Authors:
Kuschel, B
Gayther, SA
Easton, DF
Ponder, BAJ
Pharoah, PDP
Citation: B. Kuschel et al., Apparent human BRCAI knockout caused by mispriming during polymerase chainreaction: Implications for genetic testing, GENE CHROM, 31(1), 2001, pp. 96-98
Authors:
Gayther, SA
Batley, SJ
Linger, L
Bannister, A
Thorpe, K
Chin, SF
Daigo, Y
Russell, P
Wilson, A
Sowter, HM
Delhanty, JDA
Ponder, BAJ
Kouzarides, T
Caldas, C
Citation: Sa. Gayther et al., Mutations truncating the EP300 acetylase in human cancers, NAT GENET, 24(3), 2000, pp. 300-303
Authors:
Knowles, CH
Gayther, SA
Scott, M
Ramus, S
Anand, P
Williams, NS
Ponder, BA
Citation: Ch. Knowles et al., Idiopathic slow-transit constipation is not associated with mutations of the RET proto-oncogene or GDNF, DIS COL REC, 43(6), 2000, pp. 851-857
Citation: Sa. Gayther, The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer (vol 60, pg 4513, 2000), CANCER RES, 60(24), 2000, pp. 7185-7185
Authors:
Gayther, SA
de Foy, EAF
Harrington, P
Pharoah, P
Dunsmuir, WD
Edwards, SM
Gillett, C
Ardern-Jones, A
Dearnaley, DP
Easton, DF
Ford, D
Shearer, RJ
Kirby, RS
Dowe, AL
Kelly, J
Stratton, MR
Ponder, BAJ
Barnes, D
Eeles, RA
Citation: Sa. Gayther et al., The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer, CANCER RES, 60(16), 2000, pp. 4513-4518
Authors:
Mazoyer, S
Leary, J
Kirk, J
Fleischmann, E
Wagner, T
Claes, K
Messiaen, L
Foulkes, W
Desrochers, M
Simard, J
Phelan, CM
Kwan, E
Narod, SA
Vahteristo, P
Nevanlinna, H
Durando, X
Bignon, YJ
Peyrat, JP
Bonnardel, C
Sinilnikova, OM
Puget, N
Lenoir, GM
Mazoyer, S
Audoynaud, C
Goldgar, D
Maugard, C
Caux, V
Gad, S
Stoppa-Lyonnet, D
Nogues, C
Lidereau, R
Machavoine, C
Bressac-de Paillerets, B
Kuschel, B
Betz, B
Niederacher, D
Beckmann, MW
Hamann, U
Gayther, SA
Ponder, BAP
Robinson, M
Taylor, GR
Bishop, T
Catteau, A
Solomon, E
Cohen, B
Steel, M
Collins, N
Stratton, M
van der Looij, M
Olah, E
Miller, NJ
Barton, DE
Sverdlov, RS
Friedman, E
Radice, P
Montagna, M
Sensi, E
Caligo, M
van Eijk, R
Devilee, P
van der Luijt, R
Heimdal, K
Moller, P
Borg, A
Diez, O
Cortes, J
Domenech, M
Baiget, M
Osorio, A
Benitez, J
Borg, A
Maillet, P
Sappino, AP
Ozdag, H
Ozcelik, T
Ozturk, M
Rohlfs, EM
Boyd, J
McDermott, D
Offit, K
Unger, M
Nathanson, K
Weber, BL
Sellers, TA
Hampton, E
Couch, FJ
Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212
Authors:
Caldas, C
Carneiro, F
Lynch, HT
Yokota, J
Wiesner, GL
Powell, SM
Lewis, FR
Huntsman, DG
Pharoah, PDP
Jankowski, JA
MacLeod, P
Vogelsang, H
Keller, G
Park, KGM
Richards, FM
Maher, ER
Gayther, SA
Oliveira, C
Grehan, N
Wight, D
Seruca, R
Roviello, F
Ponder, BAJ
Jackson, CE
Citation: C. Caldas et al., Familial gastric cancer: overview and guidelines for management, J MED GENET, 36(12), 1999, pp. 873-880
Authors:
Gayther, SA
Russell, P
Harrington, P
Antoniou, AC
Easton, DF
Ponder, BAJ
Citation: Sa. Gayther et al., The contribution of germline BRCA1 and BRCA2 mutations to familial ovariancancer: No evidence for other ovarian cancer-susceptibility genes, AM J HU GEN, 65(4), 1999, pp. 1021-1029