Zobrazeno 1 - 10
of 332
pro vyhledávání: '"Jonasson, F."'
Autor:
Jonasson, F.1 fridbert@landspitali.is, Damji, K.F.2, Arnarsson, A.1, Sverrisson, T.1, Wang, L.2, Sasaki, H.3, Sasaki, K.3
Publikováno v:
Eye. Aug2003, Vol. 17 Issue 6, p747. 7p.
Autor:
Jonasson, F.
Publikováno v:
The British Medical Journal, 1977 Apr 01. 1(6065), 881-881.
Externí odkaz:
https://www.jstor.org/stable/20413901
Akademický článek
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Autor:
Jonasson, F, Fisher, D, Eiriksdottir, G, Sigurdsson, S, Klein, R, Loner, L, Harris, T, Gudnason, V, Cotch, MF
Publikováno v:
VI. International Symposium on AMD-Age-Related Macular Degeneration-Emerging Concepts-Exploring known and Identifying new Pathways; 20150911-20150912; Baden-Baden; DOC15amd09 /20151001/
Background: The Age, Gene/Environment Susceptibility Reykjavik Study includes a random population sample including persons 67 years and older at baseline, mean age 76 years. This is an older cohort than in most studies and therefore higher numbers of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf05128a5182880bbd69d8ec0a951442
Autor:
Ikram MK, Sim X, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, Rivadeneira F, Hofman A, de Jong PT, van Duijn CM, Kao L, Cheng CY, Smith AV, Glazer NL, Lumley T, McKnight B, Psaty BM, Jonasson F, Eiriksdottir G, Aspelund T, Newton Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L, Najjar S, Zhao JH, Heath SC, Eyheramendy S, Wallace C, Chambers JC, Khaw KT, Polidoro S, Grobbee DE, Onland Moret NC, Allione A, Di Gregorio A, Guarrera S, Ricceri F, Romanazzi V, Sacerdote C, Vineis P, Barroso I, O'Reilly PF, Peltonen L, Pouta A, de Jong PE, Snieder P, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger D, Scuteri A, Galan P, Gut IV, Hercberg S, van der Schouw YT, Numans ME, Matullo G, Navis G, Berglund G, Bandinelli S, Ferrucci L, Watkins H, Tuomilehto J, Altshuler D, Wareham NJ, Uda M, Jarvelin MR, Mooser V, Melander O, Loos RFJ, Elliott P, Abecasis GR, Caulfield M, Munroe PB, Harris TB, Launer LJ, Taylor KD, Li X, Iyengar SK, Xi Q, Sivakumaran TA, Mackey DA, Macgregor S, Martin NG, Young TL, Bis JC, Wiggins KL, Heckbert SR, Hammond CJ, Andrew T, Fahy S, Attia J, Holliday EG, Scott RJ, Islam FM, Rotter JI, McAuley AK, Boerwinkle E, Tai ES, Gudnason V, Siscovick DS, Vingerling JR, Wong TY, PANICO, SALVATORE
Publikováno v:
PLoS Genetics (print), 6(10). Public Library of Science
PLOS Genetics, 6(10). Public Library of Science
PLoS genetics, 6(10). Public Library of Science
PLoS Genetics
PLoS Genetics, Vol 6, Iss 10, p e1001184 (2010)
PLoS Genet. 6:e1001184 (2010)
PLOS Genetics, 6(10). Public Library of Science
PLoS genetics, 6(10). Public Library of Science
PLoS Genetics
PLoS Genetics, Vol 6, Iss 10, p e1001184 (2010)
PLoS Genet. 6:e1001184 (2010)
There is increasing evidence that the microcirculation plays an important role in the pathogenesis of cardiovascular diseases. Changes in retinal vascular caliber reflect early microvascular disease and predict incident cardiovascular events. We perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7358a58ef20d2f442c9d2f1082f2f0aa
http://hdl.handle.net/10722/183600
http://hdl.handle.net/10722/183600
Autor:
Springelkamp, H, Höhn, R, Mishra, A, Hysi, PG, Khor, CC, Loomis, SJ, Bailey, JNC, Gibson, J, Thorleifsson, G, Janssen, SF, Luo, X, Ramdas, WD, Vithana, E, Nongpiur, ME, Montgomery, GW, Xu, L, Mountain, JE, Gharahkhani, P, Lu, Y, Amin, N, Karssen, LC, Sim, KS, Van Leeuwen, EM, Iglesias, AI, Verhoeven, VJM, Hauser, MA, Loon, SC, Despriet, DDG, Nag, A, Venturini, C, Sanfilippo, PG, Schillert, A, Kang, JH, Landers, J, Jonasson, F, Cree, AJ, Van Koolwijk, LME, Rivadeneira, F, Souzeau, E, Jonsson, V, Menon, G, Mitchell, P, Wang, JJ, Rochtchina, E, Attia, J, Scott, R, Holliday, EG, Baird, PN, Xie, J, Inouye, M, Viswanathan, A, Sim, X, Weinreb, RN, De Jong, PTVM, Oostra, BA, Uitterlinden, AG, Hofman, A, Ennis, S, Thorsteinsdottir, U, Burdon, KP, Allingham, RR, Brilliant, MH, Budenz, DL, Christen, WG, Fingert, J, Friedman, DS, Gaasterland, D, Gaasterland, T, Haines, JL, Kraft, P, Lee, RK, Lichter, PR, Liu, Y
Publikováno v:
Springelkamp, H; Höhn, R; Mishra, A; Hysi, PG; Khor, CC; Loomis, SJ; et al.(2014). Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications, 5. doi: 10.1038/ncomms5883. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/8tq3b2r0
© 2014 Macmillan Publishers Limited. All rights reserved. Glaucoma is characterized by irreversible optic nerve degeneration and is the most frequent cause of irreversible blindness worldwide. Here, the International Glaucoma Genetics Consortium con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::432a7734471df3879f32c6d2d291d0b9
http://www.escholarship.org/uc/item/8tq3b2r0
http://www.escholarship.org/uc/item/8tq3b2r0
Autor:
Seielstad, Mark, Jensen, RA, Sim, X, Li, X, Cotch, MF, Ikram, MK, Holliday, EG, Eiriksdottir, G, Harris, TB, Jonasson, F, Klein, BEK
Publikováno v:
Seielstad, Mark; Jensen, RA; Sim, X; Li, X; Cotch, MF; Ikram, MK; et al.(2013). Genome-Wide Association Study of Retinopathy in Individuals without Diabetes. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/71h8p274
Background: Mild retinopathy (microaneurysms or dot-blot hemorrhages) is observed in persons without diabetes or hypertension and may reflect microvascular disease in other organs. We conducted a genome-wide association study (GWAS) of mild retinopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::2126424440700409d142f30fc1c3f14e
http://www.escholarship.org/uc/item/71h8p274
http://www.escholarship.org/uc/item/71h8p274
Autor:
Vance, J. M., Jonasson, F., Lennon, F., Sarrica, J., Damji, K. F., Stauffer, J., Pericak-Vance, M. A., Klintworth, G. K.
Autosomal recessive macular corneal dystrophy (MCD) is a heterogeneous disorder leading to visual impairment. Sixteen American and Icelandic families (11 type I and 5 type II) were analyzed for linkage, by use of 208 polymorphic microsatellite marker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3409dd21dbc32aae8c382de2c80a1c4
https://europepmc.org/articles/PMC1914688/
https://europepmc.org/articles/PMC1914688/
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.