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Year Number of Results
2002 2
2003 1
2006 1
2008 2
2009 1
2011 3
2012 1
2013 1
2015 2
2016 1
2017 2
2018 1
2020 4
2021 1
2022 10
2023 5
2024 2

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38 results

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Page 1
Single-sperm typing.
Lien S, Szyda J, Leeflang EP, Hubert R, Zhang L, Schmitt K, Arnheim N. Lien S, et al. Among authors: szyda j. Curr Protoc Hum Genet. 2002 May;Chapter 1:Unit 1.6. doi: 10.1002/0471142905.hg0106s32. Curr Protoc Hum Genet. 2002. PMID: 18428321
Genetics, Genomics and Emerging Molecular Therapies of Pancreatic Cancer.
Liu J, Mroczek M, Mach A, Stępień M, Aplas A, Pronobis-Szczylik B, Bukowski S, Mielczarek M, Gajewska E, Topolski P, Król ZJ, Szyda J, Dobosz P. Liu J, et al. Among authors: szyda j. Cancers (Basel). 2023 Jan 27;15(3):779. doi: 10.3390/cancers15030779. Cancers (Basel). 2023. PMID: 36765737 Free PMC article. Review.
An effect of large-scale deletions and duplications on transcript expression.
Mielczarek M, Frąszczak M, Zielak-Steciwko AE, Nowak B, Hofman B, Pierścińska J, Kruszyński W, Szyda J. Mielczarek M, et al. Among authors: szyda j. Funct Integr Genomics. 2022 Dec 23;23(1):19. doi: 10.1007/s10142-022-00946-5. Funct Integr Genomics. 2022. PMID: 36564645 Free PMC article.
The Thousand Polish Genomes-A Database of Polish Variant Allele Frequencies.
Kaja E, Lejman A, Sielski D, Sypniewski M, Gambin T, Dawidziuk M, Suchocki T, Golik P, Wojtaszewska M, Mroczek M, Stępień M, Szyda J, Lisiak-Teodorczyk K, Wolbach F, Kołodziejska D, Ferdyn K, Dąbrowski M, Woźna A, Żytkiewicz M, Bodora-Troińska A, Elikowski W, Król ZJ, Zaczyński A, Pawlak A, Gil R, Wierzba W, Dobosz P, Zawadzka K, Zawadzki P, Sztromwasser P. Kaja E, et al. Among authors: szyda j. Int J Mol Sci. 2022 Apr 20;23(9):4532. doi: 10.3390/ijms23094532. Int J Mol Sci. 2022. PMID: 35562925 Free PMC article.
Long non-coding RNA variability in porcine skeletal muscle.
Hofman B, Szyda J, Frąszczak M, Mielczarek M. Hofman B, et al. Among authors: szyda j. J Appl Genet. 2024 Mar 27. doi: 10.1007/s13353-024-00860-5. Online ahead of print. J Appl Genet. 2024. PMID: 38539022
Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19.
Słomian D, Szyda J, Dobosz P, Stojak J, Michalska-Foryszewska A, Sypniewski M, Liu J, Kotlarz K, Suchocki T, Mroczek M, Stępień M, Sztromwasser P, Król ZJ. Słomian D, et al. Among authors: szyda j. PLoS One. 2023 Jan 20;18(1):e0279356. doi: 10.1371/journal.pone.0279356. eCollection 2023. PLoS One. 2023. PMID: 36662838 Free PMC article.
38 results