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Pediatrics|November 21, 2020
Severe Lymphatic Disorder Resolved With MEK Inhibition in a Patient With Noonan Syndrome and SOS1 MutationYoav Dori, Chris Smith, Erin Pinto, et al.Journal of Assisted Reproduction and Genetics|November 7, 2016
Copy number variation analysis reveals additional variants contributing to endometriosis developmentFernanda Mafra, Diego Mazzotti, Renata Pellegrino, et al.Plos One|February 14, 2009
Genomic landscape of a three-generation pedigree segregating affective disorderShuzhang Yang, Kai Wang, Brittany Gregory, et al.Brain, Behavior, and Immunity|February 25, 2026
Neuroinflammation as a driver of Down syndrome-associated Alzheimer's diseaseHui-Qi Qu, Asbjorg Osk Snorradottir, Alvaro Gutierrez-Uzquiza, et al.Scientific Reports|April 2, 2025
Sex-specific spirometry effects of adult COPD polygenic score in children with asthmaJelte Kelchtermans, Joseph M Collaco, Huiqi Qu, et al.Translational Psychiatry|February 3, 2018
Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the diseaseYichuan Liu, Xiao Chang, Chang-Gyu Hahn, et al.Psychiatric Genetics|April 9, 2009
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1AJosephine Elia, Mario Capasso, Zafar Zaheer, et al.Biochimica Et Biophysica Acta|June 19, 2016
Understanding the genetic and epigenetic basis of common variable immunodeficiency disorder through omics approachesJin Li, Zhi Wei, Yun R Li, et al.American Journal of Human Genetics|May 4, 2010
Interpretation of association signals and identification of causal variants from genome-wide association studiesKai Wang, Samuel P Dickson, Catherine A Stolle, et al.HGG Advances|March 29, 2022
Maternal effect genes as risk factors for congenital heart defectsFadi I Musfee, Omobola O Oluwafemi, A J Agopian, et al.Pageof 91