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A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.

Hannula K, Lipsanen-Nyman M, Kontiokari T, Kere J. Hannula K, et al. Am J Hum Genet. 2001 Jan;68(1):247-53. doi: 10.1086/316937. Epub 2000 Dec 8. Am J Hum Genet. 2001. PMID: 11112662 Free PMC article.

Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause.

Hannula K, Lipsanen-Nyman M, Kristo P, Kaitila I, Simola KO, Lenko HL, Tapanainen P, Holmberg C, Kere J. Hannula K, et al. Pediatrics. 2002 Mar;109(3):441-8. doi: 10.1542/peds.109.3.441. Pediatrics. 2002. PMID: 11875139

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.

Hannula K, Lipsanen-Nyman M, Scherer SW, Holmberg C, Höglund P, Kere J. Hannula K, et al. Genomics. 2001 Apr 1;73(1):1-9. doi: 10.1006/geno.2001.6502. Genomics. 2001. PMID: 11352560

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.

Höglund P, Haila S, Gustavson KH, Taipale M, Hannula K, Popinska K, Holmberg C, Socha J, de la Chapelle A, Kere J. Höglund P, et al. Among authors: hannula k. Hum Mutat. 1998;11(4):321-7. doi: 10.1002/(SICI)1098-1004(1998)11:4<321::AID-HUMU10>3.0.CO;2-A. Hum Mutat. 1998. PMID: 9554749

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

Hannula K, Kere J, Pirinen S, Holmberg C, Lipsanen-Nyman M. Hannula K, et al. J Med Genet. 2001 Apr;38(4):273-8. doi: 10.1136/jmg.38.4.273. J Med Genet. 2001. PMID: 11370636 Free PMC article. No abstract available.

Differential prognostic impact of comorbidity in head and neck cancer.

Alho OP, Hannula K, Luokkala A, Teppo H, Koivunen P, Kantola S. Alho OP, et al. Among authors: hannula k. Head Neck. 2007 Oct;29(10):913-8. doi: 10.1002/hed.20608. Head Neck. 2007. PMID: 17510970

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