Ignatius J - Search Results

1

Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.

Silander K, Meretoja P, Juvonen V, Ignatius J, Pihko H, Saarinen A, Wallden T, Herrgård E, Aula P, Savontaus ML. Silander K, et al. Among authors: ignatius j. Hum Mutat. 1998;12(1):59-68. doi: 10.1002/(SICI)1098-1004(1998)12:1<59::AID-HUMU9>3.0.CO;2-A. Hum Mutat. 1998. PMID: 9633821

2

Dissecting the epidemiology of a trinucleotide repeat disease - example of FRDA in Finland.

Juvonen V, Kulmala SM, Ignatius J, Penttinen M, Savontaus ML. Juvonen V, et al. Among authors: ignatius j. Hum Genet. 2002 Jan;110(1):36-40. doi: 10.1007/s00439-001-0642-x. Epub 2001 Nov 14. Hum Genet. 2002. PMID: 11810294

3

A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophy.

Sankila EM, Joensuu TH, Hämäläinen RH, Raitanen N, Valle O, Ignatius J, Cormand B. Sankila EM, et al. Among authors: ignatius j. Hum Mutat. 2000 Jul;16(1):94. doi: 10.1002/1098-1004(200007)16:1<94::AID-HUMU25>3.0.CO;2-T. Hum Mutat. 2000. PMID: 10874321 No abstract available.

4

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.

Jonasson J, Juvonen V, Sistonen P, Ignatius J, Johansson D, Björck EJ, Wahlström J, Melberg A, Holmgren G, Forsgren L, Holmberg M. Jonasson J, et al. Among authors: ignatius j. Eur J Hum Genet. 2000 Dec;8(12):918-22. doi: 10.1038/sj.ejhg.5200557. Eur J Hum Genet. 2000. PMID: 11175279

5

Huntington disease in Finland: a molecular and genealogical study.

Ikonen E, Ignatius J, Norio R, Palo J, Peltonen L. Ikonen E, et al. Among authors: ignatius j. Hum Genet. 1992 May;89(3):275-80. doi: 10.1007/BF00220539. Hum Genet. 1992. PMID: 1351031

6

Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals.

Mäkelä-Bengs P, Järvinen N, Vuopala K, Suomalainen A, Ignatius J, Sipilä M, Herva R, Palotie A, Peltonen L. Mäkelä-Bengs P, et al. Among authors: ignatius j. Am J Hum Genet. 1998 Aug;63(2):506-16. doi: 10.1086/301968. Am J Hum Genet. 1998. PMID: 9683599 Free PMC article.

7

Dissecting a population genome for targeted screening of disease mutations.

Pastinen T, Perola M, Ignatius J, Sabatti C, Tainola P, Levander M, Syvänen AC, Peltonen L. Pastinen T, et al. Among authors: ignatius j. Hum Mol Genet. 2001 Dec 15;10(26):2961-72. doi: 10.1093/hmg/10.26.2961. Hum Mol Genet. 2001. PMID: 11751678

8

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.

Laiho E, Ignatius J, Mikkola H, Yee VC, Teller DC, Niemi KM, Saarialho-Kere U, Kere J, Palotie A. Laiho E, et al. Among authors: ignatius j. Am J Hum Genet. 1997 Sep;61(3):529-38. doi: 10.1086/515498. Am J Hum Genet. 1997. PMID: 9326318 Free PMC article.

9

Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.

Laitinen T, Kauppi P, Ignatius J, Ruotsalainen T, Daly MJ, Kääriäinen H, Kruglyak L, Laitinen H, de la Chapelle A, Lander ES, Laitinen LA, Kere J. Laitinen T, et al. Among authors: ignatius j. Hum Mol Genet. 1997 Nov;6(12):2069-76. doi: 10.1093/hmg/6.12.2069. Hum Mol Genet. 1997. PMID: 9328470

10

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: ignatius j. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

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