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List of works by Colin J. Ross

A Novel Mouse Model for Pyridoxine-Dependent Epilepsy Due to Antiquitin Deficiency

scientific article published on 24 September 2020

A Tetra-Primer Amplification Refractory System Technique for the Cost-Effective and Novel Genotyping of Eight Single-Nucleotide Polymorphisms of the Catechol-O-Methyltransferase Gene

article

A case of splenomegaly in CBL syndrome

scientific article

A case study of comorbidities: vocal cord dysfunction, asthma, and panic disorder

scientific article published in August 2002

A clinical tool for reducing central nervous system depression among neonates exposed to codeine through breast milk.

scientific article

A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder

scientific article published in August 2017

A girl with developmental delay, ataxia, cranial nerve palsies, severe respiratory problems in infancy-Expanding NDST1 syndrome.

scientific article

A pharmacogenetic signature of high response to Copaxone in late-phase clinical-trial cohorts of multiple sclerosis.

scientific article

A prospective study to explore the relationship between MTHFR C677T genotype, physiological folate levels, and postpartum psychopathology in at-risk women

scientific article published on 14 December 2020

A single bout of high-intensity aerobic exercise facilitates response to paired associative stimulation and promotes sequence-specific implicit motor learning.

scientific article

A systematic review of the effects of CYP2D6 phenotypes on risperidone treatment in children and adolescents

scientific article published on 16 July 2018

AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset

scientific article published on 24 June 2014

Acute hypertriglyceridemic pancreatitis during pregnancy due to homozygous lipoprotein lipase gene mutation

article

Adverse drug reaction active surveillance: developing a national network in Canada's children's hospitals.

scientific article

Age and alcoholism

scientific article published in June 1971

Alterations of plasma lipids in mice via adenoviral-mediated hepatic overexpression of human ABCA1.

scientific article published on May 2003

Amelioration of Hypertriglyceridemia with Hypo-Alpha-Cholesterolemia in LPL Deficient Mice by Hematopoietic Cell-Derived LPL ⬇️

scientific article published on September 29, 2011

An initial health economic evaluation of pharmacogenomic testing in patients treated for childhood cancer with anthracyclines.

scientific article published on 22 December 2017

An investigation of the glycosaminoglycan contribution to biaxial mechanical behaviours of porcine atrioventricular heart valve leaflets

scientific article published on 03 July 2019

Analyses of Adverse Drug Reactions-Nationwide Active Surveillance Network: Canadian Pharmacogenomics Network for Drug Safety Database

scientific article published on 19 November 2018

Apnea and oxygen desaturations in children treated with opioids after adenotonsillectomy for obstructive sleep apnea syndrome: a prospective pilot study.

scientific article published in December 2012

Application of pharmacogenomics to investigate adverse drug reactions to the disease-modifying treatments for multiple sclerosis: a case-control study protocol for dimethyl fumarate-induced lymphopenia

scientific article published on 2 June 2017

Application of principal component analysis to pharmacogenomic studies in Canada

article

Association Between SLC16A5 Genetic Variation and Cisplatin-Induced Ototoxic Effects in Adult Patients With Testicular Cancer.

scientific article published on 27 April 2017

Association between regulatory advisories and codeine prescribing to postpartum women

scientific article published in May 2015

Atypical cerebral palsy: genomics analysis enables precision medicine

scientific article published on 13 December 2018

Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy

scientific article published on 15 August 2019

Blood culture in the diagnosis of leptospirosis in North Queensland

article

CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelines

scientific article published on 08 November 2018

CYP2D6 polymorphisms and codeine analgesia in postpartum pain management: a pilot study.

scientific article

Cancer pharmacogenomics in children: research initiatives and progress to date.

scientific article published on April 2013

Case-Control Studies Are Not Familial Studies

scientific article

Cases: Cocaine adulterant linked to neutropenia

scientific article

Cellular metabolism constrains innate immune responses in early human ontogeny

scientific article published in Nature Communications

Characterization of microvascularization of liver tumor lesions with high resolution linear ultrasound and contrast enhanced ultrasound (CEUS) during surgery: First results

scientific article published on 01 January 2010

Clinical Practice Recommendations for the Management and Prevention of Cisplatin-Induced Hearing Loss Using Pharmacogenetic Markers

scientific article published on 5 March 2016

Clinical Practice Recommendations on Genetic Testing of CYP2C9 and VKORC1 Variants in Warfarin Therapy

scientific article

Codeine-related deaths: The role of pharmacogenetics and drug interactions

scientific article published on 26 March 2014

Cognitive-Behavioral Treatment Combined With Asthma Education for Adults With Asthma and Coexisting Panic Disorder

scientific article published on 01 May 2005

Common variants of the oxytocin receptor gene do not predict the positive mood benefits of prosocial spending

scientific article published on 25 April 2019

Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis

scientific article published on 16 July 2018

Communicating pharmacogenetic research results to breastfeeding mothers taking codeine: a pilot study of perceptions and benefits.

scientific article

Comparisons of pulmonary artery pressure measurements in supine and 30 degree lateral positions

scientific article published on 01 January 1995

Complete rescue of lipoprotein lipase-deficient mice by somatic gene transfer of the naturally occurring LPLS447X beneficial mutation

scientific article published on 7 July 2005

Correction of feline lipoprotein lipase deficiency with adeno-associated virus serotype 1-mediated gene transfer of the lipoprotein lipase S447X beneficial mutation

scientific article published in May 2006

Corrigendum: NANS-mediated synthesis of sialic acid is required for brain and skeletal development

scientific article published in May 2017

Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis

scientific article

DNAJC13 mutations in Parkinson disease

scientific article (publication date: April 2014)

De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome

scientific article

Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms

scientific article published on 28 March 2015

Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure

scientific article published on 15 January 2019

Delivery of recombinant gene products to the central nervous system with nonautologous cells in alginate microcapsules

scientific article published on January 1999

Design and Methods of the Pan-Canadian Applying Biomarkers to Minimize Long-Term Effects of Childhood/Adolescent Cancer Treatment (ABLE) Nephrotoxicity Study: A Prospective Observational Cohort Study

scientific article published on 16 February 2017

Development of a broad-based ADME panel for use in pharmacogenomic studies

scientific article published on June 2014

Development of a cost-efficient novel method for rapid, concurrent genotyping of five common single nucleotide polymorphisms of the brain derived neurotrophic factor (BDNF) gene by tetra-primer amplification refractory mutation system.

scientific article published on 29 June 2015

Development of small alginate microcapsules for recombinant gene product delivery to the rodent brain

scientific article published on January 2002

Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.

scientific article published on 18 January 2011

Economic impact of a genetic test for cisplatin-induced ototoxicity

scientific article published on 19 April 2011

Editorial Note to:Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

scientific article published on 01 October 2016

Elevated plasma triglyceride levels precede amyloid deposition in Alzheimer's disease mouse models with abundant A beta in plasma

scientific article published on 8 August 2006

Encapsulation of various recombinant mammalian cell types in different alginate microcapsules

scientific article published on December 1998

Enhanced atherothrombotic formation after oxidative injury by FeCl3 to the common carotid artery in severe combined hyperlipidemic mice.

scientific article published on 28 May 2009

Enhanced susceptibility to pancreatitis in severe hypertriglyceridaemic lipoprotein lipase-deficient mice and agonist-like function of pancreatic lipase in pancreatic cells.

scientific article

Exome Sequencing and the Management of Neurometabolic Disorders.

scientific article published on 25 May 2016

Exome sequencing pilot study in children with carbamazepine-induced serious skin reactions

scientific article

Expansion of the QARS deficiency phenotype with report of a family with isolated supratentorial brain abnormalities

scientific article published on 30 November 2014

Exploring genetic influences underlying acute aerobic exercise effects on motor learning.

scientific article

Expression of LPL in Endothelial-Intact Artery Results in Lipid Deposition and Vascular Cell Adhesion Molecule-1 Upregulation in Both LPL and ApoE-Deficient Mice

scientific article published on 12 October 2006

Fatal hydrocodone overdose in a child: pharmacogenetics and drug interactions.

scientific article

Forensic Investigation of Methadone Concentrations in Deceased Breastfed Infants.

scientific article published on 29 October 2015

From mutation identification to therapy: discovery and origins of the first approved gene therapy in the Western world

scientific article

Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy

scientific article

Further investigation of the role of ACYP2 and WFS1 pharmacogenomic variants in the development of cisplatin-induced ototoxicity in testicular cancer patients

scientific article published on 22 January 2018

Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype

scientific article published on 29 May 2018

Gene therapy for lipoprotein lipase deficiency: working toward clinical application

scientific article

Genetic determinants of cocaine-associated agranulocytosis.

scientific article published on 13 June 2015

Genetic diversity of variants involved in drug response and metabolism in Sri Lankan populations: implications for clinical implementation of pharmacogenomics

scientific article

Genetic markers of cisplatin-induced hearing loss in children

scientific article published in September 2014

Genetic variants inSLC22A17 and SLC22A7are associated with anthracycline-induced cardiotoxicity in children

scientific article published on 31 July 2015

Genome sequencing reveals a novel genetic mechanism underlying dihydropyrimidine dehydrogenase deficiency: A novel missense variant c.1700G > A and a large intragenic inversion in DPYD spanning intron 8 to intron 12.

scientific article

Genome-Wide Association Studies of Drug-Induced Liver Injury Make Progress Beyond the HLA Region

scientific article published on 23 July 2019

Genotypic Approaches to Therapy in Children (GATC): using information technology to improve drug safety

scientific article published on 01 January 2009

Genotypic approaches to therapy in children: a national active surveillance network (GATC) to study the pharmacogenomics of severe adverse drug reactions in children.

scientific article

Glucose intolerance and decreased early insulin response in mice with severe hypertriglyceridemia

scientific article published in January 2010

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in

scientific article published on 01 April 2019

HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia

scientific article published on 19 January 2011

HUME: large-scale detection of causal genetic factors of adverse drug reactions

scientific article published on 01 December 2018

Hearing loss in Mexican children treated with cisplatin

scientific article published on 16 June 2014

Hemorheological abnormalities in lipoprotein lipase deficient mice with severe hypertriglyceridemia

scientific article published on 25 January 2006

Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European Ancestry.

scientific article published on 23 July 2015

Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric Vasculitis

scientific article published on 26 August 2019

Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease

scientific article

Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous PAK3 Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome

scientific article published in January 2018

Infant serotonin transporter (SLC6A4) promoter genotype is associated with adverse neonatal outcomes after prenatal exposure to serotonin reuptake inhibitor medications

scientific article published on 22 May 2007

Informational coping styles: a validity study.

scientific article published in January 1995

Instructor comfort level in high-fidelity simulation.

scientific article published on 29 September 2012

Intramuscular administration of AAV1-lipoprotein lipase S447X lowers triglycerides in lipoprotein lipase-deficient patients

scientific article published on 18 September 2008

Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease

scientific article published on 16 May 2019

Les tests pharmacogénomiques: Améliorer le recours personnalisé aux médicaments pour les patients

scientific article published on 01 April 2020

Life-threatening adverse events following therapeutic opioid administration in adults: is pharmacogenetic analysis useful?

scientific article published on May 2013

Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region

scientific article published on 30 November 2020

Lipoprotein lipase S447X: a naturally occurring gain-of-function mutation

scientific article published on 30 March 2006

Long-term correction of murine lipoprotein lipase deficiency with AAV1-mediated gene transfer of the naturally occurring LPL(S447X) beneficial mutation

scientific article published in September 2004

Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes

scientific article

Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood

scientific article published on 13 February 2014

More codeine fatalities after tonsillectomy in North American children

scientific article published on 9 April 2012

Morphine biotransformation genes and neonatal clinical factors predicted behaviour problems in very preterm children at 18 months

article

NANS-mediated synthesis of sialic acid is required for brain and skeletal development

scientific article published on 23 May 2016

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

scientific article

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

scientific article published on 01 October 2016

Of children and liberty: an historian's view

scientific article published on 01 July 1982

Outcome Definition Influences the Relationship Between Genetic Polymorphisms of ERCC1, ERCC2, SLC22A2 and Cisplatin Nephrotoxicity in Adult Testicular Cancer Patients.

scientific article

Output from the CIHR Canadian HIV Trials Network international postdoctoral fellowship for capacity building in HIV clinical trials

article

PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights

scientific article published on 01 March 2019

Paediatric cardio-oncology: epidemiology, screening, prevention, and treatment

scientific article published on 01 April 2019

Perceptions About Self-Management Among People with Severe Asthma

scientific article published on 01 April 2010

Pharmacogenetic variants in TPMT alter cellular responses to cisplatin in inner ear cell lines

scientific article

Pharmacogenetic-based efavirenz dose modification: suggestions for an African population and the different CYP2B6 genotypes

scientific article

Pharmacogenetics of neonatal opioid toxicity following maternal use of codeine during breastfeeding: a case-control study

scientific article

Pharmacogenomic Prediction of Anthracycline-Induced Cardiotoxicity in Children

Pharmacogenomic Variability of Oral Baclofen Clearance and Clinical Response in Children With Cerebral Palsy.

scientific article

Pharmacogenomic diversity in Singaporean populations and Europeans

scientific article

Pharmacogenomic investigation of adverse drug reactions(ADRs): the ADR prioritization tool, APT.

scientific article

Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer.

scientific article published on 19 March 2017

Pharmacogenomic testing: Enhancing personalized medication use for patients

scientific article published on 01 April 2020

Pharmacogenomics and active surveillance for serious adverse drug reactions in children.

scientific article published on September 2010

Pharmacogenomics and its implications for autoimmune disease

scientific article published on 01 March 2007

Pharmacogenomics of Cisplatin-Induced Ototoxicity: Successes, Shortcomings, and Future Avenues of Research

scientific article published on 12 June 2019

Pharmacogenomics of Vincristine-Induced Peripheral Neuropathy Implicates Pharmacokinetic and Inherited Neuropathy Genes.

scientific article

Pharmacogenomics of cardiovascular drugs and adverse effects in pediatrics

scientific article published on September 2011

Pharmacogenomics of serious adverse drug reactions in pediatric oncology.

scientific article published on 21 March 2011

Pharmacogenomics strategies to optimize treatments for multiple sclerosis: Insights from clinical research

scientific article published on 4 March 2016

Pharmacokinetic-Pharmacogenomic Model for Chinese Children treated with Lamotrigine also Applies for Mexican Children

scientific article published on 16 July 2020

Plasma apolipoprotein AV levels in mice are positively associated with plasma triglyceride levels.

scientific article published on 13 January 2009

Postpartum Maternal Codeine Therapy and the Risk of Adverse Neonatal Outcomes

scientific article published on 01 August 2012

Prediction of codeine toxicity in infants and their mothers using a novel combination of maternal genetic markers.

scientific article published on 7 March 2012

Prenatal effects of selective serotonin reuptake inhibitor antidepressants, serotonin transporter promoter genotype (SLC6A4), and maternal mood on child behavior at 3 years of age.

scientific article published in May 2010

Presynaptic defects underlying impaired learning and memory function in lipoprotein lipase-deficient mice.

scientific article published in April 2009

Project head start

scientific article published on 01 May 1980

Promoting Neuroplasticity for Motor Rehabilitation After Stroke: Considering the Effects of Aerobic Exercise and Genetic Variation on Brain-Derived Neurotrophic Factor ⬇️

scientific article published on August 1, 2013

Putative association of ABCB1 2677G>T/A with oxycodone-induced central nervous system depression in breastfeeding mothers

scientific article published on August 2013

RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement

scientific article

Reducing anthracycline-induced cardiotoxicity through pharmacogenetics

scientific article published on 14 September 2018

Response to "evaluation of pharmacogenetic markers to predict the risk of Cisplatin-induced ototoxicity".

scientific article published on 22 April 2014

Rocky Mountain spotted fever; case report and discussion of therapy

scientific article published on March 1947

Role of TPMT and COMT genetic variation in cisplatin-induced ototoxicity.

scientific article published on 5 November 2013

S100A12 Serum Levels and PMN Counts Are Elevated in Childhood Systemic Vasculitides Especially Involving Proteinase 3 Specific Anti-neutrophil Cytoplasmic Antibodies

scientific article published on 23 November 2018

Screening and Assessing Adolescent Asthmatics for Anxiety Disorders

scientific article published on 01 February 2007

Screening and assessing adult asthmatics for anxiety disorders

scientific article published on 01 May 2002

Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?

scientific article published on 17 November 2015

Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function

scientific article published on 20 December 2018

Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic trafficking

scientific article

Somatic gene therapy for a neurodegenerative disease using microencapsulated recombinant cells

scientific article

Spontaneous atherosclerosis in aged lipoprotein lipase-deficient mice with severe hypertriglyceridemia on a normal chow diet

scientific article published on 21 November 2007

Suspected opioid overdose case resolved by CYP2D6 genotyping

scientific article published in April 2012

The Salmonella type III effector SspH2 specifically exploits the NLR co-chaperone activity of SGT1 to subvert immunity

scientific article

The emerging era of pharmacogenomics: current successes, future potential, and challenges

scientific article published on 09 May 2014

The genotypic and phenotypic spectrum of MTO1 deficiency.

scientific article published on 15 November 2017

The genotypic and phenotypic spectrum of PIGA deficiency

scientific article

The global spectrum of protein-coding pharmacogenomic diversity.

scientific article published on 25 October 2016

The importance of XRCC2 in RAD51-related DNA damage repair.

scientific article

The influence of the noradrenergic/stress system on perceptual biases for reward

article

The pharmacogenetics of codeine pain relief in the postpartum period.

scientific article published on 10 March 2015

The role of free fatty acids, pancreatic lipase and Ca+ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient mice

scientific article

The serological classification of 89 strains of Leptospirae from North Queensland, including five serotypes new to Australia

article

The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.

scientific article published on 21 December 2016

Transcriptome-wide association study uncovers the role of essential genes in anthracycline-induced cardiotoxicity

scientific article published on 21 May 2021

Treatment of a lysosomal storage disease, mucopolysaccharidosis VII, with microencapsulated recombinant cells

scientific article

Treatment of hemophilia B in mice with nonautologous somatic gene therapeutics

scientific article

Use of pharmacogenomics in pediatric renal transplant recipients

scientific article

VKORC1 and CYP2C9 genotypes are predictors of warfarin-related outcomes in children.

scientific article published on 29 January 2014

Vincristine-induced peripheral neurotoxicity: A prospective cohort

scientific article published on 04 November 2019

Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro

scientific journal article

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