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Human Molecular Genetics|December 26, 2015
Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagusPuya Gharahkhani, Joyce Tung, David Hinds, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian populationSrujana Sahebjada, Maria Schache, Andrea J Richardson, et al.
Nucleic Acids Research|February 16, 2008
Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arraysStuart Macgregor, Zhen Zhen Zhao, Anjali Henders, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 18, 2026
Multi-Ancestry, Multitrait Polygenic Risk Scores for Myopia: Improved Accuracy and Clinical PotentialBenyapa Insawang, Guiyan Ni, Nicholas Clark, et al.
Psychological Medicine|September 19, 2019
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9Jackson G Thorp, Andries T Marees, Jue-Sheng Ong, et al.
Human Heredity|May 29, 2008
Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriagesMuhammad Ayub, Muhammad Irfan, Alan Maclean, et al.
Medrxiv : the Preprint Server for Health Sciences|February 23, 2026
Genome-wide association study of corneal dystrophy uncovers novel risk loci and enables improved polygenic prediction of Fuchs endothelial corneal dystrophyBenyapa Insawang, David A Mackey, Alex W Hewitt, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 3, 2009
Neuregulin 1 and age of onset in the major psychosesDaphne Voineskos, Vincenzo De Luca, Stuart Macgregor, et al.
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