The genetics of psoriasis, psoriatic arthritis and atopic dermatitisBOWCOCK, Anne M; COOKSON, William O. C. M.Human molecular genetics (Print). 2004, Vol 13, pp R43-R55, issn 0964-6906, NS1Article

Psoriasis genetics: breaking the barrierROBERSON, Elisha D. O; BOWCOCK, Anne M.Trends in genetics (Regular ed.). 2010, Vol 26, Num 9, pp 415-423, issn 0168-9525, 9 p.Article

Genetics of psoriasis: The potential impact on new therapiesBOWCOCK, Anne M; BARKER, Jonathan N.Journal of the American Academy of Dermatology. 2003, Vol 49, Num 2, pp S51-S56, issn 0190-9622, SUPAArticle

Multisystem dystrophy syndrome due to Novel missense Mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C geneGARG, Abhimanyu; SPECKMAN, Rebecca A; BOWCOCK, Anne M et al.The American journal of medicine. 2002, Vol 112, Num 7, pp 549-555, issn 0002-9343Article

Pathogenesis and therapy of psoriasis : Skin biologyLOWES, Michelle A; BOWCOCK, Anne M; KRUEGER, James G et al.Nature (London). 2007, Vol 445, Num 7130, pp 866-873, issn 0028-0836, 8 p.Article

Phenotypic heterogeneity in patients with familial partial lipodystrophy (Dunnigan variety) related to the site of missense mutations in lamin A/C geneGARG, Abhimanyu; VINAITHEERTHAN, Maheswari; WEATHERALL, Paul T et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 1, pp 59-65, issn 0021-972XArticle

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus : Genetics in OrthopaedicsGURNETT, Christina A; KEPPEL, Cassie; BICK, Jennifer et al.Clinical orthopaedics and related research. 2007, Num 462, pp 27-31, issn 0009-921X, 5 p.Article

Localization of A gene for familial recurrent arthritisWISE, Carol A; BENNETT, Lynda B; PASCUAL, Virginia et al.Arthritis and rheumatism. 2000, Vol 43, Num 9, pp 2041-2045, issn 0004-3591Article

A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parentsGORDON, Derek; HAYNES, Chad; JOHNNIDIS, Christopher et al.European journal of human genetics. 2004, Vol 12, Num 9, pp 752-761, issn 1018-4813, 10 p.Article

Loss of heterozygosity of chromosome 3 detected with single nucleotide polymorphisms is superior to monosomy 3 for predicting metastasis in uveal melanomaONKEN, Michael D; WORLEY, Lori A; PERSON, Erica et al.Clinical cancer research. 2007, Vol 13, Num 10, pp 2923-2927, issn 1078-0432, 5 p.Article

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasisHELMS, Cynthia; CAO, Li; KWOK, Pui-Yan et al.Nature genetics. 2003, Vol 35, Num 4, pp 349-356, issn 1061-4036, 8 p.Article

Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at RELELLINGHAUS, Eva; STUART, Philip E; ONKEN, Anna T et al.Journal of investigative dermatology. 2012, Vol 132, Num 4, pp 1133-1140, issn 0022-202X, 8 p.Article

Asymmetric Lower-Limb Malformations in Individuals with Homeobox PITX1 Gene MutationGURNETT, Christina A; ALAEE, Farhang; KRUSE, Lisa M et al.American journal of human genetics. 2008, Vol 83, Num 5, pp 616-622, issn 0002-9297, 7 p.Article

SNTG1, the gene encoding γ1-syntrophin: a candidate gene for idiopathic scoliosisBASHIARDES, Stavros; VEILE, Rose; ALLEN, Missy et al.Human genetics. 2004, Vol 115, Num 1, pp 81-89, issn 0340-6717, 9 p.Article

Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibilitySPECKMAN, Rebecca A; DAW, Jil A; HELMS, Cynthia et al.Human genetics. 2003, Vol 112, Num 1, pp 34-41, issn 0340-6717, 8 p.Article

A Subset of Methylated CpG Sites Differentiate Psoriatic from Normal SkinROBERSON, Elisha D. O; YING LIU; RYAN, Caitriona et al.Journal of investigative dermatology. 2012, Vol 132, Num 3, pp 583-592, issn 0022-202X, 10 p., 1Article

Further Genetic Evidence for Three Psoriasis-Risk Genes : ADAM33, CDKAL1, and PTPN22YONGHONG LI; LIAO, Wilson; BOWCOCK, Anne M et al.Journal of investigative dermatology. 2009, Vol 129, Num 3, pp 629-634, issn 0022-202X, 6 p.Article

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3GURNETT, Christina A; DOBBS, Matthew B; NORDSIECK, Eric J et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 16, pp 1744-1748, issn 1552-4825, 5 p.Article

PSORS2 Is Due to Mutations in CARD 14JORDAN, Catherine T; LI CAO; YONGQING CHEN et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 784-795, issn 0002-9297, 12 p.Article

Protective Effect of Human Endogenous Retrovirus K dUTPase Variants on Psoriasis SusceptibilityLAI, Olivia Y; HAOYAN CHEN; FOERSTER, John et al.Journal of investigative dermatology. 2012, Vol 132, Num 7, pp 1833-1840, issn 0022-202X, 8 p.Article

Frequent Mutation of BAP1 in Metastasizing Uveal MelanomasHARBOUR, J. William; ONKEN, Michael D; ROBERSON, Elisha D. O et al.Science (Washington, D.C.). 2010, Vol 330, Num 6009, pp 1410-1413, issn 0036-8075, 4 p.Article

Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactylyGURNETT, Christina A; BOWCOCK, Anne M; DIETZ, Frederick R et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 1, pp 27-32, issn 1552-4825, 6 p.Article

Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitisMORAR, Nilesh; BOWCOCK, Anne M; HARPER, John I et al.Journal of investigative dermatology. 2006, Vol 126, Num 3, pp 603-606, issn 0022-202X, 4 p.Article

Risk factors for diabetes in familial partial lipodystrophy, Dunnigan varietyHAQUE, Wasim A; ORAL, Elif Arioglu; DIETZ, Kelly et al.Diabetes care. 2003, Vol 26, Num 5, pp 1350-1355, issn 0149-5992, 6 p.Article

Insights into psoriasis and other inflammatory diseases from large-scale gene expression studiesBOWCOCK, Anne M; SHANNON, William; FENGHE DU et al.Human molecular genetics (Print). 2001, Vol 10, Num 17, pp 1793-1805, issn 0964-6906Article