Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder von Natera‐de Benito, Daniel, Jurgens, Julie A., Yeung, Alison, Zaharieva, Irina T., Manzur, Adnan, DiTroia, Stephanie P., Di Gioia, Silvio Alessandro, Pais, Lynn, Pini, Veronica, Barry, Brenda J., Chan, Wai‐Man, Elder, James E., Christodoulou, John, Hay, Eleanor, England, Eleina M., Munot, Pinki, Hunter, David G., Feng, Lucy, Ledoux, Danielle, O'Donnell‐Luria, Anne, Phadke, Rahul, Engle, Elizabeth C., Sarkozy, Anna, Muntoni, Francesco

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Graft‐versus‐host‐disease‐like disease in a patient with thymic lipomatosis von Lau, Yuk‐Ming, Trendell‐Smith, Nigel‐Jeremy, Yeung, Chi‐Keung, Wong, Sze‐Man, Chan, Hin‐Lee Henry, Chan, Wai‐Man Mandy

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Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance von Tischfield, Max A., Baris, Hagit N., Wu, Chen, Rudolph, Guenther, Van Maldergem, Lionel, He, Wei, Chan, Wai-Man, Andrews, Caroline, Demer, Joseph L., Robertson, Richard L., Mackey, David A., Ruddle, Jonathan B., Bird, Thomas D., Gottlob, Irene, Pieh, Christina, Traboulsi, Elias I., Pomeroy, Scott L., Hunter, David G., Soul, Janet S., Newlin, Anna, Sabol, Louise J., Doherty, Edward J., de Uzcátegui, Clara E., de Uzcátegui, Nicolas, Collins, Mary Louise Z., Sener, Emin C., Wabbels, Bettina, Hellebrand, Heide, Meitinger, Thomas, de Berardinis, Teresa, Magli, Adriano, Schiavi, Costantino, Pastore-Trossello, Marco, Koc, Feray, Wong, Agnes M., Levin, Alex V., Geraghty, Michael T., Descartes, Maria, Flaherty, Maree, Jamieson, Robyn V., Møller, H.U., Meuthen, Ingo, Callen, David F., Kerwin, Janet, Lindsay, Susan, Meindl, Alfons, Gupta, Mohan L., Pellman, David, Engle, Elizabeth C.

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Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome von MacKinnon, Sarah, MSc, OC(C), Oystreck, Darren T., MMedSci, OC(C), Andrews, Caroline, MS, Chan, Wai-Man, MS, Hunter, David G., MD, PhD, Engle, Elizabeth C., MD

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A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome von Di Gioia, Silvio Alessandro, Connors, Samantha, Matsunami, Norisada, Cannavino, Jessica, Rose, Matthew F., Gilette, Nicole M., Artoni, Pietro, de Macena Sobreira, Nara Lygia, Chan, Wai-Man, Webb, Bryn D., Robson, Caroline D., Cheng, Long, Van Ryzin, Carol, Ramirez-Martinez, Andres, Mohassel, Payam, Leppert, Mark, Scholand, Mary Beth, Grunseich, Christopher, Ferreira, Carlos R., Hartman, Tyler, Hayes, Ian M., Morgan, Tim, Markie, David M., Fagiolini, Michela, Swift, Amy, Chines, Peter S., Speck-Martins, Carlos E., Collins, Francis S., Jabs, Ethylin Wang, Bönnemann, Carsten G., Olson, Eric N., Carey, John C., Robertson, Stephen P., Manoli, Irini, Engle, Elizabeth C.

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Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects von Park, Jong G., Tischfield, Max A., Nugent, Alicia A., Cheng, Long, Di Gioia, Silvio Alessandro, Chan, Wai-Man, Maconachie, Gail, Bosley, Thomas M., Summers, C. Gail, Hunter, David G., Robson, Caroline D., Gottlob, Irene, Engle, Elizabeth C.

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Human CFEOM1 Mutations Attenuate KIF21A Autoinhibition and Cause Oculomotor Axon Stalling von Cheng, Long, Desai, Jigar, Miranda, Carlos J., Duncan, Jeremy S., Qiu, Weihong, Nugent, Alicia A., Kolpak, Adrianne L., Wu, Carrie C., Drokhlyansky, Eugene, Delisle, Michelle M., Chan, Wai-Man, Wei, Yan, Propst, Friedrich, Reck-Peterson, Samara L., Fritzsch, Bernd, Engle, Elizabeth C.

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Walking for transportation in Hong Kong Chinese urban elders: a cross-sectional study on what destinations matter and when von Cerin, Ester, Lee, Ka-yiu, Barnett, Anthony, Sit, Cindy H P, Cheung, Man-chin, Chan, Wai-man, Johnston, Janice M

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An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation von CEDERQUIST, Gustav Y, LUCHNIAK, Anna, GOMES, Lavier, FLAHERTY, Maree, GRANT, Patricia Ellen, GUPTA, Mohan L, ENGLE, Elizabeth C, TISCHFIELD, Max A, PEEVA, Maya, YUYU SONG, MENEZES, Manoj P, CHAN, Wai-Man, ANDREWS, Caroline, CHEW, Sheena, JAMIESON, Robyn V

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Aqueous Humor Levels of Vascular Endothelial Growth Factor and Pigment Epithelium–Derived Factor in Polypoidal Choroidal Vasculopathy and Choroidal Neovascularization von Tong, Jian-Ping, Chan, Wai-Man, Liu, David T.L., Lai, Timothy Y.Y., Choy, Kwong-Wai, Pang, Chi-Pui, Lam, Dennis S.C.

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Walking for Recreation and Perceptions of the Neighborhood Environment in Older Chinese Urban Dwellers von Cerin, Ester, Sit, Cindy H. P., Barnett, Anthony, Cheung, Man-chin, Chan, Wai-man

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Human Schwann cells exhibit long‐term cell survival, are not tumorigenic and promote repair when transplanted into the contused spinal cord von Bastidas, Johana, Athauda, Gagani, De La Cruz, Gabriela, Chan, Wai‐Man, Golshani, Roozbeh, Berrocal, Yerko, Henao, Martha, Lalwani, Anil, Mannoji, Chikato, Assi, Mazen, Otero, P. Anthony, Khan, Aisha, Marcillo, Alexander E., Norenberg, Michael, Levi, Allan D., Wood, Patrick M., Guest, James D., Dietrich, W. Dalton, Bartlett Bunge, Mary, Pearse, Damien D.

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Biallelic mutations in human DCC cause developmental split-brain syndrome von Jamuar, Saumya S, Schmitz-Abe, Klaus, D'Gama, Alissa M, Drottar, Marie, Chan, Wai-Man, Peeva, Maya, Servattalab, Sarah, Lam, Anh-Thu N, Delgado, Mauricio R, Clegg, Nancy J, Zayed, Zayed Al, Dogar, Mohammad Asif, Alorainy, Ibrahim A, Jamea, Abdullah Abu, Abu-Amero, Khaled, Griebel, May, Ward, Wendy, Lein, Ed S, Markianos, Kyriacos, Barkovich, A James, Robson, Caroline D, Grant, P Ellen, Bosley, Thomas M, Engle, Elizabeth C, Walsh, Christopher A, Yu, Timothy W

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Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development von Whitman, Mary C., Andrews, Caroline, Chan, Wai-Man, Tischfield, Max A., Stasheff, Steven F., Brancati, Francesco, Ortiz-Gonzalez, Xilma, Nuovo, Sara, Garaci, Francesco, MacKinnon, Sarah E., Hunter, David G., Grant, P. Ellen, Engle, Elizabeth C.

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Reliable and valid NEWS for Chinese seniors: measuring perceived neighborhood attributes related to walking von Cerin, Ester, Sit, Cindy Hp, Cheung, Man-Chin, Ho, Sai-Yin, Lee, Lok-Chun Janet, Chan, Wai-Man

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The therapeutic profile of rolipram, PDE target and mechanism of action as a neuroprotectant following spinal cord injury von Schaal, Sandra Marie, Garg, Maneesh Sen, Ghosh, Mousumi, Lovera, Lilie, Lopez, Michael, Patel, Monal, Louro, Jack, Patel, Samik, Tuesta, Luis, Chan, Wai-Man, Pearse, Damien Daniel

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Regional Variations in the Relationship between Macular Thickness Measurements and Myopia von Lam, Dennis Shun Chiu, Leung, King Sai, Mohamed, Shaheeda, Chan, Wai-man, Palanivelu, Mahesh Shanmugam, Cheung, Carol Yim Lui, Li, Emmy Yuen Mei, Lai, Ricky Yiu Kwong, Leung, Christopher Kai-shun

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Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles von Thomas, Mervyn G, Maconachie, Gail D E, Kuht, Helen J, Chan, Wai-Man, Sheth, Viral, Hisaund, Michael, McLean, Rebecca J, Barry, Brenda, Al-Diri, Bashir, Proudlock, Frank A, Tu, Zhanhan, Engle, Elizabeth C, Gottlob, Irene

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The effects of exposure to scenarios about dementia on stigma and attitudes toward dementia care in a Chinese community von Cheng, Sheung-Tak, Lam, Linda C. W., Chan, Liliane C. K., Law, Alexander C. B., Fung, Ada W. T., Chan, Wai-chi, Tam, Cindy W. C., Chan, Wai-man

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The well-being of community-dwelling near-centenarians and centenarians in Hong Kong: a qualitative study von Wong, Wai-Ching Paul, Lau, Hi-Po Bobo, Kwok, Chun-Fong Noel, Leung, Yee-Man Angela, Chan, Man-Yee Grace, Chan, Wai-Man, Cheung, Siu-Lan Karen

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