-
1
-
-
1842422281
-
The genetics of psoriasis, psoriatic arthritis and atopic dermatitis
-
(Spec No 1)
-
Bowcock AM, Cookson WO (2004) The genetics of psoriasis, psoriatic arthritis and atopic dermatitis. Hum Mol Genet 13(Spec No 1):R43-55
-
(2004)
Hum Mol Genet
, vol.13
-
-
Bowcock, A.M.1
Cookson, W.O.2
-
2
-
-
0034120666
-
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome
-
Chavanas S, Bodemer C, Rochat A et al. (2000) Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome. Nat Genet 25:141-142
-
(2000)
Nat Genet
, vol.25
, pp. 141-142
-
-
Chavanas, S.1
Bodemer, C.2
Rochat, A.3
-
3
-
-
10244250341
-
The immunogenetics of asthma and eczema: A new focus on the epithelium
-
Cookson W (2004) The immunogenetics of asthma and eczema: a new focus on the epithelium. Nat Rev Immunol 4:978-988
-
(2004)
Nat Rev Immunol
, vol.4
, pp. 978-988
-
-
Cookson, W.1
-
4
-
-
59149098800
-
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis
-
De Cid R, Riveira-Munoz E, Zeeuwen PL et al. (2009) Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. Nat Genet 41:211-215
-
(2009)
Nat Genet
, vol.41
, pp. 211-215
-
-
De Cid, R.1
Riveira-Munoz, E.2
Zeeuwen, P.L.3
-
5
-
-
67349252610
-
A common variant on chromosome 11q13 is associated with atopic dermatitis
-
Esparza-Gordillo J, Weidinger S, Folster-Holst R et al. (2009) A common variant on chromosome 11q13 is associated with atopic dermatitis. Nat Genet 41:596-601
-
(2009)
Nat Genet
, vol.41
, pp. 596-601
-
-
Esparza-Gordillo, J.1
Weidinger, S.2
Folster-Holst, R.3
-
6
-
-
66749163178
-
A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming
-
Fallon PG, Sasaki T, Sandilands A et al. (2009) A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming. Nat Genet 41:602-608
-
(2009)
Nat Genet
, vol.41
, pp. 602-608
-
-
Fallon, P.G.1
Sasaki, T.2
Sandilands, A.3
-
7
-
-
37549033125
-
Psoriasis is associated with increased beta-defensin genomic copy number
-
Hollox EJ, Huffmeier U, Zeeuwen PL, et al. (2008) Psoriasis is associated with increased beta-defensin genomic copy number. Nat Genet 40:23-25
-
(2008)
Nat Genet
, vol.40
, pp. 23-25
-
-
Hollox, E.J.1
Huffmeier, U.2
Zeeuwen, P.L.3
-
8
-
-
34250828434
-
Cytokine modulation of atopic dermatitis filaggrin skin expression
-
Howell MD, Kim BE, Gao P et al. (2007) Cytokine modulation of atopic dermatitis filaggrin skin expression. J Allergy Clin Immunol 120:150-155
-
(2007)
J Allergy Clin Immunol
, vol.120
, pp. 150-155
-
-
Howell, M.D.1
Kim, B.E.2
Gao, P.3
-
9
-
-
77949542167
-
Replication of LCE3C-LCE3B CNV as a risk factor for psoriasis and analysis of interaction with other genetic risk factors
-
Huffmeier U, Bergboer JG, Becker T, et al. (2009) Replication of LCE3C-LCE3B CNV as a risk factor for psoriasis and analysis of interaction with other genetic risk factors. JInvest Dermatol 130:979-984
-
(2009)
J Invest Dermatol
, vol.130
, pp. 979-984
-
-
Huffmeier, U.1
Bergboerjg, J.G.2
Becker, T.3
-
10
-
-
34248585440
-
Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patients
-
Huffmeier U, Traupe H, Oji V et al. (2007) Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patients. J Invest Dermatol 127:1367-1370
-
(2007)
J Invest Dermatol
, vol.127
, pp. 1367-1370
-
-
Huffmeier, U.1
Traupe, H.2
Oji, V.3
-
11
-
-
33745524911
-
Breaking the (un)sound barrier: Filaggrin is a major gene for atopic dermatitis
-
Irvine AD, McLean WH (2006) Breaking the (un)sound barrier: filaggrin is a major gene for atopic dermatitis. JInvest Dermatol 126:1200-1202
-
(2006)
J Invest Dermatol
, vol.126
, pp. 1200-1202
-
-
Irvine, A.D.1
McLean, W.H.2
-
12
-
-
43049143055
-
Mapping and sequencing of structural variation from eight human genomes
-
Kidd JM, Cooper GM, Donahue WF et al. (2008) Mapping and sequencing of structural variation from eight human genomes. Nature 453:56-64
-
(2008)
Nature
, vol.453
, pp. 56-64
-
-
Kidd, J.M.1
Cooper, G.M.2
Donahue, W.F.3
-
13
-
-
35348988679
-
Paired-end mapping reveals extensive structural variation in the human genome
-
Korbel JO, Urban AE, Affourtit JP et al. (2007) Paired-end mapping reveals extensive structural variation in the human genome. Science 318:420-426
-
(2007)
Science
, vol.318
, pp. 420-426
-
-
Korbel, J.O.1
Urban, A.E.2
Affourtit, J.P.3
-
14
-
-
14244258610
-
Psoriasis pathophysiology: Current concepts of pathogenesis
-
KruegerJG, Bowcock A (2005) Psoriasis pathophysiology: current concepts of pathogenesis. Ann Rheum Dis 64(Suppl 2):ii30-6
-
(2005)
Ann Rheum Dis
, vol.64
, Issue.2 SUPPL.
-
-
Kruegerjg Bowcock, A.1
-
15
-
-
0037431756
-
Atopic dermatitis
-
DOI 10.1016/S0140-6736(03)12193-9
-
Leung DY, Bieber T (2003) Atopic dermatitis. Lancet 361:151-160 (Pubitemid 36092023)
-
(2003)
Lancet
, vol.361
, Issue.9352
, pp. 151-160
-
-
Leung, D.Y.M.1
Bieber, T.2
-
16
-
-
0039702803
-
LEKTI, a novel 15-domain type of human serine proteinase inhibitor
-
Magert HJ, Standker L, Kreutzmann P et al. (1999) LEKTI, a novel 15-domain type of human serine proteinase inhibitor. JBiol Chem 274:21499-21502
-
(1999)
J Biol Chem
, vol.274
, pp. 21499-21502
-
-
Magert, H.J.1
Standker, L.2
Kreutzmann, P.3
-
17
-
-
0035818472
-
Differentially expressed late constituents of the epidermal cornified envelope
-
Marshall D, Hardman MJ, Nield KM et al. (2001) Differentially expressed late constituents of the epidermal cornified envelope. Proc Natl Acad Sci USA 98:13031-13036
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 13031-13036
-
-
Marshall, D.1
Hardman, M.J.2
Nield, K.M.3
-
18
-
-
0029932799
-
Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21
-
Mischke D, Korge BP, Marenholz I et al. (1996) Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21. J Invest Dermatol 106:989-992
-
(1996)
J Invest Dermatol
, vol.106
, pp. 989-992
-
-
Mischke, D.1
Korge, B.P.2
Marenholz, I.3
-
19
-
-
34247579998
-
Filaggrin mutations in children with severe atopic dermatitis
-
Morar N, Cookson WO, Harper JI et al. (2007) Filaggrin mutations in children with severe atopic dermatitis. JInvest Dermatol 127:1667-1672
-
(2007)
JInvest Dermatol
, vol.127
, pp. 1667-1672
-
-
Morar, N.1
Cookson, W.O.2
Harper, J.I.3
-
21
-
-
33645399288
-
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
-
Palmer CN, Irvine AD, Terron-Kwiatkowski A et al. (2006) Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet 38:441-446
-
(2006)
Nat Genet
, vol.38
, pp. 441-446
-
-
Palmer, C.N.1
Irvine, A.D.2
Terron-Kwiatkowski, A.3
-
22
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon R, Ishikawa S, Fitch KR et al. (2006) Global variation in copy number in the human genome. Nature 444:444-454 (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
23
-
-
33947697092
-
Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levels
-
Sharma M, Mehla K, Batra J et al. (2007) Association of a chromosome 1q21 locus in close proximity to a late cornified envelope-like proline-rich 1 (LELP1) gene with total serum IgE levels. JHum Genet 52:378-383
-
(2007)
J Hum Genet
, vol.52
, pp. 378-383
-
-
Sharma, M.1
Mehla, K.2
Batra, J.3
-
24
-
-
33644622891
-
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris
-
Smith FJ, Irvine AD, Terron-Kwiatkowski A et al. (2006) Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat Genet 38:337-342
-
(2006)
Nat Genet
, vol.38
, pp. 337-342
-
-
Smith, F.J.1
Irvine, A.D.2
Terron-Kwiatkowski, A.3
-
25
-
-
50649101129
-
Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk
-
Weidinger S, Baurecht H, Wagenpfeil S, et al. (2008) Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk. J Allergy Clin Immunol 122:560-568
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 560-568
-
-
Weidinger, S.1
Baurecht, H.2
Wagenpfeil, S.3
-
26
-
-
33745353511
-
Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations
-
Weidinger S, Illig T, Baurecht H et al. (2006) Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations. J Allergy Clin Immunol 118:214-219
-
(2006)
J Allergy Clin Immunol
, vol.118
, pp. 214-219
-
-
Weidinger, S.1
Illig, T.2
Baurecht, H.3
-
27
-
-
34447261676
-
Atopic dermatitis: Insights from linkage overlap and disease co-morbidity
-
Willis-Owen SA, Morar N, Willis-Owen CA (2007) Atopic dermatitis: insights from linkage overlap and disease co-morbidity. Expert Rev Mol Med 9:1-13
-
(2007)
Expert Rev Mol Med
, vol.9
, pp. 1-13
-
-
Willis-Owen, S.A.1
Morar, N.2
Willis-Owen, C.A.3
-
28
-
-
59149096149
-
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21
-
Zhang XJ, Huang W, Yang S et al. (2009) Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. Nat Genet 41:205-210
-
(2009)
Nat Genet
, vol.41
, pp. 205-210
-
-
Zhang, X.J.1
Huang, W.2
Yang, S.3
-
29
-
-
34447580008
-
Filaggrin null alleles are not associated with psoriasis
-
Zhao Y, Terron-Kwiatkowski A, Liao H, et al. (2007) Filaggrin null alleles are not associated with psoriasis. JInvest Dermatol 127:1878-1882
-
(2007)
J Invest Dermatol
, vol.127
, pp. 1878-1882
-
-
Zhao, Y.1
Terron-Kwiatkowski, A.2
Liao, H.3
|