-
1
-
-
84857369126
-
-
American Cancer Society. Atlanta, GA: American Cancer Society. Accessed May 25, 2011
-
American Cancer Society. Breast Cancer Overview. Atlanta, GA: American Cancer Society; 2011. Available at:. Accessed May 25, 2011.
-
(2011)
Breast Cancer Overview
-
-
-
2
-
-
36448996703
-
Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations
-
DOI 10.1038/nrc2054, PII NRC2054
-
Fackenthal JD, Olopade OI,. Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations. Nat Rev Cancer. 2007; 7: 937-948. (Pubitemid 350165853)
-
(2007)
Nature Reviews Cancer
, vol.7
, Issue.12
, pp. 937-948
-
-
Fackenthal, J.D.1
Olopade, O.I.2
-
3
-
-
52949096470
-
Genetic predisposition to breast cancer: Past, present, and future
-
Turnbull C, Rahman N,. Genetic predisposition to breast cancer: past, present, and future. Annu Rev Genomics Hum Genet. 2008; 9: 321-345.
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 321-345
-
-
Turnbull, C.1
Rahman, N.2
-
4
-
-
77957329128
-
PALB2/FANCN: Recombining cancer and Fanconi anemia
-
Tischkowitz M, Xia B,. PALB2/FANCN: recombining cancer and Fanconi anemia. Cancer Res. 2010; 70: 7353-7359.
-
(2010)
Cancer Res
, vol.70
, pp. 7353-7359
-
-
Tischkowitz, M.1
Xia, B.2
-
5
-
-
77952600845
-
Susceptibility pathways in Fanconi's anemia and breast cancer
-
D'Andrea AD,. Susceptibility pathways in Fanconi's anemia and breast cancer. N Engl J Med. 2010; 362: 1909-1919.
-
(2010)
N Engl J Med
, vol.362
, pp. 1909-1919
-
-
D'Andrea, A.D.1
-
6
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
DOI 10.1038/ng1947, PII NG1947
-
Reid S, Schindler D, Hanenberg H, et al. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet. 2007; 39: 162-164. (Pubitemid 46184345)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
Neveling, K.7
Kelly, P.8
Seal, S.9
Freund, M.10
Wurm, M.11
Batish, S.D.12
Lach, F.P.13
Yetgin, S.14
Neitzel, H.15
Ariffin, H.16
Tischkowitz, M.17
Mathew, C.G.18
Auerbach, A.D.19
Rahman, N.20
more..
-
7
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
DOI 10.1038/ng1942, PII NG1942
-
Xia B, Dorsman JC, Ameziane N, et al. Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet. 2007; 39: 159-161. (Pubitemid 46184344)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
De Vries, Y.4
Rooimans, M.A.5
Sheng, Q.6
Pals, G.7
Errami, A.8
Gluckman, E.9
Llera, J.10
Wang, W.11
Livingston, D.M.12
Joenje, H.13
De Winter, J.P.14
-
8
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
DOI 10.1038/ng1959, PII NG1959
-
Rahman N, Seal S, Thompson D, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet. 2007; 39: 165-167. (Pubitemid 46184346)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
9
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
DOI 10.1038/nature05609, PII NATURE05609
-
Erkko H, Xia B, Nikkila J, et al. A recurrent mutation in PALB2 in Finnish cancer families. Nature. 2007; 446: 316-319. (Pubitemid 46426155)
-
(2007)
Nature
, vol.446
, Issue.7133
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
Schleutker, J.4
Syrjakoski, K.5
Mannermaa, A.6
Kallioniemi, A.7
Pylkas, K.8
Karppinen, S.-M.9
Rapakko, K.10
Miron, A.11
Sheng, Q.12
Li, G.13
Mattila, H.14
Bell, D.W.15
Haber, D.A.16
Grip, M.17
Reiman, M.18
Jukkola-Vuorinen, A.19
Mustonen, A.20
Kere, J.21
Aaltonen, L.A.22
Kosma, V.-M.23
Kataja, V.24
Soini, Y.25
Drapkin, R.I.26
Livingston, D.M.27
Winqvist, R.28
more..
-
10
-
-
34249857115
-
Analysis of PALB2/FANCN-associated breast cancer families
-
DOI 10.1073/pnas.0701724104
-
Tischkowitz M, Xia B, Sabbaghian N, et al. Analysis of PALB2/FANCN-associated breast cancer families. Proc Natl Acad Sci U S A. 2007; 104: 6788-6793. (Pubitemid 47175579)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.16
, pp. 6788-6793
-
-
Tischkowitz, M.1
Xia, B.2
Sabbaghian, N.3
Reis-Filho, J.S.4
Hamel, N.5
Li, G.6
Van Beers, E.H.7
Li, L.8
Khalil, T.9
Quenneville, L.A.10
Omeroglu, A.11
Poll, A.12
Lepage, P.13
Wong, N.14
Nederlof, P.M.15
Ashworth, A.16
Tonin, P.N.17
Narod, S.A.18
Livingston, D.M.19
Foulkes, W.D.20
more..
-
11
-
-
40349111045
-
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early onset breast cancer in French-Canadian women [serial online]
-
Foulkes WD, Ghadirian P, Akbari MR, et al. Identification of a novel truncating PALB2 mutation and analysis of its contribution to early onset breast cancer in French-Canadian women [serial online]. Breast Cancer Res. 2007; 9: R83.
-
(2007)
Breast Cancer Res
, vol.9
-
-
Foulkes, W.D.1
Ghadirian, P.2
Akbari, M.R.3
-
12
-
-
58549086980
-
Analysis of FANCB and FANCN/PALB2 Fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families
-
Garcia MJ, Fernandez V, Osorio A, et al. Analysis of FANCB and FANCN/PALB2 Fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families. Breast Cancer Res Treat. 2009; 113: 545-551.
-
(2009)
Breast Cancer Res Treat
, vol.113
, pp. 545-551
-
-
Garcia, M.J.1
Fernandez, V.2
Osorio, A.3
-
13
-
-
61449204036
-
The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives
-
Cao AY, Huang J, Hu Z, et al. The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives. Breast Cancer Res Treat. 2009; 114: 457-462.
-
(2009)
Breast Cancer Res Treat
, vol.114
, pp. 457-462
-
-
Cao, A.Y.1
Huang, J.2
Hu, Z.3
-
14
-
-
70449523582
-
PALB2 sequence variants in young South African breast cancer patients
-
Sluiter M, Mew S, van Rensburg EJ,. PALB2 sequence variants in young South African breast cancer patients. Fam Cancer. 2009; 8: 347-353.
-
(2009)
Fam Cancer
, vol.8
, pp. 347-353
-
-
Sluiter, M.1
Mew, S.2
Van Rensburg, E.J.3
-
15
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
Heikkinen T, Karkkainen H, Aaltonen K, et al. The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res. 2009; 15: 3214-3222.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 3214-3222
-
-
Heikkinen, T.1
Karkkainen, H.2
Aaltonen, K.3
-
16
-
-
77955053607
-
A PALB2 germline mutation associated with hereditary breast cancer in Italy
-
Papi L, Putignano AL, Congregati C, et al. A PALB2 germline mutation associated with hereditary breast cancer in Italy. Fam Cancer. 2010; 9: 181-185.
-
(2010)
Fam Cancer
, vol.9
, pp. 181-185
-
-
Papi, L.1
Putignano, A.L.2
Congregati, C.3
-
17
-
-
77649148280
-
A novel germline PALB2 deletion in Polish breast and ovarian cancer patients [serial online]
-
Dansonka-Mieszkowska A, Kluska A, Moes J, et al. A novel germline PALB2 deletion in Polish breast and ovarian cancer patients [serial online]. BMC Med Genet. 2010; 11: 20.
-
(2010)
BMC Med Genet
, vol.11
, pp. 20
-
-
Dansonka-Mieszkowska, A.1
Kluska, A.2
Moes, J.3
-
18
-
-
79958211506
-
PALB2 analysis in BRCA2-like families
-
Adank MA, van Mil SE, Gille JJ, Waisfisz Q, Meijers- Heijboer H,. PALB2 analysis in BRCA2-like families. Breast Cancer Res Treat. 2011; 127: 357-362.
-
(2011)
Breast Cancer Res Treat
, vol.127
, pp. 357-362
-
-
Adank, M.A.1
Van Mil, S.E.2
Gille, J.J.3
Waisfisz, Q.4
Meijers- Heijboer, H.5
-
19
-
-
78650201265
-
PALB2: A novel inactivating mutation in a Italian breast cancer family
-
Balia C, Sensi E, Lombardi G, Roncella M, Bevilacqua G, Caligo MA,. PALB2: a novel inactivating mutation in a Italian breast cancer family. Fam Cancer. 2010; 9: 531-536.
-
(2010)
Fam Cancer
, vol.9
, pp. 531-536
-
-
Balia, C.1
Sensi, E.2
Lombardi, G.3
Roncella, M.4
Bevilacqua, G.5
Caligo, M.A.6
-
20
-
-
79958732548
-
PALB2 mutations in German and Russian patients with bilateral breast cancer
-
Bogdanova N, Sokolenko AP, Iyevleva AG, et al. PALB2 mutations in German and Russian patients with bilateral breast cancer. Breast Cancer Res Treat. 2011; 126: 545-550.
-
(2011)
Breast Cancer Res Treat.
, vol.126
, pp. 545-550
-
-
Bogdanova, N.1
Sokolenko, A.P.2
Iyevleva, A.G.3
-
21
-
-
78650389153
-
A PALB2 mutation associated with high risk of breast cancer [serial online]
-
Southey MC, Teo ZL, Dowty JG, et al. A PALB2 mutation associated with high risk of breast cancer [serial online]. Breast Cancer Res. 2010; 12: R109.
-
(2010)
Breast Cancer Res
, vol.12
-
-
Southey, M.C.1
Teo, Z.L.2
Dowty, J.G.3
-
22
-
-
79958709462
-
PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer
-
Peterlongo P, Catucci I, Pasquini G, et al. PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer. Breast Cancer Res Treat. 2011; 126: 825-828.
-
(2011)
Breast Cancer Res Treat
, vol.126
, pp. 825-828
-
-
Peterlongo, P.1
Catucci, I.2
Pasquini, G.3
-
23
-
-
79952741549
-
Contribution to familial breast cancer of inherited mutations in the BRCA2-interacting protein PALB2
-
Casadei S, Norquist BM, Walsh T, et al. Contribution to familial breast cancer of inherited mutations in the BRCA2-interacting protein PALB2. Cancer Res. 2011; 71: 2222-2229.
-
(2011)
Cancer Res
, vol.71
, pp. 2222-2229
-
-
Casadei, S.1
Norquist, B.M.2
Walsh, T.3
-
24
-
-
79958123341
-
PALB2 mutations in familial breast and pancreatic cancer
-
Hofstatter EW, Domchek SM, Miron A, et al. PALB2 mutations in familial breast and pancreatic cancer. Fam Cancer. 2011; 10: 225-231.
-
(2011)
Fam Cancer
, vol.10
, pp. 225-231
-
-
Hofstatter, E.W.1
Domchek, S.M.2
Miron, A.3
-
25
-
-
84857374078
-
Occurrence of germline PALB2 mutations in ovarian cancer [abstract]
-
October 23-27, San Diego, Calif. Abstract A404/F. Accessed April 10, 2010
-
Erkko H, Nikkila J, Butzow R, et al. Occurrence of germline PALB2 mutations in ovarian cancer [abstract]. Proceedings of the 57th Annual Meeting of the American Society of Human Genetics; October 23-27, 2007; San Diego, Calif. Abstract A404/F. Available at:. Accessed April 10, 2010.
-
(2007)
Proceedings of the 57th Annual Meeting of the American Society of Human Genetics
-
-
Erkko, H.1
Nikkila, J.2
Butzow, R.3
-
26
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene [serial online]
-
Jones S, Hruban RH, Kamiyama M, et al. Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene [serial online]. Science. 2009; 324: 217.
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
-
27
-
-
69349092943
-
Analysis of the gene coding for the BRCA2-interacting protein PALB2 in familial and sporadic pancreatic cancer
-
Tischkowitz MD, Sabbaghian N, Hamel N, et al. Analysis of the gene coding for the BRCA2-interacting protein PALB2 in familial and sporadic pancreatic cancer. Gastroenterology. 2009; 137: 1183-1186.
-
(2009)
Gastroenterology.
, vol.137
, pp. 1183-1186
-
-
Tischkowitz, M.D.1
Sabbaghian, N.2
Hamel, N.3
-
28
-
-
77957333720
-
PALB2 mutations in European familial pancreatic cancer families
-
Slater EP, Langer P, Niemczyk E, et al. PALB2 mutations in European familial pancreatic cancer families. Clin Genet. 2010; 78: 490-494.
-
(2010)
Clin Genet
, vol.78
, pp. 490-494
-
-
Slater, E.P.1
Langer, P.2
Niemczyk, E.3
-
29
-
-
74849119957
-
PALB2 variants in hereditary and unselected Finnish prostate cancer cases [serial online]
-
Pakkanen S, Wahlfors T, Siltanen S, et al. PALB2 variants in hereditary and unselected Finnish prostate cancer cases [serial online]. J Negat Results Biomed. 2009; 8: 12.
-
(2009)
J Negat Results Biomed
, vol.8
, pp. 12
-
-
Pakkanen, S.1
Wahlfors, T.2
Siltanen, S.3
-
30
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Krawetz S., Misener S., Totowa, NJ: Humana Press
-
Rozen S, Skaletsky HJ,. Primer3 on the WWW for general users and for biologist programmers. In:, Krawetz S, Misener S, eds. Bioinformatics Methods and Protocols: Methods in Molecular Biology. Totowa, NJ: Humana Press; 2000: 365-386.
-
(2000)
Bioinformatics Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.J.2
-
31
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
DOI 10.1101/gr.176601
-
Ng PC, Henikoff S,. Predicting deleterious amino acid substitutions. Genome Res. 2001; 11: 863-874. (Pubitemid 32447869)
-
(2001)
Genome Research
, vol.11
, Issue.5
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
32
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky V, Bork P, Sunyaev S,. Human non-synonymous SNPs: server and survey. Nucleic Acids Res. 2002; 30: 3894-3900. (Pubitemid 35012462)
-
(2002)
Nucleic Acids Research
, vol.30
, Issue.17
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
33
-
-
25144496606
-
PMUT: A web-based tool for the annotation of pathological mutations on proteins
-
DOI 10.1093/bioinformatics/bti486
-
Ferrer-Costa C, Gelpi JL, Zamakola L, Parraga I, de la Cruz X, Orozco M,. PMUT: a web-based tool for the annotation of pathological mutations on proteins. Bioinformatics. 2005; 21: 3176-3178. (Pubitemid 41418475)
-
(2005)
Bioinformatics
, vol.21
, Issue.14
, pp. 3176-3178
-
-
Ferrer-Costa, C.1
Gelpi, J.L.2
Zamakola, L.3
Parraga, I.4
De La Cruz, X.5
Orozco, M.6
-
34
-
-
0141742293
-
PANTHER: A library of protein families and subfamilies indexed by function
-
DOI 10.1101/gr.772403
-
Thomas PD, Campbell MJ, Kejariwal A, et al. PANTHER: a library of protein families and subfamilies indexed by function. Genome Res. 2003; 13: 2129-2141. (Pubitemid 37161770)
-
(2003)
Genome Research
, vol.13
, Issue.9
, pp. 2129-2141
-
-
Thomas, P.D.1
Campbell, M.J.2
Kejariwal, A.3
Mi, H.4
Karlak, B.5
Daverman, R.6
Diemer, K.7
Muruganujan, A.8
Narechania, A.9
-
35
-
-
33644537810
-
Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of 8 recurrent substitutions as neutral
-
Tavtigian SV, Deffenbaugh AM, Yin L, et al. Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of 8 recurrent substitutions as neutral. J Med Genet. 2006; 43: 295-305.
-
(2006)
J Med Genet
, vol.43
, pp. 295-305
-
-
Tavtigian, S.V.1
Deffenbaugh, A.M.2
Yin, L.3
-
36
-
-
0034623005
-
T-Coffee: A novel method for fast and accurate multiple sequence alignment
-
Notredame C, Higgins DG, Heringa J,. T-Coffee: a novel method for fast and accurate multiple sequence alignment. J Mol Biol. 2000; 302: 205-217.
-
(2000)
J Mol Biol
, vol.302
, pp. 205-217
-
-
Notredame, C.1
Higgins, D.G.2
Heringa, J.3
-
37
-
-
18444402182
-
The Ensembl genome database project
-
Hubbard T, Barker D, Birney E, et al. The ENSEMBL genome database project. Nucleic Acids Res. 2002; 30: 38-41. (Pubitemid 34679498)
-
(2002)
Nucleic Acids Research
, vol.30
, Issue.1
, pp. 38-41
-
-
Hubbard, T.1
Barker, D.2
Birney, E.3
Cameron, G.4
Chen, Y.5
Clark, L.6
Cox, T.7
Cuff, J.8
Curwen, V.9
Down, T.10
Durbin, R.11
Eyras, E.12
Gilbert, J.13
Hammond, M.14
Huminiecki, L.15
Kasprzyk, A.16
Lehvaslaiho, H.17
Lijnzaad, P.18
Melsopp, C.19
Mongin, E.20
Pettett, R.21
Pocock, M.22
Potter, S.23
Rust, A.24
Schmidt, E.25
Searle, S.26
Slater, G.27
Smith, J.28
Spooner, W.29
Stabenau, A.30
Stalker, J.31
Stupka, E.32
Ureta-Vidal, A.33
Vastrik, I.34
Clamp, M.35
more..
-
38
-
-
0033987736
-
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
-
DOI 10.1002/(SICI)1098-1004(200001)15:1<7::AID-HUMU4>3.0.CO;2-N
-
den Dunnen JT, Antonarakis SE,. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000; 15: 7-12. (Pubitemid 30036162)
-
(2000)
Human Mutation
, vol.15
, Issue.1
, pp. 7-12
-
-
Den Dunnen, J.T.1
Antonarakis, S.E.2
-
39
-
-
38149063754
-
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker
-
Wildeman M, van Ophuizen E, den Dunnen JT, Taschner PE,. Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker. Hum Mutat. 2008; 29: 6-13.
-
(2008)
Hum Mutat
, vol.29
, pp. 6-13
-
-
Wildeman, M.1
Van Ophuizen, E.2
Den Dunnen, J.T.3
Taschner, P.E.4
-
40
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry ST, Ward MH, Kholodov M, et al. dbSNP: the NCBI database of genetic variation. Nucleic Acids Res. 2001; 29: 308-311. (Pubitemid 32054478)
-
(2001)
Nucleic Acids Research
, vol.29
, Issue.1
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.-H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
Sirotkin, K.7
-
41
-
-
79958282990
-
BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer
-
Wong MW, Nordfors C, Mossman D, et al. BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer. Breast Cancer Res Treat. 2011; 127: 853-859.
-
(2011)
Breast Cancer Res Treat
, vol.127
, pp. 853-859
-
-
Wong, M.W.1
Nordfors, C.2
Mossman, D.3
-
42
-
-
79151476244
-
Germline mutations in PALB2 in African American breast cancer cases
-
Ding YC, Steele L, Chu LH, et al. Germline mutations in PALB2 in African American breast cancer cases. Breast Cancer Res Treat. 2011; 126: 227-230.
-
(2011)
Breast Cancer Res Treat
, vol.126
, pp. 227-230
-
-
Ding, Y.C.1
Steele, L.2
Chu, L.H.3
-
43
-
-
69249088889
-
MRG15 is a novel PALB2-interacting factor involved in homologous recombination
-
Sy SM, Huen MS, Chen J,. MRG15 is a novel PALB2-interacting factor involved in homologous recombination. J Biol Chem. 2009; 284: 21127-21131.
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(2009)
J Biol Chem
, vol.284
, pp. 21127-21131
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Sy, S.M.1
Huen, M.S.2
Chen, J.3
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