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Thomas D. Dyer

Researcher at University of Texas at Austin

Publications -  224
Citations -  11995

Thomas D. Dyer is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Quantitative trait locus & Population. The author has an hindex of 51, co-authored 224 publications receiving 10985 citations. Previous affiliations of Thomas D. Dyer include University of Texas Health Science Center at San Antonio & Griffith University.

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Common genetic variants influence human subcortical brain structures.

Derrek P. Hibar, +344 more
- 09 Apr 2015 - 
TL;DR: In this paper, the authors conduct genome-wide association studies of the volumes of seven subcortical regions and the intracranial volume derived from magnetic resonance images of 30,717 individuals from 50 cohorts.
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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Paul M. Thompson, +332 more
TL;DR: The ENIGMA Consortium has detected factors that affect the brain that no individual site could detect on its own, and that require larger numbers of subjects than any individual neuroimaging study has currently collected.
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Identification of common variants associated with human hippocampal and intracranial volumes

Jason L. Stein, +237 more
- 01 May 2012 - 
TL;DR: In this article, the authors report genome-wide association meta-analyses and replication for mean bilateral hippocampal, total brain and intracranial volumes from a large multinational consortium.
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Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.

TL;DR: To highlight the usefulness of this much-enlarged map of cis-regulated transcripts for the discovery of genes that influence complex traits in humans, as an example, high-density lipoprotein cholesterol concentration is selected as a phenotype of clinical importance and the cis- regulated vanin 1 (VNN1) gene is identified as harboring sequence variants that influence high- density lipop protein cholesterol concentrations.
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A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

TL;DR: The results show strong evidence of linkage of this region of chromosome 2 with serum leptin levels and indicate that this region could contain an important human obesity gene.