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A reference panel of 64,976 haplotypes for genotype imputation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/gepi.20533openalex-snapshot
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
inferredcites →https://doi.org/10.1016/0014-5793(84)81279-xopenalex-snapshot
Structural and functional characterization of the abnormal Z α1‐antitrypsin isolated from human liver
inferredcites →https://doi.org/10.1038/nature06258openalex-snapshot
A second generation human haplotype map of over 3.1 million SNPs
inferredcites →https://doi.org/10.1038/nature13997openalex-snapshot
The African Genome Variation Project shapes medical genetics in Africa
inferredcites →https://doi.org/10.1038/nature14659openalex-snapshot
Sparse whole-genome sequencing identifies two loci for major depressive disorder
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/ncomms9111openalex-snapshot
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
inferredcites →https://doi.org/10.1038/ng.2354openalex-snapshot
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
inferredcites →https://doi.org/10.1038/ng.3021openalex-snapshot
Whole-genome sequence variation, population structure and demographic history of the Dutch population
inferredcites →https://doi.org/10.1038/ng.3368openalex-snapshot
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
inferredcites →https://doi.org/10.1038/ng.3583openalex-snapshot
Haplotype estimation for biobank-scale data sets
inferredcites →https://doi.org/10.1038/ng2088openalex-snapshot
A new multipoint method for genome-wide association studies by imputation of genotypes
inferredcites →https://doi.org/10.1038/nrg2796openalex-snapshot
Genotype imputation for genome-wide association studies
inferredcites →https://doi.org/10.1093/bioinformatics/btu704openalex-snapshot
minimac2: faster genotype imputation
inferredcites →https://doi.org/10.1093/bioinformatics/btw065openalex-snapshot
Phasing for medical sequencing using rare variants and large haplotype reference panels
inferredcites →https://doi.org/10.1093/ije/dyp394openalex-snapshot
Cohort Profile: The Study of Health in Pomerania
inferredcites →https://doi.org/10.1101/gr.146084.112openalex-snapshot
An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data
inferredcites →https://doi.org/10.1111/j.1532-5415.2000.tb03873.xopenalex-snapshot
Subsystems Contributing to the Decline in Ability to Walk: Bridging the Gap Between Epidemiology and Geriatric Practice in the InCHIANTI Study
inferredcites →https://doi.org/10.1126/science.1078311openalex-snapshot
Genetic Structure of Human Populations
inferredcites →https://doi.org/10.1136/thoraxjnl-2011-201321openalex-snapshot
Serum levels and genotype distribution of α 1 -antitrypsin in the general population
inferredcites →https://doi.org/10.1371/journal.pgen.1000072openalex-snapshot
A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
inferredcites →https://doi.org/10.1371/journal.pgen.1000529openalex-snapshot
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
inferredcites →https://doi.org/10.1371/journal.pone.0064343openalex-snapshot
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Association analysis of exome variants and refraction, axial length, and corneal curvature in a European-American population
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Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data
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Genetic determinants of IgG antibody response to COVID-19 vaccination
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Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population
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Socioeconomic inequalities, genetic susceptibility, and risks of depression and anxiety: A large-observational study
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Genetic adaptation to historical pathogen burdens
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Disadvantaged social status contributed to sleep disorders: An observational and genome-wide gene-environment interaction analysis
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Interpretation of risk loci from genome-wide association studies of Alzheimer's disease
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Genomics Research of Lifetime Depression in the Netherlands: The BIObanks Netherlands Internet Collaboration (BIONIC) Project
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Using DNA to predict educational trajectories in early adulthood.
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Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
inferred← citeshttps://doi.org/10.1038/mp.2017.203openalex-snapshot
Erratum: Predicting educational achievement from DNA
inferred← citeshttps://doi.org/10.1038/ng.3583openalex-snapshot
Haplotype estimation for biobank-scale data sets
inferred← citeshttps://doi.org/10.1038/nrg.2016.56openalex-snapshot
Type 2 diabetes: genetic data sharing to advance complex disease research
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Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes
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The reliability and heritability of cortical folds and their genetic correlations across hemispheres
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Prevalence and Effect of Genetic Risk of Thromboembolic Disease in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1093/bioinformatics/btw097openalex-snapshot
Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributions
inferred← citeshttps://doi.org/10.1093/bioinformatics/btw125openalex-snapshot
Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility loci
inferred← citeshttps://doi.org/10.1093/hmg/ddaa083openalex-snapshot
Population-specific reference panels are crucial for genetic analyses: an example of the CREBRF locus in Native Hawaiians
inferred← citeshttps://doi.org/10.1093/hmg/ddw174openalex-snapshot
Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
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Integrative Omics for Women’s Health
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Survey of the Heritability and Sparse Architecture of Gene Expression Traits Across Human Tissues
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Correcting subtle stratification in summary association statistics
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Genome-wide association studies of brain structure and function in the UK Biobank
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Genetic association and machine learning improves discovery and prediction of type 1 diabetes
inferred← citeshttps://doi.org/10.1101/542035openalex-snapshot
Fast and scalable genome-wide inference of local tree topologies from large number of haplotypes based on tree consistent PBWT data structure
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Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD
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Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study
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Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis
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Data from Tumor Mutational Burden Is Polygenic and Genetically Associated with Complex Traits and Diseases
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6513064openalex-snapshot
Data from A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility
inferred← citeshttps://doi.org/10.1158/1078-0432.c.6529577openalex-snapshot
Data from Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors
inferred← citeshttps://doi.org/10.1158/1078-0432.c.6529577.v1openalex-snapshot
Data from Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors
inferred← citeshttps://doi.org/10.1158/2767-9764.22546487openalex-snapshot
Supplementary Materials and Methods, Tables and Figures SM1 from Multiregional Sequencing Analysis Reveals Extensive Genetic Heterogeneity in Gastric Tumors from Latinos
inferred← citeshttps://doi.org/10.1158/2767-9764.22546487.v1openalex-snapshot
Supplementary Materials and Methods, Tables and Figures SM1 from Multiregional Sequencing Analysis Reveals Extensive Genetic Heterogeneity in Gastric Tumors from Latinos
inferred← citeshttps://doi.org/10.1158/2767-9764.c.6683111.v2openalex-snapshot
Data from A Mendelian Randomization Analysis of 55 Genetically Predicted Metabolic Traits with Breast Cancer Survival Outcomes in the Pathways Study
inferred← citeshttps://doi.org/10.1164/rccm.201905-1017ocopenalex-snapshot
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis
inferred← citeshttps://doi.org/10.1210/clinem/dgab215openalex-snapshot
A Polygenic Risk Score to Predict Future Adult Short Stature Among Children
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002782openalex-snapshot
Integration of estimated regional gene expression with neuroimaging and clinical phenotypes at biobank scale
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007739openalex-snapshot
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009021openalex-snapshot
Evaluation of polygenic prediction methodology within a reference-standardized framework
inferred← citeshttps://doi.org/10.1371/journal.pone.0166994openalex-snapshot
Associations between a Genetic Risk Score for Clinical CAD and Early Stage Lesions in the Coronary Artery and the Aorta
inferred← citeshttps://doi.org/10.1371/journal.pone.0178700openalex-snapshot
Frameshift indels introduced by genome editing can lead to in-frame exon skipping
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Serotonin transporter (5-HTT) gene network moderates the impact of prenatal maternal adversity on orbitofrontal cortical thickness in middle childhood
inferred← citeshttps://doi.org/10.14722/ndss.2020.23049openalex-snapshot
Genotype Extraction and False Relative Attacks: Security Risks to Third-Party Genetic Genealogy Services Beyond Identity Inference
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DCC gene network in the prefrontal cortex is associated with total brain volume in childhood
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Analysis of overlapping genetic association in type 1 and type 2 diabetes
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Trans-ethnic follow-up of breast cancer GWAS hits using the preferential linkage disequilibrium approach
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Overcoming the challenges of imputation of rare variants in a Taiwanese cohort
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Manifestations of Alzheimer’s Disease Genetic Risk in the Blood: A Cross-Sectional Multi-Omic Analysis in Healthy Adults Aged 18-90+
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I’am hiQ – A Novel Accuracy Index for Imputed Genotypes
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Transferability of a European-derived Alzheimer’s Disease Genetic Risk Score across Multi-Ancestry Populations.
inferred← citeshttps://doi.org/10.21203/rs.3.rs-707867/v1openalex-snapshot
Cognitive Capacity Genome-wide Polygenic Scores Identify Individuals Resilient to Cognitive Decline in Aging
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Social-Science Genomics: Progress, Challenges, and Future Directions
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Faculty Opinions recommendation of Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk.
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A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing
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