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PubPharm (162)
1
Correction : A genetic risk score to predict treatment nonresponse in psychotic depression
enthalten in:
Translational psychiatry
| 2024
von
Ter Hark, S.
|
Coenen, M.
|
Vos, C.
| +7
ErratumFor: Transl Psychiatry. 2024 Mar 2;14(1):132. - PMID 38431658
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2
A genetic risk score to predict treatment nonresponse in psychotic depression
enthalten in:
Translational psychiatry
| 2024
von
Ter Hark, S.
|
Coenen, M.
|
Vos, C.
| +7
ErratumIn: Transl Psychiatry. 2024 Apr 26;14(1):198. - PMID 38671038
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3
A common germline variant in CYP11B1 is associated with adverse clinical outcome of treatment with abiraterone or enzalutamide
enthalten in:
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
| 2023
von
Buck, S.
|
Meertens, M.
|
van Ooijen, F.
| +9
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4
Genome-wide association study on pharmacological outcomes of musculoskeletal pain in UK Biobank
enthalten in:
The pharmacogenomics journal
| 2023
von
Li, S.
|
Poelmans, G.
|
van Boekel, R.
| +1
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5
Genome-wide association study of nociceptive musculoskeletal pain treatment response in UK Biobank
enthalten in:
bioRxiv.org
| 2023
von
Li, S.
|
Poelmans, G.
|
van Boekel, R.
| +1
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6
Drug interaction potential of high-dose rifampicin in patients with pulmonary tuberculosis
enthalten in:
Antimicrobial agents and chemotherapy
| 2023
von
Stemkens, R.
|
Jager, V.
|
Dawson, R.
| +13
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7
A systematic review of genome-wide association studies for pain, nociception, neuropathy, and pain treatment responses
enthalten in:
Pain
| 2023
von
Li, S.
|
Brimmers, A.
|
van Boekel, R.
| +2
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8
Effectiveness of Genotype-Specific Tricyclic Antidepressant Dosing in Patients With Major Depressive Disorder : A Randomized Clinical Trial
enthalten in:
JAMA network open
| 2023
von
Vos, C.
|
Ter Hark, S.
|
Schellekens, A.
| +9
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9
Genetic variants of genes involved in thiopurine metabolism pathway are associated with 6-mercaptopurine toxicity in pediatric acute lymphoblastic leukemia patients from Ethiopia
enthalten in:
Frontiers in pharmacology
| 2023
von
Ali, A.
|
Adam, H.
|
Hailu, D.
| +4
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10
Evaluating the Frequencies of CNOT3, GRIA1, NFATC2, and PNPLA3 Variant Alleles and Their Association with L-Asparaginase Hypersensitivity in Pediatric Acute Lymphoblastic Leukemia in Addis Ababa, Ethiopia
enthalten in:
The application of clinical genetics
| 2023
von
Ali, A.
|
Adam, H.
|
Hailu, D.
| +3
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