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Pharmacogenetics of chemotherapy treatment response and -toxicities in patients with osteosarcoma: a systematic review

BMC cancer, 2022-12, Vol.22 (1), p.1326-1326, Article 1326

2022

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Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts

PloS one, 2014-12, Vol.9 (12), p.e115869

2014

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GNA11‐mutated Sturge–Weber syndrome has distinct neurological and dermatological features

European journal of neurology, 2022-10, Vol.29 (10), p.3061-3070

2022

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Quality of Active versus Spontaneous Reporting of Adverse Drug Reactions in Pediatric Patients: Relevance for Pharmacovigilance and Knowledge in Pediatric Medical Care

Pharmaceuticals (Basel, Switzerland), 2022-09, Vol.15 (9), p.1148

2022

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Role of SHP2 (PTPN11) in glycoprotein VI-dependent thrombus formation: Improved platelet responsiveness by the allosteric drug SHP099 in Noonan syndrome patients

Thrombosis research, 2023-08, Vol.228, p.105-116

2023

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Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma

Pharmacogenetics and genomics, 2016-05, Vol.26 (5), p.243-247

2016

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Evaluation of the pharmacokinetics of prednisolone in paediatric patients with acute lymphoblastic leukaemia treated according to Dutch Childhood Oncology Group protocols and its relation to treatment response

British journal of haematology, 2021-07, Vol.194 (2), p.423-432

2021

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The role of AXL and the in vitro activity of the receptor tyrosine kinase inhibitor BGB324 in Ewing sarcoma

Oncotarget, 2014-12, Vol.5 (24), p.12753-12768

2014

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TropicALL study: Thromboprophylaxis in Children treated for Acute Lymphoblastic Leukemia with Low-molecular-weight heparin: a multicenter randomized controlled trial

BMC pediatrics, 2017-05, Vol.17 (1), p.122-122, Article 122

2017

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A prospective study on drug monitoring of PEGasparaginase and Erwinia asparaginase and asparaginase antibodies in pediatric acute lymphoblastic leukemia

Blood, 2014-03, Vol.123 (13), p.2026-2033

2014

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The role of pharmacogenetics in the treatment of osteosarcoma

Drug discovery today, 2016-11, Vol.21 (11), p.1775-1786

2016

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Age as prognostic factor in patients with osteosarcoma

Bone (New York, N.Y.), 2011-12, Vol.49 (6), p.1173-1177

2011

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Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities

Frontiers in pharmacology, 2020-08, Vol.11, p.1241-1241

2020

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Effective low–dose sirolimus regimen for kaposiform haemangioendothelioma with Kasabach–Merritt phenomenon in young infants

British journal of clinical pharmacology, 2022-06, Vol.88 (6), p.2769-2781

2022

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High-Quality Genotyping Data from Formalin-Fixed, Paraffin-Embedded Tissue on the Drug Metabolizing Enzymes and Transporters Plus Array

The Journal of molecular diagnostics : JMD, 2015, Vol.17 (1), p.4-9

2015

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Prognostic Significance of Blasts in the Cerebrospinal Fluid Without Pleiocytosis or a Traumatic Lumbar Puncture in Children With Acute Lymphoblastic Leukemia: Experience of the Dutch Childhood Oncology Group

Journal of clinical oncology, 2006-05, Vol.24 (15), p.2332-2336

2006

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Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury

Journal of personalized medicine, 2022-05, Vol.12 (6), p.892

2022

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Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients

British journal of clinical pharmacology, 2022-07, Vol.88 (7), p.3463-3473

2022

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Magnitude and relevance of change in health-related quality of life in patients with vascular malformations treated with sirolimus

Frontiers in medicine, 2023-04, Vol.10, p.1155476-1155476

2023

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Is there a role for the MTHFR 677C>T and 1298A>C polymorphisms in methotrexate-induced liver toxicity?

Pharmacogenomics, 2014-08, Vol.15 (11), p.1401-1403

2014

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Is there a place for prophylaxis with DOACs in Klippel-Trenaunay syndrome and other low-flow vascular malformations with intravascular coagulopathy and thromboembolic events?

Thrombosis research, 2022-05, Vol.213, p.30-33

2022

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Aberrant venous anatomy as a risk factor for thromboembolic events in patients with Klippel-Trénaunay syndrome: Case-control study within a cohort study

Journal of the American Academy of Dermatology, 2021-05, Vol.84 (5), p.1470-1472

2021

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Dosage of 6-Mercaptopurine in Relation to Genetic TPMT and ITPA Variants: Toward Individualized Pediatric Acute Lymphoblastic Leukemia Maintenance Treatment

Journal of pediatric hematology/oncology, 2020-03, Vol.42 (2), p.e94-e97

2020

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The role of germline variants in chemotherapy outcome in brain tumors: a systematic review of pharmacogenetic studies

Pharmacogenomics, 2017-04, Vol.18 (5), p.501-513

2017

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Survival Trends and Long-Term Toxicity in Pediatric Patients with Osteosarcoma

Complexity (New York, N.Y.), 2012, Vol.2012 (2012), p.447-451

2012

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Pharmacogenetics of chemotherapy treatment response and -toxicities in patients with osteosarcoma: a systematic review

Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts

GNA11‐mutated Sturge–Weber syndrome has distinct neurological and dermatological features

Quality of Active versus Spontaneous Reporting of Adverse Drug Reactions in Pediatric Patients: Relevance for Pharmacovigilance and Knowledge in Pediatric Medical Care

Role of SHP2 (PTPN11) in glycoprotein VI-dependent thrombus formation: Improved platelet responsiveness by the allosteric drug SHP099 in Noonan syndrome patients

Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma

Evaluation of the pharmacokinetics of prednisolone in paediatric patients with acute lymphoblastic leukaemia treated according to Dutch Childhood Oncology Group protocols and its relation to treatment response

The role of AXL and the in vitro activity of the receptor tyrosine kinase inhibitor BGB324 in Ewing sarcoma

TropicALL study: Thromboprophylaxis in Children treated for Acute Lymphoblastic Leukemia with Low-molecular-weight heparin: a multicenter randomized controlled trial

A prospective study on drug monitoring of PEGasparaginase and Erwinia asparaginase and asparaginase antibodies in pediatric acute lymphoblastic leukemia

The role of pharmacogenetics in the treatment of osteosarcoma

Age as prognostic factor in patients with osteosarcoma

Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities

Effective low–dose sirolimus regimen for kaposiform haemangioendothelioma with Kasabach–Merritt phenomenon in young infants

High-Quality Genotyping Data from Formalin-Fixed, Paraffin-Embedded Tissue on the Drug Metabolizing Enzymes and Transporters Plus Array

Prognostic Significance of Blasts in the Cerebrospinal Fluid Without Pleiocytosis or a Traumatic Lumbar Puncture in Children With Acute Lymphoblastic Leukemia: Experience of the Dutch Childhood Oncology Group

Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury

Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients

Magnitude and relevance of change in health-related quality of life in patients with vascular malformations treated with sirolimus

Is there a role for the MTHFR 677C>T and 1298A>C polymorphisms in methotrexate-induced liver toxicity?

Is there a place for prophylaxis with DOACs in Klippel-Trenaunay syndrome and other low-flow vascular malformations with intravascular coagulopathy and thromboembolic events?

Aberrant venous anatomy as a risk factor for thromboembolic events in patients with Klippel-Trénaunay syndrome: Case-control study within a cohort study

Dosage of 6-Mercaptopurine in Relation to Genetic TPMT and ITPA Variants: Toward Individualized Pediatric Acute Lymphoblastic Leukemia Maintenance Treatment

The role of germline variants in chemotherapy outcome in brain tumors: a systematic review of pharmacogenetic studies

Survival Trends and Long-Term Toxicity in Pediatric Patients with Osteosarcoma

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