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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 26, 2018
Biomarkers of agitation and aggression in Alzheimer's disease: A systematic reviewMyuri Ruthirakuhan, Krista L Lanctôt, Matteo Di Scipio, et al.Current Atherosclerosis Reports|April 4, 2024
What Causes Premature Coronary Artery Disease?Ann Le, Helen Peng, Danielle Golinsky, et al.The Canadian Journal of Cardiology|April 5, 2024
Genetic Determinants of Vascular DementiaNazia Pathan, Muskaan Kaur Kharod, Sajjha Nawab, et al.Genes|March 28, 2024
The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future DirectionsAlice Man, Matteo Di Scipio, Shan Grewal, et al.Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|March 15, 2018
CDC42 regulates the expression of superficial zone molecules in part through the actin cytoskeleton and myocardin-related transcription factor-AElizabeth Delve, Justin Parreno, Vivian Co, et al.Ophthalmic Genetics|July 22, 2020
CRB1-related retinopathy overlapping the ocular phenotype of S-adenosylhomocysteine hydrolase deficiencyMonika K Grudzinska Pechhacker, Matteo Di Scipio, Anjali Vig, et al.American Journal of Medical Genetics. Part A|September 26, 2024
Diagnosis of TET3-Related Beck-Fahrner Syndrome in an Individual With Chorioretinal and Iris Colobomata Using a DNA Methylation SignatureAlice Man, Matteo Di Scipio, Haley McConkey, et al.Pediatric Neurology|October 9, 2024
Severe Epilepsy in an Individual With a TSC2 R905Q Variant Prompting Late Diagnosis in Affected Family MembersAlice Man, Matteo Di Scipio, Breanne Dale, et al.European Journal of Epidemiology|March 12, 2025
Identification of effect modifiers using a stratified Mendelian randomization algorithmic frameworkAlice Man, Leona Knüsel, Josef Graf, et al.Nature Communications|February 9, 2024
A method to estimate the contribution of rare coding variants to complex trait heritabilityNazia Pathan, Wei Q Deng, Matteo Di Scipio, et al.Pageof 2