Search Results - "ROEHR, J. T"

Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer’s disease with OSBPL6, PTPRG, and PDCL3 by Herold, C, Hooli, B V, Mullin, K, Liu, T, Roehr, J T, Mattheisen, M, Parrado, A R, Bertram, L, Lange, C, Tanzi, R E

“…The genetic basis of Alzheimer's disease (AD) is complex and heterogeneous. Over 200 highly penetrant pathogenic variants in the genes APP , PSEN1 , and PSEN2…”
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No association between CTNNBL1 and episodic memory performance by Liu, T, Li, S-C, Papenberg, G, Schröder, J, Roehr, J T, Nietfeld, W, Lindenberger, U, Bertram, L

“…Polymorphisms in the gene encoding catenin-β-like 1 ( CTNNBL1 ) were recently reported to be associated with verbal episodic memory performance—in particular,…”
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Role of common and rare APP DNA sequence variants in Alzheimer disease by Hooli, B V, Mohapatra, G, Mattheisen, M, Parrado, A R, Roehr, J T, Shen, Y, Gusella, J F, Moir, R, Saunders, A J, Lange, C, Tanzi, R E, Bertram, L

“…More than 30 different rare mutations, including copy number variants (CNVs), in the amyloid precursor protein gene (APP) cause early-onset familial Alzheimer…”
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Activation of the major immediate early gene of human cytomegalovirus by cis-acting elements in the promoter-regulatory sequence and by virus-specific trans-acting components by STINSKI, M. F, ROEHR, T. J

“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Comprehensive Field Synopsis and Systematic Meta-analyses of Genetic Association Studies in Cutaneous Melanoma by Chatzinasiou, Foteini, Lill, Christina M., Kypreou, Katerina, Stefanaki, Irene, Nicolaou, Vasiliki, Spyrou, George, Evangelou, Evangelos, Roehr, Johannes T., Kodela, Elizabeth, Katsambas, Andreas, Tsao, Hensin, Ioannidis, John P.A., Bertram, Lars, Stratigos, Alexander J.

“…Background Although genetic studies have reported a number of loci associated with cutaneous melanoma (CM) risk, a comprehensive synopsis of genetic…”
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Kole ot common and rare APP DNA sequence variants in Alzheimer disease by HOOLI, B. V, MOHAPATRA, G, TANZI, R. E, BERTRAM, L, MATTHEISEN, M, PARRADO, A. R, ROEHR, J. T, SHEN, Y, GUSELLA, J. F, MOIR, R, SAUNDERS, A. J, LANGE, C

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Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects by Lill, Christina M, Liu, Tian, Schjeide, Brit-Maren M, Roehr, Johannes T, Akkad, Denis A, Damotte, Vincent, Alcina, Antonio, Ortiz, Miguel A, Arroyo, Rafa, Lopez de Lapuente, Aitzkoa, Blaschke, Paul, Winkelmann, Alexander, Gerdes, Lisa-Ann, Luessi, Felix, Fernadez, Oscar, Izquierdo, Guillermo, Antigüedad, Alfredo, Hoffjan, Sabine, Cournu-Rebeix, Isabelle, Gromöller, Silvana, Faber, Hans, Liebsch, Maria, Meissner, Esther, Chanvillard, Coralie, Touze, Emmanuel, Pico, Fernando, Corcia, Philippe, Dörner, Thomas, Steinhagen-Thiessen, Elisabeth, Baeckman, Lars, Heekeren, Hauke R, Li, Shu-Chen, Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Kümpfel, Tania, Kubisch, Christian, Epplen, Joerg T, Zettl, Uwe K, Fontaine, Bertrand, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena, Bertram, Lars, Zipp, Frauke

“…Single nucleotide polymorphisms (SNPs) rs429358 (ε4) and rs7412 (ε2), both invoking changes in the amino-acid sequence of the apolipoprotein E (APOE) gene,…”
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