Bassem A. Bejjani

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Paweł Stankiewicz, Partha Sen, Samarth Bhatt et al. · The American Journal of Human Genetics · 2009 · 513 citations · Full text

Detection of low‐level mosaicism by array CGH in routine diagnostic specimens

Blake C. Ballif, Emily A. Rorem, Kyle Sundin et al. · American Journal of Medical Genetics Part A · 2006 · 359 citations

Array Cgh, Genetic Testing, Microscopy +28

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

Bassem A. Bejjani, Richard A. Lewis, Karim F. Tomey et al. · The American Journal of Human Genetics · 1998 · 319 citations · Full text

Ocular Disease, Ophthalmology, Genetic Disorder +9

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker, Blake C. Ballif, Erawati V. Bawle et al. · European Journal of Human Genetics · 2010 · 316 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

Blake C. Ballif, Aaron Theisen, Justine Coppinger et al. · Molecular Cytogenetics · 2008 · 303 citations · Full text