Paranchai Boonsawat

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 · 82 citations · Full text

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 · 79 citations · Full text

Neurodevelopmental Disorders, Syndromic Autism, Medicine +13

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 · 51 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, F-box Protein Fbxo11 +15

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 · 35 citations · Full text

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 · 29 citations · Full text