Attje S. Hoekstra
Leiden, ZH 2300RC, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA.
Journal: NPJ genomic medicine
Published: February 25, 2022
IDH1 or -2 mutations do not predict outcome and do not cause loss of 5-hydroxymethylcytosine or altered histone modifications in central chondrosarcomas.
Journal: Clinical sarcoma research
Published: February 16, 2017
Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.
Journal: Oncotarget
Published: September 06, 2016
Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiers.
Journal: Human molecular genetics
Published: April 22, 2016
Models of parent-of-origin tumorigenesis in hereditary paraganglioma.
Journal: Seminars in cell & developmental biology
Published: March 20, 2015
Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.
Journal: BMC medical genetics
Published: January 14, 2014
DRAM-1 encodes multiple isoforms that regulate autophagy.
Journal: Autophagy
Published: November 16, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026