-
1
-
-
34648843900
-
Chronic inflammatory autoimmune disorders and atherosclerosis
-
Abou-Raya, S., A. Abou-Raya, A. Naim, and H. Abuelkheir, 2007 Chronic inflammatory autoimmune disorders and atherosclerosis. Ann. N. Y. Acad. Sci. 1107: 56-67.
-
(2007)
Ann. N. Y. Acad. Sci
, vol.1107
, pp. 56-67
-
-
Abou-Raya, S.1
Abou-Raya, A.2
Naim, A.3
Abuelkheir, H.4
-
2
-
-
34447316408
-
Efficient multilocus association testing for whole genome association studies using localized haplotype clustering
-
Browning, B. L., and S. R. Browning, 2007 Efficient multilocus association testing for whole genome association studies using localized haplotype clustering. Genet. Epidemiol. 31(5): 365-375.
-
(2007)
Genet. Epidemiol
, vol.31
, Issue.5
, pp. 365-375
-
-
Browning, B.L.1
Browning, S.R.2
-
3
-
-
84859588748
-
Detecting rare variant associations by identity-by-descent mapping in case-control studies
-
Browning, S. R., and E. A. Thompson, 2012 Detecting rare variant associations by identity-by-descent mapping in case-control studies. Genetics 190: 1521-1531.
-
(2012)
Genetics
, vol.190
, pp. 1521-1531
-
-
Browning, S.R.1
Thompson, E.A.2
-
4
-
-
0036715398
-
Glutamatergic regulation of bone resorption
-
Chenu, C., 2002 Glutamatergic regulation of bone resorption. J. Musculoskelet. Neuronal Interact. 2(5): 423-431.
-
(2002)
J. Musculoskelet. Neuronal Interact
, vol.2
, Issue.5
, pp. 423-431
-
-
Chenu, C.1
-
5
-
-
10044254265
-
The role of haplotypes in candidate gene studies
-
Clark, A. G., 2004 The role of haplotypes in candidate gene studies. Genet. Epidemiol. 27: 321-333.
-
(2004)
Genet. Epidemiol
, vol.27
, pp. 321-333
-
-
Clark, A.G.1
-
6
-
-
84856478855
-
A linear complexity phasing method for thousands of genomes
-
Delaneau, O., J. Marchini, and J. Zagury, 2012 A linear complexity phasing method for thousands of genomes. Nat. Methods 9(1): 179-181.
-
(2012)
Nat. Methods
, vol.9
, Issue.1
, pp. 179-181
-
-
Delaneau, O.1
Marchini, J.2
Zagury, J.3
-
7
-
-
0034641736
-
Complex promoter and coding region b2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness
-
Drysdale, C. M., D. W. McGraw, C. B. Stack, J. C. Stephens, R. S. Judson et al., 2000 Complex promoter and coding region b2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness. Proc. Natl. Acad. Sci. USA 97: 10483-10488.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 10483-10488
-
-
Drysdale, C.M.1
McGraw, D.W.2
Stack, C.B.3
Stephens, J.C.4
Judson, R.S.5
-
8
-
-
77952557918
-
Missing heritability and strategies for finding the underlying causes of complex disease
-
Eichler, E. E., J. Flint, G. Gibson, A. Kong, S. M. Leal et al., 2010 Missing heritability and strategies for finding the underlying causes of complex disease. Nat. Rev. Genet. 11(6): 446-450.
-
(2010)
Nat. Rev. Genet
, vol.11
, Issue.6
, pp. 446-450
-
-
Eichler, E.E.1
Flint, J.2
Gibson, G.3
Kong, A.4
Leal, S.M.5
-
9
-
-
77956059154
-
Genome-wide searching of rare genetic variants in WTCCC data
-
Feng, T., and X. Zhu, 2010 Genome-wide searching of rare genetic variants in WTCCC data. Hum. Genet. 128(3): 269-280.
-
(2010)
Hum. Genet
, vol.128
, Issue.3
, pp. 269-280
-
-
Feng, T.1
Zhu, X.2
-
10
-
-
85067754932
-
The role of glutamate signalling in rheumatoid arthritis
-
Flood, S., V. Duance, and D. Mason, 2004 The role of glutamate signalling in rheumatoid arthritis. Int. J. Exp. Pathol. 85(1): A19-A20.
-
(2004)
Int. J. Exp. Pathol
, vol.85
, Issue.1
-
-
Flood, S.1
Duance, V.2
Mason, D.3
-
11
-
-
0031018689
-
Autoantibodies to glutamate receptor subunit glur2 in nonfamilial olivopontocer-ebellar degeneration
-
Gahring, L., S. Rogers, and R. Twyman, 1997 Autoantibodies to glutamate receptor subunit glur2 in nonfamilial olivopontocer-ebellar degeneration. Neurology 48(2): 494-500.
-
(1997)
Neurology
, vol.48
, Issue.2
, pp. 494-500
-
-
Gahring, L.1
Rogers, S.2
Twyman, R.3
-
12
-
-
0032527491
-
Molecular and immunochemical characterization of the ionotropic glutamate receptors in the rat heart
-
Gill, S. S., O. M. Pulido, R. W. Mueller, and P. F. McGuire, 1998 Molecular and immunochemical characterization of the ionotropic glutamate receptors in the rat heart. Brain Res. Bull. 46(5): 429-434.
-
(1998)
Brain Res. Bull
, vol.46
, Issue.5
, pp. 429-434
-
-
Gill, S.S.1
Pulido, O.M.2
Mueller, R.W.3
McGuire, P.F.4
-
13
-
-
84901335340
-
Detecting structure of haplotypes and local ancestry
-
Guan, Y., 2014 Detecting structure of haplotypes and local ancestry. Genetics 196: 625-642.
-
(2014)
Genetics
, vol.196
, pp. 625-642
-
-
Guan, Y.1
-
14
-
-
58149175796
-
Practical issues in imputation-based association mapping
-
Guan, Y., and M. Stephens, 2008 Practical issues in imputation-based association mapping. PLoS Genet. 4(12): e1000279.
-
(2008)
PLoS Genet
, vol.4
, Issue.12
-
-
Guan, Y.1
Stephens, M.2
-
15
-
-
82955223524
-
Bayesian variable selection regression for genome-wide association studies, and other large-scale problems
-
Guan, Y., and M. Stephens, 2011 Bayesian variable selection regression for genome-wide association studies, and other large-scale problems. Ann. Appl. Stat. 5(3): 1780-1815.
-
(2011)
Ann. Appl. Stat
, vol.5
, Issue.3
, pp. 1780-1815
-
-
Guan, Y.1
Stephens, M.2
-
16
-
-
34547621758
-
A genome-wide association study identifies kiaa0350 as a type 1 diabetes gene
-
Hakonarson, H., S. F. A. Grant, J. P. Bradfield, L. Marchand, C. E. Kim et al., 2007 A genome-wide association study identifies kiaa0350 as a type 1 diabetes gene. Nature 448(7153): 591-594.
-
(2007)
Nature
, vol.448
, Issue.7153
, pp. 591-594
-
-
Hakonarson, H.1
Grant, S.F.A.2
Bradfield, J.P.3
Marchand, L.4
Kim, C.E.5
-
17
-
-
0036184745
-
Generating samples under a Wright-Fisher neutral model
-
Hudson, R. R., 2002 Generating samples under a Wright-Fisher neutral model. Bioinformatics 18: 337-338.
-
(2002)
Bioinformatics
, vol.18
, pp. 337-338
-
-
Hudson, R.R.1
-
18
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
International HapMap Consortium
-
International HapMap Consortium, 2010 Integrating common and rare genetic variation in diverse human populations. Nature 467(7311): 52-58.
-
(2010)
Nature
, vol.467
, Issue.7311
, pp. 52-58
-
-
-
19
-
-
0035136746
-
Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects
-
Joosten, P. H., M. Toepoel, E. C. Mariman, and E. J. Van Zoelen, 2001 Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects. Nat. Genet. 27: 215-217.
-
(2001)
Nat. Genet
, vol.27
, pp. 215-217
-
-
Joosten, P.H.1
Toepoel, M.2
Mariman, E.C.3
van Zoelen, E.J.4
-
20
-
-
45149105926
-
Efficient control of population structure in model organism association mapping
-
Kang, H. M., N. A. Zaitlen, C. M. Wade, A. Kirby, D. Heckerman et al., 2008 Efficient control of population structure in model organism association mapping. Genetics 178: 1709-1723.
-
(2008)
Genetics
, vol.178
, pp. 1709-1723
-
-
Kang, H.M.1
Zaitlen, N.A.2
Wade, C.M.3
Kirby, A.4
Heckerman, D.5
-
21
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
-
Li, B., and S. M. Leal, 2008 Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am. J. Hum. Genet. 83(3): 311-321.
-
(2008)
Am. J. Hum. Genet
, vol.83
, Issue.3
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
22
-
-
84872033833
-
A genome-wide association study identifies grk5 and rasgrp1 as type 2 diabetes loci in Chinese Hans
-
Li, H., W. Gan, L. Lu, X. Dong, X. Han et al., 2013 A genome-wide association study identifies grk5 and rasgrp1 as type 2 diabetes loci in Chinese Hans. Diabetes 62(1): 291-298.
-
(2013)
Diabetes
, vol.62
, Issue.1
, pp. 291-298
-
-
Li, H.1
Gan, W.2
Lu, L.3
Dong, X.4
Han, X.5
-
23
-
-
78249272314
-
To identify associations with rare variants, just whait: Weighted haplotype and imputation-based tests
-
Li, Y., A. E. Byrnes, and M. Li, 2010a To identify associations with rare variants, just whait: weighted haplotype and imputation-based tests. Am. J. Hum. Genet. 87(5): 728-735.
-
(2010)
Am. J. Hum. Genet
, vol.87
, Issue.5
, pp. 728-735
-
-
Li, Y.1
Byrnes, A.E.2
Li, M.3
-
24
-
-
78649508578
-
Mach: Using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li, Y., C. J. Willer, J. Ding, P. Scheet, and G. R. Abecasis, 2010b Mach: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet. Epidemiol. 34(8): 816-834.
-
(2010)
Genet. Epidemiol
, vol.34
, Issue.8
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
Scheet, P.4
Abecasis, G.R.5
-
25
-
-
79953753220
-
Genome-wide interaction-based association analysis identified multiple new susceptibility loci for common diseases
-
Liu, Y., H. Xu, S. Chen, X. Chen, Z. Zhang et al., 2011 Genome-wide interaction-based association analysis identified multiple new susceptibility loci for common diseases. PLoS Genet. 7(3): e1001338.
-
(2011)
PLoS Genet
, vol.7
, Issue.3
-
-
Liu, Y.1
Xu, H.2
Chen, S.3
Chen, X.4
Zhang, Z.5
-
26
-
-
55549147191
-
Personal genomes: The case of the missing heri-tability
-
Maher, B., 2008 Personal genomes: the case of the missing heri-tability. Nature 456: 18-21.
-
(2008)
Nature
, vol.456
, pp. 18-21
-
-
Maher, B.1
-
27
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T. A., F. S. Collins, N. J. Cox, D. B. Goldstein, L. A. Hindorff et al., 2009 Finding the missing heritability of complex diseases. Nature 461: 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
-
28
-
-
34548084895
-
Association of grik4 with outcome of antidepressant treatment in the star*d cohort
-
Paddock, S., G. Laje, D. Charney, A. J. Rush, A. F. Wilson et al., 2007 Association of grik4 with outcome of antidepressant treatment in the star*d cohort. Am. J. Psychiatry 164: 1181-1188.
-
(2007)
Am. J. Psychiatry
, vol.164
, pp. 1181-1188
-
-
Paddock, S.1
Laje, G.2
Charney, D.3
Rush, A.J.4
Wilson, A.F.5
-
29
-
-
33748057791
-
Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, grik4, in schizophrenia and bipolar disorder
-
Pickard, B. S., M. P. Malloy, A. Christoforou, P. A. Thomson, K. L. Evans et al., 2006 Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, grik4, in schizophrenia and bipolar disorder. Mol. Psychiatry 11(9): 847-857.
-
(2006)
Mol. Psychiatry
, vol.11
, Issue.9
, pp. 847-857
-
-
Pickard, B.S.1
Malloy, M.P.2
Christoforou, A.3
Thomson, P.A.4
Evans, K.L.5
-
30
-
-
54449094448
-
A common variant in the 39 UTR of the grik4 glutamate receptor gene affects transcript abundance and protects against bipolar disorder
-
Pickard, B. S., H. M. Knight, R. S. Hamilton, D. C. Soares, R. Walker et al., 2008 A common variant in the 39 UTR of the grik4 glutamate receptor gene affects transcript abundance and protects against bipolar disorder. Proc. Natl. Acad. Sci. USA 105(39): 14940-14945.
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, Issue.39
, pp. 14940-14945
-
-
Pickard, B.S.1
Knight, H.M.2
Hamilton, R.S.3
Soares, D.C.4
Walker, R.5
-
31
-
-
80052311755
-
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases
-
Plagnol, V., J. M. M. Howson, D. J. Smyth, N. Walker, J. P. Hafler et al., 2011 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. PLoS Genet. 7(8): e1002216.
-
(2011)
PLoS Genet
, vol.7
, Issue.8
-
-
Plagnol, V.1
Howson, J.M.M.2
Smyth, D.J.3
Walker, N.4
Hafler, J.P.5
-
32
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases
-
Pritchard, J. K., 2001 Are rare variants responsible for susceptibility to complex diseases? Am. J. Hum. Genet. 69(1): 124-137.
-
(2001)
Am. J. Hum. Genet
, vol.69
, Issue.1
, pp. 124-137
-
-
Pritchard, J.K.1
-
33
-
-
10044294770
-
Evaluating associations of haplotypes with traits
-
Schaid, D. J., 2004 Evaluating associations of haplotypes with traits. Genet. Epidemiol. 27: 348-364.
-
(2004)
Genet. Epidemiol
, vol.27
, pp. 348-364
-
-
Schaid, D.J.1
-
34
-
-
33644974019
-
A fast and flexible statistical model for large-scale population genotype data: Applications to inferring missing genotypes and haplotypic phase
-
Scheet, P., and M. Stephens, 2006 A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am. J. Hum. Genet. 78: 629-644.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 629-644
-
-
Scheet, P.1
Stephens, M.2
-
35
-
-
50849117166
-
Linkage disequilibrium-based quality control for large-scale genetic studies
-
Scheet, P., and M. Stephens, 2008 Linkage disequilibrium-based quality control for large-scale genetic studies. PLoS Genet. 4(8): e1000147.
-
(2008)
PLoS Genet
, vol.4
, Issue.8
-
-
Scheet, P.1
Stephens, M.2
-
36
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott, L., K. Mohlke, L. Bonnycastle, C. Willer, Y. Li et al., 2007 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316: 1341-1345.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.1
Mohlke, K.2
Bonnycastle, L.3
Willer, C.4
Li, Y.5
-
37
-
-
33749033869
-
Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases
-
Seferovic, P. M., A. D. Ristic, R. Maksimovic, D. S. Simeunovic, G. G. Ristic et al., 2006 Cardiac arrhythmias and conduction disturbances in autoimmune rheumatic diseases. Rheumatology 45(Suppl. 4): iv39-iv42.
-
(2006)
Rheumatology
, vol.45
, Issue.SUPPL. 4
-
-
Seferovic, P.M.1
Ristic, A.D.2
Maksimovic, R.3
Simeunovic, D.S.4
Ristic, G.G.5
-
38
-
-
34547622688
-
Efficient multipoint analysis of association studies: Candidate regions and quantitative traits
-
Servin, B., and M. Stephens, 2007 Efficient multipoint analysis of association studies: candidate regions and quantitative traits. PLoS Genet. 3(7): e114.
-
(2007)
PLoS Genet
, vol.3
, Issue.7
-
-
Servin, B.1
Stephens, M.2
-
39
-
-
70349303959
-
Bayesian statistical methods for genetic association studies
-
Stephens, M., and D. J. Balding, 2009 Bayesian statistical methods for genetic association studies. Nat. Rev. Genet. 10: 681-690.
-
(2009)
Nat. Rev. Genet
, vol.10
, pp. 681-690
-
-
Stephens, M.1
Balding, D.J.2
-
40
-
-
0032786521
-
Hla-dr and -dq phenotypes in inflammatory bowel disease: A meta-analysis
-
Stokkers, P. C. F., P. H. Reitsma, G. N. J. Tytgat, and S. J. H. van Deventer, 1999 Hla-dr and -dq phenotypes in inflammatory bowel disease: a meta-analysis. Gut 45: 395-401.
-
(1999)
Gut
, vol.45
, pp. 395-401
-
-
Stokkers, P.C.F.1
Reitsma, P.H.2
Tytgat, G.N.J.3
van Deventer, S.J.H.4
-
41
-
-
84874418247
-
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21
-
Tabassum, R., G. Chauhan, O. P. Dwivedi, A. Mahajan, A. Jaiswal et al., 2013 Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Diabetes 62(3): 977-986.
-
(2013)
Diabetes
, vol.62
, Issue.3
, pp. 977-986
-
-
Tabassum, R.1
Chauhan, G.2
Dwivedi, O.P.3
Mahajan, A.4
Jaiswal, A.5
-
42
-
-
67650248695
-
Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
-
Takeuchi, F., M. Serizawa, K. Yamamoto, T. Fujisawa, E. Nakashima et al., 2009 Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Diabetes 58(7): 1690-1699.
-
(2009)
Diabetes
, vol.58
, Issue.7
, pp. 1690-1699
-
-
Takeuchi, F.1
Serizawa, M.2
Yamamoto, K.3
Fujisawa, T.4
Nakashima, E.5
-
43
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight, B. F., L. J. Scott, V. Steinthorsdottir, A. P. Morris, C. Dina et al., 2010 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet. 42(7): 579-589.
-
(2010)
Nat. Genet
, vol.42
, Issue.7
, pp. 579-589
-
-
Voight, B.F.1
Scott, L.J.2
Steinthorsdottir, V.3
Morris, A.P.4
Dina, C.5
-
44
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium, 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
-
-
-
45
-
-
0026342212
-
Do infectious agents cause rheumatoid arthritis
-
Wilder, R. L., and L. J. Corfford, 1991 Do infectious agents cause rheumatoid arthritis? Clin. Orthop. Relat. Res. 265: 36-41.
-
(1991)
Clin. Orthop. Relat. Res
, vol.265
, pp. 36-41
-
-
Wilder, R.L.1
Corfford, L.J.2
-
46
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer, C., S. Sanna, A. Jackson, A. Scuteri, L. Bonnycastle et al., 2008 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat. Genet. 40: 161-169.
-
(2008)
Nat. Genet
, vol.40
, pp. 161-169
-
-
Willer, C.1
Sanna, S.2
Jackson, A.3
Scuteri, A.4
Bonnycastle, L.5
-
47
-
-
77954140531
-
Common SNPs explain a large proportion of the herita-bility for human height
-
Yang, J., B. Benyamin, B. P. McEvoy, S. Gordon, A. K. Henders et al., 2010 Common SNPs explain a large proportion of the herita-bility for human height. Nat. Genet. 42(7): 565-569.
-
(2010)
Nat. Genet
, vol.42
, Issue.7
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
-
48
-
-
84863003734
-
Genome-wide efficient mixed model analysis for association studies
-
Zhou, X., and M. Stephens, 2012 Genome-wide efficient mixed model analysis for association studies. Nat. Genet. 44(4): 821-824.
-
(2012)
Nat. Genet
, vol.44
, Issue.4
, pp. 821-824
-
-
Zhou, X.1
Stephens, M.2
-
49
-
-
84874783818
-
Polygenic modeling with Bayesian sparse linear mixed models
-
Zhou, X., P. Carbonetto, and M. Stephens, 2013 Polygenic modeling with Bayesian sparse linear mixed models. PLoS Genet. 9(2): e1003264.
-
(2013)
PLoS Genet
, vol.9
, Issue.2
-
-
Zhou, X.1
Carbonetto, P.2
Stephens, M.3
-
50
-
-
15544365509
-
Coalescent-based association mapping and fine mapping of complex trait loci
-
Zöllner, S., and J. K. Pritchard, 2005 Coalescent-based association mapping and fine mapping of complex trait loci. Genetics 169: 1071-1092.
-
(2005)
Genetics
, vol.169
, pp. 1071-1092
-
-
Zöllner, S.1
Pritchard, J.K.2
|