1. Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11. Issue 4 (22nd January 2018) Authors: Baert, Annelot; Machackova, Eva; Coene, Ilse; Cremin, Carol; Turner, Kristin; Portigal‐Todd, Cheryl; Asrat, Marie Jill; Nuk, Jennifer; Mindlin, Allison; Young, Sean; MacMillan, Andree; Van Maerken, Tom; Trbusek, Martin; McKinnon, Wendy; Wood, Marie E.; Foulkes, William D.; Santamariña, Marta; de ... Journal: Human mutation Issue: Volume 39:Issue 4(2018) Page Start: 515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗
3. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status. Issue 5 (1st March 2020) Authors: Feng, Helian; Gusev, Alexander; Pasaniuc, Bogdan; Wu, Lang; Long, Jirong; Abu‐full, Zomoroda; Aittomäki, Kristiina; Andrulis, Irene L.; Anton‐Culver, Hoda; Antoniou, Antonis C.; Arason, Adalgeir; Arndt, Volker; Aronson, Kristan J.; Arun, Banu K.; Asseryanis, Ella; Auer, Paul L.; Azzollini, Jacopo... Journal: Genetic epidemiology Issue: Volume 44:Issue 5(2020) Page Start: 442 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. 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) ↗
6. 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) ↗
7. 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) ↗
8. 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) ↗
9. 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) ↗
10. 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) ↗