Asma Sunker

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 · 479 citations

Life Sciences, Genetics, Molecular Genetics +14

Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome

Ranad Shaheen, Eissa Faqeih, Asma Sunker et al. · The American Journal of Human Genetics · 2011 · 141 citations · Full text

Life Sciences, Genetics, Molecular Biology +13

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies

Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya et al. · Genetics in Medicine · 2015 · 109 citations · Full text

Medicine, Genetics, Molecular Genetics +14

POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism

Ranad Shaheen, Eissa Faqeih, Hanan E. Shamseldin et al. · The American Journal of Human Genetics · 2012 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

A TCTN2 mutation defines a novel Meckel Gruber syndrome locus

Ranad Shaheen, Eissa Faqeih, Mohammed Zain Seidahmed et al. · Human Mutation · 2011 · 80 citations

Life Sciences, Genetics, Molecular Genetics +17