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Page 1
Genetic variation associated with chromosomal aberration frequency: A genome-wide association study.
Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dušinská M, Musak L, Vodicka P, Hemminki K, Försti A. Niazi Y, et al. Environ Mol Mutagen. 2019 Jan;60(1):17-28. doi: 10.1002/em.22236. Epub 2018 Oct 3. Environ Mol Mutagen. 2019. PMID: 30368896
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.
Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dusinska M, Musak L, Vodicka P, Hemminki K, Försti A. Niazi Y, et al. Mutagenesis. 2019 Dec 19;34(4):323-330. doi: 10.1093/mutage/gez024. Mutagenesis. 2019. PMID: 31586183
Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium.
Sánchez-Maldonado JM, Campa D, Springer J, Badiola J, Niazi Y, Moñiz-Díez A, Hernández-Mohedo F, González-Sierra P, Ter Horst R, Macauda A, Brezina S, Cunha C, Lackner M, López-Nevot MA, Fianchi L, Pagano L, López-Fernández E, Potenza L, Luppi M, Moratalla L, Rodríguez-Sevilla JJ, Fonseca JE, Tormo M, Solano C, Clavero E, Romero A, Li Y, Lass-Flörl C, Einsele H, Vazquez L, Loeffler J, Hemminki K, Carvalho A, Netea MG, Gsur A, Dumontet C, Canzian F, Försti A, Jurado M, Sainz J. Sánchez-Maldonado JM, et al. Among authors: niazi y. Blood Cancer J. 2020 Jul 16;10(7):75. doi: 10.1038/s41408-020-00341-y. Blood Cancer J. 2020. PMID: 32678078 Free PMC article.
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans.
Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dusinska M, Musak L, Vodicka P, Hemminki K, Försti A. Niazi Y, et al. Mutat Res Genet Toxicol Environ Mutagen. 2020 Oct-Dec;858-860:503253. doi: 10.1016/j.mrgentox.2020.503253. Epub 2020 Sep 15. Mutat Res Genet Toxicol Environ Mutagen. 2020. PMID: 33198934
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population.
Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dusinska M, Musak L, Vodicka P, Försti A, Hemminki K. Niazi Y, et al. DNA Repair (Amst). 2021 May;101:103079. doi: 10.1016/j.dnarep.2021.103079. Epub 2021 Feb 27. DNA Repair (Amst). 2021. PMID: 33676360
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations.
Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dusinska M, Musak L, Vodicka P, Hemminki K, Försti A. Niazi Y, et al. Front Genet. 2021 Jun 16;12:691947. doi: 10.3389/fgene.2021.691947. eCollection 2021. Front Genet. 2021. PMID: 34220964 Free PMC article.
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study.
García-Martín P, Díez AM, Maldonado JMS, Serrano AJC, Ter Horst R, Benavente Y, Landi S, Macauda A, Clay-Gilmour A, Hernández-Mohedo F, Niazi Y, González-Sierra P, Espinet B, Rodríguez-Sevilla JJ, Maffei R, Blanco G, Giaccherini M, Puiggros A, Cerhan J, Marasca R, Cañadas-Garre M, López-Nevot MÁ, Chen-Liang T, Thomsen H, Gámez I, Moreno V, Marcos-Gragera R, García-Álvarez M, Llorca J, Jerez A, Berndt S, Butrym A, Norman AD, Casabonne D, Luppi M, Slager SL, Hemminki K, Li Y, Alcoceba M, Campa D, Canzian F, de Sanjosé S, Försti A, Netea MG, Jurado M, Sainz J. García-Martín P, et al. Among authors: niazi y. Blood Cancer J. 2022 May 17;12(5):79. doi: 10.1038/s41408-022-00676-8. Blood Cancer J. 2022. PMID: 35581176 Free PMC article. No abstract available.
Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.
Niazi Y, Paramasivam N, Blocka J, Kumar A, Huhn S, Schlesner M, Weinhold N, Sijmons R, De Jong M, Durie B, Goldschmidt H, Hemminki K, Försti A. Niazi Y, et al. Cells. 2022 Dec 26;12(1):96. doi: 10.3390/cells12010096. Cells. 2022. PMID: 36611892 Free PMC article.
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
Cabrera-Serrano AJ, Sánchez-Maldonado JM, Ter Horst R, Macauda A, García-Martín P, Benavente Y, Landi S, Clay-Gilmour A, Niazi Y, Espinet B, Rodríguez-Sevilla JJ, Pérez EM, Maffei R, Blanco G, Giaccherini M, Cerhan JR, Marasca R, López-Nevot MÁ, Chen-Liang T, Thomsen H, Gámez I, Campa D, Moreno V, de Sanjosé S, Marcos-Gragera R, García-Álvarez M, Dierssen-Sotos T, Jerez A, Butrym A, Norman AD, Luppi M, Slager SL, Hemminki K, Li Y, Berndt SI, Casabonne D, Alcoceba M, Puiggros A, Netea MG, Försti A, Canzian F, Sainz J. Cabrera-Serrano AJ, et al. Among authors: niazi y. Int J Mol Sci. 2023 Apr 28;24(9):8005. doi: 10.3390/ijms24098005. Int J Mol Sci. 2023. PMID: 37175717 Free PMC article.
14 results