Sanaa Muheisen

Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes

Linda M. Reis, Rebecca C. Tyler, Sanaa Muheisen et al. · Human Genetics · 2013 · 84 citations · Full text

Biology, Dominant Cataract, Allelic Variant +6

Mutations in MAB21L2 Result in Ocular Coloboma, Microcornea and Cataracts

Brett Deml, Ariana Kariminejad, Razieh H. R. Borujerdi et al. · PLoS Genetics · 2015 · 60 citations · Full text

Ocular Coloboma Results, Ocular Disease, Family Members +19

PITX2 deficiency and associated human disease: insights from the zebrafish model

Kathryn Hendee, Sanaa Muheisen, Linda M. Reis et al. · Human Molecular Genetics · 2018 · 58 citations · Full text

Genetics, Experimental Pathology, Pathology +21

Immobilized probe and glass surface chemistry as variables in microarray fabrication

Martin J. Hessner, Lisa Meyer, Jennifer Tackes et al. · BMC Genomics · 2004 · 42 citations · Full text

<i>EFTUD2</i> deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish model

Brett Deml, Linda M. Reis, Sanaa Muheisen et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2015 · 39 citations · Full text