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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: thomsen h. Int J Mol Sci. 2023 Apr 28;24(9):8005. doi: 10.3390/ijms24098005. Int J Mol Sci. 2023. PMID: 37175717 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: thomsen h. 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.
Runs of homozygosity and inbreeding in thyroid cancer.
Thomsen H, Chen B, Figlioli G, Elisei R, Romei C, Cipollini M, Cristaudo A, Bambi F, Hoffmann P, Herms S, Landi S, Hemminki K, Gemignani F, Försti A. Thomsen H, et al. BMC Cancer. 2016 Mar 16;16:227. doi: 10.1186/s12885-016-2264-7. BMC Cancer. 2016. PMID: 26984635 Free PMC article.
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
Chattopadhyay S, Thomsen H, da Silva Filho MI, Weinhold N, Hoffmann P, Nöthen MM, Marina A, Jöckel KH, Schmidt B, Pechlivanis S, Langer C, Goldschmidt H, Hemminki K, Försti A. Chattopadhyay S, et al. Among authors: thomsen h. Mol Med. 2018 Jun 11;24(1):30. doi: 10.1186/s10020-018-0031-8. Mol Med. 2018. PMID: 30134812 Free PMC article.
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. Among authors: thomsen h. 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. Among authors: thomsen h. Mutagenesis. 2019 Dec 19;34(4):323-330. doi: 10.1093/mutage/gez024. Mutagenesis. 2019. PMID: 31586183
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. Among authors: thomsen h. DNA Repair (Amst). 2021 May;101:103079. doi: 10.1016/j.dnarep.2021.103079. Epub 2021 Feb 27. DNA Repair (Amst). 2021. PMID: 33676360
781 results