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

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

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 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 Ziętkiewicz

Instytut Genetyki Człowieka PAN

Exome-sequencing-based analyses for searching of genetic modifiers of Wilson's disease phenotypes.

Call: OPUS 6 , Panel: NZ2

Principal investigator: prof. Anna Członkowska

Instytut Psychiatrii i Neurologii

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 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 PAN

Exome-wide search for somatic mutations in pathogenesis of endometriosis.

Call: OPUS 5 , Panel: NZ5

Principal investigator: dr hab. Paweł Włodarski

Warszawski Uniwersytet Medyczny, I Wydział Lekarski

Characterization of mutational profile in hypopharyngeal cancers by exome enrichment and massive parallel sequencing.

Call: PRELUDIUM 5 , Panel: NZ2

Principal investigator: Marcin Machnicki

Warszawski Uniwersytet Medyczny, I Wydział Lekarski

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 Krajewska-Walasek

Instytut "Pomnik - Centrum Zdrowia Dziecka"

Interactions of U6 snRNA within the catalytic center of the spliceosome – modulation of pre-mRNA splicing by U6-like exo...

Call: MAESTRO 4 , Panel: NZ1

Principal investigator: prof. Maria Konarska

Uniwersytet Warszawski, Centrum Nowych Technologii Uniwersytetu Warszawskiego

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

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

Call: HARMONIA 2 , Panel: NZ5

Principal investigator: dr Bartłomiej Budny

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

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 Szczawińska-Popłonyk

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu

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

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

Genomic basis of successful invasion - the case of the common raccoon.

Call: OPUS 19 , Panel: NZ8

Principal investigator: dr hab. Aleksandra Biedrzycka

Instytut Ochrony Przyrody Polskiej Akademii Nauk

Development of CNV detection methods based on depth of coverage

Call: PRELUDIUM 18 , Panel: ST6

Principal investigator: Wiktor Kuśmirek

Politechnika Warszawska

Exome-based study for the establishment of clinically relevant genetic variants of pelvic organ prolapse in young women.

Call: OPUS 16 , Panel: NZ5

Principal investigator: dr hab. Anna Sadakierska-Chudy

Krakowska Akademia im. Andrzeja Frycza Modrzewskiego, Wydział Lekarski i Nauk o Zdrowiu

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

Call: OPUS 14 , Panel: NZ5

Principal investigator: dr hab. Robert Śmigiel

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

In search for genetic determinants of coincidence of Hashimoto thyroiditis in women with polycystic ovary syndrome by us...

Call: OPUS 12 , Panel: NZ2

Principal investigator: prof. Ewa Hennig

Centrum Medyczne Kształcenia Podyplomowego

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

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