Mais Hashem

Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus

Sulaiman M. Al‐Mayouf, Asma Sunker, Reem Abdwani et al. · Nature Genetics · 2011 · 463 citations

Chromatin, Genome Instability, Autoimmune Disease +13

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

Leen Abu‐Safieh, May Alrashed, Shamsa Anazi et al. · Genome Research · 2012 · 277 citations · Full text

Rd Families, Genetics, Genetic Epidemiology +18

Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield

Shams Anazi, Sateesh Maddirevula, Eissa Faqeih et al. · Molecular Psychiatry · 2016 · 254 citations

Intellectual Impairment, Medicine, Genetics +6

Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes

Hanan E. Shamseldin, Muneera Alshammari, Tarfa Al‐Sheddi et al. · Journal of Medical Genetics · 2012 · 180 citations

Expanding the genetic heterogeneity of intellectual disability

Shams Anazi, Sateesh Maddirevula, Vincenzo Salpietro et al. · Human Genetics · 2017 · 173 citations

Intellectual Impairment, Genetics, Disability +6