Published in Nat Genet on August 29, 2016
Reference-based phasing using the Haplotype Reference Consortium panel. Nat Genet (2016) 0.98
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Nat Genet (2016) 0.78
A Fast and Accurate Algorithm to Test for Binary Phenotypes and Its Application to PheWAS. Am J Hum Genet (2017) 0.76
Gene-based association study of genes linked to hippocampal sclerosis of aging neuropathology: GRN, TMEM106B, ABCC9, and KCNMB2. Neurobiol Aging (2017) 0.75
Psychophysiological endophenotypes to characterize mechanisms of known schizophrenia genetic loci. Psychol Med (2016) 0.75
Evaluation of the accuracy of imputed sequence variant genotypes and their utility for causal variant detection in cattle. Genet Sel Evol (2017) 0.75
Identification of a novel locus associated with skin colour in African-admixed populations. Sci Rep (2017) 0.75
Identification of breast cancer associated variants that modulate transcription factor binding. PLoS Genet (2017) 0.75
Haplotype-based stratification of Huntington's disease. Eur J Hum Genet (2017) 0.75
Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1. J Am Soc Nephrol (2017) 0.75
Design and rationale for examining neuroimaging genetics in ischemic stroke: The MRI-GENIE study. Neurol Genet (2017) 0.75
A phased SNP-based classification of sickle cell anemia HBB haplotypes. BMC Genomics (2017) 0.75
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiol Aging (2017) 0.75
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet (2017) 0.75
A map of human genome variation from population-scale sequencing. Nature (2010) 121.13
The International HapMap Project. Nature (2003) 73.65
An integrated map of genetic variation from 1,092 human genomes. Nature (2012) 59.82
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet (2001) 53.16
A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet (2007) 52.68
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet (2009) 30.09
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol (2010) 26.41
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N Engl J Med (2006) 23.83
Worldwide human relationships inferred from genome-wide patterns of variation. Science (2008) 22.44
Genotype imputation. Annu Rev Genomics Hum Genet (2009) 18.64
Linkage disequilibrium in humans: models and data. Am J Hum Genet (2001) 14.97
Genotype imputation for genome-wide association studies. Nat Rev Genet (2010) 14.59
A global reference for human genetic variation. Nature (2015) 12.85
A systematic survey of loss-of-function variants in human protein-coding genes. Science (2012) 12.25
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet (2012) 11.29
A linear complexity phasing method for thousands of genomes. Nat Methods (2011) 8.30
Tabix: fast retrieval of sequence features from generic TAB-delimited files. Bioinformatics (2011) 5.86
Improved whole-chromosome phasing for disease and population genetic studies. Nat Methods (2013) 5.43
Inactivating mutations in NPC1L1 and protection from coronary heart disease. N Engl J Med (2014) 4.94
Large-scale whole-genome sequencing of the Icelandic population. Nat Genet (2015) 4.54
Whole-genome sequence variation, population structure and demographic history of the Dutch population. Nat Genet (2014) 4.33
Possible ancestral structure in human populations. PLoS Genet (2006) 3.56
Efficient multipoint linkage analysis through reduction of inheritance space. Am J Hum Genet (2001) 2.58
Phasing of many thousands of genotyped samples. Am J Hum Genet (2012) 2.47
Identification of a large set of rare complete human knockouts. Nat Genet (2015) 2.28
minimac2: faster genotype imputation. Bioinformatics (2014) 1.88
A reference panel of 64,976 haplotypes for genotype imputation. Nat Genet (2016) 1.61
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nat Genet (2015) 1.55
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers. Nat Genet (2015) 1.52
Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds. BMC Bioinformatics (2012) 1.21
Genotype Imputation with Millions of Reference Samples. Am J Hum Genet (2016) 1.15
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs. Eur J Hum Genet (2014) 1.01
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Psychophysiology (2014) 0.91
Blockwise HMM computation for large-scale population genomic inference. Bioinformatics (2012) 0.83
Multi-platform assessment of transcriptome profiling using RNA-seq in the ABRF next-generation sequencing study. Nat Biotechnol (2014) 1.68
Development and validation of a predictive mortality risk score from a European hemodialysis cohort. Kidney Int (2015) 1.65
A reference panel of 64,976 haplotypes for genotype imputation. Nat Genet (2016) 1.61
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nat Genet (2015) 1.43
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence. Nat Genet (2017) 1.43
Association of atopic dermatitis with cardiovascular risk factors and diseases. J Invest Dermatol (2016) 1.41
High cardiovascular event rates occur within the first weeks of starting hemodialysis. Kidney Int (2015) 1.08
Fast and accurate long-range phasing in a UK Biobank cohort. Nat Genet (2016) 1.00
Reference-based phasing using the Haplotype Reference Consortium panel. Nat Genet (2016) 0.98
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels. Nat Genet (2015) 0.95
Physical and neurobehavioral determinants of reproductive onset and success. Nat Genet (2016) 0.94
Genome-wide scans of genetic variants for psychophysiological endophenotypes: a methodological overview. Psychophysiology (2014) 0.87
Genome-wide associations for birth weight and correlations with adult disease. Nature (2016) 0.87
Knowns and unknowns for psychophysiological endophenotypes: integration and response to commentaries. Psychophysiology (2014) 0.85
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet (2016) 0.84
Implementation of the KDIGO guideline on lipid management requires a substantial increase in statin prescription rates. Kidney Int (2015) 0.83
Influence of DNA extraction methods on relative telomere length measurements and its impact on epidemiological studies. Sci Rep (2016) 0.81
Left ventricular ejection fraction is associated with prevalent and incident cardiovascular disease in patients with intermittent claudication - results from the CAVASIC Study. Atherosclerosis (2015) 0.81
Association of relative telomere length with progression of chronic kidney disease in two cohorts: effect modification by smoking and diabetes. Sci Rep (2015) 0.81
Lipoprotein(a) concentrations, apolipoprotein(a) isoforms and clinical endpoints in haemodialysis patients with type 2 diabetes mellitus: results from the 4D Study. Nephrol Dial Transplant (2016) 0.78
Association of relative telomere length with cardiovascular disease in a large chronic kidney disease cohort: the GCKD study. Atherosclerosis (2015) 0.78
Lack of association of rs3798220 with small apolipoprotein(a) isoforms and high lipoprotein(a) levels in East and Southeast Asians. Atherosclerosis (2015) 0.77
Serum concentrations of L-arginine and L-homoarginine in male patients with intermittent claudication: a cross-sectional and prospective investigation in the CAVASIC Study. Atherosclerosis (2015) 0.77
High-sensitivity cardiac troponin T in patients with intermittent claudication and its relation with cardiovascular events and all-cause mortality--the CAVASIC Study. Atherosclerosis (2014) 0.77
P300 amplitude reduction is associated with early-onset and late-onset pathological substance use in a prospectively studied cohort of 14-year-old adolescents. Psychophysiology (2013) 0.77
Genomic Methods and Microbiological Technologies for Profiling Novel and Extreme Environments for the Extreme Microbiome Project (XMP). J Biomol Tech (2017) 0.76
Do telomeres have a higher plasticity than thought? Results from the German Chronic Kidney Disease (GCKD) study as a high-risk population. Exp Gerontol (2015) 0.76
MASP1, THBS1, GPLD1 and ApoA-IV are novel biomarkers associated with prediabetes: the KORA F4 study. Diabetologia (2016) 0.76
Achieving success with the Research Domain Criteria (RDoC): Going beyond the matrix. Psychophysiology (2016) 0.76
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies. Nephrol Dial Transplant (2016) 0.76
One-year developmental stability and covariance among oddball, novelty, go/no-go, and flanker event-related potentials in adolescence: A monozygotic twin study. Psychophysiology (2016) 0.75
The authors reply. Kidney Int (2015) 0.75
Effect of diet-induced weight loss on lipoprotein(a) levels in obese individuals with and without type 2 diabetes. Diabetologia (2017) 0.75
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations. Hum Mol Genet (2016) 0.75
Common SIRT1 variants modify the effect of abdominal adipose tissue on aging-related lung function decline. Age (Dordr) (2016) 0.75
Genome-wide scans of genetic variants for psychophysiological endophenotypes: introduction to this special issue of Psychophysiology. Psychophysiology (2014) 0.75
What is the impact of different spirometric criteria on the prevalence of spirometrically defined COPD and its comorbidities? Results from the population-based KORA study. Int J Chron Obstruct Pulmon Dis (2016) 0.75
The fate of patients with intermittent claudication in the 21st century revisited - results from the CAVASIC Study. Sci Rep (2017) 0.75
Measures of chronic kidney disease and risk of incident peripheral artery disease: a collaborative meta-analysis of individual participant data. Lancet Diabetes Endocrinol (2017) 0.75
Air pollution and diabetes association: Modification by type 2 diabetes genetic risk score. Environ Int (2016) 0.75
Approaches to detect genetic effects that differ between two strata in genome-wide meta-analyses: Recommendations based on a systematic evaluation. PLoS One (2017) 0.75
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nat Genet (2019) 0.75
Theta- and delta-band EEG network dynamics during a novelty oddball task. Psychophysiology (2017) 0.75
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLoS Med (2017) 0.75
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. PLoS Genet (2017) 0.75
What is normal trauma healing and what is complex regional pain syndrome I? An analysis of clinical and experimental biomarkers. Pain (2019) 0.75
Anti-parathyroid treatment effectiveness and persistence in incident haemodialysis patients with secondary hyperparathyroidism. Nefrologia (2015) 0.75
Associations between genetic risk variants for kidney diseases and kidney disease etiology. Sci Rep (2017) 0.75
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies. Nephrol Dial Transplant (2017) 0.75
Development and validation of cardiovascular risk scores for haemodialysis patients. Int J Cardiol (2016) 0.75