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List of works by Alexander F Wilson

A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin

scientific article published on 26 April 2016

A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits

scientific article published on 4 July 2016

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

scientific article

A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing

scientific article published on 5 December 2016

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

scientific journal article

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q.

scientific article published on 14 June 2006

A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability

scientific article published on 29 May 2008

A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element

article by Cristina M Justice et al published November 2017 in American Journal of Medical Genetics

Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment

scientific article published on 20 April 2006

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

scientific article

CHD7 Gene Polymorphisms and Familial Idiopathic Scoliosis ⬇️

scientific article published on October 15, 2013

ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available

scientific article published on 18 October 2018

Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults

scientific article published on 13 May 2015

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression

scientific article

Comparison of sib-pair and variance-components methods for genomic screening

scientific article published on 01 January 1997

Comparison of sib‐pair and variance‐components methods for genomic screening

Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data

scientific article

Correlates of sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus in asthma in Barbados

scientific article published on June 2003

Cover Image, Volume 173A, Number 11, November 2017.

scientific article published in November 2017

Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method

scientific article published on 30 December 2005

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis

scientific article published on 13 April 2016

Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus

scientific article published in March 2003

Functional linear models for association analysis of quantitative traits

scientific article

Generalized functional linear models for gene-based case-control association studies

scientific article

Genetic associations with childhood brain growth, defined in two longitudinal cohorts.

scientific article published on 22 April 2018

Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis

scientific article

Gene‐based analysis of bi‐variate survival traits via functional regressions with applications to eye diseases

scientific article published in 2021

Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity

scientific article

Intra-Familial Tests of Association between Familial Idiopathic Scoliosis and Linked Regions on 9q31.3–q34.3 and 16p12.3–q22.2 ⬇️

scientific article published on November 13, 2012

Lack of association between the aggrecan gene and familial idiopathic scoliosis.

scientific article

Linear mixed models for association analysis of quantitative traits with next-generation sequencing data

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

scientific article

Linkage analysis in the next-generation sequencing era

scientific article

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

scientific article (publication date: 29 November 2011)

Performance of random forests and logic regression methods using mini-exome sequence data

scientific article

Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models

scientific article

Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses

scientific article published on 24 October 2006

Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods

scientific article published on 20 August 2003

Society for Social Medicine and the International Epidemiological Association European Group. Abstracts of oral presentations

article

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

scientific article

The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine

scientific article published on 14 July 2009

The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation ⬇️

scientific article published on 12 October 2017

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

scholarly article published November 2015

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

scientific article

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