-
1
-
-
0023683531
-
Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
-
Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Covenee WK. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 1988;336:374-6.
-
(1988)
Nature
, vol.336
, pp. 374-376
-
-
Grundy, P.1
Koufos, A.2
Morgan, K.3
Li, F.P.4
Meadows, A.T.5
Covenee, W.K.6
-
2
-
-
0030017174
-
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21
-
Rahman N, Arbour L, Tonin P, Renshaw J, Pelletier J, Baruchel S, Pritchard-Jones K, Stratton MR, Narod SA. Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21. Nat Genet 1996;13:461-3.
-
(1996)
Nat Genet
, vol.13
, pp. 461-463
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Renshaw, J.4
Pelletier, J.5
Baruchel, S.6
Pritchard-Jones, K.7
Stratton, M.R.8
Narod, S.A.9
-
3
-
-
0032053822
-
Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors
-
McDonald JM, Douglass EC, Fisher R, Geiser CF, Krill CE, Strong LC, Virshup D, Huff V. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. Cancer Res 1998;58:1387-90.
-
(1998)
Cancer Res
, vol.58
, pp. 1387-1390
-
-
McDonald, J.M.1
Douglass, E.C.2
Fisher, R.3
Geiser, C.F.4
Krill, C.E.5
Strong, L.C.6
Virshup, D.7
Huff, V.8
-
4
-
-
0034131510
-
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
-
Rapley EA, Barfoot R, Bonaiti-Pellie C, Chompret A, Foulkes W, Perusinghe N, Reeve A, Royer-Pokora B, Schumacher V, Shelling A, Skeen J, de Tourreil S, Weirich A, Pritchard-Jones K, Stratton MR, Rahman N. Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2. Br J Cancer 2000;83:177-83.
-
(2000)
Br J Cancer
, vol.83
, pp. 177-183
-
-
Rapley, E.A.1
Barfoot, R.2
Bonaiti-Pellie, C.3
Chompret, A.4
Foulkes, W.5
Perusinghe, N.6
Reeve, A.7
Royer-Pokora, B.8
Schumacher, V.9
Shelling, A.10
Skeen, J.11
De Tourreil, S.12
Weirich, A.13
Pritchard-Jones, K.14
Stratton, M.R.15
Rahman, N.16
-
7
-
-
12144288675
-
Heterogeneity in Fanconi anemia: Evidence for 2 new genetic subtypes
-
Levitus M, Rooimans MA, Steltenpool J, Cool NF, Oostra AB, Mathew CG, Hoatlin ME, Waisfisz Q, Arwert F, de Winter JP, Joenje H. Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes. Blood 2004;103:2498-503.
-
(2004)
Blood
, vol.103
, pp. 2498-2503
-
-
Levitus, M.1
Rooimans, M.A.2
Steltenpool, J.3
Cool, N.F.4
Oostra, A.B.5
Mathew, C.G.6
Hoatlin, M.E.7
Waisfisz, Q.8
Arwert, F.9
De Winter, J.P.10
Joenje, H.11
-
8
-
-
0141484612
-
A novel ubiquitin ligase is deficient in Fanconi anemia
-
Meetei AR, de Winter JP, Medhurst AL, Wallisch M, Waisfisz Q, van de Vrugt HJ, Oostra AB, Yan Z, Ling C, Bishop CE, Hoatlin ME, Joenje H, Wang W. A novel ubiquitin ligase is deficient in Fanconi anemia. Nat Genet 2003;35:165-70.
-
(2003)
Nat Genet
, vol.35
, pp. 165-170
-
-
Meetei, A.R.1
De Winter, J.P.2
Medhurst, A.L.3
Wallisch, M.4
Waisfisz, Q.5
Van De Vrugt, H.J.6
Oostra, A.B.7
Yan, Z.8
Ling, C.9
Bishop, C.E.10
Hoatlin, M.E.11
Joenje, H.12
Wang, W.13
-
9
-
-
1942502234
-
Tracing the network connecting BRCA and Fanconi anaemia proteins
-
Venkitaraman AR. Tracing the network connecting BRCA and Fanconi anaemia proteins. Nat Rev Cancer 2004;4:266-76.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 266-276
-
-
Venkitaraman, A.R.1
-
10
-
-
18444362122
-
Biallelic inactivation of BRCA2 in Fanconi anemia
-
Howlett NG, Taniguchi T, Olson S, Cox B, Waisfisz Q, Die-Smulders C, Persky N, Grompe M, Joenje H, Pals G, Ikeda H, Fox EA, D'Andrea AD. Biallelic inactivation of BRCA2 in Fanconi anemia. Science 2002;297:606-9.
-
(2002)
Science
, vol.297
, pp. 606-609
-
-
Howlett, N.G.1
Taniguchi, T.2
Olson, S.3
Cox, B.4
Waisfisz, Q.5
Die-Smulders, C.6
Persky, N.7
Grompe, M.8
Joenje, H.9
Pals, G.10
Ikeda, H.11
Fox, E.A.12
D'Andrea, A.D.13
-
11
-
-
0142054687
-
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia
-
Offit K, Levran O, Mullaney B, Mah K, Nafa K, Batish SD, Diotti R, Schneider H, Deffenbaugh A, Scholl T, Proud VK, Robson M, Norton L, Ellis N, Hanenberg H, Auerbach AD. Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia. J Natl Cancer Inst 2003;95:1548-51.
-
(2003)
J Natl Cancer Inst
, vol.95
, pp. 1548-1551
-
-
Offit, K.1
Levran, O.2
Mullaney, B.3
Mah, K.4
Nafa, K.5
Batish, S.D.6
Diotti, R.7
Schneider, H.8
Deffenbaugh, A.9
Scholl, T.10
Proud, V.K.11
Robson, M.12
Norton, L.13
Ellis, N.14
Hanenberg, H.15
Auerbach, A.D.16
-
12
-
-
1642315917
-
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood
-
Hirsch B, Shimamura A, Moreau L, Baldinger S, Hag-Alshiekh M, Bostrom B, Sencer S, D'Andrea AD. Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood. Blood 2004;103:2554-9.
-
(2004)
Blood
, vol.103
, pp. 2554-2559
-
-
Hirsch, B.1
Shimamura, A.2
Moreau, L.3
Baldinger, S.4
Hag-Alshiekh, M.5
Bostrom, B.6
Sencer, S.7
D'Andrea, A.D.8
-
13
-
-
11144353924
-
Germline mutations in BRCA2: Shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia
-
Wagner JE, Tolar J, Levran O, Scholl T, Deffenbaugh A, Satagopan J, Ben Porat L, Mah K, Batish SD, Kutler DI, MacMillan ML, Hanenberg H, Auerbach AD. Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. Blood 2004;103:3226-9.
-
(2004)
Blood
, vol.103
, pp. 3226-3229
-
-
Wagner, J.E.1
Tolar, J.2
Levran, O.3
Scholl, T.4
Deffenbaugh, A.5
Satagopan, J.6
Ben Porat, L.7
Mah, K.8
Batish, S.D.9
Kutler, D.I.10
MacMillan, M.L.11
Hanenberg, H.12
Auerbach, A.D.13
-
14
-
-
0028902528
-
Association of Wilms' tumor with primary brain tumor in siblings
-
Rainov NG, Lubbe J, Renshaw J, Pritchard-Jones K, Luthy AR, Aguzzi A. Association of Wilms' tumor with primary brain tumor in siblings. J Neuropathol Exp Neurol 1995;54:214-23.
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 214-223
-
-
Rainov, N.G.1
Lubbe, J.2
Renshaw, J.3
Pritchard-Jones, K.4
Luthy, A.R.5
Aguzzi, A.6
-
15
-
-
0031736957
-
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1
-
Rahman N, Abidi F, Ford D, Arbour L, Rapley E, Tonin P, Barton D, Batcup G, Berry J, Cotter F, Davison V, Gerrard M, Gray E, Grundy R, Hanafy M, King D, Lewis I, Ridolfi LA, Madlensky L, Mann J, O'Meara A, Oakhill T, Skolnick M, Strong L, Stratton MR. Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1. Hum Genet 1998;103:547-56.
-
(1998)
Hum Genet
, vol.103
, pp. 547-556
-
-
Rahman, N.1
Abidi, F.2
Ford, D.3
Arbour, L.4
Rapley, E.5
Tonin, P.6
Barton, D.7
Batcup, G.8
Berry, J.9
Cotter, F.10
Davison, V.11
Gerrard, M.12
Gray, E.13
Grundy, R.14
Hanafy, M.15
King, D.16
Lewis, I.17
Ridolfi, L.A.18
Madlensky, L.19
Mann, J.20
O'Meara, A.21
Oakhill, T.22
Skolnick, M.23
Strong, L.24
Stratton, M.R.25
more..
-
16
-
-
0036199856
-
An update on conformation sensitive gel electrophoresis
-
Ganguly A. An update on conformation sensitive gel electrophoresis. Hum Mutat 2002;19:334-42.
-
(2002)
Hum Mutat
, vol.19
, pp. 334-342
-
-
Ganguly, A.1
-
17
-
-
0038697601
-
Cell cycle and genetic background dependence of the effect of loss of BRCA2 on ionizing radiation sensitivity
-
Tutt A, Connor F, Bertwistle D, Kerr P, Peacock J, Ross G, Ashworth A. Cell cycle and genetic background dependence of the effect of loss of BRCA2 on ionizing radiation sensitivity. Oncogene 2003;22:2926-31.
-
(2003)
Oncogene
, vol.22
, pp. 2926-2931
-
-
Tutt, A.1
Connor, F.2
Bertwistle, D.3
Kerr, P.4
Peacock, J.5
Ross, G.6
Ashworth, A.7
-
18
-
-
0036893150
-
The relationship between the roles of BRCA genes in DNA repair and cancer predisposition
-
Tutt A, Ashworth A. The relationship between the roles of BRCA genes in DNA repair and cancer predisposition. Trends Mol Med 2002;8:571-6.
-
(2002)
Trends Mol Med
, vol.8
, pp. 571-576
-
-
Tutt, A.1
Ashworth, A.2
-
19
-
-
16144368180
-
A polymorphic stop codon in BRCA2
-
Mazoyer S, Dunning AM, Serova O, Dearden J, Puget N, Healey CS, Gayther SA, Mangion J, Stratton MR, Lynch HT, Goldgar DE, Ponder BA, Lenoir GM. A polymorphic stop codon in BRCA2. Nat Genet 1996;14:253-4.
-
(1996)
Nat Genet
, vol.14
, pp. 253-254
-
-
Mazoyer, S.1
Dunning, A.M.2
Serova, O.3
Dearden, J.4
Puget, N.5
Healey, C.S.6
Gayther, S.A.7
Mangion, J.8
Stratton, M.R.9
Lynch, H.T.10
Goldgar, D.E.11
Ponder, B.A.12
Lenoir, G.M.13
-
20
-
-
0033768238
-
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability
-
Healey CS, Dunning AM, Teare MD, Chase D, Parker L, Burn J, Chang-Claude J, Mannermaa A, Kataja V, Huntsman DG, Pharoah PD, Luben RN, Easton DF, Ponder BA. A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability. Nat Genet 2000;26:362-4.
-
(2000)
Nat Genet
, vol.26
, pp. 362-364
-
-
Healey, C.S.1
Dunning, A.M.2
Teare, M.D.3
Chase, D.4
Parker, L.5
Burn, J.6
Chang-Claude, J.7
Mannermaa, A.8
Kataja, V.9
Huntsman, D.G.10
Pharoah, P.D.11
Luben, R.N.12
Easton, D.F.13
Ponder, B.A.14
-
21
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
The Breast Cancer Linkage Consortium
-
Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, Bishop DT, Weber B, Lenoir G, Chang-Claude J, Sobol H, Teare MD, Struewing J, Arason A, Scherneck S, Peto J, Rebbeck TR, Tonin P, Neuhausen S, Barkardottir R, Eyfjord J, Lynch H, Ponder BA, Gayther SA, Zelada-Hedman M, and the Breast Cancer Linkage Consortium. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Am J Hum Genet 1998;62:676-89.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
Narod, S.4
Goldgar, D.5
Devilee, P.6
Bishop, D.T.7
Weber, B.8
Lenoir, G.9
Chang-Claude, J.10
Sobol, H.11
Teare, M.D.12
Struewing, J.13
Arason, A.14
Scherneck, S.15
Peto, J.16
Rebbeck, T.R.17
Tonin, P.18
Neuhausen, S.19
Barkardottir, R.20
Eyfjord, J.21
Lynch, H.22
Ponder, B.A.23
Gayther, S.A.24
Zelada-Hedman, M.25
more..
-
22
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 1996;41:188-90.
-
(1996)
Nat Genet
, vol.41
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
Neuhausen, S.4
Brody, L.C.5
Kaback, M.6
Haas, B.7
Norton, L.8
Borgen, P.9
Jhanwar, S.10
Goldgar, D.11
Ostrer, H.12
Offit, K.13
|