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Annals of Medicine|July 1, 2004
Triallelic inheritance: a bridge between Mendelian and multifactorial traitsErica R Eichers, Richard Alan Lewis, Nicholas Katsanis, 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.American Journal of Human Genetics|February 28, 2002
Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1Erica R Eichers, Jane S Green, David W Stockton, et al.Nature Genetics|August 24, 2004
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouseHeather M Kulaga, Carmen C Leitch, Erica R Eichers, et al.Vision Research|November 21, 2007
Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndromeMuhammad M Abd-El-Barr, Kristen Sykoudis, Sara Andrabi, et al.Human Genetics|June 24, 2006
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivityErica R Eichers, Muhammad M Abd-El-Barr, Richard Paylor, et al.Nature|October 2, 2003
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndromeStephen J Ansley, Jose L Badano, Oliver E Blacque, et al.Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.Pageof 1