Maja Dembić

457 total citations
22 papers, 319 citations indexed

About

Maja Dembić is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Maja Dembić has authored 22 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 4 papers in Genetics. Recurrent topics in Maja Dembić's work include Cardiac electrophysiology and arrhythmias (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (3 papers). Maja Dembić is often cited by papers focused on Cardiac electrophysiology and arrhythmias (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (3 papers). Maja Dembić collaborates with scholars based in Denmark, Italy and Spain. Maja Dembić's co-authors include Brage Storstein Andresen, Gitte Hoffmann Bruun, Thomas Koed Doktor, Spartaco Santi, Henriette S. Andersen, Massimo Riccio, Yimin Hua, Ying Hsiu Liu, Adrian R. Krainer and Anna Więckowska and has published in prestigious journals such as Nucleic Acids Research, PLoS Genetics and Cancer Letters.

In The Last Decade

Maja Dembić

18 papers receiving 316 citations

Peers

Maja Dembić
Leigh B. Waddell Australia
C R Müller Germany
Monica Piccini Italy
Eyby Leon United States
Florence Renaldo France
Ivana Dabaj France
Dina Marek‐Yagel Israel
Christin Collins United States
Amy Knight Johnson United States
Sheng Yao China
Leigh B. Waddell Australia
Maja Dembić
Citations per year, relative to Maja Dembić Maja Dembić (= 1×) peers Leigh B. Waddell

Countries citing papers authored by Maja Dembić

Since Specialization
Citations

This map shows the geographic impact of Maja Dembić's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Maja Dembić with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maja Dembić more than expected).

Fields of papers citing papers by Maja Dembić

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maja Dembić. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Maja Dembić. The network helps show where Maja Dembić may publish in the future.

Co-authorship network of co-authors of Maja Dembić

This figure shows the co-authorship network connecting the top 25 collaborators of Maja Dembić. A scholar is included among the top collaborators of Maja Dembić based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Maja Dembić. Maja Dembić is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Steffensen, Lasse Bach, Martin Bjerregård Pedersen, Martin J. Larsen, et al.. (2025). Mutational landscape of atherosclerotic plaques reveals large clonal cell populations. JCI Insight. 10(10). 3 indexed citations
2.
Álvarez, Mar, Maja Dembić, Margarita Castro, et al.. (2024). Splice-Switching Antisense Oligonucleotides Correct Phenylalanine Hydroxylase Exon 11 Skipping Defects and Rescue Enzyme Activity in Phenylketonuria. Nucleic Acid Therapeutics. 34(3). 134–142. 2 indexed citations
3.
Dembić, Maja, Eva Richard, Jesper F. Havelund, et al.. (2023). Regulating PCCA gene expression by modulation of pseudoexon splicing patterns to rescue enzyme activity in propionic acidemia. Molecular Therapy — Nucleic Acids. 35(1). 102101–102101. 7 indexed citations
4.
Dembić, Maja, et al.. (2022). Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. Molecular Genetics and Genomics. 298(2). 329–342. 5 indexed citations
5.
Deyneko, Igor V., Gitte Hoffmann Bruun, Maja Dembić, et al.. (2022). Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing. Frontiers in Genetics. 13. 969895–969895. 2 indexed citations
6.
Dembić, Maja, Mads Thomassen, Karin de Stricker, et al.. (2021). Synchronous detection of pancreatic adenocarcinoma and paraganglioma in a Whipple resection specimen. Pathology - Research and Practice. 226. 153590–153590.
7.
Guerra, Bárbara, Maja Dembić, Aarif Siddiqui, et al.. (2020). Down-Regulation of CK2α Leads toUp-Regulation of the Cyclin-Dependent Kinase Inhibitor p27KIP1 in Conditions Unfavorable for the Growth of Myoblast Cells. Cellular Physiology and Biochemistry. 54(6). 1177–1198. 5 indexed citations
8.
Dembić, Maja, Henriette S. Andersen, Jean Bastin, et al.. (2018). Next generation sequencing of RNA reveals novel targets of resveratrol with possible implications for Canavan disease. Molecular Genetics and Metabolism. 126(1). 64–76. 14 indexed citations
9.
Dembić, Maja, et al.. (2018). Intronic PAH gene mutations cause a splicing defect by a novel mechanism involving U1snRNP binding downstream of the 5’ splice site. PLoS Genetics. 14(4). e1007360–e1007360. 22 indexed citations
10.
Mosegaard, Signe, Gitte Hoffmann Bruun, Yngve Thomas Bliksrud, et al.. (2017). An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. Molecular Genetics and Metabolism. 122(4). 182–188. 42 indexed citations
11.
Dembić, Maja, Paula L. Hedley, Christian Torp‐Pedersen, Lars Køber, & Michael Christiansen. (2017). Pregnancy-associated plasma protein-A (PAPP-A) and the proform of the eosinophil major basic protein (ProMBP) are associated with increased risk of death in heart failure patients. Scandinavian Journal of Clinical and Laboratory Investigation. 77(5). 352–357. 7 indexed citations
12.
Doktor, Thomas Koed, Yimin Hua, Henriette S. Andersen, et al.. (2016). RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns. Nucleic Acids Research. 45(1). 395–416. 82 indexed citations
13.
14.
Kanters, Jørgen K., Lasse Skibsbye, Paula L. Hedley, et al.. (2015). Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder family. Scandinavian Journal of Clinical and Laboratory Investigation. 75(8). 699–709. 7 indexed citations
15.
Brusich, Sandro, Maja Dembić, Paula L. Hedley, et al.. (2013). First results of genetic testing in Croatian arrhythmia patients. Cardiologia Croatica. 8(9). 297–297.
16.
Hedley, Paula L., Jørgen K. Kanters, Maja Dembić, et al.. (2013). The Role of CAV3 in Long–QT Syndrome. Circulation Cardiovascular Genetics. 6(5). 452–461. 16 indexed citations
17.
Riccio, Massimo, Rossella Di Giaimo, Fabrizio Dal Piaz, et al.. (2007). Cystatin B and its EPM1 mutants are polymeric and aggregate prone in vivo. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783(2). 312–322. 29 indexed citations
18.
Riccio, Michele, Spartaco Santi, Maja Dembić, et al.. (2005). Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellum. Neurobiology of Disease. 20(1). 104–114. 22 indexed citations
19.
Carraresi, Laura, Rosanna Martinelli, Massimo Riccio, et al.. (2005). Establishment and characterization of murine small cell lung carcinoma cell lines derived from HPV-16 E6/E7 transgenic mice. Cancer Letters. 231(1). 65–73. 8 indexed citations
20.
Riccio, Massimo, Maja Dembić, Caterina Cinti, & Spartaco Santi. (2004). Multifluorescence Labeling and Colocalization Analyses. Humana Press eBooks. 285. 171–178. 21 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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