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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2005 3
2006 1
2007 1
2008 2
2009 1
2010 1
2011 5
2012 2
2014 2
2015 7
2016 2
2017 2
2018 6
2019 5
2020 3
2021 5
2022 6
2023 8
2024 4
2025 0

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62 results

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Page 1
Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model.
Makkonen K, Jännäri M, Crisóstomo L, Kuusi M, Patyra K, Melnyk V, Linnossuo V, Ojala J, Ravi R, Löf C, Mäkelä JA, Miettinen P, Laakso S, Ojaniemi M, Jääskeläinen J, Laakso M, Bossowski F, Sawicka B, Stożek K, Bossowski A, Kleinau G, Scheerer P, FinnGen F, Reeve MP, Kero J. Makkonen K, et al. Among authors: ojaniemi m. JCI Insight. 2024 Jan 9;9(4):e167092. doi: 10.1172/jci.insight.167092. JCI Insight. 2024. PMID: 38194289 Free PMC article.
Genes and environment in common neonatal lung disease.
Hallman M, Marttila R, Pertile R, Ojaniemi M, Haataja R. Hallman M, et al. Among authors: ojaniemi m. Neonatology. 2007;91(4):298-302. doi: 10.1159/000101345. Epub 2007 Jun 7. Neonatology. 2007. PMID: 17575473 Review.
Early disc degeneration in radiotherapy-treated childhood brain tumor survivors.
Grahn P, Remes T, Kivisaari R, Suo-Palosaari MH, Arikoski PM, Koskenkorva PKT, Lähteenmäki PM, Lönnqvist TRI, Ojaniemi MK, Sirkiä KH, Sutela AK, Toiviainen-Salo SM, Rantala HMJ, Harila AH, Niinimäki J, Karppinen J, Ahonen M. Grahn P, et al. Among authors: ojaniemi mk. BMC Musculoskelet Disord. 2023 May 31;24(1):441. doi: 10.1186/s12891-023-06509-4. BMC Musculoskelet Disord. 2023. PMID: 37259117 Free PMC article.
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
Cangul H, Liao XH, Schoenmakers E, Kero J, Barone S, Srichomkwun P, Iwayama H, Serra EG, Saglam H, Eren E, Tarim O, Nicholas AK, Zvetkova I, Anderson CA, Frankl FEK, Boelaert K, Ojaniemi M, Jääskeläinen J, Patyra K, Löf C, Williams ED; UK10K Consortium; Soleimani M, Barrett T, Maher ER, Chatterjee VK, Refetoff S, Schoenmakers N. Cangul H, et al. Among authors: ojaniemi m. JCI Insight. 2018 Oct 18;3(20):e99631. doi: 10.1172/jci.insight.99631. JCI Insight. 2018. PMID: 30333321 Free PMC article.
Cytosolic phosphoenolpyruvate carboxykinase deficiency: Expanding the clinical phenotype and novel laboratory findings.
Vieira P, Nagy II, Rahikkala E, Väisänen ML, Latva K, Kaunisto K, Valmari P, Keski-Filppula R, Haanpää MK, Sidoroff V, Miettinen PJ, Arkkola T, Ojaniemi M, Nuutinen M, Uusimaa J, Myllynen P. Vieira P, et al. Among authors: ojaniemi m. J Inherit Metab Dis. 2022 Mar;45(2):223-234. doi: 10.1002/jimd.12446. Epub 2021 Nov 11. J Inherit Metab Dis. 2022. PMID: 34622459
Radiotherapy-induced vascular cognitive impairment 20 years after childhood brain tumor.
Remes TM, Suo-Palosaari MH, Arikoski PM, Harila M, Koskenkorva PKT, Lähteenmäki PM, Lönnqvist TRI, Ojaniemi MK, Pohjasniemi H, Puosi R, Ritari N, Sirkiä KH, Sutela AK, Toiviainen-Salo SM, Rantala HMJ, Harila AH. Remes TM, et al. Among authors: ojaniemi mk. Neuro Oncol. 2024 Feb 2;26(2):362-373. doi: 10.1093/neuonc/noad186. Neuro Oncol. 2024. PMID: 37758202 Free PMC article.
62 results