-
1
-
-
0029980777
-
Number of people with glaucoma worldwide
-
Quigley HA. Number of people with glaucoma worldwide. Br J Ophthalmol, 80(5): 389-93. (1996) (Pubitemid 26158268)
-
(1996)
British Journal of Ophthalmology
, vol.80
, Issue.5
, pp. 389-393
-
-
Quigley, H.A.1
-
3
-
-
79959702717
-
-
Beijing: People's medical publishing house
-
Li Meiyu. Glaucoma. Beijing: People's medical publishing house, 515-9. (2004)
-
(2004)
Glaucoma
, pp. 515-519
-
-
Li, M.1
-
4
-
-
79959708501
-
-
Beijing:People's medical publishing house
-
Li Fengming. YANKEQUANSHU. Beijing:People's medical publishing house, 1962-74. (1996)
-
(1996)
Yankequanshu
, pp. 1962-1974
-
-
Li, F.1
-
5
-
-
0023230020
-
Prevalence and mode of inheritance of major genetic eye diseases in China
-
Hu DN. Prevalence and mode of inheritance of major genetic eye diseases in China. J Med Genet, 24(10):584-8. (1987)
-
(1987)
J Med Genet
, vol.24
, Issue.10
, pp. 584-588
-
-
Hu, D.N.1
-
6
-
-
0019936088
-
Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset
-
DOI 10.1007/BF00296440
-
Gencik A, Gencikova A and Ferak V. Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset. Hum Genet, 61(3):193-7. (1982) (Pubitemid 12004521)
-
(1982)
Human Genetics
, vol.61
, Issue.3
, pp. 193-197
-
-
Gencik, A.1
Gencikova, A.2
Ferak, V.3
-
7
-
-
0028880039
-
Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity (J)
-
Sarfarazi M, Akarsu AN and Hossain A. Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity (J). Genomics, 30(2):171-7. (1995)
-
(1995)
Genomics
, vol.30
, Issue.2
, pp. 171-177
-
-
Sarfarazi, M.1
Akarsu, A.N.2
Hossain, A.3
-
8
-
-
0029836678
-
A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region
-
Akarsu AN, Turacli ME, Aktan SG, Barsoum-Homsy M, Chevrette L, Sayli BS and Sarfarazi M. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Hum Mol Genet, 5(8):1199-203. (1996) (Pubitemid 26318561)
-
(1996)
Human Molecular Genetics
, vol.5
, Issue.8
, pp. 1199-1203
-
-
Akarsu, A.N.1
Turacli, M.E.2
Aktan, S.G.3
Barsoum-Homsy, M.4
Chevrette, L.5
Sayli, B.S.6
Sarfarazi, M.7
-
10
-
-
33644848333
-
Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds
-
DOI 10.1167/iovs.05-0912
-
Chakrabarti S, Kaur K, Kaur I, Mandal AK, Parikh RS, Thomas R and Majumder PP. Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds. Invest Ophthalmol Vis Sci, 47(1):43-7. (2006) (Pubitemid 46780793)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.1
, pp. 43-47
-
-
Chakrabarti, S.1
Kaur, K.2
Kaur, I.3
Mandal, A.K.4
Parikh, R.S.5
Thomas, R.6
Majumder, P.P.7
-
11
-
-
0034639693
-
Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus
-
Bejjani BA, Stockton DW, Lewis RA, Tomey KF, Dueker DK, Jabak M, Astle WF and Lupski JR. Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus. Hum Mol Genet, 9(3):367-74. (2000) (Pubitemid 30098730)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.3
, pp. 367-374
-
-
Bejjani, B.A.1
Stockton, D.W.2
Lewis, R.A.3
Tomey, K.F.4
Dueker, D.K.5
Jabak, M.6
Astle, W.F.7
Lupski, J.R.8
-
12
-
-
18344398251
-
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients
-
Sitorus R, Ardjo SM, Lorenz B and Preising M. CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients. J Med Genet, 40(1):e9. (2003)
-
(2003)
J Med Genet
, vol.40
, Issue.1
-
-
Sitorus, R.1
Ardjo, S.M.2
Lorenz, B.3
Preising, M.4
-
13
-
-
0036821466
-
A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco
-
DOI 10.1034/j.1399-0004.2002.620415.x
-
Belmouden A, Melki R and Hamdani M. A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco. Clin Genet, 62(4):334-9. (2002) (Pubitemid 36372753)
-
(2002)
Clinical Genetics
, vol.62
, Issue.4
, pp. 334-339
-
-
Belmouden, A.1
Melki, R.2
Hamdani, M.3
Zaghloul, K.4
Amraoui, A.5
Nadifi, S.6
Akhayat, O.7
Garchon, H.-J.8
-
14
-
-
15844383248
-
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients
-
Reddy AB, Kaur K, Mandal AK, Panicker SG, Thomas R, Hasnain SE, Balasubramanian D, Chakrabarti S. Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Mol Vis, 10: 696-702. (2004) (Pubitemid 41358225)
-
(2004)
Molecular Vision
, vol.10
, pp. 696-702
-
-
Reddy, A.B.M.1
Kaur, K.2
Mandal, A.K.3
Panicker, S.G.4
Thomas, R.5
Hasnain, S.E.6
Balasubramanian, D.7
Chakrabarti, S.8
-
15
-
-
2142702294
-
Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma
-
DOI 10.1167/iovs.03-0404
-
Panicker SG, Mandal AK, Reddy AB, Gothwal VK and Hasnain SE. Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma. Invest Ophthalmol Vis Sci, 45(4):1149-56. (2004) (Pubitemid 38869020)
-
(2004)
Investigative Ophthalmology and Visual Science
, vol.45
, Issue.4
, pp. 1149-1156
-
-
Panicker, S.G.1
Mandal, A.K.2
Reddy, A.B.M.3
Gothwal, V.K.4
Hasnain, S.E.5
-
16
-
-
0034854849
-
Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma
-
Mashima Y, Suzuki Y, Sergeev Y, Ohtake Y, Tanino T, Kimura I, Miyata H, Aihara M, Tanihara H, Inatani M, Azuma N, Iwata T and Araie M. Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma. Invest Ophthalmol Vis Sci, 42(10): 2211-6. (2001) (Pubitemid 32848848)
-
(2001)
Investigative Ophthalmology and Visual Science
, vol.42
, Issue.10
, pp. 2211-2216
-
-
Mashima, Y.1
Suzuki, Y.2
Sergeev, Y.3
Ohtake, Y.4
Tanino, T.5
Kimura, I.6
Miyata, H.7
Aihara, M.8
Tanihara, H.9
Inatani, M.10
Azuma, N.11
Iwata, T.12
Araie, M.13
-
17
-
-
54049126558
-
CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma
-
Chen Y, Jiang D, Yu L, Katz B, Zhang K, Wan B and Sun X. CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma. Arch Ophthalmol, 126(10): 1443-7. (2008)
-
(2008)
Arch Ophthalmol
, vol.126
, Issue.10
, pp. 1443-1447
-
-
Chen, Y.1
Jiang, D.2
Yu, L.3
Katz, B.4
Zhang, K.5
Wan, B.6
Sun, X.7
-
18
-
-
0029836678
-
AN Akarsu, ME Turacli, SG Aktan, M Barsoum-Homsy, L Chevrette, BS Sayli and M Sarfarazi. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region (J)
-
AN Akarsu, ME Turacli, SG Aktan, M Barsoum-Homsy, L Chevrette, BS Sayli and M Sarfarazi. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region (J). Hum Mol Genet, 1996, 5(8):1199-203
-
(1996)
Hum Mol Genet
, vol.5
, Issue.8
, pp. 1199-1203
-
-
-
19
-
-
0037809408
-
Gene expression profile of the human trabecular meshwork: NEIBank sequence tag analysis
-
DOI 10.1167/iovs.02-1099
-
Tomarev SI, Wistow G, Raymond V, Dubois S and Malyukova I. Gene Expression Profile of the Human Trabecular Meshwork: NEIBank Sequence Tag Analysis. Invest Ophthalmol Vis Sci, 44(6): 2588-96. (2003) (Pubitemid 36618418)
-
(2003)
Investigative Ophthalmology and Visual Science
, vol.44
, Issue.6
, pp. 2588-2596
-
-
Tomarev, S.I.1
Wistow, G.2
Raymond, V.3
Dubois, S.4
Malyukova, I.5
-
20
-
-
49049104205
-
Angiopoietin-like 7 secretion is induced by glaucoma stimuli and its concentration is elevated in glaucomatous aqueous humor
-
Kuchtey J, Kallberg ME, Gelatt KN, Rinkoski T, Komaromy AM and Kuchtey RW. Angiopoietin-like 7 Secretion Is Induced by Glaucoma Stimuli and Its Concentration Is Elevated in Glaucomatous Aqueous Humor. Invest Ophthalmol Vis Sci, 49(8): 3438-48. (2008)
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, Issue.8
, pp. 3438-3448
-
-
Kuchtey, J.1
Kallberg, M.E.2
Gelatt, K.N.3
Rinkoski, T.4
Komaromy, A.M.5
Kuchtey, R.W.6
-
21
-
-
51549087751
-
Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani families
-
Sabika Firasat, S. Amer Riazuddin, J. Fielding Hejtmancik and Sheikh Riazuddin. Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani families. Mol Vis, 14:1659-65. (2008)
-
(2008)
Mol Vis
, vol.14
, pp. 1659-1665
-
-
Firasat, S.1
Amer Riazuddin, S.2
Fielding Hejtmancik, J.3
Riazuddin, S.4
-
22
-
-
70349578331
-
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
-
Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E and Paisán-Ruiz C. Loss of Function Mutations in the Gene Encoding Latent Transforming Growth Factor Beta Binding Protein 2, LTBP2, Cause Primary Congenital Glaucoma. Human Molecular Genetics, 18(20), 3969-77. (2009)
-
(2009)
Human Molecular Genetics
, vol.18
, Issue.20
, pp. 3969-3977
-
-
Narooie-Nejad, M.1
Paylakhi, S.H.2
Shojaee, S.3
Fazlali, Z.4
Rezaei Kanavi, M.5
Nilforushan, N.6
Yazdani, S.7
Babrzadeh, F.8
Suri, F.9
Ronaghi, M.10
Elahi, E.11
Paisán-Ruiz, C.12
-
23
-
-
0034463562
-
Family-based association studies
-
DOI 10.1191/096228000668447080
-
Zhao H. Family-based association studies. Stat MethodsMed Res, 9(6): 563-87. (2000) (Pubitemid 32229170)
-
(2000)
Statistical Methods in Medical Research
, vol.9
, Issue.6
, pp. 563-587
-
-
Zhao, H.1
-
24
-
-
0842285687
-
Matching Strategies for Genetic Association Studies in Structured Populations
-
DOI 10.1086/381716
-
Hinds DA, Stokowski RP, Patil N, Konvicka K, Kershenobich D, Cox DR and Ballinger DG. Matching strategies for genetic association studies in structured populations. Am J Hum Genet, 74(2): 317-25. (2004) (Pubitemid 38168619)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.2
, pp. 317-325
-
-
Hinds, D.A.1
Stokowski, R.P.2
Patil, N.3
Konvicka, K.4
Kershenobich, D.5
Cox, D.R.6
Ballinger, D.G.7
-
25
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE and Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet, 52(3): 506-13. (1993)
-
(1993)
Am J Hum Genet
, vol.52
, Issue.3
, pp. 506-513
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
27
-
-
59149096149
-
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21
-
Zhang XJ, Huang W, Yang S, Sun LD, Zhang FY, Zhu QX, Zhang FR, Zhang C, Du WH, Pu XM, Li H, Xiao FL, Wang ZX, Cui Y, Hao F, Zheng J, Yang XQ, Cheng H, He CD, Liu XM, Xu LM, Zheng HF, Zhang SM, Zhang JZ, Wang HY, Cheng YL, Ji BH, Fang QY, Li YZ, Zhou FS, Han JW, Quan C, Chen B, Liu JL, Lin D, Fan L, Zhang AP, Liu SX, Yang CJ, Wang PG, Zhou WM, Lin GS, Wu WD, Fan X, Gao M, Yang BQ, Lu WS, Zhang Z, Zhu KJ, Shen SK, Li M, Zhang XY, Cao TT, Ren W, Zhang X, He J, Tang XF, Lu S, Yang JQ, Zhang L, Wang DN, Yuan F, Yin XY, Huang HJ, Wang HF, Lin XY and Liu JJ. Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. Nat Genet, 41(2):205-10. (2009)
-
(2009)
Nat Genet
, vol.41
, Issue.2
, pp. 205-210
-
-
Zhang, X.J.1
Huang, W.2
Yang, S.3
Sun, L.D.4
Zhang, F.Y.5
Zhu, Q.X.6
Zhang, F.R.7
Zhang, C.8
Du, W.H.9
Pu, X.M.10
Li, H.11
Xiao, F.L.12
Wang, Z.X.13
Cui, Y.14
Hao, F.15
Zheng, J.16
Yang, X.Q.17
Cheng, H.18
He, C.D.19
Liu, X.M.20
Xu, L.M.21
Zheng, H.F.22
Zhang, S.M.23
Zhang, J.Z.24
Wang, H.Y.25
Cheng, Y.L.26
Ji, B.H.27
Fang, Q.Y.28
Li, Y.Z.29
Zhou, F.S.30
Han, J.W.31
Quan, C.32
Chen, B.33
Liu, J.L.34
Lin, D.35
Fan, L.36
Zhang, A.P.37
Liu, S.X.38
Yang, C.J.39
Wang, P.G.40
Zhou, W.M.41
Lin, G.S.42
Wu, W.D.43
Fan, X.44
Gao, M.45
Yang, B.Q.46
Lu, W.S.47
Zhang, Z.48
Zhu, K.J.49
Shen, S.K.50
Li, M.51
Zhang, X.Y.52
Cao, T.T.53
Ren, W.54
Zhang, X.55
He, J.56
Tang, X.F.57
Lu, S.58
Yang, J.Q.59
Zhang, L.60
Wang, D.N.61
Yuan, F.62
Yin, X.Y.63
Huang, H.J.64
Wang, H.F.65
Lin, X.Y.66
Liu, J.J.67
more..
-
29
-
-
0036594904
-
A strategy for the rapid discovery of disease markers using the MassARRAY system
-
68-69
-
Rodi CP, Darnhofer-Patel B, Stanssens P, Zabeau M and van den Boom D. A strategy for the rapid discovery of disease markers using the MassARRAY system. Biotechniques, Suppl: 62-6, 68-9. (2002)
-
(2002)
Biotechniques
, Issue.SUPPL.
, pp. 62-66
-
-
Rodi, C.P.1
Darnhofer-Patel, B.2
Stanssens, P.3
Zabeau, M.4
Van Den Boom, D.5
-
30
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
DOI 10.1002/gepi.10252
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol, 25(2):115-21. (2003) (Pubitemid 37064867)
-
(2003)
Genetic Epidemiology
, vol.25
, Issue.2
, pp. 115-121
-
-
Dudbridge, F.1
-
31
-
-
41649094148
-
Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data
-
DOI 10.1159/000119108
-
Dudbridge F. Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data. Hum Hered, 66(2):87-98. (2008) (Pubitemid 351482562)
-
(2008)
Human Heredity
, vol.66
, Issue.2
, pp. 87-98
-
-
Dudbridge, F.1
-
32
-
-
79959503826
-
The international HapMap project (J)
-
Gibbs, RA, Belmont, JW, Hardenbol, P, Willis, TD, Yu, FL, Yang, HM, Ch'ang, LY, Huang, W, Liu, B, Shen, Y, Tam, PKH, Tsui, LC, Waye, MMY, Wong, JTF, Zeng, CQ, Zhang, QR, Chee, MS, Galver, LM, Kruglyak, S, Murray, SS, Oliphant, AR, Montpetit, A, Hudson, TJ, Chagnon, F, Ferretti, V, Leboeuf, M, Phillips, MS, Verner, A, Kwok, PY, Duan, SH, Lind, DL, Miller, RD, Rice, JP, Saccone, NL, Taillon-Miller, P, Xiao, M, Nakamura, Y, Sekine, A, Sorimachi, K, Tanaka, T; Tanaka, Y, Tsunoda, T, Yoshino, E, Bentley, DR, Deloukas, P, Hunt, S, Powell, D, Altshuler, D, Gabriel, SB, Qiu, RZ, Ken, A, Dunston, GM, Kato, K, Niikawa, N, Knoppers, BM, Foster, MW, Clayton, EW, Wang, VO, Watkin, J, Gibbs, RA, Belmont, JW, Sodergren, E, Weinstock, GM, Wilson, RK, Fulton, LL, Rogers, J, Birren, BW, Han, H, Wang, HG, Godbout, M, Wallenburg, JC, L'Archeveque, P, Bellemare, G, Todani, K, Fujita, T, Tanaka, S, Holden, AL, Lai, EH, Collins, FS, Brooks, LD, McEwen, JE, Guyer, MS, Jordan, E, Peterson, JL, Spiegel, J, Sung, LM, Zacharia, LF, Kennedy, K, Dunn, MG, Seabrook, R, Shillito, M, Skene, B, Stewart, JG, Valle, DL, Clayton, EW, Jorde, LB, Belmont, JW, Chakravarti, A, Cho, MK, Duster, T, Foster, MW, Jasperse, M, Knoppers, BM, Kwok, PY, Licinio, J, Long, JC, Marshall, PA, Ossorio, PN, Wang, VO, Rotimi, CN, Royal, CDM, Spallone, P, Terry, SF, Lander, ES, Lai, EH, Nickerson, DA, Abecasis, GR, Altshuler, D, Bentley, DR, Boehnke, M, Cardon, LR, Daly, MJ, Deloukas, P, Douglas, JA, Gabriel, SB, Hudson, RR, Hudson, TJ, Kruglyak, L, Kwok, PY, Nakamura, Y, Nussbaum, RL, Royal, CDM, Schaffner, SF, Sherry, ST; Stein, LD and Tanaka, T. The International HapMap Project (J). Nature, 2003, 426(6968): 789-96.
-
(2003)
Nature
, vol.426
, Issue.6968
, pp. 789-796
-
-
Gibbs, R.A.1
Belmont, J.W.2
Hardenbol, P.3
Willis, T.D.4
Yu, F.L.5
Yang, H.M.6
Chang, L.Y.7
Huang, W.8
Liu, B.9
Shen, Y.10
Pkh, T.11
Tsui, L.C.12
Mmy, W.13
Jtf, W.14
Zeng, C.Q.15
Zhang, Q.R.16
Chee, M.S.17
Galver, L.M.18
Kruglyak, S.19
Murray, S.S.20
Oliphant, A.R.21
Montpetit, A.22
Hudson, T.J.23
Chagnon, F.24
Ferretti, V.25
Leboeuf, M.26
Phillips, M.S.27
Verner, A.28
Kwok, P.Y.29
Duan, S.H.30
Lind, D.L.31
Miller, R.D.32
Rice, J.P.33
Saccone, N.L.34
Taillon-Miller, P.35
Xiao, M.36
Nakamura, Y.37
Sekine, A.38
Sorimachi, K.39
Tanaka, T.40
Tanaka, Y.41
Tsunoda, T.42
Yoshino, E.43
Bentley, D.R.44
Deloukas, P.45
Hunt, S.46
Powell, D.47
Altshuler, D.48
Gabriel, S.B.49
Qiu, R.Z.50
Ken, A.51
Dunston, G.M.52
Kato, K.53
Niikawa, N.54
Knoppers, B.M.55
Foster, M.W.56
Clayton, E.W.57
Wang, V.O.58
Watkin, J.59
Gibbs, R.A.60
Belmont, J.W.61
Sodergren, E.62
Weinstock, G.M.63
Wilson, R.K.64
Fulton, L.L.65
Rogers, J.66
Birren, B.W.67
Han, H.68
Wang, H.G.69
Godbout, M.70
Wallenburg, J.C.71
L'Archeveque, P.72
Bellemare, G.73
Todani, K.74
Fujita, T.75
Tanaka, S.76
Holden, A.L.77
Lai, E.H.78
Collins, F.S.79
Brooks, L.D.80
McEwen, J.E.81
Guyer, M.S.82
Jordan, E.83
Peterson, J.L.84
Spiegel, J.85
Sung, L.M.86
Zacharia, L.F.87
Kennedy, K.88
Dunn, M.G.89
Seabrook, R.90
Shillito, M.91
Skene, B.92
Stewart, J.G.93
Valle, D.L.94
Clayton, E.W.95
Jorde, L.B.96
Belmont, J.W.97
Chakravarti, A.98
Cho, M.K.99
more..
-
33
-
-
0035094764
-
Variation is the spice of life
-
DOI 10.1038/85776
-
Kruglyak L and Nickerson DA. Variation is the spice of life. Nat Genet, (3): 234-6. (2001) (Pubitemid 32201838)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 234-236
-
-
Kruglyak, L.1
Nickerson, D.A.2
-
34
-
-
0030688004
-
Variations on a theme: Cataloging human DNA sequence variation
-
DOI 10.1126/science.278.5343.1580
-
Collins FS, Guyer MS, and Charkravarti A. Variations on a theme: cataloging human DNA sequence variation. Science, 278 (5343): 1580-1. (1997) (Pubitemid 27516268)
-
(1997)
Science
, vol.278
, Issue.5343
, pp. 1580-1581
-
-
Collins, F.S.1
Guyer, M.S.2
Chakravarti, A.3
-
35
-
-
0033832928
-
Usefulness of single nucleotide polymorphism data for estimating population parameters (J)
-
Mary K. Kuhnera, Peter Beerlia, Jon Yamatoa, and Joseph Felsenstein. Usefulness of single nucleotide polymorphism data for estimating population parameters (J). Genetics, 156 (1): 439-47. 2000
-
(2000)
Genetics
, vol.156
, Issue.1
, pp. 439-447
-
-
Kuhnera, M.K.1
Beerlia, P.2
Yamatoa, J.3
Felsenstein, J.4
-
37
-
-
0242380286
-
Genome scans and candidate gene approaches in the study of common diseases and variable drug responses
-
DOI 10.1016/j.tig.2003.09.006
-
Goldstein DB, Ahmadi KR, Weale ME and Wood NW. Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends Genet, 19(11): 615-22. (2003) (Pubitemid 37338381)
-
(2003)
Trends in Genetics
, vol.19
, Issue.11
, pp. 615-622
-
-
Goldstein, D.B.1
Ahmadi, K.R.2
Weale, M.E.3
Wood, N.W.4
-
38
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
DOI 10.1038/ng1001-233
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG and Todd JA. Haplotype tagging for the identification of common disease genes. Nat Genet, 29(2): 233-7. (2001) (Pubitemid 32952665)
-
(2001)
Nature Genetics
, vol.29
, Issue.2
, pp. 233-237
-
-
Johnson, G.C.L.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.J.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.L.19
Clayton, D.G.20
Todd, J.A.21
more..
-
39
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
DOI 10.1126/science.1069424
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ and Altshuler D. The structure of haplotype blocks in the human genome. Science, 296(5576): 2225-9. (2002) (Pubitemid 34680308)
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
40
-
-
0033237816
-
The critical region for Behcet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA- B, by association analysis using refined microsatellite mapping
-
DOI 10.1086/302364
-
Ota M., Katsuyama Y., Tamiya G., Shiina T., Oka A., Ando H. Kimura M., Goto K., Ohno S., Inoko H. and Mizuki N. The Critical Region for Behcet Disease in the Human Major Histocompatibility Complex Is Reduced to a 46-kb Segment Centromeric of HLA-B, by Association Analysis Using Refined Microsatellite Mapping. Am J Hum Genet, 64(5):1406-10. (1999) (Pubitemid 30468760)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.5
, pp. 1406-1410
-
-
Ota, M.1
Mizuki, N.2
Katsuyama, Y.3
Tamiya, G.4
Shiina, T.5
Oka, A.6
Ando, H.7
Kimura, M.8
Goto, K.9
Ohno, S.10
Inoko, H.11
-
41
-
-
0037603549
-
Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma
-
DOI 10.1038/ng1166
-
Zhang Y, Leaves NI, Anderson GG, Ponting CP, Broxholme J, Holt R, Edser P, Bhattacharyya S, Dunham A, Adcock IM, Pulleyn L, Barnes PJ, Harper JI, Abecasis G, Cardon L, White M, Burton J, Matthews L, Mott R, Ross M, Cox R, Moffatt MF and Cookson WO. Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma (J). Nat Genet, 2003, 34(2):181-6. (Pubitemid 36666929)
-
(2003)
Nature Genetics
, vol.34
, Issue.2
, pp. 181-186
-
-
Zhang, Y.1
Leaves, N.I.2
Anderson, G.G.3
Ponting, C.P.4
Broxholme, J.5
Holt, R.6
Edser, P.7
Bhattacharyya, S.8
Dunham, A.9
Adcock, I.M.10
Pulleyn, L.11
Barnes, P.J.12
Harper, J.I.13
Abecasis, G.14
Cardon, L.15
White, M.16
Burton, J.17
Matthews, L.18
Mott, R.19
Ross, M.20
Cox, R.21
Moffatt, M.F.22
Cookson, W.O.C.M.23
more..
-
42
-
-
0033747061
-
Localization of the pathogenic gene of Behçet's disease by microsatellite analysis of three different populations
-
Mizuki N, Ota M, Yabuki K, Katsuyama Y, Ando H, Palimeris GD, Kaklamani E, Accorinti M, Pivetti-Pezzi P, Ohno S and Inoko H. Localization of the Pathogenic Gene of Behçet's Disease by Microsatellite Analysis of Three Different Populations. Invest Ophthalmol Vis Sci, 41(12): 3702-8. (2000)
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, Issue.12
, pp. 3702-3708
-
-
Mizuki, N.1
Ota, M.2
Yabuki, K.3
Katsuyama, Y.4
Ando, H.5
Palimeris, G.D.6
Kaklamani, E.7
Accorinti, M.8
Pivetti-Pezzi, P.9
Ohno, S.10
Inoko, H.11
-
43
-
-
0033927565
-
Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis
-
DOI 10.1086/302786
-
Keicho N, Ohashi J, Tamiya G, Nakata K, Taguchi Y, Azuma A, Ohishi N, Emi M, Park MH, Inoko H, Tokunaga K and Kudoh S. Fine Localization of a Major Disease-Susceptibility Locus for Diffuse Panbronchiolitis. Am J Hum Genet, 66(2):501-7. (2000) (Pubitemid 30468828)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.2
, pp. 501-507
-
-
Keicho, N.1
Ohashi, J.2
Tamiya, G.3
Nakata, K.4
Taguchi, Y.5
Azuma, A.6
Ohishi, N.7
Emi, M.8
Park, M.H.9
Inoko, H.10
Tokunaga, K.11
Kudoh, S.12
-
44
-
-
0035251794
-
A second susceptibility gene for developing rheumatoid arthritis in the human MHC is localized within a 70-kb interval telomeric of the TNF genes in the HLA class III region
-
DOI 10.1006/geno.2000.6371
-
Ota M, Katsuyama Y, Kimura A, Tsuchiya K, Kondo M, Naruse T, Mizuki N, Itoh K, Sasazuki T and Inoko H. A Second Susceptibility Gene for Developing Rheumatoid Arthritis in the Human MHC is Localized within a 70-kb Interval Telomeric of the TNF Genes in the HLA Class III Region. Genomics, 71(3): 263-70. (2001) (Pubitemid 32174821)
-
(2001)
Genomics
, vol.71
, Issue.3
, pp. 263-270
-
-
Ota, M.1
Katsuyama, Y.2
Kimura, A.3
Tsuchiya, K.4
Kondo, M.5
Naruse, T.6
Mizuki, N.7
Itoh, K.8
Sasazuki, T.9
Inoko, H.10
-
45
-
-
18444396271
-
A first-generation linkage disequilibrium map of human chromosome 22
-
DOI 10.1038/nature00864
-
Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, Dibling T, Tinsley E, Kirby S, Carter D, Papaspyridonos M, Livingstone S, Ganske R, Lõhmussaar E, Zernant J, Tõnisson N, Remm M, Mägi R, Puurand T, Vilo J, Kurg A, Rice K, Deloukas P, Mott R, Metspalu A, Bentley DR, Cardon LR and Dunham I. A first-generation linkage disequilibrium map of human chromosome 22. Nature, 418(6897): 544-8. (2002) (Pubitemid 34851401)
-
(2002)
Nature
, vol.418
, Issue.6897
, pp. 544-548
-
-
Dawson, E.1
Abecasis, G.R.2
Bumpstead, S.3
Chen, Y.4
Hunt, S.5
Beare, D.M.6
Pabial, J.7
Dibling, T.8
Tinsley, E.9
Kirby, S.10
Carter, D.11
Papaspyridonos, M.12
Livingstone, S.13
Ganske, R.14
Lohmussaar, E.15
Zernant, J.16
Tonisson, N.17
Remm, M.18
Magi, R.19
Puurand, T.20
Vilo, J.21
Kurg, A.22
Rice, K.23
Deloukas, P.24
Mott, R.25
Metspalu, A.26
Bentley, D.R.27
Cardon, L.R.28
Dunham, I.29
more..
-
46
-
-
0025886262
-
ABC1, a novel yeast nuclear gene has a dual function in mitochondria: It suppresses a cytochrome b mRNA translation defect and is essential for the electron transfer in the bc1 complex
-
Bousquet I, Dujardin G and Slonimski PP. ABC1, a novel yeast nuclear gene has a dual function in mitochondria: it suppresses a cytochrome b mRNA translation defect and is essential for the electron transfer in the bc 1 complex (J). EMBO J, 10(8): 2023-31. (1991) (Pubitemid 21905672)
-
(1991)
EMBO Journal
, vol.10
, Issue.8
, pp. 2023-2031
-
-
Bousquet, I.1
Dujardin, G.2
Slonimski, P.P.3
-
47
-
-
0031983781
-
Identification and characterization of aarF, a locus required for production of ubiquinone in Providencia stuartii and Escherichia coli and for expression of 2'-N-acetyltransferase in P. stuartii
-
Macinga DR, Cook GM, Poole RK and Rather,PN. Identification and characterization of aarF, a locus required for production of ubiquinone in Providencia stuartii and Escherichia coli and for expression of 2′-Nacetyltransferase in P. stuartii. J Bacteriol, 180(1):128-35. (1998) (Pubitemid 28023792)
-
(1998)
Journal of Bacteriology
, vol.180
, Issue.1
, pp. 128-135
-
-
Macinga, D.R.1
Cook, G.M.2
Poole, R.K.3
Rather, P.N.4
|