Arif O. Khan

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 · 283 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

Mohammed A. Aldahmesh, Arif O. Khan, Hisham Alkuraya et al. · The American Journal of Human Genetics · 2013 · 128 citations · Full text

Medicine, Genetics, Molecular Genetics +12

In search of triallelism in Bardet–Biedl syndrome

Leen Abu‐Safieh, Shamsa Al-Anazi, Lama AlAbdi et al. · European Journal of Human Genetics · 2012 · 124 citations

Life Sciences, Genetics, Human Genetics +1

Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract

Nisha Patel, Deepti Anand, Dorota Monies et al. · Human Genetics · 2016 · 89 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

Julie C. Van De Weghe, Tamara D. S. Rusterholz, Brooke Latour et al. · The American Journal of Human Genetics · 2017 · 89 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10