Projects funded by the NCN

Identification of novel genetic factors involved in congenital disorders of endocrine gland using advanced methods of ge...

Call: SONATA 2 , Panel: NZ5

Principal investigator: dr Bartłomiej Budny

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

Identification on novel copy-number variations (CNVs) in patients affected by bilateral congenital limb malformations by...

Call: SONATA 2 , Panel: NZ2

Principal investigator: dr hab. Aleksander Jamsheer

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski I, Katedra i Zakład Genetyki Medycznej

Array-based genomic and transcriptomic profiling in pediatric acute myeloblastic leukemia in search of genes resposible ...

Call: SONATA 2 , Panel: NZ5

Principal investigator: dr Joanna Szczepanek

Uniwersytet Mikołaja Kopernika

Application of array comparative genomic hybridization (aCGH) to identify submicroscopic aberration and lethal genes in ...

Call: PRELUDIUM 12 , Panel: NZ2

Principal investigator: Katarzyna Kowalczyk

Instytut Matki i Dziecka

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

Studies on non-coding regulatory copy-number variations as a cause of bilateral limb malformations in humans

Call: SONATA BIS 6 , Panel: NZ5

Principal investigator: prof. Aleksander Jamsheer

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Lekarski

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