-
1
-
-
0027537583
-
A population-based study of multiple sclerosis in twins: update
-
Sadovnick AD, Armstrong H, Rice GP, Bulman D, Hashimoto L, et al. (1993) A population-based study of multiple sclerosis in twins: update. Ann Neurol 33: 281-285.
-
(1993)
Ann Neurol
, vol.33
, pp. 281-285
-
-
Sadovnick, A.D.1
Armstrong, H.2
Rice, G.P.3
Bulman, D.4
Hashimoto, L.5
-
2
-
-
25844442849
-
Concordance for multiple sclerosis in Danish twins: an update of a nationwide study
-
Hansen T, Skytthe A, Stenager E, Petersen HC, Bronnum-Hansen H, et al. (2005) Concordance for multiple sclerosis in Danish twins: an update of a nationwide study. Mult Scler 11: 504-510.
-
(2005)
Mult Scler
, vol.11
, pp. 504-510
-
-
Hansen, T.1
Skytthe, A.2
Stenager, E.3
Petersen, H.C.4
Bronnum-Hansen, H.5
-
3
-
-
67649881102
-
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
-
The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)
-
The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene) (2009) Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nat Genet 41: 824-828.
-
(2009)
Nat Genet
, vol.41
, pp. 824-828
-
-
-
4
-
-
70349629969
-
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
-
Ban M, Goris A, Lorentzen AR, Baker A, Mihalova T, et al. (2009) Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. Eur J Hum Genet 17: 1309-1313.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1309-1313
-
-
Ban, M.1
Goris, A.2
Lorentzen, A.R.3
Baker, A.4
Mihalova, T.5
-
5
-
-
78649699944
-
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis
-
Ban M, McCauley JL, Zuvich R, Baker A, Bergamaschi L, et al. (2010) A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis. Genes Immun 11: 660-664.
-
(2010)
Genes Immun
, vol.11
, pp. 660-664
-
-
Ban, M.1
McCauley, J.L.2
Zuvich, R.3
Baker, A.4
Bergamaschi, L.5
-
6
-
-
58949099391
-
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
-
Baranzini SE, Wang J, Gibson RA, Galwey N, Naegelin Y, et al. (2009) Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Hum Mol Genet 18: 767-778.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 767-778
-
-
Baranzini, S.E.1
Wang, J.2
Gibson, R.A.3
Galwey, N.4
Naegelin, Y.5
-
7
-
-
67649876123
-
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
-
De Jager PL, Jia X, Wang J, de Bakker PI, Ottoboni L, et al. (2009) Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Nat Genet 41: 776-782.
-
(2009)
Nat Genet
, vol.41
, pp. 776-782
-
-
De Jager, P.L.1
Jia, X.2
Wang, J.3
de Bakker, P.I.4
Ottoboni, L.5
-
8
-
-
34548299105
-
Risk alleles for multiple sclerosis identified by a genomewide study
-
Hafler DA, Compston A, Sawcer S, Lander ES, Daly MJ, et al. (2007) Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med 357: 851-862.
-
(2007)
N Engl J Med
, vol.357
, pp. 851-862
-
-
Hafler, D.A.1
Compston, A.2
Sawcer, S.3
Lander, E.S.4
Daly, M.J.5
-
9
-
-
59149098926
-
CD226 Gly307Ser association with multiple autoimmune diseases
-
Hafler JP, Maier LM, Cooper JD, Plagnol V, Hinks A, et al. (2009) CD226 Gly307Ser association with multiple autoimmune diseases. Genes Immun 10: 5-10.
-
(2009)
Genes Immun
, vol.10
, pp. 5-10
-
-
Hafler, J.P.1
Maier, L.M.2
Cooper, J.D.3
Plagnol, V.4
Hinks, A.5
-
10
-
-
77950544633
-
Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci
-
The International Multiple Sclerosis Genetics Consortium (IMSGC)
-
The International Multiple Sclerosis Genetics Consortium (IMSGC) (2010) Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. Hum Mol Genet 19: 953-962.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 953-962
-
-
-
11
-
-
76049083598
-
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
-
Jakkula E, Leppa V, Sulonen AM, Varilo T, Kallio S, et al. (2010) Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Am J Hum Genet 86: 285-291.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 285-291
-
-
Jakkula, E.1
Leppa, V.2
Sulonen, A.M.3
Varilo, T.4
Kallio, S.5
-
12
-
-
77952884985
-
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
-
Sanna S, Pitzalis M, Zoledziewska M, Zara I, Sidore C, et al. (2010) Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. Nat Genet 42: 495-497.
-
(2010)
Nat Genet
, vol.42
, pp. 495-497
-
-
Sanna, S.1
Pitzalis, M.2
Zoledziewska, M.3
Zara, I.4
Sidore, C.5
-
13
-
-
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
-
14
-
-
84859499759
-
Alzheimer Disease Susceptibility Loci: Evidence for a Protein Network under Natural Selection
-
Raj T, Shulman JM, Keenan BT, Chibnik LB, Evans DA, et al. (2012) Alzheimer Disease Susceptibility Loci: Evidence for a Protein Network under Natural Selection. Am J Hum Genet 90: 720-726.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 720-726
-
-
Raj, T.1
Shulman, J.M.2
Keenan, B.T.3
Chibnik, L.B.4
Evans, D.A.5
-
15
-
-
0016592183
-
Histocompatibility determinants in multiple sclerosis
-
Jersild C, Dupont B, Fog T, Platz PJ, Svejgaard A, (1975) Histocompatibility determinants in multiple sclerosis. Transplant Rev 22: 148-163.
-
(1975)
Transplant Rev
, vol.22
, pp. 148-163
-
-
Jersild, C.1
Dupont, B.2
Fog, T.3
Platz, P.J.4
Svejgaard, A.5
-
16
-
-
0015465865
-
Histocompatibility (HL-A) antigens associated with multiple sclerosis
-
Jersild C, Fog T, (1972) Histocompatibility (HL-A) antigens associated with multiple sclerosis. Acta neurologica Scandinavica Supplementum 51: 377.
-
(1972)
Acta Neurologica Scandinavica Supplementum
, vol.51
, pp. 377
-
-
Jersild, C.1
Fog, T.2
-
17
-
-
84866347085
-
Modelling Genetic Susceptibility to Multiple Sclerosis with Family Data
-
O'Gorman C, Lin R, Stankovich J, Broadley SA, (2012) Modelling Genetic Susceptibility to Multiple Sclerosis with Family Data. Neuroepidemiology 40: 1-12.
-
(2012)
Neuroepidemiology
, vol.40
, pp. 1-12
-
-
O'Gorman, C.1
Lin, R.2
Stankovich, J.3
Broadley, S.A.4
-
18
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S, Walker N, Riches D, Egholm M, Todd JA, (2009) Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 324: 387-389.
-
(2009)
Science
, vol.324
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
19
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, et al. (2011) Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet 43: 519-525.
-
(2011)
Nat Genet
, vol.43
, pp. 519-525
-
-
Yang, J.1
Manolio, T.A.2
Pasquale, L.R.3
Boerwinkle, E.4
Caporaso, N.5
-
20
-
-
42649084334
-
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
-
Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, et al. (2008) Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 40: 592-599.
-
(2008)
Nat Genet
, vol.40
, pp. 592-599
-
-
Ji, W.1
Foo, J.N.2
O'Roak, B.J.3
Zhao, H.4
Larson, M.G.5
-
21
-
-
79953200132
-
PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats
-
Yu Z, Zhu Y, Chen-Plotkin AS, Clay-Falcone D, McCluskey L, et al. (2011) PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats. PLoS One 6: e17951.
-
(2011)
PLoS One
, vol.6
-
-
Yu, Z.1
Zhu, Y.2
Chen-Plotkin, A.S.3
Clay-Falcone, D.4
McCluskey, L.5
-
22
-
-
33846438189
-
Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease
-
Kang SJ, Scott WK, Li YJ, Hauser MA, van der Walt JM, et al. (2006) Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease. Mov Disord 21: 2175-2180.
-
(2006)
Mov Disord
, vol.21
, pp. 2175-2180
-
-
Kang, S.J.1
Scott, W.K.2
Li, Y.J.3
Hauser, M.A.4
van der Walt, J.M.5
-
23
-
-
45849112925
-
Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes
-
Browning SR, (2008) Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes. Genetics 178: 2123-2132.
-
(2008)
Genetics
, vol.178
, pp. 2123-2132
-
-
Browning, S.R.1
-
24
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (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
-
25
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Altshuler DM, Gibbs RA, Peltonen L, Dermitzakis E, Schaffner SF, et al. (2010) Integrating common and rare genetic variation in diverse human populations. Nature 467: 52-58.
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
Altshuler, D.M.1
Gibbs, R.A.2
Peltonen, L.3
Dermitzakis, E.4
Schaffner, S.F.5
-
26
-
-
31544449191
-
Using Linkage Genome Scans to Improve Power of Association in Genome Scans
-
Roeder K, Bacanu SA, Wasserman L, Devlin B, (2006) Using Linkage Genome Scans to Improve Power of Association in Genome Scans. Am J Hum Genet 78: 243-252.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 243-252
-
-
Roeder, K.1
Bacanu, S.A.2
Wasserman, L.3
Devlin, B.4
-
27
-
-
59949088494
-
Whole population, genome-wide mapping of hidden relatedness
-
Gusev A, Lowe JK, Stoffel M, Daly MJ, Altshuler D, et al. (2009) Whole population, genome-wide mapping of hidden relatedness. Genome Res 19: 318-326.
-
(2009)
Genome Res
, vol.19
, pp. 318-326
-
-
Gusev, A.1
Lowe, J.K.2
Stoffel, M.3
Daly, M.J.4
Altshuler, D.5
-
28
-
-
77950332127
-
High-resolution detection of identity by descent in unrelated individuals
-
Browning SR, Browning BL, (2010) High-resolution detection of identity by descent in unrelated individuals. Am J Hum Genet 86: 526-539.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 526-539
-
-
Browning, S.R.1
Browning, B.L.2
-
29
-
-
79851497145
-
A fast, powerful method for detecting identity by descent
-
Browning BL, Browning SR, (2011) A fast, powerful method for detecting identity by descent. Am J Hum Genet 88: 173-182.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 173-182
-
-
Browning, B.L.1
Browning, S.R.2
-
30
-
-
33646869900
-
Multilocus Association Mapping Using Variable-Length Markov Chains
-
Browning SR, (2006) Multilocus Association Mapping Using Variable-Length Markov Chains. Am J Hum Genet 78: 903-913.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 903-913
-
-
Browning, S.R.1
-
31
-
-
84859588748
-
Detecting rare variant associations by identity-by-descent mapping in case-control studies
-
Browning SR, Thompson EA, (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
-
32
-
-
71849088051
-
Common variants in the trichohyalin gene are associated with straight hair in Europeans
-
Medland SE, Nyholt DR, Painter JN, McEvoy BP, McRae AF, et al. (2009) Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet 85: 750-755.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 750-755
-
-
Medland, S.E.1
Nyholt, D.R.2
Painter, J.N.3
McEvoy, B.P.4
McRae, A.F.5
-
33
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, et al. (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
-
34
-
-
34548134145
-
A whole-genome association study of major determinants for host control of HIV-1
-
Fellay J, Shianna KV, Ge D, Colombo S, Ledergerber B, et al. (2007) A whole-genome association study of major determinants for host control of HIV-1. Science 317: 944-947.
-
(2007)
Science
, vol.317
, pp. 944-947
-
-
Fellay, J.1
Shianna, K.V.2
Ge, D.3
Colombo, S.4
Ledergerber, B.5
-
35
-
-
84863304598
-
-
R Development Core Team, Vienana, Australia: R Foundation for Statistical Computing. Available
-
R Development Core Team (2010) R: A language and envirnment for statistical computing. Vienana, Australia: R Foundation for Statistical Computing. Available: http://www.R-project.org.
-
(2010)
R: A language and envirnment for statistical computing
-
-
-
36
-
-
80054993342
-
Spatio-temporal transcriptome of the human brain
-
Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, et al. (2011) Spatio-temporal transcriptome of the human brain. Nature 478: 483-489.
-
(2011)
Nature
, vol.478
, pp. 483-489
-
-
Kang, H.J.1
Kawasawa, Y.I.2
Cheng, F.3
Zhu, Y.4
Xu, X.5
-
37
-
-
78651339534
-
NCBI GEO: archive for functional genomics data sets - 10 years on
-
Barrett T, Troup DB, Wilhite SE, Ledoux P, Evangelista C, et al. (2011) NCBI GEO: archive for functional genomics data sets - 10 years on. Nucleic Acids Res 39: D1005-1010.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Barrett, T.1
Troup, D.B.2
Wilhite, S.E.3
Ledoux, P.4
Evangelista, C.5
-
38
-
-
0036079158
-
The human genome browser at UCSC
-
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, et al. (2002) The human genome browser at UCSC. Genome Res 12: 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
-
39
-
-
0347755531
-
The UCSC Table Browser data retrieval tool
-
Karolchik D, Hinrichs AS, Furey TS, Roskin KM, Sugnet CW, et al. (2004) The UCSC Table Browser data retrieval tool. Nucleic Acids Res 32: D493-496.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Karolchik, D.1
Hinrichs, A.S.2
Furey, T.S.3
Roskin, K.M.4
Sugnet, C.W.5
-
40
-
-
78650081714
-
ZNF274 recruits the histone methyltransferase SETDB1 to the 3′ ends of ZNF genes
-
Frietze S, O'Geen H, Blahnik KR, Jin VX, Farnham PJ, (2010) ZNF274 recruits the histone methyltransferase SETDB1 to the 3′ ends of ZNF genes. PLoS One 5: e15082.
-
(2010)
PLoS One
, vol.5
-
-
Frietze, S.1
O'Geen, H.2
Blahnik, K.R.3
Jin, V.X.4
Farnham, P.J.5
-
41
-
-
0028877463
-
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L, (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11: 241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
42
-
-
42249087793
-
Estimation of significance thresholds for genomewide association scans
-
Dudbridge F, Gusnanto A, (2008) Estimation of significance thresholds for genomewide association scans. Genet Epidemiol 32: 227-234.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 227-234
-
-
Dudbridge, F.1
Gusnanto, A.2
-
43
-
-
0346274978
-
KRAB-containing zinc-finger repressor proteins
-
Urrutia R, (2003) KRAB-containing zinc-finger repressor proteins. Genome Biol 4: 231.
-
(2003)
Genome Biol
, vol.4
, pp. 231
-
-
Urrutia, R.1
-
44
-
-
33745179207
-
A comprehensive catalog of human KRAB-associated zinc finger genes: insights into the evolutionary history of a large family of transcriptional repressors
-
Huntley S, Baggott DM, Hamilton AT, Tran-Gyamfi M, Yang S, et al. (2006) A comprehensive catalog of human KRAB-associated zinc finger genes: insights into the evolutionary history of a large family of transcriptional repressors. Genome Res 16: 669-677.
-
(2006)
Genome Res
, vol.16
, pp. 669-677
-
-
Huntley, S.1
Baggott, D.M.2
Hamilton, A.T.3
Tran-Gyamfi, M.4
Yang, S.5
-
45
-
-
62549128139
-
A census of human transcription factors: function, expression and evolution
-
Vaquerizas JM, Kummerfeld SK, Teichmann SA, Luscombe NM, (2009) A census of human transcription factors: function, expression and evolution. Nat Rev Genet 10: 252-263.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 252-263
-
-
Vaquerizas, J.M.1
Kummerfeld, S.K.2
Teichmann, S.A.3
Luscombe, N.M.4
-
46
-
-
34347353316
-
Genome-wide analysis of KAP1 binding suggests autoregulation of KRAB-ZNFs
-
O'Geen H, Squazzo SL, Iyengar S, Blahnik K, Rinn JL, et al. (2007) Genome-wide analysis of KAP1 binding suggests autoregulation of KRAB-ZNFs. PLoS Genet 3: e89.
-
(2007)
PLoS Genet
, vol.3
-
-
O'Geen, H.1
Squazzo, S.L.2
Iyengar, S.3
Blahnik, K.4
Rinn, J.L.5
-
47
-
-
0033231183
-
The zinc finger protein NRIF interacts with the neurotrophin receptor p75(NTR) and participates in programmed cell death
-
Casademunt E, Carter BD, Benzel I, Frade JM, Dechant G, et al. (1999) The zinc finger protein NRIF interacts with the neurotrophin receptor p75(NTR) and participates in programmed cell death. Embo J 18: 6050-6061.
-
(1999)
Embo J
, vol.18
, pp. 6050-6061
-
-
Casademunt, E.1
Carter, B.D.2
Benzel, I.3
Frade, J.M.4
Dechant, G.5
-
48
-
-
79960856255
-
Comprehensive gene expression analysis of human embryonic stem cells during differentiation into neural cells
-
Fathi A, Hatami M, Hajihosseini V, Fattahi F, Kiani S, et al. (2011) Comprehensive gene expression analysis of human embryonic stem cells during differentiation into neural cells. PLoS One 6: e22856.
-
(2011)
PLoS One
, vol.6
-
-
Fathi, A.1
Hatami, M.2
Hajihosseini, V.3
Fattahi, F.4
Kiani, S.5
-
49
-
-
0036293353
-
Identification of a KRAB-containing zinc finger protein, ZNF304, by AU-motif-directed display method and initial characterization in lymphocyte activation
-
Sabater L, Ashhab Y, Caro P, Kolkowski EC, Pujol-Borrell R, et al. (2002) Identification of a KRAB-containing zinc finger protein, ZNF304, by AU-motif-directed display method and initial characterization in lymphocyte activation. Biochem Biophys Res Commun 293: 1066-1072.
-
(2002)
Biochem Biophys Res Commun
, vol.293
, pp. 1066-1072
-
-
Sabater, L.1
Ashhab, Y.2
Caro, P.3
Kolkowski, E.C.4
Pujol-Borrell, R.5
-
50
-
-
33646192473
-
Positive regulation of immune cell function and inflammatory responses by phosphatase PAC-1
-
Jeffrey KL, Brummer T, Rolph MS, Liu SM, Callejas NA, et al. (2006) Positive regulation of immune cell function and inflammatory responses by phosphatase PAC-1. Nat Immunol 7: 274-283.
-
(2006)
Nat Immunol
, vol.7
, pp. 274-283
-
-
Jeffrey, K.L.1
Brummer, T.2
Rolph, M.S.3
Liu, S.M.4
Callejas, N.A.5
-
51
-
-
52649097448
-
The Immunological Genome Project: networks of gene expression in immune cells
-
Heng TS, Painter MW, (2008) The Immunological Genome Project: networks of gene expression in immune cells. Nat Immunol 9: 1091-1094.
-
(2008)
Nat Immunol
, vol.9
, pp. 1091-1094
-
-
Heng, T.S.1
Painter, M.W.2
-
52
-
-
77952663268
-
The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues
-
Lorenz P, Dietmann S, Wilhelm T, Koczan D, Autran S, et al. (2010) The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues. BMC Genomics 11: 206.
-
(2010)
BMC Genomics
, vol.11
, pp. 206
-
-
Lorenz, P.1
Dietmann, S.2
Wilhelm, T.3
Koczan, D.4
Autran, S.5
-
53
-
-
70349532764
-
Genomic regulatory blocks in vertebrates and implications in human disease
-
Navratilova P, Becker TS, (2009) Genomic regulatory blocks in vertebrates and implications in human disease. Brief Funct Genomic Proteomic 8: 333-342.
-
(2009)
Brief Funct Genomic Proteomic
, vol.8
, pp. 333-342
-
-
Navratilova, P.1
Becker, T.S.2
-
54
-
-
80052610245
-
Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis
-
Simpson S Jr, Blizzard L, Otahal P, Van der Mei I, Taylor B, (2011) Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis. J Neurol Neurosurg Psychiatry 82: 1132-1141.
-
(2011)
J Neurol Neurosurg Psychiatry
, vol.82
, pp. 1132-1141
-
-
Simpson Jr., S.1
Blizzard, L.2
Otahal, P.3
Van der Mei, I.4
Taylor, B.5
-
55
-
-
18344385134
-
Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis
-
Rubio JP, Bahlo M, Butzkueven H, van Der Mei IA, Sale MM, et al. (2002) Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis. Am J Hum Genet 70: 1125-1137.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1125-1137
-
-
Rubio, J.P.1
Bahlo, M.2
Butzkueven, H.3
van Der Mei, I.A.4
Sale, M.M.5
-
56
-
-
0038744296
-
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies
-
Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, et al. (2003) Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet 72: 1117-1130.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.D.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
|