Projects funded by the NCN

Building a genomic atlas of human inner ear malformations: focus on novel genes and functional non-coding regions

Call: OPUS 21 , Panel: NZ5

Principal investigator: dr hab. Monika Ołdak

Instytut Fizjologii i Patologii Słuchu

Computational methods for genomic structural variants interpretation

Call: HARMONIA 10 , Panel: NZ2

Principal investigator: prof. Anna Gambin

Uniwersytet Warszawski, Wydział Matematyki, Informatyki i Mechaniki

Development of novel bioinformatics software for analysis of genetic variation in non-coding elements of the human genom...

Call: POLONEZ 3 , Panel: NZ2

Principal investigator: dr Paweł Sztromwasser

Uniwersytet Medyczny w Łodzi, I Katedra Pediatrii

Identification of novel genetics variants as the cause of the premature closure of the cranial sutures in children using...

Call: PRELUDIUM 12 , Panel: NZ5

Principal investigator: Ewelina Bukowska-Olech

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

Identification of novel genetics variants as the cause of the premature closure of the cranial sutures in children using...

Call: PRELUDIUM 12 , Panel: NZ5

Principal investigator: Ewelina Bukowska-Olech

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

Identification of novel structural variants in patients presenting with congenital limb malformations by means of the ge...

Call: PRELUDIUM 12 , Panel: NZ2

Principal investigator: dr Magdalena Socha

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski