Lista de obras - Alexander F Wilson - Dominio Público Uruguay

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 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.

artículo científico publicado en 2006

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

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2005

CHD7 Gene Polymorphisms and Familial Idiopathic Scoliosis ⬇️

artículo científico publicado el 15 de octubre de 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 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

artículo científico publicado en 2003

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

artículo científico publicado en 2003

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

artículo científico publicado en 2017

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

artículo científico publicado en 2005

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

artículo científico publicado en 2016

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

artículo científico publicado en 2003

Functional linear models for association analysis of quantitative traits

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2018

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

artículo científico publicado en 2014

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

artículo científico publicado en 2021

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

artículo científico publicado en 2009

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

artículo científico publicado el 13 de noviembre de 2012

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

artículo científico publicado en 2006

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

artículo científico publicado en 2012

Linkage analysis in the next-generation sequencing era

artículo científico publicado en 2011

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

artículo científico publicado en 2011

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2006

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

artículo científico publicado en 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

artículo científico publicado en 2013

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

artículo científico publicado en 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 ⬇️

artículo científico publicado en 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

artículo científico publicado en 2016

Lista de obras de Alexander F Wilson

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

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

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

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

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

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

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

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

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

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

CHD7 Gene Polymorphisms and Familial Idiopathic Scoliosis ⬇️

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

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

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

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

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

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

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

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

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

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

Functional linear models for association analysis of quantitative traits

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

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

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

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

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

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

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

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

Linkage analysis in the next-generation sequencing era

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

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

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

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

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

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

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

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

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

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

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