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Browsing by Author "Hoogerbrugge-van der Linden, N."
Now showing items 1-50 of 224
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TRIM28 haploinsufficiency predisposes to Wilms tumor ; Hoyer, J.; Ekici, A.B.; Popp, B.; ; ; Bhaskaran, R.; Hadjihannas, M.; Vasileiou, G.; Thiel, C.T.; et al.2019, Article / Letter to editor (International Journal of Cancer, vol. 145, iss. 4, (2019), pp. 941-951)
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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype Grolleman, J.E.; Voer, R.M. de; Elsayed, F.A.; Nielsen, Maartje; Weren, R.D.A.; Palles, Claire; ; Vos, J.R.; ; ; et al.2019, Article / Letter to editor (Cancer Cell, vol. 35, iss. 2, (2019), pp. 256-+)
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Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families Lakeman, I.M.M.; Hilbers, F.S.; Rodriguez-Girondo, M.; Lee, A.; Vreeswijk, M.P.G.; Hollestelle, A.; Seynaeve, C.; Meijers-Heijboer, H.; Oosterwijk, J.C; ; et al.2019, Article / Letter to editor (Journal of Medical Genetics, vol. 56, iss. 9, (2019), pp. 581-589)
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De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism ; Donk, R. van der; Baltrunaite, K.; ; ; Dingemans, A.J.; ; ; Wiel, L.J.M. van de; ; et al.2019, Article / Letter to editor (American Journal of Human Genetics, vol. 104, iss. 4, (2019), pp. 758-766)
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Cancer Risks for PMS2-Associated Lynch Syndrome Broeke, S.W. ten; Klift, H.M. van der; Tops, Carli M.J.; Aretz, Stefan; Bernstein, I.; Buchanan, Daniel D.; ; ; ; Nielsen, M.; et al.2018, Article / Letter to editor (Journal of Clinical Oncology, vol. 36, iss. 29, (2018), pp. 2961-2968)
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Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility Weren, R.D.A.; Post, R.S. van der; Vogelaar, I.P.; ; ; Lubinski, J.; Jakubowska, A.; Teodorczyk, U.; Aalfs, C.M.; Hest, L.P. van; et al.2018, Article / Letter to editor (Journal of Medical Genetics, vol. 55, iss. 10, (2018), pp. 669-674)
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High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer ; ; ; ; ; ; Hopman, S.; Olderode-Berends, M.J.; Gerkes, E.H.; ; et al.2018, Article / Letter to editor (Clinical Cancer Research, vol. 24, iss. 7, (2018), pp. 1594-1603)
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Germline activating TYK2 mutations in pediatric patients with two primary acute lymphoblastic leukemia occurrences ; ; ; ; ; ; Pastorczak, A.; Weren, R.D.A.; Schoot, C.E. van der; Vorst, J.M. van de; et al.2017, Article / Letter to editor (Leukemia, vol. 31, iss. 4, (2017), pp. 821-828)
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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing Vogelaar, I.P.; Post, R.S. van der; ; ; Zelst-Stams, W.A.G. van; ; Lubinski, J.; Jakubowska, A.; Teodorczyk, U.; Aalfs, C.M.; et al.2017, Article / Letter to editor (European Journal of Human Genetics, vol. 25, iss. 11, (2017), pp. 1246-1252)
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A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients. Zhang, J.; Wang, W.; Voer, R.M. de; ; ; Weren, R.D.A.; Nelen, M.; ; ; ; et al.2017, Article / Letter to editor (Oncotarget, vol. 8, (2017), pp. 24533-24547)
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Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas. Weren, R.D.A.; ; Simons, M.; Eijkelenboom, A.; Sie, A.S.; Ouchene, H.; Asseldonk, M. van; Gomez-Garcia, E.B.; Blok, M.J.; ; et al.2017, Article / Letter to editor (Human Mutation, vol. 38, iss. 2, (2017), pp. 226-235)
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Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers Ghorbanoghli, Z.; Nieuwenhuis, M.H.; Houwing-Duistermaat, J.J.; Jagmohan-Changur, S.; Hes, F.J.; Tops, C.M.; Wagner, A.; Aalfs, C.M.; Verhoef, S.; Gomez Garcia, E.B.; et al.2016, Article / Letter to editor (Familial Cancer, vol. 15, iss. 4, (2016), pp. 563-570)
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The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers Suerink, M.; Klift, H.M. van der; Broeke, S.W. ten; Dekkers, O.M.; Bernstein, I.; Capella Munar, G.; Garcia, E.; ; Letteboer, T.G.; Menko, F.H.; et al.2016, Article / Letter to editor (Genetics in Medicine, vol. 18, iss. 4, (2016), pp. 405-409)
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BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study Hoberg-Vetti, H.; Bjorvatn, C.; Fiane, B.E.; Aas, T.; Woie, K.; Espelid, H.; Rusken, T.; Eikesdal, H.P.; Listol, W.; Haavind, M.T.; et al.2016, Article / Letter to editor (European Journal of Human Genetics, vol. 24, iss. 6, (2016), pp. 881-888)
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Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility Voer, R.M. de; Hahn, M.M.; Weren, R.D.A.; ; ; Zelst-Stams, W.A. van; ; ; Zhang, J.Z; ; et al.2016, Article / Letter to editor (Plos Genetics, vol. 12, iss. 2, (2016), pp. e1005880)
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Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect Vogelaar, I.P.; ; Post, R.S. van der; Voer, R.M. de; ; ; ; ; ; ; et al.2016, Article / Letter to editor (Familial Cancer, vol. 15, iss. 2, (2016), pp. 289-296)
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Now showing items 1-50 of 224
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