On the public citation graph

Relationship between LD Score and Haseman-Elston Regression

https://doi.org/10.1101/018283
0 signed · 51 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1098-2272(200007)19:1<1::aid-gepi1>3.0.co;2-eopenalex-snapshot
Haseman and Elston revisited
inferredcites →https://doi.org/10.1007/bf01066731openalex-snapshot
The investigation of linkage between a quantitative trait and a marker locus
inferredcites →https://doi.org/10.1016/j.ajhg.2010.11.011openalex-snapshot
GCTA: A Tool for Genome-wide Complex Trait Analysis
inferredcites →https://doi.org/10.1038/nature09298openalex-snapshot
Integrating common and rare genetic variation in diverse human populations
inferredcites →https://doi.org/10.1038/nature11632openalex-snapshot
An integrated map of genetic variation from 1,092 human genomes
inferredcites →https://doi.org/10.1038/ng.2742openalex-snapshot
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
inferredcites →https://doi.org/10.1038/ng.3211openalex-snapshot
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot
An atlas of genetic correlations across human diseases and traits
inferredcites →https://doi.org/10.1038/ng.608openalex-snapshot
Common SNPs explain a large proportion of the heritability for human height
inferredcites →https://doi.org/10.1038/ng1847openalex-snapshot
Principal components analysis corrects for stratification in genome-wide association studies
inferredcites →https://doi.org/10.1073/pnas.1419064111openalex-snapshot
Measuring missing heritability: Inferring the contribution of common variants
inferredcites →https://doi.org/10.1080/00220970109600656openalex-snapshot
Estimating R 2 Shrinkage in Multiple Regression: A Comparison of Different Analytical Methods
inferredcites →https://doi.org/10.1093/bioinformatics/bts474openalex-snapshot
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood
inferredcites →https://doi.org/10.2307/1907330openalex-snapshot
Partial Time Regressions as Compared with Individual Trends
inferredcites →https://doi.org/10.2307/3001775openalex-snapshot
Tests for Linear Trends in Proportions and Frequencies
inferredcites →https://doi.org/10.3389/fgene.2014.00107openalex-snapshot
Estimating heritability of complex traits from genome-wide association studies using IBS-based Haseman–Elston regression

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/9781119487845.ch24openalex-snapshot
Improving Genetic Association Analysis through Integration of Functional Annotations of the Human Genome
inferred← citeshttps://doi.org/10.1007/s10519-018-9942-yopenalex-snapshot
Type I Error Rates and Parameter Bias in Multivariate Behavioral Genetic Models
inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.11.001openalex-snapshot
A Powerful Approach to Estimating Annotation-Stratified Genetic Covariance via GWAS Summary Statistics
inferred← citeshttps://doi.org/10.1016/j.ajhg.2018.06.002openalex-snapshot
Estimating SNP-Based Heritability and Genetic Correlation in Case-Control Studies Directly and with Summary Statistics
inferred← citeshttps://doi.org/10.1016/j.semcancer.2020.06.001openalex-snapshot
Dissecting the heritable risk of breast cancer: From statistical methods to susceptibility genes
inferred← citeshttps://doi.org/10.1038/ng.3529openalex-snapshot
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
inferred← citeshttps://doi.org/10.1038/ng.3865openalex-snapshot
Reevaluation of SNP heritability in complex human traits
inferred← citeshttps://doi.org/10.1038/s41431-020-00712-wopenalex-snapshot
Sex-specific genetic effects across biomarkers
inferred← citeshttps://doi.org/10.1038/s41467-022-28294-9openalex-snapshot
Assortative mating biases marker-based heritability estimators
inferred← citeshttps://doi.org/10.1038/s41598-025-04421-6openalex-snapshot
Population screening of adults identifies novel genetic variants associated with celiac disease
inferred← citeshttps://doi.org/10.1038/srep27644openalex-snapshot
A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics
inferred← citeshttps://doi.org/10.1073/pnas.2533909123openalex-snapshot
Observational epidemiological studies can mitigate genetic confounding with a genetic relatedness matrix
inferred← citeshttps://doi.org/10.1093/bioinformatics/bty253openalex-snapshot
A scalable estimator of SNP heritability for biobank-scale data
inferred← citeshttps://doi.org/10.1093/genetics/iyac015openalex-snapshot
Estimating SNP heritability in presence of population substructure in biobank-scale datasets
inferred← citeshttps://doi.org/10.1101/2019.12.18.879916openalex-snapshot
Imputed Genomic Data Reveals a Moderate Effect of Low Frequency Variants to the Heritability of Complex Human Traits
inferred← citeshttps://doi.org/10.1101/2024.03.09.584258openalex-snapshot
Scalable summary statistics-based heritability estimation method with individual genotype level accuracy
inferred← citeshttps://doi.org/10.1101/2024.12.09.24318711openalex-snapshot
Genome-wide association study identifies novel risk variants for celiac disease in the 5p15.33 locus: insights from a population-based screening of adults, the HUNT study
inferred← citeshttps://doi.org/10.1101/2025.03.18.25324091openalex-snapshot
Leveraging nationwide health care records in Estonia to identify the genetic background of understudied disease phenotypes
inferred← citeshttps://doi.org/10.1101/2025.04.07.25324946openalex-snapshot
LDSC++: Improving linkage disequilibrium score regression estimation of heritability and genetic correlation for multivariate GWAS analysis
inferred← citeshttps://doi.org/10.1101/2025.11.15.25340310openalex-snapshot
A photoplethysmography-based aging clock reveals genetic determinants of arterial aging
inferred← citeshttps://doi.org/10.1101/211821openalex-snapshot
Equivalence of LD-Score Regression and Individual-Level-Data Methods
inferred← citeshttps://doi.org/10.1101/242776openalex-snapshot
The Shared Genetic Basis of Educational Attainment and Cerebral Cortical Morphology
inferred← citeshttps://doi.org/10.1101/gr.279207.124openalex-snapshot
Scalable summary-statistics-based heritability estimation method with individual genotype level accuracy
inferred← citeshttps://doi.org/10.1126/science.abo2059openalex-snapshot
Cross-trait assortative mating is widespread and inflates genetic correlation estimates
inferred← citeshttps://doi.org/10.1186/s12864-024-10600-yopenalex-snapshot
Evaluation of heritability partitioning approaches in livestock populations
inferred← citeshttps://doi.org/10.1214/17-aoas1052openalex-snapshot
A unified framework for variance component estimation with summary statistics in genome-wide association studies
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002511openalex-snapshot
Interpreting population- and family-based genome-wide association studies in the presence of confounding
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1005589openalex-snapshot
Leveraging functional annotations in genetic risk prediction for human complex diseases
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006711openalex-snapshot
Phenome-wide heritability analysis of the UK Biobank
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006836openalex-snapshot
Joint modeling of genetically correlated diseases and functional annotations increases accuracy of polygenic risk prediction
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008124openalex-snapshot
Estimating variance components in population scale family trees
inferred← citeshttps://doi.org/10.1534/genetics.120.303161openalex-snapshot
On Negative Heritability and Negative Estimates of Heritability
inferred← citeshttps://doi.org/10.64898/2026.03.04.709666openalex-snapshot
GWAS Summary Statistic Tool: A Meta-Analysis and Parsing Tool for Polygenic Risk Score Calculation
inferred← citeshttps://doi.org/10.64898/2026.05.13.724972openalex-snapshot
When can whole-genome SNP heritability be reliably estimated from summary statistics?
inferred← citeshttps://doi.org/10.64898/2026.08.04.742829openalex-snapshot
The Genome-Wide Effect of Drift and Selection over a Single Generation
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.