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Clinical and molecular risk factors for repeat interventions due to symptomatic uterine leiomyomas.
Am J Obstet Gynecol. 2025 Jan;232(1):110.e1-110.e23. doi: 10.1016/j.ajog.2024.06.051. Epub 2024 Jul 31.
Am J Obstet Gynecol. 2025.
PMID: 39094728
Free article.
Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis.
Nousiainen S, Kuismin O, Reinikka S, Manninen R, Khamaiseh S, Kuivalainen M, Terho A, Koivurova S, Niinimäki M, Salokas K, Varjosalo M, Ahtikoski A, Bützow R, Lindgren O, Uimari O, Vahteristo P.
Nousiainen S, et al. Among authors: reinikka s.
Hum Genomics. 2023 Oct 3;17(1):88. doi: 10.1186/s40246-023-00538-9.
Hum Genomics. 2023.
PMID: 37789421
Free PMC article.
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A novel uterine leiomyoma subtype exhibits NRF2 activation and mutations in genes associated with neddylation of the Cullin 3-RING E3 ligase.
Mehine M, Ahvenainen T, Khamaiseh S, Härkönen J, Reinikka S, Heikkinen T, Äyräväinen A, Pakarinen P, Härkki P, Pasanen A, Levonen AL, Bützow R, Vahteristo P.
Mehine M, et al. Among authors: reinikka s.
Oncogenesis. 2022 Sep 7;11(1):52. doi: 10.1038/s41389-022-00425-3.
Oncogenesis. 2022.
PMID: 36068196
Free PMC article.
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3'RNA and whole-genome sequencing of archival uterine leiomyomas reveal a tumor subtype with chromosomal rearrangements affecting either HMGA2, HMGA1, or PLAG1.
Jokinen V, Mehine M, Reinikka S, Khamaiseh S, Ahvenainen T, Äyräväinen A, Härkki P, Bützow R, Pasanen A, Vahteristo P.
Jokinen V, et al. Among authors: reinikka s.
Genes Chromosomes Cancer. 2023 Jan;62(1):27-38. doi: 10.1002/gcc.23088. Epub 2022 Aug 1.
Genes Chromosomes Cancer. 2023.
PMID: 35822448
Free PMC article.
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