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Thordur Sigmundsson

Researcher at University of Iceland

Publications -  56
Citations -  10942

Thordur Sigmundsson is an academic researcher from University of Iceland. The author has contributed to research in topics: Psychosis & Schizophrenia (object-oriented programming). The author has an hindex of 29, co-authored 56 publications receiving 10561 citations. Previous affiliations of Thordur Sigmundsson include King's College London & University College London.

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Brain anatomy and sensorimotor gating in Asperger’s syndrome

TL;DR: It is hypothesized that Asperger's syndrome is associated with abnormalities in fronto-striatal pathways resulting in defective sensorimotor gating, and consequently characteristic difficulties inhibiting repetitive thoughts, speech and actions.
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Structural abnormalities in frontal, temporal, and limbic regions and interconnecting white matter tracts in schizophrenic patients with prominent negative symptoms.

TL;DR: Anatomical abnormalities in these schizophrenic patients with marked negative symptoms were most evident in left hemispheric neocortical and limbic regions and related white matter tracts, compatible with models that depict schizophrenia as a supraregional disorder of multiple, distributed brain regions and the axonal connections between them.
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Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

TL;DR: The weight of evidence for linkage to the chromosome 1q22, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci and is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium.
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Meta-analysis of 32 genome-wide linkage studies of schizophrenia

Mandy Y.M. Ng, +85 more
- 01 Aug 2009 - 
TL;DR: The primary analysis met empirical criteria for ‘aggregate’ genome-wide significance, indicating that some or all of 10 bins are likely to contain loci linked to SCZ, including regions of chromosomes 1, 2q, 3q, 4q, 5q, 8p and 10q.