Evidence for additional FREM1 heterogeneity in Manitoba oculotrichoanal syndrome

por Mateo, Robertino Karlo, Johnson, Royce, Lehmann, Ordan J.
Publicado 2012

Genetics and therapy for pediatric eye diseases

por Chen, Holly.Y., Lehmann, Ordan J., Swaroop, Anand
Publicado 2021

Longitudinal fluorescent observation of retinal degeneration and regeneration in zebrafish using fundus lens imaging

por Duval, Michèle G., Chung, Helen, Lehmann, Ordan J., Allison, W. Ted
Publicado 2013

A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness

por Benson, Matthew D., Khor, Chiea C., Gage, Philip J., Lehmann, Ordan J.
Publicado 2017

Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I

por Zhou, Qi, Lenger, Chaeli, Smith, Richard, Kimberling, William J, Ye, Ming, Lehmann, Ordan, MacDonald, Ian
Publicado 2012

Disparities in Healthcare Utilisation Rates for Aboriginal and Non-Aboriginal Albertan Residents, 1997–2006: A Population Database Study

por Chung, Helen, Ye, Ming, Hanson, Chris, Oladokun, Oluwaseun, Campbell, Michael J., Kramer, Gordon, Lehmann, Ordan J.
Publicado 2012

Sox11 Is Required to Maintain Proper Levels of Hedgehog Signaling during Vertebrate Ocular Morphogenesis

por Pillai-Kastoori, Lakshmi, Wen, Wen, Wilson, Stephen G., Strachan, Erin, Lo-Castro, Adriana, Fichera, Marco, Musumeci, Sebastiano A., Lehmann, Ordan J., Morris, Ann C.
Publicado 2014

Morphogenetic defects underlie Superior Coloboma, a newly identified closure disorder of the dorsal eye

por Hocking, Jennifer C., Famulski, Jakub K., Yoon, Kevin H., Widen, Sonya A., Bernstein, Cassidy S., Koch, Sophie, Weiss, Omri, Agarwala, Seema, Inbal, Adi, Lehmann, Ordan J., Waskiewicz, Andrew J.
Publicado 2018

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning

por Chrystal, Paul W., French, Curtis R., Jean, Francesca, Havrylov, Serhiy, van Baarle, Suey, Peturson, Ann-Marie, Xu, Pengfei, Crump, J. Gage, Pilgrim, David B., Lehmann, Ordan J., Waskiewicz, Andrew J.
Publicado 2021

Mutation of SALL2 causes recessive ocular coloboma in humans and mice

por Kelberman, Daniel, Islam, Lily, Lakowski, Jörn, Bacchelli, Chiara, Chanudet, Estelle, Lescai, Francesco, Patel, Aara, Stupka, Elia, Buck, Anja, Wolf, Stephan, Beales, Philip L., Jacques, Thomas S., Bitner-Glindzicz, Maria, Liasis, Alki, Lehmann, Ordan J., Kohlhase, Jürgen, Nischal, Ken K., Sowden, Jane C.
Publicado 2014