-
1
-
-
0026047218
-
Linkage analysis of quantitative traits: Increased power by using selected samples
-
1:STN:280:DyaK3MznslOnsw%3D%3D 1683186 1897525
-
Carey G, Williamson J (1991) Linkage analysis of quantitative traits: increased power by using selected samples. Am J Hum Genet 49:786-796
-
(1991)
Am J Hum Genet
, vol.49
, pp. 786-796
-
-
Carey, G.1
Williamson, J.2
-
2
-
-
34347335669
-
The population genetics of structural variation
-
1:CAS:528:DC%2BD2sXmvFKmsbY%3D 2716079 17597779 10.1038/ng2042
-
Conrad DF, Hurles ME (2007) The population genetics of structural variation. Nat Genet 39:S30-S36
-
(2007)
Nat Genet
, vol.39
-
-
Conrad, D.F.1
Hurles, M.E.2
-
3
-
-
70149107883
-
Osteo-chondroprogenitor-specific deletion of the selenocysteine tRNA gene, Trsp, leads to chondronecrosis and abnormal skeletal development: A putative model for Kashin-Beck disease
-
2721633 19696890 10.1371/journal.pgen.1000616
-
Downey CM, Horton CR, Carlson BA, Parsons TE, Hatfield DL, Hallgrimsson B, Jirik FR (2009) Osteo-chondroprogenitor-specific deletion of the selenocysteine tRNA gene, Trsp, leads to chondronecrosis and abnormal skeletal development: a putative model for Kashin-Beck disease. PLoS Genet 5:e1000616
-
(2009)
PLoS Genet
, vol.5
, pp. 1000616
-
-
Downey, C.M.1
Horton, C.R.2
Carlson, B.A.3
Parsons, T.E.4
Hatfield, D.L.5
Hallgrimsson, B.6
Jirik, F.R.7
-
4
-
-
84855947492
-
SNP and mRNA expression for glutathione peroxidase 4 in Kashin-Beck disease
-
21733339 10.1017/S0007114511002704
-
Du XH, Dai XX, Xia Song R, Zou XZ, Yan Sun W, Mo XY, Lu Bai G, Xiong YM (2012) SNP and mRNA expression for glutathione peroxidase 4 in Kashin-Beck disease. Br J Nutr 107:164-169
-
(2012)
Br J Nutr
, vol.107
, pp. 164-169
-
-
Du, X.H.1
Dai, X.X.2
Xia Song, R.3
Zou, X.Z.4
Yan Sun, W.5
Mo, X.Y.6
Lu Bai, G.7
Xiong, Y.M.8
-
5
-
-
77649146061
-
Comparative analysis of gene expression profiles between primary knee osteoarthritis and an osteoarthritis endemic to Northwestern China, Kashin-Beck disease
-
20131229 10.1002/art.27282
-
Duan C, Guo X, Zhang XD, Yu HJ, Yan H, Gao Y, Ma WJ, Gao ZQ, Xu P, Lammi M (2010) Comparative analysis of gene expression profiles between primary knee osteoarthritis and an osteoarthritis endemic to Northwestern China, Kashin-Beck disease. Arthritis Rheum 62:771-780
-
(2010)
Arthritis Rheum
, vol.62
, pp. 771-780
-
-
Duan, C.1
Guo, X.2
Zhang, X.D.3
Yu, H.J.4
Yan, H.5
Gao, Y.6
Ma, W.J.7
Gao, Z.Q.8
Xu, P.9
Lammi, M.10
-
6
-
-
84874766536
-
Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study
-
1:CAS:528:DC%2BC3sXpt1Knsg%3D%3D 3682481 23108985 10.1007/s00439-012- 1236-5
-
Guo YF, Zhang LS, Liu YJ, Hu HG, Li J, Tian Q, Yu P, Zhang F, Yang TL, Guo Y, Peng XL, Dai M, Chen W, Deng HW (2013) Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study. Hum Genet 132:189-199
-
(2013)
Hum Genet
, vol.132
, pp. 189-199
-
-
Guo, Y.F.1
Zhang, L.S.2
Liu, Y.J.3
Hu, H.G.4
Li, J.5
Tian, Q.6
Yu, P.7
Zhang, F.8
Yang, T.L.9
Guo, Y.10
Peng, X.L.11
Dai, M.12
Chen, W.13
Deng, H.W.14
-
7
-
-
68949103876
-
Inferring weak population structure with the assistance of sample group information
-
3518025 21564903 10.1111/j.1755-0998.2009.02591.x
-
Hubisz MJ, Falush D, Stephens M, Pritchard JK (2009) Inferring weak population structure with the assistance of sample group information. Mol Ecol Resour 9:1322-1332
-
(2009)
Mol Ecol Resour
, vol.9
, pp. 1322-1332
-
-
Hubisz, M.J.1
Falush, D.2
Stephens, M.3
Pritchard, J.K.4
-
8
-
-
78751700313
-
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
-
1:CAS:528:DC%2BC3MXpsFyhtw%3D%3D 3024044 21131291 10.1093/hmg/ddq518
-
Jarick I, Vogel CI, Scherag S, Schafer H, Hebebrand J, Hinney A, Scherag A (2011) Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis. Hum Mol Genet 20:840-852
-
(2011)
Hum Mol Genet
, vol.20
, pp. 840-852
-
-
Jarick, I.1
Vogel, C.I.2
Scherag, S.3
Schafer, H.4
Hebebrand, J.5
Hinney, A.6
Scherag, A.7
-
9
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
1:CAS:528:DC%2BD1cXhtFKhtrfL 2756534 18776909 10.1038/ng.237
-
Korn JM, Kuruvilla FG, McCarroll SA, Wysoker A, Nemesh J, Cawley S, Hubbell E, Veitch J, Collins PJ, Darvishi K, Lee C, Nizzari MM, Gabriel SB, Purcell S, Daly MJ, Altshuler D (2008) Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 40:1253-1260
-
(2008)
Nat Genet
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
Kuruvilla, F.G.2
McCarroll, S.A.3
Wysoker, A.4
Nemesh, J.5
Cawley, S.6
Hubbell, E.7
Veitch, J.8
Collins, P.J.9
Darvishi, K.10
Lee, C.11
Nizzari, M.M.12
Gabriel, S.B.13
Purcell, S.14
Daly, M.J.15
Altshuler, D.16
-
10
-
-
0024508964
-
Mapping Mendelian factors underlying quantitative traits using RFLP linkage maps
-
1:STN:280:DyaL1M7jsl2nug%3D%3D 1203601 2563713
-
Lander ES, Botstein D (1989) Mapping Mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics 121:185-199
-
(1989)
Genetics
, vol.121
, pp. 185-199
-
-
Lander, E.S.1
Botstein, D.2
-
11
-
-
82355169007
-
Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies
-
21922541 10.1002/gepi.20628
-
Li D, Lewinger JP, Gauderman WJ, Murcray CE, Conti D (2011) Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies. Genet Epidemiol 35:790-799
-
(2011)
Genet Epidemiol
, vol.35
, pp. 790-799
-
-
Li, D.1
Lewinger, J.P.2
Gauderman, W.J.3
Murcray, C.E.4
Conti, D.5
-
12
-
-
78650979009
-
Kashin-Beck disease and Sayiwak disease in China: Prevalence and a comparison of the clinical manifestations, familial aggregation, and heritability
-
Lu AL, Guo X, Aisha MM, Shi XW, Zhang YZ, Zhang YY (2010) Kashin-Beck disease and Sayiwak disease in China: Prevalence and a comparison of the clinical manifestations, familial aggregation, and heritability. Bone 48:347-353
-
(2010)
Bone
, vol.48
, pp. 347-353
-
-
Lu, A.L.1
Guo, X.2
Aisha, M.M.3
Shi, X.W.4
Zhang, Y.Z.5
Zhang, Y.Y.6
-
13
-
-
0034879525
-
Cloning and sequencing of a novel human gene that encodes a putative target protein of Nesh-SH3
-
1:CAS:528:DC%2BD3MXmtVynt7w%3D 11501947 10.1007/s100380170049
-
Matsuda S, Iriyama C, Yokozaki S, Ichigotani Y, Shirafuji N, Yamaki K, Hayakawa T, Hamaguchi M (2001) Cloning and sequencing of a novel human gene that encodes a putative target protein of Nesh-SH3. J Hum Genet 46:483-486
-
(2001)
J Hum Genet
, vol.46
, pp. 483-486
-
-
Matsuda, S.1
Iriyama, C.2
Yokozaki, S.3
Ichigotani, Y.4
Shirafuji, N.5
Yamaki, K.6
Hayakawa, T.7
Hamaguchi, M.8
-
14
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
1:CAS:528:DC%2BD1cXhtFKht7%2FN 18776908 10.1038/ng.238
-
McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, Wysoker A, Shapero MH, de Bakker PI, Maller JB, Kirby A, Elliott AL, Parkin M, Hubbell E, Webster T, Mei R, Veitch J, Collins PJ, Handsaker R, Lincoln S, Nizzari M, Blume J, Jones KW, Rava R, Daly MJ, Gabriel SB, Altshuler D (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40:1166-1174
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
Cawley, S.4
Nemesh, J.5
Wysoker, A.6
Shapero, M.H.7
De Bakker, P.I.8
Maller, J.B.9
Kirby, A.10
Elliott, A.L.11
Parkin, M.12
Hubbell, E.13
Webster, T.14
Mei, R.15
Veitch, J.16
Collins, P.J.17
Handsaker, R.18
Lincoln, S.19
Nizzari, M.20
Blume, J.21
Jones, K.W.22
Rava, R.23
Daly, M.J.24
Gabriel, S.B.25
Altshuler, D.26
more..
-
15
-
-
0032531956
-
Kashin-Beck osteoarthropathy in rural Tibet in relation to selenium and iodine status
-
1:STN:280:DyaK1cvjt1Cmsw%3D%3D 9770558 10.1056/NEJM199810153391604
-
Moreno-Reyes R, Suetens C, Mathieu F, Begaux F, Zhu D, Rivera MT, Boelaert M, Neve J, Perlmutter N, Vanderpas J (1998) Kashin-Beck osteoarthropathy in rural Tibet in relation to selenium and iodine status. N Engl J Med 339:1112-1120
-
(1998)
N Engl J Med
, vol.339
, pp. 1112-1120
-
-
Moreno-Reyes, R.1
Suetens, C.2
Mathieu, F.3
Begaux, F.4
Zhu, D.5
Rivera, M.T.6
Boelaert, M.7
Neve, J.8
Perlmutter, N.9
Vanderpas, J.10
-
16
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
1:CAS:528:DC%2BD28XnsVCgsrg%3D 16862161 10.1038/ng1847
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38:904-909
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
17
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
1:STN:280:DC%2BD3cvislKrtA%3D%3D 1461096 10835412
-
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945-959
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
18
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
1:CAS:528:DC%2BD2sXhtVSqurrL 1950838 17701901 10.1086/519795
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81:559-575
-
(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
-
19
-
-
0029001682
-
Extreme discordant sib pairs for mapping quantitative trait loci in humans
-
1:CAS:528:DyaK2MXmtlarsbw%3D 7777857 10.1126/science.7777857
-
Risch N, Zhang H (1995) Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science 268:1584-1589
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
20
-
-
77951799598
-
Heritability estimates and linkage analysis of 23 short tandem repeat loci on chromosomes 2, 11, and 12 in an endemic osteochondropathy in China
-
1:CAS:528:DC%2BC3cXltlyru7k%3D 20166850 10.3109/03009740903270599
-
Shi XW, Guo X, Lv AL, Kang L, Zhou YL, Zhang YZ, Wu XM, Bai YD (2010) Heritability estimates and linkage analysis of 23 short tandem repeat loci on chromosomes 2, 11, and 12 in an endemic osteochondropathy in China. Scand J Rheumatol 39:259-265
-
(2010)
Scand J Rheumatol
, vol.39
, pp. 259-265
-
-
Shi, X.W.1
Guo, X.2
Lv, A.L.3
Kang, L.4
Zhou, Y.L.5
Zhang, Y.Z.6
Wu, X.M.7
Bai, Y.D.8
-
21
-
-
80155128007
-
Genetic variants in the HLA-DRB1 gene are associated with Kashin-Beck disease in the Tibetan population
-
1:CAS:528:DC%2BC3MXhtlOksLrE 21739420 10.1002/art.30526
-
Shi Y, Lu F, Liu X, Wang Y, Huang L, Long W, Lv B, Zhang K, Ma S, Lin H, Cheng J, Zhou B, Hu M, Deng J, Zhu J, Hao P, Yang X, Zeng M, Wang X, Shen S, Yang Z (2011) Genetic variants in the HLA-DRB1 gene are associated with Kashin-Beck disease in the Tibetan population. Arthritis Rheum 63:3408-3416
-
(2011)
Arthritis Rheum
, vol.63
, pp. 3408-3416
-
-
Shi, Y.1
Lu, F.2
Liu, X.3
Wang, Y.4
Huang, L.5
Long, W.6
Lv, B.7
Zhang, K.8
Ma, S.9
Lin, H.10
Cheng, J.11
Zhou, B.12
Hu, M.13
Deng, J.14
Zhu, J.15
Hao, P.16
Yang, X.17
Zeng, M.18
Wang, X.19
Shen, S.20
Yang, Z.21
more..
-
22
-
-
84863116416
-
Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD
-
3601404 22420046 10.1176/appi.ajp.2011.11040551
-
Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A (2012) Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Am J Psychiatry 169:186-194
-
(2012)
Am J Psychiatry
, vol.169
, pp. 186-194
-
-
Stergiakouli, E.1
Hamshere, M.2
Holmans, P.3
Langley, K.4
Zaharieva, I.5
Hawi, Z.6
Kent, L.7
Gill, M.8
Williams, N.9
Owen, M.J.10
O'Donovan, M.11
Thapar, A.12
-
23
-
-
67149102421
-
Diseases. A medical mystery in middle China
-
1:CAS:528:DC%2BD1MXns12nu7s%3D 19520932 10.1126/science.324-1378
-
Stone R (2009) Diseases. A medical mystery in middle China. Science 324:1378-1381
-
(2009)
Science
, vol.324
, pp. 1378-1381
-
-
Stone, R.1
-
24
-
-
33846978695
-
Relative impact of nucleotide and copy number variation on gene expression phenotypes
-
1:CAS:528:DC%2BD2sXhsVShs7Y%3D 2665772 17289997 10.1126/science.1136678
-
Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Thorne N, Redon R, Bird CP, de Grassi A, Lee C, Tyler-Smith C, Carter N, Scherer SW, Tavare S, Deloukas P, Hurles ME, Dermitzakis ET (2007) Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 315:848-853
-
(2007)
Science
, vol.315
, pp. 848-853
-
-
Stranger, B.E.1
Forrest, M.S.2
Dunning, M.3
Ingle, C.E.4
Beazley, C.5
Thorne, N.6
Redon, R.7
Bird, C.P.8
De Grassi, A.9
Lee, C.10
Tyler-Smith, C.11
Carter, N.12
Scherer, S.W.13
Tavare, S.14
Deloukas, P.15
Hurles, M.E.16
Dermitzakis, E.T.17
-
25
-
-
57549091805
-
Comparative analysis of gene expression profiles between the normal human cartilage and the one with endemic osteoarthritis
-
1:STN:280:DC%2BD1M%2FhsVOqtw%3D%3D 18579416 10.1016/j.joca.2008.05.008
-
Wang WZ, Guo X, Duan C, Ma WJ, Zhang YG, Xu P, Gao ZQ, Wang ZF, Yan H, Zhang YF, Yu YX, Chen JC, Lammi MJ (2009) Comparative analysis of gene expression profiles between the normal human cartilage and the one with endemic osteoarthritis. Osteoarthr Cartil 17:83-90
-
(2009)
Osteoarthr Cartil
, vol.17
, pp. 83-90
-
-
Wang, W.Z.1
Guo, X.2
Duan, C.3
Ma, W.J.4
Zhang, Y.G.5
Xu, P.6
Gao, Z.Q.7
Wang, Z.F.8
Yan, H.9
Zhang, Y.F.10
Yu, Y.X.11
Chen, J.C.12
Lammi, M.J.13
-
26
-
-
77952882390
-
Association study between polymorphisms in selenoprotein genes and susceptibility to Kashin-Beck disease
-
1:STN:280:DC%2BC3czjvFOmtw%3D%3D 20178852 10.1016/j.joca.2010.02.004
-
Xiong YM, Mo XY, Zou XZ, Song RX, Sun WY, Lu W, Chen Q, Yu YX, Zang WJ (2010) Association study between polymorphisms in selenoprotein genes and susceptibility to Kashin-Beck disease. Osteoarthr Cartil 18:817-824
-
(2010)
Osteoarthr Cartil
, vol.18
, pp. 817-824
-
-
Xiong, Y.M.1
Mo, X.Y.2
Zou, X.Z.3
Song, R.X.4
Sun, W.Y.5
Lu, W.6
Chen, Q.7
Yu, Y.X.8
Zang, W.J.9
-
27
-
-
77955374501
-
The effect of Kashin-Beck disease-affected feed and T-2 toxin on the bone development of Wistar rats
-
20704625 10.1111/j.1756-185X.2010.01530.x
-
Yan D, Kang P, Yang J, Shen B, Zhou Z, Duan L, Deng J, Huang H, Pei FX (2010) The effect of Kashin-Beck disease-affected feed and T-2 toxin on the bone development of Wistar rats. Int J Rheum Dis 13:266-272
-
(2010)
Int J Rheum Dis
, vol.13
, pp. 266-272
-
-
Yan, D.1
Kang, P.2
Yang, J.3
Shen, B.4
Zhou, Z.5
Duan, L.6
Deng, J.7
Huang, H.8
Pei, F.X.9
-
28
-
-
57149123783
-
Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis
-
1:CAS:528:DC%2BD1MXit1Gg 2667994 18992858 10.1016/j.ajhg.2008.10.006
-
Yang TL, Chen XD, Guo Y, Lei SF, Wang JT, Zhou Q, Pan F, Chen Y, Zhang ZX, Dong SS, Xu XH, Yan H, Liu X, Qiu C, Zhu XZ, Chen T, Li M, Zhang H, Zhang L, Drees BM, Hamilton JJ, Papasian CJ, Recker RR, Song XP, Cheng J, Deng HW (2008) Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis. Am J Hum Genet 83:663-674
-
(2008)
Am J Hum Genet
, vol.83
, pp. 663-674
-
-
Yang, T.L.1
Chen, X.D.2
Guo, Y.3
Lei, S.F.4
Wang, J.T.5
Zhou, Q.6
Pan, F.7
Chen, Y.8
Zhang, Z.X.9
Dong, S.S.10
Xu, X.H.11
Yan, H.12
Liu, X.13
Qiu, C.14
Zhu, X.Z.15
Chen, T.16
Li, M.17
Zhang, H.18
Zhang, L.19
Drees, B.M.20
Hamilton, J.J.21
Papasian, C.J.22
Recker, R.R.23
Song, X.P.24
Cheng, J.25
Deng, H.W.26
more..
-
29
-
-
84872087895
-
Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study
-
1:CAS:528:DC%2BC3sXpsVyisw%3D%3D 3537105 23175694 10.1210/jc.2012-2751
-
Yang TL, Guo Y, Shen H, Li J, Glessner JT, Qiu C, Deng FY, Tian Q, Yu P, Liu YZ, Liu YJ, Hakonarson H, Grant SF, Deng HW (2013) Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study. J Clin Endocrinol Metab 98:E191-E195
-
(2013)
J Clin Endocrinol Metab
, vol.98
-
-
Yang, T.L.1
Guo, Y.2
Shen, H.3
Li, J.4
Glessner, J.T.5
Qiu, C.6
Deng, F.Y.7
Tian, Q.8
Yu, P.9
Liu, Y.Z.10
Liu, Y.J.11
Hakonarson, H.12
Grant, S.F.13
Deng, H.W.14
-
30
-
-
84863717547
-
Association of TNF-alpha and Fas gene promoter polymorphism with the risk of Kashin-Beck disease in Northwest Chinese population
-
22431252 10.1007/s10067-012-1975-7
-
Zhao QM, Guo X, Lai JH, Tan WH, Wang WZ, Dang XQ (2012) Association of TNF-alpha and Fas gene promoter polymorphism with the risk of Kashin-Beck disease in Northwest Chinese population. Clin Rheumatol 31:1051-1057
-
(2012)
Clin Rheumatol
, vol.31
, pp. 1051-1057
-
-
Zhao, Q.M.1
Guo, X.2
Lai, J.H.3
Tan, W.H.4
Wang, W.Z.5
Dang, X.Q.6
|