Leisti J - Search Results

1

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.

Nyström-Lahti M, Wu Y, Moisio AL, Hofstra RM, Osinga J, Mecklin JP, Järvinen HJ, Leisti J, Buys CH, de la Chapelle A, Peltomäki P. Nyström-Lahti M, et al. Among authors: leisti j. Hum Mol Genet. 1996 Jun;5(6):763-9. doi: 10.1093/hmg/5.6.763. Hum Mol Genet. 1996. PMID: 8776590

2

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

Tahvanainen E, Ranta S, Hirvasniemi A, Karila E, Leisti J, Sistonen P, Weissenbach J, Lehesjoki AE, de la Chapelle A. Tahvanainen E, et al. Among authors: leisti j. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7267-70. doi: 10.1073/pnas.91.15.7267. Proc Natl Acad Sci U S A. 1994. PMID: 8041778 Free PMC article.

3

Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers.

Kytölä S, Leisti J, Winqvist R, Salmela P. Kytölä S, et al. Among authors: leisti j. Hum Genet. 1995 Oct;96(4):449-53. doi: 10.1007/BF00191805. Hum Genet. 1995. PMID: 7557969

4

A molecular and cytogenetic study in Finnish Prader-Willi patients.

Kokkonen H, Kähkönen M, Leisti J. Kokkonen H, et al. Among authors: leisti j. Hum Genet. 1995 May;95(5):568-71. doi: 10.1007/BF00223871. Hum Genet. 1995. PMID: 7759080

5

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: leisti j. Hum Genet. 1994 Nov;94(5):479-83. doi: 10.1007/BF00211011. Hum Genet. 1994. PMID: 7959680

6

Diagnosis of fragile X syndrome by direct mutation analysis.

Väisänen ML, Kähkönen M, Leisti J. Väisänen ML, et al. Among authors: leisti j. Hum Genet. 1994 Feb;93(2):143-7. doi: 10.1007/BF00210599. Hum Genet. 1994. PMID: 8112737

7

Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission.

Väisänen ML, Haataja R, Leisti J. Väisänen ML, et al. Among authors: leisti j. Am J Hum Genet. 1996 Sep;59(3):540-6. Am J Hum Genet. 1996. PMID: 8751854 Free PMC article.

8

Genome-wide scanning for linkage in Finnish breast cancer families.

Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP. Huusko P, et al. Among authors: leisti j. Eur J Hum Genet. 2004 Feb;12(2):98-104. doi: 10.1038/sj.ejhg.5201091. Eur J Hum Genet. 2004. PMID: 14560309

9

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: leisti j. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

10

A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome.

Rekilä AM, Väisänen ML, Kähkönen M, Leisti J, Winqvist R. Rekilä AM, et al. Among authors: leisti j. Hum Genet. 1988 Oct;80(2):193. doi: 10.1007/BF00702869. Hum Genet. 1988. PMID: 2902001

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