Published in Hum Mutat on November 16, 2010
Ancient DNA reveals key stages in the formation of central European mitochondrial genetic diversity. Science (2013) 2.23
Genome flux and stasis in a five millennium transect of European prehistory. Nat Commun (2014) 1.90
Somatic mutations throughout the entire mitochondrial genome are associated with elevated PSA levels in prostate cancer patients. Am J Hum Genet (2010) 1.67
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nat Genet (2016) 1.64
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. PLoS Genet (2014) 1.64
The 5300-year-old Helicobacter pylori genome of the Iceman. Science (2016) 1.41
More comprehensive forensic genetic marker analyses for accurate human remains identification using massively parallel DNA sequencing. BMC Genomics (2016) 1.39
Ancient DNA analysis of 8000 B.C. near eastern farmers supports an early neolithic pioneer maritime colonization of Mainland Europe through Cyprus and the Aegean Islands. PLoS Genet (2014) 1.37
POPULATION GENETICS. Genomic evidence for the Pleistocene and recent population history of Native Americans. Science (2015) 1.33
mtDNA Variation and Analysis Using MITOMAP and MITOMASTER. Curr Protoc Bioinformatics (2013) 1.29
Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences. Investig Genet (2014) 1.23
Mitochondrial DNA heteroplasmy in diabetes and normal adults: role of acquired and inherited mutational patterns in twins. Hum Mol Genet (2012) 1.21
Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds. BMC Bioinformatics (2012) 1.21
Successful enrichment and recovery of whole mitochondrial genomes from ancient human dental calculus. Am J Phys Anthropol (2016) 1.19
Concept for estimating mitochondrial DNA haplogroups using a maximum likelihood approach (EMMA). Forensic Sci Int Genet (2013) 1.12
Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease. Hum Mutat (2013) 1.12
Haplogrouping mitochondrial DNA sequences in Legal Medicine/Forensic Genetics. Int J Legal Med (2012) 1.06
Uniparental markers in Italy reveal a sex-biased genetic structure and different historical strata. PLoS One (2013) 1.02
Mitochondrial DNA variants correlate with symptoms in myalgic encephalomyelitis/chronic fatigue syndrome. J Transl Med (2016) 1.01
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations. Genet Med (2014) 0.99
Maternal history of Oceania from complete mtDNA genomes: contrasting ancient diversity with recent homogenization due to the Austronesian expansion. Am J Hum Genet (2014) 0.97
The genomic landscape of polymorphic human nuclear mitochondrial insertions. Nucleic Acids Res (2014) 0.97
HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing. Nucleic Acids Res (2016) 0.96
A Common Genetic Origin for Early Farmers from Mediterranean Cardial and Central European LBK Cultures. Mol Biol Evol (2015) 0.95
Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health. Genome Biol Evol (2014) 0.95
Origin and dynamics of admixture in Brazilians and its effect on the pattern of deleterious mutations. Proc Natl Acad Sci U S A (2015) 0.95
Frequency and pattern of heteroplasmy in the complete human mitochondrial genome. PLoS One (2013) 0.95
Experiences with workflows for automating data-intensive bioinformatics. Biol Direct (2015) 0.94
Schmutzi: estimation of contamination and endogenous mitochondrial consensus calling for ancient DNA. Genome Biol (2015) 0.94
Ancient substructure in early mtDNA lineages of southern Africa. Am J Hum Genet (2013) 0.93
Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar. BMC Evol Biol (2014) 0.93
Complete mtDNA genomes of Filipino ethnolinguistic groups: a melting pot of recent and ancient lineages in the Asia-Pacific region. Eur J Hum Genet (2013) 0.93
Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™. BMC Genomics (2015) 0.92
Migration and interaction in a contact zone: mtDNA variation among Bantu-speakers in Southern Africa. PLoS One (2014) 0.92
Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean. Proc Natl Acad Sci U S A (2015) 0.91
Sequencing and analysis of a South Asian-Indian personal genome. BMC Genomics (2012) 0.91
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability. EMBO J (2016) 0.89
Investigating the prehistory of Tungusic peoples of Siberia and the Amur-Ussuri region with complete mtDNA genome sequences and Y-chromosomal markers. PLoS One (2013) 0.89
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations. Genome Res (2016) 0.88
Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier. Bioinformatics (2014) 0.88
A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nat Commun (2016) 0.87
Ancient mitochondrial DNA from the northern fringe of the Neolithic farming expansion in Europe sheds light on the dispersion process. Philos Trans R Soc Lond B Biol Sci (2015) 0.87
The Genetics of Bene Israel from India Reveals Both Substantial Jewish and Indian Ancestry. PLoS One (2016) 0.87
Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing. Croat Med J (2015) 0.87
Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. PLoS One (2015) 0.86
Genealogical relationships between early medieval and modern inhabitants of Piedmont. PLoS One (2015) 0.84
Controlling for contamination in re-sequencing studies with a reproducible web-based phylogenetic approach. Biotechniques (2014) 0.84
An integrated transcriptome and expressed variant analysis of sepsis survival and death. Genome Med (2014) 0.84
Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing. PLoS Genet (2014) 0.84
Mitochondrial DNA variants in obesity. PLoS One (2014) 0.83
Somatic mtDNA variation is an important component of Parkinson's disease. Neurobiol Aging (2015) 0.83
mtDNA from the early Bronze Age to the Roman period suggests a genetic link between the Indian subcontinent and Mesopotamian cradle of civilization. PLoS One (2013) 0.83
Mitochondrial DNA Haplogroups and Neurocognitive Impairment During HIV Infection. Clin Infect Dis (2015) 0.83
Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma. PLoS One (2015) 0.83
mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud. Nucleic Acids Res (2016) 0.83
Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry. PLoS One (2014) 0.82
Transcription factors bind negatively selected sites within human mtDNA genes. Genome Biol Evol (2014) 0.82
Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects. J Hematol Oncol (2013) 0.82
Mitochondrial haplogroups and polymorphisms reveal no association with sporadic prostate cancer in a southern European population. PLoS One (2012) 0.81
Admixture and genetic diversity distribution patterns of non-recombining lineages of Native American ancestry in Colombian populations. PLoS One (2015) 0.81
Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations. J Hum Genet (2013) 0.80
Epidermal nerve fiber density, oxidative stress, and mitochondrial haplogroups in HIV-infected Thais initiating therapy. AIDS (2014) 0.80
HLA-DRB1*14 is a protective allele for multiple sclerosis in an admixed Colombian population. Neurol Neuroimmunol Neuroinflamm (2015) 0.79
Mitochondrial haplogroups are associated with severity of diabetic retinopathy. Invest Ophthalmol Vis Sci (2014) 0.79
Genetic stratigraphy of key demographic events in Arabia. PLoS One (2015) 0.79
Genomic insights on the ethno-history of the Maya and the 'Ladinos' from Guatemala. BMC Genomics (2015) 0.79
Fine Dissection of Human Mitochondrial DNA Haplogroup HV Lineages Reveals Paleolithic Signatures from European Glacial Refugia. PLoS One (2015) 0.78
The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. PLoS One (2015) 0.78
Kuwaiti population subgroup of nomadic Bedouin ancestry-Whole genome sequence and analysis. Genom Data (2014) 0.78
Determination of population origin: a comparison of autosomal SNPs, Y-chromosomal and mtDNA haplogroups using a Malagasy population as example. Eur J Hum Genet (2013) 0.78
Mitonuclear linkage disequilibrium in human populations. Proc Biol Sci (2015) 0.78
Complete mitochondrial genomes of Thai and Lao populations indicate an ancient origin of Austroasiatic groups and demic diffusion in the spread of Tai-Kadai languages. Hum Genet (2016) 0.78
Paleogenomic Evidence for Multi-generational Mixing between Neolithic Farmers and Mesolithic Hunter-Gatherers in the Lower Danube Basin. Curr Biol (2017) 0.77
Complete mitochondrial sequences from Mesolithic Sardinia. Sci Rep (2017) 0.77
Vestiges of an Ancient Border in the Contemporary Genetic Diversity of North-Eastern Europe. PLoS One (2015) 0.77
Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry. BMC Genomics (2015) 0.77
A molecular portrait of maternal sepsis from Byzantine Troy. Elife (2017) 0.77
Bones hold the key to DNA virus history and epidemiology. Sci Rep (2015) 0.77
The mitochondrial DNA Northeast Asia CZD haplogroup is associated with good disease-free survival among male oral squamous cell carcinoma patients. PLoS One (2012) 0.77
Long-term genetic stability and a high-altitude East Asian origin for the peoples of the high valleys of the Himalayan arc. Proc Natl Acad Sci U S A (2016) 0.77
Whole mitochondrial genome genetic diversity in an Estonian population sample. Int J Legal Med (2015) 0.77
Genetic evidence of African slavery at the beginning of the trans-Atlantic slave trade. Sci Rep (2014) 0.77
Origins, admixture and founder lineages in European Roma. Eur J Hum Genet (2015) 0.77
Analysis of the Mitochondrial Genome of a Novosvobodnaya Culture Representative using Next-Generation Sequencing and Its Relation to the Funnel Beaker Culture. Acta Naturae (2014) 0.77
Mitochondrial DNA analysis of Swedish population samples. Int J Legal Med (2013) 0.77
The identification of the Romanovs: Can we (finally) put the controversies to rest? Investig Genet (2011) 0.76
Between the Baltic and Danubian Worlds: the genetic affinities of a Middle Neolithic population from central Poland. PLoS One (2015) 0.76
Identification of kinship and occupant status in Mongolian noble burials of the Yuan Dynasty through a multidisciplinary approach. Philos Trans R Soc Lond B Biol Sci (2015) 0.76
Poor Man's 1000 Genome Project: Recent Human Population Expansion Confounds the Detection of Disease Alleles in 7,098 Complete Mitochondrial Genomes. Front Genet (2013) 0.76
Assessing the genetic influence of ancient sociopolitical structure: micro-differentiation patterns in the population of Asturias (Northern Spain). PLoS One (2012) 0.76
Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania. J Hum Genet (2016) 0.76
Mitochondrial DNA sequence variation is largely conserved at birth with rare de novo mutations in neonates. Am J Obstet Gynecol (2015) 0.76
A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism. J Neurol (2016) 0.76
Ancient Out-of-Africa Mitochondrial DNA Variants Associate with Distinct Mitochondrial Gene Expression Patterns. PLoS Genet (2016) 0.76
Mitochondrial Haplogroups as a Risk Factor for Herpes Zoster. Open Forum Infect Dis (2016) 0.75
Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula. PLoS One (2016) 0.75
A European Mitochondrial Haplotype Identified in Ancient Phoenician Remains from Carthage, North Africa. PLoS One (2016) 0.75
Hunting for the LCT-13910*T allele between the Middle Neolithic and the Middle Ages suggests its absence in dairying LBK people entering the Kuyavia region in the 8th millennium BP. PLoS One (2015) 0.75
Very Short Mitochondrial DNA Fragments and Heteroplasmy in Human Plasma. Sci Rep (2016) 0.75
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Lower estimated glomerular filtration rate and higher albuminuria are associated with mortality and end-stage renal disease. A collaborative meta-analysis of kidney disease population cohorts. Kidney Int (2011) 5.25
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. PLoS Genet (2008) 5.23
A genome-wide perspective of genetic variation in human metabolism. Nat Genet (2009) 5.00
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat Genet (2008) 4.67
Fibroblast growth factor 23 (FGF23) predicts progression of chronic kidney disease: the Mild to Moderate Kidney Disease (MMKD) Study. J Am Soc Nephrol (2007) 4.59
Telomere length and risk of incident cancer and cancer mortality. JAMA (2010) 3.55
On the replication of genetic associations: timing can be everything! Am J Hum Genet (2008) 3.32
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
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet (2011) 3.03
Blockade of receptor activator of nuclear factor-κB (RANKL) signaling improves hepatic insulin resistance and prevents development of diabetes mellitus. Nat Med (2013) 2.93
Influences on the reduction of relative telomere length over 10 years in the population-based Bruneck Study: introduction of a well-controlled high-throughput assay. Int J Epidemiol (2009) 2.87
Metabolic footprint of diabetes: a multiplatform metabolomics study in an epidemiological setting. PLoS One (2010) 2.84
Serum iPTH, calcium and phosphate, and the risk of mortality in a European haemodialysis population. Nephrol Dial Transplant (2010) 2.70
CUBN is a gene locus for albuminuria. J Am Soc Nephrol (2011) 2.70
Discovery of sexual dimorphisms in metabolic and genetic biomarkers. PLoS Genet (2011) 2.68
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature (2011) 2.59
Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study. J Am Coll Cardiol (2008) 2.56
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study. PLoS One (2008) 2.37
Associations of estimated glomerular filtration rate and albuminuria with mortality and renal failure by sex: a meta-analysis. BMJ (2013) 2.24
Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians. Diabetes (2006) 2.23
Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study. Circulation (2006) 2.18
Asymmetric dimethylarginine and progression of chronic kidney disease: the mild to moderate kidney disease study. J Am Soc Nephrol (2005) 2.00
Serum creatinine, cystatin C, and beta-trace protein in diagnostic staging and predicting progression of primary nondiabetic chronic kidney disease. Clin Chem (2010) 1.95
A genome-wide association study of metabolic traits in human urine. Nat Genet (2011) 1.84
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. Circ Cardiovasc Genet (2008) 1.82
Association of ankle-brachial index and plaques in the carotid and femoral arteries with cardiovascular events and total mortality in a population-based study with 13 years of follow-up. Eur Heart J (2006) 1.82
Cellular aging reflected by leukocyte telomere length predicts advanced atherosclerosis and cardiovascular disease risk. Arterioscler Thromb Vasc Biol (2010) 1.81
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis (2009) 1.80
Oxidized phospholipids, lipoprotein(a), lipoprotein-associated phospholipase A2 activity, and 10-year cardiovascular outcomes: prospective results from the Bruneck study. Arterioscler Thromb Vasc Biol (2007) 1.79
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. Atherosclerosis (2009) 1.78
Renal insulin resistance syndrome, adiponectin and cardiovascular events in patients with kidney disease: the mild and moderate kidney disease study. J Am Soc Nephrol (2005) 1.74
Predictive performance of renal function equations for patients with chronic kidney disease and normal serum creatinine levels. J Am Soc Nephrol (2002) 1.70
Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet (2012) 1.68
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. PLoS Genet (2011) 1.68
Somatic mutations throughout the entire mitochondrial genome are associated with elevated PSA levels in prostate cancer patients. Am J Hum Genet (2010) 1.67
Differences between human plasma and serum metabolite profiles. PLoS One (2011) 1.61
Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI. Diabetes Care (2008) 1.58
Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer. Cancer Epidemiol Biomarkers Prev (2008) 1.58
Lipoprotein metabolism and lipid management in chronic kidney disease. J Am Soc Nephrol (2007) 1.53
Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson's disease in children. J Hepatol (2007) 1.44
Comparison and evaluation of cardiac biomarkers in patients with intermittent claudication: results from the CAVASIC study. Clin Chem (2013) 1.43
Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review. Exp Gerontol (2008) 1.41
Fifteen-year follow-up of association between telomere length and incident cancer and cancer mortality. JAMA (2011) 1.34
Pro-A-type natriuretic peptide and pro-adrenomedullin predict progression of chronic kidney disease: the MMKD Study. Kidney Int (2008) 1.26
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circ Cardiovasc Genet (2011) 1.26
Uric acid as a risk factor for progression of non-diabetic chronic kidney disease? The Mild to Moderate Kidney Disease (MMKD) Study. Exp Gerontol (2008) 1.25
Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes. Diabetes (2013) 1.25
INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism. Obesity (Silver Spring) (2008) 1.24
The ATGL gene is associated with free fatty acids, triglycerides, and type 2 diabetes. Diabetes (2006) 1.22
Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds. BMC Bioinformatics (2012) 1.21
Oxidized phospholipids predict the presence and progression of carotid and femoral atherosclerosis and symptomatic cardiovascular disease: five-year prospective results from the Bruneck study. J Am Coll Cardiol (2006) 1.21
Genome-wide association study of lung function decline in adults with and without asthma. J Allergy Clin Immunol (2012) 1.20
Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design? PLoS Genet (2009) 1.18
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet (2012) 1.14
Afamin is a novel human vitamin E-binding glycoprotein characterization and in vitro expression. J Proteome Res (2005) 1.13
Epidemiology of dialysis patients and heart failure patients. Semin Nephrol (2006) 1.13
DNA methylation of lipid-related genes affects blood lipid levels. Circ Cardiovasc Genet (2015) 1.12
APOA5 variants and metabolic syndrome in Caucasians. J Lipid Res (2007) 1.09
The German Chronic Kidney Disease (GCKD) study: design and methods. Nephrol Dial Transplant (2011) 1.09
A common variant in the adiponutrin gene influences liver enzyme values. J Med Genet (2009) 1.08
Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins. Hum Mol Genet (2009) 1.08
Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA Study. Obesity (Silver Spring) (2008) 1.06
Lost in the space of bioinformatic tools: a constantly updated survival guide for genetic epidemiology. The GenEpi Toolbox. Atherosclerosis (2009) 1.05
Characterization of the vitamin E-binding properties of human plasma afamin. Biochemistry (2002) 1.05
Apolipoprotein A-IV predicts progression of chronic kidney disease: the mild to moderate kidney disease study. J Am Soc Nephrol (2005) 1.01
B-type natriuretic peptide concentrations predict the progression of nondiabetic chronic kidney disease: the Mild-to-Moderate Kidney Disease Study. Clin Chem (2007) 1.00
Hemoglobin variability does not predict mortality in European hemodialysis patients. J Am Soc Nephrol (2010) 1.00
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
Increased serum lipoprotein(a) concentrations and low molecular weight phenotypes of apolipoprotein(a) are associated with symptomatic peripheral arterial disease. Clin Chem (2007) 0.96
Genetic associations with lipoprotein subfractions provide information on their biological nature. Hum Mol Genet (2011) 0.95
Different genes interact with particulate matter and tobacco smoke exposure in affecting lung function decline in the general population. PLoS One (2012) 0.95
CONAN: copy number variation analysis software for genome-wide association studies. BMC Bioinformatics (2010) 0.95
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study. Clin Chem (2008) 0.94
Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working population. PLoS Genet (2010) 0.94
Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar. BMC Evol Biol (2014) 0.93
The adiponectin gene is associated with adiponectin levels but not with characteristics of the insulin resistance syndrome in healthy Caucasians. Eur J Hum Genet (2006) 0.93
Sex and age interaction with genetic association of atherogenic uric acid concentrations. Atherosclerosis (2009) 0.93
Impact of ENPP1 genotype on arterial calcification in patients with end-stage renal failure. Nephrol Dial Transplant (2007) 0.93
Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome. J Pediatr (2003) 0.93
Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease. Exp Gerontol (2008) 0.92
eCOMPAGT -- efficient combination and management of phenotypes and genotypes for genetic epidemiology. BMC Bioinformatics (2009) 0.90
Evaluation of gene-obesity interaction effects on cholesterol levels: a genetic predisposition score on HDL-cholesterol is modified by obesity. Atherosclerosis (2012) 0.90
Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels--the Framingham Heart Study. Atherosclerosis (2009) 0.90
Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years. BMC Cancer (2008) 0.89
eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies. BMC Bioinformatics (2010) 0.89
An epidemiological study of hemodialysis patients based on the European Fresenius Medical Care hemodialysis network: results of the ARO study. Nephron Clin Pract (2010) 0.89