Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorderHolger Hengel, Lüdger Schöls, Shabab B. Hannan et al.|The American Journal of Human Genetics|2021Cited by 17
Autism-associated biomarkers: test–retest reliability and relationship to quantitative social trait variation in rhesus monkeysOzge Oztan, Karen J. Parker, Elliott H. Sherr et al.|Molecular Autism|2021Cited by 14
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disordersFranziska Langhammer, Fuad Al Mutairi, Reza Maroofian et al.|Genetics in Medicine|2023Cited by 12
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomaliesAndrea Accogli, Reza Maroofian, Maha S. Zaki et al.|Brain Communications|2023Cited by 6