-
1
-
-
0038744296
-
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
-
Antoniou A, Pharoah P, Narod S, Risch H, Eyfjord J, Hopper J, Loman N, Olsson H, Johannsson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles DM, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Gorski B, Tulinius H, Thorlacius S, Eerola H, Nevanlinna H, Syrjakoski K, Kallioniemi OP, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF. 2003. 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. Am J Hum Genet 72:1117-1130.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.2
Narod, S.3
Risch, H.4
Eyfjord, J.5
Hopper, J.6
Loman, N.7
Olsson, H.8
Johannsson, O.9
Borg, A.10
Pasini, B.11
Radice, P.12
Manoukian, S.13
Eccles, D.M.14
Tang, N.15
Olah, E.16
Anton-Culver, H.17
Warner, E.18
Lubinski, J.19
Gronwald, J.20
Gorski, B.21
Tulinius, H.22
Thorlacius, S.23
Eerola, H.24
Nevanlinna, H.25
Syrjakoski, K.26
Kallioniemi, O.P.27
Thompson, D.28
Evans, C.29
Peto, J.30
Lalloo, F.31
Evans, D.G.32
Easton, D.F.33
more..
-
2
-
-
0030482567
-
Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer
-
Athma P, Rappaport R, Swift M. 1996. Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet Cyrogenet 92:330-134.
-
(1996)
Cancer Genet Cyrogenet
, vol.92
, pp. 330-1134
-
-
Athma, P.1
Rappaport, R.2
Swift, M.3
-
3
-
-
1842591180
-
Attenuation of the p53 response to DNA damage by high cell density
-
Bar J, Cohen-Noyman E, Geiger B, Oren M. 2004. Attenuation of the p53 response to DNA damage by high cell density. Oncogene 23:2128-2137.
-
(2004)
Oncogene
, vol.23
, pp. 2128-2137
-
-
Bar, J.1
Cohen-Noyman, E.2
Geiger, B.3
Oren, M.4
-
4
-
-
0036883717
-
Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer
-
Barlund M, Monni O, Weaver JD, Kauraniemi P, Sauter G, Heiskanen M, Kallioniemi OP, Kallioniemi A. 2002. Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer. Genes Chromosomes Cancer 35:311-317.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 311-317
-
-
Barlund, M.1
Monni, O.2
Weaver, J.D.3
Kauraniemi, P.4
Sauter, G.5
Heiskanen, M.6
Kallioniemi, O.P.7
Kallioniemi, A.8
-
5
-
-
0032778345
-
Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer
-
Bebb D, Yu Z, Chen J, Telatar M, Gelmon K, Phillips N, Gatti R, Glickman B. 1999. Absence of mutations in the ATM gene in forty-seven cases of sporadic breast cancer. Br J Cancer 80:1979-1981.
-
(1999)
Br J Cancer
, vol.80
, pp. 1979-1981
-
-
Bebb, D.1
Yu, Z.2
Chen, J.3
Telatar, M.4
Gelmon, K.5
Phillips, N.6
Gatti, R.7
Glickman, B.8
-
6
-
-
0242574702
-
ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer
-
WECARE Study Collaborative Group
-
Bernstein JE, Bernstein L, Thompson WD, Lynch CF, Malone KE, Teitelbaum SL, Olsen JH, Anton-Culver H, Boice JD, Rosenstein BS, Børresen-Dale A-L, Gatti RA, Concannon P, WECARE Study Collaborative Group, Haile RW. 2003. ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer. Br J Cancer 89:1513-1516.
-
(2003)
Br J Cancer
, vol.89
, pp. 1513-1516
-
-
Bernstein, J.E.1
Bernstein, L.2
Thompson, W.D.3
Lynch, C.F.4
Malone, K.E.5
Teitelbaum, S.L.6
Olsen, J.H.7
Anton-Culver, H.8
Boice, J.D.9
Rosenstein, B.S.10
Børresen-Dale, A.-L.11
Gatti, R.A.12
Concannon, P.13
Haile, R.W.14
-
7
-
-
33750904243
-
Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the breast cancer family registry
-
in press
-
Bernstein JL, Teraoka S, Southey MC, Jenkins MA, Andrulis IL, Knight JA, John EM, Lapinski R, Wolitzer AL, Whittemore AS, West D, Seminara D, Olson ER, Spurdle AB, Chenevix-Trench G, Giles GG, Hopper JL, Concannon P. 2006. Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the breast cancer family registry. Hum Mutat, in press.
-
(2006)
Hum Mutat
-
-
Bernstein, J.L.1
Teraoka, S.2
Southey, M.C.3
Jenkins, M.A.4
Andrulis, I.L.5
Knight, J.A.6
John, E.M.7
Lapinski, R.8
Wolitzer, A.L.9
Whittemore, A.S.10
West, D.11
Seminara, D.12
Olson, E.R.13
Spurdle, A.B.14
Chenevix-Trench, G.15
Giles, G.G.16
Hopper, J.L.17
Concannon, P.18
-
8
-
-
4344675053
-
Identifying the molecular phenotype of renal progenitor cells
-
Challen G, Martinez G, Davis M, Taylor D, Crowe M, Teasdale R, Grimmond S, Little M. 2004. Identifying the molecular phenotype of renal progenitor cells. J Am Soc Nephrol 15:2344-2357.
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 2344-2357
-
-
Challen, G.1
Martinez, G.2
Davis, M.3
Taylor, D.4
Crowe, M.5
Teasdale, R.6
Grimmond, S.7
Little, M.8
-
9
-
-
0032054221
-
The role of ataxia-telangiectasia heterozygotes in familial breast cancer
-
Chen J, Birkholtz GG, Lindblom P, Rubio C, Lindblom A. 1998. The role of ataxia-telangiectasia heterozygotes in familial breast cancer. Cancer Res 58:1376-1379.
-
(1998)
Cancer Res
, vol.58
, pp. 1376-1379
-
-
Chen, J.1
Birkholtz, G.G.2
Lindblom, P.3
Rubio, C.4
Lindblom, A.5
-
10
-
-
0033531272
-
Chk1 complements the G2/M checkpoint defect and radiosensitivity of ataxia-telangiectasia cells
-
Chen P, Gatei M, O'Connell M, Khanna K, Bugg S, Hogg A, Scott S, Hobson K, Lavin M. 1999. Chk1 complements the G2/M checkpoint defect and radiosensitivity of ataxia-telangiectasia cells. Oncogene 18:249-
-
(1999)
Oncogene
, vol.18
, pp. 249
-
-
Chen, P.1
Gatei, M.2
O'Connell, M.3
Khanna, K.4
Bugg, S.5
Hogg, A.6
Scott, S.7
Hobson, K.8
Lavin, M.9
-
11
-
-
0037028740
-
Dominant negative ATM mutations in breast cancer families
-
Trench G, Spurdle A, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins M, Scott C, Pupo GM, Dörk T, Bendix R, Kirk J, Tucker K, McCredie MRE, Hopper JL, Sambrook J, Mann GJ, Khanna KK. 2002a. Dominant negative ATM mutations in breast cancer families. J Natl Cancer Inst 94:205-215.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 205-215
-
-
Trench, G.1
Spurdle, A.2
Gatei, M.3
Kelly, H.4
Marsh, A.5
Chen, X.6
Donn, K.7
Cummings, M.8
Nyholt, D.9
Jenkins, M.10
Scott, C.11
Pupo, G.M.12
Dörk, T.13
Bendix, R.14
Kirk, J.15
Tucker, K.16
McCredie, M.R.E.17
Hopper, J.L.18
Sambrook, J.19
Mann, G.J.20
Khanna, K.K.21
more..
-
12
-
-
0037134693
-
Dominant negative ATM mutations in breast cancer families: Erratum
-
Chenevix-Trench G, Spurdle A, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins M, Scott C, Pupo GM, Dork T, Bendix R, Kirk J, Tucker K, McCredie MRE, Hopper JL, Sambrook J, Mann GJ, Khanna KK. 2002b. Dominant negative ATM mutations in breast cancer families: Erratum. J Natl Cancer Inst 94:952.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 952
-
-
Chenevix-Trench, G.1
Spurdle, A.2
Gatei, M.3
Kelly, H.4
Marsh, A.5
Chen, X.6
Donn, K.7
Cummings, M.8
Nyholt, D.9
Jenkins, M.10
Scott, C.11
Pupo, G.M.12
Dork, T.13
Bendix, R.14
Kirk, J.15
Tucker, K.16
McCredie, M.R.E.17
Hopper, J.L.18
Sambrook, J.19
Mann, G.J.20
Khanna, K.K.21
more..
-
13
-
-
0042386145
-
Mammalian RanBP1 regulates centrosome cohesion during mitosis
-
Di Fiore B, Ciciarello M, Mangiacasale R, Palena A, Tassin A-M, Cundari E, Lavia P. 2003. Mammalian RanBP1 regulates centrosome cohesion during mitosis. J Cell Sci 116:3399-3411.
-
(2003)
J Cell Sci
, vol.116
, pp. 3399-3411
-
-
Di Fiore, B.1
Ciciarello, M.2
Mangiacasale, R.3
Palena, A.4
Tassin, A.-M.5
Cundari, E.6
Lavia, P.7
-
14
-
-
1642410381
-
Cellular responses to ionising radiation of at heterozygotes: Differences between missense and truncating mutation carriers
-
Fernet M, Moullan N, Lauge A, Stoppa-Lyonnet D, Hall J. 2004. Cellular responses to ionising radiation of AT heterozygotes: Differences between missense and truncating mutation carriers. Br J Cancer 90:866-873.
-
(2004)
Br J Cancer
, vol.90
, pp. 866-873
-
-
Fernet, M.1
Moullan, N.2
Lauge, A.3
Stoppa-Lyonnet, D.4
Hall, J.5
-
15
-
-
0031029676
-
Heterozygous ATM mutations do not contribute to early onset of breast cancer
-
FitzGerald M, Bean J, Hegde S, Unsal H, MacDonald D, Harkin D, Finkelstein D, Isselbacher K, Haber D. 1997. Heterozygous ATM mutations do not contribute to early onset of breast cancer. Nat Genet 15:307-310.
-
(1997)
Nat Genet
, vol.15
, pp. 307-310
-
-
Fitzgerald, M.1
Bean, J.2
Hegde, S.3
Unsal, H.4
MacDonald, D.5
Harkin, D.6
Finkelstein, D.7
Isselbacher, K.8
Haber, D.9
-
16
-
-
0035905742
-
Ataxia-telangiectasia: Chronic activation of damage-responsive functions is reduced by a-lipoic acid
-
Gatei M, Shkedy D, Khanna K, Uziel T, Shiloh Y, Pandita T, Lavin M, Rotman G. 2001. Ataxia-telangiectasia: Chronic activation of damage-responsive functions is reduced by a-lipoic acid. Oncogene 20:289-294.
-
(2001)
Oncogene
, vol.20
, pp. 289-294
-
-
Gatei, M.1
Shkedy, D.2
Khanna, K.3
Uziel, T.4
Shiloh, Y.5
Pandita, T.6
Lavin, M.7
Rotman, G.8
-
17
-
-
0033380655
-
Cancer risk in ATM Heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations
-
Gatti R, Tward A, Concannon P. 1999. Cancer risk in ATM Heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations. Mol Genet Metab 68:419-423.
-
(1999)
Mol Genet Metab
, vol.68
, pp. 419-423
-
-
Gatti, R.1
Tward, A.2
Concannon, P.3
-
18
-
-
0035879874
-
Cancer risk in heterozygotes for ataxia-telangiectasia
-
Geoffroy-Perez B, Janin N, Ossian K, Lauge A, Croquette M, Griscelli C, Debre M, Bressac-de-Paillerets B, Aurias A, Stoppa-Lyonnet D, Andrieu N. 2003. Cancer risk in heterozygotes for ataxia-telangiectasia. Int J Caneer 93:288-293.
-
(2003)
Int J Caneer
, vol.93
, pp. 288-293
-
-
Geoffroy-Perez, B.1
Janin, N.2
Ossian, K.3
Lauge, A.4
Croquette, M.5
Griscelli, C.6
Debre, M.7
Bressac-de-Paillerets, B.8
Aurias, A.9
Stoppa-Lyonnet, D.10
Andrieu, N.11
-
19
-
-
2342565206
-
Functional consequences of ATM sequence variants for chromosomal radiosensitivity
-
Gutierrez-Enriquez S, Fernet M, Dork T, Bremer M, Lauge A, Stoppa-Lyonnet D, Moullan N, Angele S, Hall J. 2004. Functional consequences of ATM sequence variants for chromosomal radiosensitivity. Genes Chromosomes Cancer 40:109-119.
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 109-119
-
-
Gutierrez-Enriquez, S.1
Fernet, M.2
Dork, T.3
Bremer, M.4
Lauge, A.5
Stoppa-Lyonnet, D.6
Moullan, N.7
Angele, S.8
Hall, J.9
-
20
-
-
0344319833
-
Identifying biological themes within lists of genes with EASE
-
Hosack D, Dennis G, Jr., Sherman B, Lane H, Lempicki R. 2003. Identifying biological themes within lists of genes with EASE. Genome Biol 4:R70.
-
(2003)
Genome Biol
, vol.4
-
-
Hosack, D.1
Dennis Jr., G.2
Sherman, B.3
Lane, H.4
Lempicki, R.5
-
21
-
-
0032983665
-
Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia
-
Inskip H, Kinlen L, Taylor A, Woods C, Arlett C. 1999. Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia. Br J Cancer 79:1304-1307.
-
(1999)
Br J Cancer
, vol.79
, pp. 1304-1307
-
-
Inskip, H.1
Kinlen, L.2
Taylor, A.3
Woods, C.4
Arlett, C.5
-
22
-
-
0032926569
-
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: Haplotype study in French at families
-
Janin N, Andrieu N, Ossian K, Laugé A, Croquette M-F, Griscelli C, Debré M, Bressac-de-Paillerets B, Aurias A, StoppaLyonnet D. 1999. Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: Haplotype study in French AT families. Br J Caneer 80:1042-1045.
-
(1999)
Br J Caneer
, vol.80
, pp. 1042-1045
-
-
Janin, N.1
Andrieu, N.2
Ossian, K.3
Laugé, A.4
Croquette, M.-F.5
Griscelli, C.6
Debré, M.7
Bressac-de-Paillerets, B.8
Aurias, A.9
Stoppalyonnet, D.10
-
23
-
-
0035093737
-
DNA double-strand breaks: Signaling, repair and the cancer connection
-
Khanna K, Jackson S. 2001. DNA double-strand breaks: Signaling, repair and the cancer connection. Nat Genet 27:247-254.
-
(2001)
Nat Genet
, vol.27
, pp. 247-254
-
-
Khanna, K.1
Jackson, S.2
-
24
-
-
0000303499
-
ATM associates with and phospharylates p53: Mapping the region of interaction
-
Khanna K, Keating K, Kozlov S, Scott S, Gatei M, Hobson K, Taya Y, Gabrielli B, Chan D, Lees-Miller S, Lavin MF. 1998. ATM associates with and phospharylates p53: Mapping the region of interaction. Nat Genet 20:398-400.
-
(1998)
Nat Genet
, vol.20
, pp. 398-400
-
-
Khanna, K.1
Keating, K.2
Kozlov, S.3
Scott, S.4
Gatei, M.5
Hobson, K.6
Taya, Y.7
Gabrielli, B.8
Chan, D.9
Lees-Miller, S.10
Lavin, M.F.11
-
25
-
-
0024190141
-
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
-
472
-
Lange K, Weeks D. Boehnke M. 1988. Programs for pedigree analysis: MENDEL, FISHER, and dGENE. Genet Epidemiol 5:471, 472.
-
(1988)
Genet Epidemiol
, vol.5
, pp. 471
-
-
Lange, K.1
Weeks, D.2
Boehnke, M.3
-
26
-
-
33644949696
-
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
-
Kathleen Cuningham Consortium for Research in Familial Breast Cancer
-
Mann G, Thorne H, Balleine R, Butow P, Clarke C, Edkins E, Evans G, Fereday S, Haan E, Gattas M, Giles GG, Goldblatt J, Hopper JL, Kirk J, Leary JA, Lindeman G, Niedermayr E, Phillips K-A, Picken S, Pupo GM, Saunders C, Scott CL, Spurdle AB, Suthers G, Tucker K, Chenevix-Trench G, Kathleen Cuningham Consortium for Research in Familial Breast Cancer. 2006. Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource. Breast Cancer Res 8:R12.
-
(2006)
Breast Cancer Res
, vol.8
-
-
Mann, G.1
Thorne, H.2
Balleine, R.3
Butow, P.4
Clarke, C.5
Edkins, E.6
Evans, G.7
Fereday, S.8
Haan, E.9
Gattas, M.10
Giles, G.G.11
Goldblatt, J.12
Hopper, J.L.13
Kirk, J.14
Leary, J.A.15
Lindeman, G.16
Niedermayr, E.17
Phillips, K.-A.18
Picken, S.19
Pupo, G.M.20
Saunders, C.21
Scott, C.L.22
Spurdle, A.B.23
Suthers, G.24
Tucker, K.25
Chenevix-Trench, G.26
more..
-
27
-
-
33644993216
-
Computational approaches for predicting the biological effect of p53 missense mutations: A comparison of 3 sequence analysis based methods
-
Mathe E, Olivier M, Kato S, Ishioka C, Hainaut P, Tavtigian S. 2006. Computational approaches for predicting the biological effect of p53 missense mutations: A comparison of 3 sequence analysis based methods. Nucleic Acids Res 5:1317-1325.
-
(2006)
Nucleic Acids Res
, vol.5
, pp. 1317-1325
-
-
Mathe, E.1
Olivier, M.2
Kato, S.3
Ishioka, C.4
Hainaut, P.5
Tavtigian, S.6
-
28
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
Ng P, Henikoff S. 2003. SIFT: Predicting amino acid changes that affect protein function. Nucleic Acids Res 31:3812-3814.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3812-3814
-
-
Ng, P.1
Henikoff, S.2
-
29
-
-
0035900911
-
Cancer in patients with ataxia-telangiectasia and in their relatives in the Nordic countries
-
Olsen J, Hahnemann J, Børresen-Dale A-L, Børndum-Nielsen K, Hammarström L, Kleinerman R, Kääriäinen H, Lönnqvist T, Sankila R, Seersholm N, Tretli S, Yuen J, Boice JD, Tucker M. 2001. Cancer in patients with ataxia-telangiectasia and in their relatives in the Nordic countries. J Natl Cancer Inst 93:121-127.
-
(2001)
J Natl Cancer Inst
, vol.93
, pp. 121-127
-
-
Olsen, J.1
Hahnemann, J.2
Børresen-Dale, A.-L.3
Børndum-Nielsen, K.4
Hammarström, L.5
Kleinerman, R.6
Kääriäinen, H.7
Lönnqvist, T.8
Sankila, R.9
Seersholm, N.10
Tretli, S.11
Yuen, J.12
Boice, J.D.13
Tucker, M.14
-
30
-
-
23644442874
-
Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia
-
Olsen J, Hahnemann J, Børrescn-Dale A-L, Tretli S, Kleinerman R, Sankila R, Hammarström L, Robsahm T, Kääriäinen H, Bregard A, Børndum-Nielsen K, Yuen J, Tucker M. 2005. Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia. Br J Cancer 93:260-265.
-
(2005)
Br J Cancer
, vol.93
, pp. 260-265
-
-
Olsen, J.1
Hahnemann, J.2
Børrescn-Dale, A.-L.3
Tretli, S.4
Kleinerman, R.5
Sankila, R.6
Hammarström, L.7
Robsahm, T.8
Kääriäinen, H.9
Bregard, A.10
Børndum-Nielsen, K.11
Yuen, J.12
Tucker, M.13
-
31
-
-
3242878412
-
3DCoffee@igs: A web server for combining sequences and structures into a multiple sequence alignment
-
Poirot O, Suhre K, Abergel C, O'Toole E, Notredame C. 2004. 3DCoffee@igs: A web server for combining sequences and structures into a multiple sequence alignment. Nucleic Acids Res 32: w37-w40.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Poirot, O.1
Suhre, K.2
Abergel, C.3
O'Toole, E.4
Notredame, C.5
-
32
-
-
0037099005
-
BioArray Software Environment (BASE): A platform for comprehensive management and analysis of microarray data
-
SOFTWARE0003
-
Saal LH, Troein C, Vallon-Christersson J, Gruvberger S, Borg A, Peterson C. 2002. BioArray Software Environment (BASE): A platform for comprehensive management and analysis of microarray data. Genome Biol 3:SOFTWARE0003.
-
(2002)
Genome Biol
, vol.3
-
-
Saal, L.H.1
Troein, C.2
Vallon-Christersson, J.3
Gruvberger, S.4
Borg, A.5
Peterson, C.6
-
33
-
-
7344226182
-
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients
-
Shayeghi M, Seal S, Regan J, Collins N, Barfoot R, Rahman N, Ashton A, Moohan M, Wooster K, Owen R, Bliss JM, Stratton MR, Yarnold J. 1998. Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients. Br J Cancer 78:922-927.
-
(1998)
Br J Cancer
, vol.78
, pp. 922-927
-
-
Shayeghi, M.1
Seal, S.2
Regan, J.3
Collins, N.4
Barfoot, R.5
Rahman, N.6
Ashton, A.7
Moohan, M.8
Wooster, K.9
Owen, R.10
Bliss, J.M.11
Stratton, M.R.12
Yarnold, J.13
-
34
-
-
4544341015
-
Linear models and empirical haves methods for assessing differential expression in microarray experiments
-
Article3
-
Smyth GK. 2004. Linear models and empirical haves methods for assessing differential expression in microarray experiments. Stat Appl Genet Mol Biol 3: Article3.
-
(2004)
Stat Appl Genet Mol Biol
, vol.3
-
-
Smyth, G.K.1
-
35
-
-
0042655147
-
ATM missense mutations are frequent in patients with breast cancer
-
Sommer S, Jiang Z, Feng J, Buzin C, Zheng J, Longmate J, Jung M, Moulds J, Dritschilo A. 2003. ATM missense mutations are frequent in patients with breast cancer. Cancer Genet Cytogenet 145:115-120.
-
(2003)
Cancer Genet Cytogenet
, vol.145
, pp. 115-120
-
-
Sommer, S.1
Jiang, Z.2
Feng, J.3
Buzin, C.4
Zheng, J.5
Longmate, J.6
Jung, M.7
Moulds, J.8
Dritschilo, A.9
-
36
-
-
9144247813
-
Microarray analysis reveals that TP53- and ATM-mutant B-CLLs share a defect in activating proapoptotic responses after DNAdamage but are distinguished by major differences in activating prosurvival responses
-
Stankovic T, Hubank M, Cronin D, Stewart G, Fletcher D, Bignell C, Alvi A, Austen B, Weston V, Fegan C, Byrd PJ, Moss PAH, Taylor AMR. 2004. Microarray analysis reveals that TP53- and ATM-mutant B-CLLs share a defect in activating proapoptotic responses after DNAdamage but are distinguished by major differences in activating prosurvival responses. Blood 103:291-300.
-
(2004)
Blood
, vol.103
, pp. 291-300
-
-
Stankovic, T.1
Hubank, M.2
Cronin, D.3
Stewart, G.4
Fletcher, D.5
Bignell, C.6
Alvi, A.7
Austen, B.8
Weston, V.9
Fegan, C.10
Byrd, P.J.11
Moss, P.A.H.12
Taylor, A.M.R.13
-
37
-
-
17344362697
-
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: Expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer
-
Stankovic T, Kidd A, Sutcliffe A, McGuire G, Robinson P, Weber P, Bedenham T, Bradwell A, Easton D, Lennox G, Haites N, Byrd PJ, Taylor AMR. 1998. ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: Expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Am J Hum Genet 62:334-345.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 334-345
-
-
Stankovic, T.1
Kidd, A.2
Sutcliffe, A.3
McGuire, G.4
Robinson, P.5
Weber, P.6
Bedenham, T.7
Bradwell, A.8
Easton, D.9
Lennox, G.10
Haites, N.11
Byrd, P.J.12
Taylor, A.M.R.13
-
38
-
-
0035839431
-
Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T3G mutations, showing a less severe phenotype
-
Stewart G, Last J, Stankovic T, Haites N, Kidd A, Byrd P, Taylor A. 2001. Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T3G mutations, showing a less severe phenotype. J Biol Chem 276:30133-30141.
-
(2001)
J Biol Chem
, vol.276
, pp. 30133-30141
-
-
Stewart, G.1
Last, J.2
Stankovic, T.3
Haites, N.4
Kidd, A.5
Byrd, P.6
Taylor, A.7
-
39
-
-
0034700243
-
Mortality rates among carriers of ataxia telangiectasia mutant allcles
-
Su Y, Swift M. 2000. Mortality rates among carriers of ataxia telangiectasia mutant allcles. Ann Int Med 133:770-778.
-
(2000)
Ann Int Med
, vol.133
, pp. 770-778
-
-
Su, Y.1
Swift, M.2
-
40
-
-
0017238344
-
Malignant neoplasms in the families of patients with ataxia- telangiectasia
-
Swift M, Sholman L, Perry M, Chase C. 1976. Malignant neoplasms in the families of patients with ataxia-telangiectasia. Cancer Res 36:209-215.
-
(1976)
Cancer Res
, vol.36
, pp. 209-215
-
-
Swift, M.1
Sholman, L.2
Perry, M.3
Chase, C.4
-
41
-
-
10744219867
-
Are ATM mutations 7271T3G and IVS10-6T3G really high-risk breast cancer-susceptibility alleles?
-
the BRCA-X Consortium, Cooperative Family Registry Breast Cancer Study, Interdisciplinary Health Research International Team on Breast Cancer Susceptibility
-
Szabo C, Schutte M, Broeks A, Houwing-Duistermaat J, Thorstenson Y, Durocher F, Oldenburg R, Wasielewski M, Odefrey F, Thompson D, Floore AN, Kraan J, Klijn JGM, van den Ouweland AMW, the BRCA-X Consortium, Cooperative Family Registry Breast Cancer Study, Interdisciplinary Health Research International Team on Breast Cancer Susceptibility. Wagner TMU, Devilee P, Simard J, van't Veer LJ, Goldgar DE, Meijers-Heijboer H. 2004. Are ATM mutations 7271T3G and IVS10-6T3G really high-risk breast cancer-susceptibility alleles? Cancer Res 64:840-843.
-
(2004)
Cancer Res
, vol.64
, pp. 840-843
-
-
Szabo, C.1
Schutte, M.2
Broeks, A.3
Houwing-Duistermaat, J.4
Thorstenson, Y.5
Durocher, F.6
Oldenburg, R.7
Wasielewski, M.8
Odefrey, F.9
Thompson, D.10
Floore, A.N.11
Kraan, J.12
Klijn, J.G.M.13
Van Den Ouweland, A.M.W.14
Wagner, T.M.U.15
Devilee, P.16
Simard, J.17
Van't Veer, L.J.18
Goldgar, D.E.19
Meijers-Heijboer, H.20
more..
-
42
-
-
33644537810
-
Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral
-
Tavtigian SV, Deffenbangh AM, Yin L, Judkins T, Scholl T, Samollow PB, de Silva D, Zharkikh A, Thomas A. 2006. Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral. J Med Genet 43:295-305.
-
(2006)
J Med Genet
, vol.43
, pp. 295-305
-
-
Tavtigian, S.V.1
Deffenbangh, A.M.2
Yin, L.3
Judkins, T.4
Scholl, T.5
Samollow, P.B.6
De Silva, D.7
Zharkikh, A.8
Thomas, A.9
-
43
-
-
34548057762
-
Two ATM variants and breast cancer risk
-
595
-
Thompson IJ, Antonion AC, Jenkins M, Marsh A, Chen X, Wayne T, Tesoriero A, Milne R, Spurdle A, Thorstenson V, Southey M, Giles GG, kConFab Investigators, Khanna KK, Sambrook J, Oefner P, Goldgar D, Hopper JL, Easton DF, Chenevix-Trench G. 2005a. Two ATM variants and breast cancer risk. Hum Mutat 25:594, 595.
-
(2005)
Hum Mutat
, vol.25
, pp. 594
-
-
Thompson, I.J.1
Antonion, A.C.2
Jenkins, M.3
Marsh, A.4
Chen, X.5
Wayne, T.6
Tesoriero, A.7
Milne, R.8
Spurdle, A.9
Thorstenson, V.10
Southey, M.11
Giles, G.G.12
Investigators, K.13
Khanna, K.K.14
Sambrook, J.15
Oefner, P.16
Goldgar, D.17
Hopper, J.L.18
Easton, D.F.19
Chenevix-Trench, G.20
more..
-
44
-
-
20544474516
-
Cancer risks and mortality in heterozygous ATM mutation carriers
-
Thompson D, Duedal S, Kirner J, McGuffog L, Last J, Reiman A, Byrd P, Taylor M, Easton D. 2005b. Cancer risks and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst 97:813-822.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 813-822
-
-
Thompson, D.1
Duedal, S.2
Kirner, J.3
McGuffog, L.4
Last, J.5
Reiman, A.6
Byrd, P.7
Taylor, M.8
Easton, D.9
-
45
-
-
0042387707
-
A full-likelihood method for the evaluation of causality of sequence variants from family data
-
Thompson D, Easton D, Goldgar D. 2003. A full-likelihood method for the evaluation of causality of sequence variants from family data. Am J Hum Genet 73:652-6555.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 652-6555
-
-
Thompson, D.1
Easton, D.2
Goldgar, D.3
-
46
-
-
9344219890
-
The ATM gene and susceptibility to breast cancer: Analysis of 38 breast tumors reveals no evidence for mutation
-
Vorechovsky I, Rasio D, Luo L, Monaco C, Hammarstrom L, Webster AD, Zaloudik J, Barhanti-Brodani G, James M, Russo G. 1996. The ATM gene and susceptibility to breast cancer: Analysis of 38 breast tumors reveals no evidence for mutation. Cancer Res 56:2726-2732.
-
(1996)
Cancer Res
, vol.56
, pp. 2726-2732
-
-
Vorechovsky, I.1
Rasio, D.2
Luo, L.3
Monaco, C.4
Hammarstrom, L.5
Webster, A.D.6
Zaloudik, J.7
Barhanti-Brodani, G.8
James, M.9
Russo, G.10
-
47
-
-
0036783355
-
Gene expression phenotype in heterozygous carriers of ataxia telangieetasia
-
Watts J, Morley M, Burdick J, Fiori J, Ewens W, Spielman R, Cheung V. 2002. Gene expression phenotype in heterozygous carriers of ataxia telangieetasia. Am J Hum Genet 71:791-800.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 791-800
-
-
Watts, J.1
Morley, M.2
Burdick, J.3
Fiori, J.4
Ewens, W.5
Spielman, R.6
Cheung, V.7
-
48
-
-
0026611233
-
Heterogeneity in the elastogenic response to X-rays in lymphocytes from ataxia-telangiectasia heterozygotes and controls
-
Wiencke J, Wara D, Little J, Kelsey K. 1992. Heterogeneity in the elastogenic response to X-rays in lymphocytes from ataxia-telangiectasia heterozygotes and controls. Cancer Causes Control 3:237-245.
-
(1992)
Cancer Causes Control
, vol.3
, pp. 237-245
-
-
Wiencke, J.1
Wara, D.2
Little, J.3
Kelsey, K.4
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