-
1
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, RiouxJD, Schaffner SF, Hudson TJ, Lander ES: High-resolution haplotype structure in the human genome. Nat Genet 2001, 29:229-232.
-
(2001)
Nat. Genet.
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
2
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D: The structure of haplotype blocks in the human genome. Science 2002, 296:2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
3
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R, Lander ES: Linkage disequilibrium in the human genome. Nature 2001, 411:199-204.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
4
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR: Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 2001, 294:1719-1723.
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
Nguyen, B.T.11
Norris, M.C.12
Sheehan, J.B.13
Shen, N.14
Stern, D.15
Stokowski, R.P.16
Thomas, D.J.17
Trulson, M.O.18
Vyas, K.R.19
Frazer, K.A.20
Fodor, S.P.21
Cox, D.R.22
more..
-
5
-
-
18444396271
-
A first-generation linkage disequilibrium map of human chromosome 22
-
Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, Dibling T, Tinsley E, Kirby S, Carter D, Papaspyridonos M, Livingstone S, Ganske R, Lohmussaar E, Zernant J, Tonisson N, Remm M, Magi R, Puurand T, Vilo J, Kurg A, Rice K, Deloukas P, Mott R, Metspalu A, Bentley DR, Cardon LR, Dunham I: A first-generation linkage disequilibrium map of human chromosome 22. Nature 2002, 418:544-548.
-
(2002)
Nature
, vol.418
, pp. 544-548
-
-
Dawson, E.1
Abecasis, G.R.2
Bumpstead, S.3
Chen, Y.4
Hunt, S.5
Beare, D.M.6
Pabial, J.7
Dibling, T.8
Tinsley, E.9
Kirby, S.10
Carter, D.11
Papaspyridonos, M.12
Livingstone, S.13
Ganske, R.14
Lohmussaar, E.15
Zernant, J.16
Tonisson, N.17
Remm, M.18
Magi, R.19
Puurand, T.20
Vilo, J.21
Kurg, A.22
Rice, K.23
Deloukas, P.24
Mott, R.25
Metspalu, A.26
Bentley, D.R.27
Cardon, L.R.28
Dunham, I.29
more..
-
6
-
-
0037370466
-
Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots
-
Phillips MS, Lawrence R, Sachidanandam R, Morris AP, Balding DJ, Donaldson MA, Studebaker JF, Ankener WM, Alfisi SV, Kuo FS, Camisa AL, Pazorov V, Scott KE, Carey BJ, Faith J, Katari G, Bhatti HA, Cyr JM, Derohannessian V, Elosua C, Forman AM, Grecco NM, Hock CR, Kuebler JM, Lathrop JA, Mockler MA, Nachtman EP, Restine SL, Varde SA, Hozza MJ, Gelfand CA, Broxholme J, Abecasis GR, Boyce-Jacino MT, Cardon LR: Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots. Nat Genet 2003, 33:382-387.
-
(2003)
Nat. Genet.
, vol.33
, pp. 382-387
-
-
Phillips, M.S.1
Lawrence, R.2
Sachidanandam, R.3
Morris, A.P.4
Balding, D.J.5
Donaldson, M.A.6
Studebaker, J.F.7
Ankener, W.M.8
Alfisi, S.V.9
Kuo, F.S.10
Camisa, A.L.11
Pazorov, V.12
Scott, K.E.13
Carey, B.J.14
Faith, J.15
Katari, G.16
Bhatti, H.A.17
Cyr, J.M.18
Derohannessian, V.19
Elosua, C.20
Forman, A.M.21
Grecco, N.M.22
Hock, C.R.23
Kuebler, J.M.24
Lathrop, J.A.25
Mockler, M.A.26
Nachtman, E.P.27
Restine, S.L.28
Varde, S.A.29
Hozza, M.J.30
Gelfand, C.A.31
Broxholme, J.32
Abecasis, G.R.33
Boyce-Jacino, M.T.34
Cardon, L.R.35
more..
-
7
-
-
12144290432
-
The impact of SNP density on fine-scale patterns of linkage disequilibrium
-
Ke X, Hunt S, Tapper W, Lawrence R, Stavrides G, Ghori J, Whittaker P, Collins A, Morris AP, Bentley D, Cardon LR, Deloukas P: The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet 2004, 13:577-588.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 577-588
-
-
Ke, X.1
Hunt, S.2
Tapper, W.3
Lawrence, R.4
Stavrides, G.5
Ghori, J.6
Whittaker, P.7
Collins, A.8
Morris, A.P.9
Bentley, D.10
Cardon, L.R.11
Deloukas, P.12
-
8
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
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: Haplotype tagging for the identification of common disease genes. Nat Genet 2001, 29:233-237.
-
(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..
-
9
-
-
0037188541
-
A dynamic programming algorithm for haplotype block partitioning
-
Zhang K, Deng M, Chen T, Waterman MS, Sun F: A dynamic programming algorithm for haplotype block partitioning. Proc Natl Acad Sci U S A 2002, 99:7335-7339.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 7335-7339
-
-
Zhang, K.1
Deng, M.2
Chen, T.3
Waterman, M.S.4
Sun, F.5
-
10
-
-
0042387804
-
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping
-
Weale ME, Depondt C, Macdonald SJ, Smith A, Lai PS, Shorvon SD, Wood NW, Goldstein DB: Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping. Am J Hum Genet 2003, 73:551-565.
-
(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
-
11
-
-
0037311771
-
Efficient selective screening of haplotype tag SNPs
-
Ke X, Cardon LR: Efficient selective screening of haplotype tag SNPs. Bioinformatics 2003, 19:287-288.
-
(2003)
Bioinformatics
, vol.19
, pp. 287-288
-
-
Ke, X.1
Cardon, L.R.2
-
12
-
-
0038728035
-
Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes
-
Meng Z, Zaykin DV, Xu CF, Wagner M, Ehm MG: Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes. Am J Hum Genet 2003, 73:115-130.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 115-130
-
-
Meng, Z.1
Zaykin, D.V.2
Xu, C.F.3
Wagner, M.4
Ehm, M.G.5
-
13
-
-
0347362608
-
Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation
-
Horne BD, Camp NJ: Principal component analysis for selection of optimal SNP-sets that capture intragenic genetic variation. Genet Epidemiol 2004, 26:11-21.
-
(2004)
Genet. Epidemiol.
, vol.26
, pp. 11-21
-
-
Horne, B.D.1
Camp, N.J.2
-
14
-
-
0346373654
-
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium
-
Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, Nickerson DA: Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. Am J Hum Genet 2004, 74:106-120.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 106-120
-
-
Carlson, C.S.1
Eberle, M.A.2
Rieder, M.J.3
Yi, Q.4
Kruglyak, L.5
Nickerson, D.A.6
-
15
-
-
15544380207
-
Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer
-
Camp NJ, Swensen J, Horne BD, Farnham JM, Thomas A, Cannon-Albright LA, Tavtigian SV: Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer. Genet Epidemiol 2004, 28:232-243.
-
(2004)
Genet. Epidemiol.
, vol.28
, pp. 232-243
-
-
Camp, N.J.1
Swensen, J.2
Horne, B.D.3
Farnham, J.M.4
Thomas, A.5
Cannon-Albright, L.A.6
Tavtigian, S.V.7
-
16
-
-
6344233909
-
Finding haplotype tagging SNPs by use of principal components analysis
-
Lin Z, Altman RB: Finding haplotype tagging SNPs by use of principal components analysis. Am J Hum Genet 2004, 75:850-861.
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 850-861
-
-
Lin, Z.1
Altman, R.B.2
-
17
-
-
1842539516
-
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other
-
Nyholt DR: A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet 2004, 74:765-769.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 765-769
-
-
Nyholt, D.R.1
-
18
-
-
26844463244
-
High Density SNP Map Reveals Interrupted and Interlaced Organization of Linkage Disequilibrium Among Markers
-
Toronto, Ontario, Canada
-
Belmont J, Yu F, Hardenbol P, Lu X, Moorhead M, Scott G, Ghose S, Pasternak S, Willis T, Faham M, Leal SM, Taylor J, Morris R, Kaplan N, Gibbs RA: High Density SNP Map Reveals Interrupted and Interlaced Organization of Linkage Disequilibrium Among Markers:; Toronto, Ontario, Canada.; 2004.
-
(2004)
-
-
Belmont, J.1
Yu, F.2
Hardenbol, P.3
Lu, X.4
Moorhead, M.5
Scott, G.6
Ghose, S.7
Pasternak, S.8
Willis, T.9
Faham, M.10
Leal, S.M.11
Taylor, J.12
Morris, R.13
Kaplan, N.14
Gibbs, R.A.15
-
19
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan D, Weinberg RA: The hallmarks of cancer. Cell 2000, 100:57-70.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
20
-
-
4644277326
-
Xeroderma pigmentosum: From symptoms and genetics to gene-based skin therapy
-
Magnaldo T, Sarasin A: Xeroderma pigmentosum: from symptoms and genetics to gene-based skin therapy. Cells Tissues Organs 2004, 177:189-198.
-
(2004)
Cells Tissues Organs
, vol.177
, pp. 189-198
-
-
Magnaldo, T.1
Sarasin, A.2
-
21
-
-
0037390446
-
The hereditary nonpolyposis colorectal cancer syndrome: Genetics and clinical implications
-
Chung DC, Rustgi AK: The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications. Ann Intern Med 2003, 138:560-570.
-
(2003)
Ann. Intern. Med.
, vol.138
, pp. 560-570
-
-
Chung, D.C.1
Rustgi, A.K.2
-
22
-
-
0035093737
-
DNA double-strand breaks: Signaling, repair and the cancer connection
-
Khanna KK, Jackson SP: DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet 2001, 27:247-254.
-
(2001)
Nat. Genet.
, vol.27
, pp. 247-254
-
-
Khanna, K.K.1
Jackson, S.P.2
-
23
-
-
84938047707
-
A computerized family history data base system
-
Skolnick M, Bean L, Dintelman SM, Mineau G: A computerized family history data base system. Social Soc Res 1979, 63:506.
-
(1979)
Social Soc. Res.
, vol.63
, pp. 506
-
-
Skolnick, M.1
Bean, L.2
Dintelman, S.M.3
Mineau, G.4
-
24
-
-
0004036330
-
The Utah genealogical database: A resource for genetic epidemiology
-
Edited by: Skolnick M. Cold Spring Harbor, NY, Cold Spring Harbor Laboratory Press
-
Skolnick M: The Utah genealogical database: A resource for genetic epidemiology. In Banbury Report No 4: Cancer Incidence in Defined Populations Edited by: Skolnick M. Cold Spring Harbor, NY, Cold Spring Harbor Laboratory Press; 1980.
-
(1980)
Banbury Report No 4: Cancer Incidence in Defined Populations
-
-
Skolnick, M.1
-
25
-
-
26844555083
-
-
Pedigree and Population Resource: Utah Population Database
-
Pedigree and Population Resource: Utah Population Database [http://www.hci.utah.edu/groups/ppr/]
-
-
-
-
26
-
-
15244341292
-
Association analyses of DNA methyltransferase-I (DNMT1) polymorphisms with systemic lupus erythematosus
-
Park BL, Kim LH, Shin HD, Park YW, Uhm WS, Bae SC: Association analyses of DNA methyltransferase-I (DNMT1) polymorphisms with systemic lupus erythematosus. J Hum Genet 2004, 49:642-646.
-
(2004)
J. Hum. Genet.
, vol.49
, pp. 642-646
-
-
Park, B.L.1
Kim, L.H.2
Shin, H.D.3
Park, Y.W.4
Uhm, W.S.5
Bae, S.C.6
-
27
-
-
2942707895
-
The effects of scale: Variation in the APOA I/C3/A4/A5 gene cluster
-
Fullerton SM, Buchanan AV, Sonpar VA, Taylor SL, Smith JD, Carlson CS, Salomaa V, Stengard JH, Boerwinkle E, Clark AG, Nickerson DA, Weiss KM: The effects of scale: variation in the APOA I/C3/A4/A5 gene cluster. Hum Genet 2004, 115:36-56.
-
(2004)
Hum. Genet.
, vol.115
, pp. 36-56
-
-
Fullerton, S.M.1
Buchanan, A.V.2
Sonpar, V.A.3
Taylor, S.L.4
Smith, J.D.5
Carlson, C.S.6
Salomaa, V.7
Stengard, J.H.8
Boerwinkle, E.9
Clark, A.G.10
Nickerson, D.A.11
Weiss, K.M.12
-
28
-
-
1242336880
-
HSD 17B1 gene polymorphisms and risk of endometrial and breast cancer
-
Setiawan VW, Hankinson SE, Colditz GA, Hunter DJ, De Vivo I: HSD 17B1 gene polymorphisms and risk of endometrial and breast cancer. Cancer Epidemiol Biomarkers Prev 2004, 13:213-219.
-
(2004)
Cancer Epidemiol. Biomarkers Prev.
, vol.13
, pp. 213-219
-
-
Setiawan, V.W.1
Hankinson, S.E.2
Colditz, G.A.3
Hunter, D.J.4
De Vivo, I.5
-
29
-
-
3242795791
-
Polymorphic variation in the CBLB gene in human type 1 diabetes
-
Kosoy R, Yokoi N, Seino S, Concannon P: Polymorphic variation in the CBLB gene in human type 1 diabetes. Genes Immun 2004, 5:232-235.
-
(2004)
Genes Immun.
, vol.5
, pp. 232-235
-
-
Kosoy, R.1
Yokoi, N.2
Seino, S.3
Concannon, P.4
-
31
-
-
0027291689
-
Allelic discrimination by nicktranslation PCR with fluorogenic probes
-
Lee LG, Connell CR, Bloch W: Allelic discrimination by nicktranslation PCR with fluorogenic probes. Nucleic Acids Res 1993, 21:3761-3766.
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 3761-3766
-
-
Lee, L.G.1
Connell, C.R.2
Bloch, W.3
-
32
-
-
26844522234
-
-
SNPHAP
-
Clayton DG: SNPHAP. [http://www-gene.cimr.cam.ac.uk/clayton/software].
-
-
-
Clayton, D.G.1
-
33
-
-
0022472723
-
Mortality and cancer incidence in 263 patients with ataxia-telangiectasia
-
Morrell D, Cromartie E, Swift M: Mortality and cancer incidence in 263 patients with ataxia-telangiectasia. J Natl Cancer Inst 1986, 77:89-92.
-
(1986)
J. Natl. Cancer Inst.
, vol.77
, pp. 89-92
-
-
Morrell, D.1
Cromartie, E.2
Swift, M.3
-
34
-
-
0026409331
-
Incidence of cancer in 161 families affected by ataxia-telangiectasia
-
Swift M, Morrell D, Massey RB, Chase CL: Incidence of cancer in 161 families affected by ataxia-telangiectasia. N Engl J Med 1991, 325:1831-1836.
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 1831-1836
-
-
Swift, M.1
Morrell, D.2
Massey, R.B.3
Chase, C.L.4
-
36
-
-
0033911566
-
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
-
Broeks A, Urbanus JH, Floore AN, Dahler EC, Klijn JG, Rutgers EJ, Devilee P, Russell NS, van Leeuwen FE, van 't Veer LJ: ATM-heterozygous germline mutations contribute to breast cancer-susceptibility. Am J Hum Genet 2000, 66:494-500.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 494-500
-
-
Broeks, A.1
Urbanus, J.H.2
Floore, A.N.3
Dahler, E.C.4
Klijn, J.G.5
Rutgers, E.J.6
Devilee, P.7
Russell, N.S.8
van Leeuwen, F.E.9
van 't Veer, L.J.10
-
37
-
-
0037028740
-
Dominant negative ATM mutations in breast cancer families
-
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: Dominant negative ATM mutations in breast cancer families. J Natl Cancer Inst 2002, 94:205-215.
-
(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..
-
38
-
-
0038745419
-
Contributions of ATM mutations to familial breast and ovarian cancer
-
Thorstenson YR, Roxas A, Kroiss R, Jenkins MA, Yu KM, Bachrich T, Muhr D, Wayne TL, Chu G, Davis RW, Wagner TM, Oefner PJ: Contributions of ATM mutations to familial breast and ovarian cancer. Cancer Res 2003, 63:3325-3333.
-
(2003)
Cancer Res.
, vol.63
, pp. 3325-3333
-
-
Thorstenson, Y.R.1
Roxas, A.2
Kroiss, R.3
Jenkins, M.A.4
Yu, K.M.5
Bachrich, T.6
Muhr, D.7
Wayne, T.L.8
Chu, G.9
Davis, R.W.10
Wagner, T.M.11
Oefner, P.J.12
-
39
-
-
0032756367
-
Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer
-
Izatt L, Greenman J, Hodgson S, Ellis D, Watts S, Scott G, Jacobs C, Liebmann R, Zvelebil MJ, Mathew C, Solomon E: Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer. Genes Chromosomes Cancer 1999, 26:286-294.
-
(1999)
Genes Chromosomes Cancer
, vol.26
, pp. 286-294
-
-
Izatt, L.1
Greenman, J.2
Hodgson, S.3
Ellis, D.4
Watts, S.5
Scott, G.6
Jacobs, C.7
Liebmann, R.8
Zvelebil, M.J.9
Mathew, C.10
Solomon, E.11
-
40
-
-
0031029676
-
Heterozygous ATM mutations do not contribute to early onset of breast cancer
-
FitzGerald MG, Bean JM, Hegde SR, Unsal H, MacDonald DJ, Harkin DP, Finkelstein DM, Isselbacher KJ, Haber DA: Heterozygous ATM mutations do not contribute to early onset of breast cancer. Nat Genet 1997, 15:307-310.
-
(1997)
Nat. Genet.
, vol.15
, pp. 307-310
-
-
FitzGerald, M.G.1
Bean, J.M.2
Hegde, S.R.3
Unsal, H.4
MacDonald, D.J.5
Harkin, D.P.6
Finkelstein, D.M.7
Isselbacher, K.J.8
Haber, D.A.9
-
41
-
-
0035900911
-
Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries
-
Olsen JH, Hahnemann JM, Borresen-Dale AL, Brondum-Nielsen K, Hammarstrom L, Kleinerman R, Kaariainen H, Lonnqvist T, Sankila R, Seersholm N, Tretli S, Yuen J, Boice JDJ, Tucker M: Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries. J Natl Cancer Inst 2001, 93:121-127.
-
(2001)
J. Natl. Cancer Inst.
, vol.93
, pp. 121-127
-
-
Olsen, J.H.1
Hahnemann, J.M.2
Borresen-Dale, A.L.3
Brondum-Nielsen, K.4
Hammarstrom, L.5
Kleinerman, R.6
Kaariainen, H.7
Lonnqvist, T.8
Sankila, R.9
Seersholm, N.10
Tretli, S.11
Yuen, J.12
Boice, J.D.J.13
Tucker, M.14
-
42
-
-
0344562925
-
Neutral sequence variants and haplotypes at the 150 Kb ataxia-telangiectasia locus
-
Li A, Huang Y, Swift M: Neutral sequence variants and haplotypes at the 150 Kb ataxia-telangiectasia locus. Am J Med Genet 1999, 86:140-144.
-
(1999)
Am. J. Med. Genet.
, vol.86
, pp. 140-144
-
-
Li, A.1
Huang, Y.2
Swift, M.3
-
43
-
-
0033658948
-
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium
-
Bonnen PE, Story MD, Ashorn CL, Buchholz TA, Weil MM, Nelson DL: Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium. Am J Hum Genet 2000, 67:1437-1451.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1437-1451
-
-
Bonnen, P.E.1
Story, M.D.2
Ashorn, C.L.3
Buchholz, T.A.4
Weil, M.M.5
Nelson, D.L.6
-
44
-
-
0034927535
-
Global analysis of ATM polymorphism reveals significant functional constraint
-
Thorstenson YR, Shen P, Tusher VG, Wayne TL, Davis RW, Chu G, Oefner PJ: Global analysis of ATM polymorphism reveals significant functional constraint. Am J Hum Genet 2001, 69:396-412.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 396-412
-
-
Thorstenson, Y.R.1
Shen, P.2
Tusher, V.G.3
Wayne, T.L.4
Davis, R.W.5
Chu, G.6
Oefner, P.J.7
-
45
-
-
7044239433
-
Common ataxia telangiectasia mutated haplotypes and risk of breast cancer: A nested case-control study
-
Tamimi RM, Hankinson SE, Spiegelman D, Kraft P, Colditz GA, Hunter DJ: Common ataxia telangiectasia mutated haplotypes and risk of breast cancer: a nested case-control study. Breast Cancer Res 2004, 6:R416-22.
-
(2004)
Breast Cancer Res.
, vol.6
-
-
Tamimi, R.M.1
Hankinson, S.E.2
Spiegelman, D.3
Kraft, P.4
Colditz, G.A.5
Hunter, D.J.6
-
46
-
-
20144371261
-
A survey of haplotype variants at several disease candidate genes: The importance of rare variants for complex diseases
-
Liu PY, Zhang YY, Lu Y, Long JR, Shen H, Zhao LJ, Xu FH, Xiao P, Xiong DH, Liu YJ, Recker RR, Deng HW: A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases. J Med Genet 2005, 42:221-227.
-
(2005)
J. Med. Genet.
, vol.42
, pp. 221-227
-
-
Liu, P.Y.1
Zhang, Y.Y.2
Lu, Y.3
Long, J.R.4
Shen, H.5
Zhao, L.J.6
Xu, F.H.7
Xiao, P.8
Xiong, D.H.9
Liu, Y.J.10
Recker, R.R.11
Deng, H.W.12
-
47
-
-
0344826588
-
Haplotype tagging single nucleotide polymorphisms and association studies
-
Thompson D, Stram D, Goldgar D, Witte JS: Haplotype tagging single nucleotide polymorphisms and association studies. Hum Hered 2003, 56:48-55.
-
(2003)
Hum. Hered.
, vol.56
, pp. 48-55
-
-
Thompson, D.1
Stram, D.2
Goldgar, D.3
Witte, J.S.4
-
48
-
-
79959503826
-
-
The International HapMap Project
-
The International HapMap Project. Nature 2003, 426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
49
-
-
26844459727
-
-
HapMap
-
HapMap [http://www.hapmap.org/]
-
-
-
-
50
-
-
14944378127
-
The effect of SNP marker density on the efficacy of haplotype tagging SNPs - A warning
-
Iles MM: The effect of SNP marker density on the efficacy of haplotype tagging SNPs - a warning. Ann Hum Genet 2005, 69:209-215.
-
(2005)
Ann. Hum. Genet.
, vol.69
, pp. 209-215
-
-
Iles, M.M.1
|