Pages that link to "Q64481879"

The following pages link to Alexander F Wilson (Q64481879):

Displaying 46 items.

• Linkage analysis in the next-generation sequencing era (Q24289003) (← links)
• Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models (Q28647065) (← links)
• Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data (Q28731717) (← links)
• A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9 (Q28943389) (← links)
• Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease (Q30447248) (← links)
• Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data (Q30907371) (← links)
• Application of the regression of offspring on mid-parent method to detect associations between single-nucleotide polymorphisms and the beta 2 electroencephalogram phenotype in the COGA data (Q31031557) (← links)
• Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method (Q33232801) (← links)
• Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment (Q33240074) (← links)
• A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q. (Q33246792) (← links)
• A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease (Q33596843) (← links)
• Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity (Q33835653) (← links)
• Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2. (Q34009591) (← links)
• Performance of random forests and logic regression methods using mini-exome sequence data (Q34177469) (← links)
• Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression (Q34177512) (← links)
• Functional linear models for association analysis of quantitative traits (Q34180342) (← links)
• Generalized functional linear models for gene-based case-control association studies (Q34307663) (← links)
• Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association (Q34319603) (← links)
• Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis (Q34350807) (← links)
• Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults (Q35775152) (← links)
• Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods (Q36226162) (← links)
• A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin (Q36891149) (← links)
• Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis (Q36958180) (← links)
• A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability (Q37336145) (← links)
• The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine (Q37363150) (← links)
• CHD7 gene polymorphisms and familial idiopathic scoliosis (Q37438133) (← links)
• A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing (Q39131328) (← links)
• Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods (Q39211782) (← links)
• Correlates of sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus in asthma in Barbados (Q39211788) (← links)
• A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits (Q39635492) (← links)
• Joan Bailey-Wilson (Q42113803) (← links)
• The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation (Q46114907) (← links)
• Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus (Q48028860) (← links)
• Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses (Q48486946) (← links)
• Genetic associations with childhood brain growth, defined in two longitudinal cohorts. (Q52570860) (← links)
• Cover Image, Volume 173A, Number 11, November 2017. (Q52934299) (← links)
• Lack of association between the aggrecan gene and familial idiopathic scoliosis. (Q54598714) (← links)
• A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element (Q56265298) (← links)
• Society for Social Medicine and the International Epidemiological Association European Group. Abstracts of oral presentations (Q57954085) (← links)
• The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population (Q58585833) (← links)
• ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available (Q58596534) (← links)
• Linear mixed models for association analysis of quantitative traits with next-generation sequencing data (Q62772008) (← links)
• Tiled regression reduces type I error rates in tests of association of rare single nucleotide variants with non-normally distributed traits, compared with simple linear regression (Q62772054) (← links)
• Comparison of sib-pair and variance-components methods for genomic screening (Q62772340) (← links)
• Comparison of sib‐pair and variance‐components methods for genomic screening (Q62772348) (← links)
• Gene‐based analysis of bi‐variate survival traits via functional regressions with applications to eye diseases (Q115242767) (← links)