-
1
-
-
54149084585
-
Multiple sclerosis
-
Compston A, Coles A (2008) Multiple sclerosis. Lancet 372: 1502-1517.
-
(2008)
Lancet
, vol.372
, pp. 1502-1517
-
-
Compston, A.1
Coles, A.2
-
2
-
-
0242268416
-
Twin concordance and sibling recurrence rates in multiple sclerosis
-
DOI 10.1073/pnas.1932604100
-
Willer CJ, Dyment DA, Risch NJ, Sadovnick AD, Ebers GC (2003) Twin concordance and sibling recurrence rates in multiple sclerosis. Proc Natl Acad Sci U S A 100: 12877-12882. (Pubitemid 37339993)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.22
, pp. 12877-12882
-
-
Willer, C.J.1
Dyment, D.A.2
Risch, N.J.3
Sadovnick, A.D.4
Ebers, G.C.5
Paty, D.W.6
Hashimoto, S.A.7
Devonshire, V.8
Hooge, J.9
Oger, J.10
Metz, L.11
Warren, S.12
Hader, W.13
Nelson, R.14
Freedman, M.15
Brunet, D.16
Paulseth, J.17
Rice, G.18
O'Connor, P.19
Duquette, P.20
Lapierre, Y.21
Bouchard, J.-P.22
Murray, T.J.23
Bhan, V.24
Maxner, C.25
Pryse-Phillips, W.26
Stefanelli, M.27
more..
-
3
-
-
0015733713
-
Histocompatibility determinants in multiple sclerosis, with special reference to clinical course
-
Jersild C, Fog T, Hansen GS, Thomsen M, Svejgaard A, et al. (1973) Histocompatibility determinants in multiple sclerosis, with special reference to clinical course. Lancet 2: 1221-1225.
-
(1973)
Lancet
, vol.2
, pp. 1221-1225
-
-
Jersild, C.1
Fog, T.2
Hansen, G.S.3
Thomsen, M.4
Svejgaard, A.5
-
4
-
-
80051684615
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
-
Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, et al. (2011) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 476: 214-219.
-
(2011)
Nature
, vol.476
, pp. 214-219
-
-
Sawcer, S.1
Hellenthal, G.2
Pirinen, M.3
Spencer, C.C.4
Patsopoulos, N.A.5
-
5
-
-
84255194782
-
Genomewide meta-analysis identifies novel multiple sclerosis susceptibility loci
-
Patsopoulos NA, Esposito F, Reischl J, Lehr S, Bauer D, et al. (2011) Genomewide meta-analysis identifies novel multiple sclerosis susceptibility loci. Ann Neurol 70: 897-912.
-
(2011)
Ann Neurol
, vol.70
, pp. 897-912
-
-
Patsopoulos, N.A.1
Esposito, F.2
Reischl, J.3
Lehr, S.4
Bauer, D.5
-
6
-
-
84887058596
-
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
-
10.1038/ng.2770
-
Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, et al. (2013) Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet 10.1038/ng.2770.
-
(2013)
Nat Genet
-
-
Beecham, A.H.1
Patsopoulos, N.A.2
Xifara, D.K.3
Davis, M.F.4
Kemppinen, A.5
-
7
-
-
71849098862
-
Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: A weighted genetic risk score
-
De Jager PL, Chibnik LB, Cui J, Reischl J, Lehr S, et al. (2009) Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: a weighted genetic risk score. Lancet Neurol 8: 1111-1119.
-
(2009)
Lancet Neurol
, vol.8
, pp. 1111-1119
-
-
De Jager, P.L.1
Chibnik, L.B.2
Cui, J.3
Reischl, J.4
Lehr, S.5
-
8
-
-
84892381360
-
Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination
-
van Pelt ED, Mescheriakova JY, Makhani N, Ketelslegers IA, Neuteboom RF, et al. (2013) Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination. Neurology.
-
(2013)
Neurology
-
-
Van Pelt, E.D.1
Mescheriakova, J.Y.2
Makhani, N.3
Ketelslegers, I.A.4
Neuteboom, R.F.5
-
9
-
-
84886727488
-
Genetic burden in multiple sclerosis families
-
Isobe N, Damotte V, Lo Re V, Ban M, Pappas D, et al. (2013) Genetic burden in multiple sclerosis families. Genes Immun 14: 434-440.
-
(2013)
Genes Immun
, vol.14
, pp. 434-440
-
-
Isobe, N.1
Damotte, V.2
Lo Re, V.3
Ban, M.4
Pappas, D.5
-
10
-
-
84871239707
-
REGENT: A risk assessment and classification algorithm for genetic and environmental factors
-
Crouch DJ, Goddard GH, Lewis CM (2013) REGENT: a risk assessment and classification algorithm for genetic and environmental factors. Eur J Hum Genet 21: 109-111.
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 109-111
-
-
Crouch, D.J.1
Goddard, G.H.2
Lewis, C.M.3
-
11
-
-
77956256212
-
Risk categorization for complex disorders according to genotype relative risk and precision in parameter estimates
-
Goddard GH, Lewis CM (2010) Risk categorization for complex disorders according to genotype relative risk and precision in parameter estimates. Genet Epidemiol 34: 624-632.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 624-632
-
-
Goddard, G.H.1
Lewis, C.M.2
-
12
-
-
0141869016
-
Understanding sensitivity and specificity with the right side of the brain
-
Loong TW (2003) Understanding sensitivity and specificity with the right side of the brain. BMJ 327: 716-719.
-
(2003)
BMJ
, vol.327
, pp. 716-719
-
-
Loong, T.W.1
-
13
-
-
84878883338
-
Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls
-
IMSGC 10.1016/j.ajhg.2013.04.019
-
IMSGC (2013) Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls. Am J Hum Genet 10.1016/j.ajhg.2013. 04.019.
-
(2013)
Am J Hum Genet
-
-
-
14
-
-
84892988063
-
DNase hypersensitive sites and association with multiple sclerosis
-
10.1093/hmg/ddt489
-
Disanto G, Sandve GK, Ricigliano VA, Pakpoor J, Berlanga-Taylor AJ, et al. (2013) DNase hypersensitive sites and association with multiple sclerosis. Hum Mol Genet 10.1093/hmg/ddt489.
-
(2013)
Hum Mol Genet
-
-
Disanto, G.1
Sandve, G.K.2
Ricigliano, V.A.3
Pakpoor, J.4
Berlanga-Taylor, A.J.5
-
15
-
-
84868212192
-
Risk in complex genetics: "all models are wrong but some are useful"
-
Sawcer S, Wason J (2012) Risk in complex genetics: "all models are wrong but some are useful". Ann Neurol 72: 502-509.
-
(2012)
Ann Neurol
, vol.72
, pp. 502-509
-
-
Sawcer, S.1
Wason, J.2
-
16
-
-
77953394241
-
Multiple sclerosis: Risk factors, prodromes, and potential causal pathways
-
Ramagopalan SV, Dobson R, Meier UC, Giovannoni G (2010) Multiple sclerosis: risk factors, prodromes, and potential causal pathways. Lancet Neurol 9: 727-739.
-
(2010)
Lancet Neurol
, vol.9
, pp. 727-739
-
-
Ramagopalan, S.V.1
Dobson, R.2
Meier, U.C.3
Giovannoni, G.4
-
17
-
-
5444259253
-
Mechanisms of non-Mendelian inheritance in genetic disease
-
Van Heyningen V, Yeyati PL (2004) Mechanisms of non-Mendelian inheritance in genetic disease. Hum Mol Genet 13 Spec No2: R225-233.
-
(2004)
Hum Mol Genet
, vol.13
, Issue.SPEC NO2
-
-
Van Heyningen, V.1
Yeyati, P.L.2
-
18
-
-
84874189972
-
Genotype to phenotype: Lessons from model organisms for human genetics
-
Lehner B (2013) Genotype to phenotype: lessons from model organisms for human genetics. Nat Rev Genet 14: 168-178.
-
(2013)
Nat Rev Genet
, vol.14
, pp. 168-178
-
-
Lehner, B.1
-
20
-
-
84883659269
-
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
-
10.1101/gr.147991.112
-
Sailani MR,Makrythanasis P, Valsesia A, Santoni FA, Deutsch S, et al. (2013) The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome. Genome Res 10.1101/gr.147991.112.
-
(2013)
Genome Res
-
-
Sailani, M.R.1
Makrythanasis, P.2
Valsesia, A.3
Santoni, F.A.4
Deutsch, S.5
-
21
-
-
80053588676
-
The major cause of multiple sclerosis is environmental: Genetics has a minor role-no
-
Sawcer S (2011) The major cause of multiple sclerosis is environmental: genetics has a minor role-no. Mult Scler 17: 1174-1175.
-
(2011)
Mult Scler
, vol.17
, pp. 1174-1175
-
-
Sawcer, S.1
|