May 01, 1998 article Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex Nature DOI: 10.1038/30764 OpenAlex Authors 0 Author list not loaded yet. Cited by 8 stored of 3,475 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access DNMT1-mediated regulation of somatostatin-positive interneuron migration impacts cortical architecture and function 2025 Nature Communications article Neuroscience Neurogenesis and neuroplasticity mechanisms Open access 13 citations Epigenetic networks coordinate DNA methylation across the genome 2025 Molecular Therapy article Biochemistry, Genetics and Molecular Biology Epigenetics and DNA Methylation Open access 16 citations DNMT1-Mediated Regulation of Somatostatin-positive Interneuron Migration Impacts Cortical Architecture and Function 2024 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Neurogenesis and neuroplasticity mechanisms 0 citations The Deuterated “Magic Methyl” Group: A Guide to Site‐Selective Trideuteromethyl Incorporation and Labeling by Using CD3 Reagents 2021 Chemistry - A European Journal article Pharmacology, Toxicology and Pharmaceutics Chemical Reactions and Isotopes Open access cited by 2 patents 112 citations Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder 2021 The American Journal of Human Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access 26 citations A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration 2021 Scientific Data data-paper Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access 37 citations Bone fragility in patients affected by congenital diseases non skeletal in origin 2021 Orphanet Journal of Rare Diseases article Medicine Bone health and osteoporosis research Open access 12 citations Epigenomic Remodeling in Huntington’s Disease—Master or Servant? 2020 Epigenomes article Neuroscience Genetic Neurodegenerative Diseases Open access 11 citations 8 results References 0