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The Journal of Clinical Endocrinology and Metabolism|August 14, 2008
Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk associationChing-Lung Cheung, Pak C Sham, Vivian Chan, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|February 13, 2009
The heritability of attitude toward economic riskSongfa Zhong, Soo Hong Chew, Eric Set, et al.
Cell Genomics|August 8, 2022
Incorporating family history of disease improves polygenic risk scores in diverse populationsMargaux L A Hujoel, Po-Ru Loh, Benjamin M Neale, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 28, 2007
An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese populationHon-Cheong So, Ronald Y L Chen, Eric Y H Chen, et al.
Elife|September 1, 2021
Human genetic analyses of organelles highlight the nucleus in age-related trait heritabilityRahul Gupta, Konrad J Karczewski, Daniel Howrigan, et al.
Investigative Ophthalmology & Visual Science|May 22, 2009
Major genetic effects in glaucoma: commingling analysis of optic disc parameters in an older Australian populationLeonieke M E van Koolwijk, Paul R Healey, Roger A Hitchings, et al.
Plos Genetics|January 24, 2013
Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studiesMiao-Xin Li, Johnny S H Kwan, Su-Ying Bao, et al.
World Journal of Stem Cells|March 8, 2019
Rational use of mesenchymal stem cells in the treatment of autism spectrum disordersQiang Liu, Mo-Xian Chen, Lin Sun, et al.
Cerebral Cortex (New York, N.Y. : 1991)|August 6, 2024
Dysfunction of thalamocortical circuits in early-onset schizophreniaJia Cai, Min Xie, Sugai Liang, et al.
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