1 - 25 of 49 results for author:"Kwok P.-Y." in Literature citations
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| Association analysis identifies ZNF750 regulatory variants in psoriasis. Birnbaum R.Y., Hayashi G., Cohen I., Poon A., Chen H., Lam E.T., Kwok P.Y., Birk O.S., Liao W. BMC Med. Genet. 12:167-167(2011) · Mapped (2) |
| Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma. Wang N.J., Sanborn Z., Arnett K.L., Bayston L.J., Liao W., Proby C.M., Leigh I.M., Collisson E.A., Gordon P.B., Jakkula L. et al. Proc. Natl. Acad. Sci. U.S.A. 108:17761-17766(2011) · Mapped (9) |
| Replication and extension of association between common genetic variants in SIM1 and human adiposity. Swarbrick M.M., Evans D.S., Valle M.I., Favre H., Wu S.H., Njajou O.T., Li R., Zmuda J.M., Miljkovic I., Harris T.B. et al. Obesity (Silver Spring) 19:2394-2403(2011) · Mapped (4) |
| Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. Slavotinek A.M., Baranzini S.E., Schanze D., Labelle-Dumais C., Short K.M., Chao R., Yahyavi M., Bijlsma E.K., Chu C., Musone S. et al. J. Med. Genet. 48:375-382(2011) · UniProtKB (1) · Mapped (1) |
| Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases. Musone S.L., Taylor K.E., Nititham J., Chu C., Poon A., Liao W., Lam E.T., Ma A., Kwok P.Y., Criswell L.A. Genes Immun. 12:176-182(2011) · Mapped (18) |
| Common variants in P2RY11 are associated with narcolepsy. Kornum B.R., Kawashima M., Faraco J., Lin L., Rico T.J., Hesselson S., Axtell R.C., Kuipers H., Weiner K., Hamacher A. et al. Nat. Genet. 43:66-71(2011) · Mapped (1) |
| Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. Riveira-Munoz E., He S.M., Escaramis G., Stuart P.E., Huffmeier U., Lee C., Kirby B., Oka A., Giardina E., Liao W. et al. J. Invest. Dermatol. 131:1105-1109(2011) · Mapped (278) |
| Carriers of rare missense variants in IFIH1 are protected from psoriasis. Li Y., Liao W., Cargill M., Chang M., Matsunami N., Feng B.J., Poon A., Callis-Duffin K.P., Catanese J.J., Bowcock A.M. et al. J. Invest. Dermatol. 130:2768-2772(2010) · Mapped (4) |
| The DNA damage-binding protein XPC is a frequent target for inactivation in squamous cell carcinomas. de Feraudy S., Ridd K., Richards L.M., Kwok P.Y., Revet I., Oh D., Feeney L., Cleaver J.E. Am. J. Pathol. 177:555-562(2010) · Mapped (12) |
| A male with unilateral microphthalmia reveals a role for TMX3 in eye development. Chao R., Nevin L., Agarwal P., Riemer J., Bai X., Delaney A., Akana M., JimenezLopez N., Bardakjian T., Schneider A. et al. PLoS ONE 5:e10565-e10565(2010) · Mapped (15) |
| Glucocorticoid receptor gene, low-grade inflammation, and heart failure: the Heart and Soul study. Otte C., Wust S., Zhao S., Pawlikowska L., Kwok P.Y., Whooley M.A. J. Clin. Endocrinol. Metab. 95:2885-2891(2010) · Mapped (12) |
| EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Weinsheimer S., Kim H., Pawlikowska L., Chen Y., Lawton M.T., Sidney S., Kwok P.Y., McCulloch C.E., Young W.L. Circ Cardiovasc Genet 2:476-482(2009) · Mapped (9) |
| Reduced expression of integrin alphavbeta8 is associated with brain arteriovenous malformation pathogenesis. Su H., Kim H., Pawlikowska L., Kitamura H., Shen F., Cambier S., Markovics J., Lawton M.T., Sidney S., Bollen A.W. et al. Am. J. Pathol. 176:1018-1027(2010) · Mapped (15) |
| Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease. Tseng Z.H., Vittinghoff E., Musone S.L., Lin F., Whiteman D., Pawlikowska L., Kwok P.Y., Olgin J.E., Aouizerat B.E. Heart Rhythm 6:1745-1750(2009) · Mapped (19) |
| Glucocorticoid receptor gene and depression in patients with coronary heart disease: the Heart and Soul Study-2009 Curt Richter Award Winner. Otte C., Wust S., Zhao S., Pawlikowska L., Kwok P.Y., Whooley M.A. Psychoneuroendocrinology 34:1574-1581(2009) · Mapped (12) |
| Human subjects are protected from mast cell tryptase deficiency despite frequent inheritance of loss-of-function mutations. Trivedi N.N., Tamraz B., Chu C., Kwok P.Y., Caughey G.H. J. Allergy Clin. Immunol. 124:1099-1105(2009) · UniProtKB (2) · Mapped (7) |
| Identification and characterization of novel polymorphisms in the basal promoter of the human transporter, MATE1. Ha Choi J., Wah Yee S., Kim M.J., Nguyen L., Ho Lee J., Kang J.O., Hesselson S., Castro R.A., Stryke D., Johns S.J. et al. Pharmacogenet. Genomics 19:770-780(2009) · Mapped (6) |
| Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Nair R.P., Duffin K.C., Helms C., Ding J., Stuart P.E., Goldgar D., Gudjonsson J.E., Li Y., Tejasvi T., Feng B.J. et al. Nat. Genet. 41:199-204(2009) · Mapped (370) |
| Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. de Cid R., Riveira-Munoz E., Zeeuwen P.L., Robarge J., Liao W., Dannhauser E.N., Giardina E., Stuart P.E., Nair R., Helms C. et al. Nat. Genet. 41:211-215(2009) · Mapped (278) |
| Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus. Musone S.L., Taylor K.E., Lu T.T., Nititham J., Ferreira R.C., Ortmann W., Shifrin N., Petri M.A., Kamboh M.I., Manzi S. et al. Nat. Genet. 40:1062-1064(2008) · Mapped (18) |
| Functional genetic variation in the basal promoter of the organic cation/carnitine transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5). Tahara H., Yee S.W., Urban T.J., Hesselson S., Castro R.A., Kawamoto M., Stryke D., Johns S.J., Ferrin T.E., Kwok P.Y. et al. J. Pharmacol. Exp. Ther. 329:262-271(2009) · Mapped (3) |
| Identification and characterization of proximal promoter polymorphisms in the human concentrative nucleoside transporter 2 (SLC28A2). Yee S.W., Shima J.E., Hesselson S., Nguyen L., De Val S., Lafond R.J., Kawamoto M., Johns S.J., Stryke D., Kwok P.Y. et al. J. Pharmacol. Exp. Ther. 328:699-707(2009) · Mapped (3) |
| Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation. Kim H., Hysi P.G., Pawlikowska L., Poon A., Burchard E.G., Zaroff J.G., Sidney S., Ko N.U., Achrol A.S., Lawton M.T. et al. Cerebrovasc. Dis. 27:176-182(2009) · Mapped (3) |
| Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships. Bodian D.L., Chan T.F., Poon A., Schwarze U., Yang K., Byers P.H., Kwok P.Y., Klein T.E. Hum. Mol. Genet. 18:463-471(2009) · UniProtKB (2) · Mapped (21) |
| Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. Li Y., Liao W., Chang M., Schrodi S.J., Bui N., Catanese J.J., Poon A., Matsunami N., Callis-Duffin K.P., Leppert M.F. et al. J. Invest. Dermatol. 129:629-634(2009) · Mapped (21) |