-
1
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Phelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, Narod S, Bristow PK, Norris FH, Helvering L, Morrison P, Rosteck P, Lai M, Barrett C, Lewis C, Neuhausen S, Cannon-Albright L, Goldgar D, Wiseman R, Kamb A, Skolnick MH. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994;266:66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
2
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Gregory S, Gumbs C, Micklem G, Barfoot R, Hamoudi R, Patel S, Rices C, Biggs P, Hashim Y, Smith A, Connor F, Arason A, Gudmundsson J, Ficenec D, Kelsell D, Fordtonin P, Bishop DT, Spurr NK, Ponder BA, Eeles R, Peto J, Devilee P, Cornelisse Cees, Lynch H, Narod S, Lenoir G, Egilsson V, Barkadottir R, Easton D, Bentley DR, Futreal A, Ashworth A, Stratton MR. Identification of the breast cancer susceptibility gene BRCA2. Nature 1995;378:789-92.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Gregory, S.7
Gumbs, C.8
Micklem, G.9
Barfoot, R.10
Hamoudi, R.11
Patel, S.12
Rices, C.13
Biggs, P.14
Hashim, Y.15
Smith, A.16
Connor, F.17
Arason, A.18
Gudmundsson, J.19
Ficenec, D.20
Kelsell, D.21
Fordtonin, P.22
Bishop, D.T.23
Spurr, N.K.24
Ponder, B.A.25
Eeles, R.26
Peto, J.27
Devilee, P.28
Cees, C.29
Lynch, H.30
Narod, S.31
Lenoir, G.32
Egilsson, V.33
Barkadottir, R.34
Easton, D.35
Bentley, D.R.36
Futreal, A.37
Ashworth, A.38
Stratton, M.R.39
more..
-
3
-
-
0037151382
-
On the use of familial aggregation in population-based case probands for calculating penetrance
-
Begg CB. On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst 2002;94:1221-6.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1221-1226
-
-
Begg, C.B.1
-
4
-
-
0036123926
-
Breast Cancer Linkage Consortium. Variation in BRCA1 cancer risks by mutation position
-
Thompson D, Easton D; Breast Cancer Linkage Consortium. Variation in BRCA1 cancer risks by mutation position. Cancer Epidemiol Biomarkers Prev 2002;11:329-36.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 329-336
-
-
Thompson, D.1
Easton, D.2
-
5
-
-
71049170380
-
Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting
-
Evans DG, Shenton A, Woodward E, Lalloo F, Maher ER. Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting. BMC Cancer 2008;8:155.
-
(2008)
BMC Cancer
, vol.8
, pp. 155
-
-
Evans, D.G.1
Shenton, A.2
Woodward, E.3
Lalloo, F.4
Maher, E.R.5
-
6
-
-
17344365851
-
Breast Cancer Linkage Consortium.Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
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, Hamann J, Haites N, Scott RJ, Maugard CM, Vasen H, Seitz S, Cannon-Albright LA, Schofield A, Zelada-Hedman M, 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)
The Breast Cancer Linkage Consortium. 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
Hamann, J.21
Haites, N.22
Scott, R.J.23
Maugard, C.M.24
Vasen, H.25
Seitz, S.26
Cannon-Albright, L.A.27
Schofield, A.28
Zelada-Hedman, M.29
more..
-
7
-
-
0033523268
-
Cancer risks in BRCA2 mutation carriers
-
The Breast Cancer Linkage Consortium
-
The Breast Cancer Linkage Consortium. Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst 1999;91:1310-6.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1310-1316
-
-
-
8
-
-
0028330276
-
Risks of cancer in BRCA1-mutation carriers
-
Breast Cancer Linkage Consortium
-
Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE. Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. Lancet 1994;343:692-5.
-
(1994)
Lancet
, vol.343
, pp. 692-695
-
-
Ford, D.1
Easton, D.F.2
Bishop, D.T.3
Narod, S.A.4
Goldgar, D.E.5
-
9
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing JP, Hartge P, Wacholder S, Baker SM, Berlin M, McAdams M, Timmerman MM, Lawrence BS, Brody C, Tucker MA. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N Engl J Med 1997;336:1401-8.
-
(1997)
N Engl J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
Baker, S.M.4
Berlin, M.5
McAdams, M.6
Timmerman, M.M.7
Lawrence, B.S.8
Brody, C.9
Tucker, M.A.10
-
10
-
-
0033591850
-
Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer
-
Warner E, Foulkes W, Goodwin P, Meshino W, Blondal J, Paterson C, Ozcelik H, Goss P, Allingham-Hawkins D, Hamel N, Di Prospero L, Contiga V, Serruya C, Klein M, Moslehi R, Honeyford J, Leide A, Glendon G, Brunet JS, Narod S. Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer. J Natl Cancer Inst 1999;91:1241-7.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1241-1247
-
-
Warner, E.1
Foulkes, W.2
Goodwin, P.3
Meshino, W.4
Blondal, J.5
Paterson, C.6
Ozcelik, H.7
Goss, P.8
Allingham-Hawkins, D.9
Hamel, N.10
Di Prospero, L.11
Contiga, V.12
Serruya, C.13
Klein, M.14
Moslehi, R.15
Honeyford, J.16
Leide, A.17
Glendon, G.18
Brunet, J.S.19
Narod, S.20
more..
-
11
-
-
0032826284
-
Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2
-
Hopper JL, Southey MC, Dite GS, Jolley DJ, Giles GG, McCredie MR, Easton DF, Venter DJ. Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study. Cancer Epidemiol Biomarkers Prev 1999;8:741-7.
-
(1999)
Australian Breast Cancer Family Study. Cancer Epidemiol Biomarkers Prev
, vol.8
, pp. 741-747
-
-
Hopper, J.L.1
Southey, M.C.2
Dite, G.S.3
Jolley, D.J.4
Giles, G.G.5
McCredie, M.R.6
Easton, D.F.7
Venter, D.J.8
-
12
-
-
33644895048
-
Characterization of BRCA1 and BRCA2 mutations in a large United States sample
-
Chen S, Iversen ES, Friebel T, Finkelstein D, Webber BL, Eisen A, Peterson LE, Schildkraut JM, Isaacs C, Peshkin BN, Corio C, Leondaris L, Tomlinson G, Dutson D, Kerber R, Amos CI, Strong LC, Berry DA, Euhus DM, Parmigiani G. Characterization of BRCA1 and BRCA2 mutations in a large United States sample. J Clin Oncol 2006;24:863-71.
-
(2006)
J Clin Oncol
, vol.24
, pp. 863-871
-
-
Chen, S.1
Iversen, E.S.2
Friebel, T.3
Finkelstein, D.4
Webber, B.L.5
Eisen, A.6
Peterson, L.E.7
Schildkraut, J.M.8
Isaacs, C.9
Peshkin, B.N.10
Corio, C.11
Leondaris, L.12
Tomlinson, G.13
Dutson, D.14
Kerber, R.15
Amos, C.I.16
Strong, L.C.17
Berry, D.A.18
Euhus, D.M.19
Parmigiani, G.20
more..
-
13
-
-
22244467729
-
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies
-
Antoniou A, Pharoah PDP, Narod S, Risch HA, Eyfjord JE, Hopper JL, 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. Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies. J Med Genet 2005;42:602-3.
-
(2005)
J Med Genet
, vol.42
, pp. 602-603
-
-
Antoniou, A.1
Pharoah, P.D.P.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
Hopper, J.L.6
Olsson, H.7
Johannsson, O.8
Borg, A.9
Pasini, B.10
Radice, P.11
Manoukian, S.12
Eccles, D.M.13
Tang, N.14
Olah, E.15
Anton-Culver, H.16
Warner, E.17
Lubinski, J.18
Gronwald, J.19
Gorski, B.20
Tulinius, H.21
Thorlacius, S.22
Eerola, H.23
Nevanlinna, H.24
Syrjakoski, K.25
Kallioniemi, O.P.26
Thompson, D.27
Evans, C.28
Peto, J.29
Lalloo, F.30
Evans, D.G.31
Easton, D.F.32
more..
-
14
-
-
0142178215
-
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
King MC, Marks JH, Mandell JB. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 2003;302:643-6.
-
(2003)
Science
, vol.302
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
15
-
-
29144509766
-
BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases
-
Pal T, Permuth-Wey J, Betts JA, Krischer JP, Fiorica J, Arango H, LaPolla J, Hoffman M, Martino MA, Wakeley K, Wilbanks G, Nicosia S, Cantor A, Sutphen R. BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer 2005;104:2807-16.
-
(2005)
Cancer
, vol.104
, pp. 2807-2816
-
-
Pal, T.1
Permuth-Wey, J.2
Betts, J.A.3
Krischer, J.P.4
Fiorica, J.5
Arango, H.6
LaPolla, J.7
Hoffman, M.8
Martino, M.A.9
Wakeley, K.10
Wilbanks, G.11
Nicosia, S.12
Cantor, A.13
Sutphen, R.14
-
16
-
-
0037087579
-
Cancer incidence in a population of Jewish women at risk of ovarian cancer
-
Liede A, Karlan BY, Baldwin RL, Platt LD, Kuperstein G, Narod SA. Cancer incidence in a population of Jewish women at risk of ovarian cancer. J Clin Oncol 2002;20:1570-7.
-
(2002)
J Clin Oncol
, vol.20
, pp. 1570-1577
-
-
Liede, A.1
Karlan, B.Y.2
Baldwin, R.L.3
Platt, L.D.4
Kuperstein, G.5
Narod, S.A.6
-
17
-
-
58749091606
-
Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation
-
Metcalfe KA, Finch A, Poll A, Horsman D, Kim-Sing C, Scott J, Royer R, Sun P, Narod SA. Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation. Br J Cancer 2009;100:421-5.
-
(2009)
Br J Cancer
, vol.100
, pp. 421-425
-
-
Metcalfe, K.A.1
Finch, A.2
Poll, A.3
Horsman, D.4
Kim-Sing, C.5
Scott, J.6
Royer, R.7
Sun, P.8
Narod, S.A.9
-
18
-
-
25144514515
-
Risk of ovarian cancer in BRCA1 and BRCA2 mutation-negative hereditary breast cancer families
-
Kauff ND, Mitra N, Robson ME, Hurley KE, Chuai S, Goldfrank D, Wadsworth E, Lee J, Cigler T, Borgen PI, Norton L, Barakat RR, Offit K. Risk of ovarian cancer in BRCA1 and BRCA2 mutation-negative hereditary breast cancer families. J Natl Cancer Inst 2005;97:1382-4.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 1382-1384
-
-
Kauff, N.D.1
Mitra, N.2
Robson, M.E.3
Hurley, K.E.4
Chuai, S.5
Goldfrank, D.6
Wadsworth, E.7
Lee, J.8
Cigler, T.9
Borgen, P.I.10
Norton, L.11
Barakat, R.R.12
Offit, K.13
-
19
-
-
58149347689
-
High risk for ovarian cancer in a prospective series is restricted to BRCA1/2 mutation carriers
-
Maehle L, Apold J, Paulsen T, Hagen B, Løvslett K, Fiane B, Van Ghelue M, Clark N, Møller P. High risk for ovarian cancer in a prospective series is restricted to BRCA1/2 mutation carriers. Clin Cancer Res 2008;14:7569-73.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 7569-7573
-
-
Maehle, L.1
Apold, J.2
Paulsen, T.3
Hagen, B.4
Løvslett, K.5
Fiane, B.6
Van Ghelue, M.7
Clark, N.8
Møller, P.9
-
20
-
-
77951720395
-
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
-
Meindl A, Hellebrand H, Wiek C, Erven V, Wappenschmidt B, Niederacher D, Freund M, Lichtner P, Hartmann L, Schaal H, Ramser J, Honisch E, Kubisch C, Wichmann HE, Kast K, Deissler H, Engel C, Muller-Myhsok B, Neveling K, Kiechle M, Mathew CG, Schindler D, Schmutzler RK, Hanenberg H. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet 2010;42:410-14.
-
(2010)
Nat Genet
, vol.42
, pp. 410-414
-
-
Meindl, A.1
Hellebrand, H.2
Wiek, C.3
Erven, V.4
Wappenschmidt, B.5
Niederacher, D.6
Freund, M.7
Lichtner, P.8
Hartmann, L.9
Schaal, H.10
Ramser, J.11
Honisch, E.12
Kubisch, C.13
Wichmann, H.E.14
Kast, K.15
Deissler, H.16
Engel, C.17
Muller-Myhsok, B.18
Neveling, K.19
Kiechle, M.20
Mathew, C.G.21
Schindler, D.22
Schmutzler, R.K.23
Hanenberg, H.24
more..
-
21
-
-
84860320440
-
Germline mutations in RAD51D confer susceptibility to ovarian cancer
-
Breast cancer susceptibility collaboration UK, Eccles D, Evans DG, Renwick A, Seal S, Lord CJ, Ashworth A, Reis-Filho JS, Antoniou AC, Rahman N.
-
Loveday C, Turnbull C, Ramsay E, Hughes D, Ruark E, Frankum JR, Bowden G, Kalmyrzaev B, Warren-Perry M, Snape K, Adlard JW, Barwell J, Berg J, Brady AF, Brewer C, Brice G, Chapman C, Cook J, Davidson R, Donadlson A, Douglas F, Greenhalgh L, Henderson A, Izatt L, Kumar A, Lalloo F, Miedzybrodzka Z, Morrison PJ, Paterson J, Porteous M, Rogers MT, Shanley S, Walker L, Breast cancer susceptibility collaboration UK, Eccles D, Evans DG, Renwick A, Seal S, Lord CJ, Ashworth A, Reis-Filho JS, Antoniou AC, Rahman N. Germline mutations in RAD51D confer susceptibility to ovarian cancer. Nat Genet 2012;44:475-6.
-
(2012)
Nat Genet
, vol.44
, pp. 475-476
-
-
Loveday, C.1
Turnbull, C.2
Ramsay, E.3
Hughes, D.4
Ruark, E.5
Frankum, J.R.6
Bowden, G.7
Kalmyrzaev, B.8
Warren-Perry, M.9
Snape, K.10
Adlard, J.W.11
Barwell, J.12
Berg, J.13
Brady, A.F.14
Brewer, C.15
Brice, G.16
Chapman, C.17
Cook, J.18
Davidson, R.19
Donadlson, A.20
Douglas, F.21
Greenhalgh, L.22
Henderson, A.23
Izatt, L.24
Kumar, A.25
Lalloo, F.26
Miedzybrodzka, Z.27
Morrison, P.J.28
Paterson, J.29
Porteous, M.30
Rogers, M.T.31
Shanley, S.32
Walker, L.33
more..
-
22
-
-
84868200604
-
High sensitivity for BRCA1/ 2 mutations in breast/ovarian kindreds: are there still other breast/ovary genes to be discovered?
-
Smith MJ, Gifford FL, Lalloo F, Newman WG, Evans DG. High sensitivity for BRCA1/ 2 mutations in breast/ovarian kindreds: are there still other breast/ovary genes to be discovered?. Breast Cancer Res Treat 2012;134:895-7.
-
(2012)
Breast Cancer Res Treat
, vol.134
, pp. 895-897
-
-
Smith, M.J.1
Gifford, F.L.2
Lalloo, F.3
Newman, W.G.4
Evans, D.G.5
-
24
-
-
1842680082
-
A breast cancer prediction model incorporating familial and personal risk factors
-
Tyrer J, Duffy SW, Cuzick J. A breast cancer prediction model incorporating familial and personal risk factors. Stat Med 2004;23:1111-30.
-
(2004)
Stat Med
, vol.23
, pp. 1111-1130
-
-
Tyrer, J.1
Duffy, S.W.2
Cuzick, J.3
-
25
-
-
40749161574
-
Mutation testing for BRCA1/ 2 in ovarian cancer families: use of histology to predict status
-
Evans DGR, Young K, Bulman M, Shenton A, Lalloo F. Mutation testing for BRCA1/ 2 in ovarian cancer families: use of histology to predict status. Clin Genet 2008;73:338-45.
-
(2008)
Clin Genet
, vol.73
, pp. 338-345
-
-
Evans, D.G.R.1
Young, K.2
Bulman, M.3
Shenton, A.4
Lalloo, F.5
-
26
-
-
33748454829
-
CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumours
-
Szymanska-Pasternak J, Szymanska A, Medrek K, Imyanitov EN, Cybulski C, Gorski B, Magnowski P, Dziuba I, Gugala K, Debniak B, Gozdz S, Sokolenko AP, Krylova NY, Lobeiko OS, Narod SA, Lubinski J. CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumours. Gynecol Oncol 2006;102:429-31.
-
(2006)
Gynecol Oncol
, vol.102
, pp. 429-431
-
-
Szymanska-Pasternak, J.1
Szymanska, A.2
Medrek, K.3
Imyanitov, E.N.4
Cybulski, C.5
Gorski, B.6
Magnowski, P.7
Dziuba, I.8
Gugala, K.9
Debniak, B.10
Gozdz, S.11
Sokolenko, A.P.12
Krylova, N.Y.13
Lobeiko, O.S.14
Narod, S.A.15
Lubinski, J.16
-
27
-
-
77951293346
-
BRCA1 gene mutations may explain more than 80% of excess number of ovarian cancer cases after breast cancer-a population based study from the Western Sweden Health Care region
-
Einbeigi Z, Enerbäck C, Wallgren A, Nordling M, Karlsson P. BRCA1 gene mutations may explain more than 80% of excess number of ovarian cancer cases after breast cancer-a population based study from the Western Sweden Health Care region. Acta Oncol 2010;49:361-7.
-
(2010)
Acta Oncol
, vol.49
, pp. 361-367
-
-
Einbeigi, Z.1
Enerbäck, C.2
Wallgren, A.3
Nordling, M.4
Karlsson, P.5
-
28
-
-
78651074177
-
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases
-
Rumilla K, Schowalter KV, Lindor NM, Thomas BC, Mensink KA, Gallinger S, Holter S, Newcomb PA, Potter JD, Jenkins MA, Hopper JL, Long TI, Weisenberger DJ, Haile RW, Casey G, Laird PW, Le March L, Thibodeau SN. Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases. J Mol Diagn 2011;13:93-9.
-
(2011)
J Mol Diagn
, vol.13
, pp. 93-99
-
-
Rumilla, K.1
Schowalter, K.V.2
Lindor, N.M.3
Thomas, B.C.4
Mensink, K.A.5
Gallinger, S.6
Holter, S.7
Newcomb, P.A.8
Potter, J.D.9
Jenkins, M.A.10
Hopper, J.L.11
Long, T.I.12
Weisenberger, D.J.13
Haile, R.W.14
Casey, G.15
Laird, P.W.16
Le March, L.17
Thibodeau, S.N.18
-
29
-
-
34249717959
-
Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review
-
Gerhardus A, Schleberger H, Schlegelberger B, Gadzicki D. Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review. Eur J Hum Genet 2007;15:619-27.
-
(2007)
Eur J Hum Genet
, vol.15
, pp. 619-627
-
-
Gerhardus, A.1
Schleberger, H.2
Schlegelberger, B.3
Gadzicki, D.4
-
30
-
-
2942726188
-
A new scoring system for the chances of identifying a BRCA1/2 mutation, outperforms existing models including BRCAPRO
-
Evans DGR, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F. A new scoring system for the chances of identifying a BRCA1/2 mutation, outperforms existing models including BRCAPRO. J Med Genet 2004;41:474-80.
-
(2004)
J Med Genet
, vol.41
, pp. 474-480
-
-
Evans, D.G.R.1
Eccles, D.M.2
Rahman, N.3
Young, K.4
Bulman, M.5
Amir, E.6
Shenton, A.7
Howell, A.8
Lalloo, F.9
-
31
-
-
79952025075
-
Development of a scoring system to screen for BRCA1/2 mutations
-
Evans GR, Lalloo F. Development of a scoring system to screen for BRCA1/2 mutations. Methods Mol Biol 2010;653:237-47.
-
(2010)
Methods Mol Biol
, vol.653
, pp. 237-247
-
-
Evans, G.R.1
Lalloo, F.2
-
32
-
-
84892627739
-
The trouble with phenocopies: are those testing negative for a family BRCA1/2 mutation really at population risk?
-
Evans DGR, Smith A, Moran A, Boyd MC, Bulman M, Woodward E, Smith L, Moran A, Lalloo F, Maher ER. The trouble with phenocopies: are those testing negative for a family BRCA1/2 mutation really at population risk? J Med Genet 2007;44:10-5.
-
(2007)
J Med Genet
, vol.44
, pp. 10-15
-
-
Evans, D.G.R.1
Smith, A.2
Moran, A.3
Boyd, M.C.4
Bulman, M.5
Woodward, E.6
Smith, L.7
Moran, A.8
Lalloo, F.9
Maher, E.R.10
|