Linda S. Weaving
University of Oxford(GB)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Epigenetics and DNA Methylation, Diabetes Treatment and Management, Family and Disability Support Research
Most-Cited Works
- → Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation(2004)498 cited
- → Rett syndrome: clinical review and genetic update(2005)212 cited
- → Effects ofMECP2mutation type, location and X‐inactivation in modulating Rett syndrome phenotype(2002)115 cited
- → Arts Syndrome Is Caused by Loss-of-Function Mutations in PRPS1(2007)104 cited
- → MECP2 and Beyond: Phenotype—Genotype Correlations in Rett Syndrome(2003)36 cited
- → Epigenetic Effects on Transgene Expression(2003)36 cited
- → Health Service Use in Rett Syndrome(2005)20 cited
- → Twist2: Role in Corneal Stromal Keratocyte Proliferation and Corneal Thickness(2010)13 cited
- → Trisomy 21 and Rett syndrome: A double burden(2004)8 cited
- → Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase α sites(2006)8 cited