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A Mutation in Sigma-1 Receptor Causes Juvenile Amyotrophic Lateral SclerosisAL-SAIF, Amr; AL-MOHANNA, Futwan; BOHLEGA, Saeed et al.Annals of neurology. 2011, Vol 70, Num 6, pp 913-919, issn 0364-5134, 7 p.Article

Linkage of a Mild Late-Onset Phenotype of Fuchs Corneal Dystrophy to a Novel Locus at 5q33.1-q35.2AMER RIAZUDDIN, S; EGHRARI, Allen O; AL-SAIF, Amr et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 12, pp 5667-5671, issn 0146-0404, 5 p.Article

Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extra pyramidal SyndromeALAZAMI, Anas M; AL-SAIF, Amr; BALTUS, Andy et al.American journal of human genetics. 2008, Vol 83, Num 6, pp 684-691, issn 0002-9297, 8 p.Article

Missense Mutations in TCF8 Cause Late-Onset Fuchs Corneal Dystrophy and Interact with FCD4 on Chromosome 9pAMER RIAZUDDIN, S; ZAGHLOUL, Norann A; AFSHARI, Natalie et al.American journal of human genetics. 2010, Vol 86, Num 1, pp 45-53, issn 0002-9297, 9 p.Article