Frequency and spectrum of cancers in the Peutz-Jeghers syndrome N Hearle, V Schumacher, FH Menko, S Olschwang, LA Boardman, ... Clinical Cancer Research 12 (10), 3209-3215, 2006 | 1070 | 2006 |
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer JMJ Piek, PJ Van Diest, RP Zweemer, JW Jansen, RJJ Poort‐Keesom, ... The Journal of Pathology: A Journal of the Pathological Society of Great …, 2001 | 1007 | 2001 |
The Cowden syndrome: a clinical and genetic study in 21 patients TM Starink, JPW Veen, F Arwert, LP Waal, GG Lange, JJP Gille, ... Clinical genetics 29 (3), 222-233, 1986 | 662 | 1986 |
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ... Jama 313 (13), 1347-1361, 2015 | 575 | 2015 |
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA JR Lo Ten Foe, MA Rooimans, L Bosnoyan-Collins, N Alon, M Wijker, ... Nature genetics 14 (3), 320-323, 1996 | 520 | 1996 |
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method FBL Hogervorst, PM Nederlof, JJP Gille, CJ McElgunn, M Grippeling, ... Cancer research 63 (7), 1449-1453, 2003 | 417 | 2003 |
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study MJE Kempers, RP Kuiper, CW Ockeloen, PO Chappuis, P Hutter, ... The lancet oncology 12 (1), 49-55, 2011 | 351 | 2011 |
Relative frequency and morphology of cancers in STK11 mutation carriers W Lim, S Olschwang, JJ Keller, AM Westerman, FH Menko, LA Boardman, ... Gastroenterology 126 (7), 1788-1794, 2004 | 335 | 2004 |
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk FJ Couch, X Wang, L McGuffog, A Lee, C Olswold, KB Kuchenbaecker, ... PLoS genetics 9 (3), e1003212, 2013 | 333 | 2013 |
Evidence for at least eight Fanconi anemia genes H Joenje, AB Oostra, M Wijker, FM di Summa, CGM van Berkel, ... The American Journal of Human Genetics 61 (4), 940-944, 1997 | 321 | 1997 |
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 | 314 | 2015 |
Cell culture models for oxidative stress: superoxide and hydrogen peroxide versus normobaric hyperoxia JJP Gille, H Joenje Mutation Research/DNAging 275 (3-6), 405-414, 1992 | 259 | 1992 |
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations RP Zweemer, PJ Van Diest, RHM Verheijen, A Ryan, JJP Gille, ... Gynecologic oncology 76 (1), 45-50, 2000 | 229 | 2000 |
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families T Peelen, M Van Vliet, A Petrij-Bosch, R Mieremet, C Szabo, ... American journal of human genetics 60 (5), 1041, 1997 | 217 | 1997 |
TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension WS Kerstjens-Frederikse, EMHF Bongers, MTR Roofthooft, EM Leter, ... Journal of medical genetics 50 (8), 500-506, 2013 | 207 | 2013 |
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach JJP Gille, FBL Hogervorst, G Pals, JT Wijnen, RJ Van Schooten, ... British Journal of Cancer 87 (8), 892-897, 2002 | 195 | 2002 |
Recurrence and variability of germline EPCAM deletions in Lynch syndrome RP Kuiper, LELM Vissers, R Venkatachalam, D Bodmer, E Hoenselaar, ... Human mutation 32 (4), 407-414, 2011 | 189 | 2011 |
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype H Joenje, JR Lo Ten Foe, AB Oostra, CG Van Berkel, MA Rooimans, ... | 188 | 1995 |
Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families AC Houweling, LM Gijezen, MA Jonker, MBA van Doorn, RA Oldenburg, ... British journal of cancer 105 (12), 1912-1919, 2011 | 179 | 2011 |
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations M Castella, R Pujol, E Callén, JP Trujillo, JA Casado, H Gille, FP Lach, ... Blood, The Journal of the American Society of Hematology 117 (14), 3759-3769, 2011 | 160 | 2011 |