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Papassotiropoulos, A; Stefanova, E; Vogler, C; Gschwind, L; Ackermann, S; Spalek, K; Rasch, Björn; Heck, A; Aerni, A; Hanser, E; Demougin, P; Huynh, K D; Luechinger, R; Klarhöfer, M; Novakovic, I; Kostic, V; Boesiger, P; Scheffler, K; de Quervain, D J F (2013). A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Molecular Psychiatry, 18(2):255-263.

de Quervain, D J F; Kolassa, I T; Ackermann, S; Aerni, A; Boesiger, P; Demougin, P; Elbert, T; Ertl, V; Gschwind, L; Hadziselimovic, N; Hanser, E; Heck, A; Hieber, P; Huynh, K D; Klarhofer, M; Luechinger, R; Rasch, B; Scheffler, K; Spalek, K; Stippich, C; Vogler, C; Vukojevic, V; Stetak, A; Papassotiropoulos, A (2012). PKCα is genetically linked to memory capacity in healthy subjects and to risk for posttraumatic stress disorder in genocide survivors. Proceedings of the National Academy of Sciences of the United States of America, 109(22):8746-8751.

Papassotiropoulos, A; Henke, K; Stefanova, E; Aerni, A; Müller, A; Demougin, P; Vogler, C; Sigmund, J C; Gschwind, L; Huynh, K D; Coluccia, D; Mondadori, C R; Hänggi, J; Buchmann, A; Kostic, V; Novakovic, I; van den Bussche, H; Kaduszkiewicz, H; Weyerer, S; Bickel, H; Riedel-Heller, S; Pentzek, M; Wiese, B; Dichgans, M; Wagner, M; Jessen, F; Maier, W; de Quervain, D J F (2011). A genome-wide survey of human short-term memory. Molecular Psychiatry, 16(2):184-192.

Kolassa, I T; Kolassa, S; Ertl, V; Papassotiropoulos, A; de Quervain, D J F (2010). The risk of posttraumatic stress disorder after trauma depends on traumatic load and the catechol-O-methyltransferase Val(158)Met polymorphism. Biological Psychiatry, 67(4):304-308.

Rasch, B; Spalek, K; Buholzer, S; Luechinger, R; Boesiger, P; de Quervain, D J F; Papassotiropoulos, A (2010). Aversive stimuli lead to differential amygdala activation and connectivity patterns depending on catechol-O-methyltransferase Val158Met genotype. NeuroImage, 52(4):1712-1719.

Rasch, B; Papassotiropoulos, A; de Quervain, D F (2010). Imaging genetics of cognitive functions: Focus on episodic memory. NeuroImage, 53(3):870-877.

Rasch, B; Spalek, K; Buholzer, S; Luechinger, R; Boesiger, P; Papassotiropoulos, A; de Quervain, D (2009). A genetic variation of the noradrenergic system is related to differential amygdala activation during encoding of emotional memories. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 106(45):19191-19196.

Hoerndli, F J; Walser, M; Fröhli Hoier, E; de Quervain, D; Papassotiropoulos, A; Hajnal, A (2009). A conserved function of c. elegans CASY-1 calsyntenin in associative learning. PLoS ONE, 4(3):e4880.

Vogler, C; Spalek, K; Aerni, A; Demougin, P; Müller, A; Huynh, K D; Papassotiropoulos, A; de Quervain, D J F (2009). CPEB3 is associated with human episodic memory. Frontiers in Behavioral Neuroscience:3:4.

Sigmund, J C; Vogler, C; Huynh, K D; de Quervain, D J F; Papassotiropoulos, A (2008). Fine-mapping at the HTR2A locus reveals multiple episodic memory-related variants. Biological Psychology, 79(2):239-242.

Tagarakis, G I; Tsolaki-Tagaraki, F; Tsolaki, M; Diegeler, A; Stylianakis, G E; Kazis, D; Tsilimingas, N B; Papassotiropoulos, A (2008). Are genetic components related to cognitive decline after coronary artery surgery? Genetics and brain function after bypass heart surgery. Journal of Cardiac Surgery, 23(3):280-281.

Buchmann, A; Montadori, C R A; Hänggi, Jürgen; Aerni, A; Vrticka, P; Luechinger, Roger; Boesiger, Peter; Hock, Christoph; Nitsch, R M; de Quervain, D J F; Papassotiropoulos, A; Henke, K (2008). Prion protein M129V polymorphism affects retrieval-related brain activity. Neuropsychologia, 46(9):2389-2402.

Webster, J A; Myers, A J; Pearson, J V; Craig, D W; Hu-Lince, D; Coon, K D; Zismann, V L; Beach, T; Leung, D; Bryden, L; Halperin, R F; Marlowe, L; Kaleem, M; Huentelman, M J; Joshipura, K; Walker, D; Heward, C B; Ravid, R; Rogers, J; Papassotiropoulos, A; Hardy, J; Reiman, E M; Stephan, D A (2008). Sorl1 as an Alzheimer's disease predisposition gene? Neurodegenerative Diseases, 5(2):60-64.

de Quervain, D J F; Kolassa, I T; Ertl, V; Onyut, P L; Neuner, F; Elbert, T; Papassotiropoulos, A (2007). A deletion variant of the alpha2b-adrenoceptor is related to emotional memory in Europeans and Africans. Nature Neuroscience, 10(9):1137-1139.

Huentelman, M J; Papassotiropoulos, A; Craig, D W; Hoerndli, F J; Pearson, J; Huynh, K; Corneveaux, J; Hänggi, Jürgen; Mondadori, C R A; Buchmann, A; Reiman, E M; Henke, K; de Quervain, D; Stephan, D A (2007). Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Human Molecular Genetics, 16(12):1469-1477.

Coon, K D; Myers, A J; Craig, D W; Webster, J A; Pearson, J V; Lince, D H; Zismann, V L; Beach, T G; Leung, D; Bryden, L; Halperin, R F; Marlowe, L; Kaleem, M; Walker, D G; Ravid, R; Heward, C B; Rogers, J; Papassotiropoulos, A; Reiman, E M; Hardy, J; Stephan, D A (2007). A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. Journal of Clinical Psychiatry, 68(4):613-618.

Hoerndli, F J; Pelech, S; Papassotiropoulos, A; Götz, J (2007). Abeta treatment and P301L tau expression in an Alzheimer's disease tissue culture model act synergistically to promote aberrant cell cycle re-entry. European Journal of Neuroscience, 26(1):60-72.

Wollmer, M A; Sleegers, K; Ingelsson, M; Zekanowski, C; Brouwers, N; Maruszak, A; Brunner, F; Huynh, K D; Kilander, L; Brundin, R M; Hedlund, M; Giedraitis, V; Glaser, A; Engelborghs, S; De Deyn, P P; Kapaki, E; Tsolaki, M; Daniilidou, M; Molyva, D; Paraskevas, G P; Thal, D R; Barcikowska, M; Kuznicki, J; Lannfelt, L; Van Broeckhoven, C; Nitsch, R M; Hock, C; Papassotiropoulos, A (2007). Association study of cholesterol-related genes in Alzheimer's disease. Neurogenetics, 8(3):179-188.

Mondadori, C R A; de Quervain, D J F; Buchmann, A; Mustovic, H; Wollmer, M A; Schmidt, C F; Boesiger, P; Hock, C; Nitsch, R M; Papassotiropoulos, A; Henke, K (2007). Better memory and neural efficiency in young apolipoprotein E epsilon4 carriers. Cerebral Cortex, 17(8):1934-1947.

De Ferrari, G V; Papassotiropoulos, A; Biechele, T; Wavrant-De Vrieze, F; Avila, M E; Major, M B; Myers, A; Sáez, K; Henríquez, J P; Zhao, A; Wollmer, M A; Nitsch, R M; Hock, C; Morris, C M; Hardy, J; Moon, R T (2007). Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 104(22):9434-3439.

Pearson, J V; Huentelman, M J; Halperin, R F; Tembe, W D; Melquist, S; Homer, N; Brun, M; Szelinger, S; Coon, K D; Zismann, V L; Webster, J A; Beach, T; Sando, S B; Aasly, J O; Heun, R; Jessen, F; Kölsch, H; Tsolaki, M; Daniilidou, M; Reiman, E M; Papassotiropoulos, A; Hutton, M L; Stephan, D A; Craig, D W (2007). Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. American Journal of Human Genetics, 80(1):126-139.

Tagarakis, G I; Tsolaki-Tagaraki, F; Tsolaki, M; Diegeler, A; Kazis, D; Rouska, E; Papassotiropoulos, A (2007). The role of SOAT-1 polymorphisms in cognitive decline and delirium after bypass heart surgery. Clinical Research in Cardiology, 96(9):600-603.

Tagarakis, G I; Tsolaki-Tagaraki, F; Tsolaki, M; Diegeler, A; Tsilimingas, N B; Papassotiropoulos, A (2007). The role of apolipoprotein E in cognitive decline and delirium after bypass heart operations. American Journal of Alzheimer's Disease and Other Dementias, 22(3):223-228.

Papassotiropoulos, A; Stephan, D A; Huentelman, M J; Hoerndli, F J; Craig, D W; Pearson, J V; Huynh, K D; Brunner, F; Corneveaux, J; Osborne, D; Wollmer, M A; Aerni, A; Coluccia, D; Hänggi, Jürgen; Mondadori, C R A; Buchmann, A; Reiman, E M; Caselli, R J; Henke, K; de Quervain, D J F (2006). Common Kibra alleles are associated with human memory performance. Science, 314(5798):475-478.

Wollmer, M A; Kapaki, E; Hersberger, M; Muntwyler, J; Brunner, F; Tsolaki, M; Akatsu, H; Kosaka, K; Michikawa, M; Molyva, D; Paraskevas, G P; Lütjohann, D; von Eckardstein, A; Hock, C; Nitsch, R M; Papassotiropoulos, A (2006). Ethnicity-dependent genetic association of ABCA2 with sporadic Alzheimer's disease. American Journal of Medical Genetics. Part B, 141B(5):534-536.

Wollmer, M A; Nitsch, R M; Hock, C; Papassotiropoulos, A (2006). Genetic association study on colony-stimulating factor 1 in Alzheimer's disease. Neurodegenerative Diseases, 3(6):334-337.

Papassotiropoulos, A; Fountoulakis, M; Dunckley, T; Stephan, D A; Reiman, E M (2006). Genetics, transcriptomics, and proteomics of Alzheimer's disease. Journal of Clinical Psychiatry, 67(4):652-670.

de Quervain, D J F; Papassotiropoulos, A (2006). Identification of a genetic cluster influencing memory performance and hippocampal activity in humans. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 103(11):4270-4274.

Coon, K D; Siegel, A M; Yee, S J; Dunckley, T L; Mueller, C; Nagra, R M; Tourtellotte, W W; Reiman, E M; Papassotiropoulos, A; Petersen, F F; Stephan, D A; Kirsch, W M (2006). Preliminary demonstration of an allelic association of the IREB2 gene with Alzheimer's disease. Journal of Alzheimer's Disease, 9(3):225-233.

Coon, K D; Valla, J; Szelinger, S; Schneider, L E; Niedzielko, T L; Brown, K M; Pearson, J V; Halperin, R; Dunckley, T L; Papassotiropoulos, A; Caselli, R J; Reiman, E M; Stephan, D A (2006). Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencing. Mitochondrion, 6(4):194-210.

Papassotiropoulos, A; Wollmer, M A; Aguzzi, A; Hock, Christoph; Nitsch, R M; de Quervain, D J F (2005). The prion gene is associated with human long-term memory. Human Molecular Genetics, 14(15):2241-2246.

Papassotiropoulos, A; Wollmer, M A; Tsolaki, M; Brunner, F; Molyva, D; Lütjohann, D; Nitsch, R M; Hock, C (2005). A cluster of cholesterol-related genes confers susceptibility for Alzheimer's disease. Journal of Clinical Psychiatry, 66(7):940-947.

Papassotiropoulos, A; Henke, K; Aerni, A; Coluccia, D; Garcia, E; Wollmer, M A; Huynh, K D; Monsch, A U; Stähelin, H B; Hock, C; Nitsch, R M; de Quervain, D J F (2005). Age-dependent effects of the 5-hydroxytryptamine-2a-receptor polymorphism (His452Tyr) on human memory. NeuroReport, 16(8):839-842.

Papassotiropoulos, A; Lambert, J C; Wavrant-De Vrièze, F; Wollmer, M A; von der Kammer, H; Streffer, J R; Maddalena, A; Huynh, K D; Wolleb, S; Lütjohann, D; Schneider, B; Thal, D R; Grimaldi, L M E; Tsolaki, M; Kapaki, E; Ravid, R; Konietzko, U; Hegi, T; Pasch, T; Jung, H; Braak, H; Amouyel, P; Rogaev, E I; Hardy, J; Hock, C; Nitsch, R M (2005). Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease. Neurodegenerative Diseases, 2(5):233-241.

Kornblum, C; Schröder, R; Müller, K; Vorgerd, M; Eggers, J; Bogdanow, M; Papassotiropoulos, A; Fabian, K; Klockgether, T; Zange, J (2005). Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover study. European Journal of Neurology, 12(4):300-309.

Koller, M F; Papassotiropoulos, A; Henke, K; Behrends, B; Noda, S; Kratzer, A; Hock, C; Hofmann, M (2005). Evidence of a genetic basis of Morgagni-Stewart-Morel syndrome. A case report of identical twins. Neurodegenerative Diseases, 2(2):56-60.

Papassotiropoulos, A; Tsolaki, M; Wollmer, M A; Molyva, D; Thal, D R; Huynh, K D; Tracy, J; Staehelin, H B; Monsch, A U; Nitsch, R M; Hock, C (2005). No association of a non-synonymous PLAU polymorphism with Alzheimer's disease and disease-related traits. American Journal of Medical Genetics. Part B, 132B(1):21-23.

Papassotiropoulos, A; Maddalena, A; Gretener, D; Nitsch, R M; Hock, C (2004). Cerebrospinal fluid biomarkers for the diagnosis of Alzheimer's disease. In: Hyman, B T; Demonet, L F; Christen, Y. The Living Brain and Alzheimer’s Disease. Berlin [etc.]: Springer Verlag , 17-24.

Maddalena, A S; Papassotiropoulos, A; Gonzalez-Agosti, C; Signorell, A; Hegi, T; Pasch, T; Nitsch, R M; Hock, C (2004). Cerebrospinal fluid profile of amyloid beta peptides in patients with Alzheimer's disease determined by protein biochip technology. Neurodegenerative Diseases, 1(4-5):231-235.

Alberici, A; Gobbo, C; Panzacchi, A; Nicosia, F; Ghidoni, R; Benussi, L; Hock, C; Papassotiropoulos, A; Liberini, P; Growdon, J H; Frisoni, G B; Villa, A; Zanetti, O; Cappa, S; Fazio, F; Binetti, G (2004). Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier. Journal of Neurology, Neurosurgery, and Psychiatry, 75(11):1607-1610.

de Quervain, D J F; Poirier, R; Wollmer, M A; Grimaldi, L M E; Tsolaki, M; Streffer, J R; Hock, C; Nitsch, R M; Mohajeri, M H; Papassotiropoulos, A (2004). Glucocorticoid-related genetic susceptibility for Alzheimer's disease. Human Molecular Genetics, 13(1):47-52.

Aerni, A; Traber, R; Hock, C; Roozendaal, B; Schelling, G; Papassotiropoulos, A; Nitsch, R M; Schnyder, U; de Quervain, D J F (2004). Low-dose cortisol for symptoms of posttraumatic stress disorder. American Journal of Psychiatry, 161(8):1488-1490.

Chen, F; Wollmer, M A; Hoerndli, F; Münch, G; Kuhla, B; Rogaev, E I; Tsolaki, M; Papassotiropoulos, A; Götz, J (2004). Role for glyoxalase I in Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 101(20):7687-7692.

de Quervain, D J F; Henke, K; Aerni, A; Coluccia, D; Wollmer, M A; Hock, C; Nitsch, R M; Papassotiropoulos, A (2003). A functional genetic variation of the 5-HT2a receptor affects human memory. Nature Neuroscience, 6(11):1141-1142.

Wollmer, M A; Streffer, J R; Lütjohann, D; Tsolaki, M; Iakovidou, V; Hegi, T; Pasch, T; Jung, H H; von Bergmann, K; Nitsch, R M; Hock, C; Papassotiropoulos, A (2003). ABCA1 modulates CSF cholesterol levels and influences the age at onset of Alzheimer's disease. Neurobiology of Aging, 24(3):421-426.

Hock, C; Konietzko, U; Streffer, J R; Tracy, J; Signorell, A; Müller-Tillmanns, B; Lemke, U; Henke, K; Moritz, E; Garcia, E; Wollmer, M A; Umbricht, D; de Quervain, D J F; Hofmann, M; Maddalena, A; Papassotiropoulos, A; Nitsch, R M (2003). Antibodies against beta-amyloid slow cognitive decline in Alzheimer's disease. Neuron, 38(4):547-554.

Maddalena, A; Papassotiropoulos, A; Müller-Tillmanns, B; Jung, H H; Hegi, T; Nitsch, R M; Hock, C (2003). Biochemical diagnosis of Alzheimer disease by measuring the cerebrospinal fluid ratio of phosphorylated tau protein to beta-amyloid peptide42. Archives of Neurology, 60(9):1202-1206.

Wollmer, M A; Streffer, J R; Tsolaki, M; Grimaldi, L M E; Lütjohann, D; Thal, D; von Bergmann, K; Nitsch, R M; Hock, C; Papassotiropoulos, A (2003). Genetic association of acyl-coenzyme A: cholesterol acyltransferase with cerebrospinal fluid cholesterol levels, brain amyloid load, and risk for Alzheimer's disease. Molecular Psychiatry, 8(6):635-638.

Schmidt, S; Marrosu, G M; Kölsch, H; Haase, C G; Ferenczik, S; Sokolowski, P; Köhler, W; Schmidt, M; Papassotiropoulos, A; Heun, R; Grosse-Wilde, H; Klockgether, T (2003). Genetic variations and humoral immune responses to myelin oligodendroglia glycoprotein in adult phenotypes of X-linked adrenoleukodystrophy. Journal of Neuroimmunology, 135(1-2):148-153.

Papassotiropoulos, A; Hock, C; Nitsch, R M (2003). Genetik gerontopsychiatrischer Erkrankungen. In: Förstl, H. Lehrbuch der Gerontopsychiatrie und –psychotherapie: Grundlagen, Klinik, Therapie. Stuttgart: Thieme, 27-36.

Papassotiropoulos, A; Streffer, J R; Tsolaki, M; Schmid, S; Thal, D; Nicosia, F; Iakovidou, V; Maddalena, A; Lütjohann, D; Ghebremedhin, E; Hegi, T; Pasch, T; Träxler, M; Brühl, A; Benussi, L; Binetti, G; Braak, H; Nitsch, R M; Hock, C (2003). Increased brain beta-amyloid load, phosphorylated tau, and risk of Alzheimer disease associated with an intronic CYP46 polymorphism. Archives of Neurology, 60(1):29-35.

Schmidt, S; Papassotiropoulos, A; Sotgiu, S; Kölsch, H; Arru, G; Fois, M L; Haase, C G; Schmitz, S; König, N; Harzheim, M; Heun, R; Klockgether, T (2003). Investigation of a genetic variation of a variable number tandem repeat polymorphism of interleukin-6 gene in patients with multiple sclerosis. Journal of Neurology, 250(5):607-611.

Bagli, M; Papassotiropoulos, A; Hampel, H; Becker, K; Jessen, F; Bürger, K; Ptok, U; Rao, M L; Möller, H J; Maier, W; Heun, R (2003). Polymorphisms of the gene encoding the inflammatory cytokine interleukin-6 determine the magnitude of the increase in soluble interleukin-6 receptor levels in Alzheimer's disease. Results of a pilot study. European Archives of Psychiatry and Clinical Neuroscience, 253(1):44-48.

Streffer, J R; Papassotiropoulos, A; Kurosinski, P; Signorell, A; Wollmer, M A; Tsolaki, M; Iakovidou, V; Hörndli, F; Bosset, J; Götz, J; Nitsch, R M; Hock, C (2003). Saitohin gene is not associated with Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry, 74(3):362-363.

Hock, C; Konietzko, U; Papassotiropoulos, A; Wollmer, A; Streffer, J; von Rotz, R C; Davey, G; Moritz, E; Nitsch, R M (2002). Generation of antibodies specific for beta-amyloid by vaccination of patients with Alzheimer disease. Nature Medicine, 8(11):1270-1275.

Wollmer, M A; Papassotiropoulos, A; Streffer, J R; Grimaldi, L M E; Kapaki, E; Salani, G; Paraskevas, G P; Maddalena, A; de Quervain, D; Bieber, C; Umbricht, D; Lemke, U; Bosshardt, S; Degonda, N; Henke, K; Hegi, T; Jung, H H; Pasch, T; Hock, C; Nitsch, R M (2002). Genetic polymorphisms and cerebrospinal fluid levels of tissue inhibitor of metalloproteinases 1 in sporadic Alzheimer's disease. Psychiatric Genetics, 12(3):155-160.

This list was generated on Mon Jul 24 05:42:36 2017 CEST.