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Fridbert Jonasson
Fridbert Jonasson
MD, Professor of Ophthalmology, Faculty of Medicine, University of Iceland
Verified email at landspitali.is
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Cited by
Cited by
Year
Genetic determinants of hair, eye and skin pigmentation in Europeans
P Sulem, DF Gudbjartsson, SN Stacey, A Helgason, T Rafnar, ...
Nature genetics 39 (12), 1443-1452, 2007
8112007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
G Thorleifsson, KP Magnusson, P Sulem, GB Walters, DF Gudbjartsson, ...
Science 317 (5843), 1397-1400, 2007
7902007
Age, gene/environment susceptibility–Reykjavik study: multidisciplinary applied phenomics
TB Harris, LJ Launer, G Eiriksdottir, O Kjartansson, PV Jonsson, ...
American journal of epidemiology 165 (9), 1076-1087, 2007
6072007
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ...
Nature genetics 42 (10), 906-909, 2010
3972010
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155-163, 2013
3162013
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD
KP Magnusson, S Duan, H Sigurdsson, H Petursson, Z Yang, Y Zhao, ...
PLoS medicine 3 (1), e5, 2006
2882006
Central corneal thickness, radius of the corneal curvature and intraocular pressure in normal subjects using non‐contact techniques: Reykjavik Eye Study
T Eysteinsson, F Jonasson, H Sasaki, A Arnarsson, T Sverrisson, ...
Acta Ophthalmologica Scandinavica 80 (1), 11-15, 2002
2442002
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126-1130, 2014
2132014
Temporal arteritis: a 14-year epidemiological, clinical and prognostic study
F Jonasson, JF Cullen, RA Elton
Scottish Medical Journal 24 (2), 111-117, 1979
1961979
Common genetic variants associated with open-angle glaucoma
WD Ramdas, LME van Koolwijk, HG Lemij, F Pasutto, AJ Cree, ...
Human molecular genetics 20 (12), 2464-2471, 2011
1782011
Prevalence of open-angle glaucoma in Iceland: Reykjavik Eye Study
F Jonasson, KF Damji, A Arnarsson, T Sverrisson, L Wang, H Sasaki, ...
Eye 17 (6), 747-753, 2003
1752003
Pseudoexfoliation syndrome in Icelandic families
RR Allingham, M Loftsdottir, MS Gottfredsdottir, E Thorgeirsson, ...
British Journal of Ophthalmology 85 (6), 702-707, 2001
1752001
Pseudoexfoliation in the Reykjavik Eye Study: prevalence and related ophthalmological variables
A Arnarsson, KF Damji, T Sverrisson, H Sasaki, F Jonasson
Acta Ophthalmologica Scandinavica 85 (8), 822-827, 2007
1732007
On the ocular refractive components: the Reykjavik Eye Study
T Olsen, A Arnarsson, H Sasaki, K Sasaki, F Jonasson
Acta Ophthalmologica Scandinavica 85 (4), 361-366, 2007
1722007
On the ocular refractive components: the Reykjavik Eye Study
T Olsen, A Arnarsson, H Sasaki, K Sasaki, F Jonasson
Acta Ophthalmologica Scandinavica 85 (4), 361-366, 2007
1722007
Is pseudoexfoliation syndrome inherited? A review of genetic and nongenetic factors and a new observation
KF Damji, HS Bains, E Stefansson, M Loftsdottir, T Sverrisson, ...
Ophthalmic genetics 19 (4), 175-185, 1998
1601998
“With the rule” astigmatism is not the rule in the elderly: Reykjavik Eye Study: a population based study of refraction and visual acuity in citizens of Reykjavik 50 years and …
E Gudmundsdottir, F Jonasson, V Jonsson, E Stefánsson, H Sasaki, ...
Acta ophthalmologica Scandinavica 78 (6), 642-646, 2000
1592000
Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo
MK Ikram, S Xueling, RA Jensen, MF Cotch, AW Hewitt, MA Ikram, ...
PLoS genetics 6 (10), e1001184, 2010
1552010
Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo
MK Ikram, S Xueling, RA Jensen, MF Cotch, AW Hewitt, MA Ikram, ...
PLoS genetics 6 (10), e1001184, 2010
1552010
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration
H Helgason, P Sulem, MR Duvvari, H Luo, G Thorleifsson, H Stefansson, ...
Nature genetics 45 (11), 1371-1374, 2013
1472013
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