Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ina S. Almdahl"'
Autor:
Jonas Alexander Jarholm, Atle Bjørnerud, Turi Olene Dalaker, Mehdi Sadat Akhavi, Bjørn Eivind Kirsebom, Lene Pålhaugen, Kaja Nordengen, Gøril Rolfseng Grøntvedt, Arne Nakling, Lisa F. Kalheim, Ina S. Almdahl, Sandra Tecelão, Tormod Fladby, Per Selnes
Publikováno v:
Journal of Alzheimer's Disease. :1-21
Background: Atrophy of the medial temporal lobe (MTL) is a biological characteristic of Alzheimer’s disease (AD) and can be measured by segmentation of magnetic resonance images (MRI). Objective: To assess the clinical utility of automated volumetr
Autor:
Ina S. Almdahl, Liva J. Martinussen, Olga Therese Ousdal, Miroslawa Kraus, Piotr Sowa, Ingrid Agartz, Maria S. Korsnes
Publikováno v:
Aging & Mental Health. :1-9
Publikováno v:
Brain and Behavior, Vol 11, Iss 5, Pp n/a-n/a (2021)
Abstract Introduction Successful inhibition of distracting emotions is important for preserving well‐being and daily functioning. There is conflicting evidence regarding the impact of healthy aging on emotional inhibition, and possible age‐relate
Externí odkaz:
https://doaj.org/article/5e71312a5ec04ec1a7d804b0f9032fb9
Autor:
Nikias Siafarikas, Tormod Fladby, Maria Stylianou-Korsnes, Maria Lage Barca, Jennifer Monereo-Sánchez, Ole A. Andreassen, Dag Aarsland, Geir Selbæk, Ina S. Almdahl, Lars T. Westlye, Karin Persson, Dag Alnæs, Martina J. Lund
Publikováno v:
International Psychogeriatrics, 33(11):1041610221000934, 1217-1228. Cambridge University Press
We present associations between neuropsychiatric symptoms (NPS) and brain morphology in a large sample of patients with mild cognitive impairment (MCI) and Alzheimer's disease with dementia (AD dementia). Several studies assessed NPS factor structure
Publikováno v:
International journal of geriatric psychiatryREFERENCES. 37(3)
Understanding the biological changes that occur prior to onset of late-life depression (LLD) is key to its prevention. To investigate potential predictors of LLD, we assessed cognitive scores and neurodegenerative and vascular biomarkers in healthy o
Autor:
Arne Nakling, Knut Waterloo, Kjell Arne Arntzen, Ragna Espenes, Sandra R.R. Tecelão, Svein Ivar Bekkelund, Carl Fredrik Eliassen, Kai Ivar Müller, Gøril Rolfseng Grøntvedt, Lene Pålhaugen, Lisa Flem Kalheim, Bjørn-Eivind Kirsebom, Ina S. Almdahl, Geir Bråthen, Krisztina Kunszt Johansen, Ramune Grambaite, Dag Aarsland, Ane Løvli Stav, Stein Harald Johnsen, Arvid Rongve, Per Selnes, Sigrid Botne Sando, Nikias Siafarikas, Erik Hessen, Tormod Fladby, Eirik Auning, Santiago Timón
Publikováno v:
Fladby, T, Palhaugen, L, Selnes, P, Waterloo, K, Brathen, G, Hessen, E, Almdahl, I S, Arntzen, K-A, Auning, E, Eliassen, C F, Espenes, R, Grambaite, R, Grontvedt, G R, Johansen, K K, Johnsen, S H, Kalheim, L F, Kirsebom, B-E, Muller, K I, Nakling, A E, Rongve, A, Sando, S B, Siafarikas, N, Stav, A L, Tecelao, S, Timon, S, Bekkelund, S I & Aarsland, D 2017, ' Detecting At-Risk Alzheimer's Disease Cases ', JOURNAL OF ALZHEIMERS DISEASE, vol. 60, no. 1, pp. 97-105 . https://doi.org/10.3233/JAD-170231
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease
While APOE ɛ4 is the major genetic risk factor for Alzheimer’s disease (AD), amyloid dysmetabolism is an initial or early event predicting clinical disease and is an important focus for secondary intervention trials. To improve identification of c
Autor:
Geir Selbæk, Daniel F. Gudbjartsson, Ina S. Almdahl, John Loughlin, Patrick Sulem, Asmundur Oddson, Unnur Thorsteinsdottir, Gudmundur L. Norddahl, Gisli Masson, Maryam S. Daneshpour, Jose I. Mayordomo, Helgi Jonsson, Lambertus A. Kiemeney, Thorunn Rafnar, Peter S. Braund, Solveig Gretarsdottir, Amanda Villalvilla, Jung Min Koh, Farhad Hosseinpanah, Anne Brækhus, Hannes Helgason, Nilesh J. Samani, Augustine Kong, Asgeir Sigurdsson, Unnur Styrkarsdottir, Hrefna Johannsdottir, Tormod Fladby, Louise N. Reynard, Hreinn Stefansson, Olafur Th Magnusson, Agnar Helgason, Gisli H. Halldorsson, Nelson L.S. Tang, Audur Magnusdottir, Florian Zink, Thorvaldur Ingvarsson, L. Stefan Lohmander, Gardar Sveinbjornsson, Arna B Agustsdottir, Ingileif Jonsdottir, Kari Stefansson, Anna Helgadottir, Aslaug Jonasdottir, Gerald Sulem, Corrine K. Welt, Claus Christiansen, Fereidoun Azizi, Ole A. Andreassen
Publikováno v:
Nature Genetics, 49, 5, pp. 801-805
Nature Genetics, 49, 801-805
Nature Genetics, 49, 801-805
Contains fulltext : 174179.pdf (Publisher’s version ) (Closed access) We performed a genome-wide association study of total hip replacements, based on variants identified through whole-genome sequencing, which included 4,657 Icelandic patients and
Autor:
Julia Sealock, Linda R. White, John Hardy, Geir Bråthen, Danielle Posthuma, Christiaan de Leeuw, Ingvild Saltvedt, Julien Bryois, Lea K. Davis, Timothy J. Hohman, Logan Dumitrescu, Nancy L. Pedersen, Petroula Proitsi, Francesco Bettella, Eystein Stordal, Dylan M. Williams, Sigrid Botne Sando, Sven Stringer, Stacy Steinberg, Jon Snaedal, Steven J. Kiddle, Jens Hjerling-Leffler, Fred Andersen, Ida K. Karlsson, Yunpeng Wang, Palmi V. Jonsson, Nicola Voyle, Jeanne E. Savage, Ingun Ulstein, Stephan Ripke, Richard Dobson, Anne Brækhus, Arvid Rongve, Sverre Bergh, Hreinn Stefansson, Dag Aarsland, Kyoko Watanabe, Patrick F. Sullivan, Maryam Shoai, Geir Selbæk, Sigurbjorn Bjornsson, Rahul S. Desikan, Srdjan Djurovic, Ina S. Almdahl, Sara Hägg, Kari Stefansson, Lavinia Athanasiu, Nathan G. Skene, Aree Witoelar, Iris E. Jansen, Ole A. Andreassen, Wiesje M. van der Flier, Tormod Fladby
Publikováno v:
Nature Genetics, 51(3), 404-413. Nature Publishing Group
Jansen, I E, Savage, J E, Watanabe, K, Bryois, J, Williams, D M, Steinberg, S, Sealock, J, Karlsson, I K, Hägg, S, Athanasiu, L, Voyle, N, Proitsi, P, Witoelar, A, Stringer, S, Aarsland, D, Almdahl, I S, Andersen, F, Bergh, S, Bettella, F, Bjornsson, S, Brækhus, A, Bråthen, G, de Leeuw, C, Desikan, R S, Djurovic, S, Dumitrescu, L, Fladby, T, Hohman, T J, Jonsson, P V, Kiddle, S J, Rongve, A, Saltvedt, I, Sando, S B, Selbæk, G, Shoai, M, Skene, N G, Snaedal, J, Stordal, E, Ulstein, I D, Wang, Y, White, L R, Hardy, J, Hjerling-Leffler, J, Sullivan, P F, van der Flier, W M, Dobson, R, Davis, L K, Stefansson, H, Stefansson, K, Pedersen, N L, Ripke, S, Andreassen, O A & Posthuma, D 2019, ' Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk ', Nature Genetics, vol. 51, no. 3, pp. 404-413 . https://doi.org/10.1038/s41588-018-0311-9
Jansen, I E, Savage, J E, Watanabe, K, Bryois, J, Williams, D M, Steinberg, S, Sealock, J, Karlsson, I K, Hägg, S, Athanasiu, L, Voyle, N, Proitsi, P, Witoelar, A, Stringer, S, Aarsland, D, Almdahl, I S, Andersen, F, Bergh, S, Bettella, F, Bjornsson, S, Brækhus, A, Bråthen, G, de Leeuw, C, Desikan, R S, Djurovic, S, Dumitrescu, L, Fladby, T, Hohman, T J, Jonsson, P V, Kiddle, S J, Rongve, A, Saltvedt, I, Sando, S B, Selbæk, G, Shoai, M, Skene, N G, Snaedal, J, Stordal, E, Ulstein, I D, Wang, Y, White, L R, Hardy, J, Hjerling-Leffler, J, Sullivan, P F, van der Flier, W M, Dobson, R, Davis, L K, Stefansson, H, Stefansson, K, Pedersen, N L, Ripke, S, Andreassen, O A & Posthuma, D 2019, ' Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk ', Nature Genetics, vol. 51, no. 3, pp. 404-413 . https://doi.org/10.1038/s41588-018-0311-9
Nature Genetics
Jansen, I E, Savage, J E, Watanabe, K, Bryois, J, Williams, D M, Steinberg, S, Sealock, J, Karlsson, I K, Hägg, S, Athanasiu, L, Voyle, N, Proitsi, P, Witoelar, A, Stringer, S, Aarsland, D, Almdahl, I S, Andersen, F, Bergh, S, Bettella, F, Bjornsson, S, Brækhus, A, Bråthen, G, de Leeuw, C, Desikan, R S, Djurovic, S, Dumitrescu, L, Fladby, T, Hohman, T J, Jonsson, P V, Kiddle, S J, Rongve, A, Saltvedt, I, Sando, S B, Selbæk, G, Shoai, M, Skene, N G, Snaedal, J, Stordal, E, Ulstein, I D, Wang, Y, White, L R, Hardy, J, Hjerling-Leffler, J, Sullivan, P F, van der Flier, W M, Dobson, R, Davis, L K, Stefansson, H, Stefansson, K, Pedersen, N L, Ripke, S, Andreassen, O A & Posthuma, D 2019, ' Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk ', Nature Genetics, vol. 51, no. 3, pp. 404-413 . https://doi.org/10.1038/s41588-018-0311-9
Jansen, I E, Savage, J E, Watanabe, K, Bryois, J, Williams, D M, Steinberg, S, Sealock, J, Karlsson, I K, Hägg, S, Athanasiu, L, Voyle, N, Proitsi, P, Witoelar, A, Stringer, S, Aarsland, D, Almdahl, I S, Andersen, F, Bergh, S, Bettella, F, Bjornsson, S, Brækhus, A, Bråthen, G, de Leeuw, C, Desikan, R S, Djurovic, S, Dumitrescu, L, Fladby, T, Hohman, T J, Jonsson, P V, Kiddle, S J, Rongve, A, Saltvedt, I, Sando, S B, Selbæk, G, Shoai, M, Skene, N G, Snaedal, J, Stordal, E, Ulstein, I D, Wang, Y, White, L R, Hardy, J, Hjerling-Leffler, J, Sullivan, P F, van der Flier, W M, Dobson, R, Davis, L K, Stefansson, H, Stefansson, K, Pedersen, N L, Ripke, S, Andreassen, O A & Posthuma, D 2019, ' Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk ', Nature Genetics, vol. 51, no. 3, pp. 404-413 . https://doi.org/10.1038/s41588-018-0311-9
Nature Genetics
Alzheimer’s disease (AD) is highly heritable and recent studies have identified over 20 disease-associated genomic loci. Yet these only explain a small proportion of the genetic variance, indicating that undiscovered loci remain. Here, we performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a962a380017ba61e1af21ea26eff5ad6
https://research.vumc.nl/en/publications/8c0567cc-6ec7-4649-a3f5-8b4da2a5f679
https://research.vumc.nl/en/publications/8c0567cc-6ec7-4649-a3f5-8b4da2a5f679
Autor:
Lene Pålhaugen, Isabel Hernández, Kari Stefansson, Alfredo Ramirez, Inger van Steenoven, Lasse Pihlstrøm, Estrella Morenas-Rodríguez, Ina S. Almdahl, Francesco Bettella, Hreinn Stefansson, Mercè Boada, Srdjan Djurovic, Dag Aarsland, Sonia Moreno-Grau, Jordi Clarimón, Jon Alm Eriksen, Sigrid Botne Sando, Tormod Fladby, Afina W. Lemstra, Aree Witoelar, Carla Abdelnour, Lluís Tárraga, Alberto Lleó, Lavinia Athanasiu, Ingun Ulstein, Olivier Bousiges, Arvid Rongve, Ane-Victoria Idland, Jon Snaedal, Rahul S. Desikan, Elisabet Londos, Ole A. Andreassen, Eystein Stordal, Stefanie Heilmann-Heimbach, Ingvild Saltvedt, Mathias Toft, Frédéric Blanc, Itziar de Rojas, Geir Bråthen, Agustín Ruiz
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientific Reports, Vol 9, Iss 1, Pp 1-2 (2019)
Universitat Autònoma de Barcelona
Scientific Reports, Vol 9, Iss 1, Pp 1-2 (2019)
“The authors would like to thank the Norwegian Dementia Genetics Network (DemGene), the European DLB Consortium (E-DLB), Dementia Genetics Spanish Consortium (DEGESCO) and Genomic Research at Fundacio ACE (GR@ACE) Consortium. Fundacio ACE would lik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c54483e0b789cc6ec1f5e682b8bdcc4a
https://ddd.uab.cat/record/253362
https://ddd.uab.cat/record/253362