosstalk: the effect of a poly(tri[ethylene glycol] ethyl ether methacrylate) thermoresponsive surface on short-term co-culture
European Journal of Dermatology·2019· 3 cited
Possible association of the TERT promoter polymorphisms rs2735940, rs7712562 and rs2853669 with diabetes mellitus in obese elderly Polish population: results from the national PolSenior study
Journal of Applied Genetics·2018· 7 citedOpen Access
Plasma Levels of Leptin and Adiponectin in Fragile X Syndrome
NeuroImmunoModulation·2016· 18 cited
Low Levels of HDL in Fragile X Syndrome Patients
Lipids·2015· 20 citedOpen Access
Erratum
Neurodegenerative Diseases·2015· 1 cited
Anti-Neuronal Antibodies in Patients with Fragile X Syndrome: Is there a Role of Autoimmunity in Its Pathogenesis?
Neurodegenerative Diseases·2014· 3 cited
Telomere length in elderly Caucasians weakly correlates with blood cell counts
European Geriatric Medicine·2013· 4 cited
Telomere Length in Elderly Caucasians Weakly Correlates with Blood Cell Counts
The Scientific World JOURNAL·2013· 15 citedOpen Access
Optimization of Genetic Engineering and Homologous Recombination of Collagen Type I Genes in Rat Bone Marrow Mesenchymal Stem Cells (MSC)
Cellular Reprogramming·2010· 11 cited
Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD
European Journal of Human Genetics·2008· 37 citedOpen Access
[Genetic determination of Wolf-Hirschhorn syndrome ].
PubMed·2002

Frequent Co-authors

Aleksander L. Sieroń(14), Małgorzata Lisik(5), Aleksandra Auguściak-Duma(5), Marta Lesiak(5), Agnieszka Fus-Kujawa(5), Karolina Stępień(4), Joanna Witecka(3), Małgorzata Szwed(3), Monika Puzianowska‐Kuźnicka(3), Andrzej Więcek(3), Jerzy Chudek(3), Karolina Bajdak-Rusinek(3), Natalia Diak(3), Anna Szydło(2), Maciej Tarnowski(2), Karolina Strzelec(2), Katarzyna Gawron(2), Magdalena Wyskida(2), Justyna Koscinska-Marczewska(2), Magdalena Owczarz(2)