Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aleksandra Stajkovska"'
Autor:
Marija Gjorgjievska, Sanja Mehandziska, Aleksandra Stajkovska, Slavica Pecioska-Dokuzovska, Anica Dimovska, Idriz Durmish, Sara Ismail, Teodora Pavlovska, Antonija Stojchevska, Haris Amedi, Jasna Andonova, Marija Nikolovska, Sara Velickovikj, Zan Mitrev, Ivan Kungulovski, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Trends from around the world suggest that the omicron BA.2 subvariant is increasing in proportion to the original BA.1 subvariant. Here we report two cases of co-infection with omicron BA.1 and omicron BA.2 in co-exposed individuals. In both individu
Externí odkaz:
https://doaj.org/article/4e68982b4a8e456286e5f9241642272a
Autor:
Sanja Mehandziska, Aleksandra Stajkovska, Margarita Stavrevska, Kristina Jakovleva, Marija Janevska, Rodney Rosalia, Ivan Kungulovski, Zan Mitrev, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
To enable the implementation of precise genomics in a local healthcare system, we devised a pipeline for filtering and reporting of relevant genetic information to healthy individuals based on exome or genome data. In our analytical pipeline, the fir
Externí odkaz:
https://doaj.org/article/d3676f7062f444bdb27d0fe8d975225e
Autor:
Aleksandra Stajkovska, Sanja Mehandziska, Rodney Rosalia, Margarita Stavrevska, Marija Janevska, Martina Markovska, Ivan Kungulovski, Zan Mitrev, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Targeted gene panel testing has the power to interrogate hundreds of genes and evaluate the genetic risk for many types of hereditary cancers simultaneously. We screened a 13-year-old male patient diagnosed with glioblastoma multiforme with the aim t
Externí odkaz:
https://doaj.org/article/caeca90a035d459c86137fbccc463cca
Autor:
Aleksandra Stajkovska, Sanja Mehandziska, Margarita Stavrevska, Kristina Jakovleva, Natasha Nikchevska, Zan Mitrev, Ivan Kungulovski, Gjorgje Zafiroski, Velibor Tasic, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Exome sequencing can interrogate thousands of genes simultaneously and it is becoming a first line diagnostic tool in genomic medicine. Herein, we applied trio clinical exome sequencing (CES) in a patient presenting with undiagnosed skeletal disorder
Externí odkaz:
https://doaj.org/article/b30d3d911db1424cbd4a4f97eb09002d
Autor:
Aleksandra Stajkovska, Kristina Jakovleva, Ivan Kungulovski, Marija Janevska, Zan Mitrev, Margarita Stavrevska, Sanja Mehandziska, Rodney A. Rosalia, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics
Frontiers in Genetics
To enable the implementation of precise genomics in a local healthcare system, we devised a pipeline for filtering and reporting of relevant genetic information to healthy individuals based on exome or genome data. In our analytical pipeline, the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9913c75190e608878ea1779506b67d96
https://www.frontiersin.org/article/10.3389/fgene.2020.00619/full
https://www.frontiersin.org/article/10.3389/fgene.2020.00619/full
Autor:
Rodney A. Rosalia, Ivan Kungulovski, Martina Markovska, Marija Janevska, Zan Mitrev, Aleksandra Stajkovska, Goran Kungulovski, Sanja Mehandziska
Background: In recent years, it has been shown that many of the pervasive genetic defects in cancer occur in chromatin modifiers. In order to obtain insights in regards to their biology and clinical relevance in cancer, we analyzed the distribution a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5163edb017c4265bedf2c4efe2eef6b9
Autor:
Sanja Mehandziska, Rodney A. Rosalia, Ivan Kungulovski, Margarita Stavrevska, Martina Markovska, Marija Janevska, Aleksandra Stajkovska, Zan Mitrev, Goran Kungulovski
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
Targeted gene panel testing has the power to interrogate hundreds of genes and evaluate the genetic risk for many types of hereditary cancers simultaneously. We screened a 13-year-old male patient diagnosed with glioblastoma multiforme with the aim t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21f19f5de4dbaeceb498456908e402e2
https://www.frontiersin.org/article/10.3389/fgene.2019.00952/full
https://www.frontiersin.org/article/10.3389/fgene.2019.00952/full
Autor:
Margarita Stavrevska, Gjorgje Zafiroski, Zan Mitrev, Kristina Jakovleva, Ivan Kungulovski, Sanja Mehandziska, Velibor Tasic, Aleksandra Stajkovska, Goran Kungulovski, Natasha Nikchevska
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)
Frontiers in Genetics, Vol 9 (2018)
Exome sequencing can interrogate thousands of genes simultaneously and it is becoming a first line diagnostic tool in genomic medicine. Herein, we applied trio clinical exome sequencing in a patient presenting with undiagnosed skeletal disorder, mino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e016bccaffe0a7cc5ab066f61c15bc
http://europepmc.org/articles/PMC5895704
http://europepmc.org/articles/PMC5895704