المؤلفون: Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L.

المساهمون: DUKE-NUS MEDICAL SCHOOL

المصدر: Unpaywall 20191101

مصطلحات موضوعية: animal experiment, animal model, animal tissue, article, CDKN2BAS gene, chromosome 14q, chromosome 8q, chromosome 9p, controlled study, disease association, disease classification, DNA sequence, exfoliation syndrome, gene, gene expression profiling, gene function, gene location, gene locus, genetic association, genetic identification, genetic susceptibility, genetic variability, human, intraocular pressure, LRP12 gene, major clinical study, mouse, nerve degeneration, nonhuman, open angle glaucoma

Relation: Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L. (2012). Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genetics 8 (4) : e1002654. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1002654; https://scholarbank.nus.edu.sg/handle/10635/161641

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/161641

المؤلفون: Altshuler, D, Gibbs, R, Peltonen, L, Dermitzakis, E, Schaffner, S, Yu, F, Bonnen, P, de Bakker, P, Deloukas, P, Gabriel, S, Gwilliam, R, Hunt, S, Inouye, M, Jia, X, Palotie, A, Parkin, M, Whittaker, P, Chang, K, Hawes, A, Lewis, L, Ren, Y, Wheeler, D, Muzny, D, Barnes, C, Darvishi, K, Hurles, M, Korn, J, Kristiansson, K, Lee, C, McCarrol, SA, Nemesh, J, Keinan, A, Montgomery, S, Pollack, S, Price, A, Soranzo, N, Gonzaga-Jauregui, C, Anttila, V, Brodeur, W, Daly, M, Leslie, S, McVean, G, Moutsianas, L, Nguyen, H, Zhang, Q, Ghori, M, McGinnis, R, McLaren, W, Takeuchi, F, Grossman, SR, Shlyakhter, I, Hostetter, E, Sabeti, P, Adebamowo, C, Foster, M, Gordon, DR, Licinio, J, Manca, M, Marshall, P, Matsuda, I, Ngare, D, Wang, V, Reddy, D, Rotimi, C, Royal, C, Sharp, R, Zeng, C, Brooks, L, McEwen, J

Relation: https://ora.ox.ac.uk/objects/uuid:5c8c7a65-5fca-45db-bbcb-53ce0ebf84df; https://doi.org/10.1038/nature09298

الاتاحة: https://doi.org/10.1038/nature09298
https://ora.ox.ac.uk/objects/uuid:5c8c7a65-5fca-45db-bbcb-53ce0ebf84df

المؤلفون: De Jager, PL, Srivastava, G.P., Lunnon, Katie, Burgess, J, Schalkwyk, Leonard, Yu, L, Eaton, ML, Keenan, BT, Ernst, J, McCabe, C, Tang, A, Raj, T, Replogle, J, Brodeur, W, Gabriel, S, Chai, HS, Younkin, C, Younkin, SG, Zou, F, Szyf, M, Epstein, CB, Schneider, J., Bernstein, BE, Meissner, A, Ertekin-Taner, N, Chibnik, LB, Kellis, M, Mill, J, Bennett, DA

مصطلحات موضوعية: Adaptor Proteins, Signal Transducing, Aged, 80 and over, Alzheimer Disease, Amyloidosis, Ankyrins, Brain, Carrier Proteins, CpG Islands, DNA Methylation, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Nuclear Proteins, Protein Interaction Maps, Tumor Suppressor Proteins

Relation: http://www.ncbi.nlm.nih.gov/pubmed/25129075; R01 AG036042; R01AG036836; R01 AG17917; R01AG15819; R01 AG032990; R01 AG18023; RC2 AG036547; P30 AG10161; P50 AG016574; U01 ES017155; KL2 RR024151; AG036039; http://hdl.handle.net/10871/19711; Nature Neuroscience

الاتاحة: http://hdl.handle.net/10871/19711
https://doi.org/10.1038/nn.3786

المؤلفون: Wiggs, JL, Yaspan, BL, Hauser, MA, Kang, JH, Allingham, RR, Olson, LM, Abdrabou, W, Fan, BJ, Wang, DY, Brodeur, W, Budenz, DL, Caprioli, J, Crenshaw, A, Crooks, K, DelBono, E, Doheny, KF, Friedman, DS, Gaasterland, D, Gaasterland, T, Laurie, C, Lee, RK, Lichter, PR, Loomis, S, Liu, Y, Medeiros, FA, McCarty, C, Mirel, D, Moroi, SE, Musch, DC, Realini, A, Rozsa, FW, Schuman, JS, Scott, K, Singh, K, Stein, JD, Trager, EH, VanVeldhuisen, P, Vollrath, D, Wollstein, G, Yoneyama, S, Zhang, K, Weinreb, RN, Ernst, J, Kellis, M, Masuda, T, Zack, D, Richards, JE, Pericak-Vance, M, Pasquale, LR, Haines, JL

وصف الملف: application/pdf; text/plain

Relation: http://d-scholarship.pitt.edu/14175/1/Common_Variants_at_9p21.pdf; http://d-scholarship.pitt.edu/14175/8/licence.txt; Wiggs, JL and Yaspan, BL and Hauser, MA and Kang, JH and Allingham, RR and Olson, LM and Abdrabou, W and Fan, BJ and Wang, DY and Brodeur, W and Budenz, DL and Caprioli, J and Crenshaw, A and Crooks, K and DelBono, E and Doheny, KF and Friedman, DS and Gaasterland, D and Gaasterland, T and Laurie, C and Lee, RK and Lichter, PR and Loomis, S and Liu, Y and Medeiros, FA and McCarty, C and Mirel, D and Moroi, SE and Musch, DC and Realini, A and Rozsa, FW and Schuman, JS and Scott, K and Singh, K and Stein, JD and Trager, EH and VanVeldhuisen, P and Vollrath, D and Wollstein, G and Yoneyama, S and Zhang, K and Weinreb, RN and Ernst, J and Kellis, M and Masuda, T and Zack, D and Richards, JE and Pericak-Vance, M and Pasquale, LR and Haines, JL (2012) Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genetics, 8 (4). ISSN 1553-7390

الاتاحة: http://d-scholarship.pitt.edu/14175/
http://d-scholarship.pitt.edu/14175/1/Common_Variants_at_9p21.pdf
http://d-scholarship.pitt.edu/14175/8/licence.txt