-
3
-
-
0035121849
-
Sibling risks in cancer: Clues to recessive or X-linked genes?
-
DOI 10.1054/bjoc.2000.1585
-
Hemminki K, Vaittinen P, Dong C, Easton D. Sibling risks in cancer: clues to recessive or X-linked genes? Br J Cancer 2001;84:388-91. (Pubitemid 32154433)
-
(2001)
British Journal of Cancer
, vol.84
, Issue.3
, pp. 388-391
-
-
Hemminki, K.1
Vaittinen, P.2
Dong, C.3
Easton, D.4
-
4
-
-
0034793635
-
A systematic review and meta-analysis of familial colorectal cancer risk
-
DOI 10.1016/S0002-9270(01)03239-7, PII S0002927001032397
-
Johns LE, Houlston RS. A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol 2001;96:2992-3003. (Pubitemid 32959544)
-
(2001)
American Journal of Gastroenterology
, vol.96
, Issue.10
, pp. 2992-3003
-
-
Johns, L.E.1
Houlston, R.S.2
-
5
-
-
0037058317
-
After hMSH2 and hMLH1 - What next? Analysis of three-generational, population-based, early-onset colorectal cancer families
-
DOI 10.1002/ijc.10670
-
Jenkins MA, Baglietto L, Dite GS, Jolley DJ, Southey MC, Whitty J, et al. After hMSH2 and hMLH1 - what next? Analysis of three-generational, population-based, early-onset colorectal cancer families. Int J Cancer 2002;102:166-71. (Pubitemid 35168030)
-
(2002)
International Journal of Cancer
, vol.102
, Issue.2
, pp. 166-171
-
-
Jenkins, M.A.1
Baglietto, L.2
Dite, G.S.3
Jolley, D.J.4
Southey, M.C.5
Whitty, J.6
Mead, L.J.7
John, D.J.B.St.8
Macrae, F.A.9
Timothy, B.D.10
Venter, D.J.11
Giles, G.G.12
Hopper, J.L.13
-
6
-
-
35348992639
-
The genetics of hereditary colon cancer
-
DOI 10.1101/gad.1593107
-
Rustgi AK. The genetics of hereditary colon cancer. Genes Dev 2007;21:2525-38. (Pubitemid 47607664)
-
(2007)
Genes and Development
, vol.21
, Issue.20
, pp. 2525-2538
-
-
Rustgi, A.K.1
-
7
-
-
0032534069
-
A National Cancer Institute Workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
-
Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, et al. A National Cancer Institute Workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998;58:5248-57.
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
Sidransky, D.4
Eshleman, J.R.5
Burt, R.W.6
-
8
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, Syngal S, Chapelle Adl, Rüschoff J, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch Syndrome) and microsatellite instability. J Natl Cancer Inst 2004;96:261-8. (Pubitemid 38256271)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.4
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
De La, C.A.5
Ruschoff, J.6
Fishel, R.7
Lindor, N.M.8
Burgart, L.J.9
Hamelin, R.10
Hamilton, S.R.11
Hiatt, R.A.12
Jass, J.13
Lindblom, A.14
Lynch, H.T.15
Peltomaki, P.16
Ramsey, S.D.17
Rodriguez-Bigas, M.A.18
Vasen, H.F.A.19
Hawk, E.T.20
Barrett, J.C.21
Freedman, A.N.22
Srivastava, S.23
more..
-
9
-
-
33749065163
-
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan
-
DOI 10.1093/hmg/ddl231
-
Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, et al. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan. Hum Mol Genet 2006;15:2903-10. (Pubitemid 44458121)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.19
, pp. 2903-2910
-
-
Kemp, Z.1
Carvajal-Carmona, L.2
Spain, S.3
Barclay, E.4
Gorman, M.5
Martin, L.6
Jaeger, E.7
Brooks, N.8
Bishop, D.T.9
Thomas, H.10
Tomlinson, I.11
Papaemmanuil, E.12
Webb, E.13
Sellick, G.S.14
Wood, W.15
Evans, G.16
Lucassen, A.17
Maher, E.R.18
Houlston, R.S.19
-
10
-
-
43549105874
-
Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q
-
Picelli S, Vandrovcova J, Jones S, Djureinovic T, Skoglund J, Zhou X-L, et al. Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q. BMC Cancer 2008;8:87.
-
(2008)
BMC Cancer
, vol.8
, pp. 87
-
-
Picelli, S.1
Vandrovcova, J.2
Jones, S.3
Djureinovic, T.4
Skoglund, J.5
Zhou, X.-L.6
-
11
-
-
77952081574
-
Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer
-
Middeldorp A, Jagmohan-Changur SC, van der Klift HM, van Puijenbroek M, Houwing-Duistermaat JJ, Webb E, et al. Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer. Genes Chromosomes Cancer 2010;49:539-48.
-
(2010)
Genes Chromosomes Cancer
, vol.49
, pp. 539-548
-
-
Middeldorp, A.1
Jagmohan-Changur, S.C.2
Van Der Klift, H.M.3
Van Puijenbroek, M.4
Houwing-Duistermaat, J.J.5
Webb, E.6
-
12
-
-
84861655606
-
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22
-
Cicek MS, Cunningham JM, Fridley BL, Serie DJ, Bamlet WR, Diergaarde B, et al. Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22. PLoS ONE 2012;7:e38175.
-
(2012)
PLoS ONE
, vol.7
-
-
Cicek, M.S.1
Cunningham, J.M.2
Fridley, B.L.3
Serie, D.J.4
Bamlet, W.R.5
Diergaarde, B.6
-
13
-
-
55349101975
-
Common familial colorectal cancer linked to chromosome 7q31: A genome-wide analysis
-
Neklason DW, Kerber RA, Nilson DB, Anton-Culver H, Schwartz AG, Griffin CA, et al. Common familial colorectal cancer linked to chromosome 7q31: a genome-wide analysis. Cancer Res 2008;68:8993-7.
-
(2008)
Cancer Res
, vol.68
, pp. 8993-8997
-
-
Neklason, D.W.1
Kerber, R.A.2
Nilson, D.B.3
Anton-Culver, H.4
Schwartz, A.G.5
Griffin, C.A.6
-
14
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
DOI 10.1038/ng.111, PII NG111
-
Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Howarth K, Pittman AM, et al. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet 2008;40:623-30. (Pubitemid 351601204)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 623-630
-
-
Tomlinson, I.P.M.1
Webb, E.2
Carvajal-Carmona, L.3
Broderick, P.4
Howarth, K.5
Pittman, A.M.6
Spain, S.7
Lubbe, S.8
Walther, A.9
Sullivan, K.10
Jaeger, E.11
Fielding, S.12
Rowan, A.13
Vijayakrishnan, J.14
Domingo, E.15
Chandler, I.16
Kemp, Z.17
Qureshi, M.18
Farrington, S.M.19
Tenesa, A.20
Prendergast, J.G.D.21
Barnetson, R.A.22
Penegar, S.23
Barclay, E.24
Wood, W.25
Martin, L.26
Gorman, M.27
Thomas, H.28
Peto, J.29
Bishop, D.T.30
Gray, R.31
Maher, E.R.32
Lucassen, A.33
Kerr, D.34
Evans, D.G.R.35
Schafmayer, C.36
Buch, S.37
Volzke, H.38
Hampe, J.39
Schreiber, S.40
John, U.41
Koessler, T.42
Pharoah, P.43
Van Wezel, T.44
Morreau, H.45
Wijnen, J.T.46
Hopper, J.L.47
Southey, M.C.48
Giles, G.G.49
Severi, G.50
Castellvi-Bel, S.51
Ruiz-Ponte, C.52
Carracedo, A.53
Castells, A.54
Forsti, A.55
Hemminki, K.56
Vodicka, P.57
Naccarati, A.58
Lipton, L.59
Ho, J.W.C.60
Cheng, K.K.61
Sham, P.C.62
Luk, J.63
Agundez, J.A.G.64
Ladero, J.M.65
De La, H.M.66
Caldes, T.67
Niittymaki, I.68
Tuupanen, S.69
Karhu, A.70
Aaltonen, L.71
Cazier, J.-B.72
Campbell, H.73
Dunlop, M.G.74
Houlston, R.S.75
more..
-
15
-
-
0242363139
-
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2
-
DOI 10.1073/pnas.2132286100
-
Wiesner GL, Daley D, Lewis S, Ticknor C, Platzer P, Lutterbaugh J, et al. A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2. Proc Natl Acad Sci U S A 2003;100:12961-5. (Pubitemid 37340008)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.22
, pp. 12961-12965
-
-
Wiesner, G.L.1
Daley, D.2
Lewis, S.3
Ticknor, C.4
Platzer, P.5
Lutterbaugh, J.6
MacMillen, M.7
Baliner, B.8
Willis, J.9
Elston, R.C.10
Markowitz, S.D.11
-
16
-
-
33744907495
-
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
-
DOI 10.1158/0008-5472.CAN-05-4074
-
Kemp ZE, Carvajal-Carmona LG, Barclay E, Gorman M, Martin L, Wood W, et al. Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom. Cancer Res 2006;66:5003-6. (Pubitemid 43844919)
-
(2006)
Cancer Research
, vol.66
, Issue.10
, pp. 5003-5006
-
-
Kemp, Z.E.1
Carvajal-Carmona, L.G.2
Barclay, E.3
Gorman, M.4
Martin, L.5
Wood, W.6
Rowan, A.7
Donohue, C.8
Spain, S.9
Jaeger, E.10
Evans, D.G.11
Maher, E.R.12
Bishop, T.13
Thomas, H.14
Houlston, R.15
Tomlinson, I.16
-
17
-
-
33746905921
-
Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1
-
Skoglund J, Djureinovic T, Zhou X-L, Vandrovcova J, Renkonen E, Iselius L, et al. Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1. J Med Genet 2006;43:e07.
-
(2006)
J Med Genet
, vol.43
-
-
Skoglund, J.1
Djureinovic, T.2
Zhou, X.-L.3
Vandrovcova, J.4
Renkonen, E.5
Iselius, L.6
-
18
-
-
77954382262
-
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22
-
Gray-McGuire C, Guda K, Adrianto I, Lin CP, Natale L, Potter JD, et al. Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. Cancer Res 2010;70:5409-18.
-
(2010)
Cancer Res
, vol.70
, pp. 5409-5418
-
-
Gray-McGuire, C.1
Guda, K.2
Adrianto, I.3
Lin, C.P.4
Natale, L.5
Potter, J.D.6
-
19
-
-
33144458558
-
A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer
-
DOI 10.1136/gut.2005.075333
-
Djureinovic T, Skoglund J, Vandrovcova J, Zhou X-L, Kalushkova A, Iselius L, et al. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer. Gut 2006;55:362-6. (Pubitemid 43268274)
-
(2006)
Gut
, vol.55
, Issue.3
, pp. 362-366
-
-
Djureinovic, T.1
Skoglund, J.2
Vandrovcova, J.3
Zhou, X.-L.4
Kalushkova, A.5
Iselius, L.6
Lindblom, A.7
-
20
-
-
66449107196
-
The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression
-
Pittman AM, Naranjo S, Webb E, Broderick P, Lips EH, van Wezel T, et al. The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression. Genome Res 2009;19:987-93.
-
(2009)
Genome Res
, vol.19
, pp. 987-993
-
-
Pittman, A.M.1
Naranjo, S.2
Webb, E.3
Broderick, P.4
Lips, E.H.5
Van Wezel, T.6
-
21
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
DOI 10.1038/ng.133, PII NG133
-
Tenesa A, Farrington SM, Prendergast JGD, Porteous ME, Walker M, Haq N, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet 2008;40:631-7. (Pubitemid 351601219)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 631-637
-
-
Tenesa, A.1
Farrington, S.M.2
Prendergast, J.G.D.3
Porteous, M.E.4
Walker, M.5
Haq, N.6
Barnetson, R.A.7
Theodoratou, E.8
Cetnarskyj, R.9
Cartwright, N.10
Semple, C.11
Clark, A.J.12
Reid, F.J.L.13
Smith, L.A.14
Kavoussanakis, K.15
Koessler, T.16
Pharoah, P.D.P.17
Buch, S.18
Schafmayer, C.19
Tepel, J.20
Schreiber, S.21
Volzke, H.22
Schmidt, C.O.23
Hampe, J.24
Chang-Claude, J.25
Hoffmeister, M.26
Brenner, H.27
Wilkening, S.28
Canzian, F.29
Capella, G.30
Moreno, V.31
Deary, I.J.32
Starr, J.M.33
Tomlinson, I.P.M.34
Kemp, Z.35
Howarth, K.36
Carvajal-Carmona, L.37
Webb, E.38
Broderick, P.39
Vijayakrishnan, J.40
Houlston, R.S.41
Rennert, G.42
Ballinger, D.43
Rozek, L.44
Gruber, S.B.45
Matsuda, K.46
Kidokoro, T.47
Nakamura, Y.48
Zanke, B.W.49
Greenwood, C.M.T.50
Rangrej, J.51
Kustra, R.52
Montpetit, A.53
Hudson, T.J.54
Gallinger, S.55
Campbell, H.56
Dunlop, M.G.57
more..
-
22
-
-
78049353079
-
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
-
Houlston RS, Cheadle J, Dobbins SE, Tenesa A, Jones AM, Howarth K, et al. Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat Genet 2010;42:973-7.
-
(2010)
Nat Genet
, vol.42
, pp. 973-977
-
-
Houlston, R.S.1
Cheadle, J.2
Dobbins, S.E.3
Tenesa, A.4
Jones, A.M.5
Howarth, K.6
-
23
-
-
34547498546
-
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
-
DOI 10.1038/ng2085, PII NG2085
-
Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Kemp Z, Spain S, et al. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet 2007;39:984-8. (Pubitemid 47185182)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 984-988
-
-
Tomlinson, I.1
Webb, E.2
Carvajal-Carmona, L.3
Broderick, P.4
Kemp, Z.5
Spain, S.6
Penegar, S.7
Chandler, I.8
Gorman, M.9
Wood, W.10
Barclay, E.11
Lubbe, S.12
Martin, L.13
Sellick, G.14
Jaeger, E.15
Hubner, R.16
Wild, R.17
Rowan, A.18
Fielding, S.19
Howarth, K.20
Silver, A.21
Atkin, W.22
Muir, K.23
Logan, R.24
Kerr, D.25
Johnstone, E.26
Sieber, O.27
Gray, R.28
Thomas, H.29
Peto, J.30
Cazier, J.-B.31
Houlston, R.32
more..
-
24
-
-
34547092701
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
-
DOI 10.1038/ng2089, PII NG2089
-
Zanke BW, Greenwood CMT, Rangrej J, Kustra R, Tenesa A, Farrington SM, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet 2007;39:989-94. (Pubitemid 47185183)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 989-994
-
-
Zanke, B.W.1
Greenwood, C.M.2
Rangrej, J.3
Kustra, R.4
Tenesa, A.5
Farrington, S.M.6
Prendergast, J.7
Olschwang, S.8
Chiang, T.9
Crowdy, E.10
Ferretti, V.11
Laflamme, P.12
Sundararajan, S.13
Roumy, S.14
Olivier, J.-F.15
Robidoux, F.16
Sladek, R.17
Montpetit, A.18
Campbell, P.19
Bezieau, S.20
O'Shea, A.M.21
Zogopoulos, G.22
Cotterchio, M.23
Newcomb, P.24
McLaughlin, J.25
Younghusband, B.26
Green, R.27
Green, J.28
Porteous, M.E.M.29
Campbell, H.30
Blanche, H.31
Sahbatou, M.32
Tubacher, E.33
Bonaiti-Pellie, C.34
Buecher, B.35
Riboli, E.36
Kury, S.37
Chanock, S.J.38
Potter, J.39
Thomas, G.40
Gallinger, S.41
Hudson, T.J.42
Dunlop, M.G.43
more..
-
25
-
-
37049032569
-
Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: Results from the colon cancer family registry
-
DOI 10.1158/0008-5472.CAN-07-3239
-
Poynter JN, Figueiredo JC, Conti DV, Kennedy K, Gallinger S, Siegmund KD, et al. Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry. Cancer Res 2007;67:11128-32. (Pubitemid 350248536)
-
(2007)
Cancer Research
, vol.67
, Issue.23
, pp. 11128-11132
-
-
Poynter, J.N.1
Figueiredo, J.C.2
Conti, D.V.3
Kennedy, K.4
Gallinger, S.5
Siegmund, K.D.6
Casey, G.7
Thibodeau, S.N.8
Jenkins, M.A.9
Hopper, J.L.10
Byrnes, G.B.11
Baron, J.A.12
Goode, E.L.13
Tiirikainen, M.14
Lindor, N.15
Grove, J.16
Newcomb, P.17
Jass, J.18
Young, J.19
Potter, J.D.20
Haile, R.W.21
Duggan, D.J.22
Le, M.L.23
more..
-
26
-
-
56749176944
-
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
-
(COGENT) CCG
-
(COGENT) CCG. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet 2008;40:1426-35.
-
(2008)
Nat Genet
, vol.40
, pp. 1426-1435
-
-
-
27
-
-
35648937584
-
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
-
DOI 10.1038/ng.2007.18, PII NG200718
-
Broderick P, Carvajal-Carmona L, Pittman AM, Webb E, Howarth K, Rowan A, et al. A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet 2007;39:1315-7. (Pubitemid 350034998)
-
(2007)
Nature Genetics
, vol.39
, Issue.11
, pp. 1315-1317
-
-
Broderick, P.1
Carvajal-Carmona, L.2
Pittman, A.M.3
Webb, E.4
Howarth, K.5
Rowan, A.6
Lubbe, S.7
Spain, S.8
Sullivan, K.9
Fielding, S.10
Jaeger, E.11
Vijayakrishnan, J.12
Kemp, Z.13
Gorman, M.14
Chandler, I.15
Papaemmanuil, E.16
Penegar, S.17
Wood, W.18
Sellick, G.19
Qureshi, M.20
Teixeira, A.21
Domingo, E.22
Barclay, E.23
Martin, L.24
Sieber, O.25
Kerr, D.26
Gray, R.27
Peto, J.28
Cazier, J.-B.29
Tomlinson, I.30
Houlston, R.S.31
more..
-
28
-
-
79955860324
-
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population
-
Cui R, Okada Y, Jang SG, Ku JL, Park JG, Kamatani Y, et al. Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. Gut 2011;60:799-805.
-
(2011)
Gut
, vol.60
, pp. 799-805
-
-
Cui, R.1
Okada, Y.2
Jang, S.G.3
Ku, J.L.4
Park, J.G.5
Kamatani, Y.6
-
29
-
-
84856703651
-
Meta-analysis of new genome-wide association studies of colorectal cancer risk
-
Peters U, Hutter C, Hsu L, Schumacher F, Conti D, Carlson C, et al. Meta-analysis of new genome-wide association studies of colorectal cancer risk. Hum Genet 2012;131:217-34.
-
(2012)
Hum Genet
, vol.131
, pp. 217-234
-
-
Peters, U.1
Hutter, C.2
Hsu, L.3
Schumacher, F.4
Conti, D.5
Carlson, C.6
-
30
-
-
84863005628
-
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk
-
Dunlop MG, Dobbins SE, Farrington SM, Jones AM, Palles C, Whiffin N, et al. Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. Nat Genet 2012;44:770-6.
-
(2012)
Nat Genet
, vol.44
, pp. 770-776
-
-
Dunlop, M.G.1
Dobbins, S.E.2
Farrington, S.M.3
Jones, A.M.4
Palles, C.5
Whiffin, N.6
-
31
-
-
76649122154
-
Detecting rare variants for complex traits using family and unrelated data
-
Zhu X, Feng T, Li Y, Lu Q, Elston RC. Detecting rare variants for complex traits using family and unrelated data. Genet Epidemiol 2010;34:171-87.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 171-187
-
-
Zhu, X.1
Feng, T.2
Li, Y.3
Lu, Q.4
Elston, R.C.5
-
32
-
-
80051827842
-
Optimum designs for next-generation sequencing to discover rare variants for common complex disease
-
Shi G, Rao DC. Optimum designs for next-generation sequencing to discover rare variants for common complex disease. Genet Epidemiol 2011;35:572-9.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 572-579
-
-
Shi, G.1
Rao, D.C.2
-
33
-
-
81255175654
-
Study designs for identification of rare disease variants in complex diseases: The utility of family-based designs
-
Ionita-Laza I, Ottman R. Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs. Genetics 2011;189:1061-8.
-
(2011)
Genetics
, vol.189
, pp. 1061-1068
-
-
Ionita-Laza, I.1
Ottman, R.2
-
34
-
-
84862152665
-
Family-based association studies for next-generation sequencing
-
Zhu Y, Xiong M. Family-based association studies for next-generation sequencing. Am J Hum Genet 2012;90:1028-45.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 1028-1045
-
-
Zhu, Y.1
Xiong, M.2
-
35
-
-
84864562836
-
Gene discovery in familial cancer syndromes by exome sequencing: Prospects for the elucidation of familial colorectal cancer type X
-
Ku C-S, Cooper DN, Wu M, Roukos DH, Pawitan Y, Soong R, et al. Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. Mod Pathol 2012;25:1055-68.
-
(2012)
Mod Pathol
, vol.25
, pp. 1055-1068
-
-
Ku, C.-S.1
Cooper, D.N.2
Wu, M.3
Roukos, D.H.4
Pawitan, Y.5
Soong, R.6
-
36
-
-
84863922124
-
Comprehensive molecular characterization of human colon and rectal cancer
-
Cancer Genome Atlas Network
-
Cancer Genome Atlas Network. Comprehensive molecular characterization of human colon and rectal cancer. Nature 2012;487:330-7.
-
(2012)
Nature
, vol.487
, pp. 330-337
-
-
-
37
-
-
38849170356
-
Colon cancer family registry: An international resource for studies of the genetic epidemiology of colon cancer
-
DOI 10.1158/1055-9965.EPI-07-0648
-
Newcomb PA, Baron J, Cotterchio M, Gallinger S, Grove J, Haile R, et al. Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. Cancer Epidemiol Biomarkers Prev 2007;16:2331-43. (Pubitemid 351196365)
-
(2007)
Cancer Epidemiology Biomarkers and Prevention
, vol.16
, Issue.11
, pp. 2331-2343
-
-
Newcomb, P.A.1
Baron, J.2
Cotterchio, M.3
Gallinger, S.4
Grove, J.5
Haile, R.6
Hall, D.7
Hopper, J.L.8
Jass, J.9
Le, M.L.10
Limburg, P.11
Lindor, N.12
Potter, J.D.13
Templeton, A.S.14
Thibodeau, S.15
Seminara, D.16
-
38
-
-
33847107140
-
Very high incidence of familial colorectal cancer in Newfoundland: A comparison with Ontario and 13 other population-based studies
-
DOI 10.1007/s10689-006-9104-x
-
Green R, Green J, Buehler S, Robb J, Daftary D, Gallinger S, et al. Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies. Fam Cancer 2007;6:53-62. (Pubitemid 46295298)
-
(2007)
Familial Cancer
, vol.6
, Issue.1
, pp. 53-62
-
-
Green, R.C.1
Green, J.S.2
Buehler, S.K.3
Robb, J.D.4
Daftary, D.5
Gallinger, S.6
McLaughlin, J.R.7
Parfrey, P.S.8
Younghusband, H.B.9
-
39
-
-
33847090714
-
The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
-
DOI 10.1007/s10689-006-0014-8
-
Stuckless S, Parfrey P, Woods M, Cox J, Fitzgerald G, Green J, et al. The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome. Fam Cancer 2007;6:1-12. (Pubitemid 46295291)
-
(2007)
Familial Cancer
, vol.6
, Issue.1
, pp. 1-12
-
-
Stuckless, S.1
Parfrey, P.S.2
Woods, M.O.3
Cox, J.4
Fitzgerald, G.W.5
Green, J.S.6
Green, R.C.7
-
40
-
-
84862929636
-
TREAT: A bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data
-
Asmann YW, Middha S, Hossain A, Baheti S, Li Y, Chai H-S, et al. TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data. Bioinformatics 2012;28:277-8.
-
(2012)
Bioinformatics
, vol.28
, pp. 277-278
-
-
Asmann, Y.W.1
Middha, S.2
Hossain, A.3
Baheti, S.4
Li, Y.5
Chai, H.-S.6
-
41
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
Li H, Durbin R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 2010;26:589-95.
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
42
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The sequence alignment/map format and SAMtools. Bioinformatics 2009;25:2078-9.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
-
43
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009;25:1754-60.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
44
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 2010;20:1297-303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
-
45
-
-
77951957381
-
SNVMix: Predicting single nucleotide variants from next-generation sequencing of tumors
-
Goya R, Sun MGF, Morin RD, Leung G, Ha G, Wiegand KC, et al. SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors. Bioinformatics 2010;26:730-6.
-
(2010)
Bioinformatics
, vol.26
, pp. 730-736
-
-
Goya, R.1
Sun, M.G.F.2
Morin, R.D.3
Leung, G.4
Ha, G.5
Wiegand, K.C.6
-
46
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium
-
1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, et al. A map of human genome variation from population-scale sequencing. Nature 2010;467:1061-73.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
Brooks, L.D.4
Durbin, R.M.5
-
47
-
-
12344280017
-
Summaries of Affymetrix GeneChip probe level data
-
Irizarry RA, Bolstad BM, Collin F, Cope LM, Hobbs B, Speed TP. Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res 2003;31:e15.
-
(2003)
Nucleic Acids Res
, vol.31
-
-
Irizarry, R.A.1
Bolstad, B.M.2
Collin, F.3
Cope, L.M.4
Hobbs, B.5
Speed, T.P.6
-
48
-
-
0036338150
-
Merlin - rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis G, Cherny S, Cookson W, Cardon L. Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.1
Cherny, S.2
Cookson, W.3
Cardon, L.4
-
49
-
-
79961151538
-
Design considerations for massively parallel sequencing studies of complex human disease
-
Feng B-J, Tavtigian SV, Southey MC, Goldgar DE. Design considerations for massively parallel sequencing studies of complex human disease. PLoS ONE 2011;6:e23221.
-
(2011)
PLoS ONE
, vol.6
-
-
Feng, B.-J.1
Tavtigian, S.V.2
Southey, M.C.3
Goldgar, D.E.4
-
50
-
-
8044228419
-
Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population
-
DOI 10.1093/hmg/6.2.285
-
Dunning AM, Chiano M, Smith NR, Dearden J, Gore M, Oakes S, et al. Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population. Hum Mol Genet 1997;6:285-9. (Pubitemid 27078085)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.2
, pp. 285-289
-
-
Dunning, A.M.1
Chiano, M.2
Smith, N.R.3
Dearden, J.4
Gore, M.5
Oakes, S.6
Wilson, C.7
Stratton, M.8
Peto, J.9
Easton, D.10
Clayton, D.11
Ponder, B.A.J.12
-
51
-
-
80051473676
-
Shroom3 and a Pitx2-N-cadherin pathway function cooperatively to generate asymmetric cell shape changes during gut morphogenesis
-
Plageman TF Jr, Zacharias AL, Gage PJ, Lang RA. Shroom3 and a Pitx2-N-cadherin pathway function cooperatively to generate asymmetric cell shape changes during gut morphogenesis. Dev Biol 2011;357:227-34.
-
(2011)
Dev Biol
, vol.357
, pp. 227-234
-
-
Plageman Jr., T.F.1
Zacharias, A.L.2
Gage, P.J.3
Lang, R.A.4
-
52
-
-
80755169008
-
A Trio-RhoA-Shroom3 pathway is required for apical constriction and epithelial invagination
-
Plageman TF, Chauhan BK, Yang C, Jaudon F, Shang X, Zheng Y, et al. A Trio-RhoA-Shroom3 pathway is required for apical constriction and epithelial invagination. Development 2011;138:5177-88.
-
(2011)
Development
, vol.138
, pp. 5177-5188
-
-
Plageman, T.F.1
Chauhan, B.K.2
Yang, C.3
Jaudon, F.4
Shang, X.5
Zheng, Y.6
-
53
-
-
80051540469
-
Identification and characterization of a set of conserved and new regulators of cytoskeletal organization, cell morphology and migration
-
Bai S, Herrera-Abreu M, Rohn J, Racine V, Tajadura V, Suryavanshi N, et al. Identification and characterization of a set of conserved and new regulators of cytoskeletal organization, cell morphology and migration. BMC Biol 2011;9:54.
-
(2011)
BMC Biol
, vol.9
, pp. 54
-
-
Bai, S.1
Herrera-Abreu, M.2
Rohn, J.3
Racine, V.4
Tajadura, V.5
Suryavanshi, N.6
-
54
-
-
0029028237
-
CDC27Hs colocalizes with CDC16Hs to the centrosome and mitotic spindle and is essential for the metaphase to anaphase transition
-
Tugendreich S, Tomkiel J, Earnshaw W, Hieter P. CDC27Hs colocalizes with CDC16Hs to the centrosome and mitotic spindle and is essential for the metaphase to anaphase transition. Cell 1995;81:261-8.
-
(1995)
Cell
, vol.81
, pp. 261-268
-
-
Tugendreich, S.1
Tomkiel, J.2
Earnshaw, W.3
Hieter, P.4
-
55
-
-
0036744787
-
Unstable kinetochore-microtubule capture and chromosomal instability following deletion of CENP-E
-
Putkey FR, Cramer T, Morphew MK, Silk AD, Johnson RS, McIntosh JR, et al. Unstable kinetochore-microtubule capture and chromosomal instability following deletion of CENP-E. Dev Cell 2002;3:351-65.
-
(2002)
Dev Cell
, vol.3
, pp. 351-365
-
-
Putkey, F.R.1
Cramer, T.2
Morphew, M.K.3
Silk, A.D.4
Johnson, R.S.5
McIntosh, J.R.6
-
56
-
-
33845657930
-
The DNA helicase ChlR1 is required for sister chromatid cohesion in mammalian cells
-
DOI 10.1242/jcs.03262
-
Parish JL, Rosa J, Wang X, Lahti JM, Doxsey SJ, Androphy EJ. The DNA helicase ChlR1 is required for sister chromatid cohesion in mammalian cells. J Cell Sci 2006;119:4857-65. (Pubitemid 46017799)
-
(2006)
Journal of Cell Science
, vol.119
, Issue.23
, pp. 4857-4865
-
-
Parish, J.L.1
Rosa, J.2
Wang, X.3
Lahti, J.M.4
Doxsey, S.J.5
Androphy, E.J.6
-
57
-
-
58149293621
-
FAM29A promotes microtubule amplification via recruitment of the NEDD1-γ-tubulin complex to the mitotic spindle
-
Zhu H, Coppinger JA, Jang C-Y, Yates JR, Fang G. FAM29A promotes microtubule amplification via recruitment of the NEDD1-γ-tubulin complex to the mitotic spindle. J Cell Biol 2008;183:835-48.
-
(2008)
J Cell Biol
, vol.183
, pp. 835-848
-
-
Zhu, H.1
Coppinger, J.A.2
Jang, C.-Y.3
Yates, J.R.4
Fang, G.5
-
58
-
-
0036429193
-
The human and mouse replication-dependent histone genes
-
DOI 10.1016/S0888-7543(02)96850-3
-
Marzluff WF, Gongidi P, Woods KR, Jin J, Maltais LJ. The human and mouse replication-dependent histone genes. Genomics 2002;80:487-98. (Pubitemid 35333791)
-
(2002)
Genomics
, vol.80
, Issue.5
, pp. 487-498
-
-
Marzluff, W.F.1
Gongidi, P.2
Woods, K.R.3
Jin, J.4
Maltais, L.J.5
-
59
-
-
4344561301
-
Molecular interactions of Polo-like-kinase 1 with the mitotic kinesin-like protein CHO1/MKLP-1
-
DOI 10.1242/jcs.01173
-
Liu X, Zhou T, Kuriyama R, Erikson RL. Molecular interactions of Polo-like-kinase 1 with themitotic kinesin-like protein CHO1/MKLP-1. JCell Sci 2004;117:3233-46. (Pubitemid 39139909)
-
(2004)
Journal of Cell Science
, vol.117
, Issue.15
, pp. 3233-3246
-
-
Liu, X.1
Zhou, T.2
Kuriyama, R.3
Erikson, R.L.4
-
60
-
-
4143116899
-
TTK kinase is essential for the centrosomal localization of TACC2
-
DOI 10.1016/j.febslet.2004.06.092, PII S0014579304008634
-
Dou Z, Ding X, Zereshki A, Zhang Y, Zhang J, Wang F, et al. TTK kinase is essential for the centrosomal localization of TACC2. FEBS Lett 2004;572:51-6. (Pubitemid 39092512)
-
(2004)
FEBS Letters
, vol.572
, Issue.1-3
, pp. 51-56
-
-
Dou, Z.1
Ding, X.2
Zereshki, A.3
Zhang, Y.4
Zhang, J.5
Wang, F.6
Sun, J.7
Huang, H.8
Yao, X.9
-
61
-
-
22144495367
-
NIPA defines an SCF-type mammalian E3 ligase that regulates mitotic entry
-
DOI 10.1016/j.cell.2005.04.034, PII S0092867405004587
-
Bassermann F, von Klitzing C, Münch S, Bai R-Y, Kawaguchi H, Morris SW, et al. NIPA defines an SCF-type mammalian E3 ligase that regulates mitotic entry. Cell 2005;122:45-57. (Pubitemid 40977939)
-
(2005)
Cell
, vol.122
, Issue.1
, pp. 45-57
-
-
Bassermann, F.1
Von Klitzing, C.2
Munch, S.3
Bai, R.-Y.4
Kawaguchi, H.5
Morris, S.W.6
Peschel, C.7
Duyster, J.8
-
62
-
-
0037134457
-
CARD-8 protein, a new CARD family member that regulates caspase-1 activation and apoptosis
-
DOI 10.1074/jbc.M107811200
-
Razmara M, Srinivasula SM, Wang L, Poyet J-L, Geddes BJ, DiStefano PS, et al. CARD-8 rrotein, a new CARD family member that regulates caspase-1 activation and apoptosis. J Biol Chem2002;277:13952-8. (Pubitemid 34968002)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.16
, pp. 13952-13958
-
-
Razmara, M.1
Srinivasula, S.M.2
Wang, L.3
Poyet, J.-L.4
Geddes, B.J.5
Distefano, P.S.6
Bertin, J.7
Alnemri, E.S.8
-
63
-
-
0033500156
-
Identification of CtBP1 and CtBP2 as corepressors of zinc finger- homeodomain factor δEF1
-
Furusawa T, Moribe H, Kondoh H, Higashi Y. Identification of CtBP1 and CtBP2 as corepressors of zinc finger-homeodomain factor δEF1. Mol Cell Biol 1999;19:8581-90. (Pubitemid 30414051)
-
(1999)
Molecular and Cellular Biology
, vol.19
, Issue.12
, pp. 8581-8590
-
-
Furusawa, T.1
Moribe, H.2
Kondoh, H.3
Higashi, Y.4
-
64
-
-
0242669199
-
Coordinated histone modifications mediated by a CtBP co-repressor complex
-
DOI 10.1038/nature01550
-
Shi Y, Sawada J-i, Sui G, Affar EB, Whetstine JR, Lan F, et al. Coordinated histone modifications mediated by a CtBP co-repressor complex. Nature 2003;422:735-8. (Pubitemid 36514114)
-
(2003)
Nature
, vol.422
, Issue.6933
, pp. 735-738
-
-
Shi, Y.1
Sawada, J.-I.2
Sui, G.3
Affar, E.B.4
Whetstine, J.R.5
Lan, F.6
Ogawa, H.7
Luke, M.P.-S.8
Nakatani, Y.9
Shi, Y.10
-
65
-
-
0036311933
-
Multiple regulatory domains of IRF-5 control activation, cellular localization, and induction of chemokines that mediate recruitment of T lymphocytes
-
DOI 10.1128/MCB.22.16.5721-5740.2002
-
Barnes BJ, Kellum MJ, Field AE, Pitha PM. Multiple regulatory domains of IRF-5 control activation, cellular localization, and induction of chemokines that mediate recruitment of T lymphocytes. Mol Cell Biol 2002;22:5721-40. (Pubitemid 34815822)
-
(2002)
Molecular and Cellular Biology
, vol.22
, Issue.16
, pp. 5721-5740
-
-
Barnes, B.J.1
Kellum, M.J.2
Field, A.E.3
Pitha, P.M.4
-
66
-
-
34548720441
-
Role of MED12 in transcription and human behavior
-
DOI 10.2217/14622416.8.8.909
-
Philibert RA, Madan A. Role of MED12 in transcription and human behavior. Pharmacogenomics 2007;8:909-16. (Pubitemid 47430441)
-
(2007)
Pharmacogenomics
, vol.8
, Issue.8
, pp. 909-916
-
-
Philibert, R.A.1
Madan, A.2
-
67
-
-
34548238145
-
Arkadia activates Smad3/Smad4-dependent transcription by triggering signal-induced SnoN degradation
-
DOI 10.1128/MCB.00664-07
-
Levy L, Howell M, Das D, Harkin S, Episkopou V, Hill CS. Arkadia activates Smad3/Smad4-dependent transcription by triggering signal-induced SnoN degradation. Mol Cell Biol 2007;27:6068-83. (Pubitemid 47326695)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.17
, pp. 6068-6083
-
-
Levy, L.1
Howell, M.2
Das, D.3
Harkin, S.4
Episkopou, V.5
Hill, C.S.6
-
68
-
-
0031010818
-
Steroidogenic factor 1: A key determinant of endocrine development and function
-
DOI 10.1210/er.18.3.361
-
Parker KL, Schimmer BP. Steroidogenic factor 1: a key determinant of endocrine development and function. Endocr Rev 1997;18:361-77. (Pubitemid 27246881)
-
(1997)
Endocrine Reviews
, vol.18
, Issue.3
, pp. 361-377
-
-
Parker, K.L.1
Schimmer, B.P.2
-
69
-
-
77749270561
-
Transcriptional corepressor TLE1 functions with Runx2 in epigenetic repression of ribosomal RNA genes
-
Ali SA, Zaidi SK, Dobson JR, Shakoori AR, Lian JB, Stein JL, et al. Transcriptional corepressor TLE1 functions with Runx2 in epigenetic repression of ribosomal RNA genes. Proc Natl Acad Sci U S A 2010;107:4165-9.
-
(2010)
Proc Natl Acad Sci U S a
, vol.107
, pp. 4165-4169
-
-
Ali, S.A.1
Zaidi, S.K.2
Dobson, J.R.3
Shakoori, A.R.4
Lian, J.B.5
Stein, J.L.6
-
70
-
-
0036040358
-
A new Groucho TLE4 protein may regulate the repressive activity of Pax5 in human B lymphocytes
-
Milili M, Gauthier L, Veran J, Mattei M-G, Schiff C. A new Groucho TLE4 protein may regulate the repressive activity of Pax5 in human B lymphocytes. Immunology 2002;106:447-55.
-
(2002)
Immunology
, vol.106
, pp. 447-455
-
-
Milili, M.1
Gauthier, L.2
Veran, J.3
Mattei, M.-G.4
Schiff, C.5
-
71
-
-
0028876893
-
Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor
-
Lee JW, Choi HS, Gyuris J, Brent R, Moore DD. Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor. Mol Endocrinol 1995;9:243-54.
-
(1995)
Mol Endocrinol
, vol.9
, pp. 243-254
-
-
Lee, J.W.1
Choi, H.S.2
Gyuris, J.3
Brent, R.4
Moore, D.D.5
-
72
-
-
33846491444
-
BTNL2, a butyrophilin/B7-like molecule, is a negative costimulatory molecule modulated in intestinal inflammation
-
Arnett HA, Escobar SS, Gonzalez-Suarez E, Budelsky AL, Steffen LA, Boiani N, et al. BTNL2, a butyrophilin/B7-like molecule, is a negative costimulatory molecule modulated in intestinal inflammation. J Immunol 2007;178:1523-33. (Pubitemid 46154623)
-
(2007)
Journal of Immunology
, vol.178
, Issue.3
, pp. 1523-1533
-
-
Arnett, H.A.1
Escobar, S.S.2
Gonzalez-Suarez, E.3
Budelsky, A.L.4
Steffen, L.A.5
Boiani, N.6
Zhang, M.7
Siu, G.8
Brewer, A.W.9
Viney, J.L.10
-
73
-
-
0028952240
-
BAGE: A new gene encoding an antigen recognized on human melanomas by cytolytic T lymphocytes
-
Boël P, Wildmann C, Sensi ML, Brasseur R, Renauld J-C, Coulie P, et al. BAGE: a new gene encoding an antigen recognized on human melanomas by cytolytic T lymphocytes. Immunity 1995;2:167-75.
-
(1995)
Immunity
, vol.2
, pp. 167-175
-
-
Boël, P.1
Wildmann, C.2
Sensi, M.L.3
Brasseur, R.4
Renauld, J.-C.5
Coulie, P.6
-
74
-
-
79958251632
-
Fank1 interacts with Jab1 and regulates cell apoptosis via the AP-1 pathway
-
Wang H, Song W, Hu T, Zhang N, Miao S, Zong S, et al. Fank1 interacts with Jab1 and regulates cell apoptosis via the AP-1 pathway. Cell Mol Life Sci 2011;68:2129-39.
-
(2011)
Cell Mol Life Sci
, vol.68
, pp. 2129-2139
-
-
Wang, H.1
Song, W.2
Hu, T.3
Zhang, N.4
Miao, S.5
Zong, S.6
-
75
-
-
0036214286
-
Structure and function of natural killer cell receptors: Multiple molecular solutions to self, nonself discrimination
-
DOI 10.1146/annurev.immunol.20.100301.064812
-
Natarajan K, Dimasi N, Wang J, Mariuzza RA, Margulies DH. Structure and function of natural killer cell receptors: multiple molecular solutions to self, nonself discrimination. Annu Rev Immunol 2002;20:853-85. (Pubitemid 34293442)
-
(2002)
Annual Review of Immunology
, vol.20
, pp. 853-885
-
-
Natarajan, K.1
Dimasi, N.2
Wang, J.3
Mariuzza, R.A.4
Margulies, D.H.5
-
76
-
-
82455184700
-
Mannose-binding lectin and the balance between immune protection and complication
-
Takahashi K. Mannose-binding lectin and the balance between immune protection and complication. Expert Rev Anti Infect Ther 2011;9:1179-90.
-
(2011)
Expert Rev Anti Infect Ther
, vol.9
, pp. 1179-1190
-
-
Takahashi, K.1
-
78
-
-
77956642100
-
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
-
Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, et al. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat Genet 2010;42:790-3.
-
(2010)
Nat Genet
, vol.42
, pp. 790-793
-
-
Ng, S.B.1
Bigham, A.W.2
Buckingham, K.J.3
Hannibal, M.C.4
McMillin, M.J.5
Gildersleeve, H.I.6
-
79
-
-
73349110071
-
Exome sequencing identifies the cause of a Mendelian disorder
-
Ng SB, Buckingham KJ, Lee C, Bigham AW, Tabor HK, Dent KM, et al. Exome sequencing identifies the cause of a Mendelian disorder. Nat Genet 2010;42:30-5.
-
(2010)
Nat Genet
, vol.42
, pp. 30-35
-
-
Ng, S.B.1
Buckingham, K.J.2
Lee, C.3
Bigham, A.W.4
Tabor, H.K.5
Dent, K.M.6
-
80
-
-
84858076515
-
Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts
-
Polvi A, Linnankivi T, Kivelä T, Herva R, Keating James P, Mäkitie O, et al. Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts. Am J Hum Genet 2012;90:540-9.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 540-549
-
-
Polvi, A.1
Linnankivi, T.2
Kivelä, T.3
Herva, R.4
Keating James, P.5
Mäkitie, O.6
-
81
-
-
77954158128
-
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene
-
Sobreira NLM, Cirulli ET, Avramopoulos D, Wohler E, Oswald GL, Stevens EL, et al. Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene. PLoS Genet 2010;6:e1000991.
-
(2010)
PLoS Genet
, vol.6
-
-
Sobreira, N.L.M.1
Cirulli, E.T.2
Avramopoulos, D.3
Wohler, E.4
Oswald, G.L.5
Stevens, E.L.6
-
82
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli ET, Goldstein DB. Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat Rev Genet 2010;11:415-25.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
83
-
-
0024602536
-
Estimating the power of a proposed linkage study for a complex genetic trait
-
Ploughman LM, Boehnke M. Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet 1989;44:543-51. (Pubitemid 19095400)
-
(1989)
American Journal of Human Genetics
, vol.44
, Issue.4
, pp. 543-551
-
-
Ploughman, L.M.1
Boehnke, M.2
-
84
-
-
0025848680
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen HFA, Mecklin JP, Khan PM, Lynch HT. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 1991;34:424-5.
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.A.1
Mecklin, J.P.2
Khan, P.M.3
Lynch, H.T.4
-
85
-
-
20244386256
-
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
DOI 10.1001/jama.293.16.1979
-
Lindor NM, Rabe K, Petersen GM, Haile R, Casey G, Baron J, et al. Lower cancer incidence in Amsterdam-i criteria families without mismatch repair deficiency: familial colorectal cancer type x. JAMA 2005;293:1979-85. (Pubitemid 40570891)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.M.3
Haile, R.4
Casey, G.5
Baron, J.6
Gallinger, S.7
Bapat, B.8
Aronson, M.9
Hopper, J.10
Jass, J.11
LeMarchand, L.12
Grove, J.13
Potter, J.14
Newcomb, P.15
Terdiman, J.P.16
Conrad, P.17
Moslein, G.18
Goldberg, R.19
Ziogas, A.20
Anton-Culver, H.21
De Andrade, M.22
Siegmund, K.23
Thibodeau, S.N.24
Boardman, L.A.25
Seminara, D.26
more..
-
86
-
-
80052825195
-
The functional spectrum of low-frequency coding variation
-
Marth G, Yu F, Indap A, Garimella K, Gravel S, Leong W, et al. The functional spectrum of low-frequency coding variation. Genome Biol 2011;12:R84.
-
(2011)
Genome Biol
, vol.12
-
-
Marth, G.1
Yu, F.2
Indap, A.3
Garimella, K.4
Gravel, S.5
Leong, W.6
|