Bayley JP - Search Results

1

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

Bayley JP, Oldenburg RA, Nuk J, Hoekstra AS, van der Meer CA, Korpershoek E, McGillivray B, Corssmit EP, Dinjens WN, de Krijger RR, Devilee P, Jansen JC, Hes FJ. Bayley JP, et al. BMC Med Genet. 2014 Oct 10;15:111. doi: 10.1186/s12881-014-0111-8. BMC Med Genet. 2014. PMID: 25300370 Free PMC article.

2

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paraganglioma.

Bayley JP, Bausch B, Rijken JA, van Hulsteijn LT, Jansen JC, Ascher D, Pires DEV, Hes FJ, Hensen EF, Corssmit EPM, Devilee P, Neumann HPH. Bayley JP, et al. J Med Genet. 2020 Feb;57(2):96-103. doi: 10.1136/jmedgenet-2019-106214. Epub 2019 Sep 6. J Med Genet. 2020. PMID: 31492822

3

Advances in paraganglioma-pheochromocytoma cell lines and xenografts.

Bayley JP, Devilee P. Bayley JP, et al. Endocr Relat Cancer. 2020 Dec;27(12):R433-R450. doi: 10.1530/ERC-19-0434. Endocr Relat Cancer. 2020. PMID: 33112800 Review.

4

SDHB variant type impacts phenotype and malignancy in pheochromocytoma-paraganglioma.

Bayley JP, Bausch B, Jansen JC, Hensen EF, van der Tuin K, Corssmit EP, Devilee P, Neumann HP. Bayley JP, et al. J Med Genet. 2023 Jan;60(1):25-32. doi: 10.1136/jmedgenet-2020-107656. Epub 2021 Nov 8. J Med Genet. 2023. PMID: 34750193

5

High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.

Heesterman BL, Bayley JP, Tops CM, Hes FJ, van Brussel BT, Corssmit EP, Hamming JF, van der Mey AG, Jansen JC. Heesterman BL, et al. Among authors: bayley jp. Eur J Hum Genet. 2013 Apr;21(4):469-70. doi: 10.1038/ejhg.2012.203. Epub 2012 Sep 5. Eur J Hum Genet. 2013. PMID: 22948026 Free PMC article.

6

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.

Bayley JP, Devilee P, Taschner PE. Bayley JP, et al. BMC Med Genet. 2005 Nov 16;6:39. doi: 10.1186/1471-2350-6-39. BMC Med Genet. 2005. PMID: 16288654 Free PMC article.

7

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.

Bayley JP, van Minderhout I, Weiss MM, Jansen JC, Oomen PH, Menko FH, Pasini B, Ferrando B, Wong N, Alpert LC, Williams R, Blair E, Devilee P, Taschner PE. Bayley JP, et al. BMC Med Genet. 2006 Jan 11;7:1. doi: 10.1186/1471-2350-7-1. BMC Med Genet. 2006. PMID: 16405730 Free PMC article.

8

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients.

Bayley JP, Grimbergen AE, van Bunderen PA, van der Wielen M, Kunst HP, Lenders JW, Jansen JC, Dullaart RP, Devilee P, Corssmit EP, Vriends AH, Losekoot M, Weiss MM. Bayley JP, et al. BMC Med Genet. 2009 Apr 15;10:34. doi: 10.1186/1471-2350-10-34. BMC Med Genet. 2009. PMID: 19368708 Free PMC article.

9

Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients.

Bayley JP, Weiss MM, Grimbergen A, van Brussel BT, Hes FJ, Jansen JC, Verhoef S, Devilee P, Corssmit EP, Vriends AH. Bayley JP, et al. Endocr Relat Cancer. 2009 Sep;16(3):929-37. doi: 10.1677/ERC-09-0084. Epub 2009 Jun 22. Endocr Relat Cancer. 2009. PMID: 19546167

10

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. Among authors: bayley jp. 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.

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