On the public citation graph
On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles
0 signed · 370 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-2272(1999)16:3<250::aid-gepi2>3.0.co;2-topenalex-snapshot
Likelihoods andTDT for the case-parents design
inferredcites →https://doi.org/10.1002/(sici)1098-2272(200002)18:2<143::aid-gepi4>3.0.co;2-5openalex-snapshot
Effect of allelic heterogeneity on the power of the transmission disequilibrium test
inferredcites →https://doi.org/10.1006/tpbi.1997.1299openalex-snapshot
Ancestral Processes with Selection
inferredcites →https://doi.org/10.1007/s00439-001-0667-1openalex-snapshot
Handbook of statistical genetics:
inferredcites →https://doi.org/10.1016/0016-0032(58)90688-4openalex-snapshot
An introduction to probability theory and its applications
inferredcites →https://doi.org/10.1016/s0065-2660(01)42023-2openalex-snapshot
14 The future of genetic case-control studies
inferredcites →https://doi.org/10.1016/s0958-1669(98)80135-3openalex-snapshot
Linkage disequilibrium mapping of complex disease: fantasy or reality?
inferredcites →https://doi.org/10.1038/sj.ejhg.5200619openalex-snapshot
Haplotypes vs single marker linkage disequilibrium tests: what do we gain?
inferredcites →https://doi.org/10.1080/00401706.1991.10484817openalex-snapshot
Categorical Data Analysis
inferredcites →https://doi.org/10.1086/302139openalex-snapshot
Genome Screens Using Linkage Disequilibrium Tests: Optimal Marker Characteristics and Feasibility
inferredcites →https://doi.org/10.1086/302781openalex-snapshot
Variation in the Interleukin 4–Receptor α Gene Confers Susceptibility to Asthma and Atopy in Ethnically Diverse Populations
inferredcites →https://doi.org/10.1086/302796openalex-snapshot
The Trimmed-Haplotype Test for Linkage Disequilibrium
inferredcites →https://doi.org/10.1086/320106openalex-snapshot
Complexity and Power in Case-Control Association Studies
inferredcites →https://doi.org/10.1086/321272openalex-snapshot
Are Rare Variants Responsible for Susceptibility to Complex Diseases?
inferredcites →https://doi.org/10.1093/genetics/145.2.519openalex-snapshot
The Genealogy of Samples in Models With Selection
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040269openalex-snapshot
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.
inferredcites →https://doi.org/10.1101/gr.148401openalex-snapshot
Genetic Analysis of Case/Control Data Using Estimated Haplotype Frequencies: Application to APOE Locus Variation and Alzheimer's Disease
inferredcites →https://doi.org/10.1111/j.1751-5823.2000.tb00385.xopenalex-snapshot
Linkage Disequilibrium Mapping of Disease Susceptibility Genes in Human Populations
inferredcites →https://doi.org/10.1126/science.8091226openalex-snapshot
Genetic Dissection of Complex Traits
inferredcites →https://doi.org/10.1177/096228020101000104openalex-snapshot
A chronology of fine-scale gene mapping by linkage disequilibrium
inferredcites →https://doi.org/10.2307/2342907openalex-snapshot
An Introduction to Probability Theory and Its Applications.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4677894openalex-extracted
Association of Adiponectin Gene Snps with Environmental Risk Factors in Type 2 Diabetes Mellitus: An Updated Evidence of Haplotype-Based Analysis Study
inferred← citeshttps://doi.org/10.1001/jama.2011.1029openalex-snapshot
Germline Mutations in MSR1, ASCC1, and CTHRC1 in Patients With Barrett Esophagus and Esophageal Adenocarcinoma
inferred← citeshttps://doi.org/10.1002/9781118398890.ch7openalex-snapshot
Discovering Multilocus Associations with Complex Pain Phenotypes
inferred← citeshttps://doi.org/10.1002/9783527619368.ch38openalex-snapshot
Association Studies of Complex Diseases
inferred← citeshttps://doi.org/10.1002/ajmg.b.32766openalex-snapshot
Genetic variability of serotonin pathway associated with schizophrenia onset, progression, and treatment
inferred← citeshttps://doi.org/10.1002/bimj.201800053openalex-snapshot
Powerful testing via hierarchical linkage disequilibrium in haplotype association studies
inferred← citeshttps://doi.org/10.1002/cbf.1661openalex-snapshot
Haplotype analysis of the CYP2J2 gene associated with myocardial infarction in a Chinese Han population
inferred← citeshttps://doi.org/10.1002/gepi.10317openalex-snapshot
Haplotype‐based association analysis in cohort studies of unrelated individuals
inferred← citeshttps://doi.org/10.1002/gepi.20005openalex-snapshot
Haplotype sharing correlation analysis using family data: A comparison with family‐based association test in the presence of allelic heterogeneity
inferred← citeshttps://doi.org/10.1002/gepi.20020openalex-snapshot
Comparison of prospective and retrospective methods for haplotype inference in case‐control studies
inferred← citeshttps://doi.org/10.1002/gepi.20022openalex-snapshot
Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes
inferred← citeshttps://doi.org/10.1002/gepi.20025openalex-snapshot
The role of haplotypes in candidate gene studies
inferred← citeshttps://doi.org/10.1002/gepi.20037openalex-snapshot
Evaluating associations of haplotypes with traits
inferred← citeshttps://doi.org/10.1002/gepi.20039openalex-snapshot
SNPs, haplotypes, and model selection in a candidate gene region: The SIMPle analysis for multilocus data
inferred← citeshttps://doi.org/10.1002/gepi.20040openalex-snapshot
Estimating haplotype-disease associations with pooled genotype data
inferred← citeshttps://doi.org/10.1002/gepi.20061openalex-snapshot
Accounting for haplotype uncertainty in matched association studies: A comparison of simple and flexible techniques
inferred← citeshttps://doi.org/10.1002/gepi.20098openalex-snapshot
Maximum likelihood estimation of haplotype effects and haplotype-environment interactions in association studies
inferred← citeshttps://doi.org/10.1002/gepi.20102openalex-snapshot
Global transmission/disequilibrium tests based on haplotype sharing in multiple candidate genes
inferred← citeshttps://doi.org/10.1002/gepi.20110openalex-snapshot
Fine mapping by linkage and association in nuclear family and case-control designs
inferred← citeshttps://doi.org/10.1002/gepi.20144openalex-snapshot
Haplotype analysis in the presence of informatively missing genotype data
inferred← citeshttps://doi.org/10.1002/gepi.20154openalex-snapshot
A comparison of several methods for haplotype frequency estimation and haplotype reconstruction for tightly linked markers from general pedigrees
inferred← citeshttps://doi.org/10.1002/gepi.20165openalex-snapshot
A sliding‐window weighted linkage disequilibrium test
inferred← citeshttps://doi.org/10.1002/gepi.20192openalex-snapshot
Simple methods for assessing haplotype‐environment interactions in case‐only and case‐control studies
inferred← citeshttps://doi.org/10.1002/gepi.20228openalex-snapshot
Sequential haplotype scan methods for association analysis
inferred← citeshttps://doi.org/10.1002/gepi.20242openalex-snapshot
Detecting haplotype effects in genomewide association studies
inferred← citeshttps://doi.org/10.1002/gepi.20259openalex-snapshot
Robust estimation and testing of haplotype effects in case‐control studies
inferred← citeshttps://doi.org/10.1002/gepi.20311openalex-snapshot
X‐LRT: a likelihood approach to estimate genetic risks and test association with X‐linked markers using a case‐parents design
inferred← citeshttps://doi.org/10.1002/gepi.20373openalex-snapshot
More powerful haplotype sharing by accounting for the mode of inheritance
inferred← citeshttps://doi.org/10.1002/gepi.20382openalex-snapshot
Generalized linear modeling with regularization for detecting common disease rare haplotype association
inferred← citeshttps://doi.org/10.1002/gepi.20448openalex-snapshot
Comparisons of multi‐marker association methods to detect association between a candidate region and disease
inferred← citeshttps://doi.org/10.1002/gepi.20450openalex-snapshot
An evaluation of statistical approaches to rare variant analysis in genetic association studies
inferred← citeshttps://doi.org/10.1002/gepi.20452openalex-snapshot
Gene, region and pathway level analyses in whole‐genome studies
inferred← citeshttps://doi.org/10.1002/gepi.21792openalex-snapshot
Imputation Without Doing Imputation: A New Method for the Detection of Non‐Genotyped Causal Variants
inferred← citeshttps://doi.org/10.1002/gepi.22258openalex-snapshot
Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes
inferred← citeshttps://doi.org/10.1002/gepi.70039openalex-snapshot
Variant Prioritization by Pedigree‐Based Haplotyping
inferred← citeshttps://doi.org/10.1002/humu.9369openalex-snapshot
Linear allele-specific long-range amplification: a novel method of long-range molecular haplotyping
inferred← citeshttps://doi.org/10.1002/jbt.22503openalex-snapshot
Correlation betweenTICAM1gene polymorphisms and community‐acquired pneumonia in children
inferred← citeshttps://doi.org/10.1002/mc.20858openalex-snapshot
Genetic variability in DNA repair and cell cycle control pathway genes and risk of smoking‐related lung cancer
inferred← citeshttps://doi.org/10.1002/sim.5540openalex-snapshot
A fast collapsed data method for estimating haplotype frequencies from pooled genotype data with applications to the study of rare variants
inferred← citeshttps://doi.org/10.1002/sim.8877openalex-snapshot
Detecting rare haplotype association with two correlated phenotypes of binary and continuous types
inferred← citeshttps://doi.org/10.1007/0-387-26288-1_16openalex-snapshot
Single Nucleotide Polymorphisms and Their Applications
inferred← citeshttps://doi.org/10.1007/978-3-540-68168-7_40openalex-snapshot
Application to Estimate Haplotypes for Multiallelic Present-Absent Loci
inferred← citeshttps://doi.org/10.1007/978-3-540-69264-5_7openalex-snapshot
Family-Based Association Studies
inferred← citeshttps://doi.org/10.1007/978-3-540-69264-5_8openalex-snapshot
Haplotype Association Analysis
inferred← citeshttps://doi.org/10.1007/978-3-642-20036-6_19openalex-snapshot
Haplotype Reconstruction in Large Pedigrees with Many Untyped Individuals
inferred← citeshttps://doi.org/10.1007/s00223-003-0087-4openalex-snapshot
Association of Estrogen Receptor a and Vitamin D Receptor Gene Polymorphisms with Bone Mineral Density in Chinese Males
inferred← citeshttps://doi.org/10.1007/s00223-004-0034-zopenalex-snapshot
APOE Haplotypes Influence Bone Mineral Density in Caucasian Males but Not Females
inferred← citeshttps://doi.org/10.1007/s00335-008-9167-0openalex-snapshot
Risk haplotype analysis for bovine paratuberculosis
inferred← citeshttps://doi.org/10.1007/s00403-012-1301-xopenalex-snapshot
Possible contribution of GSTP1 and other xenobiotic metabolizing genes to vitiligo susceptibility
inferred← citeshttps://doi.org/10.1007/s00439-005-0053-5openalex-snapshot
An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3′ haplotypes could modify circulating levels of mannose-binding lectin
inferred← citeshttps://doi.org/10.1007/s10038-005-0281-5openalex-snapshot
Estrogen receptor α gene relationship with peak bone mass and body mass index in Chinese nuclear families
inferred← citeshttps://doi.org/10.1007/s10552-011-9745-4openalex-snapshot
Genomics of the NF-κB signaling pathway: hypothesized role in ovarian cancer
inferred← citeshttps://doi.org/10.1007/s11033-013-2993-5openalex-snapshot
Association of interleukin-8 gene polymorphisms with the risk of hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s11033-022-07868-2openalex-snapshot
Association between the ELAVL1 gene single nucleotide polymorphisms and the Genetic Susceptibility to cervical cancer by high resolution melting in a Tunisian population
inferred← citeshttps://doi.org/10.1007/s11192-014-1298-3openalex-snapshot
Literature-related discovery: common factors for Parkinson’s Disease and Crohn’s Disease
inferred← citeshttps://doi.org/10.1007/s11910-016-0643-8openalex-snapshot
New Genetic Approaches to AD: Lessons from APOE-TOMM40 Phylogenetics
inferred← citeshttps://doi.org/10.1007/s12020-008-9078-6openalex-snapshot
Haplotype-based case study of human CYP4A11 gene and cerebral infarction in Japanese subject
inferred← citeshttps://doi.org/10.1007/s12041-016-0720-4openalex-snapshot
Association and expression analyses of the Ucp2 and Ucp3 gene polymorphisms with body measurement and meat quality traits in Qinchuan cattle
inferred← citeshttps://doi.org/10.1007/s12041-019-1110-5openalex-snapshot
Association between the SNPs in trace element-related metabolic genes and the risk of gastric cancer: a case–control study in Xianyou of China
inferred← citeshttps://doi.org/10.1007/s13258-015-0342-xopenalex-snapshot
Survey of computational haplotype determination methods for single individual
inferred← citeshttps://doi.org/10.1007/s13277-013-0823-yopenalex-snapshot
The potential effect of gender in CYP1A1 and GSTM1 genotype-specific associations with pediatric brain tumor
inferred← citeshttps://doi.org/10.1007/s13277-013-1351-5openalex-snapshot
Haplotype analysis of RECQL5 gene and laryngeal cancer
inferred← citeshttps://doi.org/10.1007/s13277-014-2528-2openalex-snapshot
Association between RECQL5 genetic polymorphisms and susceptibility to breast cancer
inferred← citeshttps://doi.org/10.1007/s13353-012-0129-6openalex-snapshot
Association of IGF1 and KDM5A polymorphisms with performance, fatness and carcass traits in chickens
inferred← citeshttps://doi.org/10.1007/s40865-023-00239-wopenalex-snapshot
Impact of Family Violence on Antisocial Behaviors in Two Developmental Periods: the Investigation of the Moderating Role of a Haplotypic Serotonergic Polygenic Score
inferred← citeshttps://doi.org/10.1016/b978-0-12-816473-0.00005-0openalex-snapshot
Molecular Marker–Assisted Selective Breeding of Largemouth Bass
inferred← citeshttps://doi.org/10.1016/j.ab.2014.08.021openalex-snapshot
Haplotyping using a combination of polymerase chain reaction–single-strand conformational polymorphism analysis and haplotype-specific PCR amplification
inferred← citeshttps://doi.org/10.1016/j.ajhg.2007.11.004openalex-snapshot
Simple and Efficient Analysis of Disease Association with Missing Genotype Data
inferred← citeshttps://doi.org/10.1016/j.amjhyper.2004.07.010openalex-snapshot
An association study in essential hypertension using functional polymorphisms in lymphotoxin-? gene
inferred← citeshttps://doi.org/10.1016/j.amjhyper.2005.11.015openalex-snapshot
Association Study Between C-Reactive Protein Genes and Ischemic Stroke in Japanese Subjects
inferred← citeshttps://doi.org/10.1016/j.amjhyper.2006.06.008openalex-snapshot
Association Between the Calcitonin-Related Peptide α (CALCA) Gene and Essential Hypertension in Japanese Subjects
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2022.105565openalex-snapshot
Association between genetic polymorphisms in the melatonin receptor type 1 A gene and sleep bruxism
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.01.119openalex-snapshot
Association of the ABCA1 gene polymorphisms with type 2 DM in a Japanese population
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.10.180openalex-snapshot
Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese population
inferred← citeshttps://doi.org/10.1016/j.bjoms.2014.06.003openalex-snapshot
Association study of single nucleotide polymorphisms of MAFB with non-syndromic cleft lip with or without cleft palate in a population in Heilongjiang Province, northern China
inferred← citeshttps://doi.org/10.1016/j.cca.2010.06.009openalex-snapshot
Identification of a novel IRGM promoter single nucleotide polymorphism associated with tuberculosis
inferred← citeshttps://doi.org/10.1016/j.clim.2011.02.013openalex-snapshot
Analysis of the 8.1 ancestral MHC haplotype in severe, pneumonia-related sepsis
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2009.07.016openalex-snapshot
Haplotype-based case–control study between human apurinic/apyrimidinic endonuclease 1/redox effector factor-1 gene and cerebral infarction
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2012.12.021openalex-snapshot
A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men
inferred← citeshttps://doi.org/10.1016/j.ejca.2010.04.020openalex-snapshot
Polymorphisms in the adenomatous polyposis coli (APC) gene and advanced colorectal adenoma risk
inferred← citeshttps://doi.org/10.1016/j.fsi.2014.04.009openalex-snapshot
A new anti-lipopolysaccharide factor (ALF) gene with its SNP polymorphisms related to WSSV-resistance of Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.gene.2012.04.047openalex-snapshot
Association of polymorphisms of endothelial nitric oxide synthase (eNOS) gene with the risk of primary open angle glaucoma in a Brazilian population
inferred← citeshttps://doi.org/10.1016/j.gene.2013.04.013openalex-snapshot
Haplotypes and effects on growth traits of bovine Wnt7a gene in Chinese Qinchuan cattle
inferred← citeshttps://doi.org/10.1016/j.gene.2013.11.046openalex-snapshot
Association analysis of bovine Foxa2 gene single sequence variant and haplotype combinations with growth traits in Chinese cattle
inferred← citeshttps://doi.org/10.1016/j.gene.2014.03.001openalex-snapshot
Identification of bovine NPC1 gene cSNPs and their effects on body size traits of Qinchuan cattle
inferred← citeshttps://doi.org/10.1016/j.gene.2015.03.016openalex-snapshot
Haplotype combination of the bovine CFL2 gene sequence variants and association with growth traits in Qinchuan cattle
inferred← citeshttps://doi.org/10.1016/j.gene.2018.05.073openalex-snapshot
Genetic variants of fatty acid elongase 6 in Chinese Holstein cow
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148816openalex-snapshot
Association of adiponectin gene single nucleotide polymorphisms with environmental risk factors in type 2 diabetes mellitus: An updated evidence of haplotype-based analysis study
inferred← citeshttps://doi.org/10.1016/j.humimm.2016.05.003openalex-snapshot
Polymorphisms and haplotypes of the chromosome locus 17q12-17q21.1 contribute to adult asthma susceptibility in Slovenian patients
inferred← citeshttps://doi.org/10.1016/j.jad.2020.03.059openalex-snapshot
Age-dependent association of polymorphisms in the promoter and 5′-untranslated region of the norepinephrine transporter gene with generalized anxiety disorder
inferred← citeshttps://doi.org/10.1016/j.jkss.2008.10.001openalex-snapshot
Discussion: Why do we test multiple traits in genetic association studies?
inferred← citeshttps://doi.org/10.1016/j.jkss.2008.10.008openalex-snapshot
Discussion: Why do we test multiple traits in genetic association studies
inferred← citeshttps://doi.org/10.1016/j.mcp.2015.09.007openalex-snapshot
Associations between allelic polymorphism of the BMP Binding Endothelial Regulator and phenotypic variation of cattle
inferred← citeshttps://doi.org/10.1016/j.meegid.2015.11.031openalex-snapshot
SFRP1 variations influence susceptibility and immune response to Mycobacterium tuberculosis in a Chinese Han population
inferred← citeshttps://doi.org/10.1016/j.meegid.2019.103970openalex-snapshot
Association of LEPR polymorphisms with predisposition and inflammatory response in anti-tuberculosis drug-induced liver injury: A pilot prospective investigation in Western Chinese Han population
inferred← citeshttps://doi.org/10.1016/j.metabol.2006.12.014openalex-snapshot
Lack of association of CPT1A polymorphisms or haplotypes on hepatic lipid content or insulin resistance in Japanese individuals with type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1016/j.mgene.2018.10.006openalex-snapshot
Significant associations between prolactin gene polymorphisms and growth traits in the channel catfish (Ictalurus punctatus Rafinesque, 1818) core breeding population
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2018.05.021openalex-snapshot
The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2012.10.056openalex-snapshot
Corticotropin-releasing hormone system polymorphisms are associated with children’s cortisol reactivity
inferred← citeshttps://doi.org/10.1016/j.numecd.2005.07.002openalex-snapshot
P-selectin gene genotypes or haplotypes and cardiovascular complications in type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1016/j.numecd.2014.02.007openalex-snapshot
PPARα gene polymorphisms modulate the association between physical activity and cardiometabolic risk
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112129openalex-snapshot
Haplotype-based breeding: A new insight in crop improvement
inferred← citeshttps://doi.org/10.1016/j.preghy.2017.11.010openalex-snapshot
Transforming growth factor beta 1 related gene polymorphisms in gestational hypertension and preeclampsia: A case-control candidate gene association study
inferred← citeshttps://doi.org/10.1016/j.schres.2007.03.007openalex-snapshot
A Case-control association study between the GRID1 gene and schizophrenia in the Chinese Northern Han population
inferred← citeshttps://doi.org/10.1016/j.taap.2018.04.034openalex-snapshot
Adiponectin gene polymorphisms and obesity increase the susceptibility to arsenic-related renal cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.trim.2005.03.015openalex-snapshot
Strategies in analysis of the genetic component of multifactorial diseases; biostatistical aspects
inferred← citeshttps://doi.org/10.1016/j.vaccine.2009.01.080openalex-snapshot
HLA haplotype and supertype associations with cellular immune responses and cytokine production in healthy children after rubella vaccine
inferred← citeshttps://doi.org/10.1016/j.ygeno.2018.11.028openalex-snapshot
Genetic variants and haplotype combination in the bovine CRTC3 affected conformation traits in two Chinese native cattle breeds (Bos Taurus)
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)01479-7openalex-snapshot
Estrogen receptor α and vitamin D receptor gene polymorphisms and bone mineral density: association study of healthy pre- and postmenopausal Chinese women
inferred← citeshttps://doi.org/10.1016/s0040-5809(03)00084-4openalex-snapshot
The loss of statistical power to distinguish populations when certain samples are ambiguous
inferred← citeshttps://doi.org/10.1016/s0065-2660(07)00414-2openalex-snapshot
Haplotype‐Association Analysis
inferred← citeshttps://doi.org/10.1016/s0065-2660(07)00415-4openalex-snapshot
Characterization of LD Structures and the Utility of HapMap in Genetic Association Studies
inferred← citeshttps://doi.org/10.1016/s0167-5273(08)70286-9openalex-snapshot
P375 Haplotype-based case study of human CYP4A11 gene and cerebral infarction in Japanese subjects
inferred← citeshttps://doi.org/10.1017/neu.2015.70openalex-snapshot
Association between AUTS2 haplotypes and alcohol dependence in a Japanese population
inferred← citeshttps://doi.org/10.1017/s095457941600105xopenalex-snapshot
The interactive effects of child maltreatment and the FK506 binding protein 5 gene (FKBP5) on dissociative symptoms in adolescence
inferred← citeshttps://doi.org/10.1038/ajh.2008.276openalex-snapshot
A Haplotype of the CYP4F2 Gene is Associated With Cerebral Infarction in Japanese Men
inferred← citeshttps://doi.org/10.1038/ajh.2009.221openalex-snapshot
Haplotype-Based Case-Control Study on Human Apurinic/Apyrimidinic Endonuclease 1/Redox Effector Factor-1 Gene and Essential Hypertension
inferred← citeshttps://doi.org/10.1038/aps.2012.69openalex-snapshot
Association between fibroblast growth factor 7 and the risk of chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.1038/ejhg.2009.7openalex-snapshot
Joint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power
inferred← citeshttps://doi.org/10.1038/hr.2009.136openalex-snapshot
Purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene is associated with cerebral infarction in Japanese subjects
inferred← citeshttps://doi.org/10.1038/jhg.2009.85openalex-snapshot
pHCR: a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis
inferred← citeshttps://doi.org/10.1038/jhg.2014.48openalex-snapshot
Genetic variations in RORα are associated with chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.1038/jhh.2009.67openalex-snapshot
The purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene associated with essential hypertension in Japanese men
inferred← citeshttps://doi.org/10.1038/jhh.2016.96openalex-snapshot
Haplotype-based, case–control study of the receptor (calcitonin) activity-modifying protein (RAMP) 1 gene in essential hypertension
inferred← citeshttps://doi.org/10.1038/nrd2519openalex-snapshot
Genome-wide association studies: progress and potential for drug discovery and development
inferred← citeshttps://doi.org/10.1038/s10038-022-01079-0openalex-snapshot
Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia
inferred← citeshttps://doi.org/10.1038/s41431-018-0334-9openalex-snapshot
Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia
inferred← citeshttps://doi.org/10.1038/s42003-021-02782-yopenalex-snapshot
Features and applications of haplotypes in crop breeding
inferred← citeshttps://doi.org/10.1038/sj.ejhg.5201234openalex-snapshot
Accurate determination of microsatellite allele frequencies in pooled DNA samples
inferred← citeshttps://doi.org/10.1038/sj.jhh.1001943openalex-snapshot
A haplotype in the human Sur2 gene is associated with essential hypertension
inferred← citeshttps://doi.org/10.1038/sj.mp.4001505openalex-snapshot
Molecular genetics of autism spectrum disorder
inferred← citeshttps://doi.org/10.1042/cs20050323openalex-snapshot
Searching for genetic clues to the causes of pre-eclampsia
inferred← citeshttps://doi.org/10.1046/j.1529-8817.2005.00168.xopenalex-snapshot
A Haplotype Similarity Based Transmission/Disequilibrium Test under Founder Heterogeneity
inferred← citeshttps://doi.org/10.1073/pnas.0404730102openalex-snapshot
gerbil : Genotype resolution and block identification using likelihood
inferred← citeshttps://doi.org/10.1080/03610920802696588openalex-snapshot
Modeling Informatively Missing Genotypes in Haplotype Analysis
inferred← citeshttps://doi.org/10.1080/10495398.2016.1271805openalex-snapshot
Combined Haplotypes of CaSR Gene Sequence Variants and Their Associations with Growth Traits in Cattle
inferred← citeshttps://doi.org/10.1080/10495398.2020.1769117openalex-snapshot
The polymorphism of bovine Cofilin-1 gene sequence variants and association analysis with growth traits in Qinchuan cattle
inferred← citeshttps://doi.org/10.1080/20008066.2023.2219075openalex-snapshot
Effects of prenatal exposure to the 1944–45 Dutch famine and glucocorticoid receptor polymorphisms on later life PTSD susceptibility
inferred← citeshttps://doi.org/10.1086/346117openalex-snapshot
Hierarchical Modeling of Linkage Disequilibrum: Genetic Structure and Spatial Relations
inferred← citeshttps://doi.org/10.1086/380204openalex-snapshot
Inference on Haplotype Effects in Case-Control Studies Using Unphased Genotype Data
inferred← citeshttps://doi.org/10.1086/383251openalex-snapshot
A Simple Correction for Multiple Testing for Single-Nucleotide Polymorphisms in Linkage Disequilibrium with Each Other
inferred← citeshttps://doi.org/10.1086/424390openalex-snapshot
A Powerful Strategy to Account for Multiple Testing in the Context of Haplotype Analysis
inferred← citeshttps://doi.org/10.1086/498175openalex-snapshot
The Effect of Single-Nucleotide Polymorphism Marker Selection on Patterns of Haplotype Blocks and Haplotype Frequency Estimates
inferred← citeshttps://doi.org/10.1086/507317openalex-snapshot
A Fast Method for Computing High-Significance Disease Association in Large Population-Based Studies
inferred← citeshttps://doi.org/10.1086/513205openalex-snapshot
Association Mapping via Regularized Regression Analysis of Single-Nucleotide–Polymorphism Haplotypes in Variable-Sized Sliding Windows
inferred← citeshttps://doi.org/10.1086/518670openalex-snapshot
Identification of Risk-Related Haplotypes with the Use of Multiple SNPs from Nuclear Families
inferred← citeshttps://doi.org/10.1089/cmb.2005.12.1243openalex-snapshot
A Block-Free Hidden Markov Model for Genotypes and Its Application to Disease Association
inferred← citeshttps://doi.org/10.1089/cmb.2011.0167openalex-snapshot
Haplotype Reconstruction in Large Pedigrees with Untyped Individuals through IBD Inference
inferred← citeshttps://doi.org/10.1089/dna.2010.1126openalex-snapshot
Association of PTEN Polymorphisms with Susceptibility to Hepatocellular Carcinoma in a Han Chinese Population
inferred← citeshttps://doi.org/10.1089/gtmb.2012.0034openalex-snapshot
A Haplotype of the SMTN Gene Associated with Myocardial Infarction in Japanese Women
inferred← citeshttps://doi.org/10.1089/gtmb.2012.0379openalex-snapshot
A Haplotype of the GOSR2 Gene Is Associated with Myocardial Infarction in Japanese Men
inferred← citeshttps://doi.org/10.1089/gtmb.2013.0434openalex-snapshot
Haplotype Analysis of the XRCC1 Gene and Laryngeal Cancer
inferred← citeshttps://doi.org/10.1093/bib/bbu050openalex-snapshot
Detecting associations of rare variants with common diseases: collapsing or haplotyping?
inferred← citeshttps://doi.org/10.1093/bib/bbv072openalex-snapshot
Comparison of haplotype-based statistical tests for disease association with rare and common variants
inferred← citeshttps://doi.org/10.1093/bib/bbz031openalex-snapshot
Comparison of haplotype-based tests for detecting gene–environment interactions with rare variants
inferred← citeshttps://doi.org/10.1093/bioinformatics/bti1021openalex-snapshot
Tag SNP selection in genotype data for maximizing SNP prediction accuracy
inferred← citeshttps://doi.org/10.1093/bioinformatics/btm371openalex-snapshot
Haplotype inference for present–absent genotype data using previously identified haplotypes and haplotype patterns
inferred← citeshttps://doi.org/10.1093/bioinformatics/btm435openalex-snapshot
H aplo P ool : improving haplotype frequency estimation through DNA pools and phylogenetic modeling
inferred← citeshttps://doi.org/10.1093/biostatistics/kxj021openalex-snapshot
Efficient semiparametric estimation of haplotype-disease associations in case-cohort and nested case-control studies
inferred← citeshttps://doi.org/10.1093/biostatistics/kxp023openalex-snapshot
SHARE: an adaptive algorithm to select the most informative set of SNPs for candidate genetic association
inferred← citeshttps://doi.org/10.1093/carcin/bgl198openalex-snapshot
The mannose-binding lectin (MBL2) haplotype and breast cancer: an association study in African-American and Caucasian women
inferred← citeshttps://doi.org/10.1093/hmg/ddn439openalex-snapshot
Expansion of the human μ-opioid receptor gene architecture: novel functional variants
inferred← citeshttps://doi.org/10.1093/nar/gkl742openalex-snapshot
An efficient method for multi-locus molecular haplotyping
inferred← citeshttps://doi.org/10.1093/ps/85.2.178openalex-snapshot
Single Marker and Haplotype Analysis of the Chicken Apolipoprotein B Gene T123G and D9500D9- Polymorphism Reveals Association with Body Growth and Obesity
inferred← citeshttps://doi.org/10.1093/ps/85.6.980openalex-snapshot
Association of Single Nucleotide Polymorphisms of the Insulin Gene with Chicken Early Growth and Fat Deposition
inferred← citeshttps://doi.org/10.1094/phyto-02-15-0051-ropenalex-snapshot
Association Analysis for Bacterial Spot Resistance in a Directionally Selected Complex Breeding Population of Tomato
inferred← citeshttps://doi.org/10.1097/01.ccm.0000251121.24451.76openalex-snapshot
Genetic risk factors for acute respiratory distress syndrome: Whatʼs the right direction to take?*
inferred← citeshttps://doi.org/10.1097/01.ccm.0000256845.92640.38openalex-snapshot
Inhibitor κB-α haplotype GTC is associated with susceptibility to acute respiratory distress syndrome in Caucasians*
inferred← citeshttps://doi.org/10.1097/01.hjh.0000125429.28861.58openalex-snapshot
Angiotensinogen promoter haplotypes are associated with blood pressure in untreated hypertensives
inferred← citeshttps://doi.org/10.1097/01.hjh.0000163144.74588.adopenalex-snapshot
Influence of the endothelial nitric oxide synthase gene on conventional and ambulatory blood pressure: sib-pair analysis and haplotype study
inferred← citeshttps://doi.org/10.1097/hjh.0b013e3282f2f10copenalex-snapshot
A haplotype of the CYP4A11 gene associated with essential hypertension in Japanese men
inferred← citeshttps://doi.org/10.1097/md.0000000000015090openalex-snapshot
The role of ERCC1 and AFP gene polymorphism in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1101/2020.12.04.20244251openalex-snapshot
Retrospective analysis of The Two Sister Study using haplotype-based association testing to identify loci associated with early-onset breast cancer
inferred← citeshttps://doi.org/10.1101/2024.11.18.24317486openalex-snapshot
Leveraging hierarchical structures for genetic block interaction studies using the hierarchical transformer
inferred← citeshttps://doi.org/10.1101/gr.2204604openalex-snapshot
Haplotype and Missing Data Inference in Nuclear Families
inferred← citeshttps://doi.org/10.1101/pdb.top96openalex-snapshot
Family-Based Genetic Association Tests
inferred← citeshttps://doi.org/10.1109/icece.2010.561openalex-snapshot
The Comparison of Haplotype Difference Based on the 21st Chromosome of Four Populations
inferred← citeshttps://doi.org/10.1111/age.12489openalex-snapshot
Effect of swine leukocyte antigen‐ DQA gene variation on diarrhea in Large White, Landrace, and Duroc piglets
inferred← citeshttps://doi.org/10.1111/age.12805openalex-snapshot
Genome‐wide association study reveals candidate genes associated with body measurement traits in Chinese Wagyu beef cattle
inferred← citeshttps://doi.org/10.1111/iji.12667openalex-snapshot
IKZF1 rs4132601 and rs11978267 gene polymorphisms and paediatric systemic lupus erythematosus; relation to lupus nephritis
inferred← citeshttps://doi.org/10.1111/j.1365-2052.2011.02234.xopenalex-snapshot
Optimal use of regression models in genome‐wide association studies
inferred← citeshttps://doi.org/10.1111/j.1439-0388.2008.00783.xopenalex-snapshot
Analysis of Relationship between Bovine Lymphocyte Antigen DRB3.2 Alleles, Somatic Cell Count and milk Traits in Iranian Holstein Population
inferred← citeshttps://doi.org/10.1111/j.1469-1809.2006.00306.xopenalex-snapshot
Two‐sample Comparison Based on Prediction Error, with Applications to Candidate Gene Association Studies
inferred← citeshttps://doi.org/10.1111/j.1469-1809.2009.00543.xopenalex-snapshot
A Variable‐Sized Sliding‐Window Approach for Genetic Association Studies via Principal Component Analysis
inferred← citeshttps://doi.org/10.1111/j.1469-1809.2010.00593.xopenalex-snapshot
Haplotype Misclassification Resulting from Statistical Reconstruction and Genotype Error, and Its Impact on Association Estimates
inferred← citeshttps://doi.org/10.1111/j.1469-1809.2012.00715.xopenalex-snapshot
A Unified Framework for Haplotype Inference in Nuclear Families
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2005.00193.xopenalex-snapshot
Using Tree‐Based Recursive Partitioning Methods to Group Haplotypes for Increased Power in Association Studies
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2005.00198.xopenalex-snapshot
Multiple Testing in the Context of Haplotype Analysis Revisited: Application to Case‐Control Data
inferred← citeshttps://doi.org/10.1111/j.1530-0277.2011.01623.xopenalex-snapshot
Cannabinoid Receptor 1 Gene is Associated with Alcohol Dependence
inferred← citeshttps://doi.org/10.1111/j.1541-0420.2010.01454.xopenalex-snapshot
Unbiased and Locally Efficient Estimation of Genetic Effect on Quantitative Trait in the Presence of Population Admixture
inferred← citeshttps://doi.org/10.1111/j.1601-183x.2006.00296.xopenalex-snapshot
RhoA, encoding a Rho GTPase, is associated with smoking initiation
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2008.02086.xopenalex-snapshot
Association of extracellular superoxide dismutase gene with cerebral infarction in women: a haplotype-based case-control study
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2009.02115.xopenalex-snapshot
The haplotype of the CACNA1B gene associated with cerebral infarction in a Japanese population
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2010.02174.xopenalex-snapshot
Association of the insulin-like growth factor1 gene with myocardial infarction in Japanese subjects
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2012.02242.xopenalex-snapshot
Haplotype of smoothelin gene associated with essential hypertension
inferred← citeshttps://doi.org/10.1111/j.1601-5223.2012.02247.xopenalex-snapshot
Haplotype-based case-control study of CYP4A11 gene and myocardial infarction
inferred← citeshttps://doi.org/10.1111/odi.12564openalex-snapshot
Genetic determinants and postorthodontic external apical root resorption in Czech children
inferred← citeshttps://doi.org/10.1111/pbr.12773openalex-snapshot
Single‐marker and haplotype‐based association analysis of anthracnose (Colletotrichum dematium)resistance in spinach (Spinacia oleracea)
showing the first 200 of 346 · page through all 346
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.