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The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|September 1, 2021
Gene expression analysis of MAOA and the clock gene ARNTL in individuals with bipolar disorder compared to healthy controlsS A Bengesser, H Hohenberger, B Tropper, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2015
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for careBrian T Wilson, Zornitza Stark, Ruth E Sutton, et al.
Brain Sciences|August 9, 2018
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) MutationJennifer F Gardner, Thomas D Cushion, Georgios Niotakis, et al.
PLOS Global Public Health|April 20, 2026
Community-led standards for global wastewater-based infectious disease surveillanceEmily A Smith, Maryam Ahmadi Jeshvaghane, Dylan A Pilz, et al.
Scientific Reports|October 18, 2017
A comparative study of machine learning methods for time-to-event survival data for radiomics risk modellingStefan Leger, Alex Zwanenburg, Karoline Pilz, et al.
Nature Genetics|March 12, 2014
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disabilityKatrina Tatton-Brown, Sheila Seal, Elise Ruark, et al.
Nature Genetics|November 5, 1997
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIID B Simon, R S Bindra, T A Mansfield, et al.
Brain : a Journal of Neurology|October 23, 2021
Early childhood epilepsies: epidemiology, classification, aetiology, and socio-economic determinantsJoseph D Symonds, Katherine S Elliott, Jay Shetty, et al.
Circulation. Cardiovascular Genetics|September 20, 2013
Genome-wide association study identifies 3 genomic loci significantly associated with serum levels of homoarginine: the AtheroRemo ConsortiumMarcus E Kleber, Ilkka Seppälä, Stefan Pilz, et al.
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