-
1
-
-
38749100987
-
Genome studies: Genetics by numbers
-
Baker M 2008. Genome studies: genetics by numbers. Nature 451: 516-518.
-
(2008)
Nature
, vol.451
, pp. 516-518
-
-
Baker, M.1
-
2
-
-
42449153256
-
Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease
-
Beckly JB, Hancock L, Geremia A, Cummings JR, Morris A, Cooney R, Pathan S, Guo C, Jewell DP 2008. Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease. Inflamm Bowel Dis 14: 500-507.
-
(2008)
Inflamm Bowel Dis
, vol.14
, pp. 500-507
-
-
Beckly, J.B.1
Hancock, L.2
Geremia, A.3
Cummings, J.R.4
Morris, A.5
Cooney, R.6
Pathan, S.7
Guo, C.8
Jewell, D.P.9
-
3
-
-
41149176472
-
Haplotypic analysis of Wellcome Trust Case Control Consortium data
-
Browning BL, Browning SR 2008. Haplotypic analysis of Wellcome Trust Case Control Consortium data. Hum Genet 123: 273-280.
-
(2008)
Hum Genet
, vol.123
, pp. 273-280
-
-
Browning, B.L.1
Browning, S.R.2
-
4
-
-
34547546458
-
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease
-
Buch S, Schafmayer C, Volzke H, Becker C, Franke A, von Eller Eberstein H, Kluck C, Bassmann I, Brosch M, Lammert F, Miquel JF, Nervi F, Wittig M, Rosskopf D, Timm B, Holl C, Seeger M, ElSharawy A, Lu T, Egberts J, Fandrich F, Folsch UR, Krawczak M, Schreiber S, Nurnberg P, Tepel J, Hampe J 2007. A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Nat Genet 39: 995-999.
-
(2007)
Nat Genet
, vol.39
, pp. 995-999
-
-
Buch, S.1
Schafmayer, C.2
Volzke, H.3
Becker, C.4
Franke, A.5
von Eller Eberstein, H.6
Kluck, C.7
Bassmann, I.8
Brosch, M.9
Lammert, F.10
Miquel, J.F.11
Nervi, F.12
Wittig, M.13
Rosskopf, D.14
Timm, B.15
Holl, C.16
Seeger, M.17
Elsharawy, A.18
Lu, T.19
Egberts, J.20
Fandrich, F.21
Folsch, U.R.22
Krawczak, M.23
Schreiber, S.24
Nurnberg, P.25
Tepel, J.26
Hampe, J.27
more..
-
5
-
-
33748902565
-
Genetic susceptibility to infectious diseases: Big is beautiful, but will bigger be even better?
-
Burgner D, Jamieson SE, Blackwell JM 2006. Genetic susceptibility to infectious diseases: big is beautiful, but will bigger be even better? Lancet Infect Dis 6: 653-663.
-
(2006)
Lancet Infect Dis
, vol.6
, pp. 653-663
-
-
Burgner, D.1
Jamieson, S.E.2
Blackwell, J.M.3
-
6
-
-
45749089363
-
Maternal genotype effects can alias case genotype effects in case-control studies
-
Buyske S 2008. Maternal genotype effects can alias case genotype effects in case-control studies. Eur J Hum Genet 16: 784-785.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 784-785
-
-
Buyske, S.1
-
7
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Consortium WTCC
-
Consortium WTCC 2007. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
8
-
-
38749083888
-
The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes
-
Cooper JD, Smyth DJ, Bailey R, Payne F, Downes K, Godfrey LM, Masters J, Zeitels LR, Vella A, Walker NM, Todd JA 2007. The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes. BMC Med Genet 8: 71.
-
(2007)
BMC Med Genet
, vol.8
, pp. 71
-
-
Cooper, J.D.1
Smyth, D.J.2
Bailey, R.3
Payne, F.4
Downes, K.5
Godfrey, L.M.6
Masters, J.7
Zeitels, L.R.8
Vella, A.9
Walker, N.M.10
Todd, J.A.11
-
9
-
-
1842483890
-
Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects
-
Cordell HJ, Barratt BJ, Clayton DG 2004. Case/pseudocontrol analysis in genetic association studies: a unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects. Genet Epidemiol 26: 167-185.
-
(2004)
Genet Epidemiol
, vol.26
, pp. 167-185
-
-
Cordell, H.J.1
Barratt, B.J.2
Clayton, D.G.3
-
10
-
-
25144501575
-
Genetic association studies
-
Cordell HJ, Clayton DG 2005. Genetic association studies. Lancet 366: 1121-1131.
-
(2005)
Lancet
, vol.366
, pp. 1121-1131
-
-
Cordell, H.J.1
Clayton, D.G.2
-
11
-
-
39749119374
-
A genome-wide association study of sporadic ALS in a homogenous Irish population
-
Cronin S, Berger S, Ding J, Schymick JC, Washecka N, Hernandez DG, Greenway MJ, Bradley DG, Traynor BJ, Hardiman O 2008. A genome-wide association study of sporadic ALS in a homogenous Irish population. Hum Mol Genet 17: 768-774.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 768-774
-
-
Cronin, S.1
Berger, S.2
Ding, J.3
Schymick, J.C.4
Washecka, N.5
Hernandez, D.G.6
Greenway, M.J.7
Bradley, D.G.8
Traynor, B.J.9
Hardiman, O.10
-
12
-
-
35748943204
-
The Framingham Heart Study 100K SNP genome-wide association study resource: Overview of 17 phenotype working group reports
-
Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB, Sr., Demissie S, DeStefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, Kiel DP, Laramie JM, Larson MG, Levy D, Liu CY, Lunetta KL, Mailman MD, Manning AK, Meigs JB, Murabito JM, Newton Cheh C, O'Connor GT, O'Donnell CJ, Pandey M, Seshadri S, Vasan RS, Wang ZY, Wilk JB, Wolf PA, Yang Q, Atwood LD 2007. The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet 8 (Suppl. 1): S1.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Cupples, L.A.1
Arruda, H.T.2
Benjamin, E.J.3
D'Agostino Sr., R.B.4
Demissie, S.5
DeStefano, A.L.6
Dupuis, J.7
Falls, K.M.8
Fox, C.S.9
Gottlieb, D.J.10
Govindaraju, D.R.11
Guo, C.Y.12
Heard-Costa, N.L.13
Hwang, S.J.14
Kathiresan, S.15
Kiel, D.P.16
Laramie, J.M.17
Larson, M.G.18
Levy, D.19
Liu, C.Y.20
Lunetta, K.L.21
Mailman, M.D.22
Manning, A.K.23
Meigs, J.B.24
Murabito, J.M.25
Newton cheh, C.26
O'Connor, G.T.27
O'Donnell, C.J.28
Pandey, M.29
Seshadri, S.30
Vasan, R.S.31
Wang, Z.Y.32
Wilk, J.B.33
Wolf, P.A.34
Yang, Q.35
Atwood, L.D.36
more..
-
13
-
-
52949135179
-
Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization
-
Davey Smith G, Timpson N, Ebrahim S 2008. Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization. Ann Med 40: 524-541.
-
(2007)
Ann Med
, vol.40
, pp. 524-541
-
-
Smith, G.D.1
Timpson, N.2
Ebrahim, S.3
-
14
-
-
0036917469
-
The ABCA4 gene in autosomal recessive cone-rod dystrophies
-
Ducroq D, Rozet JM, Gerber S, Perrault I, Barbet D, Hanein S, Hakiki S, Dufier JL, Munnich A, Hamel C, Kaplan J 2002. The ABCA4 gene in autosomal recessive cone-rod dystrophies. Am J Hum Genet 71: 1480-1482.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1480-1482
-
-
Ducroq, D.1
Rozet, J.M.2
Gerber, S.3
Perrault, I.4
Barbet, D.5
Hanein, S.6
Hakiki, S.7
Dufier, J.L.8
Munnich, A.9
Hamel, C.10
Kaplan, J.11
-
15
-
-
38449103390
-
Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP
-
Duggan D, Zheng SL, Knowlton M, Benitez D, Dimitrov L, Wiklund F, Robbins C, Isaacs SD, Cheng Y, Li G, Sun J, Chang BL, Marovich L, Wiley KE, Balter K, Stattin P, Adami HO, Gielzak M, Yan G, Sauvageot J, Liu W, Kim JW, Bleecker ER, Meyers DA, Trock BJ, Partin AW, Walsh PC, Isaacs WB, Gronberg H, Xu J, Carpten JD 2007. Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP. J Natl Cancer Inst 99: 1836-1844.
-
(2007)
J Natl Cancer Inst
, vol.99
, pp. 1836-1844
-
-
Duggan, D.1
Zheng, S.L.2
Knowlton, M.3
Benitez, D.4
Dimitrov, L.5
Wiklund, F.6
Robbins, C.7
Isaacs, S.D.8
Cheng, Y.9
Li, G.10
Sun, J.11
Chang, B.L.12
Marovich, L.13
Wiley, K.E.14
Balter, K.15
Stattin, P.16
Adami, H.O.17
Gielzak, M.18
Yan, G.19
Sauvageot, J.20
Liu, W.21
Kim, J.W.22
Bleecker, E.R.23
Meyers, D.A.24
Trock, B.J.25
Partin, A.W.26
Walsh, P.C.27
Isaacs, W.B.28
Gronberg, H.29
Xu, J.30
Carpten, J.D.31
more..
-
16
-
-
0033614660
-
Mother-to-child transmission of toxoplasmosis: Risk estimates for clinical counselling
-
Dunn D, Wallon M, Peyron F, Petersen E, Peckham C, Gilbert R 1999. Mother-to-child transmission of toxoplasmosis: risk estimates for clinical counselling. Lancet 353: 1829-1833.
-
(1999)
Lancet
, vol.353
, pp. 1829-1833
-
-
Dunn, D.1
Wallon, M.2
Peyron, F.3
Petersen, E.4
Peckham, C.5
Gilbert, R.6
-
17
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, Ballinger DG, Struewing JP, Morrison J, Field H, Luben R, Wareham N, Ahmed S, Healey CS, Bowman R, Meyer KB, Haiman CA, Kolonel LK, Henderson BE, Le Marchand L, Brennan P, Sangrajrang S, Gaborieau V, Odefrey F, Shen CY, Wu PE, Wang HC, Eccles D, Evans DG, Peto J, Fletcher O, Johnson N, Seal S, Stratton MR, Rahman N, Chenevix-Trench G, Bojesen SE, Nordestgaard BG, Axelsson CK, Garcia-Closas M, Brinton L, Chanock S, Lissowska J, Peplonska B, Nevanlinna H, Fagerholm R, Eerola H, Kang D, Yoo KY, Noh DY, Ahn SH, Hunter DJ, Hankinson SE, Cox DG, Hall P, Wedren S, Liu J, Low YL, Bogdanova N, Schurmann P, Dork T, Tollenaar RA, Jacobi CE, Devilee P, Klijn JG, Sigurdson AJ, Doody MM, Alexander BH, Zhang J, Cox A, Brock IW, MacPherson G, Reed MW, Couch FJ, Goode EL, Olson JE, Meijers-Heijboer H, van den Ouweland A, Uitterlinden A, Rivadeneira F, Milne RL, Ribas G, Gonzalez-Neira A, Benitez J, Hopper JL, McCredie M, Southey M, Giles GG, Schroen C, Justenhoven C, Brauch H, Hamann U, Ko YD, Spurdle AB, Beesley J, Chen X, Mannermaa A, Kosma VM, Kataja V, Hartikainen J, Day NE, Cox DR, Ponder BA 2007. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447: 1087-1093.
-
(2007)
Nature
, vol.447
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
Pharoah, P.D.4
Thompson, D.5
Ballinger, D.G.6
Struewing, J.P.7
Morrison, J.8
Field, H.9
Luben, R.10
Wareham, N.11
Ahmed, S.12
Healey, C.S.13
Bowman, R.14
Meyer, K.B.15
Haiman, C.A.16
Kolonel, L.K.17
Henderson, B.E.18
le Marchand, L.19
Brennan, P.20
Sangra jrang, S.21
Gaborieau, V.22
Odefrey, F.23
Shen, C.Y.24
Wu, P.E.25
Wang, H.C.26
Eccles, D.27
Evans, D.G.28
Peto, J.29
Fletcher, O.30
Johnson, N.31
Seal, S.32
Stratton, M.R.33
Rahman, N.34
Chenevix-Trench, G.35
Bojesen, S.E.36
Nordestgaard, B.G.37
Axelsson, C.K.38
Garcia-Closas, M.39
Brinton, L.40
Chanock, S.41
Lissowska, J.42
Peplonska, B.43
Nevanlinna, H.44
Fagerholm, R.45
Eerola, H.46
Kang, D.47
Yoo, K.Y.48
Noh, D.Y.49
Ahn, S.H.50
Hunter, D.J.51
Hankinson, S.E.52
Cox, D.G.53
Hall, P.54
Wedren, S.55
Liu, J.56
Low, Y.L.57
Bogdanova, N.58
Schurmann, P.59
Dork, T.60
Tollenaar, R.A.61
Jacobi, C.E.62
Devilee, P.63
Klijn, J.G.64
Sigurdson, A.J.65
Doody, M.M.66
Alexander, B.H.67
Zhang, J.68
Cox, A.69
Brock, I.W.70
Macpherson, G.71
Reed, M.W.72
Couch, F.J.73
Goode, E.L.74
Olson, J.E.75
Meijers-Heijboer, H.76
van den Ouweland, A.77
Uitterlinden, A.78
Rivadeneira, F.79
Milne, R.L.80
Ribas, G.81
Gonzalez-Neira, A.82
Benitez, J.83
Hopper, J.L.84
McCredie, M.85
Southey, M.86
Giles, G.G.87
Schroen, C.88
Justenhoven, C.89
Brauch, H.90
Hamann, U.91
Ko, Y.D.92
Spurdle, A.B.93
Beesley, J.94
Chen, X.95
Mannermaa, A.96
Kosma, V.M.97
Kataja, V.98
Hartikainen, J.99
more..
-
18
-
-
38949127024
-
Mendelian randomization: Can genetic epidemiology help redress the failures of observational epidemiology?
-
Ebrahim S, Davey Smith G 2008. Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology? Hum Genet 123: 15-33.
-
(2008)
Hum Genet
, vol.123
, pp. 15-33
-
-
Ebrahim, S.1
Smith, G.D.2
-
19
-
-
36849035803
-
A 100K ge nome-wide association scan for diabetes and related traits in the Framingham Heart Study: Replication and integration with other genome-wide datasets
-
Florez JC, Manning AK, Dupuis J, McAteer J, Irenze K, Gianniny L, Mirel DB, Fox CS, Cupples LA, Meigs JB 2007. A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets. Diabetes 56: 3063-3074.
-
(2007)
Diabetes
, vol.56
, pp. 3063-3074
-
-
Florez, J.C.1
Manning, A.K.2
Dupuis, J.3
McAteer, J.4
Irenze, K.5
Gianniny, L.6
Mirel, D.B.7
Fox, C.S.8
Cupples, L.A.9
Meigs, J.B.10
-
20
-
-
0037332054
-
Effect of timing and type of treatment on the risk of mother to child transmission of Toxoplasma gondii
-
Gilbert R, Gras L 2003. Effect of timing and type of treatment on the risk of mother to child transmission of Toxoplasma gondii. Bjog 110: 112-120.
-
(2003)
Bjog
, vol.110
, pp. 112-120
-
-
Gilbert, R.1
Gras, L.2
-
21
-
-
31544443587
-
Association between prenatal treatment and clinical manifestations of congenital toxoplasmosis in infancy: A cohort study in 13 European centres
-
Gras L, Wallon M, Pollak A, Cortina-Borja M, Evengard B, Hayde M, Petersen E, Gilbert R 2005. Association between prenatal treatment and clinical manifestations of congenital toxoplasmosis in infancy: a cohort study in 13 European centres. Acta Paediatr 94: 1721-1731.
-
(2005)
Acta Paediatr
, vol.94
, pp. 1721-1731
-
-
Gras, L.1
Wallon, M.2
Pollak, A.3
Cortina-Borja, M.4
Evengard, B.5
Hayde, M.6
Petersen, E.7
Gilbert, R.8
-
22
-
-
34247563453
-
Genome-wide association study identifies a second prostate cancer susceptibi lity variant at 8q24
-
Gudmundsson J, Sulem P, Manolescu A, Amundadottir LT, Gudbjartsson D, Helgason A, Rafnar T, Bergthorsson JT, Agnarsson BA, Baker A, Sigurdsson A, Benediktsdottir KR, Jakobsdottir M, Xu J, Blondal T, Kostic J, Sun J, Ghosh S, Stacey SN, Mouy M, Saemundsdottir J, Backman VM, Kristjansson K, Tres A, Partin AW, Albers-Akkers MT, Godino-Ivan Marcos J, Walsh PC, Swinkels DW, Navarrete S, Isaacs SD, Aben KK, Graif T, Cashy J, Ruiz-Echarri M, Wiley KE, Suarez BK, Witjes JA, Frigge M, Ober C, Jonsson E, Einarsson GV, Mayordomo JI, Kiemeney LA, Isaacs WB, Catalona WJ, Barkardottir RB, Gulcher JR, Thorsteinsdottir U, Kong A, Stefansson K 2007. Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat Genet 39: 631-637.
-
(2007)
Nat Genet
, vol.39
, pp. 631-637
-
-
Gudmundsson, J.1
Sulem, P.2
Manolescu, A.3
Amundadottir, L.T.4
GudbJartsson, D.5
Helgason, A.6
Rafnar, T.7
Bergthorsson, J.T.8
Agnarsson, B.A.9
Baker, A.10
Sigurdsson, A.11
Benediktsdottir, K.R.12
Jakobsdottir, M.13
Xu, J.14
Blondal, T.15
Kostic, J.16
Sun, J.17
Ghosh, S.18
Stacey, S.N.19
Mouy, M.20
Saemundsdottir, J.21
Backman, V.M.22
Kristjansson, K.23
Tres, A.24
Partin, A.W.25
Albers-Akkers, M.T.26
Godino-Ivan Marcos, J.27
Walsh, P.C.28
Swinkels, D.W.29
Navarrete, S.30
Isaacs, S.D.31
Aben, K.K.32
Graif, T.33
Cashy, J.34
Ruiz-Echarri, M.35
Wiley, K.E.36
Suarez, B.K.37
Witjes, J.A.38
Frigge, M.39
Ober, C.40
Jonsson, E.41
Einarsson, G.V.42
Mayordomo, J.I.43
Kiemeney, L.A.44
Isaacs, W.B.45
Catalona, W.J.46
Barkardottir, R.B.47
Gulcher, J.R.48
Thorsteinsdottir, U.49
Kong, A.50
Stefansson, K.51
more..
-
23
-
-
33846627302
-
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
-
Hampe J, Franke A, Rosenstiel P, Till A, Teuber M, Huse K, Albrecht M, Mayr G, De La Vega FM, Briggs J, Gunther S, Prescott NJ, Onnie CM, Hasler R, Sipos B, Folsch UR, Lengauer T, Platzer M, Mathew CG, Krawczak M, Schreiber S 2007. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet 39: 207-211.
-
(2007)
Nat Genet
, vol.39
, pp. 207-211
-
-
Hampe, J.1
Franke, A.2
Rosenstiel, P.3
Till, A.4
Teuber, M.5
Huse, K.6
Albrecht, M.7
Mayr, G.8
de la Vega, F.M.9
Briggs, J.10
Gunther, S.11
Prescott, N.J.12
Onnie, C.M.13
Hasler, R.14
Sipos, B.15
Folsch, U.R.16
Lengauer, T.17
Platzer, M.18
Mathew, C.G.19
Krawczak, M.20
Schreiber, S.21
more..
-
24
-
-
33646242987
-
The v-MFG test: Investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability
-
Hsieh HJ, Palmer CG, Harney S, Newton JL, Wordsworth P, Brown MA, Sinsheimer JS 2006. The v-MFG test: investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability. Genet Epidemiol 30: 333-347.
-
(2006)
Genet Epidemiol
, vol.30
, pp. 333-347
-
-
Hsieh, H.J.1
Palmer, C.G.2
Harney, S.3
Newton, J.L.4
Wordsworth, P.5
Brown, M.A.6
Sinsheimer, J.S.7
-
25
-
-
48449083270
-
Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis
-
Jamieson SE, de Roubaix LA, Cortina-Borja M, Tan HK, Mui EJ, Cordell HJ, Kirisits MJ, Miller EN, Peacock CS, Hargrave AC, Coyne JJ, Boyer K, Bessieres MH, Buffolano W, Ferret N, Franck J, Kieffer F, Meier P, Nowakowska DE, Paul M, Peyron F, Stray-Pedersen B, Prusa AR, Thulliez P, Wallon M, Petersen E, McLeod R, Gilbert RE, Blackwell JM 2008. Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis. PLoS ONE 3: e2285.
-
(2008)
PLoS ONE
, vol.3
-
-
Jamieson, S.E.1
de Roubaix, L.A.2
Cortina-Borja, M.3
Tan, H.K.4
Mui, E.J.5
Cordell, H.J.6
Kirisits, M.J.7
Miller, E.N.8
Peacock, C.S.9
Hargrave, A.C.10
Coyne, J.J.11
Boyer, K.12
Bessieres, M.H.13
Buffolano, W.14
Ferret, N.15
Franck, J.16
Kieffer, F.17
Meier, P.18
Nowakowska, D.E.19
Paul, M.20
Peyron, F.21
Stray-Pedersen, B.22
Prusa, A.R.23
Thulliez, P.24
Wallon, M.25
Petersen, E.26
McLeod, R.27
Gilbert, R.E.28
Blackwell, J.M.29
more..
-
26
-
-
35748938784
-
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
-
Kathiresan S, Manning AK, Demissie S, D'Agostino RB, Surti A, Guiducci C, Gianniny L, Burtt NP, Melander O, Orho-Melander M, Arnett DK, Peloso GM, Ordovas JM, Cupples LA 2007. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. BMC Med Genet 8 (Suppl. 1): S17.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Kathiresan, S.1
Manning, A.K.2
Demissie, S.3
D'Agostino, R.B.4
Surti, A.5
Guiducci, C.6
Gianniny, L.7
Burtt, N.P.8
Melander, O.9
Orho-Melander, M.10
Arnett, D.K.11
Peloso, G.M.12
Ordovas, J.M.13
Cupples, L.A.14
-
27
-
-
0037656046
-
The gene for Stargardt disease, ABCA4, is a major retinal gene: A mini-review
-
Koenekoop RK 2003. The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-review. Ophthalmic Genet 24: 75-80.
-
(2003)
Ophthalmic Genet
, vol.24
, pp. 75-80
-
-
Koenekoop, R.K.1
-
28
-
-
42149109325
-
Improved correction for population stratification in genome-wide association studies by identifying hidden popula tion structures
-
Li Q, Yu K 2008. Improved correction for population stratification in genome-wide association studies by identifying hidden population structures. Genet Epidemiol 32: 215-226.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 215-226
-
-
Li, Q.1
Yu, K.2
-
29
-
-
0032704229
-
HLA-class II genes modify outcome of Toxoplasma gondii infection
-
Mack DG, Johnson JJ, Roberts F, Roberts CW, Estes RG, David C, Grumet FC, McLeod R 1999. HLA-class II genes modify outcome of Toxoplasma gondii infection. Int J Parasitol 29: 1351-1358.
-
(1999)
Int J Parasitol
, vol.29
, pp. 1351-1358
-
-
Mack, D.G.1
Johnson, J.J.2
Roberts, F.3
Roberts, C.W.4
Estes, R.G.5
David, C.6
Grumet, F.C.7
McLeod, R.8
-
30
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P 2007. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39: 906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
31
-
-
33646462725
-
Outcome of treatment for congenital toxoplasmosis, 1981-2004: The national Collaborative Chicago-Based, Congenital Toxoplasmosis Study
-
McLeod R, Boyer K, Karrison T, Kasza K, Swisher C, Roizen N, Jalbrzikowski J, Remington J, Heydemann P, Noble AG, Mets M, Holfels E, Withers S, Latkany P, Meier P 2006. Outcome of treatment for congenital toxoplasmosis, 1981-2004: the National Collaborative Chicago-Based, Congenital Toxoplasmosis Study. Clin Infect Dis 42: 1383-1394.
-
(2006)
Clin Infect Dis
, vol.42
, pp. 1383-1394
-
-
McLeod, R.1
Boyer, K.2
Karrison, T.3
Kasza, K.4
Swisher, C.5
Roizen, N.6
Jalbrzikowski, J.7
Remington, J.8
Heydemann, P.9
Noble, A.G.10
Mets, M.11
Holfels, E.12
Withers, S.13
Latkany, P.14
Meier, P.15
-
32
-
-
14044256556
-
Detection of a novel parasite kinase activity at the Toxoplasma gondii parasitophorous vacuole membrane capable of phosphorylating host Ikappa Balpha
-
Molestina RE, Sinai AP 2005a. Detection of a novel parasite kinase activity at the Toxoplasma gondii parasitophorous vacuole membrane capable of phosphorylating host Ikappa Balpha. Cell Microbiol 7: 351-362.
-
(2005)
Cell Microbiol
, vol.7
, pp. 351-362
-
-
Molestina, R.E.1
Sinai, A.P.2
-
33
-
-
30544440755
-
Host and parasite-derived IKK activities direct distinct temporal phases of NF-kappaB activation and target gene expression following Toxoplasma gondii infection
-
Molestina RE, Sinai AP 2005b. Host and parasite-derived IKK activities direct distinct temporal phases of NF-kappaB activation and target gene expression following Toxoplasma gondii infection. J Cell Sci 118: 5785-5796.
-
(2005)
J Cell Sci
, vol.118
, pp. 5785-5796
-
-
Molestina, R.E.1
Sinai, A.P.2
-
34
-
-
36849012027
-
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
-
Nejentsev S, Howson JM, Walker NM, Szeszko J, Field SF, Stevens HE, Reynolds P, Hardy M, King E, Masters J, Hulme J, Maier LM, Smyth D, Bailey R, Cooper JD, Ribas G, Campbell RD, Clayton DG, Todd JA 2007. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature 450: 887-892.
-
(2007)
Nature
, vol.450
, pp. 887-892
-
-
Nejentsev, S.1
Howson, J.M.2
Walker, N.M.3
Szeszko, J.4
Field, S.F.5
Stevens, H.E.6
Reynolds, P.7
Hardy, M.8
King, E.9
Masters, J.10
Hulme, J.11
Maier, L.M.12
Smyth, D.13
Bailey, R.14
Cooper, J.D.15
Ribas, G.16
Campbell, R.D.17
Clayton, D.G.18
Todd, J.A.19
-
35
-
-
25844510235
-
Shaking the tree: Mapping complex disease genes with linkage disequilibrium
-
Palmer LJ, Cardon LR 2005. Shaking the tree: mapping complex disease genes with linkage disequilibrium. Lancet 366: 1223-1234.
-
(2005)
Lancet
, vol.366
, pp. 1223-1234
-
-
Palmer, L.J.1
Cardon, L.R.2
-
36
-
-
34347338690
-
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
-
Parkes M, Barrett JC, Prescott NJ, Tremelling M, Anderson CA, Fisher SA, Roberts RG, Nimmo ER, Cummings FR, Soars D, Drummond H, Lees CW, Khawaja SA, Bagnall R, Burke DA, Todhunter CE, Ahmad T, Onnie CM, McArdle W, Strachan D, Bethel G, Bryan C, Lewis CM, Deloukas P, Forbes A, Sanderson J, Jewell DP, Satsangi J, Mansfield JC, Cardon L, Mathew CG 2007. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Nat Genet 39: 830-832.
-
(2007)
Nat Genet
, vol.39
, pp. 830-832
-
-
Parkes, M.1
Barrett, J.C.2
Prescott, N.J.3
Tremelling, M.4
Anderson, C.A.5
Fisher, S.A.6
Roberts, R.G.7
Nimmo, E.R.8
Cummings, F.R.9
Soars, D.10
Drummond, H.11
Lees, C.W.12
Khawaja, S.A.13
Bagnall, R.14
Burke, D.A.15
Todhunter, C.E.16
Ahmad, T.17
Onnie, C.M.18
McArdle, W.19
Strachan, D.20
Bethel, G.21
Bryan, C.22
Lewis, C.M.23
Deloukas, P.24
Forbes, A.25
Sanderson, J.26
Jewell, D.P.27
Satsangi, J.28
Mansfield, J.C.29
Cardon, L.30
Mathew, C.G.31
more..
-
37
-
-
36549003138
-
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
-
Plenge RM, Cotsapas C, Davies L, Price AL, de Bakker PI, Maller J, Pe'er I, Burtt NP, Blumenstiel B, DeFelice M, Parkin M, Barry R, Winslow W, Healy C, Graham RR, Neale BM, Izmailova E, Roubenoff R, Parker AN, Glass R, Karlson EW, Maher N, Hafler DA, Lee DM, Seldin MF, Remmers EF, Lee AT, Padyukov L, Alfredsson L, Coblyn J, Weinblatt ME, Gabriel SB, Purcell S, Klareskog L, Gregersen PK, Shadick NA, Daly MJ, Altshuler D 2007. Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Nat Genet 39: 1477-1482.
-
(2007)
Nat Genet
, vol.39
, pp. 1477-1482
-
-
Plenge, R.M.1
Cotsapas, C.2
Davies, L.3
Price, A.L.4
de Bakker, P.I.5
Maller, J.6
Pe'er, I.7
Burtt, N.P.8
Blumenstiel, B.9
deFelice, M.10
Parkin, M.11
Barry, R.12
Winslow, W.13
Healy, C.14
Graham, R.R.15
Neale, B.M.16
Izmailova, E.17
Roubenoff, R.18
Parker, A.N.19
Glass, R.20
Karlson, E.W.21
Maher, N.22
Hafler, D.A.23
Lee, D.M.24
Seldin, M.F.25
Remmers, E.F.26
Lee, A.T.27
Padyukov, L.28
Alfredsson, L.29
Coblyn, J.30
Weinblatt, M.E.31
Gabriel, S.B.32
Purcell, S.33
Klareskog, L.34
Gregersen, P.K.35
Shadick, N.A.36
Daly, M.J.37
Altshuler, D.38
more..
-
38
-
-
35548958718
-
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci
-
Raelson JV, Little RD, Ruether A, Fournier H, Paquin B, Van Eerdewegh P, Bradley WE, Croteau P, Nguyen-Huu Q, Segal J, Debrus S, Allard R, Rosenstiel P, Franke A, Jacobs G, Nikolaus S, Vidal JM, Szego P, Laplante N, Clark HF, Paulussen RJ, Hooper JW, Keith TP, Belouchi A, Schreiber S 2007. Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. Proc Natl Acad Sci USA 104: 14747-14752.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 14747-14752
-
-
Raelson, J.V.1
Little, R.D.2
Ruether, A.3
Fournier, H.4
Paquin, B.5
van Eerdewegh, P.6
Bradley, W.E.7
Croteau, P.8
Nguyen-Huu, Q.9
Segal, J.10
Debrus, S.11
Allard, R.12
Rosenstiel, P.13
Franke, A.14
Jacobs, G.15
Nikolaus, S.16
Vidal, J.M.17
Szego, P.18
Laplante, N.19
Clark, H.F.20
Paulussen, R.J.21
Hooper, J.W.22
Keith, T.P.23
Belouchi, A.24
Schreiber, S.25
more..
-
39
-
-
84882814593
-
Toxoplasmosis
-
In JS Remington, C Baker, E Wilson, JO Klein, 6th ed., WB Saunders, Philadelphia
-
Remington JS, McLeod R, Thullie P, Desmonts G 2005. Toxoplasmosis. In JS Remington, C Baker, E Wilson, JO Klein, Infectious diseases of the fetus and newborn infant, 6th ed., WB Saunders, Philadelphia, p. 947-1091.
-
(2005)
Infectious Diseases of the Fetus and Newborn Infant
, pp. 947-1091
-
-
Remington, J.S.1
McLeod, R.2
Thullie, P.3
Desmonts, G.4
-
40
-
-
34748852627
-
Identifying genes for coronary artery disease: An idea whose time has come
-
Roberts R, Stewart AF, Wells GA, Williams KA, Kavaslar N, McPherson R 2007. Identifying genes for coronary artery disease: an idea whose time has come. Can J Cardiol 23 (Suppl. A): 7A-15A.
-
(2007)
Can J Cardiol
, vol.23
, Issue.SUPPL. A
-
-
Roberts, R.1
Stewart, A.F.2
Wells, G.A.3
Williams, K.A.4
Kavaslar, N.5
McPherson, R.6
-
41
-
-
25644433629
-
Stickler syndrome: Clinical characteristics and diagnostic criteria
-
Rose PS, Levy HP, Liberfarb RM, Davis J, Szymko-Bennett Y, Rubin BI, Tsilou E, Griffith AJ, Francomano CA 2005. Stickler syndrome: clinical characteristics and diagnostic criteria. Am J Med Genet A 138: 199-207.
-
(2005)
Am J Med Genet A
, vol.138
, pp. 199-207
-
-
Rose, P.S.1
Levy, H.P.2
Liberfarb, R.M.3
Davis, J.4
Szymko-Bennett, Y.5
Rubin, B.I.6
Tsilou, E.7
Griffith, A.J.8
Francomano, C.A.9
-
42
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, Konig IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H 2007. Genomewide association analysis of coronary artery disease. N Engl J Med 357: 443-453.
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.E.10
Barrett, J.H.11
Konig, I.R.12
Stevens, S.E.13
Szymczak, S.14
Tregouet, D.A.15
Iles, M.M.16
Pahlke, F.17
Pollard, H.18
Lieb, W.19
Cambien, F.20
Fischer, M.21
Ouwehand, W.22
Blankenberg, S.23
Balmforth, A.J.24
Baessler, A.25
Ball, S.G.26
Strom, T.M.27
Braenne, I.28
Gieger, C.29
Deloukas, P.30
Tobin, M.D.31
Ziegler, A.32
Thompson, J.R.33
Schunkert, H.34
more..
-
43
-
-
34547625955
-
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
-
Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orru M, Usala G, Dei M, Lai S, Maschio A, Busonero F, Mulas A, Ehret GB, Fink AA, Weder AB, Cooper RS, Galan P, Chakravarti A, Schlessinger D, Cao A, Lakatta E, Abecasis GR 2007. Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet 3: e115.
-
(2007)
PLoS Genet
, vol.3
-
-
Scuteri, A.1
Sanna, S.2
Chen, W.M.3
Uda, M.4
Albai, G.5
Strait, J.6
Najjar, S.7
Nagaraja, R.8
Orru, M.9
Usala, G.10
Dei, M.11
Lai, S.12
Maschio, A.13
Busonero, F.14
Mulas, A.15
Ehret, G.B.16
Fink, A.A.17
Weder, A.B.18
Cooper, R.S.19
Galan, P.20
Chakravarti, A.21
Schlessinger, D.22
Cao, A.23
Lakatta, E.24
Abecasis, G.R.25
more..
-
44
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
Sladek R, Rocheleau G, Rung J, Dina C, Shen L, Serre D, Boutin P, Vincent D, Belisle A, Hadjadj S, Balkau B, Heude B, Charpentier G, Hudson TJ, Montpetit A, Pshezhetsky AV, Prentki M, Posner BI, Balding DJ, Meyre D, Polychronakos C, Froguel P 2007. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 445: 881-885.
-
(2007)
Nature
, vol.445
, pp. 881-885
-
-
Sladek, R.1
Rocheleau, G.2
Rung, J.3
Dina, C.4
Shen, L.5
Serre, D.6
Boutin, P.7
Vincent, D.8
Belisle, A.9
Hadjadj, S.10
Balkau, B.11
Heude, B.12
Charpentier, G.13
Hudson, T.J.14
Montpetit, A.15
Pshezhetsky, A.V.16
Prentki, M.17
Posner, B.I.18
Balding, D.J.19
Meyre, D.20
Polychronakos, C.21
Froguel, P.22
more..
-
45
-
-
36549071998
-
Genetic determinants of hair, eye and skin pigmentation in Europeans
-
Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Magnusson KP, Manolescu A, Karason A, Palsson A, Thorleifsson G, Jakobsdottir M, Steinberg S, Palsson S, Jonasson F, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Kiemeney LA, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir U, Stefansson K 2007. Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 39: 1443-1452.
-
(2007)
Nat Genet
, vol.39
, pp. 1443-1452
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.N.3
Helgason, A.4
Rafnar, T.5
Magnusson, K.P.6
Manolescu, A.7
Karason, A.8
Palsson, A.9
Thorleifsson, G.10
Jakobsdottir, M.11
Steinberg, S.12
Palsson, S.13
Jonasson, F.14
Sigurgeirsson, B.15
Thorisdottir, K.16
Ragnarsson, R.17
Benediktsdottir, K.R.18
Aben, K.K.19
Kiemeney, L.A.20
Olafsson, J.H.21
Gulcher, J.22
Kong, A.23
Thorsteinsdottir, U.24
Stefansson, K.25
more..
-
46
-
-
41649087155
-
Common statistical issues in genome-wide association studies: A review on power, data quality control, genotype calling and population structure
-
Teo YY 2008. Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure. Curr Opin Lipidol 19: 133-143.
-
(2008)
Curr Opin Lipidol
, vol.19
, pp. 133-143
-
-
Teo, Y.Y.1
-
47
-
-
53849086543
-
Assessing genuine parents-offspring trios for genetic association studies
-
Teo YY, Fry AE, Sanjoaquin MA, Pederson B, Small KS, Rockett KA, Kwiatkowski DP, Clark TG 2009a. Assessing genuine parents-offspring trios for genetic association studies. Hum Hered 67: 26-37.
-
(2009)
Hum Hered
, vol.67
, pp. 26-37
-
-
Teo, Y.Y.1
Fry, A.E.2
Sanjoaquin, M.A.3
Pederson, B.4
Small, K.S.5
Rockett, K.A.6
Kwiatkowski, D.P.7
Clark, T.G.8
-
48
-
-
41449101024
-
Whole genome-amplified DNA: Insights and imputation
-
Teo YY, Inouye M, Small KS, Fry AE, Potter SC, Dunstan SJ, Seielstad M, Barroso I, Wareham NJ, Rockett KA, Kwiatkowski DP, Deloukas P 2008a. Whole genome-amplified DNA: insights and imputation. Nat Methods 5: 279-280.
-
(2008)
Nat Methods
, vol.5
, pp. 279-280
-
-
Teo, Y.Y.1
Inouye, M.2
Small, K.S.3
Fry, A.E.4
Potter, S.C.5
Dunstan, S.J.6
Seielstad, M.7
Barroso, I.8
Wareham, N.J.9
Rockett, K.A.10
Kwiatkowski, D.P.11
Deloukas, P.12
-
49
-
-
42149179227
-
Perturbation analysis: A simple method for filtering snps with erroneous genotyping in genome-wide association studies
-
Teo YY, Small KS, Clark TG, Kwiatkowski DP 2008b. Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies. Ann Hum Genet 72: 368-374.
-
(2008)
Ann Hum Genet
, vol.72
, pp. 368-374
-
-
Teo, Y.Y.1
Small, K.S.2
Clark, T.G.3
Kwiatkowski, D.P.4
-
50
-
-
63449142078
-
Power consequences of linkage disequilibrium variation between populations
-
Teo YY, Small KS, Fry AE, Wu Y, Kwiatkowski DP, Clark TG 2009b. Power consequences of linkage disequilibrium variation between populations. Genet Epidemiol Epub 33: 128-135.
-
(2009)
Genet Epidemiol Epub
, vol.33
, pp. 128-135
-
-
Teo, Y.Y.1
Small, K.S.2
Fry, A.E.3
Wu, Y.4
Kwiatkowski, D.P.5
Clark, T.G.6
-
51
-
-
36549005027
-
Rheumatoid arthritis association at 6q23
-
Thomson W, Barton A, Ke X, Eyre S, Hinks A, Bowes J, Donn R, Symmons D, Hider S, Bruce IN, Wilson AG, Marinou I, Morgan A, Emery P, Carter A, Steer S, Hocking L, Reid DM, Wordsworth P, Harrison P, Strachan D, Worthington J 2007. Rheumatoid arthritis association at 6q23. Nat Genet 39: 1431-1433.
-
(2007)
Nat Genet
, vol.39
, pp. 1431-1433
-
-
Thomson, W.1
Barton, A.2
Ke, X.3
Eyre, S.4
Hinks, A.5
Bowes, J.6
Donn, R.7
Symmons, D.8
Hider, S.9
Bruce, I.N.10
Wilson, A.G.11
Marinou, I.12
Morgan, A.13
Emery, P.14
Carter, A.15
Steer, S.16
Hocking, L.17
Reid, D.M.18
Wordsworth, P.19
Harrison, P.20
Strachan, D.21
Worthington, J.22
more..
-
52
-
-
34347341846
-
Robust associations of four new chromo some regions from genome-wide analyses of type 1 diabetes
-
Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, Lowe CE, Szeszko JS, Hafler JP, Zeitels L, Yang JH, Vella A, Nutland S, Stevens HE, Schuilenburg H, Coleman G, Maisuria M, Meadows W, Smink LJ, Healy B, Burren OS, Lam AA, Ovington NR, Allen J, Adlem E, Leung HT, Wallace C, Howson JM, Guja C, Ionescu-Tirgoviste C, Simmonds MJ, Heward JM, Gough SC, Dunger DB, Wicker LS, Clayton DG 2007. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat Genet 39: 857-864.
-
(2007)
Nat Genet
, vol.39
, pp. 857-864
-
-
Todd, J.A.1
Walker, N.M.2
Cooper, J.D.3
Smyth, D.J.4
Downes, K.5
Plagnol, V.6
Bailey, R.7
Nejentsev, S.8
Field, S.F.9
Payne, F.10
Lowe, C.E.11
Szeszko, J.S.12
Hafler, J.P.13
Zeitels, L.14
Yang, J.H.15
Vella, A.16
Nutland, S.17
Stevens, H.E.18
Schuilenburg, H.19
Coleman, G.20
Maisuria, M.21
Meadows, W.22
Smink, L.J.23
Healy, B.24
Burren, O.S.25
Lam, A.A.26
Ovington, N.R.27
Allen, J.28
Adlem, E.29
Leung, H.T.30
Wallace, C.31
Howson, J.M.32
Guja, C.33
Ionescu-Tirgoviste, C.34
Simmonds, M.J.35
Heward, J.M.36
Gough, S.C.37
Dunger, D.B.38
Wicker, L.S.39
Clayton, D.G.40
more..
-
53
-
-
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 2007. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet 39: 984-988.
-
(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
more..
-
54
-
-
22844449221
-
Genomic screening and replication using the same data set in family-based association testing
-
Van Steen K, McQueen MB, Herbert A, Raby B, Lyon H, Demeo DL, Murphy A, Su J, Datta S, Rosenow C, Christman M, Silverman EK, Laird NM, Weiss ST, Lange C 2005. Genomic screening and replication using the same data set in family-based association testing. Nat Genet 37: 683-691.
-
(2005)
Nat Genet
, vol.37
, pp. 683-691
-
-
van Steen, K.1
McQueen, M.B.2
Herbert, A.3
Raby, B.4
Lyon, H.5
Demeo, D.L.6
Murphy, A.7
Su, J.8
Datta, S.9
Rosenow, C.10
Christman, M.11
Silverman, E.K.12
Laird, N.M.13
Weiss, S.T.14
Lange, C.15
-
55
-
-
0031949066
-
A log-linear approach to caseparent-triad data: Assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
-
Weinberg CR, Wilcox AJ, Lie RT 1998. A log-linear approach to caseparent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 62: 969-978.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 969-978
-
-
Weinberg, C.R.1
Wilcox, A.J.2
Lie, R.T.3
-
56
-
-
35748981184
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC), Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Breast Cancer Susceptibility Collaboration (UK), Steering Committee
-
Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC), Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cummings FR, Jewell DP, Webster J, Brown MJ, Lathrop MG, Connell J, Dominiczak A, Marcano CA, Burke B, Dobson R, Gungadoo J, Lee KL, Munroe PB, Newhouse SJ, Onipinla A, Wallace C, Xue M, Caulfield M, Farrall M, Barton A; Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee, Bruce IN, Donovan H, Eyre S, Gilbert PD, Hilder SL, Hinks AM, John SL, Potter C, Silman AJ, Symmons DP, Thomson W, Worthington J, Dunger DB, Widmer B, Frayling TM, Freathy RM, Lango H, Perry JR, Shields BM, Weedon MN, Hattersley AT, Hitman GA, Walker M, Elliott KS, Groves CJ, Lindgren CM, Rayner NW, Timpson NJ, Zeggini E, Newport M, Sirugo G, Lyons E, Vannberg F, Hill AV, Bradbury LA, Farrar C, Pointon JJ, Wordsworth P, Brown MA, Franklyn JA, Heward JM, Simmonds MJ, Gough SC, Seal S; Breast Cancer Susceptibility Collaboration (UK), Stratton MR, Rahman N, Ban M, Goris A, Sawcer SJ, Compston A, Conway D, Jallow M, Newport M, Sirugo G, Rockett KA, Bumpstead SJ, Chaney A, Downes K, Ghori MJ, Gwilliam R, Hunt SE, Inouye M, Keniry A, King E, McGinnis R, Potter S, Ravindrarajah R, Whittaker P, Widden C, Withers D, Cardin NJ, Davison D, Ferreira T, Pereira-Gale J, Hallgrimsdo'ttir IB, Howie BN, Su Z, Teo YY, Vukcevic D, Bentley D, Brown MA, Compston A, Farrall M, Hall AS, Hattersley AT, Hill AV, Parkes M, Pembrey M, Stratton MR, Mitchell SL, Newby PR, Brand OJ, Carr-Smith J, Pearce SH, McGinnis R, Keniry A, Deloukas P, Reveille JD, Zhou X, Sims AM, Dowling A, Taylor J, Doan T, Davis JC, Savage L, Ward MM, Learch TL, Weisman MH, Brown M.2007. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 39: 1329-1337.
-
(2007)
Nat Genet
, vol.39
, pp. 1329-1337
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.P.7
McCarthy, M.I.8
Ouwehand, W.H.9
Samani, N.J.10
Todd, J.A.11
Donnelly, P.12
Barrett, J.C.13
Davison, D.14
Easton, D.15
Evans, D.M.16
Leung, H.T.17
Marchini, J.L.18
Morris, A.P.19
Spencer, C.C.20
Tobin, M.D.21
Attwood, A.P.22
Boorman, J.P.23
Cant, B.24
Everson, U.25
Hussey, J.M.26
Jolley, J.D.27
Knight, A.S.28
Koch, K.29
Meech, E.30
Nutland, S.31
Prowse, C.V.32
Stevens, H.E.33
Taylor, N.C.34
Walters, G.R.35
Walker, N.M.36
Watkins, N.A.37
Winzer, T.38
Jones, R.W.39
McArdle, W.L.40
Ring, S.M.41
Strachan, D.P.42
Pembrey, M.43
Breen, G.44
St Clair, D.45
Caesar, S.46
Gordon-Smith, K.47
Jones, L.48
Fraser, C.49
Green, E.K.50
Grozeva, D.51
Hamshere, M.L.52
Holmans, P.A.53
Jones, I.R.54
Kirov, G.55
Moskivina, V.56
Nikolov, I.57
O'Donovan, M.C.58
Owen, M.J.59
Collier, D.A.60
Elkin, A.61
Farmer, A.62
Williamson, R.63
McGuffin, P.64
Young, A.H.65
Ferrier, I.N.66
Ball, S.G.67
Balmforth, A.J.68
Barrett, J.H.69
Bishop, T.D.70
Iles, M.M.71
Maqbool, A.72
Yuldasheva, N.73
Hall, A.S.74
Braund, P.S.75
Dixon, R.J.76
Mangino, M.77
Stevens, S.78
Thompson, J.R.79
Bredin, F.80
Tremelling, M.81
Parkes, M.82
Drummond, H.83
Lees, C.W.84
Nimmo, E.R.85
Satsangi, J.86
Fisher, S.A.87
Forbes, A.88
Lewis, C.M.89
Onnie, C.M.90
Prescott, N.J.91
Sanderson, J.92
Matthew, C.G.93
Barbour, J.94
Mohiuddin, M.K.95
Todhunter, C.E.96
Mansfield, J.C.97
Ahmad, T.98
Cummings, F.R.99
more..
-
57
-
-
42249108172
-
Examining the statistical properties of fine-scale mapping in large-scale association studies
-
Wiltshire S, Morris AP, Zeggini E 2008. Examining the statistical properties of fine-scale mapping in large-scale association studies. Genet Epidemiol 32: 204-214.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 204-214
-
-
Wiltshire, S.1
Morris, A.P.2
Zeggini, E.3
-
58
-
-
34547092701
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
-
Zanke BW, Greenwood CM, Rangrej J, Kustra R, Tenesa A, Farrington SM, Prendergast J, Olschwang S, Chiang T, Crowdy E, Ferretti V, Laflamme P, Sundararajan S, Roumy S, Olivier JF, Robidoux F, Sladek R, Montpetit A, Campbell P, Bezieau S, O'Shea AM, Zogopoulos G, Cotterchio M, Newcomb P, McLaughlin J, Younghusband B, Green R, Green J, Porteous ME, Campbell H, Blanche H, Sahbatou M, Tubacher E, Bonaiti-Pellie C, Buecher B, Riboli E, Kury S, Chanock SJ, Potter J, Thomas G, Gallinger S, Hudson TJ, Dunlop MG 2007. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet 39: 989-994.
-
(2007)
Nat Genet
, vol.39
, 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.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..
-
59
-
-
34249895023
-
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
-
Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, Lango H, Timpson NJ, Perry JR, Rayner NW, Freathy RM, Barrett JC, Shields B, Morris AP, Ellard S, Groves CJ, Harries LW, Marchini JL, Owen KR, Knight B, Cardon LR, Walker M, Hitman GA, Morris AD, Doney AS, McCarthy MI, Hattersley AT 2007. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 316: 1336-1341.
-
(2007)
Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
Frayling, T.M.4
Elliott, K.S.5
Lango, H.6
Timpson, N.J.7
Perry, J.R.8
Rayner, N.W.9
Freathy, R.M.10
Barrett, J.C.11
Shields, B.12
Morris, A.P.13
Ellard, S.14
Groves, C.J.15
Harries, L.W.16
Marchini, J.L.17
Owen, K.R.18
Knight, B.19
Cardon, L.R.20
Walker, M.21
Hitman, G.A.22
Morris, A.D.23
Doney, A.S.24
McCarthy, M.I.25
Hattersley, A.T.26
more..
|