Projects funded by the NCN

Genetic factors causing increased virulence of the baculovirus infecting one of the major forest pests - the gypsy moth ...

Call: PRELUDIUM 9 , Panel: NZ2

Principal investigator: dr Martyna Krejmer-Rąbalska

Uniwersytet Gdański, Międzyuczelniany Wydział Biotechnologii Uniwersytetu Gdańskiego i Gdańskiego Uniwersytetu Medycznego

The association of common polymorphic variants of DNA repair genes OGG1, APE1 and PARP1 with cell growth and apoptosis

Call: PRELUDIUM 7 , Panel: NZ3

Principal investigator: Somayeh Shahmoradi Ghahe

Uniwersytet Warszawski, Wydział Biologii

The Dynamics of a Variant - Textological Status of Czesław Miłosz's Poems and Its Cosequences for Interpretation

Call: PRELUDIUM 6 , Panel: HS2

Principal investigator: Paweł Bem

Instytut Badań Literackich PAN

Discovery of new functional variants in platelet activation pathways genes contribiuting to risk of ischemic stroke in P...

Call: OPUS 6 , Panel: NZ7

Principal investigator: dr hab. Marek Postuła

Warszawski Uniwersytet Medyczny, I Wydział Lekarski

Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association m...

Call: SONATA 6 , Panel: NZ5

Principal investigator: dr Agnieszka Ludwig-Gałęzowska

Uniwersytet Jagielloński Collegium Medicum, Collegium Medicum, Wydział Lekarski

Primary biliary cirrhosis (PBC) in Poland - clinical characteristics, analysis of relationship between genetic and molec...

Call: OPUS 1 , Panel: NZ5

Principal investigator: prof. Andrzej Habior

CENTRUM MEDYCZNE KSZTAŁCENIA PODYPLOMOWEGO

Genetic and phenotypic contribution to variability of methane emitted by dairy cows

Call: OPUS 5 , Panel: NZ9

Principal investigator: dr hab. Tomasz Strabel

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

FUNCTIONAL STUDIES OF RARE GENETIC VARIANTS OF GENES CAUSSALLY CONNECTED WITH ALZHEIMER'S DISEASE IN THE POLISH POPULATI...

Call: SONATA 5 , Panel: NZ3

Principal investigator: dr Michalina Wężyk

Instytut Medycyny Doświadczalnej i Klinicznej im. Mirosława Mossakowskiego PAN

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

The influence of steroid hormones on the expression of genetic variance in a wild bird population

Call: SONATA 4 , Panel: NZ8

Principal investigator: dr Szymon Drobniak

Uniwersytet Jagielloński, Wydział Biologii i Nauk o Ziemi

Influence of genetic factors on development and course of Graves' disease: the variants of 11beta-hydroxysteroid dehydro...

Call: PRELUDIUM 3 , Panel: NZ5

Principal investigator: Konrad Szymański

Warszawski Uniwersytet Medyczny, I Wydział Lekarski

Selenium level and selenoprotein gene alterations as risk factors of cancers in Poland.

Call: PRELUDIUM 2 , Panel: NZ2

Principal investigator: dr Katarzyna Jaworska-Bieniek

Pomorski Uniwersytet Medyczny w Szczecinie, Wydział Lekarsko-Biotechnologiczny i Medycyny Laboratoryjnej

Uncovering the molecular background of equine erythrocyte antigens variability using serological and genetic methods

Call: OPUS 24 , Panel: NZ9

Principal investigator: dr hab. Jakub Cieślak

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

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

Solving the puzzle of deep intronic splicing variants as missing elements in the genetic landscape of Usher syndrome

Call: PRELUDIUM 19 , Panel: NZ5

Principal investigator: Natalia Bałdyga

Instytut Fizjologii i Patologii Słuchu

Systematic genomic search for novel genes/variants in consanguineous families including males with reproductive failure

Call: OPUS 19 , Panel: NZ5

Principal investigator: prof. Maciej Kurpisz

Instytut Genetyki Człowieka Polskiej Akademii Nauk

Understanding of genetic basis of lethal lung developmental disorders in newborns with the use of next generation sequen...

Call: SONATA 15 , Panel: NZ5

Principal investigator: dr Justyna Karolak

Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu, Wydział Farmaceutyczny

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

Identification of the key genetic determinants of Staphylococcus aureus assosiated with bacteraemia infections.

Call: SONATA 14 , Panel: NZ6

Principal investigator: dr Marta Zapotoczna

Uniwersytet Warszawski, Wydział Biologii

Computational methods for genomic structural variants interpretation

Call: HARMONIA 10 , Panel: NZ2

Principal investigator: prof. Anna Gambin

Uniwersytet Warszawski, Wydział Matematyki, Informatyki i Mechaniki

"Mine is more important!" - using dynamic stimuli to determine neural effects of ownership

Call: PRELUDIUM 15 , Panel: HS6

Principal investigator: dr Ilona Kotlewska

Uniwersytet Jagielloński, Wydział Filozoficzny

Alternative routs of phenylalanine disposal and their potential role in prevention of brain damage in phenylketonuria

Call: OPUS 15 , Panel: NZ5

Principal investigator: dr hab. Mirosław Bik-Multanowski

Uniwersytet Jagielloński - Collegium Medicum, Collegium Medicum, Wydział Lekarski

Disclosing chromatin accessibility in brain tumor cells after treatment by cracking a 'nucleosomal code'

Call: OPUS 14 , Panel: NZ2

Principal investigator: dr Jakub Mieczkowski

Instytut Biologii Doświadczalnej im. M. Nenckiego Polskiej Akademii Nauk

Novel causative genetic variants in azoospermia: whole genome analysis and functional in vitro studies

Call: SONATA 13 , Panel: NZ5

Principal investigator: dr Agnieszka Malcher

Instytut Genetyki Człowieka Polskiej Akademii Nauk

Promutagenic function of ubiquitin enzyme variant Mms2 in S. cerevisiae cells.

Call: PRELUDIUM 12 , Panel: NZ3

Principal investigator: Michał Krawczyk

Instytut Biochemii i Biofizyki Polskiej Akademii Nauk

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

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

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

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

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

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