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Nature Communications|September 29, 2016
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing geneGijs van Ingen, Jin Li, André Goedegebure, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 29, 2014
Hyaluronan synthase 3 variant and anthracycline-related cardiomyopathy: a report from the children's oncology groupXuexia Wang, Wei Liu, Can-Lan Sun, et al.American Journal of Human Genetics|September 17, 2024
The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infantsHadley Stevens Smith, Bethany Zettler, Casie A Genetti, et al.American Journal of Respiratory and Critical Care Medicine|January 25, 2011
ANGPT2 genetic variant is associated with trauma-associated acute lung injury and altered plasma angiopoietin-2 isoform ratioNuala J Meyer, Mingyao Li, Rui Feng, et al.Cancer Research|February 22, 2012
Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicityKristopher R Bosse, Sharon J Diskin, Kristina A Cole, et al.JAMA Psychiatry|May 11, 2022
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental CohortAaron Alexander-Bloch, Guillaume Huguet, Laura M Schultz, et al.Journal of Biomedical Informatics|April 30, 2021
Genomic considerations for FHIR®; eMERGE implementation lessonsMullai Murugan, Lawrence J Babb, Casey Overby Taylor, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humansCai Qi, Irena Feng, Ana Rita Costa, et al.Nature Biotechnology|April 12, 2016
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseasesRong Chen, Lisong Shi, Jörg Hakenberg, et al.Nature Genetics|May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastomaMario Capasso, Marcella Devoto, Cuiping Hou, et al.Pageof 91