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Frontiers in Neurology|September 14, 2020
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette SyndromeLuca Pagliaroli, Andrea Vereczkei, Shanmukha Sampath Padmanabhuni, et al.Annals of Human Genetics|June 14, 2019
Genetic history of the population of CretePetros Drineas, Fotis Tsetsos, Anna Plantinga, et al.International Journal of Legal Medicine|December 18, 2017
Ancestry inference of 96 population samples using microhaplotypesOzlem Bulbul, Andrew J Pakstis, Usha Soundararajan, et al.Annals of Human Genetics|October 16, 2012
Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studiesVasileios Stathias, Georgios R Sotiris, Iordanis Karagiannidis, et al.Scientific Reports|May 10, 2023
Aeolus winds impact on volcanic ash early warning systems for aviationVassilis Amiridis, Anna Kampouri, Antonis Gkikas, et al.Medrxiv : the Preprint Server for Health Sciences|June 10, 2025
Contextualizing molecular and structural aging across human organsJuan Shu, Yuxin Guo, Julio Chirinos, et al.Human Genetics|November 9, 2011
A global view of the OCA2-HERC2 region and pigmentationMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.Frontiers in Neuroscience|October 7, 2016
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome EtiologyJohn Alexander, Hera Potamianou, Jinchuan Xing, et al.Journal of Medical Genetics|July 5, 2013
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of familiesIordanis Karagiannidis, Sandra Dehning, Paul Sandor, et al.Translational Psychiatry|March 24, 2019
Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitryMary Mufford, Josh Cheung, Neda Jahanshad, et al.Pageof 8