Publications by authors named "Erica Eichers"

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Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome.
Jonathan L Tobin, Matt Di Franco, Erica Eichers, Helen May-Simera, Monica Garcia

Proc Natl Acad Sci U S A· May 2008

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Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome.
Muhammad M Abd-El-Barr, Kristen Sykoudis, Sara Andrabi, Erica R Eichers, Mark E Pennesi

Vision Res· December 2007

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Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity.
Erica R Eichers, Muhammad M Abd-El-Barr, Richard Paylor, Richard Alan Lewis, Weimin Bi

Hum Genet· September 2006

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Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
Alison J Ross, Helen May-Simera, Erica R Eichers, Masatake Kai, Josephine Hill

Nat Genet· October 2005

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Triallelic inheritance: a bridge between Mendelian and multifactorial traits.
Erica R Eichers, Richard Alan Lewis, Nicholas Katsanis, James R Lupski

Ann Med· October 2004

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Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse.
Heather M Kulaga, Carmen C Leitch, Erica R Eichers, Jose L Badano, Alysa Lesemann

Nat Genet· September 2004

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Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.
Stephen J Ansley, Jose L Badano, Oliver E Blacque, Josephine Hill, Bethan E Hoskins, Erica R Eichers

Nature· October 2003

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BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance.
Nicholas Katsanis, Erica R Eichers, Stephen J Ansley, Richard Alan Lewis, Hülya Kayserili

Am J Hum Genet· July 2002

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Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1.
Erica R Eichers, Jane S Green, David W Stockton, Christopher S Jackman, James Whelan

Am J Hum Genet· April 2002

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