-
1
-
-
33947582074
-
Epidemiology of Sjogren's syndrome: where are we now?
-
Binard A., Devauchelle-Pensec V., Fautrel B., Jousse S., Youinou P., Saraux A. Epidemiology of Sjogren's syndrome: where are we now?. Clinical and Experimental Rheumatology 2007, 25:1-4.
-
(2007)
Clinical and Experimental Rheumatology
, vol.25
, pp. 1-4
-
-
Binard, A.1
Devauchelle-Pensec, V.2
Fautrel, B.3
Jousse, S.4
Youinou, P.5
Saraux, A.6
-
2
-
-
38149138096
-
Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part I
-
Helmick C.G., Felson D.T., Lawrence R.C., Gabriel S., Hirsch R., Kwoh C.K., et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part I. Arthritis & Rheumatism 2008, 58:15-25.
-
(2008)
Arthritis & Rheumatism
, vol.58
, pp. 15-25
-
-
Helmick, C.G.1
Felson, D.T.2
Lawrence, R.C.3
Gabriel, S.4
Hirsch, R.5
Kwoh, C.K.6
-
3
-
-
0036092482
-
Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group
-
Vitali C., Bombardieri S., Jonsson R., Moutsopoulos H.M., Alexander E.L., Carsons S.E., et al. Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Annals of the Rheumatic Diseases 2002, 61:554-558.
-
(2002)
Annals of the Rheumatic Diseases
, vol.61
, pp. 554-558
-
-
Vitali, C.1
Bombardieri, S.2
Jonsson, R.3
Moutsopoulos, H.M.4
Alexander, E.L.5
Carsons, S.E.6
-
4
-
-
0025764467
-
Chronic bilateral dacryo-adenitis in identical twins: a possible incomplete form of Sjogren syndrome
-
Besana C., Salmaggi C., Pellegrino C., Pierro L., Vergani S., Faravelli A., et al. Chronic bilateral dacryo-adenitis in identical twins: a possible incomplete form of Sjogren syndrome. European Journal of Pediatrics 1991, 150:652-655.
-
(1991)
European Journal of Pediatrics
, vol.150
, pp. 652-655
-
-
Besana, C.1
Salmaggi, C.2
Pellegrino, C.3
Pierro, L.4
Vergani, S.5
Faravelli, A.6
-
5
-
-
0033812388
-
Monozygotic twins with primary Sjogren's syndrome
-
Bolstad A.I., Haga H.J., Wassmuth R., Jonsson R. Monozygotic twins with primary Sjogren's syndrome. The Journal of Rheumatology 2000, 27:2264-2266.
-
(2000)
The Journal of Rheumatology
, vol.27
, pp. 2264-2266
-
-
Bolstad, A.I.1
Haga, H.J.2
Wassmuth, R.3
Jonsson, R.4
-
6
-
-
23444434377
-
Primary Sjogren's syndrome in dizygotic adolescent twins: one case with lymphocytic interstitial pneumonia
-
Houghton K.M., Cabral D.A., Petty R.E., Tucker L.B. Primary Sjogren's syndrome in dizygotic adolescent twins: one case with lymphocytic interstitial pneumonia. The Journal of Rheumatology 2005, 32:1603-1606.
-
(2005)
The Journal of Rheumatology
, vol.32
, pp. 1603-1606
-
-
Houghton, K.M.1
Cabral, D.A.2
Petty, R.E.3
Tucker, L.B.4
-
7
-
-
0030993254
-
Immunologically restricted and inhibitory anti-Ro/SSA in monozygotic twins
-
Scofield R.H., Kurien B.T., Reichlin M. Immunologically restricted and inhibitory anti-Ro/SSA in monozygotic twins. Lupus 1997, 6:395-398.
-
(1997)
Lupus
, vol.6
, pp. 395-398
-
-
Scofield, R.H.1
Kurien, B.T.2
Reichlin, M.3
-
8
-
-
0026537198
-
A revised estimate of twin concordance in systemic lupus erythematosus
-
Deapen D., Escalante A., Weinrib L., Horwitz D., Bachman B., Roy-Burman P., et al. A revised estimate of twin concordance in systemic lupus erythematosus. Arthritis & Rheumatism 1992, 35:311-318.
-
(1992)
Arthritis & Rheumatism
, vol.35
, pp. 311-318
-
-
Deapen, D.1
Escalante, A.2
Weinrib, L.3
Horwitz, D.4
Bachman, B.5
Roy-Burman, P.6
-
9
-
-
0027375302
-
Twin concordance rates for rheumatoid arthritis: results from a nationwide study
-
Silman A.J., MacGregor A.J., Thomson W., Holligan S., Carthy D., Farhan A., et al. Twin concordance rates for rheumatoid arthritis: results from a nationwide study. British Journal of Rheumatology 1993, 32:903-907.
-
(1993)
British Journal of Rheumatology
, vol.32
, pp. 903-907
-
-
Silman, A.J.1
MacGregor, A.J.2
Thomson, W.3
Holligan, S.4
Carthy, D.5
Farhan, A.6
-
10
-
-
54549125740
-
Genes and Sjogren's syndrome
-
[vii]
-
Cobb B.L., Lessard C.J., Harley J.B., Moser K.L. Genes and Sjogren's syndrome. Rheumatic Disease Clinics of North America 2008, 34:847-868. [vii].
-
(2008)
Rheumatic Disease Clinics of North America
, vol.34
, pp. 847-868
-
-
Cobb, B.L.1
Lessard, C.J.2
Harley, J.B.3
Moser, K.L.4
-
11
-
-
17244373451
-
Familial aggregation of systemic lupus erythematosus, rheumatoid arthritis, and other autoimmune diseases in 1,177 lupus patients from the GLADEL cohort
-
Alarcon-Segovia D., Alarcon-Riquelme M.E., Cardiel M.H., Caeiro F., Massardo L., Villa A.R., et al. Familial aggregation of systemic lupus erythematosus, rheumatoid arthritis, and other autoimmune diseases in 1,177 lupus patients from the GLADEL cohort. Arthritis & Rheumatism 2005, 52:1138-1147.
-
(2005)
Arthritis & Rheumatism
, vol.52
, pp. 1138-1147
-
-
Alarcon-Segovia, D.1
Alarcon-Riquelme, M.E.2
Cardiel, M.H.3
Caeiro, F.4
Massardo, L.5
Villa, A.R.6
-
12
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander E.S., Linton L.M., Birren B., Nusbaum C., Zody M.C., Baldwin J., et al. Initial sequencing and analysis of the human genome. Nature 2001, 409:860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
-
13
-
-
0035895505
-
The sequence of the human genome
-
Venter J.C., Adams M.D., Myers E.W., Li P.W., Mural R.J., Sutton G.G., et al. The sequence of the human genome. Science 2001, 291:1304-1351.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
-
14
-
-
79959503826
-
The international HapMap project
-
The international HapMap project. Nature 2003, 426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
15
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
A map of human genome variation from population-scale sequencing. Nature 2010, 467:1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
16
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein R.J., Zeiss C., Chew E.Y., Tsai J.Y., Sackler R.S., Haynes C., et al. Complement factor H polymorphism in age-related macular degeneration. Science 2005, 308:385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.Y.4
Sackler, R.S.5
Haynes, C.6
-
17
-
-
84872748863
-
-
A catalog of published genome-Wide Association studies. Available at: [accessed 29.08.2011].
-
Hindorff LA JH, Hall PN, Mehta JP, and Manolio TA. A catalog of published genome-Wide Association studies. Available at: [accessed 29.08.2011]. http://www.genome.gov/gwastudies.
-
-
-
Hindorff, L.A.J.H.1
Hall, P.N.2
Mehta, J.P.3
Manolio, T.A.4
-
18
-
-
42249087793
-
Estimation of significance thresholds for genomewide association scans
-
Dudbridge F., Gusnanto A. Estimation of significance thresholds for genomewide association scans. Genetic Epidemiology 2008, 32:227-234.
-
(2008)
Genetic Epidemiology
, vol.32
, pp. 227-234
-
-
Dudbridge, F.1
Gusnanto, A.2
-
20
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch N.J. Searching for genetic determinants in the new millennium. Nature 2000, 405:847-856.
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
21
-
-
0015236430
-
Histocompatibility (HL-A) antigens associated with systemic lupus erythematosus. A possible genetic predisposition to disease
-
Grumet F.C., Coukell A., Bodmer J.G., Bodmer W.F., McDevitt H.O. Histocompatibility (HL-A) antigens associated with systemic lupus erythematosus. A possible genetic predisposition to disease. The New England Journal of Medicine 1971, 285:193-196.
-
(1971)
The New England Journal of Medicine
, vol.285
, pp. 193-196
-
-
Grumet, F.C.1
Coukell, A.2
Bodmer, J.G.3
Bodmer, W.F.4
McDevitt, H.O.5
-
22
-
-
0015197172
-
The distribution of HL-A histocompatibility factors and genes in patients with systemic lupus erythematosus
-
Waters H., Konrad P., Walford R.L. The distribution of HL-A histocompatibility factors and genes in patients with systemic lupus erythematosus. Tissue Antigens 1971, 1:68-73.
-
(1971)
Tissue Antigens
, vol.1
, pp. 68-73
-
-
Waters, H.1
Konrad, P.2
Walford, R.L.3
-
23
-
-
0015309257
-
Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus
-
Agnello V., De Bracco M.M., Kunkel H.G. Hereditary C2 deficiency with some manifestations of systemic lupus erythematosus. Journal of Immunology 1972, 108:837-840.
-
(1972)
Journal of Immunology
, vol.108
, pp. 837-840
-
-
Agnello, V.1
De Bracco, M.M.2
Kunkel, H.G.3
-
24
-
-
0016188451
-
Lupus erythematosus syndrome and complete deficiency of the fourth component of complement
-
Hauptmann G., Grosshans E., Heid E. Lupus erythematosus syndrome and complete deficiency of the fourth component of complement. Bollettino Dell'Istituto Sieroterapico Milanese 1974, 53(Suppl. 228).
-
(1974)
Bollettino Dell'Istituto Sieroterapico Milanese
, vol.53
, Issue.SUPPL. 228
-
-
Hauptmann, G.1
Grosshans, E.2
Heid, E.3
-
25
-
-
0019442485
-
Lupus erythematosus-like syndrome with selective complete deficiency of C1q
-
Nishino H., Shibuya K., Nishida Y., Mushimoto M. Lupus erythematosus-like syndrome with selective complete deficiency of C1q. Annals of Internal Medicine 1981, 95:322-324.
-
(1981)
Annals of Internal Medicine
, vol.95
, pp. 322-324
-
-
Nishino, H.1
Shibuya, K.2
Nishida, Y.3
Mushimoto, M.4
-
26
-
-
0036676085
-
Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus
-
Edberg J.C., Langefeld C.D., Wu J., Moser K.L., Kaufman K.M., Kelly J., et al. Genetic linkage and association of Fcgamma receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus. Arthritis & Rheumatism 2002, 46:2132-2140.
-
(2002)
Arthritis & Rheumatism
, vol.46
, pp. 2132-2140
-
-
Edberg, J.C.1
Langefeld, C.D.2
Wu, J.3
Moser, K.L.4
Kaufman, K.M.5
Kelly, J.6
-
27
-
-
0029866721
-
Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans
-
Salmon J.E., Millard S., Schachter L.A., Arnett F.C., Ginzler E.M., Gourley M.F., et al. Fc gamma RIIA alleles are heritable risk factors for lupus nephritis in African Americans. The Journal of Clinical Investigation 1996, 97:1348-1354.
-
(1996)
The Journal of Clinical Investigation
, vol.97
, pp. 1348-1354
-
-
Salmon, J.E.1
Millard, S.2
Schachter, L.A.3
Arnett, F.C.4
Ginzler, E.M.5
Gourley, M.F.6
-
28
-
-
13244277850
-
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
-
Prokunina L., Castillejo-Lopez C., Oberg F., Gunnarsson I., Berg L., Magnusson V., et al. A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nature Genetics 2002, 32:666-669.
-
(2002)
Nature Genetics
, vol.32
, pp. 666-669
-
-
Prokunina, L.1
Castillejo-Lopez, C.2
Oberg, F.3
Gunnarsson, I.4
Berg, L.5
Magnusson, V.6
-
29
-
-
62749182367
-
Association of programmed cell death 1 polymorphisms and systemic lupus erythematosus: a meta-analysis
-
Lee Y.H., Woo J.H., Choi S.J., Ji J.D., Song G.G. Association of programmed cell death 1 polymorphisms and systemic lupus erythematosus: a meta-analysis. Lupus 2009, 18:9-15.
-
(2009)
Lupus
, vol.18
, pp. 9-15
-
-
Lee, Y.H.1
Woo, J.H.2
Choi, S.J.3
Ji, J.D.4
Song, G.G.5
-
30
-
-
37449023760
-
PTPN22: its role in SLE and autoimmunity
-
Chung S.A., Criswell L.A. PTPN22: its role in SLE and autoimmunity. Autoimmunity 2007, 40:582-590.
-
(2007)
Autoimmunity
, vol.40
, pp. 582-590
-
-
Chung, S.A.1
Criswell, L.A.2
-
31
-
-
58849120030
-
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus
-
Orru V., Tsai S.J., Rueda B., Fiorillo E., Stanford S.M., Dasgupta J., et al. A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus. Human Molecular Genetics 2009, 18:569-579.
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 569-579
-
-
Orru, V.1
Tsai, S.J.2
Rueda, B.3
Fiorillo, E.4
Stanford, S.M.5
Dasgupta, J.6
-
32
-
-
34247125683
-
Association of IRF5 in UK SLE families identifies a variant involved in polyadenylation
-
Cunninghame Graham D.S., Manku H., Wagner S., Reid J., Timms K., Gutin A., et al. Association of IRF5 in UK SLE families identifies a variant involved in polyadenylation. Human Molecular Genetics 2007, 16:579-591.
-
(2007)
Human Molecular Genetics
, vol.16
, pp. 579-591
-
-
Cunninghame Graham, D.S.1
Manku, H.2
Wagner, S.3
Reid, J.4
Timms, K.5
Gutin, A.6
-
33
-
-
34247254495
-
Structural insertion/deletion variation in IRF5 is associated with a risk haplotype and defines the precise IRF5 isoforms expressed in systemic lupus erythematosus
-
Kozyrev S.V., Lewen S., Reddy P.M., Pons-Estel B., Witte T., Junker P., et al. Structural insertion/deletion variation in IRF5 is associated with a risk haplotype and defines the precise IRF5 isoforms expressed in systemic lupus erythematosus. Arthritis & Rheumatism 2007, 56:1234-1241.
-
(2007)
Arthritis & Rheumatism
, vol.56
, pp. 1234-1241
-
-
Kozyrev, S.V.1
Lewen, S.2
Reddy, P.M.3
Pons-Estel, B.4
Witte, T.5
Junker, P.6
-
34
-
-
42549152933
-
Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans
-
Kelly J.A., Kelley J.M., Kaufman K.M., Kilpatrick J., Bruner G.R., Merrill J.T., et al. Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans. Genes and Immunity 2008, 9:187-194.
-
(2008)
Genes and Immunity
, vol.9
, pp. 187-194
-
-
Kelly, J.A.1
Kelley, J.M.2
Kaufman, K.M.3
Kilpatrick, J.4
Bruner, G.R.5
Merrill, J.T.6
-
35
-
-
34548427925
-
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus
-
Remmers E.F., Plenge R.M., Lee A.T., Graham R.R., Hom G., Behrens T.W., et al. STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. The New England Journal of Medicine 2007, 357:977-986.
-
(2007)
The New England Journal of Medicine
, vol.357
, pp. 977-986
-
-
Remmers, E.F.1
Plenge, R.M.2
Lee, A.T.3
Graham, R.R.4
Hom, G.5
Behrens, T.W.6
-
36
-
-
49549100511
-
Trex1 prevents cell-intrinsic initiation of autoimmunity
-
Stetson D.B., Ko J.S., Heidmann T., Medzhitov R. Trex1 prevents cell-intrinsic initiation of autoimmunity. Cell 2008, 134:587-598.
-
(2008)
Cell
, vol.134
, pp. 587-598
-
-
Stetson, D.B.1
Ko, J.S.2
Heidmann, T.3
Medzhitov, R.4
-
37
-
-
38649138296
-
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus
-
Kozyrev S.V., Abelson A.K., Wojcik J., Zaghlool A., Linga Reddy M.V., Sanchez E., et al. Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. Nature Genetics 2008, 40:211-216.
-
(2008)
Nature Genetics
, vol.40
, pp. 211-216
-
-
Kozyrev, S.V.1
Abelson, A.K.2
Wojcik, J.3
Zaghlool, A.4
Linga Reddy, M.V.5
Sanchez, E.6
-
38
-
-
40049108936
-
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
-
Hom G., Graham R.R., Modrek B., Taylor K.E., Ortmann W., Garnier S., et al. Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. The New England Journal of Medicine 2008, 358:900-909.
-
(2008)
The New England Journal of Medicine
, vol.358
, pp. 900-909
-
-
Hom, G.1
Graham, R.R.2
Modrek, B.3
Taylor, K.E.4
Ortmann, W.5
Garnier, S.6
-
39
-
-
38649125210
-
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
-
Harley J.B., Alarcon-Riquelme M.E., Criswell L.A., Jacob C.O., Kimberly R.P., Moser K.L., et al. Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nature Genetics 2008, 40:204-210.
-
(2008)
Nature Genetics
, vol.40
, pp. 204-210
-
-
Harley, J.B.1
Alarcon-Riquelme, M.E.2
Criswell, L.A.3
Jacob, C.O.4
Kimberly, R.P.5
Moser, K.L.6
-
40
-
-
50449111452
-
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus
-
Graham R.R., Cotsapas C., Davies L., Hackett R., Lessard C.J., Leon J.M., et al. Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nature Genetics 2008, 40:1059-1061.
-
(2008)
Nature Genetics
, vol.40
, pp. 1059-1061
-
-
Graham, R.R.1
Cotsapas, C.2
Davies, L.3
Hackett, R.4
Lessard, C.J.5
Leon, J.M.6
-
41
-
-
70350629871
-
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
-
Han J.W., Zheng H.F., Cui Y., Sun L.D., Ye D.Q., Hu Z., et al. Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. Nature Genetics 2009, 41:1234-1237.
-
(2009)
Nature Genetics
, vol.41
, pp. 1234-1237
-
-
Han, J.W.1
Zheng, H.F.2
Cui, Y.3
Sun, L.D.4
Ye, D.Q.5
Hu, Z.6
-
42
-
-
78650862201
-
Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study
-
Lessard C.J., Adrianto I., Kelly J.A., Kaufman K.M., Grundahl K.M., Adler A., et al. Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study. American Journal of Human Genetics 2011, 88:83-91.
-
(2011)
American Journal of Human Genetics
, vol.88
, pp. 83-91
-
-
Lessard, C.J.1
Adrianto, I.2
Kelly, J.A.3
Kaufman, K.M.4
Grundahl, K.M.5
Adler, A.6
-
43
-
-
79551619981
-
Evolutionary evidence of the effect of rare variants on disease etiology
-
Gorlov I.P., Gorlova O.Y., Frazier M.L., Spitz M.R., Amos C.I. Evolutionary evidence of the effect of rare variants on disease etiology. Clinical Genetics 2011, 79:199-206.
-
(2011)
Clinical Genetics
, vol.79
, pp. 199-206
-
-
Gorlov, I.P.1
Gorlova, O.Y.2
Frazier, M.L.3
Spitz, M.R.4
Amos, C.I.5
|