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Ghazi Chabchoub et al.
ANNALS OF HUMAN BIOLOGY (2009)
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease
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CLINICAL ENDOCRINOLOGY (2009)
Association of PTPN22 C1858T and CTLA-4 A49G polymorphisms with type 1 diabetes in Croatians
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DIABETES RESEARCH AND CLINICAL PRACTICE (2009)
Frontiers and controversies in the pathobiology of vitiligo: separating the wheat from the chaff
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EXPERIMENTAL DERMATOLOGY (2009)
Cutting Edge: The PTPN22 Allelic Variant Associated with Autoimmunity Impairs B Cell Signaling
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JOURNAL OF IMMUNOLOGY (2009)
CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data
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PIGMENT CELL & MELANOMA RESEARCH (2009)
Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects
Bernadett Farago et al.
RHEUMATOLOGY INTERNATIONAL (2009)
PTPN22 C1858T polymorphism and human brucellosis
Maria Jose Bravo et al.
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES (2009)
The Protein Tyrosine Phosphatase Non-Receptor Type 22 C1858T Polymorphism Is a Joint Susceptibility Locus for Immunthyroiditis and Autoimmune Diabetes
Georg Dultz et al.
THYROID (2009)
Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population
H. Lamsyah et al.
TISSUE ANTIGENS (2009)
Mutation screening of PTPN22:: association of the 1858T-allele with Addison's disease
Beate Skinningsrud et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
PTPN22 allele polymorphisms in 15 Chinese populations
Z. -H. Zhang et al.
INTERNATIONAL JOURNAL OF IMMUNOGENETICS (2008)
Association of PTPN22 1858C/T polymorphism with vitiligo susceptibility in Gujarat population
Naresh C. Laddha et al.
JOURNAL OF DERMATOLOGICAL SCIENCE (2008)
PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not
Greggory S. LaBerge et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2008)
The PTPN22-1858C>T (R620W) functional polymorphism is associated with generalized vitiligo in the Romanian population
Greggory S. LaBerge et al.
PIGMENT CELL & MELANOMA RESEARCH (2008)
PTPN22 gene polymorphism in Takayasus arteritis
N. Sahin et al.
RHEUMATOLOGY (2008)
Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population
Michiko Ichimura et al.
THYROID (2008)
Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population
K. Douroudis et al.
TISSUE ANTIGENS (2008)
The functional R620W variant of the PTPN22 gene is associated with celiac disease
I. Santin et al.
TISSUE ANTIGENS (2008)
The association of the PTPN22 620W polymorphism with Behcet's disease
Vijay Baranathan et al.
ANNALS OF THE RHEUMATIC DISEASES (2007)
Genetic variations in NALP1 are associated with generalized vitiligo in a Romanian population
Ying Jin et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2007)
The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population
J. Wesoly et al.
RHEUMATOLOGY (2007)
NALP1 in vitiligo-associated multiple autoimmune disease
Ying Jin et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
The definition and assessment of vitiligo:: a consensus report of the Vitiligo European Task Force
Alain Taieb et al.
PIGMENT CELL RESEARCH (2007)
Genetic epidemiology of vitiligo: a study of 815 probands and their families from south China
Xiukun Sun et al.
INTERNATIONAL JOURNAL OF DERMATOLOGY (2006)
Association of the PTPN22/LYP gene with type 1 diabetes
Andrea K. Steck et al.
PEDIATRIC DIABETES (2006)
Protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene R620W variant and sporadic idiopathic hypoparathyroidism in Asian Indians
D. Ray et al.
INTERNATIONAL JOURNAL OF IMMUNOGENETICS (2006)
Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients
P. Harrison et al.
RHEUMATOLOGY (2006)
Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis
C Vandiedonck et al.
ANNALS OF NEUROLOGY (2006)
PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases
LM Gomez et al.
GENES AND IMMUNITY (2005)
A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo
I Cantón et al.
GENES AND IMMUNITY (2005)
Early disease onset and increased risk of other autoimmune diseases in familial generalized vitiligo
G Laberge et al.
PIGMENT CELL RESEARCH (2005)
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations
M van Oene et al.
ARTHRITIS AND RHEUMATISM (2005)
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection:: the PTPN22 620W allele associates with multiple autoimmune phenotypes
LA Criswell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases
A Blomhoff et al.
PIGMENT CELL RESEARCH (2005)
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE
C Kyogoku et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis
AB Begovich et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease
MR Velaga et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2004)
Epidemiology of vitiligo and associated autoimmune diseases in caucasian probands and their families
A Alkhateeb et al.
PIGMENT CELL RESEARCH (2003)
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