Colin J Ross

Ontology type: schema:Person     

Person Info


Colin J



Publications in SciGraph latest 50 shown

  • 2019-02 CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelines in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-12 A systematic review of the effects of CYP2D6 phenotypes on risperidone treatment in children and adolescents in CHILD AND ADOLESCENT PSYCHIATRY AND MENTAL HEALTH
  • 2018-08 Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis in NATURE GENETICS
  • 2016-07 NANS-mediated synthesis of sialic acid is required for brain and skeletal development in NATURE GENETICS
  • 2016-06 De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-12 The genotypic and phenotypic spectrum of PIGA deficiency in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-12 Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-12 Genetic determinants of cocaine-associated agranulocytosis in BMC RESEARCH NOTES
  • 2015-03 Detektion intrinsischer Band- und TFCC-Läsionen des Handgelenks in DER UNFALLCHIRURG
  • 2014-08 AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset in NEUROGENETICS
  • 2014-03 Role of TPMT and COMT genetic variation in cisplatin‐induced ototoxicity in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-08 Replication of TPMT and ABCC3 Genetic Variants Highly Associated With Cisplatin‐Induced Hearing Loss in Children in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-07 HLA‐A*31:01 and HLA‐B*15:02 as Genetic Markers for Carbamazepine Hypersensitivity in Children in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2013-05 Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy in NATURE GENETICS
  • 2012-12 Apnea and Oxygen Desaturations in Children Treated with Opioids after Adenotonsillectomy for Obstructive Sleep Apnea Syndrome in PEDIATRIC DRUGS
  • 2012-06 Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin in THE PHARMACOGENOMICS JOURNAL
  • 2012-04 Prediction of Codeine Toxicity in Infants and Their Mothers Using a Novel Combination of Maternal Genetic Markers in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2009-12 Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy in NATURE GENETICS
  • 2009-12 Application of principal component analysis to pharmacogenomic studies in Canada in THE PHARMACOGENOMICS JOURNAL
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