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Katie Weihbrecht
Katie Weihbrecht
Visual Sciences
Genetics
Biology
Polydactyly
Retinal degeneration
Joubert syndrome
3
Papers
202
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Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse model
2018
PLOS ONE
Katie Weihbrecht
Wesley A. Goar
Calvin S. Carter
Val C. Sheffield
Seongjin Seo
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Citations (5)
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye
2017
Medical research archives
Katie Weihbrecht
Wesley A. Goar
Thomas Pak
Janelle E. Garrison
Adam P. DeLuca
Edwin M. Stone
Todd E. Scheetz
Val C. Sheffield
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Citations (31)
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting
2012
Proceedings of the National Academy of Sciences of the United States of America
Melissa C. Humbert
Katie Weihbrecht
Charles Searby
Yalan Li
Robert M. Pope
Val C. Sheffield
Seongjin Seo
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Citations (166)
1