المؤلفون: Strunz T., Lauwen S., Kiel C., Fritsche L.G., Igl W., Bailey J.N.C., Grassmann F., Sengupta S., Bragg-Gresham J.L., Burdon K.P., Hebbring S.J., Wen C., Gorski M., Kim I.K., Cho D., Zack D., Souied E., Scholl H.P.N., Bala E., Lee K.E., Hunter D.J., Sardell R.J., Mitchell P., Merriam J.E., Cipriani V., Hoffman J.D., Schick T., Lechanteur Y.T.E., Guymer R.H., Johnson M.P., Jiang Y., Stanton C.M., Buitendijk G.H.S., Zhan X., Kwong A.M., Boleda A., Brooks M., Gieser L., Ratnapriya R., Branham K.E., Foerster J.R., Heckenlively J.R., Othman M.I., Vote B.J., Liang H.H., Souzeau E., McAllister I.L., Isaacs T., Hall J., Lake S., Mackey D.A., Constable I.J., Craig J.E., Kitchner T.E., Yang Z., Su Z., Luo H., Chen D., Ouyang H., Flagg K., Lin D., Mao G., Ferreyra H., Stark K., Strachwitz C.N., Wolf A., Brandl C., Rudolph G., Olden M., Morrison M.A., Morgan D.J., Schu M., Ahn J., Silvestri G., Tsironi E.E., Park K.H., Farrer L.A., Orlin A., Brucker A., Li M., Curcio C., Mohand-Saïd S., Sahel J.-A., Audo I., Benchaboune M., Cree A.J., Rennie C.A., Goverdhan S.V., Grunin M., Hagbi-Levi S., Campochiaro P., Katsanis N., Holz F.G., Blond F., Blanché H., Deleuze J.-F., Igo R.P., Jr., Truitt B., Peachey N.S., Meuer S.M., Myers C.E., Moore E.L., Klein R., Hauser M.A., Postel E.A., Courtenay M.D., Schwartz S.G., Kovach J.L., Scott W.K., Liew G., Tfan A.G., Gopinath B., Merriam J.C., Smith R.T., Khan J.C., Shahid H., Moore A.T., McGrath J.A., Laux R., Brantley M.A., Agarwal A., Ersoy L., Caramoy A., Langmann T., Saksens N.T.M., Jong E.K., Hoyng C.B., Cain M.S., Richardson A.J., Martin T.M., Blangero J., Weeks D.E., Dhillon B., Duijn C.M., Doheny K.F., Romm J., Klaver C.C.W., Hayward C., Gorin M.B., Klein M.L., Baird P.N., Hollander A.I., Fauser S., Yates J.R.W., Allikmets R., Wang J.J., Schaumberg D.A., Klein B.E.K., Hagstrom S.A., Chowers I., Lotery A.J., Léveillard T., Zhang K., Brilliant M.H., Hewitt A.W., Swaroop A., Chew E.Y., Pericak-Vance M.A., DeAngelis M., Stambolian D., Haines J.L., Iyengar S.K., Weber B.H.F., Abecasis G.R., Heid I.M., Hollander A., International AMD Genomics Consortium (IAMDGC)

المصدر: Scientific Reports ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85078851693&doi=10.1038%2fs41598-020-58510-9&partnerID=40&md5=1f299c56be2191781072cefdb9d2bafbTest

مصطلحات موضوعية: transcriptome, gene, gene expression profiling, gene regulatory network, genetic predisposition, genetics, genome-wide association study, human, macular degeneration, Gene Regulatory Networks, Genes, Genetic Predisposition to Disease, Humans, Nature Research

العلاقة: http://hdl.handle.net/11615/79512Test

الإتاحة: https://doi.org/10.1038/s41598-020-58510-9Test
http://hdl.handle.net/11615/79512Test

المؤلفون: Stocker A.J., Siddle D.R., Warrington E.M., Mariotti G., Silvestri D., Zeqai A., Tortora P., Argyriou A., De Vicente J., Abello R., Mercolino M.

المصدر: IET Conference Publications ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85047313321&partnerID=40&md5=21ad288059699f885bfbd1f9b910e28dTest

مصطلحات موضوعية: Engineering, Channel model, Propagation paths, Radio channels, Signal amplitude, Solar corona, Sun earth probes, X bands, Solar radiation, Institution of Engineering and Technology

العلاقة: http://hdl.handle.net/11615/79485Test

الإتاحة: http://hdl.handle.net/11615/79485Test

المؤلفون: Stocker A.J., Siddle D.R., Warrington E.M., Mariotti G., Silvestri D., Zeqaj A., Tortora P., Argyriou A., De Vicente J., Abello R., Mercolino M.

المصدر: Radio Science ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85052953702&doi=10.1029%2f2018RS006578&partnerID=40&md5=a90291d1170e0220a38452defce61f38Test

مصطلحات موضوعية: Electrical engineering, Radio, Channel model, In-phase, Propagation paths, Radio channel modeling, Signal amplitude, Solar corona, Sun earth probes, X bands, Solar radiation, Blackwell Publishing Ltd

العلاقة: http://hdl.handle.net/11615/79486Test

الإتاحة: https://doi.org/10.1029/2018RS006578Test
http://hdl.handle.net/11615/79486Test

المؤلفون: Jacobs B.C., van den Berg B., Verboon C., Chavada G., Cornblath D.R., Gorson K.C., Harbo T., Hartung H.-P., Hughes R.A.C., Kusunoki S., van Doorn P.A., Willison H.J., the IGOS Consortium, Jacobs B.C., Hartung H.P., van Woerkom M., Roodbol J., Reisin R.C., Reddel S.W., Islam Z., Islam B., Mohammad Q.D., van den Bergh P., Feasby T.E., Wang Y.Z., Péréon Y., Lehmann H.C., Dardiotis E., Nobile-Orazio E., Shahrizaila N., Bateman K., Illa I., Querol L.A., Hsieh S.T., Davidson A., Addington J.M., Ajroud-Driss S., Andersen H., Antonini G., Attarian S., Badrising U., Barroso F.A., Benedetti L., Beronio A., Bianco M., Binda D., Briani C., Bürmann J., Bella I.R., Bertorini T.E., Bhavaraju-Sanka R., Brannagan T.H., Busby M., Butterworth S., Campagnolo M., Casasnovas C., Cavaletti G., Chao C.S., Chen S., Chetty S., Claeys K.G., Cohen J.A., Conti M.E., Cosgrove J.S., Dalakas M.C., Dimachkie M.M., Dillmann U., Domínguez González C., Doppler K., Dornonville de la Cour C., Echaniz-Laguna A., Eftimov F., Faber C.G., Fazio R., Fokke C., Fujioka T., Fulgenzi E.A., Galassi G., Garcia T., Garnero M., Garssen M.P.J., Gijsbers C.J., Gilchrist J.M., Gilhuis H.J., Goldstein J.M., Goyal N., Granit V., Grapperon A., Gutiérrez Gutiérrez G., Gutmann L., Hadden R.D.M., Holbech J.V., Holt J.K.L., Homedes Pedret C., Htut M., Jellema K., Jericó Pascual I., Kaida K., Karafiath S., Katzberg H.D., Kiers L., Kieseier B.C., Kimpinski K., Kleyweg R.P., Kokubun N., Kolb N.A., Kuitwaard K., Kuwabara S., Kwan J.Y., Ladha S.S., Landschoff Lassen L., Lawson V., Ledingham D., Léon Cejas L., Luciano C.A., Lucy S.T., Lunn M.P.T., Magot A., Manji H., Marchesoni C., Marfia G.A.M., Márquez Infante C., Martinez Hernandez E., Mataluni G., Mattiazi M., McDermott C.J., Meekins G.D., Miller J., Monges M.S., Montero M.C.J., Morís de la Tassa G., Nascimbene C., Neumann C., Nowak R.J., Orizaola Balaguer P., Osei-Bonsu M., Pan E.B.L., Pardo Fernandez J., Pasnoor M., Pulley M.T., Rajabally Y.A., Rinaldi S., Ritter C., Roberts R.C., Rojas-Marcos I., Rudnicki S.A., Sachs G.M., Samijn J.P.A., Santoro L., Saperstein D.S., Savransky A., Schneider H., Schenone A., Sedano Tous M.J., Sekiguchi Y., Sheikh K.A., Silvestri N.J., Sindrup S.H., Sommer C.L., Stein B., Stino A.M., Spyropoulos A., Srinivasan J., Suzuki H., Taylor S.W., Tankisi H., Tigner D., Twydell P.T., Valzania F., van Damme P., van der Kooi A.J., van Dijk G.W., van der Ree T., van Koningsveld R., Varrato J.D., Vermeij F.H., Verschuuren J.J.G.M., Visser L.H., Vytopil M.V., Waheed W., Wilken M., Wilkerson C., Wirtz P.W., Yamagishi Y., Yiu E.M., Zhou L., Zivkovic S.

المصدر: Journal of the Peripheral Nervous System ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85020274741&doi=10.1111%2fjns.12209&partnerID=40&md5=3bcbcb1272010b750bfb9f6bf069524dTest

مصطلحات موضوعية: DNA, adult, Article, blood sampling, cerebrospinal fluid, child, clinical feature, clinical protocol, cohort analysis, demography, disease course, disease severity, electrophysiology, environmental factor, follow up, Guillain Barre syndrome, human, infection, major clinical study, observational study, outcome assessment, priority journal, prospective study, disease exacerbation, female, international cooperation, male, metabolism, pathophysiology, Cohort Studies

العلاقة: http://hdl.handle.net/11615/74071Test

الإتاحة: https://doi.org/10.1111/jns.12209Test
http://hdl.handle.net/11615/74071Test

المؤلفون: Fritsche L.G., Igl W., Bailey J.N.C., Grassmann F., Sengupta S., Bragg-Gresham J.L., Burdon K.P., Hebbring S.J., Wen C., Gorski M., Kim I.K., Cho D., Zack D., Souied E., Scholl H.P.N., Bala E., ELee K., Hunter D.J., Sardell R.J., Mitchell P., Merriam J.E., Cipriani V., Hoffman J.D., Schick T., Lechanteur Y.T.E., Guymer R.H., Johnson M.P., Jiang Y., Stanton C.M., Buitendijk G.H.S., Zhan X., Kwong A.M., Boleda A., Brooks M., Gieser L., Ratnapriya R., Branham K.E., Foerster J.R., Heckenlively J.R., Othman M.I., Vote B.J., Liang H.H., Souzeau E., McAllister I.L., Isaacs T., Hall J., Lake S., Mackey D.A., Constable I.J., Craig J.E., Kitchner T.E., Yang Z., Su Z., Luo H., Chen D., Ouyang H., Flagg K., Lin D., Mao G., Ferreyra H., Stark K., Von Strachwitz C.N., Wolf A., Brandl C., Rudolph G., Olden M., Morrison M.A., Morgan D.J., Schu M., Ahn J., Silvestri G., Tsironi E.E., Park K.H., Farrer L.A., Orlin A., Brucker A., Li M., Curcio C.A., Mohand-Sa'd S., Sahel J.-A., Audo I., Benchaboune M., Cree A.J., Rennie C.A., Goverdhan S.V., Grunin M., Hagbi-Levi S., Campochiaro P., Katsanis N., Holz F.G., Blond F., Blanché H., Deleuze J.-F., Igo R.P., Jr., Truitt B., Peachey N.S., Meuer S.M., Myers C.E., Moore E.L., Klein R., Hauser M.A., Postel E.A., Courtenay M.D., Schwartz S.G., Kovach J.L., Scott W.K., Liew G., Tan A.G., Gopinath B., Merriam J.C., Smith R.T., Khan J.C., Shahid H., Moore A.T., McGrath J.A., Laux R., Brantley M.A., Agarwal A., Ersoy L., Caramoy A., Langmann T., Saksens N.T.M., Jong E.K., Hoyng C.B., Cain M.S., Richardson A.J., Martin T.M., Blangero J., Weeks D.E., Dhillon B., Van Duijn C.M., Doheny K.F., Romm J., Klaver C.C.W., Hayward C., Gorin M.B., Klein M.L., Baird P.N., Den Hollander A.I., Fauser S., WYates J.R., Allikmets R., Wang J.J., Schaumberg D.A., Klein B.E.K., Hagstrom S.A., Chowers I., Lotery A.J., Léveillard T., Zhang K., Brilliant M.H., Hewitt A.W., Swaroop A., Chew E.Y., Pericak-Vance M.A., DeAngelis M., Stambolian D., Haines J.L., Iyengar S.K., Weber B.H.F., Abecasis G.R., Heid I.M.

المصدر: Nature Genetics ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-84981164833&doi=10.1038%2fng.3448&partnerID=40&md5=66fc1d341e310e50179402c07e0c2a01Test

مصطلحات موضوعية: gelatinase B, monocarboxylate transporter 3, age related macular degeneration, Article, controlled study, gene frequency, gene locus, genetic association, genetic susceptibility, genetic variability, genetics, genotype, heritability, human, hypothesis, priority journal, rare disease, genetic predisposition, genome-wide association study, macular degeneration, mutation, Genetic Predisposition to Disease, Humans, Nature Publishing Group

العلاقة: http://hdl.handle.net/11615/71835Test

الإتاحة: https://doi.org/10.1038/ng.3448Test
http://hdl.handle.net/11615/71835Test

المؤلفون: Ratnapriya, R., Zhan, X., Fariss, R. N., Branham, K. E., Zipprer, D., Chakarova, C. F., Sergeev, Y. V., Campos, M. M., Othman, M., Friedman, J. S., Maminishkis, A., Waseem, N. H., Brooks, M., Rajasimha, H. K., Edwards, A. O., Lotery, A., Klein, B. E., Truitt, B. J., Li, B., Schaumberg, D. A., Morgan, D. J., Morrison, M. A., Souied, E., Tsironi, E. E., Grassmann, F., Fishman, G. A., Silvestri, G., Scholl, H. P. N., Kim, I. K., Ramke, J., Tuo, J., Merriam, J. E., Merriam, J. C., Park, K. H., Olson, L. M., Farrer, L. A., Johnson, M. P., Peachey, N. S., Lathrop, M., Baron, R. V., Igo, R. P., Klein, R., Hagstrom, S. A., Kamatani, Y., Martin, T. M., Jiang, Y., Conley, Y., Sahel, J. A., Zack, D. J., Chan, C. C., Pericak-Vance, M. A., Jacobson, S. G., Gorin, M. B., Klein, M. L., Allikmets, R., Iyengar, S. K., Weber, B. H., Haines, J. L., Léveillard, T., Deangelis, M. M., Stambolian, D., Weeks, D. E., Bhattacharya, S. E., Chew, E. Y., Heckenlively, J. R., Abecasis, G. R., Swaroop, A.

المصدر: http://www.scopus.com/inward/record.url?eid=2-s2.0-84911391197&partnerID=40&md5=bff6d761c7df0727830d4d91ec1ac76aTest.

مصطلحات موضوعية: elastin, fibrillin 2, actin binding protein, fibrillin, age related macular degeneration, aged, aging, animal tissue, Article, autosomal dominant inheritance, Bruch membrane, clinical article, controlled study, exome, extracellular matrix, gene, gene expression, gene sequence, genetic variability, genotype, human, human tissue, macular degeneration, male, molecular model, nonhuman, nucleotide sequence, pedigree, phenotype, protein expression

العلاقة: 9646906; http://hdl.handle.net/11615/32604Test

الإتاحة: https://doi.org/10.1093/hmg/ddu276Test
http://hdl.handle.net/11615/32604Test

المؤلفون: Owen, L. A., Morrison, M. A., Ahn, J., Woo, S. J., Sato, H., Robinson, R., Morgan, D. J., Zacharaki, F., Simeonova, M., Uehara, H., Chakravarthy, U., Hogg, R. E., Ambati, B. K., Kotoula, M., Baehr, W., Haider, N. B., Silvestri, G., Miller, J. W., Tsironi, E. E., Farrer, L. A., Kim, I. K., Park, K. H., DeAngelis, M. M.

المصدر: ://WOS:000339485800023

مصطلحات موضوعية: age-related macular degeneration, angiogenesis, FLT1, VEGF, ENDOTHELIAL GROWTH-FACTOR, MACULAR DEGENERATION, CHOROIDAL, NEOVASCULARIZATION, OCULAR NEOVASCULARIZATION, TUMOR ANGIOGENESIS, FACTOR RECEPTOR-1, NONHUMAN PRIMATE, NR2E3 FUNCTIONS, ASSOCIATION, Ophthalmology

العلاقة: http://hdl.handle.net/11615/31517Test

الإتاحة: https://doi.org/10.1167/iovs.14-14047Test
http://hdl.handle.net/11615/31517Test

المؤلفون: Fritsche, L. G., Chen, W., Schu, M., Yaspan, B. L., Yu, Y., Thorleifsson, G., Zack, D. J., Arakawa, S., Cipriani, V., Ripke, S., Igo, R. P., Buitendijk, G. H. S., Sim, X., Weeks, D. E., Guymer, R. H., Merriam, J. E., Francis, P. J., Hannum, G., Agarwal, A., Armbrecht, A. M., Audo, I., Aung, T., Barile, G. R., Benchaboune, M., Bird, A. C., Bishop, P. N., Branham, K. E., Brooks, M., Brucker, A. J., Cade, W. H., Cain, M. S., Campochiaro, P. A., Chan, C. C., Cheng, C. Y., Chew, E. Y., Chin, K. A., Chowers, I., Clayton, D. G., Cojocaru, R., Conley, Y. P., Cornes, B. K., Daly, M. J., Dhillon, B., Edwards, A. O., Evangelou, E., Fagerness, J., Ferreyra, H. A., Friedman, J. S., Geirsdottir, A., George, R. J., Gieger, C., Gupta, N., Hagstrom, S. A., Harding, S. P., Haritoglou, C., Heckenlively, J. R., Holz, F. G., Hughes, G., Ioannidis, J. P. A., Ishibashi, T., Joseph, P., Jun, G., Kamatani, Y., Katsanis, N., N Keilhauer, C., Khan, J. C., Kim, I. K., Kiyohara, Y., Klein, B. E. K., Klein, R., Kovach, J. L., Kozak, I., Lee, C. J., Lee, K. E., Lichtner, P., Lotery, A. J., Meitinger, T., Mitchell, P., Mohand-Saïd, S., Moore, A. T., Morgan, D. J., Morrison, M. A., Myers, C. E., Naj, A. C., Nakamura, Y., Okada, Y., Orlin, A., Ortube, M. C., Othman, M. I., Pappas, C., Park, K. H., Pauer, G. J. T., Peachey, N. S., Poch, O., Priya, R. R., Reynolds, R., Richardson, A. J., Ripp, R., Rudolph, G., Ryu, E., Sahel, J. A., Schaumberg, D. A., Scholl, H. P. N., Schwartz, S. G., Scott, W. K., Shahid, H., Sigurdsson, H., Silvestri, G., Sivakumaran, T. A., Smith, R. T., Sobrin, L., Souied, E. H., Stambolian, D. E., Stefansson, H., Sturgill-Short, G. M., Takahashi, A., Tosakulwong, N., Truitt, B. J., Tsironi, E. E., Uitterlinden, A. G., Van Duijn, C. M., Vijaya, L., Vingerling, J. R., Vithana, E. N., Webster, A. R., Wichmann, H. E., Winkler, T. W., Wong, T. Y., Wright, A. F., Zelenika, D., Zhang, M., Zhao, L., Zhang, K., Klein, M. L., Hageman, G. S., Lathrop, G. M., Stefansson, K., Allikmets, R., Baird, P. N., Gorin, M. B., Wang, J. J., Klaver, C. C. W., Seddon, J. M., Pericak-Vance, M. A., Iyengar, S. K., Yates, J. R. W., Swaroop, A., Weber, B. H. F., Kubo, M., Deangelis, M. M., Léveillard, T., Thorsteinsdottir, U., Haines, J. L., Farrer, L. A., Heid, I. M., Abecasis, G. R.

المصدر: Nature Genetics ; http://www.scopus.com/inward/record.url?eid=2-s2.0-84875706378&partnerID=40&md5=e0203b979643081dc774c59da5b5aa21Test

مصطلحات موضوعية: monocarboxylate transporter 3, transforming growth factor beta1, adolescent, adult, aged, angiogenesis, article, complement system, controlled study, copy number variation, extracellular matrix, gene cluster, gene control, gene expression, gene linkage disequilibrium, gene locus, genetic association, genetic risk, geographic atrophy, human, lipid metabolism, major clinical study, meta analysis (topic), priority journal, retina macula age related degeneration, Biological Markers, Case-Control Studies, Female, Genetic Loci, Genetic Predisposition to Disease

العلاقة: http://hdl.handle.net/11615/27576Test

الإتاحة: https://doi.org/10.1038/ng.2578Test
http://hdl.handle.net/11615/27576Test

المؤلفون: Morrison, M. A., Silveira, A. C., Huynh, N., Jun, G., Smith, S. E., Zacharaki, F., Sato, H., Loomis, S., Andreoli, M. T., Adams, S. M., Radeke, M. J., Jelcick, A. S., Yuan, Y., Tsiloulis, A. N., Chatzoulis, D. Z., Silvestri, G., Kotoula, M. G., Tsironi, E. E., Hollis, B. W., Chen, R., Haider, N. B., Miller, J. W., Farrer, L. A., Hageman, G. S., Kim, I. K., Schaumberg, D. A., DeAngelis, M. M.

المصدر: http://www.scopus.com/inward/record.url?eid=2-s2.0-84860642194&partnerID=40&md5=da78e08a42baae25eed2327c9f34fb68Test.

مصطلحات موضوعية: Age-related macular degeneration, Vitamin D, calcitriol receptor, complement factor H, adult, aged, article, case control study, comparative study, epidemiology, female, follow up, genetic polymorphism, genetic predisposition, genetics, genotype, Greece, human, male, metabolism, middle aged, pathology, prognosis, prospective study, retina macula degeneration, risk factor, sibling, systems biology, vitamin D deficiency, 80 and over

العلاقة: http://hdl.handle.net/11615/31135Test

الإتاحة: https://doi.org/10.1186/1479-7364-5-6-538Test
http://hdl.handle.net/11615/31135Test