-
1
-
-
78650801916
-
Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population
-
Dinh TA, Rosner BI, Atwood JC, et al: Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila) 4:9-22, 2011
-
(2011)
Cancer Prev Res (Phila)
, vol.4
, pp. 9-22
-
-
Dinh, T.A.1
Rosner, B.I.2
Atwood, J.C.3
-
2
-
-
70350090521
-
Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome
-
Stoffel E, Mukherjee B, Raymond VM, et al: Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome. Gastroenterology 137:1621-1627, 2009
-
(2009)
Gastroenterology
, vol.137
, pp. 1621-1627
-
-
Stoffel, E.1
Mukherjee, B.2
Raymond, V.M.3
-
3
-
-
0029585997
-
Life-time risk of different cancers in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome
-
Aarnio M, Mecklin JP, Aaltonen LA, et al: Life-time risk of different cancers in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome. Int J Cancer 64:430-433, 1995
-
(1995)
Int J Cancer
, vol.64
, pp. 430-433
-
-
Aarnio, M.1
Mecklin, J.P.2
Aaltonen, L.A.3
-
4
-
-
0032941343
-
Cancer risk in mutation carriers of DNA-mismatch-repair genes
-
Aarnio M, Sankila R, Pukkala E, et al: Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 81:214-218, 1999
-
(1999)
Int J Cancer
, vol.81
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
-
5
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Järvinen HJ, Aarnio M, Mustonen H, et al: Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 118:829-834, 2000
-
(2000)
Gastroenterology
, vol.118
, pp. 829-834
-
-
Järvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
-
6
-
-
84860605783
-
Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: A prospective cohort study
-
Win AK, Young JP, Lindor NM, et al: Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: A prospective cohort study. J Clin Oncol 30:958-964, 2012
-
(2012)
J Clin Oncol
, vol.30
, pp. 958-964
-
-
Win, A.K.1
Young, J.P.2
Lindor, N.M.3
-
7
-
-
33646593777
-
Extent of disease at presentation and outcome for adrenocortical carcinoma: Have we made progress?
-
Kebebew E, Reiff E, Duh QY, et al: Extent of disease at presentation and outcome for adrenocortical carcinoma: Have we made progress? World J Surg 30:872-878, 2006
-
(2006)
World J Surg
, vol.30
, pp. 872-878
-
-
Kebebew, E.1
Reiff, E.2
Duh, Q.Y.3
-
8
-
-
0035979262
-
An inherited p53 mutation that contributes in a tissuespecific manner to pediatric adrenal cortical carcinoma
-
Ribeiro RC, Sandrini F, Figueiredo B, et al: An inherited p53 mutation that contributes in a tissuespecific manner to pediatric adrenal cortical carcinoma. Proc Natl Acad Sci U S A 98:9330-9335, 2001
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 9330-9335
-
-
Ribeiro, R.C.1
Sandrini, F.2
Figueiredo, B.3
-
9
-
-
0014037384
-
Adrenocortical neoplasms with hemihypertrophy, brain tumors, and other disorders
-
Fraumeni JF Jr, Miller RW: Adrenocortical neoplasms with hemihypertrophy, brain tumors, and other disorders. J Pediatr 70:129-138, 1967
-
(1967)
J Pediatr
, vol.70
, pp. 129-138
-
-
Fraumeni, J.F.1
Miller, R.W.2
-
10
-
-
0037222381
-
Germline TP53 mutations and Li-Fraumeni syndrome
-
Varley JM: Germline TP53 mutations and Li-Fraumeni syndrome. Hum Mutat 21:313-320, 2003
-
(2003)
Hum Mutat
, vol.21
, pp. 313-320
-
-
Varley, J.M.1
-
11
-
-
0033365202
-
Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumors
-
Varley JM, McGown G, Thorncroft M, et al: Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumors. Am J Hum Genet 65:995-1006, 1999
-
(1999)
Am J Hum Genet
, vol.65
, pp. 995-1006
-
-
Varley, J.M.1
McGown, G.2
Thorncroft, M.3
-
12
-
-
84858020426
-
TP53 germline mutations in adult patients with adrenocortical carcinoma
-
Herrmann LJ, Heinze B, Fassnacht M, et al: TP53 germline mutations in adult patients with adrenocortical carcinoma. J Clin Endocrinol Metab 97:E476-E485, 2012
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. E476-E485
-
-
Herrmann, L.J.1
Heinze, B.2
Fassnacht, M.3
-
13
-
-
84872094332
-
Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma
-
Raymond VM, Else T, Everett JN, et al: Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma. J Clin Endocrinol Metab 98:E119-E125, 2013
-
(2013)
J Clin Endocrinol Metab
, vol.98
, pp. E119-E125
-
-
Raymond, V.M.1
Else, T.2
Everett, J.N.3
-
14
-
-
67349216593
-
Screening of patients with multiple endocrine neoplasia type 1 (MEN-1): A critical analysis of its value
-
Waldmann J, Fendrich V, Habbe N, et al: Screening of patients with multiple endocrine neoplasia type 1 (MEN-1): A critical analysis of its value. World J Surg 33:1208-1218, 2009
-
(2009)
World J Surg
, vol.33
, pp. 1208-1218
-
-
Waldmann, J.1
Fendrich, V.2
Habbe, N.3
-
15
-
-
0036688509
-
Adrenal involvement in multiple endocrine neoplasia type 1
-
Langer P, Cupisti K, Bartsch DK, et al: Adrenal involvement in multiple endocrine neoplasia type 1. World J Surg 26:891-896, 2002
-
(2002)
World J Surg
, vol.26
, pp. 891-896
-
-
Langer, P.1
Cupisti, K.2
Bartsch, D.K.3
-
16
-
-
84857111277
-
Association of adrenocortical carcinoma with familial cancer susceptibility syndromes
-
Else T: Association of adrenocortical carcinoma with familial cancer susceptibility syndromes. Mol Cell Endocrinol 351:66-70, 2012
-
(2012)
Mol Cell Endocrinol
, vol.351
, pp. 66-70
-
-
Else, T.1
-
17
-
-
0035133356
-
Sensitivity and predictive value of criteria for p53 germline mutation screening
-
Chompret A, Abel A, Stoppa-Lyonnet D, et al: Sensitivity and predictive value of criteria for p53 germline mutation screening. J Med Genet 38:43-47, 2001
-
(2001)
J Med Genet
, vol.38
, pp. 43-47
-
-
Chompret, A.1
Abel, A.2
Stoppa-Lyonnet, D.3
-
18
-
-
12844262940
-
Development of a fluorescent multiplex assay for detection of MSI-high tumors
-
Bacher JW, Flanagan LA, Smalley RL, et al: Development of a fluorescent multiplex assay for detection of MSI-high tumors. Dis Markers 20:237-250, 2004
-
(2004)
Dis Markers
, vol.20
, pp. 237-250
-
-
Bacher, J.W.1
Flanagan, L.A.2
Smalley, R.L.3
-
19
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Aaltonen LA, Peltomäki P, Leach FS, et al: Clues to the pathogenesis of familial colorectal cancer. Science 260:812-816, 1993
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Leach, F.S.3
-
20
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov Y, Peinado MA, Malkhosyan S, et al: Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 363:558-561, 1993
-
(1993)
Nature
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
-
21
-
-
0027314411
-
Microsatellite instability in cancer of the proximal colon
-
Thibodeau SN, Bren G, Schaid D: Microsatellite instability in cancer of the proximal colon. Science 260:816-819, 1993
-
(1993)
Science
, vol.260
, pp. 816-819
-
-
Thibodeau, S.N.1
Bren, G.2
Schaid, D.3
-
22
-
-
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 cancer
-
Boland CR, Thibodeau SN, Hamilton SR, 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 cancer. Cancer Res 58: 5248-5257, 1998
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
-
23
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al: Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96: 261-268, 2004
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
-
24
-
-
3142748325
-
Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation
-
Nakagawa H, Lockman JC, Frankel WL, et al: Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation. Cancer Res 64:4721-4727, 2004
-
(2004)
Cancer Res
, vol.64
, pp. 4721-4727
-
-
Nakagawa, H.1
Lockman, J.C.2
Frankel, W.L.3
-
25
-
-
84862530392
-
Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results
-
Beamer LC, Grant ML, Espenschied CR, et al: Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results. J Clin Oncol 30: 1058-1063, 2012
-
(2012)
J Clin Oncol
, vol.30
, pp. 1058-1063
-
-
Beamer, L.C.1
Grant, M.L.2
Espenschied, C.R.3
-
26
-
-
85023776034
-
-
National Comprehensive Cancer Network: National Comprehensive Cancer Network Web site
-
National Comprehensive Cancer Network: National Comprehensive Cancer Network Web site. http://www.nccn.org
-
-
-
-
27
-
-
33749066191
-
Prediction of germline mutations and cancer risk in the Lynch syndrome
-
Chen S, Wang W, Lee S, et al: Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 296:1479-1487, 2006
-
(2006)
JAMA
, vol.296
, pp. 1479-1487
-
-
Chen, S.1
Wang, W.2
Lee, S.3
-
28
-
-
33747871345
-
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
-
Hampel H, Frankel W, Panescu J, et al: Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 66:7810-7817, 2006
-
(2006)
Cancer Res
, vol.66
, pp. 7810-7817
-
-
Hampel, H.1
Frankel, W.2
Panescu, J.3
-
29
-
-
17944362664
-
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
-
Hampel H, Frankel WL, Martin E, et al: Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 352: 1851-1860, 2005
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
30
-
-
84867499525
-
Identification of Lynch syndrome among patients with colorectal cancer
-
Moreira L, Balaguer F, Lindor N, et al: Identification of Lynch syndrome among patients with colorectal cancer. JAMA 308:1555-1565, 2012
-
(2012)
JAMA
, vol.308
, pp. 1555-1565
-
-
Moreira, L.1
Balaguer, F.2
Lindor, N.3
-
31
-
-
59849108362
-
Recommendations from the EGAPP Working Group: Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives
-
Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group: Recommendations from the EGAPP Working Group: Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. Genet Med 11:35-41, 2009
-
(2009)
Genet Med
, vol.11
, pp. 35-41
-
-
-
32
-
-
61449320520
-
Endometrial cancer and Lynch syndrome: Clinical and pathologic considerations
-
Meyer LA, Broaddus RR, Lu KH: Endometrial cancer and Lynch syndrome: Clinical and pathologic considerations. Cancer Control 16:14-22, 2009
-
(2009)
Cancer Control
, vol.16
, pp. 14-22
-
-
Meyer, L.A.1
Broaddus, R.R.2
Lu, K.H.3
-
33
-
-
0013878809
-
Hereditary factors in cancer: Study of two large Midwestern kindreds
-
Lynch HT, Shaw MW, Magnuson CW, et al: Hereditary factors in cancer: Study of two large Midwestern kindreds. Arch Intern Med 117:206-212, 1966
-
(1966)
Arch Intern Med
, vol.117
, pp. 206-212
-
-
Lynch, H.T.1
Shaw, M.W.2
Magnuson, C.W.3
-
34
-
-
0034526111
-
Adrenocortical adenocarcinoma in an MSH2 carrier: Coincidence or causal relation?
-
Berends MJ, Cats A, Hollema H, et al: Adrenocortical adenocarcinoma in an MSH2 carrier: Coincidence or causal relation? Hum Pathol 31:1522-1527, 2000
-
(2000)
Hum Pathol
, vol.31
, pp. 1522-1527
-
-
Berends, M.J.1
Cats, A.2
Hollema, H.3
-
35
-
-
84866500834
-
Unusual DNA mismatch repair-deficient tumors in Lynch syndrome: A report of new cases and review of the literature
-
Karamurzin Y, Zeng Z, Stadler ZK, et al: Unusual DNA mismatch repair-deficient tumors in Lynch syndrome: A report of new cases and review of the literature. Hum Pathol, 2012
-
(2012)
Hum Pathol
-
-
Karamurzin, Y.1
Zeng, Z.2
Stadler, Z.K.3
-
36
-
-
79958081637
-
Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome
-
Medina-Arana V, Delgado L, González L, et al: Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome. Fam Cancer 10:265-271, 2011
-
(2011)
Fam Cancer
, vol.10
, pp. 265-271
-
-
Medina-Arana, V.1
Delgado, L.2
González, L.3
-
37
-
-
3342984883
-
Unusual tumors associated with the hereditary nonpolyposis colorectal cancer syndrome
-
Broaddus RR, Lynch PM, Lu KH, et al: Unusual tumors associated with the hereditary nonpolyposis colorectal cancer syndrome. Mod Pathol 17: 981-989, 2004
-
(2004)
Mod Pathol
, vol.17
, pp. 981-989
-
-
Broaddus, R.R.1
Lynch, P.M.2
Lu, K.H.3
-
38
-
-
84866604260
-
MSH6 mutations are frequent in hereditary nonpolyposis colorectal cancer families with normal pMSH6 expression as detected by immunohistochemistry
-
Okkels H, Lindorff-Larsen K, Thorlasius-Ussing O, et al: MSH6 mutations are frequent in hereditary nonpolyposis colorectal cancer families with normal pMSH6 expression as detected by immunohistochemistry. Appl Immunohistochem Mol Morphol 20:470-477, 2012
-
(2012)
Appl Immunohistochem Mol Morphol
, vol.20
, pp. 470-477
-
-
Okkels, H.1
Lindorff-Larsen, K.2
Thorlasius-Ussing, O.3
-
39
-
-
3242670404
-
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6mutations: Impact on counseling and surveillance
-
Hendriks YM, Wagner A, Morreau H, et al: Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6mutations: Impact on counseling and surveillance. Gastroenterology 127:17-25, 2004
-
(2004)
Gastroenterology
, vol.127
, pp. 17-25
-
-
Hendriks, Y.M.1
Wagner, A.2
Morreau, H.3
-
40
-
-
84863609627
-
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline
-
Weissman SM, Burt R, Church J, et al: Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline. J Genet Couns 21:484-493, 2012
-
(2012)
J Genet Couns
, vol.21
, pp. 484-493
-
-
Weissman, S.M.1
Burt, R.2
Church, J.3
-
41
-
-
85023758758
-
Mismatch repair protein deficiency is common in sebaceous neoplasms and suggests the importance of screening for lynch syndrome
-
Plocharczyk EF, Frankel WL, Hampel H, et al: Mismatch repair protein deficiency is common in sebaceous neoplasms and suggests the importance of screening for lynch syndrome. Am J Dermatopathol, 2012
-
(2012)
Am J Dermatopathol
-
-
Plocharczyk, E.F.1
Frankel, W.L.2
Hampel, H.3
|