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M. Leja · SciRah

Researcher profile · Semantic Scholar

M. Leja

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M. Leja — researcher profile on SciRah

h-index: 9
Works: 19
Citations: 345

Most-cited papers

Study of novel anticancer 4-thiazolidinone derivatives.
K. A. Szychowski, M. Leja, D. Kaminskyy, U. Binduga +3 more
2017Chemico-Biological Interactions87 citations
Semantic Scholar
Tetrabromobisphenol A (TBBPA)-stimulated reactive oxygen species (ROS) production in cell-free model using the 2′,7′-dichlorodihydrofluorescein diacetate (H2DCFDA) assay—limitations of method
K. A. Szychowski, K. Rybczyńska-Tkaczyk, M. Leja, A. Wójtowicz +1 more
2016Environmental science and pollution research international74 citations Open access
Semantic Scholar
Anticancer properties of 4-thiazolidinone derivatives depend on peroxisome proliferator-activated receptor gamma (PPARγ).
K. A. Szychowski, M. Leja, D. Kaminskyy, Anna Kryshchyshyn +5 more
2017European journal of medicinal chemistry49 citations
Semantic Scholar
Cytotoxic effects of two extracts from garlic (Allium sativum L.) cultivars on the human squamous carcinoma cell line SCC-15
K. A. Szychowski, U. Binduga, K. Rybczyńska-Tkaczyk, M. Leja +1 more
2016Saudi Journal of Biological Sciences29 citations Open access
Semantic Scholar
Anticancer properties of 5Z-(4-fluorobenzylidene)-2-(4-hydroxyphenylamino)-thiazol-4-one
K. A. Szychowski, D. Kaminskyy, M. Leja, Anna Kryshchyshyn +5 more
2019Scientific Reports19 citations Open access
Semantic Scholar
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation
N. Bałdyga, D. Oziębło, Nina Gan, M. Furmanek +3 more
2023Genes18 citations Open access
Semantic Scholar
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene
D. Oziębło, A. Sarosiak, M. Leja, B. Budde +6 more
2019Journal of Translational Medicine17 citations Open access
Semantic Scholar
Hearing Loss as the Main Clinical Presentation in NLRP3-Associated Autoinflammatory Disease
D. Oziębło, M. Leja, A. Jeznach, M. Orzechowska +6 more
2022Frontiers in Immunology16 citations Open access
Semantic Scholar
TBC1D24 emerges as an important contributor to progressive postlingual dominant hearing loss
D. Oziębło, M. Leja, M. Lazniewski, A. Sarosiak +5 more
2021Scientific Reports12 citations Open access
Semantic Scholar
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss
D. Oziębło, Sang-Yeon Lee, M. Leja, A. Sarosiak +8 more
2022Human Genetics9 citations
Semantic Scholar
Zebrafish in-vivo study reveals deleterious activity of human TBC1D24 genetic variants linked with autosomal dominant hearing loss.
A. Sarosiak, J. Jędrychowska, D. Oziębło, Nina Gan +9 more
2024Biochimica et Biophysica Acta - Molecular Basis of Disease6 citations Open access
Semantic Scholar
Autosomal dominant hearing loss – literature review
M. Leja, D. Oziębło, N. Bałdyga, H. Skarżyńśki +1 more
2023Nowa Audiofonologia3 citations Open access
Semantic Scholar
Characterization of a novel GRHL2 mutation reveals molecular mechanisms underlying autosomal dominant hearing loss (DFNA28): insights from structural and functional studies.
D. Oziębło, N. Bałdyga, M. Leja, Adam Jarmuła +3 more
2025Human Molecular Genetics2 citations
Semantic Scholar
Searching for the Molecular Basis of Partial Deafness
D. Oziębło, N. Bałdyga, M. Leja, H. Skarżyńśki +1 more
2022International Journal of Molecular Sciences2 citations Open access
Semantic Scholar
Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families
D. Oziębło, M. Leja, Nina Gan, N. Bałdyga +4 more
2026Journal of molecular medicine1 citations Open access
Semantic Scholar
POSTLINGUAL SENSORINEURAL HEARING LOSS DUE TO KNOWN TBC1D24 GENE ALTERATION
D. Oziębło, M. Leja, N. Bałdyga, Sarosiak +2 more
2021Journal of hearing science1 citations Open access
Semantic Scholar
Analysis of major otosclerosis-associated variants in RELN and TGFB1 genes in Polish patients
D. Oziębło, S. Domagała, M. Leja, H. Skarżyńśki +1 more
2020Archives of medical science : AMS1 citations Open access
Semantic Scholar
Advances in genetic diagnostics and the mystery of missing heredity: Where does the genetic cause of molecularly unexplained hereditary hearing loss hide?
N. Bałdyga, D. Oziębło, M. Leja, H. Skarżyński +1 more
2026Nowa Audiofonologia0 citations Open access
Semantic Scholar
REPORT ON THE 52ND EUROPEAN HUMANGENETICS CONFERENCE, 15–18 JUNE 2019,GOTHENBURG, SWEDEN
M. Ołdak, M. Leja, Agnieszka Madejska, Beata Harasimowicz +2 more
20200 citations
Semantic Scholar

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