Ryynänen M - Search Results

1

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.

Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, Gillanders E, Syrjäkoski K, Kainu T, Vahteristo P, Krahe R, Pääkkönen K, Hartikainen J, Blomqvist C, Löppönen T, Holli K, Ryynänen M, Bützow R, Borg A, Wasteson Arver B, Holmberg E, Mannermaa A, Kere J, Kallioniemi OP, Winqvist R, Nevanlinna H. Sarantaus L, et al. Among authors: ryynanen m. Eur J Hum Genet. 2000 Oct;8(10):757-63. doi: 10.1038/sj.ejhg.5200529. Eur J Hum Genet. 2000. PMID: 11039575

2

Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families.

Hartikainen JM, Kataja V, Pirskanen M, Arffman A, Ristonmaa U, Vahteristo P, Ryynänen M, Heinonen S, Kosma VM, Mannermaa A. Hartikainen JM, et al. Among authors: ryynanen m. Clin Genet. 2007 Oct;72(4):311-20. doi: 10.1111/j.1399-0004.2007.00866.x. Clin Genet. 2007. PMID: 17850627

3

Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies.

Ryynänen M, Heinonen S, Makkonen M, Kajanoja E, Mannermaa A, Pertti K. Ryynänen M, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):212-6. doi: 10.1038/sj.ejhg.5200285. Eur J Hum Genet. 1999. PMID: 10196705

4

Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients.

Hiltunen M, Mannermaa A, Koivisto AM, Lehtovirta M, Helisalmi S, Ryynänen M, Riekkinen P Sr, Soininen H. Hiltunen M, et al. Among authors: ryynanen m. Eur J Hum Genet. 1999 Sep;7(6):652-8. doi: 10.1038/sj.ejhg.5200342. Eur J Hum Genet. 1999. PMID: 10482953

5

Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation.

Kallinen J, Heinonen S, Mannermaa A, Ryynänen M. Kallinen J, et al. Among authors: ryynanen m. Clin Genet. 2000 Aug;58(2):111-5. doi: 10.1034/j.1399-0004.2000.580204.x. Clin Genet. 2000. PMID: 11005143

6

Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.

Ryynänen M, Kirkinen P, Mannermaa A, Saarikoski S. Ryynänen M, et al. Am J Obstet Gynecol. 1995 Apr;172(4 Pt 1):1236-9. doi: 10.1016/0002-9378(95)91485-4. Am J Obstet Gynecol. 1995. PMID: 7726262

7

The fragile X syndrome in Finland: demonstration of a founder effect by analysis of microsatellite haplotypes.

Haataja R, Väisänen ML, Li M, Ryynänen M, Leisti J. Haataja R, et al. Among authors: ryynanen m. Hum Genet. 1994 Nov;94(5):479-83. doi: 10.1007/BF00211011. Hum Genet. 1994. PMID: 7959680

8

Strong family history of uterine leiomyomatosis warrants fumarate hydratase mutation screening.

Tolvanen J, Uimari O, Ryynänen M, Aaltonen LA, Vahteristo P. Tolvanen J, et al. Among authors: ryynanen m. Hum Reprod. 2012 Jun;27(6):1865-9. doi: 10.1093/humrep/des105. Epub 2012 Apr 3. Hum Reprod. 2012. PMID: 22473397

9

Deletion in the FMR1 gene in a fragile-X male.

Mannermaa A, Pulkkinen L, Kajanoja E, Ryynänen M, Saarikoski S. Mannermaa A, et al. Among authors: ryynanen m. Am J Med Genet. 1996 Aug 9;64(2):293-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<293::AID-AJMG12>3.0.CO;2-A. Am J Med Genet. 1996. PMID: 8844068

10

Antenatal genetic screening for congenital nephrosis.

Kallinen J, Heinonen S, Ryynänen M, Pulkkinen L, Mannermaa A. Kallinen J, et al. Among authors: ryynanen m. Prenat Diagn. 2001 Feb;21(2):81-4. doi: 10.1002/1097-0223(200102)21:2<81::aid-pd1>3.0.co;2-8. Prenat Diagn. 2001. PMID: 11241530

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