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au.\*:("WISE, Carol A")

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Results 1 to 19 of 19

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Familial osteofibrous dysplasia : A case seriesKAROL, Lori A; BROWN, David S; WISE, Carol A et al.Journal of bone and joint surgery. American volume. 2005, Vol 87A, Num 10, pp 2297-2307, issn 0021-9355, 11 p.Article

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorderWISE, Carol A; GILLUM, Joseph D; SEIDMAN, Christine E et al.Human molecular genetics (Print). 2002, Vol 11, Num 8, pp 961-969, issn 0964-6906Article

Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNAEDERY, Patrick; MARCAILLOU, Charles; JOUK, Pierre-Simon et al.Science (Washington, D.C.). 2011, Vol 332, Num 6026, pp 240-243, issn 0036-8075, 4 p.Article

Apoptotic gene analysis in idiopathic talipes equinovarus (Clubfoot) : Genetics in OrthopaedicsESTER, Audrey R; TYERMAN, Gayle; WISE, Carol A et al.Clinical orthopaedics and related research. 2007, Num 462, pp 32-37, issn 0009-921X, 6 p.Article

Genome-Wide Association Analysis of Juvenile Idiopathic Arthritis Identifies a New Susceptibility Locus at Chromosomal Region 3q13THOMPSON, Susan D; MARION, Miranda C; HAAS, Johannes-Peter et al.Arthritis and rheumatism. 2012, Vol 64, Num 8, pp 2781-2791, issn 0004-3591, 11 p.Article

Localization of susceptibility to familial idiopathic scoliosisWISE, Carol A; BARNES, Robert; GILLUM, T. Joseph et al.Spine (Philadelphia, PA. 1976). 2000, Vol 25, Num 18, pp 2372-2380, issn 0362-2436Article

Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosisDE MUNNIK, Sonja A; BICKNELL, Louise S; HAGEN, Johanna M.van et al.European journal of human genetics. 2012, Vol 20, Num 6, pp 598-606, issn 1018-4813, 9 p.Article

Rare and Common Variants in CARD 14, Encoding an Epidermal Regulator of NF-kappaB, in PsoriasisJORDAN, Catherine T; LI CAO; OLFSON, Emily H et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 796-808, issn 0002-9297, 13 p.Article

Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathwaysNAIR, Rajan P; CALLIS DUFFIN, Kristina; RUETHER, Andreas et al.Nature genetics. 2009, Vol 41, Num 2, pp 199-204, issn 1061-4036, 6 p.Article

Mutations in the pre-replication complex cause Meier-Gorlin syndromeBICKNELL, Louise S; BONGERS, Ernie M.h F; VAN BOKHOVEN, Hans et al.Nature genetics. 2011, Vol 43, Num 4, pp 356-359, issn 1061-4036, 4 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

NAT2 variation and idiopathic talipes equinovarus (clubfoot)HECHT, Jacqueline T; ESTER, Audrey; SCOTT, Allison et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 19, pp 2285-2291, issn 1552-4825, 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

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

Hierarchy of Risk of Childhood-Onset Rheumatoid Arthritis Conferred by HLA-DRB1 Alleles Encoding the Shared EpitopePRAHALAD, Sampath; THOMPSON, Susan D; KENNEDY, Christine et al.Arthritis and rheumatism. 2012, Vol 64, Num 3, pp 925-930, issn 0004-3591, 6 p.Article

Meier―Gorlin Syndrome: Growth and Secondary Sexual Development of a Microcephalic Primordial Dwarfism DisorderDE MUNNIK, Sonja A; OTTEN, Barto J; DEAL, Cheri L et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2733-2742, issn 1552-4825, 10 p.Article

Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSHARMA, Swarkar; XIAOCHONG GAO; GURNETT, Christina A et al.Human molecular genetics (Print). 2011, Vol 20, Num 7, pp 1456-1466, issn 0964-6906, 11 p.Article

The Susceptibility Loci Juvenile Idiopathic Arthritis Shares With Other Autoimmune Diseases Extend to PTPN2, COG6, and ANGPT1THOMPSON, Susan D; SUDMAN, Marc; MUELLER, Cornelia et al.Arthritis and rheumatism. 2010, Vol 62, Num 11, pp 3265-3276, issn 0004-3591, 12 p.Article

Altered Transmission of HOX and Apoptotic SNPs Identify a Potential Common Pathway for ClubfootESTER, Audrey R; WEYMOUTH, Katelyn S; BURT, Amber et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2745-2752, issn 1552-4825, 8 p.Article

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