| Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies A Antoniou, PDP Pharoah, S Narod, HA Risch, JE Eyfjord, JL Hopper, ... The American Journal of Human Genetics 72 (5), 1117-1130, 2003 | 4715 | 2003 |
| Gene-expression profiles in hereditary breast cancer I Hedenfalk, D Duggan, Y Chen, M Radmacher, M Bittner, R Simon, ... New England Journal of Medicine 344 (8), 539-548, 2001 | 2154 | 2001 |
| Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer SN Stacey, A Manolescu, P Sulem, T Rafnar, J Gudmundsson, ... Nature genetics 39 (7), 865-869, 2007 | 898 | 2007 |
| Parental origin of sequence variants associated with complex diseases A Kong, V Steinthorsdottir, G Masson, G Thorleifsson, P Sulem, ... Nature 462 (7275), 868-874, 2009 | 656 | 2009 |
| The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions AC Antoniou, AP Cunningham, J Peto, DG Evans, F Lalloo, SA Narod, ... British journal of cancer 98 (8), 1457-1466, 2008 | 613 | 2008 |
| Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer SN Stacey, A Manolescu, P Sulem, S Thorlacius, SA Gudjonsson, ... Nature genetics 40 (6), 703-706, 2008 | 548 | 2008 |
| Distinct Somatic Genetic Changes Associated with Tumor Progression in Carriers of BRCA1 and BRCA2 Germ-line Mutations M Tirkkonen, O Johannsson, BA Agnarsson, H Olsson, S Ingvarsson, ... Cancer research 57 (7), 1222-1227, 1997 | 483 | 1997 |
| High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families A Borg, T Sandberg, K Nilsson, O Johannsson, M Klinker, A Måsbäck, ... Journal of the National Cancer Institute 92 (15), 1260-1266, 2000 | 433 | 2000 |
| Frequent amplification of chromosomal region 20q12-q13 in ovarian cancer MM Tanner, S Grenman, A Koul, O Johannsson, P Meltzer, T Pejovic, ... Clinical Cancer Research 6 (5), 1833-1839, 2000 | 432 | 2000 |
| Tumour biological features of BRCA1-induced breast and ovarian cancer OT Johannsson, I Idvall, C Anderson, Å Borg, RB Barkardottir, V Egilsson, ... European Journal of Cancer 33 (3), 362-371, 1997 | 430 | 1997 |
| Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer N Loman, O Johannsson, U Kristoffersson, H Olsson, A Borg Journal of the National Cancer Institute 93 (16), 1215-1223, 2001 | 355 | 2001 |
| Survival of BRCA1 breast and ovarian cancer patients: a population-based study from southern Sweden OT Johannsson, J Ranstam, Å Borg, H Olsson Journal of Clinical Oncology 16 (2), 397-404, 1998 | 324 | 1998 |
| High prevalence of the 999del5 mutation in Icelandic breast and ovarian cancer patients G Johannesdottir, J Gudmundsson, JT Bergthorsson, A Arason, ... Cancer research 56 (16), 3663-3665, 1996 | 314 | 1996 |
| A germline variant in the TP53 polyadenylation signal confers cancer susceptibility SN Stacey, P Sulem, A Jonasdottir, G Masson, J Gudmundsson, ... Nature genetics 43 (11), 1098-1103, 2011 | 313 | 2011 |
| Identification of six new susceptibility loci for invasive epithelial ovarian cancer KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ... Nature genetics 47 (2), 164-171, 2015 | 307 | 2015 |
| Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study EK Bancroft, EC Page, E Castro, H Lilja, A Vickers, D Sjoberg, M Assel, ... European urology 66 (3), 489-499, 2014 | 290 | 2014 |
| Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics G Jönsson, J Staaf, J Vallon-Christersson, M Ringnér, K Holm, C Hegardt, ... Breast Cancer Research 12, 1-14, 2010 | 251 | 2010 |
| Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. S Håkansson, O Johannsson, U Johansson, G Sellberg, N Loman, ... American journal of human genetics 60 (5), 1068, 1997 | 225 | 1997 |
| Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus T Kainu, SHH Juo, R Desper, AA Schäffer, E Gillanders, E Rozenblum, ... Proceedings of the National Academy of Sciences 97 (17), 9603-9608, 2000 | 224 | 2000 |
| Steroid receptors in hereditary breast carcinomas associated with BRCA1 or BRCA2 mutations or unknown susceptibility genes N Loman, O Johannsson, PO Bendahl, Å Borg, M Fernö, H Olsson Cancer: Interdisciplinary International Journal of the American Cancer …, 1998 | 223 | 1998 |
