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Page 1
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
Carlton VE, Hu X, Chokkalingam AP, Schrodi SJ, Brandon R, Alexander HC, Chang M, Catanese JJ, Leong DU, Ardlie KG, Kastner DL, Seldin MF, Criswell LA, Gregersen PK, Beasley E, Thomson G, Amos CI, Begovich AB. Carlton VE, et al. Am J Hum Genet. 2005 Oct;77(4):567-81. doi: 10.1086/468189. Epub 2005 Aug 10. Am J Hum Genet. 2005. PMID: 16175503 Free PMC article.
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.
Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, Chokkalingam AP, Alexander HC, Ardlie KG, Huang Q, Smith AM, Spoerke JM, Conn MT, Chang M, Chang SY, Saiki RK, Catanese JJ, Leong DU, Garcia VE, McAllister LB, Jeffery DA, Lee AT, Batliwalla F, Remmers E, Criswell LA, Seldin MF, Kastner DL, Amos CI, Sninsky JJ, Gregersen PK. Begovich AB, et al. Among authors: carlton ve. Am J Hum Genet. 2004 Aug;75(2):330-7. doi: 10.1086/422827. Epub 2004 Jun 18. Am J Hum Genet. 2004. PMID: 15208781 Free PMC article.
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.
Kyogoku C, Langefeld CD, Ortmann WA, Lee A, Selby S, Carlton VE, Chang M, Ramos P, Baechler EC, Batliwalla FM, Novitzke J, Williams AH, Gillett C, Rodine P, Graham RR, Ardlie KG, Gaffney PM, Moser KL, Petri M, Begovich AB, Gregersen PK, Behrens TW. Kyogoku C, et al. Among authors: carlton ve. Am J Hum Genet. 2004 Sep;75(3):504-7. doi: 10.1086/423790. Epub 2004 Jul 23. Am J Hum Genet. 2004. PMID: 15273934 Free PMC article.
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
Criswell LA, Pfeiffer KA, Lum RF, Gonzales B, Novitzke J, Kern M, Moser KL, Begovich AB, Carlton VE, Li W, Lee AT, Ortmann W, Behrens TW, Gregersen PK. Criswell LA, et al. Among authors: carlton ve. Am J Hum Genet. 2005 Apr;76(4):561-71. doi: 10.1086/429096. Epub 2005 Feb 17. Am J Hum Genet. 2005. PMID: 15719322 Free PMC article.
Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC.
Bull LN, Juijn JA, Liao M, van Eijk MJ, Sinke RJ, Stricker NL, DeYoung JA, Carlton VE, Baharloo S, Klomp LW, Abukawa D, Barton DE, Bass NM, Bourke B, Drumm B, Jankowska I, Lovisetto P, McQuaid S, Pawlowska J, Tazawa Y, Villa E, Tygstrup N, Berger R, Knisely AS, Freimer NB, et al. Bull LN, et al. Among authors: carlton ve. Hum Genet. 1999 Mar;104(3):241-8. doi: 10.1007/pl00008714. Hum Genet. 1999. PMID: 10323248
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64.
Sinke RJ, Carlton VE, Juijn JA, Delhaas T, Bull L, van Berge Henegouwen GP, van Hattum J, Keller KM, Sinaasappel M, Bijleveld CM, Knol IE, Ploos van Amstel HK, Pearson PL, Berger R, Freimer NB, Houwen RH. Sinke RJ, et al. Among authors: carlton ve. Hum Genet. 1997 Sep;100(3-4):382-7. doi: 10.1007/s004390050520. Hum Genet. 1997. PMID: 9272159 Free article.
High-throughput, high-accuracy array-based resequencing.
Zheng J, Moorhead M, Weng L, Siddiqui F, Carlton VE, Ireland JS, Lee L, Peterson J, Wilkins J, Lin S, Kan Z, Seshagiri S, Davis RW, Faham M. Zheng J, et al. Among authors: carlton ve. Proc Natl Acad Sci U S A. 2009 Apr 21;106(16):6712-7. doi: 10.1073/pnas.0901902106. Epub 2009 Apr 2. Proc Natl Acad Sci U S A. 2009. PMID: 19342489 Free PMC article.
39 results