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Molecular Psychiatry|July 27, 2016
Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disabilityS Riazuddin, M Hussain, A Razzaq, et al.Parkinsonism & Related Disorders|August 2, 2022
Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohortDouglas P Loesch, Andrea R V R Horimoto, Elif Irem Sarihan, et al.Molecular Psychiatry|September 2, 2018
Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disabilityS Riazuddin, M Hussain, A Razzaq, et al.Nature Communications|March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencingAndreas Keller, Angela Graefen, Markus Ball, et al.Annals of Neurology|July 6, 2021
Characterizing the Genetic Architecture of Parkinson's Disease in LatinosDouglas P Loesch, Andrea R V R Horimoto, Karl Heilbron, et al.JAMA|June 21, 2001
Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis: a randomized controlled trialL Y Agodoa, L Appel, G L Bakris, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 5, 2020
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease PatientsElif Irem Sarihan, Eduardo Pérez-Palma, Lisa-Marie Niestroj, et al.Frontiers in Genetics|October 11, 2021
Tracing the Distribution of European Lactase Persistence Genotypes Along the AmericasAna Cecília Guimarães Alves, Natalie Mary Sukow, Gabriel Adelman Cipolla, et al.Nature Genetics|August 4, 2009
Mutations in PYCR1 cause cutis laxa with progeroid featuresBruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.Science (New York, N.Y.)|August 13, 2021
Population sequencing data reveal a compendium of mutational processes in the human germ lineVladimir B Seplyarskiy, Ruslan A Soldatov, Evan Koch, et al.Pageof 84