Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

179 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Potential added value of combined DPYD/DPD genotyping and phenotyping to prevent severe toxicity in patients with a DPYD variant and decreased dihydropyrimidine dehydrogenase enzyme activity.
Ockeloen CW, Raaijmakers A, Hijmans-van der Vegt M, Bierau J, de Vos-Geelen J, Willemsen AE, van den Bosch BJ, Coenen MJ. Ockeloen CW, et al. Among authors: coenen mj. J Oncol Pharm Pract. 2023 Jan;29(1):5-13. doi: 10.1177/10781552211049144. Epub 2021 Nov 19. J Oncol Pharm Pract. 2023. PMID: 34797200 Free PMC article.
Pharmacogenetics of inflammatory bowel disease.
van den Bosch BJ, Coenen MJ. van den Bosch BJ, et al. Among authors: coenen mj. Pharmacogenomics. 2021 Jan;22(1):55-66. doi: 10.2217/pgs-2020-0095. Epub 2020 Dec 11. Pharmacogenomics. 2021. PMID: 33305616 Review.
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.
de Boer E, Ockeloen CW, Matalonga L, Horvath R; Solve-RD SNV-indel working group; Rodenburg RJ, Coenen MJH, Janssen M, Henssen D, Gilissen C, Steyaert W, Paramonov I; Solve-RD-DITF-ITHACA; Trimouille A, Kleefstra T, Verloes A, Vissers LELM. de Boer E, et al. Eur J Hum Genet. 2021 Sep;29(9):1359-1368. doi: 10.1038/s41431-021-00900-2. Epub 2021 Jun 1. Eur J Hum Genet. 2021. PMID: 34075211 Free PMC article.
Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis.
de Boer E, Ockeloen CW, Matalonga L, Horvath R; Solve-RD SNV-indel working group; Rodenburg RJ, Coenen MJH, Janssen M, Henssen D, Gilissen C, Steyaert W, Paramonov I; Solve-RD-DITF-ITHACA; Trimouille A, Kleefstra T, Verloes A, Vissers LELM. de Boer E, et al. Eur J Hum Genet. 2021 Sep;29(9):1470-1471. doi: 10.1038/s41431-021-00937-3. Eur J Hum Genet. 2021. PMID: 34267341 Free PMC article. No abstract available.
Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in SULT1E1, CYP2B6 and CYP4F8 and Methotrexate Levels and Toxicities.
Hurkmans EGE, Klumpers MJ, Vermeulen SH, Hagleitner MM, Flucke U, Schreuder HWB, Gelderblom H, Bras J, Guchelaar HJ, Coenen MJH, Te Loo DMWM. Hurkmans EGE, et al. Among authors: coenen mjh. Front Pharmacol. 2020 Aug 12;11:1241. doi: 10.3389/fphar.2020.01241. eCollection 2020. Front Pharmacol. 2020. PMID: 32903464 Free PMC article.
Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury.
Klumpers MJ, Witte W, Gattuso G, Schiavello E, Terenziani M, Massimino M, Gidding CEM, Vermeulen SH, Driessen CM, Van Herpen CM, Van Meerten E, Guchelaar HJ, Coenen MJH, Te Loo DMWM. Klumpers MJ, et al. Among authors: coenen mjh. J Pers Med. 2022 May 28;12(6):892. doi: 10.3390/jpm12060892. J Pers Med. 2022. PMID: 35743677 Free PMC article.
179 results