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Molecular Genetics and Metabolism|June 4, 2011
Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutationsChristian P Schaaf, Maria Blazo, Richard Alan Lewis, et al.
Discover Mental Health|June 25, 2026
The effect of acceptance and commitment therapy on communication avoidance, emotional well-being, and hyperarousal in Iranian caregivers of women with advanced breast cancerManijeh Firoozi, Mehdi Sharifi, Christopher Alan Lewis, et al.
Investigative Ophthalmology & Visual Science|January 31, 2002
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblingsPaul S Bernstein, Mark Leppert, Nanda Singh, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
A genome-wide screen for copy number alterations in Aicardi syndromeXiaoling Wang, V Reid Sutton, Tanya N Eble, et al.
Ophthalmology|August 3, 2012
Risk of cataract in persons with cytomegalovirus retinitis and the acquired immune deficiency syndromeJohn H Kempen, Elizabeth A Sugar, Alice T Lyon, et al.
Investigative Ophthalmology & Visual Science|March 28, 2006
Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humansCarla Bidinost, Natalie Hernandez, Deepak P Edward, et al.
American Journal of Medical Genetics. Part A|February 9, 2010
Potocki-Shaffer syndrome: comprehensive clinical assessment, review of the literature, and proposals for medical managementDaniel T Swarr, Douglas Bloom, Richard Alan Lewis, et al.
American Journal of Human Genetics|May 23, 2002
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritanceNicholas Katsanis, Erica R Eichers, Stephen J Ansley, et al.
The Journal of Infectious Diseases|July 13, 2010
Effect of host genetics on the development of cytomegalovirus retinitis in patients with AIDSEfe Sezgin, Douglas A Jabs, Sher L Hendrickson, et al.
Nature|December 6, 2005
Dissection of epistasis in oligogenic Bardet-Biedl syndromeJose L Badano, Carmen C Leitch, Stephen J Ansley, et al.
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