RAG-1 sequences resolve phylogenetic relationships within Charadriiform birds

TA Paton, AJ Baker, JG Groth… - Molecular phylogenetics …, 2003 - Elsevier
The Charadriiformes is a large and diverse order of shorebirds currently classified into 19
families, including morphologically aberrant forms that are of uncertain phylogenetic …

Phylogenetic relationships and divergence times of Charadriiformes genera: multigene evidence for the Cretaceous origin of at least 14 clades of shorebirds

AJ Baker, SL Pereira, TA Paton - Biology letters, 2007 - royalsocietypublishing.org
Comparative study of character evolution in the shorebirds is presently limited because the
phylogenetic placement of some enigmatic genera remains unclear. We therefore used …

Sequences from 14 mitochondrial genes provide a well-supported phylogeny of the Charadriiform birds congruent with the nuclear RAG-1 tree

TA Paton, AJ Baker - Molecular Phylogenetics and Evolution, 2006 - Elsevier
Because of the difficulties of constructing a robust phylogeny for Charadriiform birds using
morphological characters, recent studies have turned to DNA sequences to resolve the …

[HTML][HTML] Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes

R Ammar, TA Paton, D Torti, A Shlien, GD Bader - F1000Research, 2015 - ncbi.nlm.nih.gov
Haplotypes are often critical for the interpretation of genetic laboratory observations into
medically actionable findings. Current massively parallel DNA sequencing technologies …

[HTML][HTML] Structural neuroimaging correlates of social deficits are similar in autism spectrum disorder and attention-deficit/hyperactivity disorder: analysis from the POND …

DA Baribeau, A Dupuis, TA Paton, C Hammill… - Translational …, 2019 - nature.com
Autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and
obsessive-compulsive disorder (OCD) have been associated with difficulties recognizing and …

Whole-exome sequencing and targeted copy number analysis in primary ciliary dyskinesia

…, MA Zariwala, L Lau, TA Paton… - G3: Genes …, 2015 - academic.oup.com
Primary ciliary dyskinesia (PCD) is an autosomal-recessive disorder resulting from loss of
normal ciliary function. Symptoms include neonatal respiratory distress, chronic sinusitis, …

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

…, I Cohn, N Sondheimer, RKC Yuen, B Trost, TA Paton… - Cmaj, 2018 - Can Med Assoc
BACKGROUND: The Personal Genome Project Canada is a comprehensive public data
resource that integrates whole genome sequencing data and health information. We describe …

Assessment of the implementation of pharmacogenomic testing in a pediatric tertiary care setting

…, RK Jobling, K Kalbfleisch, TA Paton… - JAMA network …, 2021 - jamanetwork.com
Importance Pharmacogenomic (PGx) testing provides preemptive pharmacotherapeutic
guidance regarding the lack of therapeutic benefit or adverse drug reactions of PGx targeted …

[HTML][HTML] Oxytocin receptor polymorphisms are differentially associated with social abilities across neurodevelopmental disorders

DA Baribeau, A Dupuis, TA Paton, SW Scherer… - Scientific Reports, 2017 - nature.com
Oxytocin is a pituitary neuropeptide that affects social behaviour. Single nucleotide
polymorphisms (SNPs) in the oxytocin receptor gene (OXTR) have been shown to explain some …

[HTML][HTML] Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study

I Cohn, TA Paton, CR Marshall, R Basran… - npj Genomic …, 2017 - nature.com
Whole-genome sequencing and whole-exome sequencing have proven valuable for
diagnosing inherited diseases, particularly in children. However, usage of sequencing data as a …