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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 3

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61 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 article.
Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci.
Pasanen A, Karjalainen MK; FinnGen; Zhang G, Tiensuu H, Haapalainen AM, Ojaniemi M, Feenstra B, Jacobsson B, Palotie A, Laivuori H, Muglia LJ, Rämet M, Hallman M. Pasanen A, et al. Among authors: ojaniemi m. PLoS Genet. 2023 Oct 23;19(10):e1010982. doi: 10.1371/journal.pgen.1010982. eCollection 2023 Oct. PLoS Genet. 2023. PMID: 37871108 Free PMC article.
Growth hormone and treatment outcomes: expert review of current clinical practice.
Cassorla F, Cianfarani S, Haverkamp F, Labarta JI, Loche S, Luo X, Maghnie M, Mericq V, Muzsnai A, Norgren S, Ojaniemi M, Pribilincova Z, Quinteiro S, Savendahl L, Spinola e Castro A, Gasteyger C. Cassorla F, et al. Among authors: ojaniemi m. Pediatr Endocrinol Rev. 2011 Dec;9(2):554-65. Pediatr Endocrinol Rev. 2011. PMID: 22397140 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.
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
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.
61 results