-
1
-
-
0037439356
-
Cancer in Fanconi anemia, 1927-2001
-
2
-
Alter BP (2003) Cancer in Fanconi anemia, 1927-2001. Cancer 97(2):425-440
-
(2003)
Cancer
, vol.97
, pp. 425-440
-
-
Alter, B.P.1
-
2
-
-
0142063079
-
Polygenic inheritance of breast cancer: Implications for design of association studies
-
Antoniou AC, Easton DF (2003) Polygenic inheritance of breast cancer: implications for design of association studies. Genet Epidemiol 25:190-202
-
(2003)
Genet Epidemiol
, vol.25
, pp. 190-202
-
-
Antoniou, A.C.1
Easton, D.F.2
-
3
-
-
33646815890
-
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families
-
INHERIT BRCAs Program Members. 1
-
Antoniou AC, Durocher F, Smith P, Simard J, Easton DF; INHERIT BRCAs Program Members (2006) BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families. Breast Cancer Res 8(1):R3
-
(2006)
Breast Cancer Res
, vol.8
, pp. 3
-
-
Antoniou, A.C.1
Durocher, F.2
Smith, P.3
Simard, J.4
Easton, D.F.5
-
4
-
-
0034848175
-
Breast cancer, Cowden disease and PTEN-MATCHS syndrome
-
6
-
Ball S, Arolker M, Purushotham AD (2001) Breast cancer, Cowden disease and PTEN-MATCHS syndrome. Eur J Surg Oncol 27(6):604-606
-
(2001)
Eur J Surg Oncol
, vol.27
, pp. 604-606
-
-
Ball, S.1
Arolker, M.2
Purushotham, A.D.3
-
5
-
-
24944434380
-
Functional promoter SNPs in cell cycle checkpoint genes
-
18
-
Belanger H, Beaulieu P, Moreau C, Labuda D, Hudson TJ, Sinnett D (2005) Functional promoter SNPs in cell cycle checkpoint genes. Hum Mol Genet 14(18):2641-2648
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2641-2648
-
-
Belanger, H.1
Beaulieu, P.2
Moreau, C.3
Labuda, D.4
Hudson, T.J.5
Sinnett, D.6
-
6
-
-
0032528315
-
Automated detection of point mutations using fluorescent sequence trace subtraction
-
14
-
Bonfield JK, Rada C, Staden R (1998) Automated detection of point mutations using fluorescent sequence trace subtraction. Nucleic Acids Res 26(14):3404-3409
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 3404-3409
-
-
Bonfield, J.K.1
Rada, C.2
Staden, R.3
-
7
-
-
0025275853
-
C-Ha-ras oncogene expression in immortalized human keratinocytes (HaCaT) alters growth potential in vivo but lacks correlation with malignancy
-
9
-
Boukamp P, Stanbridge EJ, Foo DY, Cerutti PA, Fusenig NE (1990) c-Ha-ras oncogene expression in immortalized human keratinocytes (HaCaT) alters growth potential in vivo but lacks correlation with malignancy. Cancer Res 50(9):2840-2847
-
(1990)
Cancer Res
, vol.50
, pp. 2840-2847
-
-
Boukamp, P.1
Stanbridge, E.J.2
Foo, D.Y.3
Cerutti, P.A.4
Fusenig, N.E.5
-
8
-
-
0023852747
-
Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line
-
3
-
Boukamp P, Petrussevska RT, Breitkreutz D, Hornung J, Markham A, Fusenig NE (1998) Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line. J Cell Biol 106(3):761-771
-
(1998)
J Cell Biol
, vol.106
, pp. 761-771
-
-
Boukamp, P.1
Petrussevska, R.T.2
Breitkreutz, D.3
Hornung, J.4
Markham, A.5
Fusenig, N.E.6
-
9
-
-
20644461718
-
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
-
1
-
Cantor SB, Bell DW, Ganesan S, Kass EM, Drapkin R, Grossman S, Wahrer DC, Sgroi DC, Lane WS, Haber DA, Livingston DM (2001) BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell 105(1):149-160
-
(2001)
Cell
, vol.105
, pp. 149-160
-
-
Cantor, S.B.1
Bell, D.W.2
Ganesan, S.3
Kass, E.M.4
Drapkin, R.5
Grossman, S.6
Wahrer, D.C.7
Sgroi, D.C.8
Lane, W.S.9
Haber, D.A.10
Livingston, D.M.11
-
10
-
-
1442281478
-
The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations
-
8
-
Cantor S, Drapkin R, Zhang F, Lin Y, Han J, Pamidi S, Livingston DM (2004) The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations. Proc Natl Acad Sci USA 101(8):2357-2362
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 2357-2362
-
-
Cantor, S.1
Drapkin, R.2
Zhang, F.3
Lin, Y.4
Han, J.5
Pamidi, S.6
Livingston, D.M.7
-
11
-
-
0042242582
-
ESEfinder: A web resource to identify exonic splicing enhancers
-
13
-
Cartegni L, Wang J, Zhu Z, Zhang MQ, Krainer AR (2003) ESEfinder: a web resource to identify exonic splicing enhancers. Nucleic Acids Res 31(13):3568-3571
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3568-3571
-
-
Cartegni, L.1
Wang, J.2
Zhu, Z.3
Zhang, M.Q.4
Krainer, A.R.5
-
12
-
-
21444443478
-
MatInspector and beyond: Promoter analysis based on transcription factor binding sites
-
13
-
Cartharius K, Frech K, Grote K, Klocke B, Haltmeier M, Klingenhoff A, Frisch M, Bayerlein M, Werner T (2005) MatInspector and beyond: promoter analysis based on transcription factor binding sites. Bioinformatics 21(13):2933-2942
-
(2005)
Bioinformatics
, vol.21
, pp. 2933-2942
-
-
Cartharius, K.1
Frech, K.2
Grote, K.3
Klocke, B.4
Haltmeier, M.5
Klingenhoff, A.6
Frisch, M.7
Bayerlein, M.8
Werner, T.9
-
13
-
-
3042582651
-
CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
-
CHEK2 Breast Cancer Case-Control Consortium. 6
-
CHEK2 Breast Cancer Case-Control Consortium (2004) 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 74(6):1175-1182
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1175-1182
-
-
-
14
-
-
0037028740
-
Dominant negative ATM mutations in breast cancer families
-
3
-
Chenevix-Trench G, Spurdle AB, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins MA, Scott C, Pupo GM, Dork T, Bendix R, Kirk J, Tucker K, McCredie MR, Hopper JL, Sambrook J, Mann GJ, Khanna KK (2002) Dominant negative ATM mutations in breast cancer families. J Natl Cancer Inst 94(3):205-215
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 205-215
-
-
Chenevix-Trench, G.1
Spurdle, A.B.2
Gatei, M.3
Kelly, H.4
Marsh, A.5
Chen, X.6
Donn, K.7
Cummings, M.8
Nyholt, D.9
Jenkins, M.A.10
Scott, C.11
Pupo, G.M.12
Dork, T.13
Bendix, R.14
Kirk, J.15
Tucker, K.16
McCredie, M.R.17
Hopper, J.L.18
Sambrook, J.19
Mann, G.J.20
Khanna, K.K.21
more..
-
15
-
-
0035960431
-
Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease
-
Collaborative Group on Hormonal Factors in Breast Cancer. 9291
-
Collaborative Group on Hormonal Factors in Breast Cancer (2001) Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease. Lancet 358(9291):1389-1399
-
(2001)
Lancet
, vol.358
, pp. 1389-1399
-
-
-
16
-
-
36749050267
-
Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non-BRCA1/2 French Canadian breast and ovarian cancer families
-
INHERIT BRCAs
-
Desjardins S, Belleau P, Labrie Y, Ouellette G, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Pichette R, Plante M, INHERIT BRCAs, Durocher F (2008) Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non-BRCA1/2 French Canadian breast and ovarian cancer families. Int J Cancer 122(1):108-116
-
(2008)
Int J Cancer
, vol.122
, Issue.1
, pp. 108-116
-
-
Desjardins, S.1
Belleau, P.2
Labrie, Y.3
Ouellette, G.4
Bessette, P.5
Chiquette, J.6
Laframboise, R.7
Lépine, J.8
Lespérance, B.9
Pichette, R.10
Plante, M.11
Durocher, F.12
-
17
-
-
0029150074
-
A comparison of linkage disequilibrium measures for fine-scale mapping
-
2
-
Devlin B, Risch N (1995) A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics 29(2):311-322
-
(1995)
Genomics
, vol.29
, pp. 311-322
-
-
Devlin, B.1
Risch, N.2
-
18
-
-
0242475326
-
LDA-a java-based linkage disequilibrium analyzer
-
16
-
Ding K, Zhou K, He F, Shen Y (2003) LDA-a java-based linkage disequilibrium analyzer. Bioinformatics 19(16):2147-2148
-
(2003)
Bioinformatics
, vol.19
, pp. 2147-2148
-
-
Ding, K.1
Zhou, K.2
He, F.3
Shen, Y.4
-
19
-
-
1542286160
-
A novel functional polymorphism in the uridine diphosphate- glucuronosyltransferase 2B7 promoter with significant impact on promoter activity
-
3
-
Duguay Y, Báár C, Skorpen F, Guillemette C (2004) A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity. Clin Pharmacol Ther 75(3):223-233
-
(2004)
Clin Pharmacol Ther
, vol.75
, pp. 223-233
-
-
Duguay, Y.1
Báár, C.2
Skorpen, F.3
Guillemette, C.4
-
20
-
-
33750008499
-
Inherited susceptibility to breast cancer: Accomplishments and challenges
-
Research Signpost Kerala
-
Durocher F, Guénard F, Desjardins S, Ouellette G, Labrie Y (2005) Inherited susceptibility to breast cancer: accomplishments and challenges. In: Sinnett D (ed) Molecular genetics of cancer. Research Signpost, Kerala, pp 19-93
-
(2005)
Molecular Genetics of Cancer
, pp. 19-93
-
-
Durocher, F.1
Guénard, F.2
Desjardins, S.3
Ouellette, G.4
Labrie, Y.5
Sinnett, D.6
-
21
-
-
33749998118
-
Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French-Canadian breast/ovarian cancer families
-
Durocher F, Labrie Y, Soucy P, Sinilnikova O, Labuda D, Bessette P, Chiquette J, Laframboise R, Lepine J, Lesperance B, Ouellette G, Pichette R, Plante M, Tavtigian SV, Simard J (2006) Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French-Canadian breast/ovarian cancer families. BMC Cancer 6:230
-
(2006)
BMC Cancer
, vol.6
, pp. 230
-
-
Durocher, F.1
Labrie, Y.2
Soucy, P.3
Sinilnikova, O.4
Labuda, D.5
Bessette, P.6
Chiquette, J.7
Laframboise, R.8
Lepine, J.9
Lesperance, B.10
Ouellette, G.11
Pichette, R.12
Plante, M.13
Tavtigian, S.V.14
Simard, J.15
-
22
-
-
36448968217
-
Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer
-
12
-
Durocher F, Labrie Y, Ouellette G, INHERIT BRCAs, Simard J (2007) Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer. J Hum Genet 52(12):963-977
-
(2007)
J Hum Genet
, vol.52
, pp. 963-977
-
-
Durocher, F.1
Labrie, Y.2
Ouellette, G.3
Inherit, B.4
Simard, J.5
-
23
-
-
0033281771
-
How many more breast cancer predisposition genes are there
-
1
-
Easton DF (1999) How many more breast cancer predisposition genes are there? Breast Cancer Res 1(1):14-17
-
(1999)
Breast Cancer Res
, vol.1
, pp. 14-17
-
-
Easton, D.F.1
-
24
-
-
0028785586
-
The Bloom's syndrome gene product is homologous to RecQ helicases
-
4
-
Ellis NA, Groden J, Ye TZ, Straughen J, Lennon DJ, Ciocci S, Proytcheva M, German J (1995) The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 83(4):655-666
-
(1995)
Cell
, vol.83
, pp. 655-666
-
-
Ellis, N.A.1
Groden, J.2
Ye, T.Z.3
Straughen, J.4
Lennon, D.J.5
Ciocci, S.6
Proytcheva, M.7
German, J.8
-
25
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
7133
-
Erkko H, Xia B, Nikkila J, Schleutker J, Syrjakoski K, Mannermaa A, Kallioniemi A, Pylkas K, Karppinen SM, Rapakko K, Miron A, Sheng Q, Li G, Mattila H, Bell DW, Haber DA, Grip M, Reiman M, Jukkola-Vuorinen A, Mustonen A, Kere J, Aaltonen LA, Kosma VM, Kataja V, Soini Y, Drapkin RI, Livingston DM, Winqvist R (2007) A recurrent mutation in PALB2 in Finnish cancer families. Nature 446(7133):316-319
-
(2007)
Nature
, vol.446
, 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..
-
26
-
-
34548056355
-
Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk
-
8
-
Figueroa JD, Malats N, Rothman N, Real FX, Silverman D, Kogevinas M, Chanock S, Yeager M, Welch R, Dosemeci M, Tardon A, Serra C, Carrato A, Garcia-Closas R, Castano-Vinyals G, Garcia-Closas M (2007) Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. Carcinogenesis 28(8):1788-1793
-
(2007)
Carcinogenesis
, vol.28
, pp. 1788-1793
-
-
Figueroa, J.D.1
Malats, N.2
Rothman, N.3
Real, F.X.4
Silverman, D.5
Kogevinas, M.6
Chanock, S.7
Yeager, M.8
Welch, R.9
Dosemeci, M.10
Tardon, A.11
Serra, C.12
Carrato, A.13
Garcia-Closas, R.14
Castano-Vinyals, G.15
Garcia-Closas, M.16
-
27
-
-
34447106707
-
BRIP1 (BACH1) variants and familial breast cancer risk: A case-control study
-
Frank B, Hemminki K, Meindl A, Wappenschmidt B, Sutter C, Kiechle M, Bugert P, Schmutzler RK, Bartram CR, Burwinkel B (2007) BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study. BMC Cancer 7:83
-
(2007)
BMC Cancer
, vol.7
, pp. 83
-
-
Frank, B.1
Hemminki, K.2
Meindl, A.3
Wappenschmidt, B.4
Sutter, C.5
Kiechle, M.6
Bugert, P.7
Schmutzler, R.K.8
Bartram, C.R.9
Burwinkel, B.10
-
28
-
-
33645744903
-
Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: Two population-based studies in USA and Poland, and meta-analyses
-
4
-
Garcia-Closas M, Egan KM, Newcomb PA, Brinton LA, Titus-Ernstoff L, Chanock S, Welch R, Lissowska J, Peplonska B, Szeszenia-Dabrowska N, Zatonski W, Bardin-Mikolajczak A, Struewing JP (2006) Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses. Hum Genet 119(4):376-388
-
(2006)
Hum Genet
, vol.119
, pp. 376-388
-
-
Garcia-Closas, M.1
Egan, K.M.2
Newcomb, P.A.3
Brinton, L.A.4
Titus-Ernstoff, L.5
Chanock, S.6
Welch, R.7
Lissowska, J.8
Peplonska, B.9
Szeszenia-Dabrowska, N.10
Zatonski, W.11
Bardin-Mikolajczak, A.12
Struewing, J.P.13
-
29
-
-
0037222380
-
TP53 mutations in familial breast cancer: Functional aspects
-
3
-
Gasco M, Yulug IG, Crook T (2003) TP53 mutations in familial breast cancer: functional aspects. Hum Mutat 21(3):301-306
-
(2003)
Hum Mutat
, vol.21
, pp. 301-306
-
-
Gasco, M.1
Yulug, I.G.2
Crook, T.3
-
30
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
6
-
Giardiello FM, Brensinger JD, Tersmette AC, Goodman SN, Petersen GM, Booker SV, Cruz-Correa M, Offerhaus JA (2000) Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119(6):1447-1453
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
Goodman, S.N.4
Petersen, G.M.5
Booker, S.V.6
Cruz-Correa, M.7
Offerhaus, J.A.8
-
31
-
-
35448967457
-
Germline mutations in the breast cancer susceptibility gene PTEN are rare in high-risk non-BRCA1/2 French Canadian breast cancer families
-
INHERIT BRCAs
-
Guenard F, Labrie Y, Ouellette G, Beauparlant CJ, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Pichette R, Plante M; INHERIT BRCAs, Durocher F (2007) Germline mutations in the breast cancer susceptibility gene PTEN are rare in high-risk non-BRCA1/2 French Canadian breast cancer families. Fam Cancer 6(4):483-490
-
(2007)
Fam Cancer
, vol.6
, Issue.4
, pp. 483-490
-
-
Guenard, F.1
Labrie, Y.2
Ouellette, G.3
Beauparlant, C.J.4
Bessette, P.5
Chiquette, J.6
Laframboise, R.7
Lépine, J.8
Lespérance, B.9
Pichette, R.10
Plante, M.11
Durocher, F.12
-
32
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
2
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA (2001) Haplotype tagging for the identification of common disease genes. Nat Genet 29(2):233-237
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
33
-
-
0037306114
-
No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families
-
3
-
Karppinen SM, Vuosku J, Heikkinen K, Allinen M, Winqvist R (2003) No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families. Eur J Cancer 39(3):366-371
-
(2003)
Eur J Cancer
, vol.39
, pp. 366-371
-
-
Karppinen, S.M.1
Vuosku, J.2
Heikkinen, K.3
Allinen, M.4
Winqvist, R.5
-
34
-
-
0029918651
-
Antiestrogenic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin are mediated by direct transcriptional interference with the liganded estrogen receptor. Cross-talk between aryl hydrocarbon- and estrogen-mediated signaling
-
18
-
Kharat I, Saatcioglu F (1996) Antiestrogenic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin are mediated by direct transcriptional interference with the liganded estrogen receptor. Cross-talk between aryl hydrocarbon- and estrogen-mediated signaling. J Biol Chem 271(18):10533-10537
-
(1996)
J Biol Chem
, vol.271
, pp. 10533-10537
-
-
Kharat, I.1
Saatcioglu, F.2
-
35
-
-
0032535661
-
Cloning of two new human helicase genes of the RecQ family: Biological significance of multiple species in higher eukaryotes
-
3
-
Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A (1998) Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. Genomics 54(3):443-452
-
(1998)
Genomics
, vol.54
, pp. 443-452
-
-
Kitao, S.1
Ohsugi, I.2
Ichikawa, K.3
Goto, M.4
Furuichi, Y.5
Shimamoto, A.6
-
36
-
-
0032939991
-
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
-
1
-
Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y (1999) Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nat Genet 22(1):82-84
-
(1999)
Nat Genet
, vol.22
, pp. 82-84
-
-
Kitao, S.1
Shimamoto, A.2
Goto, M.3
Miller, R.W.4
Smithson, W.A.5
Lindor, N.M.6
Furuichi, Y.7
-
37
-
-
0037471838
-
Prediction of pathogenic mutations in patients with early-onset breast cancer by family history
-
Early Onset Breast Cancer Study Group. 9363
-
Lalloo F, Varley J, Ellis D, Moran A, O'Dair L, Pharoah P, Evans DG, Early Onset Breast Cancer Study Group (2003) Prediction of pathogenic mutations in patients with early-onset breast cancer by family history. Lancet 361(9363):1101-1102
-
(2003)
Lancet
, vol.361
, pp. 1101-1102
-
-
Lalloo, F.1
Varley, J.2
Ellis, D.3
Moran, A.4
O'Dair, L.5
Pharoah, P.6
Evans, D.G.7
-
38
-
-
0037430741
-
BACH1 517C- > T transition impairs protein translocation to nucleus: A role in breast cancer susceptibility
-
3
-
Lei H, Vorechovsky I (2003) BACH1 517C- > T transition impairs protein translocation to nucleus: a role in breast cancer susceptibility? Int J Cancer 104(3):389-391
-
(2003)
Int J Cancer
, vol.104
, pp. 389-391
-
-
Lei, H.1
Vorechovsky, I.2
-
39
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
-
9
-
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H (2005) The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J. Nat Genet 37(9):934-935
-
(2005)
Nat Genet
, vol.37
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
De Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Rooimans, M.A.9
Pals, G.10
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
40
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
9
-
Levran O, Attwooll C, Henry RT, Milton KL, Neveling K, Rio P, Batish SD, Kalb R, Velleuer E, Barral S, Ott J, Petrini J, Schindler D, Hanenberg H, Auerbach AD (2005) The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat Genet 37(9):931-933
-
(2005)
Nat Genet
, vol.37
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
Milton, K.L.4
Neveling, K.5
Rio, P.6
Batish, S.D.7
Kalb, R.8
Velleuer, E.9
Barral, S.10
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
41
-
-
34447619477
-
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
-
Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer. 6
-
Lewis AG, Flanagan J, Marsh A, Pupo GM, Mann G, Spurdle AB, Lindeman GJ, Visvader JE, Brown MA, Chenevix-Trench G, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (2005) Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer. Breast Cancer Res 7(6):R1005-1016
-
(2005)
Breast Cancer Res
, vol.7
, pp. 1005-1016
-
-
Lewis, A.G.1
Flanagan, J.2
Marsh, A.3
Pupo, G.M.4
Mann, G.5
Spurdle, A.B.6
Lindeman, G.J.7
Visvader, J.E.8
Brown, M.A.9
Chenevix-Trench, G.10
-
42
-
-
0000356980
-
The interaction of selection and linkage. II. Optimum models
-
Lewontin RC (1964) The interaction of selection and linkage. II. Optimum models. Genetics 50:757-782
-
(1964)
Genetics
, vol.50
, pp. 757-782
-
-
Lewontin, R.C.1
-
43
-
-
0036533574
-
No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22
-
4
-
Luo L, Lei H, Du Q, von Wachenfeldt A, Kockum I, Luthman H, Vorechovsky I, Lindblom A (2002) No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22. Int J Cancer 98(4):638-639
-
(2002)
Int J Cancer
, vol.98
, pp. 638-639
-
-
Luo, L.1
Lei, H.2
Du, Q.3
Von Wachenfeldt, A.4
Kockum, I.5
Luthman, H.6
Vorechovsky, I.7
Lindblom, A.8
-
44
-
-
3142747089
-
The aryl hydrocarbon receptor displaces p300 from E2F-dependent promoters and represses S phase-specific gene expression
-
28
-
Marlowe JL, Knudsen ES, Schwemberger S, Puga A (2004) The aryl hydrocarbon receptor displaces p300 from E2F-dependent promoters and represses S phase-specific gene expression. J Biol Chem 279(28):29013-29022
-
(2004)
J Biol Chem
, vol.279
, pp. 29013-29022
-
-
Marlowe, J.L.1
Knudsen, E.S.2
Schwemberger, S.3
Puga, A.4
-
45
-
-
0035864856
-
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway
-
4
-
Medhurst AL, Huber PA, Waisfisz Q, de Winter JP, Mathew CG (2001) Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway. Hum Mol Genet 10(4):423-429
-
(2001)
Hum Mol Genet
, vol.10
, pp. 423-429
-
-
Medhurst, A.L.1
Huber, P.A.2
Waisfisz, Q.3
De Winter, J.P.4
Mathew, C.G.5
-
46
-
-
33745588077
-
No evidence of BRCA1/2 genomic rearrangements in high-risk French-Canadian breast/ovarian cancer families
-
2
-
Moisan AM, Fortin J, Moisan MD, Samson C, Bessette P, Chiquette J, Laframboise R, Lepine J, Lesperance B, Pichette R, Plante M, Provencher L, Voyer P, Goldgar D, Bridge P, Simard J (2006) No evidence of BRCA1/2 genomic rearrangements in high-risk French-Canadian breast/ovarian cancer families. Genet Test 10(2):104-115
-
(2006)
Genet Test
, vol.10
, pp. 104-115
-
-
Moisan, A.M.1
Fortin, J.2
Moisan, M.D.3
Samson, C.4
Bessette, P.5
Chiquette, J.6
Laframboise, R.7
Lepine, J.8
Lesperance, B.9
Pichette, R.10
Plante, M.11
Provencher, L.12
Voyer, P.13
Goldgar, D.14
Bridge, P.15
Simard, J.16
-
47
-
-
34047201701
-
Association between common variation in 120 candidate genes and breast cancer risk
-
3
-
Pharoah PD, Tyrer J, Dunning AM, Easton DF, Ponder BA; SEARCH Investigators (2007) Association between common variation in 120 candidate genes and breast cancer risk. PLoS Genet 3(3):e42
-
(2007)
PLoS Genet
, vol.3
, pp. 42
-
-
Pharoah, P.D.1
Tyrer, J.2
Dunning, A.M.3
Easton, D.F.4
Ponder Investigators, B.A.5
Search6
-
48
-
-
0035902166
-
Cancer genetics
-
6835
-
Ponder BA (2001) Cancer genetics. Nature 411(6835):336-341
-
(2001)
Nature
, vol.411
, pp. 336-341
-
-
Ponder, B.A.1
-
49
-
-
0028971143
-
MatInd and MatInspector: New fast and versatile tools for detection of consensus matches in nucleotide sequence data
-
23
-
Quandt K, Frech K, Karas H, Wingender E, Werner T (1995) MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data. Nucleic Acids Res 23(23):4878-4884
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 4878-4884
-
-
Quandt, K.1
Frech, K.2
Karas, H.3
Wingender, E.4
Werner, T.5
-
50
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
2
-
Rahman N, Seal S, Thompson D, Kelly P, Renwick A, Elliott A, Reid S, Spanova K, Barfoot R, Chagtai T, Jayatilake H, McGuffog L, Hanks S, Evans DG, Eccles D, Easton DF, Stratton MR (2007) PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet 39(2):165-167
-
(2007)
Nat Genet
, vol.39
, 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
-
52
-
-
33746491583
-
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
-
Breast Cancer Susceptibility Collaboration (UK), 8
-
Renwick A, Thompson D, Seal S, Kelly P, Chagtai T, Ahmed M, North B, Jayatilake H, Barfoot R, Spanova K, McGuffog L, Evans DG, Eccles D, Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR, Rahman N (2006) ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat Genet 38(8):873-875
-
(2006)
Nat Genet
, vol.38
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
Kelly, P.4
Chagtai, T.5
Ahmed, M.6
North, B.7
Jayatilake, H.8
Barfoot, R.9
Spanova, K.10
McGuffog, L.11
Evans, D.G.12
Eccles, D.13
-
53
-
-
10744227178
-
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early onset breast cancer cases and reference individuals
-
2
-
Rutter JL, Smith AM, Davila MR, Sigurdson AJ, Giusti RM, Pineda MA, Doody MM, Tucker MA, Greene MH, Zhang J, Struewing JP (2003) Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early onset breast cancer cases and reference individuals. Hum Mutat 22(2):121-128
-
(2003)
Hum Mutat
, vol.22
, pp. 121-128
-
-
Rutter, J.L.1
Smith, A.M.2
Davila, M.R.3
Sigurdson, A.J.4
Giusti, R.M.5
Pineda, M.A.6
Doody, M.M.7
Tucker, M.A.8
Greene, M.H.9
Zhang, J.10
Struewing, J.P.11
-
54
-
-
0004136246
-
-
Irwin N, Janssen KA, Argentine J, Curtis S, Zierler M, Dickerson M, Sialiano I, McInerny N, Brown D, Schaefer S, deBruin D, Atkeson E, Weiss D, Curtis MD (eds) Cold Spring Harbor Laboratory Press, Cold Spring Harbor
-
Sambrook J, Russell DW (2001) Irwin N, Janssen KA, Argentine J, Curtis S, Zierler M, Dickerson M, Sialiano I, McInerny N, Brown D, Schaefer S, deBruin D, Atkeson E, Weiss D, Curtis MD (eds) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor
-
(2001)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Russell, D.W.2
-
55
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
11
-
Seal S, Thompson D, Renwick A, Elliott A, Kelly P, Barfoot R, Chagtai T, Jayatilake H, Ahmed M, Spanova K, North B, McGuffog L, Evans DG, Eccles D, Easton DF, Stratton MR, Rahman N (2006) Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet 38(11):1239-1241
-
(2006)
Nat Genet
, vol.38
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
56
-
-
3042829470
-
Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes
-
Sigurdson AJ, Hauptmann M, Chatterjee N, Alexander BH, Doody MM, Rutter JL, Struewing JP (2004) Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes. BMC Cancer 4:9
-
(2004)
BMC Cancer
, vol.4
, pp. 9
-
-
Sigurdson, A.J.1
Hauptmann, M.2
Chatterjee, N.3
Alexander, B.H.4
Doody, M.M.5
Rutter, J.L.6
Struewing, J.P.7
-
57
-
-
33847259648
-
Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer
-
2
-
Simard J, Dumont M, Moisan AM, Gaborieau V, Malouin H, Durocher F, Chiquette J, Plante M, Avard D, Bessette P, Brousseau C, Dorval M, Godard B, Houde L; INHERIT BRCAs, Joly Y, Lajoie MA, Leblanc G, Lepine J, Lesperance B, Vezina H, Parboosingh J, Pichette R, Provencher L, Rheaume J, Sinnett D, Samson C, Simard JC, Tranchant M, Voyer P, Easton D, Tavtigian SV, Knoppers BM, Laframboise R, Bridge P, Goldgar D (2007) Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. J Med Genet 44(2):107-121
-
(2007)
J Med Genet
, vol.44
, pp. 107-121
-
-
Simard, J.1
Dumont, M.2
Moisan, A.M.3
Gaborieau, V.4
Malouin, H.5
Durocher, F.6
Chiquette, J.7
Plante, M.8
Avard, D.9
Bessette, P.10
Brousseau, C.11
Dorval, M.12
Godard, B.13
Houde Brcas, L.14
Inherit15
Joly, Y.16
Lajoie, M.A.17
Leblanc, G.18
Lepine, J.19
Lesperance, B.20
Vezina, H.21
Parboosingh, J.22
Pichette, R.23
Provencher, L.24
Rheaume, J.25
Sinnett, D.26
Samson, C.27
Simard, J.C.28
Tranchant, M.29
Voyer, P.30
Easton, D.31
Tavtigian, S.V.32
Knoppers, B.M.33
Laframboise, R.34
Bridge, P.35
Goldgar, D.36
more..
-
58
-
-
34247110291
-
Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
-
2
-
Smogorzewska A, Matsuoka S, Vinciguerra P, McDonald ER 3rd, Hurov KE, Luo J, Ballif BA, Gygi SP, Hofmann K, D'Andrea AD, Elledge SJ (2007) Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell 129(2):289-301
-
(2007)
Cell
, vol.129
, pp. 289-301
-
-
Smogorzewska, A.1
Matsuoka, S.2
Vinciguerra, P.3
McDonald III, E.R.4
Hurov, K.E.5
Luo, J.6
Ballif, B.A.7
Gygi, S.P.8
Hofmann, K.9
D'Andrea, A.D.10
Elledge, S.J.11
-
59
-
-
42349086525
-
Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer
-
Song H, Ramus SJ, Kjaer SK, Hogdall E, Dicioccio RA, Whittemore AS, McGuire V, Hogdall C, Jacobs IJ, Easton DF, Ponder BA, Dunning AM, Gayther SA, D P Pharoah P (2007) Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer. PLoS ONE 2:e268
-
(2007)
PLoS ONE
, vol.2
, pp. 268
-
-
Song, H.1
Ramus, S.J.2
Kjaer, S.K.3
Hogdall, E.4
Dicioccio, R.A.5
Whittemore, A.S.6
McGuire, V.7
Hogdall, C.8
Jacobs, I.J.9
Easton, D.F.10
Ponder, B.A.11
Dunning, A.M.12
Gayther, S.A.13
Pharoah, D.P.14
-
60
-
-
17344362697
-
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: Expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer
-
2
-
Stankovic T, Kidd AM, Sutcliffe A, McGuire GM, Robinson P, Weber P, Bedenham T, Bradwell AR, Easton DF, Lennox GG, Haites N, Byrd PJ, Taylor AM (1998) ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Am J Hum Genet 62(2):334-345
-
(1998)
Am J Hum Genet
, vol.62
, pp. 334-345
-
-
Stankovic, T.1
Kidd, A.M.2
Sutcliffe, A.3
McGuire, G.M.4
Robinson, P.5
Weber, P.6
Bedenham, T.7
Bradwell, A.R.8
Easton, D.F.9
Lennox, G.G.10
Haites, N.11
Byrd, P.J.12
Taylor, A.M.13
-
61
-
-
0242691208
-
A comparison of bayesian methods for haplotype reconstruction from population genotype data
-
5
-
Stephens M, Donnelly P (2003) A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet 73(5):1162-1169
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1162-1169
-
-
Stephens, M.1
Donnelly, P.2
-
62
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
4
-
Stephens M, Smith NJ, Donnelly P (2001) A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 68(4):978-989
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
63
-
-
10744219867
-
Are ATM mutations 7271T->G and IVS10-6T->G really high-risk breast cancer-susceptibility alleles
-
3
-
Szabo CI, Schutte M, Broeks A, Houwing-Duistermaat JJ, Thorstenson YR, Durocher F, Oldenburg RA, Wasielewski M, Odefrey F, Thompson D, Floore AN, Kraan J, Klijn JG, van den Ouweland AM, Wagner TM, Devilee P, Simard J, van 't Veer LJ, Goldgar DE, Meijers-Heijboer H (2004) Are ATM mutations 7271T->G and IVS10-6T->G really high-risk breast cancer-susceptibility alleles? Cancer Res 64(3):840-843
-
(2004)
Cancer Res
, vol.64
, pp. 840-843
-
-
Szabo, C.I.1
Schutte, M.2
Broeks, A.3
Houwing-Duistermaat, J.J.4
Thorstenson, Y.R.5
Durocher, F.6
Oldenburg, R.A.7
Wasielewski, M.8
Odefrey, F.9
Thompson, D.10
Floore, A.N.11
Kraan, J.12
Klijn, J.G.13
Van Den Ouweland, A.M.14
Wagner, T.M.15
Devilee, P.16
Simard, J.17
Van 'T Veer, L.J.18
Goldgar, D.E.19
Meijers-Heijboer, H.20
more..
-
64
-
-
34249857115
-
Analysis of PALB2/FANCN-associated breast cancer families
-
16
-
Tischkowitz M, Xia B, Sabbaghian N, Reis-Filho JS, Hamel N, Li G, van Beers EH, Li L, Khalil T, Quenneville LA, Omeroglu A, Poll A, Lepage P, Wong N, Nederlof PM, Ashworth A, Tonin PN, Narod SA, Livingston DM, Foulkes WD (2007) Analysis of PALB2/FANCN-associated breast cancer families. Proc Natl Acad Sci USA 104(16):6788-6793
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, 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..
-
65
-
-
0031933599
-
Infrequent mutations in the PTEN/MMAC1 gene among primary breast cancers
-
1
-
Ueda K, Nishijima M, Inui H, Watatani M, Yayoi E, Okamura J, Yasutomi M, Nakamura Y, Miyoshi Y (1998) Infrequent mutations in the PTEN/MMAC1 gene among primary breast cancers. Jpn J Cancer Res 89(1):17-21
-
(1998)
Jpn J Cancer Res
, vol.89
, pp. 17-21
-
-
Ueda, K.1
Nishijima, M.2
Inui, H.3
Watatani, M.4
Yayoi, E.5
Okamura, J.6
Yasutomi, M.7
Nakamura, Y.8
Miyoshi, Y.9
-
66
-
-
33144489382
-
BACH1 Ser919Pro variant and breast cancer risk
-
Vahteristo P, Yliannala K, Tamminen A, Eerola H, Blomqvist C, Nevanlinna H (2006) BACH1 Ser919Pro variant and breast cancer risk. BMC Cancer 6:19
-
(2006)
BMC Cancer
, vol.6
, pp. 19
-
-
Vahteristo, P.1
Yliannala, K.2
Tamminen, A.3
Eerola, H.4
Blomqvist, C.5
Nevanlinna, H.6
-
67
-
-
26844451916
-
Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families
-
2-3
-
Vezina H, Durocher F, Dumont M, Houde L, Szabo C, Tranchant M, Chiquette J, Plante M, Laframboise R, Lepine J, Nevanlinna H, Stoppa-Lyonnet D, Goldgar D, Bridge P, Simard J (2005) Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families. Hum Genet 117(2-3):119-132
-
(2005)
Hum Genet
, vol.117
, pp. 119-132
-
-
Vezina, H.1
Durocher, F.2
Dumont, M.3
Houde, L.4
Szabo, C.5
Tranchant, M.6
Chiquette, J.7
Plante, M.8
Laframboise, R.9
Lepine, J.10
Nevanlinna, H.11
Stoppa-Lyonnet, D.12
Goldgar, D.13
Bridge, P.14
Simard, J.15
-
68
-
-
0042387804
-
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping
-
3
-
Weale ME, Depondt C, Macdonald SJ, Smith A, Lai PS, Shorvon SD, Wood NW, Goldstein DB (2003) Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping. Am J Hum Genet 73(3):551-565
-
(2003)
Am J Hum Genet
, vol.73
, pp. 551-565
-
-
Weale, M.E.1
Depondt, C.2
MacDonald, S.J.3
Smith, A.4
Lai, P.S.5
Shorvon, S.D.6
Wood, N.W.7
Goldstein, D.B.8
-
69
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
5259
-
Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD (1996) Positional cloning of the Werner's syndrome gene. Science 272(5259):258-262
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Ouais, S.10
Martin, G.M.11
Mulligan, J.12
Schellenberg, G.D.13
-
70
-
-
0142147272
-
The BRCT domain is a phospho-protein binding domain
-
5645
-
Yu X, Chini CC, He M, Mer G, Chen J (2003) The BRCT domain is a phospho-protein binding domain. Science 302(5645):639-642
-
(2003)
Science
, vol.302
, pp. 639-642
-
-
Yu, X.1
Chini, C.C.2
He, M.3
Mer, G.4
Chen, J.5
|