Paranchai Boonsawat

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny Lai et al. · Genetics in Medicine · 2021 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly

Paranchai Boonsawat, Pascal Joset, Katharina Steindl et al. · Genetics in Medicine · 2019 · 86 citations · Full text

Life Sciences, Genetics, Neuroscience +17

De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder

Anne Gregor, Lynette G. Sadleir, Reza Asadollahi et al. · The American Journal of Human Genetics · 2018 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling

Reza Asadollahi, Justin E Strauss, Martin Zenker et al. · European Journal of Human Genetics · 2018 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Pathogenic <i>SCN2A</i> variants cause early-stage dysfunction in patient-derived neurons

Reza Asadollahi, Igor Delvendahl, Roman Muff et al. · Human Molecular Genetics · 2023 · 30 citations · Full text

Life Sciences, Genetics, Neuroscience +17