1. Accurate detection and quantification of epigenetic and genetic second hits in BRCA1 and BRCA2-associated hereditary breast and ovarian cancer reveals multiple co-acting second hits. (1st July 2018) Authors: Van Heetvelde, Mattias; Van Bockstal, Mieke; Poppe, Bruce; Lambein, Kathleen; Rosseel, Toon; Atanesyan, Lilit; Deforce, Dieter; Van Den Berghe, Ivo; De Leeneer, Kim; Van Dorpe, Jo; Vral, Anne; Claes, Kathleen B.M. Journal: Cancer letters Issue: Volume 425(2018) Page Start: 125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of the Novel Fanconi Anemia Gene SLX4/FANCP in Familial Breast Cancer Cases. Issue 1 (11th October 2012) Authors: Bakker, Janine L.; van Mil, Saskia E.; Crossan, Gerry; Sabbaghian, Nelly; De Leeneer, Kim; Poppe, Bruce; Adank, Muriel; Gille, Hans; Verheul, Henk; Meijers‐Heijboer, Hanne; de Winter, Johan P.; Claes, Kathleen; Tischkowitz, Marc; Waisfisz, Quinten Journal: Human mutation Issue: Volume 34:Issue 1(2013:Jan.) Page Start: 70 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Epigenetics in T‐cell acute lymphoblastic leukemia. Issue 1 (January 2015) Authors: Peirs, Sofie; Van der Meulen, Joni; Van de Walle, Inge; Taghon, Tom; Speleman, Frank; Poppe, Bruce; Van Vlierberghe, Pieter Journal: Immunological reviews Issue: Volume 263:Issue 1(2015) Page Start: 50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Future perspectives of genome-scale sequencing. Issue 1 (2nd January 2018) Authors: Steyaert, Wouter; Callens, Steven; Coucke, Paul; Dermaut, Bart; Hemelsoet, Dimitri; Terryn, Wim; Poppe, Bruce Journal: Acta clinica belgica Issue: Volume 73:Issue 1(2018) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study. (12th October 2018) Authors: Qian, Frank; Wang, Shengfeng; Mitchell, Jonathan; McGuffog, Lesley; Barrowdale, Daniel; Leslie, Goska; Oosterwijk, Jan C; Chung, Wendy K; Evans, D Gareth; Engel, Christoph; Kast, Karin; Aalfs, Cora M; Adank, Muriel A; Adlard, Julian; Agnarsson, Bjarni A; Aittomäki, Kristiina; Alducci, Elisa; Andr... Journal: Journal of the National Cancer Institute Issue: Volume 111:Number 4(2019) Page Start: 350 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation. Issue 1 (December 2016) Authors: Baert, Annelot; Depuydt, Julie; Van Maerken, Tom; Poppe, Bruce; Malfait, Fransiska; Storm, Katrien; van den Ende, Jenneke; Van Damme, Tim; De Nobele, Sylvia; Perletti, Gianpaolo; De Leeneer, Kim; Claes, Kathleen; Vral, Anne Journal: Breast cancer research Issue: Volume 18:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2. Issue 1 (December 2016) Authors: Silvestri, Valentina; Barrowdale, Daniel; Mulligan, Anna; Neuhausen, Susan; Fox, Stephen; Karlan, Beth; Mitchell, Gillian; James, Paul; Thull, Darcy; Zorn, Kristin; Carter, Natalie; Nathanson, Katherine; Domchek, Susan; Rebbeck, Timothy; Ramus, Susan; Nussbaum, Robert; Olopade, Olufunmilayo; Rant... Journal: Breast cancer research Issue: Volume 18:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutation Analysis of the BRCA1 and BRCA2 Genes in the Belgian Patient Population and Identification of a Belgian Founder Mutation BRCA1 IVS5+3A>G. Issue 1 (17th June 2013) Authors: Claes, Kathleen; Machackova, Eva; De Vos, Michel; Poppe, Bruce; De Paepe, Anne; Messiaen, Ludwine Journal: Disease markers Issue: Volume 15:Issue 1/3(1999) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Issue 4 (12th March 2011) Authors: Gardie, Betty; Remenieras, Audrey; Kattygnarath, Darouna; Bombled, Johny; Lefèvre, Sandrine; Perrier-Trudova, Victoria; Rustin, Pierre; Barrois, Michel; Slama, Abdelhamid; Avril, Marie-Françoise; Bessis, Didier; Caron, Olivier; Caux, Frédéric; Collignon, Patrick; Coupier, Isabelle; Cremin, Carol;... Journal: Journal of medical genetics Issue: Volume 48:Issue 4(2011) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Screening for Fabry Disease in Male Patients With Arrhythmia Requiring a Pacemaker or an Implantable Cardioverter–Defibrillator. Issue 8 (23rd February 2021) Authors: Hemelsoet, Dimitri; De Keyser, Jan; Van Heuverswyn, Frederic; Willems, Rik; Vandekerckhove, Hans; Bondue, Antoine; de Asmundis, Carlo; Saenen, Johan; Van de Walle, Stefaan; Godart, Pascal; Kampmann, Christoph; Stepman, Hedwig; Poppe, Bruce; Terryn, Wim Journal: Circulation Issue: Volume 143:Issue 8(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗