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Träfflista för sökning "WFRF:(Lamb F. K.) srt2:(2005-2009)"

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1.	Achterberg, A., et al. (author) The search for muon neutrinos from northern hemisphere gamma-ray bursts with AMANDA 2008 In: Astrophysical Journal. - : American Astronomical Society. - 0004-637X .- 1538-4357. ; 674:1, s. 357-370 Journal article (peer-reviewed)abstract We present the results of the analysis of neutrino observations by the Antarctic Muon and Neutrino Detector Array (AMANDA) correlated with photon observations of more than 400 gamma-ray bursts (GRBs) in the northern hemisphere from 1997 to 2003. During this time period, AMANDA's effective collection area for muon neutrinos was larger than that of any other existing detector. After the application of various selection criteria to our data, we expect similar to 1 neutrino event and <2 background events. Based on our observations of zero events during and immediately prior to the GRBs in the data set, we set the most stringent upper limit on muon neutrino emission correlated with GRBs. Assuming a Waxman-Bahcall spectrum and incorporating all systematic uncertainties, our flux upper limit has a normalization at 1 PeV of E-2 Phi(nu) <= 6.3 x 10(-9) GeV cm(-2) s(-1) sr(-1), with 90% of the events expected within the energy range of similar to 10 TeV to similar to 3 PeV. The impact of this limit on several theoretical models of GRBs is discussed, as well as the future potential for detection of GRBs by next-generation neutrino telescopes. Finally, we briefly describe several modifications to this analysis in order to apply it to other types of transient point sources.
2.	Szatmari, Peter, et al. (author) Mapping autism risk loci using genetic linkage and chromosomal rearrangements. 2007 In: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 39:3, s. 319-328 Journal article (peer-reviewed)abstract Autism spectrum disorders (ASDs) are common, heritable neurodevelopmental conditions. The genetic architecture of ASDs is complex, requiring large samples to overcome heterogeneity. Here we broaden coverage and sample size relative to other studies of ASDs by using Affymetrix 10K SNP arrays and 1,168 families with at least two affected individuals, performing the largest linkage scan to date while also analyzing copy number variation in these families. Linkage and copy number variation analyses implicate chromosome 11p12-p13 and neurexins, respectively, among other candidate loci. Neurexins team with previously implicated neuroligins for glutamatergic synaptogenesis, highlighting glutamate-related genes as promising candidates for contributing to ASDs.

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Type of publication: journal article (2)

Type of content: peer-reviewed (2)

Author/Editor: Hasegawa, Y. (1); Kolanoski, H. (1); Sander, H. G. (1); Wagner, W. (1); Burgess, T. (1); Lundberg, J. (1); show more...; Bohm, C. (1); Boeser, S. (1); Bai, X. (1); Beattie, K. (1); Landsman, H. (1); Rizzo, A. (1); Inaba, M. (1); Kowalski, M. (1); Van Eijndhoven, N. (1); Schlenstedt, S. (1); Ackermann, M. (1); Adams, J. (1); Auffenberg, J. (1); Barwick, S. W. (1); Bay, R. (1); Berghaus, P. (1); Berley, D. (1); Bernardini, E. (1); Besson, D. Z. (1); Blaufuss, E. (1); Braun, J. (1); Christy, B. (1); Cowen, D. F. (1); De Clercq, C. (1); Desiati, P. (1); DeYoung, T. (1); Diaz-Velez, J. C. (1); Evenson, P. A. (1); Fadiran, O. (1); Fazely, A. R. (1); Filimonov, K. (1); Gaisser, T. K. (1); Gallagher, J. (1); Gerhardt, L. (1); Goldschmidt, A. (1); Goodman, J. A. (1); Gross, A. (1); Halzen, F. (1); Hanson, K. (1); Helbing, K. (1); Hill, G. C. (1); Hoffman, K. D. (1); Hoshina, K. (1); Hultqvist, K. (1); show less...

University: University of Gothenburg (1); Uppsala University (1); Stockholm University (1)

Language: English (2)

Research subject (UKÄ/SCB): Natural sciences (1); Medical and Health Sciences (1)

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