Published in Biochem Biophys Res Commun on June 13, 2009
Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients. PLoS One (2011) 0.96
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy. PLoS One (2012) 0.96
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy. Neurogenetics (2010) 0.87
Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C. PLoS One (2010) 0.87
Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients. J Transl Med (2012) 0.78
Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy. Mol Vis (2012) 0.75
Multiple maternal origins of chickens: out of the Asian jungles. Mol Phylogenet Evol (2005) 2.94
Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations. Hum Mol Genet (2006) 2.89
Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences. Am J Hum Genet (2003) 2.26
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2. Am J Hum Genet (2004) 2.13
The dazzling array of basal branches in the mtDNA macrohaplogroup M from India as inferred from complete genomes. Mol Biol Evol (2005) 2.03
Obesity and risk of colorectal cancer: a systematic review of prospective studies. PLoS One (2013) 2.02
Hantavirus infections in humans and animals, China. Emerg Infect Dis (2010) 1.99
A critical reassessment of the role of mitochondria in tumorigenesis. PLoS Med (2005) 1.96
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families. Invest Ophthalmol Vis Sci (2005) 1.94
Effective small RNA destruction by the expression of a short tandem target mimic in Arabidopsis. Plant Cell (2012) 1.72
Mitochondrial genome evidence reveals successful Late Paleolithic settlement on the Tibetan Plateau. Proc Natl Acad Sci U S A (2009) 1.67
Genome of the Chinese tree shrew. Nat Commun (2013) 1.55
MitoTool: a web server for the analysis and retrieval of human mitochondrial DNA sequence variations. Mitochondrion (2010) 1.54
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. Mol Vis (2005) 1.47
Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1. J Hum Genet (2012) 1.38
Molecular characterization of rabies virus isolates in China during 2004. Virus Res (2006) 1.36
mtDNA data mining in GenBank needs surveying. Am J Hum Genet (2009) 1.36
Robot-assisted versus conventional laparoscopic surgery for colorectal disease, focusing on rectal cancer: a meta-analysis. Ann Surg Oncol (2012) 1.35
A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani family. Invest Ophthalmol Vis Sci (2005) 1.34
Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis. PLoS One (2011) 1.33
Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches. Hum Mutat (2009) 1.32
FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus. Mol Vis (2007) 1.29
Large-scale mtDNA screening reveals a surprising matrilineal complexity in east Asia and its implications to the peopling of the region. Mol Biol Evol (2010) 1.29
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation. Am J Hum Genet (2008) 1.29
Migration of Norway rats resulted in the worldwide distribution of Seoul hantavirus today. J Virol (2011) 1.27
Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy. Biochem Biophys Res Commun (2011) 1.26
Identification and association of the single nucleotide polymorphisms in calpain3 (CAPN3) gene with carcass traits in chickens. BMC Genet (2009) 1.26
Functions of the intermediate filament cytoskeleton in the eye lens. J Clin Invest (2009) 1.26
Investigation of the role of healthy dogs as potential carriers of rabies virus. Vector Borne Zoonotic Dis (2008) 1.25
Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China. Hum Genet (2003) 1.24
Low "penetrance" of phylogenetic knowledge in mitochondrial disease studies. Biochem Biophys Res Commun (2005) 1.23
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. Am J Hum Genet (2011) 1.23
Hantaviruses in rodents and humans, Inner Mongolia Autonomous Region, China. Emerg Infect Dis (2009) 1.21
Population phylogenomic analysis of mitochondrial DNA in wild boars and domestic pigs revealed multiple domestication events in East Asia. Genome Biol (2007) 1.21
Comment on "Reconstructing the origin of Andaman islanders". Science (2006) 1.19
Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gene with PACG in southern China. Mol Vis (2009) 1.16
IDH1 and IDH2 mutations are frequent in Chinese patients with acute myeloid leukemia but rare in other types of hematological disorders. Biochem Biophys Res Commun (2010) 1.15
Cooperation of Escherichia coli Hfq hexamers in DsrA binding. Genes Dev (2011) 1.15
Genetic diversity and origin of Chinese cattle revealed by mtDNA D-loop sequence variation. Mol Phylogenet Evol (2005) 1.13
Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing. Hum Genet (2014) 1.13
High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients. Biochem Biophys Res Commun (2006) 1.12
Tracing the Austronesian footprint in Mainland Southeast Asia: a perspective from mitochondrial DNA. Mol Biol Evol (2010) 1.10
Mutation analysis of 12 genes in Chinese families with congenital cataracts. Mol Vis (2011) 1.10
UHRF1 promotes cell growth and metastasis through repression of p16(ink⁴a) in colorectal cancer. Ann Surg Oncol (2012) 1.10
Immunolocalization and expression of vascular endothelial growth factor receptors (VEGFRs) and neuropilins (NRPs) on keratinocytes in human epidermis. Mol Med (2006) 1.09
[Tree shrews under the spot light: emerging model of human diseases]. Dongwuxue Yanjiu (2013) 1.07
Seoul virus and hantavirus disease, Shenyang, People's Republic of China. Emerg Infect Dis (2009) 1.07
Genetic diversity of Chinese rabies viruses: evidence for the presence of two distinct clades in China. Infect Genet Evol (2008) 1.06
Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy. J Hum Genet (2006) 1.06
Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family. Mol Vis (2004) 1.05
Distilling artificial recombinants from large sets of complete mtDNA genomes. PLoS One (2008) 1.04
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism. Mol Vis (2008) 1.04
An update to MitoTool: using a new scoring system for faster mtDNA haplogroup determination. Mitochondrion (2013) 1.03
Mutations in NYX of individuals with high myopia, but without night blindness. Mol Vis (2007) 1.03
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes. Invest Ophthalmol Vis Sci (2008) 1.02
Novel SOX2 mutation associated with ocular coloboma in a Chinese family. Arch Ophthalmol (2008) 1.02
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma. Mol Vis (2009) 1.01
Replication study supports CTNND2 as a susceptibility gene for high myopia. Invest Ophthalmol Vis Sci (2011) 1.01
The art of microRNA: various strategies leading to gene silencing via an ancient pathway. Biochim Biophys Acta (2008) 1.00
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families. Invest Ophthalmol Vis Sci (2005) 1.00
'Distorted' mitochondrial DNA sequences in schizophrenic patients. Eur J Hum Genet (2007) 0.99
Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China. Hum Genet (2013) 0.99
Evaluating the phylogenetic position of Chinese tree shrew (Tupaia belangeri chinensis) based on complete mitochondrial genome: implication for using tree shrew as an alternative experimental animal to primates in biomedical research. J Genet Genomics (2012) 0.99
Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia. Mol Vis (2009) 0.98
Mitochondrial genomes of domestic animals need scrutiny. Mol Ecol (2014) 0.98
Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studies. J Hum Genet (2009) 0.98
Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutation. Am J Med Genet A (2009) 0.98
The search of 'novel' mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor. Int J Cardiol (2007) 0.97
Novel 48-membered hexadecanuclear and 60-membered icosanuclear manganese metallamacrocycles. Inorg Chem (2008) 0.97
To trust or not to trust an idiosyncratic mitochondrial data set. Am J Hum Genet (2003) 0.97
Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic. J Hum Genet (2004) 0.97
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families. Mol Vis (2006) 0.97
Persistence of fetal vasculature in a patient with Knobloch syndrome: potential role for endostatin in fetal vascular remodeling of the eye. Ophthalmology (2004) 0.97
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes. Mol Vis (2011) 0.96
Mutation spectrum and frequency of the RHO gene in 248 Chinese families with retinitis pigmentosa. Biochem Biophys Res Commun (2010) 0.96
Protective effects of tetramethylpyrazine on rat retinal cell cultures. Neurochem Int (2007) 0.96