Sox11 is required to maintain proper levels of Hedgehog signaling during vertebrate ocular morphogenesis von Pillai-Kastoori, Lakshmi, Wen, Wen, Wilson, Stephen G, Strachan, Erin, Lo-Castro, Adriana, Fichera, Marco, Musumeci, Sebastiano A, Lehmann, Ordan J, Morris, Ann C

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Mutations in PIK3R1 Cause SHORT Syndrome von Dyment, David A., Smith, Amanda C., Alcantara, Diana, Schwartzentruber, Jeremy A., Basel-Vanagaite, Lina, Curry, Cynthia J., Temple, I. Karen, Reardon, William, Mansour, Sahar, Haq, Mushfequr R., Gilbert, Rodney, Lehmann, Ordan J., Vanstone, Megan R., Beaulieu, Chandree L., Majewski, Jacek, Bulman, Dennis E., O’Driscoll, Mark, Boycott, Kym M., Innes, A. Micheil

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease von French, Curtis R, Seshadri, Sudha, Destefano, Anita L, Fornage, Myriam, Arnold, Corey R, Gage, Philip J, Skarie, Jonathan M, Dobyns, William B, Millen, Kathleen J, Liu, Ting, Dietz, William, Kume, Tsutomu, Hofker, Marten, Emery, Derek J, Childs, Sarah J, Waskiewicz, Andrew J, Lehmann, Ordan J

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foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish von Whitesell, Thomas R., Chrystal, Paul W., Ryu, Jae-Ryeon, Munsie, Nicole, Grosse, Ann, French, Curtis R., Workentine, Matthew L., Li, Rui, Zhu, Lihua Julie, Waskiewicz, Andrew, Lehmann, Ordan J., Lawson, Nathan D., Childs, Sarah J.

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Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling von Havrylov, Serhiy, Chrystal, Paul, van Baarle, Suey, French, Curtis R., MacDonald, Ian M., Avasarala, Jagannadha, Rogers, R. Curtis, Berry, Fred B., Kume, Tsutomu, Waskiewicz, Andrew J., Lehmann, Ordan J.

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

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Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth von Seo, Seungwoon, Singh, Hardeep P., Lacal, Pedro M., Sasman, Amy, Fatima, Anees, Liu, Ting, Schultz, Kathryn M., Losordo, Douglas W., Lehmann, Ordan J., Kume, Tsutomu

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Genetics and therapy for pediatric eye diseases von Chen, Holly.Y., Lehmann, Ordan J., Swaroop, Anand

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A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma von Liu, Chunqiao, Widen, Sonya A, Williamson, Kathleen A, Ratnapriya, Rinki, Gerth-Kahlert, Christina, Rainger, Joe, Alur, Ramakrishna P, Strachan, Erin, Manjunath, Souparnika H, Balakrishnan, Archana, Floyd, James A, Li, Tiansen, Waskiewicz, Andrew, Brooks, Brian P, Lehmann, Ordan J, FitzPatrick, David R, Swaroop, Anand

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Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies von Asai-Coakwell, Mika, March, Lindsey, Dai, Xiao Hua, Duval, Michele, Lopez, Irma, French, Curtis R, Famulski, Jakub, De Baere, Elfride, Francis, Peter J, Sundaresan, Periasamy, Sauvé, Yves, Koenekoop, Robert K, Berry, Fred B, Allison, W Ted, Waskiewicz, Andrew J, Lehmann, Ordan J

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GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies von Asai-Coakwell, Mika, French, Curtis R., Berry, Karyn M., Ye, Ming, Koss, Ron, Somerville, Martin, Mueller, Rosemary, van Heyningen, Veronica, Waskiewicz, Andrew J., Lehmann, Ordan J.

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Changes at CMAJ von Lehmann, Ordan J

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Disparities in healthcare utilisation rates for Aboriginal and non-Aboriginal Albertan residents, 1997-2006: a population database study von Chung, Helen, Ye, Ming, Hanson, Chris, Oladokun, Oluwaseun, Campbell, Michael J, Kramer, Gordon, Lehmann, Ordan J

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FoxC1 activates limbal epithelial stem cells following corneal epithelial debridement von Yang, Wending, Lee, Sun Kyong, Lehmann, Ordan J., Wu, Zhijian, Hiriyanna, Suja, Swaroop, Anand, Lavker, Robert M., Peng, Han, Kume, Tsutomu

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BMP3 is a novel locus involved in the causality of ocular coloboma von Fox, Sabrina C., Widen, Sonya A., Asai-Coakwell, Mika, Havrylov, Serhiy, Benson, Matthew, Prichard, Lisa B., Baddam, Pranidhi, Graf, Daniel, Lehmann, Ordan J., Waskiewicz, Andrew J.

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FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation von Aldinger, Kimberly A, Lehmann, Ordan J, Hudgins, Louanne, Chizhikov, Victor V, Bassuk, Alexander G, Ades, Lesley C, Krantz, Ian D, Dobyns, William B, Millen, Kathleen J

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Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma von Lahola-Chomiak, Adrian A, Footz, Tim, Nguyen-Phuoc, Kim, Neil, Gavin J, Fan, Baojian, Allen, Keri F, Greenfield, David S, Parrish, Richard K, Linkroum, Kevin, Pasquale, Louis R, Leonhardt, Ralf M, Ritch, Robert, Javadiyan, Shari, Craig, Jamie E, Allison, W T, Lehmann, Ordan J, Walter, Michael A, Wiggs, Janey L

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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies von Ye, Ming, Berry-Wynne, Karyn M., Asai-Coakwell, Mika, Sundaresan, Periasamy, Footz, Tim, French, Curtis R., Abitbol, Marc, Fleisch, Valerie C., Corbett, Nathan, Allison, W. Ted, Drummond, Garry, Walter, Michael A., Underhill, T. Michael, Waskiewicz, Andrew J., Lehmann, Ordan J.

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A targeted approach to genome-wide studies reveals new genetic associations with central corneal thickness von Benson, Matthew D, Khor, Chiea C, Gage, Philip J, Lehmann, Ordan J

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Fox's in development and disease von Lehmann, Ordan J, Sowden, Jane C, Carlsson, Peter, Jordan, Tim, Bhattacharya, Shomi S

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