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Statistical power and significance testing in large-scale genetic studies

https://doi.org/10.1038/nrg3706
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Outgoing claims: the papers this work cites, builds on, or argues with.

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General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies
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Statistical analysis strategies for association studies involving rare variants
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Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix
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Searching for missing heritability: Designing rare variant association studies
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Combined Linkage and Association Sib-Pair Analysis for Quantitative Traits
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Power Comparisons of the Transmission/Disequilibrium Test and Sib–Transmission/Disequilibrium-Test Statistics
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Power of Linkage versus Association Analysis of Quantitative Traits, by Use of Variance-Components Models, for Sibship Data
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A Note on the Calculation of Empirical P Values from Monte Carlo Procedures
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A Simple Correction for Multiple Testing for Single-Nucleotide Polymorphisms in Linkage Disequilibrium with Each Other
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Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies
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SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits
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Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
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What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations
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Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
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Rare Variants of IFIH1 , a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
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Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies
inferredcites →https://doi.org/10.1186/1753-6561-5-s9-s33openalex-snapshot
Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data
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Combining effects from rare and common genetic variants in an exome-wide association study of sequence data
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Computational and statistical approaches to analyzing variants identified by exome sequencing
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Analysis of copy number variations at 15 schizophrenia-associated loci
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A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
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Discovery of Rare Variants via Sequencing: Implications for the Design of Complex Trait Association Studies
inferredcites →https://doi.org/10.1371/journal.pgen.1001322openalex-snapshot
Testing for an Unusual Distribution of Rare Variants
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The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals
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Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes
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Bootstrap Methods and Their Application

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Identification and Genomic Localization of Autosomal sdY Locus in a Population of Atlantic Salmon (Salmo salar)
inferred← citeshttps://doi.org/10.1007/s10238-018-0529-yopenalex-snapshot
Association of the CYP4V2 polymorphism rs13146272 with venous thromboembolism in a Chinese population
inferred← citeshttps://doi.org/10.1007/s10353-026-00938-wopenalex-snapshot
Understanding and applying statistical methods in surgical research: a comprehensive guide for clinicians
inferred← citeshttps://doi.org/10.1007/s10519-017-9837-3openalex-snapshot
The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations
inferred← citeshttps://doi.org/10.1007/s10519-024-10187-wopenalex-snapshot
Using Alternative Definitions of Controls to Increase Statistical Power in GWAS
inferred← citeshttps://doi.org/10.1007/s11065-015-9281-1openalex-snapshot
Genetics and Brain Morphology
inferred← citeshttps://doi.org/10.1007/s11065-020-09426-8openalex-snapshot
Bilingualism Is Associated with a Delayed Onset of Dementia but Not with a Lower Risk of Developing it: a Systematic Review with Meta-Analyses
inferred← citeshttps://doi.org/10.1007/s11103-018-0754-5openalex-snapshot
Coexpression network revealing the plasticity and robustness of population transcriptome during the initial stage of domesticating energy crop Miscanthus lutarioriparius
inferred← citeshttps://doi.org/10.1007/s11357-024-01196-yopenalex-snapshot
Hepatic WDR23 proteostasis mediates insulin homeostasis by regulating insulin-degrading enzyme capacity
inferred← citeshttps://doi.org/10.1007/s12031-021-01805-xopenalex-snapshot
Genome-Wide Detection of m6A-Associated Genetic Polymorphisms Associated with Ischemic Stroke
inferred← citeshttps://doi.org/10.1007/s12035-018-0877-3openalex-snapshot
Implication of Genes for the N-Methyl-d-Aspartate (NMDA) Receptor in Substance Addictions
inferred← citeshttps://doi.org/10.1007/s12035-025-05582-1openalex-snapshot
Beyond Single Variants: A Pathway-Based Approach to Explore the Genetic Basis of Memory
inferred← citeshttps://doi.org/10.1007/s12041-018-0936-6openalex-snapshot
A multiple regression method for genomewide association studies using only linkage information
inferred← citeshttps://doi.org/10.1007/s12665-016-6148-6openalex-snapshot
Spatiotemporal dynamics of the climatic impacts on greenup date in the Tibetan Plateau
inferred← citeshttps://doi.org/10.1007/s13311-020-00838-1openalex-snapshot
Translational Genomics in Neurocritical Care: a Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-802395-2.00022-5openalex-snapshot
Genetics of neurodegenerative diseases: an overview
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20356-7openalex-snapshot
Hypothesis Testing
inferred← citeshttps://doi.org/10.1016/b978-0-12-812537-3.00011-1openalex-snapshot
Multifactorial Inheritance and Complex Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-813176-3.00023-7openalex-snapshot
Current progress and future direction in the genetics of PTSD: Focus on the development and contributions of the PGC-PTSD working group
inferred← citeshttps://doi.org/10.1016/b978-0-12-813176-3.00034-1openalex-snapshot
Genomic treatment response prediction in schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-815298-0.00027-7openalex-snapshot
Genetics, imaging, and cognition
inferred← citeshttps://doi.org/10.1016/b978-0-12-817218-6.00012-7openalex-snapshot
Rigor and reproducibility in genetic research and the effects on scientific reporting and public discourse
inferred← citeshttps://doi.org/10.1016/b978-0-12-819978-7.00009-9openalex-snapshot
Next-Generation Omics Technologies for Exploring Complex Metabolic Regulation During Plant-Microbe Interaction
inferred← citeshttps://doi.org/10.1016/b978-0-12-821375-9.00005-0openalex-snapshot
Genetics and epigenetics of human aggression
inferred← citeshttps://doi.org/10.1016/b978-0-12-849886-6.00009-4openalex-snapshot
Nutrigenomics and personalized nutrition for the prevention of hyperglycemia and type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1016/b978-0-323-91259-4.00050-3openalex-snapshot
Power
inferred← citeshttps://doi.org/10.1016/b978-0-323-95502-7.00015-4openalex-snapshot
Hypothesis Testing
inferred← citeshttps://doi.org/10.1016/j.ajhg.2015.02.009openalex-snapshot
A Large-Scale Genetic Analysis Reveals a Strong Contribution of the HLA Class II Region to Giant Cell Arteritis Susceptibility
inferred← citeshttps://doi.org/10.1016/j.ajhg.2017.04.015openalex-snapshot
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource
inferred← citeshttps://doi.org/10.1016/j.ajhg.2022.03.005openalex-snapshot
Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries
inferred← citeshttps://doi.org/10.1016/j.ajhg.2025.07.002openalex-snapshot
Rare-variant association studies: When are aggregation tests more powerful than single-variant tests?
inferred← citeshttps://doi.org/10.1016/j.bandl.2017.03.012openalex-snapshot
Multimodal imaging of language reorganization in patients with left temporal lobe epilepsy
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.11.030openalex-snapshot
Pathway analysis of complex diseases for GWAS, extending to consider rare variants, multi-omics and interactions
inferred← citeshttps://doi.org/10.1016/j.beha.2017.07.007openalex-snapshot
Pharmacogenomics in acute lymphoblastic leukemia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2014.08.005openalex-snapshot
Genetics of Complex Traits in Psychiatry
inferred← citeshttps://doi.org/10.1016/j.biopsych.2016.02.033openalex-snapshot
Multimodal Brain Imaging Reveals Structural Differences in Alzheimer’s Disease Polygenic Risk Carriers: A Study in Healthy Young Adults
inferred← citeshttps://doi.org/10.1016/j.biopsych.2017.11.006openalex-snapshot
Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3′UTRome
inferred← citeshttps://doi.org/10.1016/j.burns.2018.10.027openalex-snapshot
Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study
inferred← citeshttps://doi.org/10.1016/j.cbd.2026.101764openalex-snapshot
Genome-wide association analysis to identify novel candidate genes and genomic model optimization to predict acute low-temperature stress resilience in olive flounder (Paralichthys olivaceus)
inferred← citeshttps://doi.org/10.1016/j.cels.2017.10.016openalex-snapshot
An Integrated Systems Genetics and Omics Toolkit to Probe Gene Function
inferred← citeshttps://doi.org/10.1016/j.cels.2019.03.013openalex-snapshot
Strategies for Network GWAS Evaluated Using Classroom Crowd Science
inferred← citeshttps://doi.org/10.1016/j.cels.2020.11.006openalex-snapshot
SECAT: Quantifying Protein Complex Dynamics across Cell States by Network-Centric Analysis of SEC-SWATH-MS Profiles
inferred← citeshttps://doi.org/10.1016/j.cll.2020.02.004openalex-snapshot
The Clinical Application of RNA Sequencing in Genetic Diagnosis of Mendelian Disorders
inferred← citeshttps://doi.org/10.1016/j.crmeth.2023.100515openalex-snapshot
EpiMix is an integrative tool for epigenomic subtyping using DNA methylation
inferred← citeshttps://doi.org/10.1016/j.ctrv.2016.12.005openalex-snapshot
Strategies to design clinical studies to identify predictive biomarkers in cancer research
inferred← citeshttps://doi.org/10.1016/j.ebiom.2019.01.041openalex-snapshot
Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
inferred← citeshttps://doi.org/10.1016/j.gde.2017.08.002openalex-snapshot
Natural diversity facilitates the discovery of conserved chemotherapeutic response mechanisms
inferred← citeshttps://doi.org/10.1016/j.genrep.2020.100729openalex-snapshot
Genetic analysis and epistatic interaction association of lipid traits in a C57xBalb/c F2 mice
inferred← citeshttps://doi.org/10.1016/j.genrep.2026.102666openalex-snapshot
Association of genetic risk score (GRS) constructed from THADA gene variants with polycystic ovary syndrome risk in Punjabi women
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2016.11.008openalex-snapshot
What can time-frequency and phase coherence measures tell us about the genetic basis of P3 amplitude?
inferred← citeshttps://doi.org/10.1016/j.isci.2026.114953openalex-snapshot
Platform-dependent effects of genetic variants on plasma APOL1
inferred← citeshttps://doi.org/10.1016/j.isci.2026.117256openalex-snapshot
Form and function of actin impacts actin health and aging
inferred← citeshttps://doi.org/10.1016/j.jaci.2024.11.033openalex-snapshot
A genome-wide meta-analysis reveals shared and population-specific variants for allergic sensitization
inferred← citeshttps://doi.org/10.1016/j.jpeds.2019.12.036openalex-snapshot
Association between CNTF Polymorphisms and Adiposity Markers in European Adolescents
inferred← citeshttps://doi.org/10.1016/j.jstrokecerebrovasdis.2016.08.002openalex-snapshot
Association of Rare Nonsynonymous Variants in PKD1 and PKD2 with Familial Intracranial Aneurysms in a Japanese Population
inferred← citeshttps://doi.org/10.1016/j.jtha.2024.12.030openalex-snapshot
Applying artificial intelligence to uncover the genetic landscape of coagulation factors
inferred← citeshttps://doi.org/10.1016/j.kint.2021.05.037openalex-snapshot
A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis
inferred← citeshttps://doi.org/10.1016/j.landurbplan.2018.07.006openalex-snapshot
Understanding avian assemblage change within anthropogenic environments using citizen science data
inferred← citeshttps://doi.org/10.1016/j.mayocp.2016.09.008openalex-snapshot
Neurology Individualized Medicine: When to Use Next-Generation Sequencing Panels
inferred← citeshttps://doi.org/10.1016/j.mcp.2016.09.001openalex-snapshot
Genomics of Alzheimer's disease: Value of high-throughput genomic technologies to dissect its etiology
inferred← citeshttps://doi.org/10.1016/j.medcle.2018.05.036openalex-snapshot
Biomedical research at the crossroads and ways through
inferred← citeshttps://doi.org/10.1016/j.medcli.2017.12.013openalex-snapshot
La investigación biomédica en la encrucijada y vías de salida
inferred← citeshttps://doi.org/10.1016/j.mib.2018.05.003openalex-snapshot
Host genetics and microbiome associations through the lens of genome wide association studies
inferred← citeshttps://doi.org/10.1016/j.micpath.2023.106115openalex-snapshot
Community detection in Epstein-Barr virus associated carcinomas and role of tyrosine kinase in etiological mechanisms for oncogenesis
inferred← citeshttps://doi.org/10.1016/j.micpath.2023.106386openalex-snapshot
Over-representation analysis of angiogenic factors in immunosuppressive mechanisms in neoplasms and neurological conditions during COVID-19
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.135315openalex-snapshot
Genome-wide identification of m6A-associated single-nucleotide polymorphisms in Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2023.120049openalex-snapshot
Both fine-grained and coarse-grained spatial patterns of neural activity measured by functional MRI show preferential encoding of pain in the human brain
inferred← citeshttps://doi.org/10.1016/j.neuron.2025.10.014openalex-snapshot
From variants to mechanisms: Neurogenomics in the post-GWAS era
inferred← citeshttps://doi.org/10.1016/j.patter.2020.100115openalex-snapshot
Statistical Hypothesis Testing versus Machine Learning Binary Classification: Distinctions and Guidelines
inferred← citeshttps://doi.org/10.1016/j.pbb.2018.02.005openalex-snapshot
Reproducibility and replicability in zebrafish behavioral neuroscience research
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2020.101898openalex-snapshot
Alterations in nicotinic receptor alpha5 subunit gene differentially impact early and later stages of cocaine addiction: a translational study in transgenic rats and patients
inferred← citeshttps://doi.org/10.1016/j.psj.2024.103666openalex-snapshot
Genetic parameter estimation and molecular foundation of chicken beak shape
inferred← citeshttps://doi.org/10.1016/j.psj.2025.105069openalex-snapshot
Genetic parameter estimation and molecular foundation of Double-yolk eggs trait in white leghorn
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2018.05.040openalex-snapshot
The association between cortisol, oxytocin, and immune cell mitochondrial oxygen consumption in postpartum women with childhood maltreatment
inferred← citeshttps://doi.org/10.1016/j.pt.2019.01.004openalex-snapshot
Genome-wide Approaches to Investigate Anthelmintic Resistance
inferred← citeshttps://doi.org/10.1016/j.pt.2024.02.007openalex-snapshot
Exploiting integrative metabolomics to study host–parasite interactions in Plasmodium infections
inferred← citeshttps://doi.org/10.1016/j.schres.2017.09.031openalex-snapshot
Genetic analysis of deep phenotyping projects in common disorders
inferred← citeshttps://doi.org/10.1016/j.schres.2017.12.012openalex-snapshot
Complement system biomarkers in first episode psychosis
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114767openalex-snapshot
Whole-genome resequencing-based GWAS reveals loci associated with yellow leaf disease resistance in Phalaenopsis
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/10.1016/j.theriogenology.2021.12.025openalex-snapshot
Meta-analysis of genome-wide association studies for litter size in sheep
inferred← citeshttps://doi.org/10.1016/j.tig.2014.08.006openalex-snapshot
Sex differences in disease genetics: evidence, evolution, and detection
inferred← citeshttps://doi.org/10.1016/j.xops.2022.100113openalex-snapshot
Genome-wide Association Study of Axial Length in Population-based Cohorts in Japan
inferred← citeshttps://doi.org/10.1016/j.yamp.2018.06.004openalex-snapshot
The Clinical Application of RNA Sequencing in Genetic Diagnosis of Mendelian Disorders
inferred← citeshttps://doi.org/10.1016/s1474-4422(14)70266-2openalex-snapshot
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
inferred← citeshttps://doi.org/10.1016/s1474-4422(17)30161-8openalex-snapshot
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
inferred← citeshttps://doi.org/10.1016/s2213-2600(18)30101-2openalex-snapshot
Adrenal insufficiency and ICS: genetics takes a breath
inferred← citeshttps://doi.org/10.1016/s2213-8587(16)00113-3openalex-snapshot
Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population
inferred← citeshttps://doi.org/10.1016/s2352-3026(18)30107-8openalex-snapshot
Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association study
inferred← citeshttps://doi.org/10.1017/9781139924771.006openalex-snapshot
Genetic approaches to neurodegenerative disease
inferred← citeshttps://doi.org/10.1017/cbo9781107337459.009openalex-snapshot
Admixture mapping for disease gene discovery
inferred← citeshttps://doi.org/10.1017/thg.2017.12openalex-snapshot
Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations
inferred← citeshttps://doi.org/10.1021/acs.est.3c02231openalex-snapshot
Separating Measurement Error and Signal in Environmental Data: Use of Replicates to Address Uncertainty
inferred← citeshttps://doi.org/10.1038/ejhg.2015.244openalex-snapshot
Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases
inferred← citeshttps://doi.org/10.1038/ejhg.2015.269openalex-snapshot
The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants
inferred← citeshttps://doi.org/10.1038/jhg.2017.75openalex-snapshot
Genetic variants underlying vitamin D metabolism and VDR–TGFβ-1–SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study
inferred← citeshttps://doi.org/10.1038/mp.2016.20openalex-snapshot
Pathways to smoking behaviours: biological insights from the Tobacco and Genetics Consortium meta-analysis
inferred← citeshttps://doi.org/10.1038/mp.2016.222openalex-snapshot
Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism
inferred← citeshttps://doi.org/10.1038/mp.2016.67openalex-snapshot
Converging findings from linkage and association analyses on susceptibility genes for smoking and other addictions
inferred← citeshttps://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferred← citeshttps://doi.org/10.1038/ncomms14946openalex-snapshot
Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania
inferred← citeshttps://doi.org/10.1038/ncomms15930openalex-snapshot
Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource
inferred← citeshttps://doi.org/10.1038/ng.3507openalex-snapshot
Weighting sequence variants based on their annotation increases power of whole-genome association studies
inferred← citeshttps://doi.org/10.1038/ng.3843openalex-snapshot
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
inferred← citeshttps://doi.org/10.1038/ng.3975openalex-snapshot
Covariate selection for association screening in multiphenotype genetic studies
inferred← citeshttps://doi.org/10.1038/nm.4071openalex-snapshot
Advancing the understanding of autism disease mechanisms through genetics
inferred← citeshttps://doi.org/10.1038/nn.4409openalex-snapshot
The road to precision psychiatry: translating genetics into disease mechanisms
inferred← citeshttps://doi.org/10.1038/nn.4618openalex-snapshot
Analysis of genome-wide association data highlights candidates for drug repositioning in psychiatry
inferred← citeshttps://doi.org/10.1038/nrc.2017.82openalex-snapshot
Genome-wide association studies of cancer: current insights and future perspectives
inferred← citeshttps://doi.org/10.1038/nrg3934openalex-snapshot
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders
inferred← citeshttps://doi.org/10.1038/s10038-022-01051-yopenalex-snapshot
Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot
inferred← citeshttps://doi.org/10.1038/s41380-020-0670-3openalex-snapshot
GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size
inferred← citeshttps://doi.org/10.1038/s41390-019-0735-7openalex-snapshot
Association of UCP1, UCP2 and UCP3 gene polymorphisms with cardiovascular disease risk factors in European adolescents: the HELENA study
inferred← citeshttps://doi.org/10.1038/s41390-021-01519-1openalex-snapshot
Interplay of physical activity and genetic variants of the endothelial lipase on cardiovascular disease risk factors
inferred← citeshttps://doi.org/10.1038/s41390-022-02377-1openalex-snapshot
Association between PTPN1 polymorphisms and obesity-related phenotypes in European adolescents: influence of physical activity
inferred← citeshttps://doi.org/10.1038/s41397-018-0055-zopenalex-snapshot
Genome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid loci
inferred← citeshttps://doi.org/10.1038/s41397-019-0099-8openalex-snapshot
Genes and variants in hematopoiesis-related pathways are associated with gemcitabine/carboplatin-induced thrombocytopenia
inferred← citeshttps://doi.org/10.1038/s41397-020-0148-3openalex-snapshot
SWEDEGENE—a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions
inferred← citeshttps://doi.org/10.1038/s41397-020-0165-2openalex-snapshot
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment
inferred← citeshttps://doi.org/10.1038/s41398-017-0010-9openalex-snapshot
Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank
inferred← citeshttps://doi.org/10.1038/s41398-017-0088-0openalex-snapshot
Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorder
inferred← citeshttps://doi.org/10.1038/s41398-018-0175-xopenalex-snapshot
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder
inferred← citeshttps://doi.org/10.1038/s41398-018-0343-zopenalex-snapshot
Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene
inferred← citeshttps://doi.org/10.1038/s41416-018-0141-7openalex-snapshot
Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease
inferred← citeshttps://doi.org/10.1038/s41431-020-00800-xopenalex-snapshot
Semi-parametric empirical Bayes factor for genome-wide association studies
inferred← citeshttps://doi.org/10.1038/s41435-018-0013-4openalex-snapshot
Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2)
inferred← citeshttps://doi.org/10.1038/s41437-024-00733-xopenalex-snapshot
Multi-population GWAS detects robust marker associations in a newly established six-rowed winter barley breeding program
inferred← citeshttps://doi.org/10.1038/s41437-025-00783-9openalex-snapshot
Machine learning reveals complex genetics of fungal resistance in sorghum grain mold
inferred← citeshttps://doi.org/10.1038/s41467-018-03082-6openalex-snapshot
Exploiting genetic variation to uncover rules of transcription factor binding and chromatin accessibility
inferred← citeshttps://doi.org/10.1038/s41467-018-03109-yopenalex-snapshot
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference
inferred← citeshttps://doi.org/10.1038/s41467-018-06805-xopenalex-snapshot
Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes
inferred← citeshttps://doi.org/10.1038/s41467-019-12760-yopenalex-snapshot
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
inferred← citeshttps://doi.org/10.1038/s41467-021-27930-0openalex-snapshot
DeepNull models non-linear covariate effects to improve phenotypic prediction and association power
inferred← citeshttps://doi.org/10.1038/s41467-023-41210-zopenalex-snapshot
ADuLT: An efficient and robust time-to-event GWAS
inferred← citeshttps://doi.org/10.1038/s41467-025-67277-4openalex-snapshot
Cost-effective non-additive GWAS across 2329 diseases in 500,349 individuals
inferred← citeshttps://doi.org/10.1038/s41556-025-01801-yopenalex-snapshot
Ten essential tips for robust statistics in cell biology
inferred← citeshttps://doi.org/10.1038/s41568-018-0087-3openalex-snapshot
Post-GWAS in prostate cancer: from genetic association to biological contribution
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