Lucy R. Osborne
0000-0003-1152-1568
Publication & Citation Trends
Publications
0 total
367. Inspire 7: Intellectual Disability Polygenic Risk Evaluation in 7q11.23 Deletion Syndrome
Cited by 0
Semantic Scholar
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders
Cited by 2
Semantic Scholar
Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome OA
Cited by 1
Semantic Scholar
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotyping OA
Cited by 0
Semantic Scholar
DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number OA
Cited by 4
Semantic Scholar
Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome OA
Cited by 45
Semantic Scholar
Behavioral Genetics of the Mouse: Williams syndrome
Cited by 0
Semantic Scholar
Research Topics
Williams Syndrome Research
(54)
Congenital heart defects research
(20)
Genetics and Neurodevelopmental Disorders
(12)
Genomic variations and chromosomal abnormalities
(11)
Nuclear Receptors and Signaling
(9)
Affiliations
University of New Brunswick
Institute of Molecular Biotechnology
Mount Sinai Hospital
National Institutes of Health
Austrian Academy of Sciences