-
1
-
-
33645307434
-
Pathogenetic mechanisms in thyroid follicular-cell neoplasia
-
Kondo T, Ezzat S, Asa SL. Pathogenetic mechanisms in thyroid follicular-cell neoplasia. Nat Rev Cancer 2006;6:292-306.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 292-306
-
-
Kondo, T.1
Ezzat, S.2
Asa, S.L.3
-
2
-
-
0028143018
-
Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands
-
Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst 1994;86:1600-8.
-
(1994)
J Natl Cancer Inst
, vol.86
, pp. 1600-1608
-
-
Goldgar, D.E.1
Easton, D.F.2
Cannon-Albright, L.A.3
Skolnick, M.H.4
-
3
-
-
63449092713
-
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
-
Gudmundsson J, Sulem P, Gudbjartsson DF, Jonasson JG, Sigurdsson A, Bergthorsson JT, He H, Blondal T, Geller F, Jakobsdottir M, Magnusdottir DN, Matthiasdottir S, Stacey SN, Skarphedinsson OB, Helgadottir H, Li W, Nagy R, Aguillo E, Faure E, Prats E, Saez B, Martinez M, Eyjolfsson GI, Bjornsdottir US, Holm H, Kristjansson K, Frigge ML, Kristvinsson H, Gulcher JR, Jonsson T, Rafnar T, Hjartarsson H, Mayordomo JI, de la Chapelle A, Hrafnkelsson J, Thorsteinsdottir U, Kong A, Stefansson K. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet 2009;41:460-4.
-
(2009)
Nat Genet
, vol.41
, pp. 460-464
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
Jonasson, J.G.4
Sigurdsson, A.5
Bergthorsson, J.T.6
He, H.7
Blondal, T.8
Geller, F.9
Jakobsdottir, M.10
Magnusdottir, D.N.11
Matthiasdottir, S.12
Stacey, S.N.13
Skarphedinsson, O.B.14
Helgadottir, H.15
Li, W.16
Nagy, R.17
Aguillo, E.18
Faure, E.19
Prats, E.20
Saez, B.21
Martinez, M.22
Eyjolfsson, G.I.23
Bjornsdottir, U.S.24
Holm, H.25
Kristjansson, K.26
Frigge, M.L.27
Kristvinsson, H.28
Gulcher, J.R.29
Jonsson, T.30
Rafnar, T.31
Hjartarsson, H.32
Mayordomo, J.I.33
de la Chapelle, A.34
Hrafnkelsson, J.35
Thorsteinsdottir, U.36
Kong, A.37
Stefansson, K.38
more..
-
4
-
-
60849084449
-
Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancer
-
Jazdzewski K, Liyanarachchi S, Swierniak M, Pachucki J, Ringel MD, Jarzab B, de la Chapelle A. Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancer. Proc Natl Acad Sci U S A 2009;106:1502-5.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 1502-1505
-
-
Jazdzewski, K.1
Liyanarachchi, S.2
Swierniak, M.3
Pachucki, J.4
Ringel, M.D.5
Jarzab, B.6
de la Chapelle, A.7
-
5
-
-
35148844645
-
Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma
-
Ruiz-Llorente S, Montero-Conde C, Milne RL, Moya CM, Cebrian A, Leton R, Cascon A, Mercadillo F, Landa I, Borrego S, Perez de Nanclares G, Alvarez-Escola C, Diaz-Perez JA, Carracedo A, Urioste M, Gonzalez-Neira A, Benitez J, Santisteban P, Dopazo J, Ponder BA, Robledo M. Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma. Cancer Res 2007;67:9561-7.
-
(2007)
Cancer Res
, vol.67
, pp. 9561-9567
-
-
Ruiz-Llorente, S.1
Montero-Conde, C.2
Milne, R.L.3
Moya, C.M.4
Cebrian, A.5
Leton, R.6
Cascon, A.7
Mercadillo, F.8
Landa, I.9
Borrego, S.10
Perez de Nanclares, G.11
Alvarez-Escola, C.12
Diaz-Perez, J.A.13
Carracedo, A.14
Urioste, M.15
Gonzalez-Neira, A.16
Benitez, J.17
Santisteban, P.18
Dopazo, J.19
Ponder, B.A.20
Robledo, M.21
more..
-
6
-
-
57149102908
-
A range of cancers is associated with the rs6983267 marker on chromosome 8
-
Wokolorczyk D, Gliniewicz B, Sikorski A, Zlowocka E, Masojc B, Debniak T, Matyjasik J, Mierzejewski M, Medrek K, Oszutowska D, Suchy J, Gronwald J, Teodorczyk U, Huzarski T, Byrski T, Jakubowska A, Gorski B, van de Wetering T, Walczak S, Narod SA, Lubinski J, Cybulski C. A range of cancers is associated with the rs6983267 marker on chromosome 8. Cancer Res 2008;68:9982-6.
-
(2008)
Cancer Res
, vol.68
, pp. 9982-9986
-
-
Wokolorczyk, D.1
Gliniewicz, B.2
Sikorski, A.3
Zlowocka, E.4
Masojc, B.5
Debniak, T.6
Matyjasik, J.7
Mierzejewski, M.8
Medrek, K.9
Oszutowska, D.10
Suchy, J.11
Gronwald, J.12
Teodorczyk, U.13
Huzarski, T.14
Byrski, T.15
Jakubowska, A.16
Gorski, B.17
van de Wetering, T.18
Walczak, S.19
Narod, S.A.20
Lubinski, J.21
Cybulski, C.22
more..
-
8
-
-
77950405093
-
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E, Holmes C, Marchini JL, Stirrups K, Tobin MD, Wain LV, Yau C, Aerts J, Ahmad T, Andrews TD, Arbury H, Attwood A, Auton A, Ball SG, Balmforth AJ, Barrett JC, Barroso I, Barton A, Bennett AJ, Bhaskar S, Blaszczyk K, Bowes J, Brand OJ, Braund PS, Bredin F, Breen G, Brown MJ, Bruce IN, Bull J, Burren OS, Burton J, Byrnes J, Caesar S, Clee CM, Coffey AJ, Connell JM, Cooper JD, Dominiczak AF, Downes K, Drummond HE, Dudakia D, Dunham A, Ebbs B, Eccles D, Edkins S, Edwards C, Elliot A, Emery P, Evans DM, Evans G, Eyre S, Farmer A, Ferrier IN, Feuk L, Fitzgerald T, Flynn E, Forbes A, Forty L, Franklyn JA, Freathy RM, Gibbs P, Gilbert P, Gokumen O, Gordon-Smith K, Gray E, Green E, Groves CJ, Grozeva D, Gwilliam R, Hall A, Hammond N, Hardy M, Harrison P, Hassanali N, Hebaishi H, Hines S, Hinks A, Hitman GA, Hocking L, Howard E, Howard P, Howson JM, Hughes D, Hunt S, Isaacs JD, Jain M, Jewell DP, Johnson T, Jolley JD, Jones IR, Jones LA, Kirov G, Langford CF, Lango-Allen H, Lathrop GM, Lee J, Lee KL, Lees C, Lewis K, Lindgren CM, Maisuria-Armer M, Maller J, Mansfield J, Martin P, Massey DC, McArdle WL, McGuffin P, McLay KE, Mentzer A, Mimmack ML, Morgan AE, Morris AP, Mowat C, Myers S, Newman W, Nimmo ER, O'Donovan MC, Onipinla A, Onyiah I, Ovington NR, Owen MJ, Palin K, Parnell K, Pernet D, Perry JR, Phillips A, Pinto D, Prescott NJ, Prokopenko I, Quail MA, Rafelt S, Rayner NW, Redon R, Reid DM, Renwick A, Ring SM, Robertson N, Russell E, St Clair D, Sambrook JG, Sanderson JD, Schuilenburg H, Scott CE, Scott R, Seal S, Shaw-Hawkins S, Shields BM, Simmonds MJ, Smyth DJ, Somaskantharajah E, Spanova K, Steer S, Stephens J, Stevens HE, Stone MA, Su Z, Symmons DP, Thompson JR, Thomson W, Travers ME, Turnbull C, Valsesia A, Walker M, Walker NM, Wallace C, Warren-Perry M, Watkins NA, Webster J, Weedon MN, Wilson AG, Woodburn M, Wordsworth BP, Young AH, Zeggini E, Carter NP, Frayling TM, Lee C, McVean G, Munroe PB, Palotie A, Sawcer SJ, Scherer SW, Strachan DP, Tyler-Smith C, Brown MA, Burton PR, Caulfield MJ, Compston A, Farrall M, Gough SC, Hall AS, Hattersley AT, Hill AV, Mathew CG, Pembrey M, Satsangi J, Stratton MR, Worthington J, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand W, Parkes M, Rahman N, Todd JA, Samani NJ, Donnelly P; Wellcome Trust Case Control Consortium. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 2010;464:713-20.
-
(2010)
Nature
, vol.464
, pp. 713-720
-
-
Craddock, N.1
Hurles, M.E.2
Cardin, N.3
Pearson, R.D.4
Plagnol, V.5
Robson, S.6
Vukcevic, D.7
Barnes, C.8
Conrad, D.F.9
Giannoulatou, E.10
Holmes, C.11
Marchini, J.L.12
Stirrups, K.13
Tobin, M.D.14
Wain, L.V.15
Yau, C.16
Aerts, J.17
Ahmad, T.18
Andrews, T.D.19
Arbury, H.20
Attwood, A.21
Auton, A.22
Ball, S.G.23
Balmforth, A.J.24
Barrett, J.C.25
Barroso, I.26
Barton, A.27
Bennett, A.J.28
Bhaskar, S.29
Blaszczyk, K.30
Bowes, J.31
Brand, O.J.32
Braund, P.S.33
Bredin, F.34
Breen, G.35
Brown, M.J.36
Bruce, I.N.37
Bull, J.38
Burren, O.S.39
Burton, J.40
Byrnes, J.41
Caesar, S.42
Clee, C.M.43
Coffey, A.J.44
Connell, J.M.45
Cooper, J.D.46
Dominiczak, A.F.47
Downes, K.48
Drummond, H.E.49
Dudakia, D.50
Dunham, A.51
Ebbs, B.52
Eccles, D.53
Edkins, S.54
Edwards, C.55
Elliot, A.56
Emery, P.57
Evans, D.M.58
Evans, G.59
Eyre, S.60
Farmer, A.61
Ferrier, I.N.62
Feuk, L.63
Fitzgerald, T.64
Flynn, E.65
Forbes, A.66
Forty, L.67
Franklyn, J.A.68
Freathy, R.M.69
Gibbs, P.70
Gilbert, P.71
Gokumen, O.72
Gordon-Smith, K.73
Gray, E.74
Green, E.75
Groves, C.J.76
Grozeva, D.77
Gwilliam, R.78
Hall, A.79
Hammond, N.80
Hardy, M.81
Harrison, P.82
Hassanali, N.83
Hebaishi, H.84
Hines, S.85
Hinks, A.86
Hitman, G.A.87
Hocking, L.88
Howard, E.89
Howard, P.90
Howson, J.M.91
Hughes, D.92
Hunt, S.93
Isaacs, J.D.94
Jain, M.95
Jewell, D.P.96
Johnson, T.97
Jolley, J.D.98
Jones, I.R.99
Jones, L.A.100
Kirov, G.101
Langford, C.F.102
Lango-Allen, H.103
Lathrop, G.M.104
Lee, J.105
Lee, K.L.106
Lees, C.107
Lewis, K.108
Lindgren, C.M.109
Maisuria-Armer, M.110
Maller, J.111
Mansfield, J.112
Martin, P.113
Massey, D.C.114
McArdle, W.L.115
McGuffin, P.116
McLay, K.E.117
Mentzer, A.118
Mimmack, M.L.119
Morgan, A.E.120
Morris, A.P.121
Mowat, C.122
Myers, S.123
Newman, W.124
Nimmo, E.R.125
O'Donovan, M.C.126
Onipinla, A.127
Onyiah, I.128
Ovington, N.R.129
Owen, M.J.130
Palin, K.131
Parnell, K.132
Pernet, D.133
Perry, J.R.134
Phillips, A.135
Pinto, D.136
Prescott, N.J.137
Prokopenko, I.138
Quail, M.A.139
Rafelt, S.140
Rayner, N.W.141
Redon, R.142
Reid, D.M.143
Renwick, A.144
Ring, S.M.145
Robertson, N.146
Russell, E.147
St Clair, D.148
Sambrook, J.G.149
Sanderson, J.D.150
Schuilenburg, H.151
Scott, C.E.152
Scott, R.153
Seal, S.154
Shaw-Hawkins, S.155
Shields, B.M.156
Simmonds, M.J.157
Smyth, D.J.158
Somaskantharajah, E.159
Spanova, K.160
Steer, S.161
Stephens, J.162
Stevens, H.E.163
Stone, M.A.164
Su, Z.165
Symmons, D.P.166
Thompson, J.R.167
Thomson, W.168
Travers, M.E.169
Turnbull, C.170
Valsesia, A.171
Walker, M.172
Walker, N.M.173
Wallace, C.174
Warren-Perry, M.175
Watkins, N.A.176
Webster, J.177
Weedon, M.N.178
Wilson, A.G.179
Woodburn, M.180
Wordsworth, B.P.181
Young, A.H.182
Zeggini, E.183
Carter, N.P.184
Frayling, T.M.185
Lee, C.186
McVean, G.187
Munroe, P.B.188
Palotie, A.189
Sawcer, S.J.190
Scherer, S.W.191
Strachan, D.P.192
Tyler-Smith, C.193
Brown, M.A.194
Burton, P.R.195
Caulfield, M.J.196
Compston, A.197
Farrall, M.198
Gough, S.C.199
Hall, A.S.200
Hattersley, A.T.201
Hill, A.V.202
Mathew, C.G.203
Pembrey, M.204
Satsangi, J.205
Stratton, M.R.206
Worthington, J.207
Deloukas, P.208
Duncanson, A.209
Kwiatkowski, D.P.210
McCarthy, M.I.211
Ouwehand, W.212
Parkes, M.213
Rahman, N.214
Todd, J.A.215
Samani, N.J.216
Donnelly, P.217
more..
-
9
-
-
34547498546
-
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
-
Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Kemp Z, Spain S, Penegar S, Chandler I, Gorman M, Wood W, Barclay E, Lubbe S, Martin L, Sellick G, Jaeger E, Hubner R, Wild R, Rowan A, Fielding S, Howarth K, Silver A, Atkin W, Muir K, Logan R, Kerr D, Johnstone E, Sieber O, Gray R, Thomas H, Peto J, Cazier JB, Houlston R. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet 2007;39:984-8.
-
(2007)
Nat Genet
, vol.39
, 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..
-
10
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 2009;5:e1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
11
-
-
79959789728
-
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes
-
Carvajal-Carmona LG, Cazier JB, Jones AM, Howarth K, Broderick P, Pittman A, Dobbins S, Tenesa A, Farrington S, Prendergast J, Theodoratou E, Barnetson R, Conti D, Newcomb P, Hopper JL, Jenkins MA, Gallinger S, Duggan DJ, Campbell H, Kerr D, Casey G, Houlston R, Dunlop M, Tomlinson I. Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes. Hum Mol Genet 2011;20:2879-88.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2879-2888
-
-
Carvajal-Carmona, L.G.1
Cazier, J.B.2
Jones, A.M.3
Howarth, K.4
Broderick, P.5
Pittman, A.6
Dobbins, S.7
Tenesa, A.8
Farrington, S.9
Prendergast, J.10
Theodoratou, E.11
Barnetson, R.12
Conti, D.13
Newcomb, P.14
Hopper, J.L.15
Jenkins, M.A.16
Gallinger, S.17
Duggan, D.J.18
Campbell, H.19
Kerr, D.20
Casey, G.21
Houlston, R.22
Dunlop, M.23
Tomlinson, I.24
more..
-
12
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81:559-75.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
13
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 2007;39:906-13.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
14
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005;21:263-5.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
-
15
-
-
56749176944
-
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
-
Houlston RS, Webb E, Broderick P, Pittman AM, Di Bernardo MC, Lubbe S, Chandler I, Vijayakrishnan J, Sullivan K, Penegar S, Carvajal-Carmona L, Howarth K, Jaeger E, Spain SL, Walther A, Barclay E, Martin L, Gorman M, Domingo E, Teixeira AS, Kerr D, Cazier JB, Niittymaki I, Tuupanen S, Karhu A, Aaltonen LA, Tomlinson IP, Farrington SM, Tenesa A, Prendergast JG, Barnetson RA, Cetnarskyj R, Porteous ME, Pharoah PD, Koessler T, Hampe J, Buch S, Schafmayer C, Tepel J, Schreiber S, Volzke H, Chang-Claude J, Hoffmeister M, Brenner H, Zanke BW, Montpetit A, Hudson TJ, Gallinger S, Campbell H, Dunlop MG. 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
-
-
Houlston, R.S.1
Webb, E.2
Broderick, P.3
Pittman, A.M.4
Di Bernardo, M.C.5
Lubbe, S.6
Chandler, I.7
Vijayakrishnan, J.8
Sullivan, K.9
Penegar, S.10
Carvajal-Carmona, L.11
Howarth, K.12
Jaeger, E.13
Spain, S.L.14
Walther, A.15
Barclay, E.16
Martin, L.17
Gorman, M.18
Domingo, E.19
Teixeira, A.S.20
Kerr, D.21
Cazier, J.B.22
Niittymaki, I.23
Tuupanen, S.24
Karhu, A.25
Aaltonen, L.A.26
Tomlinson, I.P.27
Farrington, S.M.28
Tenesa, A.29
Prendergast, J.G.30
Barnetson, R.A.31
Cetnarskyj, R.32
Porteous, M.E.33
Pharoah, P.D.34
Koessler, T.35
Hampe, J.36
Buch, S.37
Schafmayer, C.38
Tepel, J.39
Schreiber, S.40
Volzke, H.41
Chang-Claude, J.42
Hoffmeister, M.43
Brenner, H.44
Zanke, B.W.45
Montpetit, A.46
Hudson, T.J.47
Gallinger, S.48
Campbell, H.49
Dunlop, M.G.50
more..
-
16
-
-
77953614624
-
Challenges in the identification and use of rare diseaseassociated predisposition variants
-
Carvajal-Carmona LG. Challenges in the identification and use of rare diseaseassociated predisposition variants. Curr Opin Genet Dev 2010;20:5.
-
(2010)
Curr Opin Genet Dev
, vol.20
, pp. 5
-
-
Carvajal-Carmona, L.G.1
-
17
-
-
68149170044
-
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling
-
Tuupanen S, Turunen M, Lehtonen R, Hallikas O, Vanharanta S, Kivioja T, Bjorklund M, Wei G, Yan J, Niittymaki I, Mecklin JP, Jarvinen H, Ristimaki A, Di-Bernardo M, East P, Carvajal-Carmona L, Houlston RS, Tomlinson I, Palin K, Ukkonen E, Karhu A, Taipale J, Aaltonen LA. The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. Nat Genet 2009;41:885-90.
-
(2009)
Nat Genet
, vol.41
, pp. 885-890
-
-
Tuupanen, S.1
Turunen, M.2
Lehtonen, R.3
Hallikas, O.4
Vanharanta, S.5
Kivioja, T.6
Bjorklund, M.7
Wei, G.8
Yan, J.9
Niittymaki, I.10
Mecklin, J.P.11
Jarvinen, H.12
Ristimaki, A.13
Di-Bernardo, M.14
East, P.15
Carvajal-Carmona, L.16
Houlston, R.S.17
Tomlinson, I.18
Palin, K.19
Ukkonen, E.20
Karhu, A.21
Taipale, J.22
Aaltonen, L.A.23
more..
-
18
-
-
30044436911
-
The role of microRNA genes in papillary thyroid carcinoma
-
He H, Jazdzewski K, Li W, Liyanarachchi S, Nagy R, Volinia S, Calin GA, Liu CG, Franssila K, Suster S, Kloos RT, Croce CM, de la Chapelle A. The role of microRNA genes in papillary thyroid carcinoma. Proc Natl Acad Sci U S A 2005;102:19075-80.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 19075-19080
-
-
He, H.1
Jazdzewski, K.2
Li, W.3
Liyanarachchi, S.4
Nagy, R.5
Volinia, S.6
Calin, G.A.7
Liu, C.G.8
Franssila, K.9
Suster, S.10
Kloos, R.T.11
Croce, C.M.12
de la Chapelle, A.13
|