Palmi V. Jonsson
Palmi V. Jonsson
Professor
Verified email at landspitali.is
Title
Cited by
Cited by
Year
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
26442013
Variant of TREM2 associated with the risk of Alzheimer's disease
T Jonsson, H Stefansson, S Steinberg, I Jonsdottir, PV Jonsson, ...
New England Journal of Medicine 368 (2), 107-116, 2013
16502013
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429-435, 2011
15802011
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
T Jonsson, JK Atwal, S Steinberg, J Snaedal, PV Jonsson, S Bjornsson, ...
Nature 488 (7409), 96-99, 2012
15192012
Genome-wide analysis of genetic loci associated with Alzheimer disease
S Seshadri, AL Fitzpatrick, MA Ikram, AL DeStefano, V Gudnason, ...
Jama 303 (18), 1832-1840, 2010
11682010
Potentially inappropriate medication use among elderly home care patients in Europe
D Fialová, E Topinková, G Gambassi, H Finne-Soveri, PV Jónsson, ...
Jama 293 (11), 1348-1358, 2005
9272005
Causes and correlates of recurrent falls in ambulatory frail elderly
LA Lipsitz, PV Jonsson, MM Kelley, JS Koestner
Journal of gerontology 46 (4), M114-M122, 1991
5421991
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
5192007
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk
IE Jansen, JE Savage, K Watanabe, J Bryois, DM Williams, S Steinberg, ...
Nature genetics 51 (3), 404-413, 2019
4352019
Mapping of a familial essential tremor gene, FET1, to chromosome 3q13
JR Gulcher, Ţ Jónsson, A Kong, K Kristjánsson, ML Frigge, A Kárason, ...
Nature genetics 17 (1), 84-87, 1997
3341997
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
2762014
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 Med 3 (1), e5, 2005
2702005
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
S Steinberg, H Stefansson, T Jonsson, H Johannsdottir, A Ingason, ...
Nature genetics 47 (5), 445-447, 2015
2302015
International variation in the incidence of hip fractures: cross-national project on osteoporosis for the World Health Organization Program for Research on Aging
AV Schwartz, JL Kelsey, S Maggi, M Tuttleman, SC Ho, PV Jonsson, ...
Osteoporosis international 9 (3), 242-253, 1999
2301999
Cerebral microbleeds in the population based AGES-Reykjavik study: prevalence and location
S Sveinbjornsdottir, S Sigurdsson, T Aspelund, O Kjartansson, ...
Journal of Neurology, Neurosurgery & Psychiatry 79 (9), 1002-1006, 2008
2252008
Cerebral microbleeds, retinopathy, and dementia: the AGES-Reykjavik Study
C Qiu, MF Cotch, S Sigurdsson, PV Jonsson, MK Jonsdottir, ...
Neurology 75 (24), 2221-2228, 2010
2232010
Integrated health information systems based on the RAI/MDS series of instruments
JP Hirdes, BE Fries, JN Morris, K Steel, V Mor, D Frijters, S LaBine, ...
Healthcare management forum 12 (4), 30-40, 1999
2111999
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
J Deelen, M Beekman, HW Uh, L Broer, KL Ayers, Q Tan, Y Kamatani, ...
Human molecular genetics 23 (16), 4420-4432, 2014
2082014
Efforts to establish the reliability of the Resident Assessment Instrument
A Sgadari, JN Morris, BE Fries, G Ljunggren, PV JÓNsson, JN DuPaquier, ...
Age and Ageing 26 (suppl_2), 27-30, 1997
2071997
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
1882016
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