Basamat Almoallem

Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus

Basamat Almoallem, Miriam Bauwens, Sophie Walraedt et al. · Investigative Ophthalmology & Visual Science · 2015 · 48 citations · Full text

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56

Basamat Almoallem, Gavin Arno, Julie De Zaeytijd et al. · Scientific Reports · 2020 · 34 citations · Full text

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement

Sabrina Méchaussier, Basamat Almoallem, Christina Zeitz et al. · The American Journal of Human Genetics · 2020 · 34 citations · Full text

Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus

Anja K. Mayer, Muhammad Mahajnah, Mervyn G. Thomas et al. · Brain · 2019 · 31 citations · Full text

Thumb Hypoplasia, Ocular Disease, Developmental Biology +12