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European Journal of Endocrinology|April 25, 2014
Adiponectin gene variants and the risk of coronary heart disease: a 16-year longitudinal studyChloe Y Y Cheung, Elaine Y L Hui, Bernard M Y Cheung, et al.Cell Genomics|February 13, 2023
Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversityKristin Tsuo, Wei Zhou, Ying Wang, et al.Spine|December 24, 2005
The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degenerationJeffrey J T Jim, Noora Noponen-Hietala, Kenneth M C Cheung, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 16, 2009
Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese populationHon-Cheong So, Pui Y Fong, Ronald Y L Chen, et al.BMC Medical Genetics|July 17, 2015
Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicismWei Liu, John K L Wong, Qiuming He, et al.Cell Reports|February 27, 2020
Directed Differentiation of Notochord-like and Nucleus Pulposus-like Cells Using Human Pluripotent Stem CellsYuelin Zhang, Zhao Zhang, Peikai Chen, et al.Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.Gigascience|August 31, 2018
PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statisticsJie Zheng, Tom G Richardson, Louise A C Millard, et al.BMC Cancer|May 13, 2020
Knowledge-based analyses reveal new candidate genes associated with risk of hepatitis B virus related hepatocellular carcinomaDeke Jiang, Jiaen Deng, Changzheng Dong, et al.Human Genetics|June 3, 2019
Estimation of metabolic syndrome heritability in three large populations including full pedigree and genomic informationFrancesca Graziano, Ginevra Biino, Maria Teresa Bonati, et al.Pageof 50