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 …
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 …
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 …
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
Haplotypes are often critical for the interpretation of genetic laboratory observations into
medically actionable findings. Current massively parallel DNA sequencing technologies …
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 …
Autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and
obsessive-compulsive disorder (OCD) have been associated with difficulties recognizing 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, …
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
BACKGROUND: The Personal Genome Project Canada is a comprehensive public data
resource that integrates whole genome sequencing data and health information. We describe …
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 …
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
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 …
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 …
diagnosing inherited diseases, particularly in children. However, usage of sequencing data as a …