Jazin E - Search Results

1

MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions.

Cavelier L, Jazin E, Jalonen P, Gyllensten U. Cavelier L, et al. Among authors: jazin e. Hum Genet. 2000 Jul;107(1):45-50. doi: 10.1007/s004390000305. Hum Genet. 2000. PMID: 10982034

2

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E. Lindholm E, et al. Among authors: jazin e. Am J Hum Genet. 2001 Jul;69(1):96-105. doi: 10.1086/321288. Epub 2001 May 25. Am J Hum Genet. 2001. PMID: 11389481 Free PMC article.

3

MtDNA mutations in maternally inherited diabetes: presence of the 3397 ND1 mutation previously associated with Alzheimer's and Parkinson's disease.

Cavelier L, Erikson I, Tammi M, Jalonen P, Lindholm E, Jazin E, Smith P, Luthman H, Gyllensten U. Cavelier L, et al. Among authors: jazin e. Hereditas. 2001;135(1):65-70. doi: 10.1111/j.1601-5223.2001.00065.x. Hereditas. 2001. PMID: 12035616 Free article.

4

Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes.

Balciuniene J, Dahl N, Jalonen P, Verhoeven K, Van Camp G, Borg E, Pettersson U, Jazin EE. Balciuniene J, et al. Among authors: jazin ee. Hum Genet. 1999 Sep;105(3):211-6. doi: 10.1007/s004390051091. Hum Genet. 1999. PMID: 10987647

5

Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.

Jazin EE, Cavelier L, Eriksson I, Oreland L, Gyllensten U. Jazin EE, et al. Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12382-7. doi: 10.1073/pnas.93.22.12382. Proc Natl Acad Sci U S A. 1996. PMID: 8901590 Free PMC article.

6

Mitochondrial sequence variants in patients with schizophrenia.

Lindholm E, Cavelier L, Howell WM, Eriksson I, Jalonen P, Adolfsson R, Blackwood DH, Muir WJ, Brookes AJ, Gyllensten U, Jazin EE. Lindholm E, et al. Among authors: jazin ee. Eur J Hum Genet. 1997 Nov-Dec;5(6):406-12. Eur J Hum Genet. 1997. PMID: 9450186

7

Mitochondrial mutation rate revisited: hot spots and polymorphism.

Jazin E, Soodyall H, Jalonen P, Lindholm E, Stoneking M, Gyllensten U. Jazin E, et al. Nat Genet. 1998 Feb;18(2):109-10. doi: 10.1038/ng0298-109. Nat Genet. 1998. PMID: 9462737 No abstract available.

8

Decreased cytochrome-c oxidase activity and lack of age-related accumulation of mitochondrial DNA deletions in the brains of schizophrenics.

Cavelier L, Jazin EE, Eriksson I, Prince J, Båve U, Oreland L, Gyllensten U. Cavelier L, et al. Among authors: jazin ee. Genomics. 1995 Sep 1;29(1):217-24. doi: 10.1006/geno.1995.1234. Genomics. 1995. PMID: 8530074

9

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

Balciuniene J, Dahl N, Borg E, Samuelsson E, Koisti MJ, Pettersson U, Jazin EE. Balciuniene J, et al. Among authors: jazin ee. Am J Hum Genet. 1998 Sep;63(3):786-93. doi: 10.1086/302012. Am J Hum Genet. 1998. PMID: 9718342 Free PMC article.

10

Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23.

Lindholm E, Ekholm B, Balciuniene J, Johansson G, Castensson A, Koisti M, Nylander PO, Pettersson U, Adolfsson R, Jazin E. Lindholm E, et al. Among authors: jazin e. Am J Med Genet. 1999 Aug 20;88(4):369-77. Am J Med Genet. 1999. PMID: 10402504

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