Nieminen P - Search Results

1

Recessively inherited lower incisor hypodontia.

Pirinen S, Kentala A, Nieminen P, Varilo T, Thesleff I, Arte S. Pirinen S, et al. Among authors: nieminen p. 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

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. Hum Genet. 1995 Sep;96(3):305-8. doi: 10.1007/BF00210412. Hum Genet. 1995. PMID: 7649547

3

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: nieminen p. J Dent Res. 2001 May;80(5):1445-50. doi: 10.1177/00220345010800051201. J Dent Res. 2001. PMID: 11437217

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: nieminen p. 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: nieminen p. 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: nieminen p. 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

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: nieminen p. J Dent Res. 1996 Jun;75(6):1346-52. doi: 10.1177/00220345960750060401. J Dent Res. 1996. PMID: 8831628

8

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. Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715. Eur J Hum Genet. 2001. PMID: 11781684

9

Blepharocheilodontic (BCD) syndrome: New insights on craniofacial and dental features.

Awadh W, Kiukkonen A, Nieminen P, Arte S, Hurmerinta K, Rice DP. Awadh W, et al. Among authors: nieminen p. Am J Med Genet A. 2017 Apr;173(4):905-913. doi: 10.1002/ajmg.a.38088. Epub 2017 Feb 9. Am J Med Genet A. 2017. PMID: 28181393

10

MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.

Nieminen P, Kotilainen J, Aalto Y, Knuutila S, Pirinen S, Thesleff I. Nieminen P, et al. J Dent Res. 2003 Dec;82(12):1013-7. doi: 10.1177/154405910308201215. J Dent Res. 2003. PMID: 14630905

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