Published in Hum Mol Genet on July 06, 2007
High-throughput sequencing of complete human mtDNA genomes from the Caucasus and West Asia: high diversity and demographic inferences. Eur J Hum Genet (2011) 1.80
High-throughput sequencing of complete human mtDNA genomes from the Philippines. Genome Res (2010) 1.56
A Bayesian evaluation of human mitochondrial substitution rates. Am J Hum Genet (2008) 1.38
Climate shaped the worldwide distribution of human mitochondrial DNA sequence variation. Proc Biol Sci (2009) 1.20
Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins. BMC Evol Biol (2011) 1.16
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
Evolution of the mitochondrial genome in mammals living at high altitude: new insights from a study of the tribe Caprini (Bovidae, Antilopinae). J Mol Evol (2009) 1.09
Ancient mitochondrial DNA provides high-resolution time scale of the peopling of the Americas. Sci Adv (2016) 1.07
Analysis of the evolutionary forces shaping mitochondrial genomes of a Neotropical malaria vector complex. Mol Phylogenet Evol (2011) 1.06
Explaining the imperfection of the molecular clock of hominid mitochondria. PLoS One (2009) 0.93
Understanding phylogenetic incongruence: lessons from phyllostomid bats. Biol Rev Camb Philos Soc (2012) 0.91
Mitochondrial genome sequences illuminate maternal lineages of conservation concern in a rare carnivore. BMC Ecol (2011) 0.91
Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans. BMC Evol Biol (2010) 0.91
Tracing the legacy of the early Hainan Islanders--a perspective from mitochondrial DNA. BMC Evol Biol (2011) 0.84
Revision of the mtDNA tree and corresponding haplogroup nomenclature. Proc Natl Acad Sci U S A (2010) 0.83
Mutation rate switch inside Eurasian mitochondrial haplogroups: impact of selection and consequences for dating settlement in Europe. PLoS One (2011) 0.82
Comparative analysis of mitochondrial genomes in Bombina (Anura; Bombinatoridae). J Mol Evol (2008) 0.81
Estimate of within population incremental selection through branch imbalance in lineage trees. Nucleic Acids Res (2015) 0.76
Selection on the mitochondrial ATP synthase 6 and the NADH dehydrogenase 2 genes in hares (Lepus capensis L., 1758) from a steep ecological gradient in North Africa. BMC Evol Biol (2017) 0.75
Ancient mitochondrial genome reveals trace of prehistoric migration in the east Pamir by pastoralists. J Hum Genet (2015) 0.75
MtDNA genomes reveal a relaxation of selective constraints in low-BMI individuals in a Uyghur population. Hum Genet (2017) 0.75
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet (2010) 7.94
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet (2009) 4.97
Genome-wide association study identifies five loci associated with lung function. Nat Genet (2009) 4.10
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet (2013) 3.25
mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res (2006) 3.23
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLoS Genet (2009) 3.18
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet (2012) 3.04
Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet (2013) 2.92
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet (2013) 2.83
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain. Nat Struct Mol Biol (2011) 2.73
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum Mol Genet (2008) 2.66
Global and unbiased detection of splice junctions from RNA-seq data. Genome Biol (2010) 2.32
Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines. Genome Res (2003) 2.12
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. PLoS Genet (2012) 1.79
Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet (2009) 1.77
Continuous Aging of the Human DNA Methylome Throughout the Human Lifespan. PLoS One (2013) 1.74
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet (2013) 1.72
A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One (2012) 1.72
Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet (2012) 1.68
Genes predict village of origin in rural Europe. Eur J Hum Genet (2010) 1.61
Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins. PLoS Genet (2011) 1.60
Major gender difference in association of FTO gene variant among severely obese children with obesity and obesity related phenotypes. Biochem Biophys Res Commun (2008) 1.55
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. PLoS Genet (2013) 1.52
Real-time PCR-based system for simultaneous quantification of human papillomavirus types associated with high risk of cervical cancer. J Clin Microbiol (2003) 1.52
SNP frequency estimation using massively parallel sequencing of pooled DNA. Eur J Hum Genet (2008) 1.51
Genome-wide linkage analysis of serum creatinine in three isolated European populations. Kidney Int (2009) 1.48
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. PLoS Genet (2010) 1.43
Use of FTA card for dry collection, transportation and storage of cervical cell specimen to detect high-risk HPV. J Clin Virol (2009) 1.41
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. Circ Cardiovasc Genet (2009) 1.35
Type-specific associations of human papillomavirus load with risk of developing cervical carcinoma in situ. Int J Cancer (2004) 1.33
TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies. Lancet Oncol (2009) 1.26
Genome-wide association study of susceptibility loci for cervical cancer. J Natl Cancer Inst (2013) 1.22
Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors. Proc Natl Acad Sci U S A (2012) 1.17
Evidence of inbreeding depression on human height. PLoS Genet (2012) 1.16
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet (2012) 1.14
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids. Am J Hum Genet (2012) 1.13
Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing. Genome Biol (2010) 1.13
A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample. PLoS One (2011) 1.13
Long noncoding RNA-mediated maintenance of DNA methylation and transcriptional gene silencing. Development (2012) 1.11
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. PLoS Genet (2010) 1.10
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations. Eur J Hum Genet (2009) 1.05
Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data. BMC Genomics (2010) 1.02
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Hum Mol Genet (2014) 1.02
HPV test shows low sensitivity of Pap screen in older women. Lancet Oncol (2010) 1.01
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. BMC Med Genet (2010) 1.00
Identification of genetic variants influencing the human plasma proteome. Proc Natl Acad Sci U S A (2013) 1.00
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults. Hum Mol Genet (2011) 0.99
High-risk human papilloma virus (HPV) and survival in patients with esophageal carcinoma: a pilot study. BMC Cancer (2006) 0.98
Full-length sequence analysis of the HLA-DRB1 locus suggests a recent origin of alleles. Immunogenetics (2007) 0.98
Affected sib-pair analysis of the contribution of HLA class I and class II loci to development of cervical cancer. Hum Mol Genet (2004) 0.98
Type-specific detection of high-risk human papillomavirus (HPV) in self-sampled cervicovaginal cells applied to FTA elute cartridge. J Clin Virol (2011) 0.97
A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genet (2011) 0.97
Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels. PLoS Genet (2013) 0.97
A recent genetic link between Sami and the Volga-Ural region of Russia. Eur J Hum Genet (2006) 0.96
Adherence to a traditional lifestyle affects food and nutrient intake among modern Swedish Sami. Int J Circumpolar Health (2009) 0.96
Linkage disequilibrium between microsatellite markers in the Swedish Sami relative to a worldwide selection of populations. Hum Genet (2004) 0.95
Comparison between the Hybrid Capture 2 and the hpVIR real-time PCR for detection of human papillomavirus in women with ASCUS or low grade dysplasia. J Clin Virol (2009) 0.94
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Obesity (Silver Spring) (2009) 0.93
Lifestyle, genetics, and disease in Sami. Croat Med J (2006) 0.93
Evaluation of the SNP tagging approach in an independent population sample--array-based SNP discovery in Sami. Hum Genet (2007) 0.92
Real-time DNA quantification of nuclear and mitochondrial DNA in forensic analysis. Biotechniques (2002) 0.91
Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemia. Am J Hematol (2012) 0.91
Fas and FasL gene polymorphisms are not associated with cervical cancer but differ among Black and Mixed-ancestry South Africans. BMC Res Notes (2009) 0.88
Genetic architecture of circulating lipid levels. Eur J Hum Genet (2011) 0.88
Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics study. J Psychiatr Res (2012) 0.87
Mutations in HNF1A result in marked alterations of plasma glycan profile. Diabetes (2012) 0.87
Identification of local selective sweeps in human populations since the exodus from Africa. Hereditas (2008) 0.87
The Northern Swedish Population Health Study (NSPHS)--a paradigmatic study in a rural population combining community health and basic research. Rural Remote Health (2010) 0.86
Detection of human papillomavirus among women in Laos: feasibility of using filter paper card and prevalence of high-risk types. Int J Gynecol Cancer (2012) 0.86
Genome-wide analysis of chimpanzee genes with premature termination codons. BMC Genomics (2009) 0.85
A Fas gene polymorphism influences herpes simplex virus type 2 infection in South African women. J Med Virol (2010) 0.82
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits. Eur J Hum Genet (2011) 0.82
Common variants in Mendelian kidney disease genes and their association with renal function. J Am Soc Nephrol (2013) 0.82
A cis-eQTL of HLA-DRB1 and a frameshift mutation of MICA contribute to the pattern of association of HLA alleles with cervical cancer. Cancer Med (2014) 0.81
Glycomics meets lipidomics--associations of N-glycans with classical lipids, glycerophospholipids, and sphingolipids in three European populations. Mol Biosyst (2011) 0.81
Extended haplotypes in the growth hormone releasing hormone receptor gene (GHRHR) are associated with normal variation in height. PLoS One (2009) 0.81
A variant upstream of HLA-DRB1 and multiple variants in MICA influence susceptibility to cervical cancer in a Swedish population. Cancer Med (2014) 0.80
Genetic origin of the Swedish Sami inferred from HLA class I and class II allele frequencies. Eur J Hum Genet (2008) 0.80
Multiply-primed rolling circle amplification of human papillomavirus using sequence-specific primers. Virology (2012) 0.80
Human enterovirus species B in ileocecal Crohn's disease. Clin Transl Gastroenterol (2013) 0.80
A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition. Hum Genet (2003) 0.80
Polymorphisms in sh2b1 and spns1 loci are associated with triglyceride levels in a healthy population in northern Sweden. J Genet (2012) 0.78
Animal source food intake and association with blood cholesterol, glycerophospholipids and sphingolipids in a northern Swedish population. Int J Circumpolar Health (2013) 0.78
Prevalence and sensitization of atopic allergy and coeliac disease in the Northern Sweden Population Health Study. Int J Circumpolar Health (2013) 0.78
Increased alpha-9 human papillomavirus species viral load in human immunodeficiency virus positive women. BMC Infect Dis (2014) 0.78
Projected cost-effectiveness of repeat high-risk human papillomavirus testing using self-collected vaginal samples in the Swedish cervical cancer screening program. Acta Obstet Gynecol Scand (2013) 0.76
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet (2016) 0.75
[Is the HPV test to supplement vaginal smears in menopausal women?]. Lakartidningen (2010) 0.75
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep (2017) 0.75
Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. PLoS Genet (2017) 0.75
Variants in STAT5B associate with serum TC and LDL-C levels. J Clin Endocrinol Metab (2011) 0.75
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes. J Mol Neurosci (2012) 0.75