Amy Lawson‐Yuen

Familial deletion within NLGN4 associated with autism and Tourette syndrome

Amy Lawson‐Yuen, Juan‐Sebastian Saldivar, Steve S. Sommer et al. · European Journal of Human Genetics · 2008 · 270 citations · Full text

Neurodevelopmental Disorders, Psychiatry, Syndromic Autism +10

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı et al. · The Lancet Diabetes & Endocrinology · 2020 · 107 citations

Disease Characteristics, Disease Mechanism, Genetic Disorder +10

Ube3a mRNA and protein expression are not decreased in Mecp2 mutant mice

Amy Lawson‐Yuen, Daniel Liu, Liqun Han et al. · Brain Research · 2007 · 70 citations · Full text

Mecp2 Mutant Mice, Systems Biology, Signal Transduction +10

Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

Ferdy S. van Geest, Stefan Groeneweg, Erica L T van den Akker et al. · The Journal of Clinical Endocrinology & Metabolism · 2021 · 45 citations · Full text

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition

Mitchell R. Vollger, Jonas Korlach, Kiara C. Eldred et al. · Nature Genetics · 2025 · 27 citations · Full text

Biology, Bioinformatics, Chromatin +13