Jakub Piotr Fichna (Jakub P Fichna)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Topics

Dna Methylation

Top Venues

International journal of molecular sciences

Journal of clinical medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Jakub Piotr Fichna, Mateusz Chilinski, Anup Kumar Halder, Paweł Cieszczyk, Dariusz Plewczyński, Cezary Zekanowski, Piotr Janik
Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome. International journal of molecular sciences 25 (11) (2024)
Jakub Piotr Fichna, Mateusz Chilinski, Anup Kumar Halder, Paweł Cieszczyk, Dariusz Plewczyński, Cezary Zekanowski, Piotr Janik
Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome. International journal of molecular sciences 25 (11) (2024)
Jakub Piotr Fichna, Kinga Humińska-Lisowska, Krzysztof Safranow, Jakub Grzegorz Adamczyk, Paweł Cięszczyk, Cezary Zekanowski, Mariusz Berdyński
Rare Variant in the SLC6A2 Encoding a Norepinephrine Transporter Is Associated with Elite Athletic Performance in the Polish Population. Genes 12 (6) (2021)
Anna Potulska-Chromik, Maria Jędrzejowska, Monika Gos, Edyta Rosiak, Monika Grudzińska, Aleksandra Maruszak, Andrzej Opuchlik, Cezary Zekanowski, Jakub Piotr Fichna
Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients. Journal of clinical medicine 10 (5) (2021)
Jakub Piotr Fichna, Anna Macias, Marcin Piechota, Michał Korostyński, Anna Potulska-Chromik, Maria Jolanta Redowicz, Cezary Zekanowski
Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients. Human genomics 12 (1) (2018)
Jakub Piotr Fichna, Aleksandra Maruszak, Cezary Żekanowski
Myofibrillar myopathy in the genomic context. Journal of applied genetics 59 (4) (2018)