Michael J. Lyons
Greenwood Genetic Center(US)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, RNA modifications and cancer, Epigenetics and DNA Methylation
Most-Cited Works
- → Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome(2007)445 cited
- → Health Supervision for Children With Neurofibromatosis Type 1(2019)228 cited
- → Health Care Supervision for Children With Williams Syndrome(2020)202 cited
- → Clinical spectrum of individuals with pathogenic N F1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1(2019)131 cited
- → Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome(2019)125 cited
- → Health Supervision for People With Achondroplasia(2020)114 cited
- → BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects(2009)108 cited
- → Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A(2015)104 cited
- → Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients(2020)96 cited
- → Efficient and Robust Paramyxoviridae Reverse Genetics Systems(2017)92 cited