-
1
-
-
84884582201
-
Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning?
-
Ghoussaini M, Pharoah PD, Easton DF. Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning? AmJPathol 2013;183:1038-51
-
(2013)
AmJPathol
, vol.183
, pp. 1038-1051
-
-
Ghoussaini, M.1
Pharoah, P.D.2
Easton, D.F.3
-
2
-
-
84930531402
-
Gene-panel sequencing and the prediction of breast-cancer risk
-
Easton DF, Pharoah PD, Antoniou AC, Tischkowitz M, Tavtigian SV, Nathanson KL, Devilee P, Meindl A, Couch FJ, Southey M, Goldgar DE, Evans DG, Chenevix-Trench G, Rahman N, Robson M, Domchek SM, Foulkes WD. Gene-panel sequencing and the prediction of breast-cancer risk. N Engl J Med 2015;372:2243-57
-
(2015)
N Engl J Med
, vol.372
, pp. 2243-2257
-
-
Easton, D.F.1
Pharoah, P.D.2
Antoniou, A.C.3
Tischkowitz, M.4
Tavtigian, S.V.5
Nathanson, K.L.6
Devilee, P.7
Meindl, A.8
Couch, F.J.9
Southey, M.10
Goldgar, D.E.11
Evans, D.G.12
Chenevix-Trench, G.13
Rahman, N.14
Robson, M.15
Domchek, S.M.16
Foulkes, W.D.17
-
3
-
-
20644461718
-
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
-
Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, Grossman S, Wahrer DC, Sgroi DC, Lane WS, Haber DA, Livingston DM. BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell 2001;105:149-60
-
(2001)
Cell
, vol.105
, pp. 149-160
-
-
Cantor, S.B.1
Bell, D.W.2
Ganesan, S.3
Kass, E.M.4
Drapkin, R.5
Grossman, S.6
Wahrer, D.C.7
Sgroi, D.C.8
Lane, W.S.9
Haber, D.A.10
Livingston, D.M.11
-
4
-
-
24944575242
-
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ
-
Litman R, Peng M, Jin Z, Zhang F, Zhang J, Powell S, Andreassen PR, Cantor SB. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer cell 2005;8:255-65
-
(2005)
Cancer cell
, vol.8
, pp. 255-265
-
-
Litman, R.1
Peng, M.2
Jin, Z.3
Zhang, F.4
Zhang, J.5
Powell, S.6
Andreassen, P.R.7
Cantor, S.B.8
-
5
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet 2005;37:934-5
-
(2005)
Nat Genet
, vol.37
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
de Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Rooimans, M.A.9
Pals, G.10
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
6
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
Seal S, Thompson D, Renwick A, Elliott A, Kelly P, Barfoot R, Chagtai T, Jayatilake H, Ahmed M, Spanova K, North B, McGuffog L, Evans DG, Eccles D, Breast Cancer Susceptibility C, Easton DF, Stratton MR, Rahman N. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet 2006;38:1239-41
-
(2006)
Nat Genet
, vol.38
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Breast Cancer Susceptibility, C.15
Easton, D.F.16
Stratton, M.R.17
Rahman, N.18
-
7
-
-
34447106707
-
BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study
-
Frank B, Hemminki K, Meindl A, Wappenschmidt B, Sutter C, Kiechle M, Bugert P, Schmutzler RK, Bartram CR, Burwinkel B. BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study. BMC Cancer 2007;7:83
-
(2007)
BMC Cancer
, vol.7
, pp. 83
-
-
Frank, B.1
Hemminki, K.2
Meindl, A.3
Wappenschmidt, B.4
Sutter, C.5
Kiechle, M.6
Bugert, P.7
Schmutzler, R.K.8
Bartram, C.R.9
Burwinkel, B.10
-
8
-
-
84870417701
-
Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families
-
Catucci I, Milgrom R, Kushnir A, Laitman Y, Paluch-Shimon S, Volorio S, Ficarazzi F, Bernard L, Radice P, Friedman E, Peterlongo P. Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families. Fam Cancer 2012;11:483-91
-
(2012)
Fam Cancer
, vol.11
, pp. 483-491
-
-
Catucci, I.1
Milgrom, R.2
Kushnir, A.3
Laitman, Y.4
Paluch-Shimon, S.5
Volorio, S.6
Ficarazzi, F.7
Bernard, L.8
Radice, P.9
Friedman, E.10
Peterlongo, P.11
-
9
-
-
79958282990
-
BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer
-
Wong MW, Nordfors C, Mossman D, Pecenpetelovska G, Avery-Kiejda KA, Talseth-Palmer B, Bowden NA, Scott RJ. BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer. Breast Cancer Res Treat 2011;127:853-9
-
(2011)
Breast Cancer Res Treat
, vol.127
, pp. 853-859
-
-
Wong, M.W.1
Nordfors, C.2
Mossman, D.3
Pecenpetelovska, G.4
Avery-Kiejda, K.A.5
Talseth-Palmer, B.6
Bowden, N.A.7
Scott, R.J.8
-
10
-
-
84860389325
-
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals
-
Kuusisto KM, Bebel A, Vihinen M, Schleutker J, Sallinen SL. Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals. Breast Cancer Res 2011;13:R20
-
(2011)
Breast Cancer Res
, vol.13
, pp. R20
-
-
Kuusisto, K.M.1
Bebel, A.2
Vihinen, M.3
Schleutker, J.4
Sallinen, S.L.5
-
11
-
-
67349212342
-
Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives
-
Cao AY, Huang J, Hu Z, Li WF, Ma ZL, Tang LL, Zhang B, Su FX, Zhou J, Di GH, Shen KW, Wu J, Lu JS, Luo JM, Yuan WT, Shen ZZ, Huang W, Shao ZM. Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives. Breast Cancer Res Treat 2009;115:51-5
-
(2009)
Breast Cancer Res Treat
, vol.115
, pp. 51-55
-
-
Cao, A.Y.1
Huang, J.2
Hu, Z.3
Li, W.F.4
Ma, Z.L.5
Tang, L.L.6
Zhang, B.7
Su, F.X.8
Zhou, J.9
Di, G.H.10
Shen, K.W.11
Wu, J.12
Lu, J.S.13
Luo, J.M.14
Yuan, W.T.15
Shen, Z.Z.16
Huang, W.17
Shao, Z.M.18
-
12
-
-
46149124073
-
Mutational analysis of the breast cancer susceptibility gene BRIP1/BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families
-
Guénard F, Labrie Y, Ouellette G, Joly Beauparlant C, Simard J, Durocher F, BRCAs I. Mutational analysis of the breast cancer susceptibility gene BRIP1/BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families. J Hum Genet 2008;53:579-91
-
(2008)
J Hum Genet
, vol.53
, pp. 579-591
-
-
Guénard, F.1
Labrie, Y.2
Ouellette, G.3
Joly Beauparlant, C.4
Simard, J.5
Durocher, F.6
-
13
-
-
84875703379
-
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
-
361e1-2
-
Michailidou K, Hall P, Gonzalez-Neira A, Ghoussaini M, Dennis J, Milne RL, Schmidt MK, Chang-Claude J, Bojesen SE, Bolla MK, Wang Q, Dicks E, Lee A, Turnbull C, Rahman N, Breast, Ovarian Cancer Susceptibility C, Fletcher O, Peto J, Gibson L, Dos Santos Silva I, Nevanlinna H, Muranen TA, Aittomaki K, Blomqvist C, Czene K, Irwanto A, Liu J, Waisfisz Q, Meijers-Heijboer H, Adank M, Hereditary B, Ovarian Cancer Research Group N, van der Luijt RB, Hein R, Dahmen N, Beckman L, Meindl A, Schmutzler RK, Muller-Myhsok B, Lichtner P, Hopper JL, Southey MC, Makalic E, Schmidt DF, Uitterlinden AG, Hofman A, Hunter DJ, Chanock SJ, Vincent D, Bacot F, Tessier DC, Canisius S, Wessels LF, Haiman CA, Shah M, Luben R, Brown J, Luccarini C, Schoof N, Humphreys K, Li J, Nordestgaard BG, Nielsen SF, Flyger H, Couch FJ, Wang X, Vachon C, Stevens KN, Lambrechts D, Moisse M, Paridaens R, Christiaens MR, Rudolph A, Nickels S, Flesch-Janys D, Johnson N, Aitken Z, Aaltonen K, Heikkinen T, Broeks A, Veer LJ, van der Schoot CE, Guenel P, Truong T, Laurent-Puig P, Menegaux F, Marme F, Schneeweiss A, Sohn C, Burwinkel B, Zamora MP, Perez JI, Pita G, Alonso MR, Cox A, Brock IW, Cross SS, Reed MW, Sawyer EJ, Tomlinson I, Kerin MJ, Miller N, Henderson BE, Schumacher F, Le Marchand L, Andrulis IL, Knight JA, Glendon G, Mulligan AM, kConFab I, Australian Ovarian Cancer Study G, Lindblom A, Margolin S, Hooning MJ, Hollestelle A, van den Ouweland AM, Jager A, Bui QM, Stone J, Dite GS, Apicella C, Tsimiklis H, Giles GG, Severi G, Baglietto L, Fasching PA, Haeberle L, Ekici AB, Beckmann MW, Brenner H, Muller H, Arndt V, Stegmaier C, Swerdlow A, Ashworth A, Orr N, Jones M, Figueroa J, Lissowska J, Brinton L, Goldberg MS, Labreche F, Dumont M, Winqvist R, Pylkas K, Jukkola-Vuorinen A, Grip M, Brauch H, Hamann U, Bruning T, Network G, Radice P, Peterlongo P, Manoukian S, Bonanni B, Devilee P, Tollenaar RA, Seynaeve C, van Asperen CJ, Jakubowska A, Lubinski J, Jaworska K, Durda K, Mannermaa A, Kataja V, Kosma VM, Hartikainen JM, Bogdanova NV, Antonenkova NN, Dork T, Kristensen VN, Anton-Culver H, Slager S, Toland AE, Edge S, Fostira F, Kang D, Yoo KY, Noh DY, Matsuo K, Ito H, Iwata H, Sueta A, Wu AH, Tseng CC, Van Den Berg D, Stram DO, Shu XO, Lu W, Gao YT, Cai H, Teo SH, Yip CH, Phuah SY, Cornes BK, Hartman M, Miao H, Lim WY, Sng JH, Muir K, Lophatananon A, Stewart-Brown S, Siriwanarangsan P, Shen CY, Hsiung CN, Wu PE, Ding SL, Sangrajrang S, Gaborieau V, Brennan P, McKay J, Blot WJ, Signorello LB, Cai Q, Zheng W, Deming-Halverson S, Shrubsole M, Long J, Simard J, Garcia-Closas M, Pharoah PD, Chenevix-Trench G, Dunning AM, Benitez J, Easton DF. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet 2013;45:353-61, 361e1-2
-
(2013)
Nat Genet
, vol.45
, pp. 353-361
-
-
Michailidou, K.1
Hall, P.2
Gonzalez-Neira, A.3
Ghoussaini, M.4
Dennis, J.5
Milne, R.L.6
Schmidt, M.K.7
Chang-Claude, J.8
Bojesen, S.E.9
Bolla, M.K.10
Wang, Q.11
Dicks, E.12
Lee, A.13
Turnbull, C.14
Rahman, N.15
Fletcher, O.16
Peto, J.17
Gibson, L.18
Dos Santos Silva, I.19
Nevanlinna, H.20
Muranen, T.A.21
Aittomaki, K.22
Blomqvist, C.23
Czene, K.24
Irwanto, A.25
Liu, J.26
Waisfisz, Q.27
Meijers-Heijboer, H.28
Adank, M.29
Hereditary, B.30
van der Luijt, R.B.31
Hein, R.32
Dahmen, N.33
Beckman, L.34
Meindl, A.35
Schmutzler, R.K.36
Muller-Myhsok, B.37
Lichtner, P.38
Hopper, J.L.39
Southey, M.C.40
Makalic, E.41
Schmidt, D.F.42
Uitterlinden, A.G.43
Hofman, A.44
Hunter, D.J.45
Chanock, S.J.46
Vincent, D.47
Bacot, F.48
Tessier, D.C.49
Canisius, S.50
Wessels, L.F.51
Haiman, C.A.52
Shah, M.53
Luben, R.54
Brown, J.55
Luccarini, C.56
Schoof, N.57
Humphreys, K.58
Li, J.59
Nordestgaard, B.G.60
Nielsen, S.F.61
Flyger, H.62
Couch, F.J.63
Wang, X.64
Vachon, C.65
Stevens, K.N.66
Lambrechts, D.67
Moisse, M.68
Paridaens, R.69
Christiaens, M.R.70
Rudolph, A.71
Nickels, S.72
Flesch-Janys, D.73
Johnson, N.74
Aitken, Z.75
Aaltonen, K.76
Heikkinen, T.77
Broeks, A.78
Veer, L.J.79
van der Schoot, C.E.80
Guenel, P.81
Truong, T.82
Laurent-Puig, P.83
Menegaux, F.84
Marme, F.85
Schneeweiss, A.86
Sohn, C.87
Burwinkel, B.88
Zamora, M.P.89
Perez, J.I.90
Pita, G.91
Alonso, M.R.92
Cox, A.93
Brock, I.W.94
Cross, S.S.95
Reed, M.W.96
Sawyer, E.J.97
Tomlinson, I.98
Kerin, M.J.99
more..
-
14
-
-
49149112491
-
Risk factors for the incidence of breast cancer: do they affect survival from the disease?
-
Barnett GC, Shah M, Redman K, Easton DF, Ponder BA, Pharoah PD. Risk factors for the incidence of breast cancer: do they affect survival from the disease? J Clin Oncol 2008;26:3310-6
-
(2008)
J Clin Oncol
, vol.26
, pp. 3310-3316
-
-
Barnett, G.C.1
Shah, M.2
Redman, K.3
Easton, D.F.4
Ponder, B.A.5
Pharoah, P.D.6
-
15
-
-
66649125208
-
Genetic models for the familial aggregation of mammographic breast density
-
Kataoka M, Antoniou A, Warren R, Leyland J, Brown J, Audley T, Easton D. Genetic models for the familial aggregation of mammographic breast density. Cancer Epidemiol Biomarkers Prev 2009;18:1277-84
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 1277-1284
-
-
Kataoka, M.1
Antoniou, A.2
Warren, R.3
Leyland, J.4
Brown, J.5
Audley, T.6
Easton, D.7
-
16
-
-
80255127234
-
Cutadapt removes adapter sequences from high-throughput sequencing reads
-
Martin M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnetjournal 2011;17:10-2
-
(2011)
EMBnetjournal
, vol.17
, pp. 10-12
-
-
Martin, M.1
-
17
-
-
84864119729
-
Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly
-
Li H. Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly. Bioinformatics 2012;28:1838-44
-
(2012)
Bioinformatics
, vol.28
, pp. 1838-1844
-
-
Li, H.1
-
18
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 2010;20:1297-303
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
DePristo, M.A.11
-
19
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 2011;43:491-8
-
(2011)
Nat Genet
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
del Angel, G.8
Rivas, M.A.9
Hanna, M.10
McKenna, A.11
Fennell, T.J.12
Kernytsky, A.M.13
Sivachenko, A.Y.14
Cibulskis, K.15
Gabriel, S.B.16
Altshuler, D.17
Daly, M.J.18
-
20
-
-
84895858942
-
A general framework for estimating the relative pathogenicity of human genetic variants
-
Kircher M, Witten DM, Jain P, O'Roak BJ, Cooper GM, Shendure J. A general framework for estimating the relative pathogenicity of human genetic variants. Nat Genet 2014;46:310-15
-
(2014)
Nat Genet
, vol.46
, pp. 310-315
-
-
Kircher, M.1
Witten, D.M.2
Jain, P.3
O'Roak, B.J.4
Cooper, G.M.5
Shendure, J.6
-
21
-
-
7044272596
-
The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer
-
John EM, Hopper JL, Beck JC, Knight JA, Neuhausen SL, Senie RT, Ziogas A, Andrulis IL, Anton-Culver H, Boyd N, Buys SS, Daly MB, O'Malley FP, Santella RM, Southey MC, Venne VL, Venter DJ, West DW, Whittemore AS, Seminara D, Breast Cancer Family R. The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer. Breast Cancer Res 2004;6:R375-89
-
(2004)
Breast Cancer Res
, vol.6
, pp. R375-R389
-
-
John, E.M.1
Hopper, J.L.2
Beck, J.C.3
Knight, J.A.4
Neuhausen, S.L.5
Senie, R.T.6
Ziogas, A.7
Andrulis, I.L.8
Anton-Culver, H.9
Boyd, N.10
Buys, S.S.11
Daly, M.B.12
O'Malley, F.P.13
Santella, R.M.14
Southey, M.C.15
Venne, V.L.16
Venter, D.J.17
West, D.W.18
Whittemore, A.S.19
Seminara, D.20
Breast Cancer Family, R.21
more..
-
22
-
-
70350490327
-
Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer
-
Tavtigian SV, Oefner PJ, Babikyan D, Hartmann A, Healey S, Le Calvez-Kelm F, Lesueur F, Byrnes GB, Chuang SC, Forey N, Feuchtinger C, Gioia L, Hall J, Hashibe M, Herte B, McKay-Chopin S, Thomas A, Vallee MP, Voegele C, Webb PM, Whiteman DC, Australian Cancer S, Breast Cancer Family R, Kathleen Cuningham Foundation Consortium for Research into Familial Aspects of Breast C, Sangrajrang S, Hopper JL, Southey MC, Andrulis IL, John EM, Chenevix-Trench G. Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer. Am J Hum Genet 2009;85:427-46
-
(2009)
Am J Hum Genet
, vol.85
, pp. 427-446
-
-
Tavtigian, S.V.1
Oefner, P.J.2
Babikyan, D.3
Hartmann, A.4
Healey, S.5
Le Calvez-Kelm, F.6
Lesueur, F.7
Byrnes, G.B.8
Chuang, S.C.9
Forey, N.10
Feuchtinger, C.11
Gioia, L.12
Hall, J.13
Hashibe, M.14
Herte, B.15
McKay-Chopin, S.16
Thomas, A.17
Vallee, M.P.18
Voegele, C.19
Webb, P.M.20
Whiteman, D.C.21
Australian Cancer, S.22
Breast Cancer Family, R.23
Sangrajrang, S.24
Hopper, J.L.25
Southey, M.C.26
Andrulis, I.L.27
John, E.M.28
Chenevix-Trench, G.29
more..
-
23
-
-
84860389647
-
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study
-
Le Calvez-Kelm F, Lesueur F, Damiola F, Vallee M, Voegele C, Babikyan D, Durand G, Forey N, McKay-Chopin S, Robinot N, Nguyen-Dumont T, Thomas A, Byrnes GB, Breast Cancer Family R, Hopper JL, Southey MC, Andrulis IL, John EM, Tavtigian SV. Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study. Breast Cancer Res 2011;13:R6
-
(2011)
Breast Cancer Res
, vol.13
, pp. R6
-
-
Le Calvez-Kelm, F.1
Lesueur, F.2
Damiola, F.3
Vallee, M.4
Voegele, C.5
Babikyan, D.6
Durand, G.7
Forey, N.8
McKay-Chopin, S.9
Robinot, N.10
Nguyen-Dumont, T.11
Thomas, A.12
Byrnes, G.B.13
Breast Cancer Family, R.14
Hopper, J.L.15
Southey, M.C.16
Andrulis, I.L.17
John, E.M.18
Tavtigian, S.V.19
-
24
-
-
84859479737
-
Rare mutations in XRCC2 increase the risk of breast cancer
-
Park DJ, Lesueur F, Nguyen-Dumont T, Pertesi M, Odefrey F, Hammet F, Neuhausen SL, John EM, Andrulis IL, Terry MB, Daly M, Buys S, Le Calvez-Kelm F, Lonie A, Pope BJ, Tsimiklis H, Voegele C, Hilbers FM, Hoogerbrugge N, Barroso A, Osorio A, Breast Cancer Family R, Kathleen Cuningham Foundation Consortium for Research into Familial Breast C, Giles GG, Devilee P, Benitez J, Hopper JL, Tavtigian SV, Goldgar DE, Southey MC. Rare mutations in XRCC2 increase the risk of breast cancer. Am J Hum Genet 2012;90:734-9
-
(2012)
Am J Hum Genet
, vol.90
, pp. 734-739
-
-
Park, D.J.1
Lesueur, F.2
Nguyen-Dumont, T.3
Pertesi, M.4
Odefrey, F.5
Hammet, F.6
Neuhausen, S.L.7
John, E.M.8
Andrulis, I.L.9
Terry, M.B.10
Daly, M.11
Buys, S.12
Le Calvez-Kelm, F.13
Lonie, A.14
Pope, B.J.15
Tsimiklis, H.16
Voegele, C.17
Hilbers, F.M.18
Hoogerbrugge, N.19
Barroso, A.20
Osorio, A.21
Breast Cancer Family, R.22
Giles, G.G.23
Devilee, P.24
Benitez, J.25
Hopper, J.L.26
Tavtigian, S.V.27
Goldgar, D.E.28
Southey, M.C.29
more..
-
25
-
-
84871644687
-
RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study
-
Le Calvez-Kelm F, Oliver J, Damiola F, Forey N, Robinot N, Durand G, Voegele C, Vallee MP, Byrnes G, Registry BC, Hopper JL, Southey MC, Andrulis IL, John EM, Tavtigian SV, Lesueur F. RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study. PLoS ONE 2012;7:e52374
-
(2012)
PLoS ONE
, vol.7
-
-
Le Calvez-Kelm, F.1
Oliver, J.2
Damiola, F.3
Forey, N.4
Robinot, N.5
Durand, G.6
Voegele, C.7
Vallee, M.P.8
Byrnes, G.9
Registry, B.C.10
Hopper, J.L.11
Southey, M.C.12
Andrulis, I.L.13
John, E.M.14
Tavtigian, S.V.15
Lesueur, F.16
-
26
-
-
84904049854
-
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers
-
Park DJ, Tao K, Le Calvez-Kelm F, Nguyen-Dumont T, Robinot N, Hammet F, Odefrey F, Tsimiklis H, Teo ZL, Thingholm LB, Young EL, Voegele C, Lonie A, Pope BJ, Roane TC, Bell R, Hu H, Shankaracharya, HuffCD, Ellis J, Li J, Makunin IV, John EM, Andrulis IL, Terry MB, Daly M, Buys SS, Snyder C, Lynch HT, Devilee P, Giles GG, Hopper JL, Feng BJ, Lesueur F, Tavtigian SV, Southey MC, Goldgar DE. Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers. Cancer Discov 2014;4:804-15
-
(2014)
Cancer Discov
, vol.4
, pp. 804-815
-
-
Park, D.J.1
Tao, K.2
Le Calvez-Kelm, F.3
Nguyen-Dumont, T.4
Robinot, N.5
Hammet, F.6
Odefrey, F.7
Tsimiklis, H.8
Teo, Z.L.9
Thingholm, L.B.10
Young, E.L.11
Voegele, C.12
Lonie, A.13
Pope, B.J.14
Roane, T.C.15
Bell, R.16
Hu, H.17
Shankaracharya18
Huff, C.D.19
Ellis, J.20
Li, J.21
Makunin, I.V.22
John, E.M.23
Andrulis, I.L.24
Terry, M.B.25
Daly, M.26
Buys, S.S.27
Snyder, C.28
Lynch, H.T.29
Devilee, P.30
Giles, G.G.31
Hopper, J.L.32
Feng, B.J.33
Lesueur, F.34
Tavtigian, S.V.35
Southey, M.C.36
Goldgar, D.E.37
more..
-
27
-
-
84905731318
-
Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study
-
Damiola F, Pertesi M, Oliver J, Le Calvez-Kelm F, Voegele C, Young EL, Robinot N, Forey N, Durand G, Vallee MP, Tao K, Roane TC, Williams GJ, Hopper JL, Southey MC, Andrulis IL, John EM, Goldgar DE, Lesueur F, Tavtigian SV. Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study. Breast Cancer Res 2014;16:R58
-
(2014)
Breast Cancer Res
, vol.16
, pp. R58
-
-
Damiola, F.1
Pertesi, M.2
Oliver, J.3
Le Calvez-Kelm, F.4
Voegele, C.5
Young, E.L.6
Robinot, N.7
Forey, N.8
Durand, G.9
Vallee, M.P.10
Tao, K.11
Roane, T.C.12
Williams, G.J.13
Hopper, J.L.14
Southey, M.C.15
Andrulis, I.L.16
John, E.M.17
Goldgar, D.E.18
Lesueur, F.19
Tavtigian, S.V.20
more..
-
28
-
-
61849100599
-
Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus
-
Garritano S, Gemignani F, Voegele C, Nguyen-Dumont T, Le Calvez-Kelm F, De Silva D, Lesueur F, Landi S, Tavtigian SV. Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus. BMC Genet 2009;10:5
-
(2009)
BMC Genet
, vol.10
, pp. 5
-
-
Garritano, S.1
Gemignani, F.2
Voegele, C.3
Nguyen-Dumont, T.4
Le Calvez-Kelm, F.5
De Silva, D.6
Lesueur, F.7
Landi, S.8
Tavtigian, S.V.9
-
29
-
-
84870748167
-
A role for common genomic variants in the assessment of familial breast cancer
-
Sawyer S, Mitchell G, McKinley J, Chenevix-Trench G, Beesley J, Chen XQ, Bowtell D, Trainer AH, Harris M, Lindeman GJ, James PA. A role for common genomic variants in the assessment of familial breast cancer. J Clin Oncol 2012;30: 4330-6
-
(2012)
J Clin Oncol
, vol.30
, pp. 4330-4336
-
-
Sawyer, S.1
Mitchell, G.2
McKinley, J.3
Chenevix-Trench, G.4
Beesley, J.5
Chen, X.Q.6
Bowtell, D.7
Trainer, A.H.8
Harris, M.9
Lindeman, G.J.10
James, P.A.11
-
30
-
-
84939443187
-
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls
-
Thompson ER, Gorringe KL, Rowley SM, Wong-Brown MW, McInerny S, Li N, Trainer AH, Devereux L, Doyle MA, Li J, Lupat R, Delatycki MB, LifePool I, Mitchell G, James PA, Scott RJ, Campbell IG. Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls. Breast Cancer Res 2015;17:111
-
(2015)
Breast Cancer Res
, vol.17
, pp. 111
-
-
Thompson, E.R.1
Gorringe, K.L.2
Rowley, S.M.3
Wong-Brown, M.W.4
McInerny, S.5
Li, N.6
Trainer, A.H.7
Devereux, L.8
Doyle, M.A.9
Li, J.10
Lupat, R.11
Delatycki, M.B.12
LifePool, I.13
Mitchell, G.14
James, P.A.15
Scott, R.J.16
Campbell, I.G.17
-
31
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009;25:1754-60
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
32
-
-
84856478855
-
A linear complexity phasing method for thousands of genomes
-
Delaneau O, Marchini J, Zagury JF. A linear complexity phasing method for thousands of genomes. Nat Methods 2012;9:179-81
-
(2012)
Nat Methods
, vol.9
, pp. 179-181
-
-
Delaneau, O.1
Marchini, J.2
Zagury, J.F.3
-
33
-
-
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 DF. Cancer risks and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst 2005;97:813-22
-
(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.F.9
-
34
-
-
33746491583
-
ATM mutations that cause ataxiatelangiectasia are breast cancer susceptibility alleles
-
Renwick A, Thompson D, Seal S, Kelly P, Chagtai T, Ahmed M, North B, Jayatilake H, Barfoot R, Spanova K, McGuffog L, Evans DG, Eccles D, Breast Cancer Susceptibility C, Easton DF, Stratton MR, Rahman N. ATM mutations that cause ataxiatelangiectasia are breast cancer susceptibility alleles. Nat Genet 2006;38:873-5
-
(2006)
Nat Genet
, vol.38
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
Kelly, P.4
Chagtai, T.5
Ahmed, M.6
North, B.7
Jayatilake, H.8
Barfoot, R.9
Spanova, K.10
McGuffog, L.11
Evans, D.G.12
Eccles, D.13
Breast Cancer Susceptibility, C.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
35
-
-
3042582651
-
CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10. studies
-
Consortium CBCC-C. CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10. studies. Am J Hum Genet 2004;74:1175-82
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1175-1182
-
-
-
36
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N, Stratton MR, Consortium CH-BC. Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 2002;31:55-9
-
(2002)
Nat Genet
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
van den Ouweland, A.2
Klijn, J.3
Wasielewski, M.4
de Snoo, A.5
Oldenburg, R.6
Hollestelle, A.7
Houben, M.8
Crepin, E.9
van Veghel-Plandsoen, M.10
Elstrodt, F.11
van Duijn, C.12
Bartels, C.13
Meijers, C.14
Schutte, M.15
McGuffog, L.16
Thompson, D.17
Easton, D.18
Sodha, N.19
Seal, S.20
Barfoot, R.21
Mangion, J.22
Chang-Claude, J.23
Eccles, D.24
Eeles, R.25
Evans, D.G.26
Houlston, R.27
Murday, V.28
Narod, S.29
Peretz, T.30
Peto, J.31
Phelan, C.32
Zhang, H.X.33
Szabo, C.34
Devilee, P.35
Goldgar, D.36
Futreal, P.A.37
Nathanson, K.L.38
Weber, B.39
Rahman, N.40
Stratton, M.R.41
more..
-
37
-
-
84905842087
-
Breast-cancer risk in families with mutations in PALB2
-
Antoniou AC, Casadei S, Heikkinen T, Barrowdale D, Pylkas K, Roberts J, Lee A, Subramanian D, De Leeneer K, Fostira F, Tomiak E, Neuhausen SL, Teo ZL, Khan S, Aittomaki K, Moilanen JS, Turnbull C, Seal S, Mannermaa A, Kallioniemi A, Lindeman GJ, Buys SS, Andrulis IL, Radice P, Tondini C, Manoukian S, Toland AE, Miron P, Weitzel JN, Domchek SM, Poppe B, Claes KB, Yannoukakos D, Concannon P, Bernstein JL, James PA, Easton DF, Goldgar DE, Hopper JL, Rahman N, Peterlongo P, Nevanlinna H, King MC, Couch FJ, Southey MC, Winqvist R, Foulkes WD, Tischkowitz M. Breast-cancer risk in families with mutations in PALB2. N Engl J Med 2014;371:497-506
-
(2014)
N Engl J Med
, vol.371
, pp. 497-506
-
-
Antoniou, A.C.1
Casadei, S.2
Heikkinen, T.3
Barrowdale, D.4
Pylkas, K.5
Roberts, J.6
Lee, A.7
Subramanian, D.8
De Leeneer, K.9
Fostira, F.10
Tomiak, E.11
Neuhausen, S.L.12
Teo, Z.L.13
Khan, S.14
Aittomaki, K.15
Moilanen, J.S.16
Turnbull, C.17
Seal, S.18
Mannermaa, A.19
Kallioniemi, A.20
Lindeman, G.J.21
Buys, S.S.22
Andrulis, I.L.23
Radice, P.24
Tondini, C.25
Manoukian, S.26
Toland, A.E.27
Miron, P.28
Weitzel, J.N.29
Domchek, S.M.30
Poppe, B.31
Claes, K.B.32
Yannoukakos, D.33
Concannon, P.34
Bernstein, J.L.35
James, P.A.36
Easton, D.F.37
Goldgar, D.E.38
Hopper, J.L.39
Rahman, N.40
Peterlongo, P.41
Nevanlinna, H.42
King, M.C.43
Couch, F.J.44
Southey, M.C.45
Winqvist, R.46
Foulkes, W.D.47
Tischkowitz, M.48
more..
-
38
-
-
80054973810
-
Mutations in BRIP1 confer high risk of ovarian cancer
-
Rafnar T, Gudbjartsson DF, Sulem P, Jonasdottir A, Sigurdsson A, Jonasdottir A, Besenbacher S, Lundin P, Stacey SN, Gudmundsson J, Magnusson OT, le Roux L, Orlygsdottir G, Helgadottir HT, Johannsdottir H, Gylfason A, Tryggvadottir L, Jonasson JG, de Juan A, Ortega E, Ramon-Cajal JM, Garcia-Prats MD, Mayordomo C, Panadero A, Rivera F, Aben KK, van Altena AM, Massuger LF, Aavikko M, Kujala PM, StaffS, Aaltonen LA, Olafsdottir K, Bjornsson J, Kong A, Salvarsdottir A, Saemundsson H, Olafsson K, Benediktsdottir KR, Gulcher J, Masson G, Kiemeney LA, Mayordomo JI, Thorsteinsdottir U, Stefansson K. Mutations in BRIP1 confer high risk of ovarian cancer. Nat Genet 2011;43:1104-7
-
(2011)
Nat Genet
, vol.43
, pp. 1104-1107
-
-
Rafnar, T.1
Gudbjartsson, D.F.2
Sulem, P.3
Jonasdottir, A.4
Sigurdsson, A.5
Jonasdottir, A.6
Besenbacher, S.7
Lundin, P.8
Stacey, S.N.9
Gudmundsson, J.10
Magnusson, O.T.11
le Roux, L.12
Orlygsdottir, G.13
Helgadottir, H.T.14
Johannsdottir, H.15
Gylfason, A.16
Tryggvadottir, L.17
Jonasson, J.G.18
de Juan, A.19
Ortega, E.20
Ramon-Cajal, J.M.21
Garcia-Prats, M.D.22
Mayordomo, C.23
Panadero, A.24
Rivera, F.25
Aben, K.K.26
van Altena, A.M.27
Massuger, L.F.28
Aavikko, M.29
Kujala, P.M.30
Staff, S.31
Aaltonen, L.A.32
Olafsdottir, K.33
Bjornsson, J.34
Kong, A.35
Salvarsdottir, A.36
Saemundsson, H.37
Olafsson, K.38
Benediktsdottir, K.R.39
Gulcher, J.40
Masson, G.41
Kiemeney, L.A.42
Mayordomo, J.I.43
Thorsteinsdottir, U.44
Stefansson, K.45
more..
-
39
-
-
84952641661
-
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN genes in Women with Ovarian Cancer
-
Ramus SJ, Song H, Dicks E, Tyrer JP, Rosenthal AN, Intermaggio MP, Fraser L, Gentry-Maharaj A, Hayward J, Philpott S, Anderson C, Edlund CK, Conti D, Harrington P, Barrowdale D, Bowtell DD, Alsop K, Mitchell G, Group AS, Cicek MS, Cunningham JM, Fridley BL, Alsop J, Jimenez-Linan M, Poblete S, Lele S, Sucheston-Campbell L, Moysich KB, Sieh W, McGuire V, Lester J, Bogdanova N, Durst M, Hillemanns P, Ovarian Cancer Association C, Odunsi K, Whittemore AS, Karlan BY, Dork T, Goode EL, Menon U, Jacobs IJ, Antoniou AC, Pharoah PD, Gayther SA. Germline Mutations in the BRIP1, BARD1, PALB2, and NBN genes in Women with Ovarian Cancer. J Natl Cancer Inst 2015;107:djv214
-
(2015)
J Natl Cancer Inst
, vol.107
-
-
Ramus, S.J.1
Song, H.2
Dicks, E.3
Tyrer, J.P.4
Rosenthal, A.N.5
Intermaggio, M.P.6
Fraser, L.7
Gentry-Maharaj, A.8
Hayward, J.9
Philpott, S.10
Anderson, C.11
Edlund, C.K.12
Conti, D.13
Harrington, P.14
Barrowdale, D.15
Bowtell, D.D.16
Alsop, K.17
Mitchell, G.18
Group, A.S.19
Cicek, M.S.20
Cunningham, J.M.21
Fridley, B.L.22
Alsop, J.23
Jimenez-Linan, M.24
Poblete, S.25
Lele, S.26
Sucheston-Campbell, L.27
Moysich, K.B.28
Sieh, W.29
McGuire, V.30
Lester, J.31
Bogdanova, N.32
Durst, M.33
Hillemanns, P.34
Ovarian Cancer Association, C.35
Odunsi, K.36
Whittemore, A.S.37
Karlan, B.Y.38
Dork, T.39
Goode, E.L.40
Menon, U.41
Jacobs, I.J.42
Antoniou, A.C.43
Pharoah, P.D.44
Gayther, S.A.45
more..
-
40
-
-
84921898753
-
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
-
Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, Olson JE, Godwin AK, Pankratz VS, Olswold C, Slettedahl S, Hallberg E, Guidugli L, Davila JI, Beckmann MW, Janni W, Rack B, Ekici AB, Slamon DJ, Konstantopoulou I, Fostira F, Vratimos A, Fountzilas G, Pelttari LM, Tapper WJ, Durcan L, Cross SS, Pilarski R, Shapiro CL, Klemp J, Yao S, Garber J, Cox A, Brauch H, Ambrosone C, Nevanlinna H, Yannoukakos D, Slager SL, Vachon CM, Eccles DM, Fasching PA. Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. J Clin Oncol 2015;33:304-11
-
(2015)
J Clin Oncol
, vol.33
, pp. 304-311
-
-
Couch, F.J.1
Hart, S.N.2
Sharma, P.3
Toland, A.E.4
Wang, X.5
Miron, P.6
Olson, J.E.7
Godwin, A.K.8
Pankratz, V.S.9
Olswold, C.10
Slettedahl, S.11
Hallberg, E.12
Guidugli, L.13
Davila, J.I.14
Beckmann, M.W.15
Janni, W.16
Rack, B.17
Ekici, A.B.18
Slamon, D.J.19
Konstantopoulou, I.20
Fostira, F.21
Vratimos, A.22
Fountzilas, G.23
Pelttari, L.M.24
Tapper, W.J.25
Durcan, L.26
Cross, S.S.27
Pilarski, R.28
Shapiro, C.L.29
Klemp, J.30
Yao, S.31
Garber, J.32
Cox, A.33
Brauch, H.34
Ambrosone, C.35
Nevanlinna, H.36
Yannoukakos, D.37
Slager, S.L.38
Vachon, C.M.39
Eccles, D.M.40
Fasching, P.A.41
more..
-
41
-
-
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 AM, Sutcliffe A, McGuire GM, Robinson P, Weber P, Bedenham T, Bradwell AR, Easton DF, Lennox GG, Haites N, Byrd PJ, Taylor AM. 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 1998;62:334-45
-
(1998)
Am J Hum Genet
, vol.62
, pp. 334-345
-
-
Stankovic, T.1
Kidd, A.M.2
Sutcliffe, A.3
McGuire, G.M.4
Robinson, P.5
Weber, P.6
Bedenham, T.7
Bradwell, A.R.8
Easton, D.F.9
Lennox, G.G.10
Haites, N.11
Byrd, P.J.12
Taylor, A.M.13
-
42
-
-
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
-
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. 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 2006;27:1122-8
-
(2006)
Hum Mutat
, vol.27
, pp. 1122-1128
-
-
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
-
43
-
-
80053100604
-
Rare variants in the ATM gene and risk of breast cancer
-
Goldgar DE, Healey S, Dowty JG, Da Silva L, Chen X, Spurdle AB, Terry MB, Daly MJ, Buys SM, Southey MC, Andrulis I, John EM, Bcfr, kConFab, Khanna KK, Hopper JL, Oefner PJ, Lakhani S, Chenevix-Trench G. Rare variants in the ATM gene and risk of breast cancer. Breast Cancer Res 2011;13:R73
-
(2011)
Breast Cancer Res
, vol.13
, pp. R73
-
-
Goldgar, D.E.1
Healey, S.2
Dowty, J.G.3
Da Silva, L.4
Chen, X.5
Spurdle, A.B.6
Terry, M.B.7
Daly, M.J.8
Buys, S.M.9
Southey, M.C.10
Andrulis, I.11
John, E.M.12
Khanna, K.K.13
Hopper, J.L.14
Oefner, P.J.15
Lakhani, S.16
Chenevix-Trench, G.17
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