Projects funded by the NCN

Nuclear genes involved in mitochondrial diseases caused by mitochondrial DNA instability

Call: OPUS 8 , Panel: NZ5

Principal investigator: dr hab. Katarzyna Tońska

Uniwersytet Warszawski, Wydział Biologii

Identification of new, clinically relevant genetic and epigenetic aberrations by next-generation sequencing in chronic m...

Call: HARMONIA 6 , Panel: NZ5

Principal investigator: dr Tomasz Artur Stokłosa

Warszawski Uniwersytet Medyczny, Wydział Lekarski

Whole exome sequencing in Polish population of patients - search for the genetic basis of primary ciliary dyskinesia, PC...

Call: OPUS 7 , Panel: NZ2

Principal investigator: prof. Ewa Maria Ziętkiewicz

Instytut Genetyki Człowieka Polskiej Akademii Nauk

Whole-exome sequencing for identification of genetic factors associated with early mortality of adults in Polish populat...

Call: OPUS 6 , Panel: NZ7

Principal investigator: prof. Rafał Tomasz Płoski

Warszawski Uniwersytet Medyczny, I Wydział Lekarski

Whole exome sequencing in Polish patients with sporadic keratoconus and a pilot study of keratoconus proteomic and metab...

Call: HARMONIA 5 , Panel: NZ2

Principal investigator: dr hab. Marzena Gajęcka

Instytut Genetyki Człowieka Polskiej Akademii Nauk

The application of whole exome sequencing for disease gene identification in a group of sporadic intellectual disability...

Call: HARMONIA 4 , Panel: NZ5

Principal investigator: prof. Małgorzata Antonina Krajewska-Walasek

Instytut "Pomnik - Centrum Zdrowia Dziecka"

Search for novel genes involved in pathogenesis of combied pituitary hormone deficiency

Call: HARMONIA 2 , Panel: NZ5

Principal investigator: dr Bartłomiej Marcin Budny

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski II

In search of the causes of type 1 diabetes in children with coexisting neurodevelopmental and neurological disorders - g...

Call: PRELUDIUM 23 , Panel: NZ5

Principal investigator: Hanna Maria Kuśmierczyk-Kozieł

Uniwersytet Medyczny w Łodzi

GENETIC AND EPIGENETIC BACKGROUND OF ANTIBODY PRODUCTION DEFECTS IN CHILDREN– IN SEARCH OF A PATHOPHYSIOLOGICAL MODEL OF...

Call: OPUS 24 , Panel: NZ6

Principal investigator: dr hab. Aleksandra Anna Szczawińska-Popłonyk

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu

Genetic Background of Overgrowth Syndromes in Polish and Lithuanian Populations: basis for rapid genetic testing to prev...

Call: DAINA 2 , Panel: NZ2

Principal investigator: dr Renata Posmyk

Uniwersytet Medyczny w Białymstoku

Development of CNV detection methods based on depth of coverage

Call: PRELUDIUM 18 , Panel: ST6

Principal investigator: dr Wiktor Tomasz Kuśmirek

Politechnika Warszawska

Searching genetic causes of new severe/lethal multidefect congenital syndromes in human fetuses.

Call: OPUS 14 , Panel: NZ5

Principal investigator: dr hab. Robert Stanisław Śmigiel

Uniwersytet Medyczny im. Piastów Śląskich we Wrocławiu, Wydział Nauk o Zdrowiu

Identification of novel genetic variants associated with risk of chronic pancreatitis by whole exome sequencing.

Call: OPUS 10 , Panel: NZ5

Principal investigator: dr hab. Agnieszka Magdalena Rygiel

Instytut Matki i Dziecka

Identification of new breast cancer susceptibility genes by whole-exome sequencing in the genetically homogeneous Polish...

Call: OPUS 9 , Panel: NZ5

Principal investigator: prof. Cezary Cybulski

Pomorski Uniwersytet Medyczny w Szczecinie, Wydział Farmacji, Biotechnologii Medycznej i Medycyny Laboratoryjnej