Projects funded by the NCN

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

Molecular basis of isolated hearing loss in group of Polish patients - using of Next Generation Sequencing to identify g...

Call: PRELUDIUM 7 , Panel: NZ5

Principal investigator: Katarzyna Niepokój

Instytut Matki i Dziecka

Identification of genes controlling neuronal migration in development of the human nervous system

Call: HARMONIA 3 , Panel: NZ2

Principal investigator: dr hab. Wojciech Wiszniewski

Instytut Matki i Dziecka

micro-RNAs related to cardiac hypertrophy and fibrosis in the molecular mechanisms of the left ventricular response to v...

Call: PRELUDIUM 6 , Panel: NZ5

Principal investigator: Ewa Szczerba

Instytut Matki i Dziecka

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

Dissecting the clinical complexity of 22q11 Deletion Syndrome by deep phenotyping and functional genomics.

Call: OPUS 19 , Panel: NZ5

Principal investigator: dr hab. Beata Nowakowska

Instytut Matki i Dziecka

Identification and characterization of new genetic variants associated with disturbances in the metabolism of biogenic a...

Call: OPUS 22 , Panel: NZ5

Principal investigator: dr hab. Agnieszka Rygiel

Instytut Matki i Dziecka

Attempt to identify and define the functional changes of genes related to intellectual and cognitive abilities.

Call: OPUS 4 , Panel: NZ4

Principal investigator: prof. Jerzy Bal

Instytut Matki i Dziecka

Phenotypical variability of the epileptic syndromes due to Nav1.1 ion channel mutations.

Call: OPUS 9 , Panel: NZ4

Principal investigator: dr Dorota Hoffman-Zacharska

Instytut Matki i Dziecka

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

Change in global gene expression versus keratin and lipid profile in rare skin disorders from the group of ichthyosis.

Call: SONATA 7 , Panel: NZ5

Principal investigator: dr Katarzyna Wertheim-Tysarowska

Instytut Matki i Dziecka

Molecular variation of RAS-MAPK pathway genes and phenotypic expression of Noonan syndrome

Call: SONATA 1 , Panel: NZ5

Principal investigator: dr Jakub Klapecki

Instytut Matki i Dziecka

Research on a pathogenesis of cognitive and neurofunctioning impairments in patients with Noonan syndrome. A role of RAS...

Call: PRELUDIUM 11 , Panel: HS6

Principal investigator: Natalia Braun-Walicka

Instytut Matki i Dziecka

Physical and social school environment and quality of school performance in relation to adolescent subjective health and...

Call: OPUS 5 , Panel: HS6

Principal investigator: dr hab. Joanna Mazur

Instytut Matki i Dziecka

Genetic risk factors in the Kashubian population and their involvement in the pathogenesis of autosomal recessive intell...

Call: SONATA 8 , Panel: NZ5

Principal investigator: dr Agnieszka Charzewska

Instytut Matki i Dziecka

The identification of new genes related to Noonan syndrome pathogenesis - functional analysis of identified variants in ...

Call: OPUS 5 , Panel: NZ2

Principal investigator: dr Monika Gos

Instytut Matki i Dziecka

Identification of genes controlling brain development through genomic analysis of patients with microcephaly

Call: OPUS 10 , Panel: NZ2

Principal investigator: dr hab. Wojciech Wiszniewski

Instytut Matki i Dziecka