Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy von Poulter, James A., Ali, Manir, Gilmour, David F., Rice, Aine, Kondo, Hiroyuki, Hayashi, Kenshi, Mackey, David A., Kearns, Lisa S., Ruddle, Jonathan B., Craig, Jamie E., Pierce, Eric A., Downey, Louise M., Mohamed, Moin D., Markham, Alexander F., Inglehearn, Chris F., Toomes, Carmel

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Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta von Parry, David A., Mighell, Alan J., El-Sayed, Walid, Shore, Roger C., Jalili, Ismail K., Dollfus, Hélène, Bloch-Zupan, Agnes, Carlos, Roman, Carr, Ian M., Downey, Louise M., Blain, Katharine M., Mansfield, David C., Shahrabi, Mehdi, Heidari, Mansour, Aref, Parissa, Abbasi, Mohsen, Michaelides, Michel, Moore, Anthony T., Kirkham, Jennifer, Inglehearn, Chris F.

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Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy von Poulter, James A., Ali, Manir, Gilmour, David F., Rice, Aine, Kondo, Hiroyuki, Hayashi, Kenshi, Mackey, David A., Kearns, Lisa S., Ruddle, Jonathan B., Craig, Jamie E., Pierce, Eric A., Downey, Louise M., Mohamed, Moin D., Markham, Alexander F., Inglehearn, Chris F., Toomes, Carmel

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Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q von Toomes, Carmel, Bottomley, Helen M., Jackson, Richard M., Towns, Katherine V., Scott, Sheila, Mackey, David A., Craig, Jamie E., Jiang, Li, Yang, Zhenglin, Trembath, Richard, Woodruff, Geoffrey, Gregory-Evans, Cheryl Y., Gregory-Evans, Kevin, Parker, Michael J., Black, Graeme C.M., Downey, Louise M., Zhang, Kang, Inglehearn, Chris F.

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Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR von Panagiotou, Evangelia S., Sanjurjo Soriano, Carla, Poulter, James A., Lord, Emma C., Dzulova, Denisa, Kondo, Hiroyuki, Hiyoshi, Atsushi, Chung, Brian Hon-Yin, Chu, Yoyo Wing-Yiu, Lai, Connie H.Y., Tafoya, Mark E., Karjosukarso, Dyah, Collin, Rob W.J., Topping, Joanne, Downey, Louise M., Ali, Manir, Inglehearn, Chris F., Toomes, Carmel

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Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR) von Poulter, James A, Davidson, Alice E, Ali, Manir, Gilmour, David F, Parry, David A, Mintz-Hittner, Helen A, Carr, Ian M, Bottomley, Helen M, Long, Vernon W, Downey, Louise M, Sergouniotis, Panagiotis I, Wright, Genevieve A, MacLaren, Robert E, Moore, Anthony T, Webster, Andrew R, Inglehearn, Chris F, Toomes, Carmel

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Importance of Anatomical Efficacy for Disease Control in Neovascular AMD: An Expert Opinion von Balaskas, Konstantinos, Amoaku, Winfried M., Cudrnak, Tomas, Downey, Louise M., Groppe, Markus, Mahmood, Sajjad, Mehta, Hemal, Mohamed, Quresh, Mushtaq, Bushra, Severn, Philip, Vardarinos, Athanasios, Yang, Yit C.

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Spectrum and Frequency of FZD4 Mutations in Familial Exudative Vitreoretinopathy von Toomes, Carmel, Bottomley, Helen M, Scott, Sheila, Mackey, David A, Craig, Jamie E, Appukuttan, Binoy, Stout, J. Timothy, Flaxel, Christina J, Zhang, Kang, Black, Graeme C. M, Fryer, Alan, Downey, Louise M, Inglehearn, Chris F

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Familial Exudative Vitreoretinopathy and DiGeorge Syndrome: A New Locus for Familial Exudative Vitreoretinopathy on Chromosome 22q11.2? von GILMOUR, David F, DOWNEY, Louise M, SHERIDAN, Eamonn, LONG, Vernon, BRADBURY, John, INGLEHEARN, Chris F, TOOMES, Carmel

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Familial Exudative Vitreoretinopathy and DiGeorge Syndrome von Gilmour, David F., FRCOphth, Downey, Louise M., FRCOphth, PhD, Sheridan, Eamonn, MBChB, Long, Vernon, FRCOphth, Bradbury, John, FRCOphth, Inglehearn, Chris F., PhD, Toomes, Carmel, PhD

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Comment on 'cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy' von Bottomley, Helen M, Downey, Louise M, Inglehearn, Chris F, Toomes, Carmel

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Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate von Downey, Louise M, Keen, T Jeffrey, Jalili, Ismail K, McHale, John, Aldred, Michael J, Robertson, Steven P, Mighell, Alan, Fayle, Steven, Wissinger, Bernd, Inglehearn, Chris F

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Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR) von Toomes, Carmel, Downey, Louise M, Bottomley, Helen M, Scott, Sheila, Woodruff, Geoffrey, Trembath, Richard C, Inglehearn, Chris F

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Analysis of the rdd locus in chicken: a model for human retinitis pigmentosa von Burt, David W, Morrice, David R, Lester, Douglas H, Robertson, Graeme W, Mohamed, Moin D, Simmons, Ian, Downey, Louise M, Thaung, Caroline, Bridges, Leslie R, Paton, Ian R, Gentle, Mike, Smith, Jacqueline, Hocking, Paul M, Inglehearn, Chris F

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Genetic, ophthalmic, morphometric and histopathological analysis of the Retinopathy Globe Enlarged (rge) chicken von Inglehearn, Chris F, Morrice, David R, Lester, Douglas H, Robertson, Graeme W, Mohamed, Moin D, Simmons, Ian, Downey, Louise M, Thaung, Caroline, Bridges, Leslie R, Paton, Ian R, Smith, Jacqueline, Petersen-Jones, Simon, Hocking, Paul M, Burt, David W

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Importance of Anatomical Efficacy for Disease Control in Neovascular AMD: An Expert Opinion von Of, Adis Journals On Behalf, Balaskas, Konstantinos, Amoaku, Winfried M, Cudrnak, Tomas, Downey, Louise M, Groppe, Markus, Mahmood, Sajjad, Hemal Mehta, Quresh Mohamed, Mushtaq, Bushra, Severn, Philip, Vardarinos, Athanasios, Yit C Yang

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Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal- Recessive ConeRod Dystrophy and Amelogenesis Imperfecta von Parry, David A, Mighell, Alan J, El-Sayed, Walid, Shore, Roger C, Jalili, Ismail K, Dollfus, Hélène, Bloch-Zupan, Agnes, Carlos, Roman, Carr, Ian M, Downey, Louise M, Blain, Katharine M, Mansfield, David C, Shahrabi, Mehdi, Heidari, Mansour, Aref, Parissa, Abbasi, Mohsen, Michaelides, Michel, Moore, Anthony T, Kirkham, Jennifer, Inglehearn, Chris F

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Importance of Anatomical Efficacy for Disease Control in Neovascular AMD: An Expert Opinion von Balaskas, Konstantinos, Amoaku, Winfried M, Cudrnak, Tomas, Downey, Louise M, Groppe, Markus, Mahmood, Sajjad, Mehta, Hemal, Mohamed, Quresh, Mushtaq, Bushra, Severn, Philip, Vardarinos, Athanasios, Yang, Yit C

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Spectrum and frequency of FZD4 mutations in fasnilial exudative vitreoretinopathy von TOOMES, Carmel, BOTTOMLEY, Helen M, FRYER, Alan, DOWNEY, Louise M, INGLEHEARN, Chris F, SCOTT, Sheila, MACKEY, David A, CRAIG, Jamie E, APPUKUTTAN, Binoy, STOUT, J. Timothy, FLAXEL, Christina J, KANG ZHANG, BLACK, Graeme C. M

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The ADVANCE study: a randomized study to evaluate the effects of cinacalcet plus low-dose vitamin D on vascular calcification in patients on hemodialysis von RAGGI, Paolo, CHERTOW, Glenn M, DEHMEL, Bastian, FLOEGE, Jiirgen, URENA TORRES, Pablo, CSIKY, Botond, NASO, Agostino, NOSSULI, Kaldun, MOUSTAFA, Moustafa, GOODMAN, William G, LOPEZ, Nicole, DOWNEY, Gerry

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