Pirinen S - Search Results

1

Recessively inherited lower incisor hypodontia.

Pirinen S, Kentala A, Nieminen P, Varilo T, Thesleff I, Arte S. Pirinen S, et al. J Med Genet. 2001 Aug;38(8):551-6. doi: 10.1136/jmg.38.8.551. J Med Genet. 2001. PMID: 11494968 Free PMC article. No abstract available.

2

Characteristics of incisor-premolar hypodontia in families.

Arte S, Nieminen P, Apajalahti S, Haavikko K, Thesleff I, Pirinen S. Arte S, et al. Among authors: pirinen s. J Dent Res. 2001 May;80(5):1445-50. doi: 10.1177/00220345010800051201. J Dent Res. 2001. PMID: 11437217

3

Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.

Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I. Nieminen P, et al. Among authors: pirinen s. Hum Genet. 1995 Sep;96(3):305-8. doi: 10.1007/BF00210412. Hum Genet. 1995. PMID: 7649547

4

A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.

Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P. Lammi L, et al. Among authors: pirinen s. Eur J Hum Genet. 2003 Nov;11(11):866-71. doi: 10.1038/sj.ejhg.5201060. Eur J Hum Genet. 2003. PMID: 14571272

5

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.

Lammi L, Arte S, Somer M, Jarvinen H, Lahermo P, Thesleff I, Pirinen S, Nieminen P. Lammi L, et al. Among authors: pirinen s. Am J Hum Genet. 2004 May;74(5):1043-50. doi: 10.1086/386293. Epub 2004 Mar 23. Am J Hum Genet. 2004. PMID: 15042511 Free PMC article.

6

Premolar hypodontia is a common feature in Sotos syndrome with a mutation in the NSD1 gene.

Kotilainen J, Pohjola P, Pirinen S, Arte S, Nieminen P. Kotilainen J, et al. Among authors: pirinen s. Am J Med Genet A. 2009 Nov;149A(11):2409-14. doi: 10.1002/ajmg.a.33062. Am J Med Genet A. 2009. PMID: 19876911

7

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S. Nieminen P, et al. Among authors: pirinen s. Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715. Eur J Hum Genet. 2001. PMID: 11781684

8

Gene defect in hypodontia: exclusion of EGF, EGFR, and FGF-3 as candidate genes.

Arte S, Nieminen P, Pirinen S, Thesleff I, Peltonen L. Arte S, et al. Among authors: pirinen s. J Dent Res. 1996 Jun;75(6):1346-52. doi: 10.1177/00220345960750060401. J Dent Res. 1996. PMID: 8831628

9

Craniofacial and dental characteristics of Silver-Russell syndrome.

Kotilainen J, Hölttä P, Mikkonen T, Arte S, Sipilä I, Pirinen S. Kotilainen J, et al. Among authors: pirinen s. Am J Med Genet. 1995 Mar 27;56(2):229-36. doi: 10.1002/ajmg.1320560223. Am J Med Genet. 1995. PMID: 7625451

10

Short root anomaly in families and its association with other dental anomalies.

Apajalahti S, Arte S, Pirinen S. Apajalahti S, et al. Among authors: pirinen s. Eur J Oral Sci. 1999 Apr;107(2):97-101. doi: 10.1046/j.0909-8836.1999.eos107204.x. Eur J Oral Sci. 1999. PMID: 10232457

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