Projects funded by the NCN


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61 projects found matching your search criteria :

  1. Identification and comprehensive characterization of genomic variants associated with Gilles de la Tourette syndrome

    Call: OPUS 12 , Panel: NZ2

    Principal investigator: prof. Cezary Żekanowski

    Instytut Medycyny Doświadczalnej i Klinicznej im. Mirosława Mossakowskiego Polskiej Akademii Nauk

  2. Identification of obesity risk variants in the dog genome using whole-genome sequencing

    Call: OPUS 12 , Panel: NZ2

    Principal investigator: prof. Maciej Szydłowski

    Uniwersytet Przyrodniczy w Poznaniu, Wydział Medycyny Weterynaryjnej i Nauk o Zwierzętach

  3. 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

  4. 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

  5. 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

  6. The effect of Differential Speed Rolling processing combined with multi-variant heat treatment on structure and properti...

    Call: SONATA 12 , Panel: ST8

    Principal investigator: dr Wojciech Polkowski

    Sieć Badawcza ŁUKASIEWICZ - Krakowski Instytut Technologiczny

  7. 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

  8. The APOBEC3B deletion - analysis of its role in familial breast cancer predisposition and determination of its consequen...

    Call: PRELUDIUM 10 , Panel: NZ5

    Principal investigator: dr Katarzyna Klonowska

    Instytut Chemii Bioorganicznej Polskiej Akademii Nauk

  9. 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 Rygiel

    Instytut Matki i Dziecka

  10. Non-stationary signal-dependent noise modelling in parallel magnetic resonance imaging

    Call: PRELUDIUM 10 , Panel: ST7

    Principal investigator: Tomasz Pięciak

    Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie, Wydział Elektrotechniki, Automatyki, Informatyki i Inżynierii Biomedycznej

  11. Investigation of genetic variants underlying variability in patients with 22q11 Deletion Syndrome.

    Call: OPUS 9 , Panel: NZ5

    Principal investigator: dr Beata Nowakowska

    Instytut Matki i Dziecka