-
1
-
-
84894595574
-
Modest familial risk for multiple sclerosis - A registry based study of the population of Sweden
-
Westerlind H, Ramanujam R, Uvehag D et al: Modest familial risk for multiple sclerosis - a registry based study of the population of Sweden. Brain 2014; 137:Pt 3 770-778.
-
(2014)
Brain
, vol.137
, pp. 770-778
-
-
Westerlind, H.1
Ramanujam, R.2
Uvehag, D.3
-
2
-
-
84887058596
-
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
-
International Multiple Sclerosis Genetics Consortium (IMSGC)
-
International Multiple Sclerosis Genetics Consortium (IMSGC)Beecham AH, Patsopoulos NA, Xifara DK et al: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet 2013; 45: 1353-1360.
-
(2013)
Nat Genet
, vol.45
, pp. 1353-1360
-
-
Beecham, A.H.1
Patsopoulos, N.A.2
Xifara, D.K.3
-
3
-
-
0141577138
-
Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland
-
Pihlaja H, Rantamäki T, Wikström J et al: Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland. Genes Immun 2003; 4: 138-146.
-
(2003)
Genes Immun
, vol.4
, pp. 138-146
-
-
Pihlaja, H.1
Rantamäki, T.2
Wikström, J.3
-
4
-
-
56749098072
-
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
-
Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV et al: Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Nat Genet 2008; 40: 1402-1403.
-
(2008)
Nat Genet
, vol.40
, pp. 1402-1403
-
-
Aulchenko, Y.S.1
Hoppenbrouwers, I.A.2
Ramagopalan, S.V.3
-
5
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K et al: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
6
-
-
80051684615
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
-
Sawcer S, Hellenthal G, Pirinen M et al: Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011; 476: 214-219.
-
(2011)
Nature
, vol.476
, pp. 214-219
-
-
Sawcer, S.1
Hellenthal, G.2
Pirinen, M.3
-
8
-
-
59949088494
-
Whole population, genome-wide mapping of hidden relatedness
-
Gusev A, Lowe JK, Stoffel M et al: Whole population, genome-wide mapping of hidden relatedness. Genome Res 2009; 19: 318-326.
-
(2009)
Genome Res
, vol.19
, pp. 318-326
-
-
Gusev, A.1
Lowe, J.K.2
Stoffel, M.3
-
9
-
-
77950332127
-
High-resolution detection of identity by descent in unrelated individuals
-
Browning SR, Browning BL: High-resolution detection of identity by descent in unrelated individuals. Am J Hum Genet 2010; 86: 526-539.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 526-539
-
-
Browning, S.R.1
Browning, B.L.2
-
10
-
-
79851497145
-
A fast, powerful method for detecting identity by descent
-
Browning BL, Browning SR: A fast, powerful method for detecting identity by descent. Am J Hum Genet 2011; 88: 173-182.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 173-182
-
-
Browning, B.L.1
Browning, S.R.2
-
11
-
-
84901035063
-
Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population
-
Gauvin H, Moreau C, Lefebvre J-F et al: Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population. Eur J Hum Genet 2014; 22: 814-821.
-
(2014)
Eur J Hum Genet
, vol.22
, pp. 814-821
-
-
Gauvin, H.1
Moreau, C.2
Lefebvre, J.-F.3
-
12
-
-
82355190213
-
Identity-by-descent-based phasing and imputation in founder populations using graphical models
-
Palin K, Campbell H, Wright AF, Wilson JF, Durbin R: Identity-by-descent-based phasing and imputation in founder populations using graphical models. Genet Epidemiol 2011; 35: 853-860.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 853-860
-
-
Palin, K.1
Campbell, H.2
Wright, A.F.3
Wilson, J.F.4
Durbin, R.5
-
13
-
-
80051816176
-
Identity by descent estimation with dense genome-wide genotype data
-
Han L, Abney M: Identity by descent estimation with dense genome-wide genotype data. Genet Epidemiol 2011; 35: 557-567.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 557-567
-
-
Han, L.1
Abney, M.2
-
14
-
-
84878589007
-
Improving the accuracy and efficiency of identity by descent detection in population data
-
Browning BL, Browning SR: Improving the accuracy and efficiency of identity by descent detection in population data. Genetics 2013; 194: 459-471.
-
(2013)
Genetics
, vol.194
, pp. 459-471
-
-
Browning, B.L.1
Browning, S.R.2
-
15
-
-
7044220607
-
Oestrogen receptor alpha gene haplotype and postmenopausal breast cancer risk: A case control study
-
Wedrén S, Lovmar L, Humphreys K et al: Oestrogen receptor alpha gene haplotype and postmenopausal breast cancer risk: a case control study. Breast Cancer Res 2004; 6: R437-R449.
-
(2004)
Breast Cancer Res
, vol.6
, pp. R437-R449
-
-
Wedrén, S.1
Lovmar, L.2
Humphreys, K.3
-
16
-
-
33744900610
-
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17
-
Farrall M, Green FR, Peden JF et al: Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17. PLoS Genet 2006; 2: e72.
-
(2006)
PLoS Genet
, vol.2
, pp. e72
-
-
Farrall, M.1
Green, F.R.2
Peden, J.F.3
-
17
-
-
40549109924
-
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
-
Broadbent HM, Peden JF, Lorkowski S et al: Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 2008; 17: 806-814.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 806-814
-
-
Broadbent, H.M.1
Peden, J.F.2
Lorkowski, S.3
-
18
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 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
-
20
-
-
79956146364
-
-
The MathWorks Inc., Natick, MA, USA: The MathWorks Inc.
-
The MathWorks Inc.. MATLAB. version 7.10.0 (R2010a)Natick, MA, USA: The MathWorks Inc. 2010.
-
(2010)
MATLAB. Version 7.10.0 (R2010a)
-
-
-
21
-
-
84859588748
-
Detecting rare variant associations by identity-by-descent mapping in case-control studies
-
Browning SR, Thompson EA: Detecting rare variant associations by identity-by-descent mapping in case-control studies. Genetics 2012; 190: 1521-1531.
-
(2012)
Genetics
, vol.190
, pp. 1521-1531
-
-
Browning, S.R.1
Thompson, E.A.2
-
22
-
-
70450173127
-
High prevalence of multiple sclerosis in the Swedish county of Värmland
-
Boström I, Callander M, Kurtzke JF, Landtblom AM: High prevalence of multiple sclerosis in the Swedish county of Värmland. Mult Scler 2009; 15: 1253-1262.
-
(2009)
Mult Scler
, vol.15
, pp. 1253-1262
-
-
Boström, I.1
Callander, M.2
Kurtzke, J.F.3
Landtblom, A.M.4
-
23
-
-
0028220775
-
Familial clustering of multiple sclerosis in a northern Swedish rural district
-
Binzer M, Forsgren L, Holmgren G, Drugge U, Fredrikson S: Familial clustering of multiple sclerosis in a northern Swedish rural district. J Neurol Neurosurg Psychiatry 1994; 57: 497-499.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 497-499
-
-
Binzer, M.1
Forsgren, L.2
Holmgren, G.3
Drugge, U.4
Fredrikson, S.5
-
24
-
-
23944499790
-
A high-density screen for linkage in multiple sclerosis
-
Sawcer S, Ban M, Maranian M et al: A high-density screen for linkage in multiple sclerosis. Am J Hum Genet 2005; 77: 454-467.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 454-467
-
-
Sawcer, S.1
Ban, M.2
Maranian, M.3
-
25
-
-
61849139440
-
An investigation of susceptibility loci in benign, aggressive and primary progressive multiple sclerosis in Northern Irish population
-
Gray OM, Abdeen H, McDonnell GV, Patterson CC, Graham CA, Hawkins SA: An investigation of susceptibility loci in benign, aggressive and primary progressive multiple sclerosis in Northern Irish population. Mult Scler 2009; 15: 299-303.
-
(2009)
Mult Scler
, vol.15
, pp. 299-303
-
-
Gray, O.M.1
Abdeen, H.2
McDonnell, G.V.3
Patterson, C.C.4
Graham, C.A.5
Hawkins, S.A.6
-
26
-
-
0030800775
-
Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients
-
Barcellos LF, Thomson G, Carrington M et al: Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients. JAMA 1997; 278: 1256-1261.
-
(1997)
JAMA
, vol.278
, pp. 1256-1261
-
-
Barcellos, L.F.1
Thomson, G.2
Carrington, M.3
-
27
-
-
18044401069
-
Linkage and association analysis of chromosome 19q13 in multiple sclerosis
-
Pericak-Vance MA, Rimmler JB, Martin ER et al: Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics 2001; 3: 195-201.
-
(2001)
Neurogenetics
, vol.3
, pp. 195-201
-
-
Pericak-Vance, M.A.1
Rimmler, J.B.2
Martin, E.R.3
-
28
-
-
0035985723
-
Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3
-
Lucotte GL: Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3. Genet Couns 2002; 13: 133-138.
-
(2002)
Genet Couns
, vol.13
, pp. 133-138
-
-
Lucotte, G.L.1
-
29
-
-
10744231697
-
Investigation of seven proposed regions of linkage in multiple sclerosis: An American and French collaborative study
-
Pericak-Vance MA, Rimmler JB, Haines JL et al: Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study. Neurogenetics 2004; 5: 45-48.
-
(2004)
Neurogenetics
, vol.5
, pp. 45-48
-
-
Pericak-Vance, M.A.1
Rimmler, J.B.2
Haines, J.L.3
-
30
-
-
84874636721
-
Identity-bydescent mapping to detect rare variants conferring susceptibility to multiple sclerosis
-
Lin R, Charlesworth J, Stankovich J, Perreau VM, Brown MA, Taylor BV: Identity-bydescent mapping to detect rare variants conferring susceptibility to multiple sclerosis. PLoS One 2013; 8: e56379.
-
(2013)
PLoS One
, vol.8
, pp. e56379
-
-
Lin, R.1
Charlesworth, J.2
Stankovich, J.3
Perreau, V.M.4
Brown, M.A.5
Taylor, B.V.6
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