Published in Am J Hum Genet on September 01, 1993
Origin and evolution of Native American mtDNA variation: a reappraisal. Am J Hum Genet (1996) 7.34
Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet (2000) 7.06
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups. Am J Hum Genet (2002) 6.02
mtDNA variation among Greenland Eskimos: the edge of the Beringian expansion. Am J Hum Genet (2000) 5.17
The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs. Am J Hum Genet (1999) 4.80
The role of selection in the evolution of human mitochondrial genomes. Genetics (2005) 4.56
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet (1994) 4.47
mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans. Am J Hum Genet (1993) 4.46
Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups. Am J Hum Genet (1995) 4.30
mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe. Am J Hum Genet (1998) 3.94
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet (1997) 3.48
Investigation of heteroplasmy in the human mitochondrial DNA control region: a synthesis of observations from more than 5000 global population samples. J Mol Evol (2009) 3.47
The ancestry of Brazilian mtDNA lineages. Am J Hum Genet (2000) 3.46
Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome Res (2004) 3.34
A "Copernican" reassessment of the human mitochondrial DNA tree from its root. Am J Hum Genet (2012) 3.31
A signal, from human mtDNA, of postglacial recolonization in Europe. Am J Hum Genet (2001) 3.28
1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging. Am J Hum Genet (1995) 3.22
Beringian standstill and spread of Native American founders. PLoS One (2007) 3.10
Mitochondrial DNA sequence variation in human evolution and disease. Proc Natl Acad Sci U S A (1994) 2.96
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes. Am J Hum Genet (1999) 2.89
Ethnic India: a genomic view, with special reference to peopling and structure. Genome Res (2003) 2.88
Do the four clades of the mtDNA haplogroup L2 evolve at different rates? Am J Hum Genet (2001) 2.88
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America. Proc Natl Acad Sci U S A (1994) 2.86
Mitochondrial DNA analysis of Mongolian populations and implications for the origin of New World founders. Genetics (1996) 2.80
mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico. Am J Hum Genet (1994) 2.68
Genetic relationship of populations in China. Proc Natl Acad Sci U S A (1998) 2.65
Admixture dynamics in Hispanics: a shift in the nuclear genetic ancestry of a South American population isolate. Proc Natl Acad Sci U S A (2006) 2.65
Founder mitochondrial haplotypes in Amerindian populations. Am J Hum Genet (1994) 2.56
A three-stage colonization model for the peopling of the Americas. PLoS One (2008) 2.40
Ice Ages and the mitochondrial DNA chronology of human dispersals: a review. Philos Trans R Soc Lond B Biol Sci (2004) 2.39
Most of the extant mtDNA boundaries in south and southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans. BMC Genet (2004) 2.37
mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. Am J Hum Genet (2000) 2.35
Natural selection and molecular evolution in PTC, a bitter-taste receptor gene. Am J Hum Genet (2004) 2.33
mtDNA sequence diversity in Africa. Am J Hum Genet (1996) 2.28
Different genetic components in the Ethiopian population, identified by mtDNA and Y-chromosome polymorphisms. Am J Hum Genet (1998) 2.16
mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America? Am J Hum Genet (1998) 2.16
A single and early migration for the peopling of the Americas supported by mitochondrial DNA sequence data. Proc Natl Acad Sci U S A (1997) 2.15
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia. Proc Natl Acad Sci U S A (1994) 2.07
The central Siberian origin for native American Y chromosomes. Am J Hum Genet (1999) 2.03
mtDNA analysis of a prehistoric Oneota population: implications for the peopling of the New World. Am J Hum Genet (1998) 2.01
Compilation of human mtDNA control region sequences. Nucleic Acids Res (1998) 2.00
Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest Colombia. Am J Hum Genet (2000) 1.94
Admixture in Mexico City: implications for admixture mapping of type 2 diabetes genetic risk factors. Hum Genet (2006) 1.93
mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World. Am J Hum Genet (1998) 1.91
The phylogeny of the four pan-American MtDNA haplogroups: implications for evolutionary and disease studies. PLoS One (2008) 1.87
The Genographic Project public participation mitochondrial DNA database. PLoS Genet (2007) 1.86
Y-chromosome evidence for differing ancient demographic histories in the Americas. Am J Hum Genet (2003) 1.84
The dual origin and Siberian affinities of Native American Y chromosomes. Am J Hum Genet (2001) 1.65
Updating phylogeny of mitochondrial DNA macrohaplogroup m in India: dispersal of modern human in South Asian corridor. PLoS One (2009) 1.58
Origin and diffusion of mtDNA haplogroup X. Am J Hum Genet (2003) 1.57
Evidence that a West-East admixed population lived in the Tarim Basin as early as the early Bronze Age. BMC Biol (2010) 1.55
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups. Ann Hum Genet (2005) 1.54
The initial peopling of the Americas: a growing number of founding mitochondrial genomes from Beringia. Genome Res (2010) 1.50
Nuclear and mitochondrial DNA analysis of a 2,000-year-old necropolis in the Egyin Gol Valley of Mongolia. Am J Hum Genet (2003) 1.50
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA. Am J Hum Genet (1996) 1.46
Autosomal, mtDNA, and Y-chromosome diversity in Amerinds: pre- and post-Columbian patterns of gene flow in South America. Am J Hum Genet (2000) 1.45
mtDNA variation indicates Mongolia may have been the source for the founding population for the New World. Am J Hum Genet (1996) 1.44
mtDNA and the peopling of the Americas. Am J Hum Genet (1993) 1.40
Virologic and genetic studies relate Amerind origins to the indigenous people of the Mongolia/Manchuria/southeastern Siberia region. Proc Natl Acad Sci U S A (1994) 1.40
Diversity and age of the four major mtDNA haplogroups, and their implications for the peopling of the New World. Am J Hum Genet (1997) 1.39
Genetic evidence for the proto-Austronesian homeland in Asia: mtDNA and nuclear DNA variation in Taiwanese aboriginal tribes. Am J Hum Genet (1998) 1.39
mtDNA affinities of the peoples of North-Central Mexico. Am J Hum Genet (2000) 1.34
Reconstructing Native American migrations from whole-genome and whole-exome data. PLoS Genet (2013) 1.34
Mitochondrial DNA and Y chromosome variation provides evidence for a recent common ancestry between Native Americans and Indigenous Altaians. Am J Hum Genet (2012) 1.31
Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats. Philos Trans R Soc Lond B Biol Sci (1998) 1.30
Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia. Am J Hum Genet (2002) 1.29
Reconciling migration models to the Americas with the variation of North American native mitogenomes. Proc Natl Acad Sci U S A (2013) 1.23
Linguistic diversity of the Americas can be reconciled with a recent colonization. Proc Natl Acad Sci U S A (1999) 1.23
mtDNA and Native Americans: a Southern perspective. Am J Hum Genet (1994) 1.23
mtDNA variation in the Yanomami: evidence for additional New World founding lineages. Am J Hum Genet (1996) 1.22
mtDNA haplogroups and frequency patterns in Europe. Am J Hum Genet (2000) 1.22
Evidence for mitochondrial DNA recombination in a human population of island Melanesia. Proc Biol Sci (1999) 1.21
Gene flow across linguistic boundaries in Native North American populations. Proc Natl Acad Sci U S A (2005) 1.21
Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity. Am J Hum Genet (2003) 1.21
Mitochondrial and nuclear DNA diversity in the Chocó and Chibcha Amerinds of Panamá. Genetics (1997) 1.14
The structure of diversity within New World mitochondrial DNA haplogroups: implications for the prehistory of North America. Am J Hum Genet (2002) 1.12
mtDNA history of the Cayapa Amerinds of Ecuador: detection of additional founding lineages for the Native American populations. Am J Hum Genet (1999) 1.12
FMR1 in global populations. Am J Hum Genet (1996) 1.11
Mitochondrial genome diversity in arctic Siberians, with particular reference to the evolutionary history of Beringia and Pleistocenic peopling of the Americas. Am J Hum Genet (2008) 1.10
mtDNA and Y chromosome-specific polymorphisms in modern Ojibwa: implications about the origin of their gene pool. Am J Hum Genet (1997) 1.09
Rapid coastal spread of First Americans: novel insights from South America's Southern Cone mitochondrial genomes. Genome Res (2012) 1.08
Mitochondrial control-region sequence variation in aboriginal Australians. Am J Hum Genet (1998) 1.08
The Basque paradigm: genetic evidence of a maternal continuity in the Franco-Cantabrian region since pre-Neolithic times. Am J Hum Genet (2012) 1.07
Mitochondrial genome diversity of Native Americans supports a single early entry of founder populations into America. Am J Hum Genet (2002) 1.06
The first peopling of South America: new evidence from Y-chromosome haplogroup Q. PLoS One (2013) 1.03
A defective Vkappa A2 allele in Navajos which may play a role in increased susceptibility to haemophilus influenzae type b disease. J Clin Invest (1996) 1.03
Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. BMC Evol Biol (2013) 1.02
About the "Asian"-specific 9-bp deletion of mtDNA.... Am J Hum Genet (1995) 1.01
Human beta-globin gene polymorphisms characterized in DNA extracted from ancient bones 12,000 years old. Am J Hum Genet (1995) 1.01
Normal variation at the myotonic dystrophy locus in global human populations. Am J Hum Genet (1995) 1.00
Stable isotope and DNA evidence for ritual sequences in Inca child sacrifice. Proc Natl Acad Sci U S A (2007) 0.99
MtDNA haplogroups in Native Americans. Am J Hum Genet (1995) 0.98
Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy. Am J Hum Genet (1996) 0.95
Lack of ancient Polynesian-Amerindian contact. Am J Hum Genet (1996) 0.95
Mitochondrial echoes of first settlement and genetic continuity in El Salvador. PLoS One (2009) 0.95
Do species populations really start small? New perspectives from the Late Neogene fossil record of African mammals. Philos Trans R Soc Lond B Biol Sci (2004) 0.94
Problematic use of Greenberg's linguistic classification of the Americas in studies of Native American genetic variation. Am J Hum Genet (2004) 0.94
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans. Am J Hum Genet (1995) 0.94
HLA class II linkage disequilibrium and haplotype evolution in the Cayapa Indians of Ecuador. Am J Hum Genet (1995) 0.93
Clan, language, and migration history has shaped genetic diversity in Haida and Tlingit populations from Southeast Alaska. Am J Phys Anthropol (2012) 0.93
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science (1985) 95.08
Sequence and organization of the human mitochondrial genome. Nature (1981) 57.39
Mitochondrial DNA and human evolution. Nature (1987) 22.33
Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA. Nucleic Acids Res (1987) 10.38
Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci U S A (1980) 9.48
Extensive mitochondrial diversity within a single Amerindian tribe. Proc Natl Acad Sci U S A (1991) 9.35
Mitochondrial DNA sequences in single hairs from a southern African population. Proc Natl Acad Sci U S A (1989) 6.92
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. J Mol Evol (1983) 6.80
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell (1990) 6.80
Maximum likelihood estimation of the number of nucleotide substitutions from restriction sites data. Genetics (1983) 5.48
Geographic variation in human mitochondrial DNA from Papua New Guinea. Genetics (1990) 5.44
Diabetes incidence and prevalence in Pima Indians: a 19-fold greater incidence than in Rochester, Minnesota. Am J Epidemiol (1978) 5.22
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages. Am J Hum Genet (1990) 5.17
Length mutations in human mitochondrial DNA. Genetics (1983) 4.81
Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations. Genetics (1992) 4.78
Dramatic founder effects in Amerindian mitochondrial DNAs. Am J Phys Anthropol (1985) 4.56
mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans. Am J Hum Genet (1993) 4.46
Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations. Genetics (1992) 4.12
Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition. Hum Genet (1986) 3.93
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci U S A (1981) 3.71
An Asian-specific 9-bp deletion of mitochondrial DNA is frequently found in Polynesians. Am J Hum Genet (1989) 3.13
Human origins and analysis of mitochondrial DNA sequences. Science (1992) 3.10
Genetic studies on the Senegal population. I. Mitochondrial DNA polymorphisms. Am J Hum Genet (1988) 3.05
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics (1992) 2.94
The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians. Am J Phys Anthropol (1970) 2.59
The powers and pitfalls of parsimony. Nature (1993) 2.47
Human origins and analysis of mitochondrial DNA sequences. Science (1992) 2.43
Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations. Curr Genet (1987) 2.42
The genetic structure of a tribal population, the Yanomama Indians XI. Gene frequencies for 10 blood groups and the ABH-Le secretor traits in the Yanomama and their neighbors; the uniqueness of the tribe. Am J Hum Genet (1975) 2.28
American Indian prehistory as written in the mitochondrial DNA: a review. Hum Biol (1992) 2.28
Rate of sequence divergence estimated from restriction maps of mitochondrial DNAs from Papua New Guinea. Cold Spring Harb Symp Quant Biol (1986) 2.13
GM allotypes in Native Americans: evidence for three distinct migrations across the Bering land bridge. Am J Phys Anthropol (1985) 2.11
Founder effect and number of private polymorphisms observed in Amerindian tribes. Proc Natl Acad Sci U S A (1978) 2.06
Genetic variation of the mitochondrial DNA genome in American Indians is at mutation-drift equilibrium. Am J Phys Anthropol (1991) 2.04
Rare variants, private polymorphisms, and locus heterozygosity in Amerindian populations. Am J Hum Genet (1978) 1.96
Microevolution in lower Central America: genetic characterization of the Chibcha-speaking groups of Costa Rica and Panama, and a consensus taxonomy based on genetic and linguistic affinity. Am J Hum Genet (1990) 1.86
Absence of the Asian-specific region V mitochondrial marker in Native Beringians. Am J Hum Genet (1992) 1.77
Gene frequencies and microdifferentiation among the Makiritare Indians. I. Eleven blood group systems and the ABH-Le secretor traits: a note on Rh gene frequency determinations. Am J Hum Genet (1970) 1.72
The genetic structure of a tribal population, the Yanomama Indians. IX. Gene frequencies for 18 serum protein and erythrocyte enzyme systems in the Yanomama and five neighboring tribes: nine new variants. Am J Hum Genet (1973) 1.59
Genetic studies on the Ticuna, an enigmatic tribe of Central Amazonas. Ann Hum Genet (1980) 1.49
Genetic studies of the Macushi and Wapishana Indians. I. Rare genetic variants and a "private polymorphism' of esterase A. Hum Genet (1977) 1.41
Intra and intertribal genetic variation within a linguistic group: the Ge-speaking indians of Brazil. Am J Phys Anthropol (1977) 1.27
Dietary change and plasma glucose levels in an Amerindian population undergoing cultural transition. Soc Sci Med (1987) 1.23
Study of HLA alloantigens of the Navajo Indians of North America. II. HLA-A, B, C, DR and other genetic markers. Tissue Antigens (1982) 1.16
HL-A27 and ankylosing spondylitis in B.C. Indians. J Rheumatol (1975) 1.08
Genetic studies of the Macushi and Wapishana Indians. II. Data on 12 genetic polymorphisms of the red cell and serum proteins: gene flor between the tribes. Hum Genet (1977) 1.08
Electrophoretic variants in three Amerindian tribes: the Baniwa, Kanamari, and Central Pano of western Brazil. Am J Phys Anthropol (1979) 1.03
Distribution of albumin variants Naskapi amd Mexico among Aleuts, Frobisher Bay Eskimos, and Micmac, Naskapi, Mohawk, Omaha, and Apache Indians. Am J Phys Anthropol (1978) 1.01
The HLA loci of th Hopi and Navajo. Am J Phys Anthropol (1981) 1.00
The Northern and Southeastern Ojibwa: serum proteins and red cell enzyme systems. Am J Phys Anthropol (1974) 0.96
Dogrib Indians of the Northwest Territories, Canada: genetic diversity and genetic relationship among subarctic Indians. Ann Hum Biol (1983) 0.95
Study of HLA system in a Mataco population: a geographically isolated American Indian tribe. Tissue Antigens (1984) 0.89
Immunoglobulin (GM and KM) allotypes and relation to population history in native peoples of British Columbia: Haida and Bella Coola. Am J Phys Anthropol (1988) 0.85
The detection of the genetic carriers of hereditary disease. Am J Hum Genet (1949) 15.66
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science (1988) 11.76
Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci U S A (1980) 9.48
Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat Genet (1995) 7.17
Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. J Mol Evol (1983) 6.80
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell (1990) 6.80
Classification of European mtDNAs from an analysis of three European populations. Genetics (1996) 6.28
The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations. Am J Hum Genet (1949) 5.72
Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription. Chem Biol (2000) 5.55
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines. Methods Enzymol (1996) 5.40
The Inheritance of Sickle Cell Anemia. Science (1949) 5.26
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages. Am J Hum Genet (1990) 5.17
The genetic structure of a tirbal population, the Vanomama Indians. II. Eleven blood-group systems and the ABH-Le secretor traits. Ann Hum Genet (1972) 4.87
Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations. Genetics (1992) 4.78
Chronic enterovirus infection in patients with postviral fatigue syndrome. Lancet (1988) 4.69
Dramatic founder effects in Amerindian mitochondrial DNAs. Am J Phys Anthropol (1985) 4.56
mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet (1994) 4.47
mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans. Am J Hum Genet (1993) 4.46
Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups. Am J Hum Genet (1995) 4.30
Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations. Genetics (1992) 4.12
Mitochondrial mutations in cancer. Oncogene (2006) 3.86
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci U S A (1981) 3.71
The costs of human inbreeding and their implications for variations at the DNA level. Nat Genet (1994) 3.69
Patient perception of involvement in medical care: relationship to illness attitudes and outcomes. J Gen Intern Med (1990) 3.56
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. Nat Genet (1992) 3.53
Extension of life-span with superoxide dismutase/catalase mimetics. Science (2000) 3.41
A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase. Nat Genet (1998) 3.41
Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude. Am J Phys Anthropol (1994) 3.40
Prognosis of diabetics with diabetes onset before the age of thirty-one. I. Survival, causes of death, and complications. Diabetologia (1978) 3.40
The genetic structure of a tribal population, the Yanomama Indians. XII. Biodemographic studies. Am J Phys Anthropol (1975) 3.40
Indirect estimates of mutation rates in tribal Amerindians. Proc Natl Acad Sci U S A (1978) 3.36
Causal pathways for incident lower-extremity ulcers in patients with diabetes from two settings. Diabetes Care (1999) 3.27
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. Nat Genet (1997) 3.26
Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. Am J Hum Genet (1986) 3.17
Lower-extremity amputation in diabetes. The independent effects of peripheral vascular disease, sensory neuropathy, and foot ulcers. Diabetes Care (1999) 3.06
Use of metronidazole in equine acute idiopathic toxaemic colitis. Vet Rec (1998) 2.97
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics (1992) 2.94
Genome size and evolution. Chromosoma (1973) 2.93
Mitochondrial disease in superoxide dismutase 2 mutant mice. Proc Natl Acad Sci U S A (1999) 2.91
Prognosis of diabetics with diabetes onset before the age of thirty-one. II. Factors influencing the prognosis. Diabetologia (1978) 2.90
Regional linguistic and genetic differences among Yanomama indians. Science (1974) 2.87
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America. Proc Natl Acad Sci U S A (1994) 2.86
The NAS-NRC twin panel: methods of construction of the panel, zygosity diagnosis, and proposed use. Am J Hum Genet (1967) 2.81
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mitochondrial DNA. Am J Hum Genet (1986) 2.80
The structure of human mitochondrial DNA variation. J Mol Evol (1991) 2.78
Patients' Perceived Involvement in Care Scale: relationship to attitudes about illness and medical care. J Gen Intern Med (1990) 2.72
Mitochondrial DNA variation in human evolution and disease. Gene (1999) 2.72
Risk factors for diabetic peripheral sensory neuropathy. Results of the Seattle Prospective Diabetic Foot Study. Diabetes Care (1997) 2.70
mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico. Am J Hum Genet (1994) 2.68
Cyclosporine for plaque-type psoriasis. Results of a multidose, double-blind trial. N Engl J Med (1991) 2.66
"Private" genetic variants and the frequency of mutation among South American Indians. Proc Natl Acad Sci U S A (1973) 2.64
Increased mitochondrial oxidative stress in the Sod2 (+/-) mouse results in the age-related decline of mitochondrial function culminating in increased apoptosis. Proc Natl Acad Sci U S A (2001) 2.63
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Proc Natl Acad Sci U S A (1989) 2.63
The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians. Am J Phys Anthropol (1970) 2.59
Mitochondrial disease in mouse results in increased oxidative stress. Proc Natl Acad Sci U S A (1999) 2.58
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol (1991) 2.57
Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain. Ann Neurol (1993) 2.56
Congenital Aniridia. Am J Hum Genet (1960) 2.50
A prospective study of risk factors for diabetic foot ulcer. The Seattle Diabetic Foot Study. Diabetes Care (1999) 2.49
A benefit-based copay for prescription drugs: patient contribution based on total benefits, not drug acquisition cost. Am J Manag Care (2001) 2.44
Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic. Am J Phys Anthropol (1999) 2.43
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics (1993) 2.39
mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. Am J Hum Genet (2000) 2.35
The relationship between patients' satisfaction with their physicians and perceptions about interventions they desired and received. Med Care (1989) 2.32
Children of incest. Pediatrics (1967) 2.32
Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease. JAMA (1991) 2.31
A randomized controlled trial of implant-retained mandibular overdentures. J Dent Res (2006) 2.31
Probability of founder effect in a tribal population. Proc Natl Acad Sci U S A (1978) 2.29
The genetic structure of a tribal population, the Yanomama Indians XI. Gene frequencies for 10 blood groups and the ABH-Le secretor traits in the Yanomama and their neighbors; the uniqueness of the tribe. Am J Hum Genet (1975) 2.28
Genetic effects of the atomic bombs: a reappraisal. Science (1981) 2.27
Enhanced optical coherence tomography imaging by multiple scan averaging. Br J Ophthalmol (2005) 2.27
Likelihood ratio: A powerful tool for incorporating the results of a diagnostic test into clinical decisionmaking. Ann Emerg Med (1999) 2.23
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet (1997) 2.21
The genetic structure of a tribal population, the Yanomama Indians. XV. Patterns inferred by autocorrelation analysis. Genetics (1986) 2.18
Blood pressure, sodium intake, and sodium related hormones in the Yanomamo Indians, a "no-salt" culture. Circulation (1975) 2.17
mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America? Am J Hum Genet (1998) 2.16
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nat Genet (1992) 2.15
Allelic disequilibrium and allele frequency distribution as a function of social and demographic history. Am J Hum Genet (1997) 2.14
Amino acid change associated with the major polymorphic Hinc II site of Oriental and Caucasian mitochondrial DNAs. Am J Hum Genet (1983) 2.13
Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America. Am J Hum Genet (1988) 2.13
Structure and evolution of organelle genomes. Microbiol Rev (1982) 2.11
Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation. J Biol Chem (1992) 2.08
Cytoplasmic inheritance of chloramphenicol resistance in mouse tissue culture cells. Proc Natl Acad Sci U S A (1974) 2.08
JC virus DNA is present in the mucosa of the human colon and in colorectal cancers. Proc Natl Acad Sci U S A (1999) 2.08
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia. Proc Natl Acad Sci U S A (1994) 2.07
Founder effect and number of private polymorphisms observed in Amerindian tribes. Proc Natl Acad Sci U S A (1978) 2.06
Mitochondrial oxidative phosphorylation defects in Parkinson's disease. Ann Neurol (1991) 2.06