-
1
-
-
0031958466
-
BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: Relationship to family history and implications for genetic testing
-
Rubin SC, Blackwood MA, Bandera CM, Behbakht K, Benjamin I, Rebbeck RH, et al. BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing. Am J Obstet Gynecol 1998;178:670-5.
-
(1998)
Am J Obstet Gynecol
, vol.178
, pp. 670-675
-
-
Rubin, S.C.1
Blackwood, M.A.2
Bandera, C.M.3
Behbakht, K.4
Benjamin, I.5
Rebbeck, R.H.6
-
2
-
-
0036095495
-
Contribution of BRCA1 and BRCA2 to familial ovarian cancer: A gynecologic oncology group study
-
Reedy M, Gallion H, Fowler JM, Kryscio R, Smith SA. Contribution of BRCA1 and BRCA2 to familial ovarian cancer: a gynecologic oncology group study. Gynecol Oncol 2002;85:255-9.
-
(2002)
Gynecol Oncol
, vol.85
, pp. 255-259
-
-
Reedy, M.1
Gallion, H.2
Fowler, J.M.3
Kryscio, R.4
Smith, S.A.5
-
3
-
-
0031025322
-
Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: Results from three U.S. population-based case-control studies of ovarian cancer
-
Whittemore AS, Gong G, Itnyre J. Prevalence and contribution of BRCA1 mutations in breast cancer and ovarian cancer: results from three U.S. population-based case-control studies of ovarian cancer. Am J Hum Genet 1997;60:496-504.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 496-504
-
-
Whittemore, A.S.1
Gong, G.2
Itnyre, J.3
-
4
-
-
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, et al. 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
-
5
-
-
0035098503
-
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
-
Risch HA, McLaughlin JR, Cole DE, Rosen B, Bradley L, Kwan E, et al. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. Am J Hum Genet 2001;68:700-10.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 700-710
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.3
Rosen, B.4
Bradley, L.5
Kwan, E.6
-
6
-
-
0142178215
-
The New York Breast Cancer Study Group. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
King M-C, Marks JH, Mandell JB; The New York Breast Cancer Study Group. 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
-
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
-
-
0033927850
-
BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer
-
Moslehi R, Chu W, Karlan B, Fishman D, Risch H, Fields A, et al. BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer. Am J Hum Genet 2000;66:1259-72.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1259-1272
-
-
Moslehi, R.1
Chu, W.2
Karlan, B.3
Fishman, D.4
Risch, H.5
Fields, A.6
-
9
-
-
0030902227
-
Population Genetics of BRCA1 and BRCA2
-
Szabo CI, King MC. Population Genetics of BRCA1 and BRCA2. Am J Hum Genet 1997;60:1013-20.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1013-1020
-
-
Szabo, C.I.1
King, M.C.2
-
10
-
-
0036591552
-
Characterization of Common BRCA1 and BRCA2 Variants
-
Deffenbaugh AM, Frank TS, Hoffman M, Cannon-Albright L, Neuhausen SL. Characterization of Common BRCA1 and BRCA2 Variants. Genet Test 2002;6:119-21.
-
(2002)
Genet Test
, vol.6
, pp. 119-121
-
-
Deffenbaugh, A.M.1
Frank, T.S.2
Hoffman, M.3
Cannon-Albright, L.4
Neuhausen, S.L.5
-
11
-
-
0033865651
-
Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer
-
Payne SR, Newman B, King MC. Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer. Genes Chromosomes Cancer 2000;29:58-62.
-
(2000)
Genes Chromosomes Cancer
, vol.29
, pp. 58-62
-
-
Payne, S.R.1
Newman, B.2
King, M.C.3
-
12
-
-
0037162110
-
Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations
-
Rebbeck TR, Lynch HT, Neuhausen SL, Narod SA, Van't Veer L, Garber JE, et al. Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations. N Engl J Med 2002;346:1616-22.
-
(2002)
N Engl J Med
, vol.346
, pp. 1616-1622
-
-
Rebbeck, T.R.1
Lynch, H.T.2
Neuhausen, S.L.3
Narod, S.A.4
Van't Veer, L.5
Garber, J.E.6
-
13
-
-
0037162115
-
Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation
-
Kauff ND, Satagopan JM, Robson ME, Scheuer L, Hensley M, Hudis CA, et al. Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation. N Engl J Med 2002;346:1609-15.
-
(2002)
N Engl J Med
, vol.346
, pp. 1609-1615
-
-
Kauff, N.D.1
Satagopan, J.M.2
Robson, M.E.3
Scheuer, L.4
Hensley, M.5
Hudis, C.A.6
-
14
-
-
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
-
15
-
-
0028844202
-
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for genotype-phenotype correlation
-
Gayther SA, Warren W, Mazoyer S, Russell PA, Harrington PA, Chiano M, et al. Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for genotype-phenotype correlation. Nat Genet 1995;11:428-33.
-
(1995)
Nat Genet
, vol.11
, pp. 428-433
-
-
Gayther, S.A.1
Warren, W.2
Mazoyer, S.3
Russell, P.A.4
Harrington, P.A.5
Chiano, M.6
-
16
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
Gayther SA, Mangion J, Russell P, Seal S, Barfoot R, Ponder BA, et al. Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. Nat Genet 1997;15:103-5.
-
(1997)
Nat Genet
, vol.15
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russell, P.3
Seal, S.4
Barfoot, R.5
Ponder, B.A.6
-
17
-
-
0030852505
-
BRCA1 sequence analysis in women at high risk for susceptibility mutations: Risk factor analysis and implications for genetic testing
-
Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, et al. BRCA1 sequence analysis in women at high risk for susceptibility mutations: risk factor analysis and implications for genetic testing. JAMA 1997;278:1242-50.
-
(1997)
JAMA
, vol.278
, pp. 1242-1250
-
-
Shattuck-Eidens, D.1
Oliphant, A.2
McClure, M.3
McBride, C.4
Gupte, J.5
Rubano, T.6
-
18
-
-
0008195461
-
A descriptive study of BRCA1 testing and reactions to disclosure of test results
-
Lynch HT, Lemon SJ, Durham C, Tinley ST, Connolly C, Lynch JF, et al. A descriptive study of BRCA1 testing and reactions to disclosure of test results. Cancer 1997;79:2219-28.
-
(1997)
Cancer
, vol.79
, pp. 2219-2228
-
-
Lynch, H.T.1
Lemon, S.J.2
Durham, C.3
Tinley, S.T.4
Connolly, C.5
Lynch, J.F.6
-
19
-
-
18544381115
-
Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutations
-
Kauff ND, Scheuer L, Robson ME, Glogowski E, Kelly B, Barakat R, et al. Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA2 mutations. Genet Med 2001;3:422-5.
-
(2001)
Genet Med
, vol.3
, pp. 422-425
-
-
Kauff, N.D.1
Scheuer, L.2
Robson, M.E.3
Glogowski, E.4
Kelly, B.5
Barakat, R.6
-
20
-
-
33745881036
-
Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 mutation. Hereditary Ovarian Cancer Clinical Study Group
-
Finch A, Beiner M, Lubinski J, Lynch HT, Moller P, Rosen B, et al. Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 mutation. Hereditary Ovarian Cancer Clinical Study Group. JAMA 2006;296:185-92.
-
(2006)
JAMA
, vol.296
, pp. 185-192
-
-
Finch, A.1
Beiner, M.2
Lubinski, J.3
Lynch, H.T.4
Moller, P.5
Rosen, B.6
-
21
-
-
0032514413
-
Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group
-
Narod SA, Risch H, Moslehi R, Dorum A, Neuhausen S, Olsson H, et al. Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group. N Engl J Med 1998;339:424-8.
-
(1998)
N Engl J Med
, vol.339
, pp. 424-428
-
-
Narod, S.A.1
Risch, H.2
Moslehi, R.3
Dorum, A.4
Neuhausen, S.5
Olsson, H.6
-
22
-
-
0037093059
-
Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations: An updated decision analysis
-
Grann VR, Jacobson JS, Thomason D, Hershman D, Heitjan DF, Neugut AI. Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations: an updated decision analysis. J Clin Oncol 2002;20:2520-9.
-
(2002)
J Clin Oncol
, vol.20
, pp. 2520-2529
-
-
Grann, V.R.1
Jacobson, J.S.2
Thomason, D.3
Hershman, D.4
Heitjan, D.F.5
Neugut, A.I.6
-
23
-
-
0029889525
-
Hormone replacement therapy in breast cancer survivors: A cohort study
-
DiSaia PJ, Grosen EA, Kurosaki T, Gildea M, Cowan B, Anton-Culver H. Hormone replacement therapy in breast cancer survivors: a cohort study. Am J Obstet Gynecol 1996;174:1494-8.
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 1494-1498
-
-
DiSaia, P.J.1
Grosen, E.A.2
Kurosaki, T.3
Gildea, M.4
Cowan, B.5
Anton-Culver, H.6
-
24
-
-
0031003498
-
Contribution of BRCA1 mutations to ovarian cancer
-
Stratton JF, Gayther SA, Russell P, Dearden J, Gore M, Blake P, et al. Contribution of BRCA1 mutations to ovarian cancer. N Engl J Med 1997;336:1125-30.
-
(1997)
N Engl J Med
, vol.336
, pp. 1125-1130
-
-
Stratton, J.F.1
Gayther, S.A.2
Russell, P.3
Dearden, J.4
Gore, M.5
Blake, P.6
-
25
-
-
0035095962
-
Risk of endometrial carcinoma associated with BRCA mutation
-
Levine DA, Lin O, Barakat RR, Robson ME, McDermott D, Cohen L, et al. Risk of endometrial carcinoma associated with BRCA mutation. Gynecol Oncol 2001;80:395-8.
-
(2001)
Gynecol Oncol
, vol.80
, pp. 395-398
-
-
Levine, D.A.1
Lin, O.2
Barakat, R.R.3
Robson, M.E.4
McDermott, D.5
Cohen, L.6
-
26
-
-
0034039265
-
BRCA1 germline mutations in women with uterine serous papillary carcinoma
-
Lavie O, Hornreich G, Ben Arie A, Renbaum P, Levy-Lahad E, Beller U. BRCA1 germline mutations in women with uterine serous papillary carcinoma. Obstet Gynecol 2000;96:28-32.
-
(2000)
Obstet Gynecol
, vol.96
, pp. 28-32
-
-
Lavie, O.1
Hornreich, G.2
Ben Arie, A.3
Renbaum, P.4
Levy-Lahad, E.5
Beller, U.6
-
27
-
-
0033976892
-
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations
-
Zweemer RP, van Diest PJ, Verheijen RH, Ryan A, Gille JJ, Sijmons RH, et al. Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations. Gynecol Oncol 2000;76:45-50.
-
(2000)
Gynecol Oncol
, vol.76
, pp. 45-50
-
-
Zweemer, R.P.1
van Diest, P.J.2
Verheijen, R.H.3
Ryan, A.4
Gille, J.J.5
Sijmons, R.H.6
-
28
-
-
0035093053
-
A genetic epidemiological study of carcinoma of the fallopian tube
-
Aziz S, Kuperstein G, Rosen B, Cole D, Nedelcu R, McLaughlin J, et al. A genetic epidemiological study of carcinoma of the fallopian tube. Gynecol Oncol 2001;80:341-5.
-
(2001)
Gynecol Oncol
, vol.80
, pp. 341-345
-
-
Aziz, S.1
Kuperstein, G.2
Rosen, B.3
Cole, D.4
Nedelcu, R.5
McLaughlin, J.6
-
29
-
-
0037130889
-
Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program
-
Brose MS, Rebbeck TR, Calzone KA, Stopfer JE, Nathanson KL, Weber BL. Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. J Natl Cancer Inst 2002;94:1365-72.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1365-1372
-
-
Brose, M.S.1
Rebbeck, T.R.2
Calzone, K.A.3
Stopfer, J.E.4
Nathanson, K.L.5
Weber, B.L.6
-
30
-
-
0019960002
-
Intra-abdominal carcinomatosis after prophylactic oophorectomy in ovarian-cancer-prone families
-
Tobacman JK, Greene MH, Tucker MA, Costa J, Kase R, Fraumeni JF Jr. Intra-abdominal carcinomatosis after prophylactic oophorectomy in ovarian-cancer-prone families. Lancet 1982;2:795-7.
-
(1982)
Lancet
, vol.2
, pp. 795-797
-
-
Tobacman, J.K.1
Greene, M.H.2
Tucker, M.A.3
Costa, J.4
Kase, R.5
Fraumeni Jr., J.F.6
-
31
-
-
0027483251
-
Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer: A report of the Gilda Radner Familial Ovarian Cancer Registry
-
Piver MS, Jishi MF, Tsukada Y, Nava G. Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer: a report of the Gilda Radner Familial Ovarian Cancer Registry. Cancer 1993;71:2751-5.
-
(1993)
Cancer
, vol.71
, pp. 2751-2755
-
-
Piver, M.S.1
Jishi, M.F.2
Tsukada, Y.3
Nava, G.4
-
32
-
-
0029441577
-
Prophylactic oophorectomy in inherited breast/ovarian cancer families
-
Struewing JP, Watson P, Easton DF, Ponder BA, Lynch HT, Tucker MA. Prophylactic oophorectomy in inherited breast/ovarian cancer families. J Natl Cancer Inst Monogr 1995:33-5.
-
(1995)
J Natl Cancer Inst Monogr
, pp. 33-35
-
-
Struewing, J.P.1
Watson, P.2
Easton, D.F.3
Ponder, B.A.4
Lynch, H.T.5
Tucker, M.A.6
-
33
-
-
0033942547
-
Occult ovarian tumors in women with BRCA1 or BRCA2 mutations undergoing prophylactic oophorectomy
-
Lu KH, Garber JE, Cramer DW, Welch WR, Niloff J, Schrag D, et al. Occult ovarian tumors in women with BRCA1 or BRCA2 mutations undergoing prophylactic oophorectomy. J Clin Oncol 2000;18:2728-32.
-
(2000)
J Clin Oncol
, vol.18
, pp. 2728-2732
-
-
Lu, K.H.1
Garber, J.E.2
Cramer, D.W.3
Welch, W.R.4
Niloff, J.5
Schrag, D.6
-
34
-
-
0034810223
-
Occult carcinoma in prophylactic oophorectomy specimens: Prevalence and association with BRCA germline mutation status
-
Colgan TJ, Murphy J, Cole DE, Narod S, Rosen B. Occult carcinoma in prophylactic oophorectomy specimens: prevalence and association with BRCA germline mutation status. Am J Surg Pathol 2001;25:1283-9.
-
(2001)
Am J Surg Pathol
, vol.25
, pp. 1283-1289
-
-
Colgan, T.J.1
Murphy, J.2
Cole, D.E.3
Narod, S.4
Rosen, B.5
-
35
-
-
16644400609
-
Risk-reducing salpingo-oophorectomy in BRCA mutation carriers: Role of serial sectioning in the detection of occult malignancy
-
Powell CB, Kenley E, Chen L-M, Crawford B, McLennan J, Zaloudek C, et al. Risk-reducing salpingo-oophorectomy in BRCA mutation carriers: Role of serial sectioning in the detection of occult malignancy. J Clin Oncol 2005;23:127-32.
-
(2005)
J Clin Oncol
, vol.23
, pp. 127-132
-
-
Powell, C.B.1
Kenley, E.2
Chen, L.-M.3
Crawford, B.4
McLennan, J.5
Zaloudek, C.6
-
36
-
-
0022386154
-
Peritoneal carcinomatosis after prophylactic oophorectomy in familial ovarian cancer syndrome
-
Chen KT, Schooley JL, Flam MS. Peritoneal carcinomatosis after prophylactic oophorectomy in familial ovarian cancer syndrome. Obstet Gynecol 1985;66:93S-4S.
-
(1985)
Obstet Gynecol
, vol.66
-
-
Chen, K.T.1
Schooley, J.L.2
Flam, M.S.3
-
37
-
-
0035137888
-
Occult cancer of the fallopian tube in BRCA-1 germline mutation carriers at prophylactic oophorectomy: A case for recommending hysterectomy at surgical prophylaxis
-
Paley PJ, Swisher EM, Garcia RL, Agoff SN, Greer BE, Peters KL, et al. Occult cancer of the fallopian tube in BRCA-1 germline mutation carriers at prophylactic oophorectomy: a case for recommending hysterectomy at surgical prophylaxis. Gynecol Oncol 2001;80:176-80.
-
(2001)
Gynecol Oncol
, vol.80
, pp. 176-180
-
-
Paley, P.J.1
Swisher, E.M.2
Garcia, R.L.3
Agoff, S.N.4
Greer, B.E.5
Peters, K.L.6
-
38
-
-
0036080703
-
Peritoneal lavage cytology: An assessment of its value during prophylactic oophorectomy
-
Colgan TJ, Boerner SL, Murphy J, Cole DE, Narod S, Rosen B. Peritoneal lavage cytology: an assessment of its value during prophylactic oophorectomy. Gynecol Oncol 2002;85:397-403.
-
(2002)
Gynecol Oncol
, vol.85
, pp. 397-403
-
-
Colgan, T.J.1
Boerner, S.L.2
Murphy, J.3
Cole, D.E.4
Narod, S.5
Rosen, B.6
-
39
-
-
33645225423
-
The tubal fimbria is a preferred site for early adenocarcinoma in women with familial ovarian cancer syndrome
-
Medeiros F, Muto MG, Lee Y, Elvin JA, Callahan MJ, Feltmate C, et al. The tubal fimbria is a preferred site for early adenocarcinoma in women with familial ovarian cancer syndrome. Am J Surg Pathol 2006;30:230-6.
-
(2006)
Am J Surg Pathol
, vol.30
, pp. 230-236
-
-
Medeiros, F.1
Muto, M.G.2
Lee, Y.3
Elvin, J.A.4
Callahan, M.J.5
Feltmate, C.6
-
40
-
-
0029585997
-
Lifetime risk of different cancers in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome
-
Aarnio M, Mecklin JP, Aaltonen LA, Nystrom-Lahti M, Jarvinen HJ. Lifetime risk of different cancers in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome. Int J Cancer 1995;64:430-3.
-
(1995)
Int J Cancer
, vol.64
, pp. 430-433
-
-
Aarnio, M.1
Mecklin, J.P.2
Aaltonen, L.A.3
Nystrom-Lahti, M.4
Jarvinen, H.J.5
-
41
-
-
0032941343
-
Cancer risk in mutation carriers of DNA-mismatch-repair genes
-
Aarnio M, Sankila R, Pukkala E, Salovaara R, Aaltonen LA, de la Chapelle A, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 1999;81:214-8.
-
(1999)
Int J Cancer
, vol.81
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
Salovaara, R.4
Aaltonen, L.A.5
de la Chapelle, A.6
-
42
-
-
0033458843
-
Clinical impact of molecular and genetic diagnosis, genetic counseling, and management of hereditary cancer. Part I: Studies of cancer in families
-
Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, et al. Clinical impact of molecular and genetic diagnosis, genetic counseling, and management of hereditary cancer. Part I: Studies of cancer in families. Cancer 1999;86:2449-56.
-
(1999)
Cancer
, vol.86
, pp. 2449-2456
-
-
Lynch, H.T.1
Watson, P.2
Shaw, T.G.3
Lynch, J.F.4
Harty, A.E.5
Franklin, B.A.6
-
43
-
-
0028108802
-
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families available by linkage
-
Nystrom-Lahti M, Parsons R, Sistonen P, Pylkkanen L, Aaltonen LA, Leach FS, et al. Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families available by linkage. Am J Hum Genet 1994;55:659-65.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 659-665
-
-
Nystrom-Lahti, M.1
Parsons, R.2
Sistonen, P.3
Pylkkanen, L.4
Aaltonen, L.A.5
Leach, F.S.6
-
44
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, et al. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 1996;2:169-74.
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
-
46
-
-
0025773554
-
Mutator phenotype may be required for multistage carcinogenesis
-
Loeb LA. Mutator phenotype may be required for multistage carcinogenesis. Cancer Res 1991;51:3075-9.
-
(1991)
Cancer Res
, vol.51
, pp. 3075-3079
-
-
Loeb, L.A.1
-
47
-
-
0027205395
-
Nucleotide repeats: Slippery DNA and diseases
-
Kunkel TA. Nucleotide repeats: slippery DNA and diseases. Nature 1993;365:207-8.
-
(1993)
Nature
, vol.365
, pp. 207-208
-
-
Kunkel, T.A.1
-
48
-
-
0032534069
-
A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal caner
-
Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, et al. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal caner. Cancer Res 1998;58:5248-57.
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
Sidransky, D.4
Eshleman, J.R.5
Burt, R.W.6
-
49
-
-
33750515665
-
Improved survival with an intact DNA mismatch repair system in endometrial cancer
-
Cohn DE, Frankel WL, Resnick KE, Zanagnolo VL, Copeland LJ, Hampel H, et al. Improved survival with an intact DNA mismatch repair system in endometrial cancer. Obstet Gynecol 2006;108:1208-15.
-
(2006)
Obstet Gynecol
, vol.108
, pp. 1208-1215
-
-
Cohn, D.E.1
Frankel, W.L.2
Resnick, K.E.3
Zanagnolo, V.L.4
Copeland, L.J.5
Hampel, H.6
-
50
-
-
17944362664
-
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
-
Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 2005;352:1851-60.
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
Arnold, M.4
Khanduja, K.5
Kuebler, P.6
-
51
-
-
0030997158
-
Mutational analysis of MLH1 and MSH2 in 25 prospectively acquired RER+ endometrial cancers
-
Kowalski LD, Mutch DG, Herzog TJ, Rader JS, Goodfellow PJ. Mutational analysis of MLH1 and MSH2 in 25 prospectively acquired RER+ endometrial cancers. Genes Chromosomes Cancer 1997;18:219-27.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 219-227
-
-
Kowalski, L.D.1
Mutch, D.G.2
Herzog, T.J.3
Rader, J.S.4
Goodfellow, P.J.5
-
52
-
-
0032870838
-
-
Basil JB, Swisher EM, Herzog TJ, Rader JS, Elbendary A, Mutch DG, et al. Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability [published erratum appears in Gynecol Oncol 2001;80:109]. Gynecol Oncol 1999;74:395-9.
-
Basil JB, Swisher EM, Herzog TJ, Rader JS, Elbendary A, Mutch DG, et al. Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability [published erratum appears in Gynecol Oncol 2001;80:109]. Gynecol Oncol 1999;74:395-9.
-
-
-
-
53
-
-
0032487831
-
MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas
-
Esteller M, Levine R, Baylin SB, Ellenson LH, Herman JG. MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas. Oncogene 1998;17:2413-7.
-
(1998)
Oncogene
, vol.17
, pp. 2413-2417
-
-
Esteller, M.1
Levine, R.2
Baylin, S.B.3
Ellenson, L.H.4
Herman, J.G.5
-
54
-
-
0037609660
-
Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers
-
Goodfellow PJ, Buttin BM, Herzog TJ, Rader JS, Gibb RK, Swisher E, et al. Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. Proc Natl Acad Sci U S A 2003;100:5908-13.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 5908-5913
-
-
Goodfellow, P.J.1
Buttin, B.M.2
Herzog, T.J.3
Rader, J.S.4
Gibb, R.K.5
Swisher, E.6
-
55
-
-
33746794561
-
Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinomas): A guide for clinicians
-
Hendriks YM, de Jong AE, Morreau H, Tops CM, Vasen HF, Wijnen JT, et al. Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinomas): a guide for clinicians. CA Cancer J Clin 2006;56:213-25.
-
(2006)
CA Cancer J Clin
, vol.56
, pp. 213-225
-
-
Hendriks, Y.M.1
de Jong, A.E.2
Morreau, H.3
Tops, C.M.4
Vasen, H.F.5
Wijnen, J.T.6
-
56
-
-
0033825587
-
Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1
-
Syngal S, Fox EA, Eng C, Kolodner RD, Garber JE. Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1. J Med Genet 2000;37:641-5.
-
(2000)
J Med Genet
, vol.37
, pp. 641-645
-
-
Syngal, S.1
Fox, E.A.2
Eng, C.3
Kolodner, R.D.4
Garber, J.E.5
-
57
-
-
18644386133
-
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel detection approach
-
Gille JJ, Hogervorst FB, Pals G, Wijnen JT, van Schooten RJ, Dommering CJ, et al. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel detection approach. Br J Cancer 2002;87:892-7.
-
(2002)
Br J Cancer
, vol.87
, pp. 892-897
-
-
Gille, J.J.1
Hogervorst, F.B.2
Pals, G.3
Wijnen, J.T.4
van Schooten, R.J.5
Dommering, C.J.6
-
58
-
-
0032552239
-
Clinical findings with implications for genetic testing in families with clustering of colorectal cancers
-
Wijnen JT, Vasen HF, Khan PM, Zwinderman AH, van der Klift H, Mulder A, et al. Clinical findings with implications for genetic testing in families with clustering of colorectal cancers. N Engl J Med 1998;339:511-8.
-
(1998)
N Engl J Med
, vol.339
, pp. 511-518
-
-
Wijnen, J.T.1
Vasen, H.F.2
Khan, P.M.3
Zwinderman, A.H.4
van der Klift, H.5
Mulder, A.6
-
59
-
-
16944364360
-
Hereditary non-polyposis colorectal cancer families not complying with the Amsterdam criteria show an extremely low frequency of mismatch repair gene mutations
-
Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, et al. Hereditary non-polyposis colorectal cancer families not complying with the Amsterdam criteria show an extremely low frequency of mismatch repair gene mutations. Am J Hum Genet 1997;61:329-35.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 329-335
-
-
Wijnen, J.1
Khan, P.M.2
Vasen, H.3
van der Klift, H.4
Mulder, A.5
van Leeuwen-Cornelisse, I.6
-
60
-
-
0037730214
-
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: High mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene
-
Wagner A, Barrows Wijnen JT, van der Klift H, Franken PF, Verkuijlen P, et al. Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. Am J Hum Genet 2003;72:1088-100.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1088-1100
-
-
Wagner, A.1
Barrows Wijnen, J.T.2
van der Klift, H.3
Franken, P.F.4
Verkuijlen, P.5
-
61
-
-
3242670404
-
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance
-
Hendriks YM, Wagner A, Morreau H, Menko F, Stormorken A, Quehenberger F, et al. Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. Gastroenterology 2004;127:17-25.
-
(2004)
Gastroenterology
, vol.127
, pp. 17-25
-
-
Hendriks, Y.M.1
Wagner, A.2
Morreau, H.3
Menko, F.4
Stormorken, A.5
Quehenberger, F.6
-
62
-
-
1642574368
-
Accuracy of reporting of family history of colorectal cancer
-
Mitchell RJ, Brewster D, Campbell H, Porteous MDM, Wyllie AH, Bird CC, et al. Accuracy of reporting of family history of colorectal cancer. Gut 2004;53:291-5.
-
(2004)
Gut
, vol.53
, pp. 291-295
-
-
Mitchell, R.J.1
Brewster, D.2
Campbell, H.3
Porteous, M.D.M.4
Wyllie, A.H.5
Bird, C.C.6
-
63
-
-
0036284436
-
Evaluation of the family history of collection process and the accuracy of cancer reporting among a series of women with endometrial cancer
-
Ivanovich J, Babb S, Goodfellow P, Mutch D, Herzog T, Rader J, et al. Evaluation of the family history of collection process and the accuracy of cancer reporting among a series of women with endometrial cancer. Clin Cancer Res 2002;8:1849-56.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 1849-1856
-
-
Ivanovich, J.1
Babb, S.2
Goodfellow, P.3
Mutch, D.4
Herzog, T.5
Rader, J.6
-
64
-
-
33747871345
-
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
-
Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, et al. Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 2006;66:7810-7.
-
(2006)
Cancer Res
, vol.66
, pp. 7810-7817
-
-
Hampel, H.1
Frankel, W.2
Panescu, J.3
Lockman, J.4
Sotamaa, K.5
Fix, D.6
-
65
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Jarvinen HJ, Aarnio M, Mustonen H, Aktan-Collan K, Aaltonen LA, Peltomaki P, et al. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 2000;118:829-34.
-
(2000)
Gastroenterology
, vol.118
, pp. 829-834
-
-
Jarvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
Aktan-Collan, K.4
Aaltonen, L.A.5
Peltomaki, P.6
-
66
-
-
0037086654
-
The outcome of endometrial cancer surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma
-
Dove-Edwin I, Boks D, Goff S, Kenter GG, Carpenter R, Vasen HF, et al. The outcome of endometrial cancer surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma. Cancer 2002;94:1708-12.
-
(2002)
Cancer
, vol.94
, pp. 1708-1712
-
-
Dove-Edwin, I.1
Boks, D.2
Goff, S.3
Kenter, G.G.4
Carpenter, R.5
Vasen, H.F.6
-
67
-
-
30944457531
-
Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome
-
Schmeler KM, Lynch HT, Chen L-M, Munsell MF, Soliman PT, Clark MB, et al. Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 2006;354:261-9.
-
(2006)
N Engl J Med
, vol.354
, pp. 261-269
-
-
Schmeler, K.M.1
Lynch, H.T.2
Chen, L.-M.3
Munsell, M.F.4
Soliman, P.T.5
Clark, M.B.6
-
68
-
-
0038501057
-
genetic testing for cancer susceptibility
-
American Society of Clinical Oncology policy statement update
-
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. J Clin Oncol 2003;21:2397-406.
-
(2003)
J Clin Oncol
, vol.21
, pp. 2397-2406
-
-
-
69
-
-
33750594611
-
Cancer genetic testing and assisted reproduction
-
Offit K, Kohut K, Clagett B, Wadsworth EA, Lafaro KJ, Cummings S, et al. Cancer genetic testing and assisted reproduction. J Clin Oncol 2006;24:4775-82.
-
(2006)
J Clin Oncol
, vol.24
, pp. 4775-4782
-
-
Offit, K.1
Kohut, K.2
Clagett, B.3
Wadsworth, E.A.4
Lafaro, K.J.5
Cummings, S.6
-
70
-
-
33845472926
-
Preimplantation genetic diagnosis for cancer syndromes: A new challenge for preventive medicine
-
Offit K, Sagi M, Hurley K. Preimplantation genetic diagnosis for cancer syndromes: a new challenge for preventive medicine. JAMA 2006;296:2727-30.
-
(2006)
JAMA
, vol.296
, pp. 2727-2730
-
-
Offit, K.1
Sagi, M.2
Hurley, K.3
|