-
2
-
-
0032730774
-
Genetic susceptibility to non-polyposis colorectal cancer
-
Lynch HT, de la Chapelle A. Genetic susceptibility to non-polyposis colorectal cancer. J Med Genet 1999; 36(11): 801-818.
-
(1999)
J Med Genet
, vol.36
, Issue.11
, pp. 801-818
-
-
Lynch, H.T.1
De La Chapelle, A.2
-
3
-
-
0034330224
-
Lynch syndrome: Genetics, natural history, genetic counseling, and prevention
-
Lynch HT, Lynch J. Lynch syndrome: genetics, natural history, genetic counseling, and prevention. J Clin Oncol 2000;18(Suppl):19S-31S.
-
(2000)
J Clin Oncol
, vol.18
, Issue.SUPPL.
-
-
Lynch, H.T.1
Lynch, J.2
-
4
-
-
0027248156
-
Genetics, natural history, tumor spectrum and patology of hereditary non-polyposis colorectal cancer: An updated review
-
Lynch HT, Smyrk TC, Watson P et al. Genetics, natural history, tumor spectrum and patology of hereditary non-polyposis colorectal cancer: an updated review. Gastroenterology 1993; 104:1535-1549.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
-
5
-
-
0037422027
-
Hereditary colorectal cancer
-
Lynch HT, Chapelle A. Hereditary colorectal cancer. N Eng J Med 2003; 348(10): 919-932.
-
(2003)
N Eng J Med
, vol.348
, Issue.10
, pp. 919-932
-
-
Lynch, H.T.1
Chapelle, A.2
-
6
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene
-
Miki Y, Swensen J, Shattuck-Eldens D et al. A strong candidate for the breast and ovarian cancer susceptibility gene. Science 1994; 266(5182): 66-71.
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eldens, D.3
-
7
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J et al. Identification of the breast cancer susceptibility gene BRCA2. Nature 1995; 378(6559): 789-792.
-
(1995)
Nature
, vol.378
, Issue.6559
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
-
8
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarkoma
-
Friend SH, Bernards R, Rogelj S. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarkoma. Nature 1986; 323(6089): 643-646.
-
(1986)
Nature
, vol.323
, Issue.6089
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
-
9
-
-
0026254581
-
Testing for germline p53 mutations in cancer families
-
Li FP, Correa P, Fraumeni JF jr. Testing for germline p53 mutations in cancer families. Cancer Epidemiol Biomark Prev 1991; 1:91-94.
-
(1991)
Cancer Epidemiol Biomark Prev
, vol.1
, pp. 91-94
-
-
Li, F.P.1
Correa, P.2
-
10
-
-
0025648762
-
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
-
Srivastava S, Zou Z, Pirrollo K et al. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 1990; 348(6303): 747-749.
-
(1990)
Nature
, vol.348
, Issue.6303
, pp. 747-749
-
-
Srivastava, S.1
Zou, Z.2
Pirrollo, K.3
-
11
-
-
33751027938
-
Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology
-
Goetz P, Foretova L, Puchmajerova A. Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology. Klin Onkol 2006; 19 (Suppl)-44-48
-
(2006)
Klin Onkol
, vol.19
, pp. 44-48
-
-
Goetz, P.1
Foretova, L.2
Puchmajerova, A.3
-
12
-
-
13744263782
-
Hereditary cancer predisposition syndromes
-
Garber JE, Offit K. Hereditary cancer predisposition syndromes. J Clin Oncol 2005; 23(2): 276-292
-
(2005)
J Clin Oncol
, vol.23
, Issue.2
, pp. 276-292
-
-
Garber, J.E.1
Offit, K.2
-
13
-
-
33645745489
-
Genetic and preventive services for hereditary breast and ovarian cancer in the Czech Republic
-
Foretová L, Petráková K, Palácová M et al. Genetic and preventive services for hereditary breast and ovarian cancer in the Czech Republic. Hereditary Cancer in Clinical Practice 2006; 4(1): 3-6.
-
(2006)
Hereditary Cancer in Clinical Practice
, vol.4
, Issue.1
, pp. 3-6
-
-
Foretová, L.1
Petráková, K.2
Palácová, M.3
-
14
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
Ford D, Easton DF, Stratton M et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 1998; 62(3): 676-689.
-
(1998)
Am J Hum Genet
, vol.62
, Issue.3
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
15
-
-
77952981208
-
Hereditary breast and ovarian cancer (HBOC): Clinical features and Counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li.-Fraumeni
-
Shulman LP. Hereditary breast and ovarian cancer (HBOC): Clinical features and Counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li.-Fraumeni. Obstet Gynecol Clin N Am 2010; 37(1): 109-133.
-
Obstet Gynecol Clin N Am 2010
, vol.37
, Issue.1
, pp. 109-133
-
-
Shulman, L.P.1
-
16
-
-
77951206427
-
Triple-negative breast cancer: Molecular features, pathogenesis, treatment and current lines of research
-
Bosch A, Eroles P, Zaragoza R et al. Triple-negative breast cancer: Molecular features, pathogenesis, treatment and current lines of research. Cancer Treatment Reviews 2010; 36(3): 206-215.
-
(2010)
Cancer Treatment Reviews
, vol.36
, Issue.3
, pp. 206-215
-
-
Bosch, A.1
Eroles, P.2
Zaragoza, R.3
-
17
-
-
68149163711
-
Triple-negative breast cancers are increased in black women regardless of age or body mass index
-
Stead LA, Lash TL, Sobieraj JE et al Triple-negative breast cancers are increased in black women regardless of age or body mass index. Breast Cancer Research 2009; 11:R18.
-
(2009)
Breast Cancer Research
, vol.11
-
-
Stead, L.A.1
Lash, T.L.2
Sobieraj, J.E.3
-
20
-
-
0038036629
-
The recommendation of clinical care for patients with breast and ovarian cancer and for healthy people with germline mutations in BRCA and BRCA2 genes
-
Bartoňková H, Foretová L, Helmichová E et al. The recommendation of clinical care for patients with breast and ovarian cancer and for healthy people with germline mutations In BRCA] and BRCA2 genes. KIm Onkol 2003; 16(1): 28-34.
-
(2003)
KIm Onkol
, vol.16
, Issue.1
, pp. 28-34
-
-
Bartoňková, H.1
Foretová, L.2
Helmichová, E.3
-
21
-
-
78650642385
-
Syndrom hereditárního karcinomu prsu a ovarií
-
Plevová P, Novotný J, Petráková K et al. Syndrom hereditárního karcinomu prsu a ovarií. Klin Onkol 2009 (Suppl S1):S6-S11.
-
(2009)
Klin Onkol
, Issue.SUPPL. S1
-
-
Plevová, P.1
Novotný, J.2
Petráková, K.3
-
22
-
-
77954654101
-
Population based study of BRCA 1/2 mutations: Family history based criteria identify minority of mutation carriers
-
Mateju J, Stribrna M, Zikan M et al. Population based study of BRCA 1/2 mutations: family history based criteria identify minority of mutation carriers. Neoplasma 2010; 57(3): 280-285.
-
(2010)
Neoplasma
, vol.57
, Issue.3
, pp. 280-285
-
-
Mateju, J.1
Stribrna, M.2
Zikan, M.3
-
23
-
-
8844220451
-
CHEK2 is a multiorgan cancer susceptibility gene
-
Cybulski C, Górskl T, Huzarski T et al. CHEK2 is a multiorgan cancer susceptibility gene. Am J Hum Genet 2004; 75(6):1131-1135.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.6
, pp. 1131-1135
-
-
Cybulski, C.1
Górskl, T.2
Huzarski, T.3
-
24
-
-
3042582651
-
CHEK2 1100delC and susceptibility to breast cancer. a collaborative analysis involving 10, 860 breast cancer cases and 9,065 controls from 10 studies
-
The CHEK2 Breast Cancer Case-Control Consortium
-
The CHEK2 Breast Cancer Case-Control Consortium. 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(6): 1175-1182.
-
(2004)
Am J Hum Genet
, vol.74
, Issue.6
, pp. 1175-1182
-
-
-
25
-
-
33645084562
-
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
-
Walsh T, Casadei S, Coats KH et al. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 In families at high risk of breast cancer. JAMA 2006; 295(12): 1379-1388.
-
(2006)
JAMA
, vol.295
, Issue.12
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.H.3
-
26
-
-
44949263899
-
Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer
-
Machackova E, Foretova L, Lukesova M et al. Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer. BMC Cancer 2008, 8(140): 12.
-
(2008)
BMC Cancer
, vol.8
, Issue.140
, pp. 12
-
-
Machackova, E.1
Foretova, L.2
Lukesova, M.3
-
27
-
-
66349115872
-
Diagnostic guidelines for High-Resolution Melting curve (HRM) analysis: A validation of BRCA1 mutation scanning using the 96-well LightScanner
-
Stoep N, Paridon Ch, Janssens T et al Diagnostic guidelines for High-Resolution Melting curve (HRM) analysis: A validation of BRCA1 mutation scanning using the 96-well LightScanner. Human Mutation 2009; 30(6): 899-909.
-
(2009)
Human Mutation
, vol.30
, Issue.6
, pp. 899-909
-
-
Stoep, N.1
Paridon, C.2
Janssens, T.3
-
28
-
-
2342516899
-
BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic
-
Foretova L, Machackova E, Navratilova M et al. BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic. Human Mutation 2004; 23(4): 397-398.
-
(2004)
Human Mutation
, vol.23
, Issue.4
, pp. 397-398
-
-
Foretova, L.1
Machackova, E.2
Navratilova, M.3
-
29
-
-
34347223992
-
High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic
-
Vasickova P, Machackova E, Lukesova M et al. High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic. BMC Med Genet 2007; 8:32.
-
(2007)
BMC Med Genet
, vol.8
, pp. 32
-
-
Vasickova, P.1
Machackova, E.2
Lukesova, M.3
-
30
-
-
48549084778
-
A syngeneic variance library for functional annotation of human variation: Application to BRCA2
-
Hucl T, Rago C, Gallmeier E et al. A syngeneic variance library for functional annotation of human variation: application to BRCA2. Cancer Res 2008; 68(13): 5023-5030.
-
(2008)
Cancer Res
, vol.68
, Issue.13
, pp. 5023-5030
-
-
Hucl, T.1
Rago, C.2
Gallmeier, E.3
-
31
-
-
20244378377
-
The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic
-
Kleibl Z, Novotny J, Bezdickova D et al. The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic. Breast Cancer Research and Treatment 2005; 90(2): 165-167.
-
(2005)
Breast Cancer Research and Treatment
, vol.90
, Issue.2
, pp. 165-167
-
-
Kleibl, Z.1
Novotny, J.2
Bezdickova, D.3
-
32
-
-
78650630880
-
Magnetic resonance of breast as a screening method in women with high risk of breast cancer
-
Schneiderova M, Belanova R, Lidakova J et al. Magnetic resonance of breast as a screening method In women with high risk of breast cancer. Educational Proceedings. BOD 2009:91-92.
-
(2009)
Educational Proceedings. BOD
, pp. 91-92
-
-
Schneiderova, M.1
Belanova, R.2
Lidakova, J.3
-
33
-
-
33751045766
-
Breast magnetic resonance imaging in surveillance of women at high risk for breast cancer
-
Schneiderova M, Bartonkova H. Breast magnetic resonance imaging in surveillance of women at high risk for breast cancer. Klin Onkol 2006; 19 (Suppl): 91-96.
-
(2006)
Klin Onkol
, vol.19
, Issue.SUPPL.
, pp. 91-96
-
-
Schneiderova, M.1
Bartonkova, H.2
-
34
-
-
71049170380
-
Penetrance estimated for BRCA1 and BRCA2 based on genetic testing in a clinical cancer genetics service setting: Risk of breast/ovarian cancer quoted should reflect the cancer burden in the family
-
Evans DG, Shenton A, Woodward E. Penetrance estimated for BRCA1 and BRCA2 based on genetic testing in a clinical cancer genetics service setting: Risk of breast/ovarian cancer quoted should reflect the cancer burden in the family. BMC Cancer 2008; 8:155.
-
(2008)
BMC Cancer
, vol.8
, pp. 155
-
-
Evans, D.G.1
Shenton, A.2
Woodward, E.3
-
35
-
-
0034236361
-
Prophylactic surgery for women at high risk for breast cancer
-
Blanchard DK, Hartmann LC. Prophylactic surgery for women at high risk for breast cancer. Clin Breast Cancer 2000; 1(2): 127-134.
-
(2000)
Clin Breast Cancer
, vol.1
, Issue.2
, pp. 127-134
-
-
Blanchard, D.K.1
Hartmann, L.C.2
-
36
-
-
0034017713
-
Prophylactic surgery in women with a hereditary predisposition to breast and ovarian cancer 2000
-
Eisen A Rebbeck TR, Wood WC et al. Prophylactic Surgery in Women With a Hereditary Predisposition to Breast and Ovarian Cancer 2000; J Clin Oncol 2000; 18(9): 1980-1995.
-
(2000)
J Clin Oncol
, vol.18
, Issue.9
, pp. 1980-1995
-
-
Rebbeck Tr, E.A.1
Wood, W.C.2
-
37
-
-
0033452876
-
Prophylactic mastectomy and inherited predisposition to breast carcinoma
-
Hughes KS, Papa MZ, Whitney T et al. Prophylactic mastectomy and inherited predisposition to breast carcinoma. Cancer Supplement 1999; 86:2502-2515.
-
(1999)
Cancer Supplement
, vol.86
, pp. 2502-2515
-
-
Hughes, K.S.1
Papa, M.Z.2
Whitney, T.3
-
38
-
-
0034631316
-
Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
-
Meijers-Heijboer EJ, Verhoog LC, Brekelmans CTM et al. Presymptomatic DNA testing and prophylactic surgery In families with a BRCA1 or BRCA2 mutation. Lancet 2000; 355(9220): 2015-2020.
-
(2000)
Lancet
, vol.355
, Issue.9220
, pp. 2015-2020
-
-
Meijers-Heijboer, E.J.1
Verhoog, L.C.2
Brekelmans, C.T.M.3
-
39
-
-
0035913275
-
Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation
-
Meijers-Heijboer H, van Geel B, van Putten WU et al. Breast cancer after prophylactic bilateral mastectomy In women with a BRCA1 or BRCA2 mutation. N Engl J Med 2001;345:159-163.
-
(2001)
N Engl J Med
, vol.345
, pp. 159-163
-
-
Meijers-Heijboer, H.1
Van Geel, B.2
Van Putten, W.U.3
-
40
-
-
33751048090
-
Prophylactic mastectomy and its Indications in high-risk women
-
Drazan L Prophylactic mastectomy and its Indications In high-risk women Klin Onkol 2006; 19 (Suppl): 97-100.
-
(2006)
Klin Onkol
, vol.19
, pp. 97-100
-
-
Drazan, L.1
-
41
-
-
68649097351
-
Oboustranná rekonstrukce prsů dvěma DIEP laloky: Jak ji hodnoti pacientky?
-
Dražan L, Hýža R Stupka I et al. Oboustranná rekonstrukce prsů dvěma DIEP laloky: Jak ji hodnoti pacientky? Praktický lékař 2009; 89(6): 306-311.
-
(2009)
Praktický Lékař
, vol.89
, Issue.6
, pp. 306-311
-
-
Dražan, L.1
Stupka I, H.R.2
-
42
-
-
0033166374
-
A practical approach to familial and hereditary colorectal cancer
-
Ivanovich JL, Reed TE, Ciske DJ et al. A practical approach to familial and hereditary colorectal cancer. Am J Med 1999; 107(1)-68-77.
-
(1999)
Am J Med
, vol.107
, Issue.1
, pp. 68-77
-
-
Ivanovich, J.L.1
Reed, T.E.2
Ciske, D.J.3
-
43
-
-
33751060446
-
Plevová R Diagnostika Lynchova syndromu - Nové geny a metody
-
Křepelová A, Pavlíková K, Plevová R Diagnostika Lynchova syndromu - nové geny a metody. Klin Onkol 2006; 19 (Suppl): 76-81.
-
(2006)
Klin Onkol
, vol.19
, Issue.SUPPL.
, pp. 76-81
-
-
Křepelová, A.1
Pavlíková, K.2
-
44
-
-
67650872601
-
Hereditární nepolypózní kolorektá lní karcinom (HNPCC, Lynchův syndrom)
-
Plevová P, Novotný J, Šachlová M et al. Hereditární nepolypózní kolorektální karcinom (HNPCC, Lynchův syndrom). Klin Onkol 2009; (Suppl S1): S12-S15.
-
(2009)
Klin Onkol
, Issue.SUPPL. S1
-
-
Plevová, P.1
Novotný, J.2
Šachlová, M.3
-
45
-
-
0032522623
-
Multiple primary cancers in familles with Li-Fraumenl syndrome
-
Hisada M, Garber JE, Fung CY et al. Multiple primary cancers in familles with Li-Fraumenl syndrome. J Natl Cancer Inst 1998; 90(8)- 606-611.
-
(1998)
J Natl Cancer Inst
, vol.90
, Issue.8
, pp. 606-611
-
-
Hisada, M.1
Garber, J.E.2
Fung, C.Y.3
-
47
-
-
33751053516
-
Kasuistiky Li-Fraumeni syndromu: Diagnostické a preventivní možnosti
-
Foretová L, Navrátilová M, Petrákova K. Kasuistiky Li-Fraumeni syndromu: diagnostické a preventivní možnosti. Klin Onkol 2006; 19 (Suppl): 85-87
-
(2006)
Klin Onkol
, vol.19
, Issue.SUPPL.
, pp. 85-87
-
-
Foretová, L.1
Navrátilová, M.2
Petrákova, K.3
-
49
-
-
67650921129
-
Syndrom familiárního melanomu (s dysplastickými naevy či bez nich)
-
Foretová L, Macháčková E, Šachlová M et al. Syndrom familiárního melanomu (s dysplastickými naevy či bez nich). Kim Onkol 2009; (Suppl S1): S32-S33.
-
(2009)
Kim Onkol
, Issue.SUPPL. S1
-
-
Foretová, L.1
Macháčková, E.2
Šachlová, M.3
-
53
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
Giardiello FM, Brenslnger JD, Tersmett AC et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000; 119(6): 1447-1453.
-
(2000)
Gastroenterology
, vol.119
, Issue.6
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brenslnger, J.D.2
Tersmett, A.C.3
-
55
-
-
77956412331
-
MUTYH-associated polyposls-variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations
-
Morak M, Laner A, Bacher U et al. MUTYH-associated polyposls-variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations. Clim Genet 2010; 78(4): 353-363.
-
(2010)
Clim Genet
, vol.78
, Issue.4
, pp. 353-363
-
-
Morak, M.1
Laner, A.2
Bacher, U.3
-
56
-
-
77956326790
-
Genome-wide association studies of cancer predisposition
-
Stadler ZK, Vijai J, Thom P et al Genome-wide association studies of cancer predisposition. Hematol Oncol Clin N Am 2010; 24:973-996.
-
(2010)
Hematol Oncol Clin N Am
, Issue.24
, pp. 973-996
-
-
Stadler, Z.K.1
Vijai, J.2
Thom, P.3
-
57
-
-
77956305912
-
Inherited predisposition to cancer. Introduction and overview
-
Robson M, Offit K. Inherited predisposition to cancer. Introduction and overview. Hematol Oncol Clin N Am 2010, 24(5):793-797.
-
(2010)
Hematol Oncol Clin N Am
, vol.24
, Issue.5
, pp. 793-797
-
-
Robson, M.1
Offit, K.2
-
58
-
-
67349222061
-
Breast cancer susceptibility: Current knowledge and implications for genetic counselling
-
Ripperger T, Gadzicki D, Meindl A et al. Breast cancer susceptibility: current knowledge and implications for genetic counselling Eur J Hum Genet 2009; 17(6): 722-731.
-
(2009)
Eur J Hum Genet
, vol.17
, Issue.6
, pp. 722-731
-
-
Ripperger, T.1
Gadzicki, D.2
Meindl, A.3
|