P Devilee
Overview
Explore the profile of P Devilee including associated specialties, affiliations and a list of published articles.
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116
Citations
4696
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Recent Articles
1.
Hoekstra A, van den Ende B, Julia X, van Breemen L, Scheurwater K, Tops C, et al.
Clin Genet
. 2016 Aug;
91(4):536-544.
PMID: 27485256
Germline mutations in genes encoding subunits of succinate dehydrogenase (SDH) are associated with hereditary paraganglioma and pheochromocytoma. Although most mutations in SDHB, SDHC and SDHD are intraexonic variants, large germline...
2.
Kriege M, Hollestelle A, Jager A, Huijts P, Berns E, Sieuwerts A, et al.
Br J Cancer
. 2014 Jun;
111(5):1004-13.
PMID: 24918820
Background: We assessed the sensitivity to adjuvant chemotherapy in cell cycle checkpoint kinase 2 (CHEK2) vs non-CHEK2 breast cancer patients by comparing the contralateral breast cancer incidence and distant disease-free...
3.
Agarwal D, Pineda S, Michailidou K, Herranz J, Pita G, Moreno L, et al.
Br J Cancer
. 2014 Feb;
110(4):1088-100.
PMID: 24548884
Background: Breast cancer is one of the most common malignancies in women. Genome-wide association studies have identified FGFR2 as a breast cancer susceptibility gene. Common variation in other fibroblast growth...
4.
Hilbers F, Vreeswijk M, van Asperen C, Devilee P
Clin Genet
. 2013 Sep;
84(5):407-14.
PMID: 24025038
Women with a family history of breast cancer have an approximately twofold elevated risk of the disease. Even though an array of genes has been associated with breast cancer risk...
5.
Jakubowska A, Rozkrut D, Antoniou A, Hamann U, Scott R, McGuffog L, et al.
Br J Cancer
. 2012 Jun;
106(12):2016-24.
PMID: 22669161
Background: The variable penetrance of breast cancer in BRCA1/2 mutation carriers suggests that other genetic or environmental factors modify breast cancer risk. Two genes of special interest are prohibitin (PHB)...
6.
Park D, Lesueur F, Nguyen-Dumont T, Pertesi M, Odefrey F, Hammet F, et al.
Am J Hum Genet
. 2012 Apr;
90(4):734-9.
PMID: 22464251
An exome-sequencing study of families with multiple breast-cancer-affected individuals identified two families with XRCC2 mutations, one with a protein-truncating mutation and one with a probably deleterious missense mutation. We performed...
7.
Hensen E, Siemers M, Jansen J, Corssmit E, Romijn J, Tops C, et al.
Clin Endocrinol (Oxf)
. 2011 May;
75(5):650-5.
PMID: 21561462
Objective: Head and neck paragangliomas (HNPGL) are associated with mutations in genes encoding subunits of succinate dehydrogenase (SDH). The aim of this study was to evaluate SDH mutations, family history...
8.
Hensen E, van Duinen N, Jansen J, Corssmit E, Tops C, Romijn J, et al.
Clin Genet
. 2011 Feb;
81(3):284-8.
PMID: 21348866
Mutations in four genes encoding subunits or cofactors of succinate dehydrogenase (SDH) cause hereditary paraganglioma and pheochromocytoma syndromes. Mutations in SDHB and SDHD are generally the most common, whereas mutations...
9.
Didraga M, van Beers E, Joosse S, Brandwijk K, Oldenburg R, Wessels L, et al.
Breast Cancer Res Treat
. 2011 Feb;
130(2):425-36.
PMID: 21286804
Germline mutations in BRCA1 and BRCA2 explain approximately 25% of all familial breast cancers. Despite intense efforts to find additional high-risk breast cancer genes (BRCAx) using linkage analysis, none have...
10.
Tomlinson I, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, et al.
Br J Cancer
. 2009 Nov;
102(2):447-54.
PMID: 19920828
It is now recognised that a part of the inherited risk of colorectal cancer (CRC) can be explained by the co-inheritance of low-penetrance genetic variants. The accumulated experience to date...