Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease von Fujinami, Kaoru, MD, Zernant, Jana, MS, Chana, Ravinder K., BSc, Wright, Genevieve A., BSc, Tsunoda, Kazushige, MD, PhD, Ozawa, Yoko, MD, PhD, Tsubota, Kazuo, MD, PhD, Robson, Anthony G., PhD, Holder, Graham E., PhD, Allikmets, Rando, PhD, Michaelides, Michel, MD, FRCOphth, Moore, Anthony T., FRCS, FRCOphth

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Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom von Pontikos, Nikolas, Arno, Gavin, Jurkute, Neringa, Schiff, Elena, Ba-Abbad, Rola, Malka, Samantha, Gimenez, Ainoa, Georgiou, Michalis, Wright, Genevieve, Armengol, Monica, Knight, Hannah, Katz, Menachem, Moosajee, Mariya, Yu-Wai-Man, Patrick, Moore, Anthony T., Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.

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Running off the road: roadside non-native plants invading mountain vegetation von McDougall, Keith L., Lembrechts, Jonas, Rew, Lisa J., Haider, Sylvia, Cavieres, Lohengrin A., Kueffer, Christoph, Milbau, Ann, Naylor, Bridgett J., Nuñez, Martin A., Pauchard, Anibal, Seipel, Tim, Speziale, Karina L., Wright, Genevieve T., Alexander, Jake M.

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Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans von Li, Zheng, Sergouniotis, Panagiotis I., Michaelides, Michel, Mackay, Donna S., Wright, Genevieve A., Devery, Sophie, Moore, Anthony T., Holder, Graham E., Robson, Anthony G., Webster, Andrew R.

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IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History von SEN, SAGNIK, FABOZZI, LORENZO, FUJINAMI, KAORU, FUJINAMI-YOKOKAWA, YU, WRIGHT, GENEVIEVE A., WEBSTER, ANDREW, MAHROO, OMAR, ROBSON, ANTHONY G., GEORGIOU, MICHALIS, MICHAELIDES, MICHEL

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Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans von Burgess, Rosemary, Millar, Ian D., Leroy, Bart P., Urquhart, Jill E., Fearon, Ian M., De Baere, Elfrida, Brown, Peter D., Robson, Anthony G., Wright, Genevieve A., Kestelyn, Philippe, Holder, Graham E., Webster, Andrew R., Manson, Forbes D.C., Black, Graeme C.M.

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Rapid upwards spread of non-native plants in mountains across continents von Iseli, Evelin, Chisholm, Chelsea, Lenoir, Jonathan, Haider, Sylvia, Seipel, Tim, Barros, Agustina, Hargreaves, Anna L., Kardol, Paul, Lembrechts, Jonas J., McDougall, Keith, Rashid, Irfan, Rumpf, Sabine B., Arévalo, José Ramón, Cavieres, Lohengrin, Daehler, Curtis, Dar, Pervaiz A., Endress, Bryan, Jakobs, Gabi, Jiménez, Alejandra, Küffer, Christoph, Mihoc, Maritza, Milbau, Ann, Morgan, John W., Naylor, Bridgett J., Pauchard, Aníbal, Ratier Backes, Amanda, Reshi, Zafar A., Rew, Lisa J., Righetti, Damiano, Shannon, James M., Valencia, Graciela, Walsh, Neville, Wright, Genevieve T., Alexander, Jake M.

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Phenotypic Variability in RDH5 Retinopathy (Fundus Albipunctatus) von Sergouniotis, Panagiotis I., MD, Sohn, Elliott H., MD, Li, Zheng, PhD, McBain, Vikki A., PhD, Wright, Genevieve A., BSc, Moore, Anthony T., MA, FRCOphth, Robson, Anthony G., PhD, Holder, Graham E., PhD, Webster, Andrew R., MD, FRCOphth

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Social Calls Predict Foraging Success in Big Brown Bats von Wright, Genevieve Spanjer, Chiu, Chen, Xian, Wei, Wilkinson, Gerald S., Moss, Cynthia F.

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Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly von Hull, Sarah, Arno, Gavin, Ostergaard, Pia, Pontikos, Nikolas, Robson, Anthony G., Webster, Andrew R., Hogg, Chris R., Wright, Genevieve A., Henderson, Robert H.H., Martin, Carol-Anne, Jackson, Andrew P., Mansour, Sahar, Moore, Anthony T., Michaelides, Michel

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RP1L1 Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy von Davidson, Alice E., Sergouniotis, Panagiotis I., Mackay, Donna S., Wright, Genevieve A., Waseem, Naushin H., Michaelides, Michel, Holder, Graham E., Robson, Anthony G., Moore, Anthony T., Plagnol, Vincent, Webster, Andrew R.

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Enhanced Learning and Memory in Patients with CRB1 Retinopathy von Wright, Genevieve A, Rodriguez-Martinez, Ana Catalina, Conn, Hanne, Matarin, Mar, Thompson, Pamela, Moore, Anthony T, Ba-Abbad, Rola, Webster, Andrew R, Moosajee, Mariya

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ABCA4 gene screening by next-generation sequencing in a British cohort von Fujinami, Kaoru, Zernant, Jana, Chana, Ravinder K, Wright, Genevieve A, Tsunoda, Kazushige, Ozawa, Yoko, Tsubota, Kazuo, Webster, Andrew R, Moore, Anthony T, Allikmets, Rando, Michaelides, Michel

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Conservation and genomic diversity of a rare tree, Eucalyptus imlayensis (Myrtaceae), regenerating after wildfire von Simmons, C. Laura, Wright, Genevieve T, Mcdougall, Keith L, James, Elizabeth A

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Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy von Tan, Mei Hong, Mackay, Donna S, Cowing, Jill, Tran, Hoai Viet, Smith, Alexander J, Wright, Genevieve A, Dev-Borman, Arundhati, Henderson, Robert H, Moradi, Phillip, Russell-Eggitt, Isabelle, MacLaren, Robert E, Robson, Anthony G, Cheetham, Michael E, Thompson, Dorothy A, Webster, Andrew R, Michaelides, Michel, Ali, Robin R, Moore, Anthony T

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Think globally, measure locally: The MIREN standardized protocol for monitoring plant species distributions along elevation gradients von Haider, Sylvia, Lembrechts, Jonas J., McDougall, Keith, Pauchard, Aníbal, Alexander, Jake M., Barros, Agustina, Cavieres, Lohengrin A., Rashid, Irfan, Rew, Lisa J., Aleksanyan, Alla, Arévalo, José R., Aschero, Valeria, Chisholm, Chelsea, Clark, V. Ralph, Clavel, Jan, Daehler, Curtis, Dar, Pervaiz A., Dietz, Hansjörg, Dimarco, Romina D., Edwards, Peter, Essl, Franz, Fuentes‐Lillo, Eduardo, Guisan, Antoine, Gwate, Onalenna, Hargreaves, Anna L., Jakobs, Gabi, Jiménez, Alejandra, Kardol, Paul, Kueffer, Christoph, Larson, Christian, Lenoir, Jonathan, Lenzner, Bernd, Padrón Mederos, Miguel A., Mihoc, Maritza, Milbau, Ann, Morgan, John W., Müllerová, Jana, Naylor, Bridgett J., Nijs, Ivan, Nuñez, Martin A., Otto, Rüdiger, Preuk, Niels, Ratier Backes, Amanda, Reshi, Zafar A., Rumpf, Sabine B., Sandoya, Verónica, Schroder, Mellesa, Speziale, Karina L., Urbach, Davnah, Valencia, Graciela, Vandvik, Vigdis, Vitková, Michaela, Vorstenbosch, Tom, Walker, Tom W. N., Walsh, Neville, Wright, Genevieve, Zong, Shengwei, Seipel, Tim

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Social learning of a novel foraging task by big brown bats, Eptesicus fuscus von Wright, Genevieve Spanjer, Wilkinson, Gerald S., Moss, Cynthia F.

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Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for Therapy von Wright, Genevieve A., Georgiou, Michalis, Robson, Anthony G., Ali, Naser, Kalhoro, Ambreen, Holthaus, SM Kleine, Pontikos, Nikolas, Oluonye, Ngozi, de Carvalho, Emanuel R., Neveu, Magella M., Weleber, Richard G., Michaelides, Michel

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Investigating Splice Defects in USH2A Using Targeted Long-Read Sequencing von Chandrasekhar, Shwetha, Lin, Siying, Jurkute, Neringa, Oprych, Kathryn, Estramiana Elorrieta, Leire, Schiff, Elena, Malka, Samantha, Wright, Genevieve, Michaelides, Michel, Mahroo, Omar A, Webster, Andrew R, Arno, Gavin

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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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