Published in Am J Hum Genet on April 01, 1998
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The distribution of mitochondrial DNA heteroplasmy due to random genetic drift. Am J Hum Genet (2008) 1.22
Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene. Am J Hum Genet (1999) 1.13
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Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice. Nat Genet (1997) 2.69
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Proc Natl Acad Sci U S A (1992) 2.62
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res (1990) 2.47
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Heteroplasmic point mutations in the human mtDNA control region. Am J Hum Genet (1996) 1.78
Mitochondrial gene segregation in mammals: is the bottleneck always narrow? Hum Genet (1992) 1.77
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet (1992) 1.73
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle. Am J Hum Genet (1997) 1.68
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes. Proc Natl Acad Sci U S A (1995) 1.66
Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes. Am J Hum Genet (1997) 1.66
Rearranged mitochondrial genomes are present in human oocytes. Am J Hum Genet (1995) 1.63
Mitochondrial genotype segregation in a mouse heteroplasmic lineage produced by embryonic karyoplast transplantation. Genetics (1997) 1.62
Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck. Am J Hum Genet (1997) 1.56
Prenatal diagnosis of mitochondrial DNA8993 T----G disease. Am J Hum Genet (1992) 1.38
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Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues. J Med Genet (1994) 1.26
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Behaviour of a population of partially duplicated mitochondrial DNA molecules in cell culture: segregation, maintenance and recombination dependent upon nuclear background. Hum Mol Genet (1997) 1.03
Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome. Diabetologia (1995) 0.96
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Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet (2000) 7.06
Paleolithic and neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet (1996) 4.23
A signal, from human mtDNA, of postglacial recolonization in Europe. Am J Hum Genet (2001) 3.28
Do the four clades of the mtDNA haplogroup L2 evolve at different rates? Am J Hum Genet (2001) 2.88
Detecting errors in mtDNA data by phylogenetic analysis. Int J Legal Med (2001) 1.97
Prehistoric and historic traces in the mtDNA of Mozambique: insights into the Bantu expansions and the slave trade. Ann Hum Genet (2001) 1.74
Median networks: speedy construction and greedy reduction, one simulation, and two case studies from human mtDNA. Mol Phylogenet Evol (2000) 1.52
The mitochondrial gene tree comes of age. Am J Hum Genet (2001) 1.43
Identification of Native American founder mtDNAs through the analysis of complete mtDNA sequences: some caveats. Ann Hum Genet (2003) 1.41
Evidence from human oocytes for a genetic bottleneck in an mtDNA disease. Am J Hum Genet (1998) 1.34
Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region. Hum Immunol (2001) 1.31
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility. Nat Genet (2001) 1.31
Phylogeographic investigations: the role of trees in forensic genetics. Forensic Sci Int (2006) 1.29
mtDNA haplogroups and frequency patterns in Europe. Am J Hum Genet (2000) 1.22
A common mitochondrial DNA variant is associated with insulin resistance in adult life. Diabetologia (1998) 1.12
Human origins and ancient human DNA. Science (2001) 1.07
Phase II study of the antifolate N10-propargyl-5,8-dideazafolic acid (CB 3717) in advanced breast cancer. Eur J Cancer Clin Oncol (1988) 1.00
Somatostatin receptors are present in small-cell but not in non-small-cell primary lung carcinomas: relationship to EGF-receptors. Int J Cancer (1990) 0.97
Does a common mitochondrial DNA polymorphism underlie susceptibility to diabetes and the thrifty genotype? Trends Genet (1998) 0.95
A phase II study of bryostatin 1 in metastatic malignant melanoma. Br J Cancer (1998) 0.91
Molecular genetic characterization of an X-linked form of Leigh's syndrome. Ann Neurol (1993) 0.90
Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta. J Med Genet (2009) 0.90
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients. Brain (1994) 0.85
Importance of mitochondrial haplotypes and maternal lineage in sprint performance among individuals of West African ancestry. Scand J Med Sci Sports (2011) 0.82
Regulation of hepatic tyrosine aminotransferase in genetically obese rats. Biochim Biophys Acta (1983) 0.81
Control of aromatase in breast cancer cells and its importance for tumor growth. J Steroid Biochem Mol Biol (1993) 0.81
Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases. Neuromuscul Disord (2000) 0.80
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Comparison of different endocrine therapies in management of bone metastases from breast carcinoma. J R Soc Med (1985) 0.79
Prospects for DNA-based prenatal diagnosis of mitochondrial disorders. Prenat Diagn (1996) 0.77
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation. Neuromuscul Disord (2005) 0.77