Hensen EF - Search Results

1

Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-Paraganglioma.

Buffet A, Zhang J, Rebel H, Corssmit EPM, Jansen JC, Hensen EF, Bovée JVMG, Morini A, Gimenez-Roqueplo AP, Hes FJ, Devilee P, Favier J, Bayley JP. Buffet A, et al. Among authors: hensen ef. J Clin Endocrinol Metab. 2021 Jan 23;106(2):459-471. doi: 10.1210/clinem/dgaa819. J Clin Endocrinol Metab. 2021. PMID: 33180916

2

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

Hensen EF, Jordanova ES, van Minderhout IJ, Hogendoorn PC, Taschner PE, van der Mey AG, Devilee P, Cornelisse CJ. Hensen EF, et al. Oncogene. 2004 May 20;23(23):4076-83. doi: 10.1038/sj.onc.1207591. Oncogene. 2004. PMID: 15064708

3

Hensen EF, Goeman JJ, Oosting J, Van der Mey AG, Hogendoorn PC, Cremers CW, Devilee P, Cornelisse CJ. Hensen EF, et al. BMC Med Genomics. 2009 May 11;2:25. doi: 10.1186/1755-8794-2-25. BMC Med Genomics. 2009. PMID: 19432956 Free PMC article.

4

The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.

Hensen EF, Jansen JC, Siemers MD, Oosterwijk JC, Vriends AH, Corssmit EP, Bayley JP, van der Mey AG, Cornelisse CJ, Devilee P. Hensen EF, et al. Eur J Hum Genet. 2010 Jan;18(1):62-6. doi: 10.1038/ejhg.2009.112. Eur J Hum Genet. 2010. PMID: 19584903 Free PMC article.

5

Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma.

Hensen EF, Bayley JP. Hensen EF, et al. Fam Cancer. 2011 Jun;10(2):355-63. doi: 10.1007/s10689-010-9402-1. Fam Cancer. 2011. PMID: 21082267 Free PMC article. Review.

6

High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands.

Hensen EF, van Duinen N, Jansen JC, Corssmit EP, Tops CM, Romijn JA, Vriends AH, van der Mey AG, Cornelisse CJ, Devilee P, Bayley JP. Hensen EF, et al. Clin Genet. 2012 Mar;81(3):284-8. doi: 10.1111/j.1399-0004.2011.01653.x. Epub 2011 Mar 15. Clin Genet. 2012. PMID: 21348866

7

Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients.

Hensen EF, Siemers MD, Jansen JC, Corssmit EP, Romijn JA, Tops CM, van der Mey AG, Devilee P, Cornelisse CJ, Bayley JP, Vriends AH. Hensen EF, et al. Clin Endocrinol (Oxf). 2011 Nov;75(5):650-5. doi: 10.1111/j.1365-2265.2011.04097.x. Clin Endocrinol (Oxf). 2011. PMID: 21561462

8

Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion.

Rijken JA, Niemeijer ND, Corssmit EP, Jonker MA, Leemans CR, Menko FH, Hensen EF. Rijken JA, et al. Among authors: hensen ef. Clin Genet. 2016 Jan;89(1):128-32. doi: 10.1111/cge.12591. Epub 2015 Apr 27. Clin Genet. 2016. PMID: 25827221

9

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.

Hoekstra AS, Hensen EF, Jordanova ES, Korpershoek E, van der Horst-Schrivers AN, Cornelisse C, Corssmit EP, Hes FJ, Jansen JC, Kunst HP, Timmers HJ, Bateman A, Eccles D, Bovée JV, Devilee P, Bayley JP. Hoekstra AS, et al. Among authors: hensen ef. Oncotarget. 2017 Feb 28;8(9):14525-14536. doi: 10.18632/oncotarget.14649. Oncotarget. 2017. PMID: 28099933 Free PMC article.

10

The phenotype of SDHB germline mutation carriers: a nationwide study.

Niemeijer ND, Rijken JA, Eijkelenkamp K, van der Horst-Schrivers ANA, Kerstens MN, Tops CMJ, van Berkel A, Timmers HJLM, Kunst HPM, Leemans CR, Bisschop PH, Dreijerink KMA, van Dooren MF, Bayley JP, Pereira AM, Jansen JC, Hes FJ, Hensen EF, Corssmit EPM. Niemeijer ND, et al. Among authors: hensen ef. Eur J Endocrinol. 2017 Aug;177(2):115-125. doi: 10.1530/EJE-17-0074. Epub 2017 May 10. Eur J Endocrinol. 2017. PMID: 28490599

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