Anthony T. Moore
1985–2025 年に発表
- 別表記
- Anthony T Moore
- 155
- 論文数
- 24,549
- 被引用数
- 90
- h 指数
- 153
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Biochemistry, Genetics and Molecular Biology67.5%
- Medicine24.4%
- Neuroscience4.9%
- Immunology and Microbiology1.6%
- Nursing0.5%
- Engineering0.4%
- その他0.7%
トピック
- Retinal Development and Disorders12.2%
- Retinal Diseases and Treatments7.9%
- Mitochondrial Function and Pathology5%
- CRISPR and Genetic Engineering2.3%
- ATP Synthase and ATPases Research2.2%
- Connexins and lens biology2.2%
- その他68.2%
共著者
- Andrew R. Webster53
- Michel Michaelides50
- Anthony G. Robson28
- Graham E. Holder26
- Alan C. Bird19
- Shomi S. Bhattacharya19
- Gavin Arno18
- David M. Hunt15
- John R.W. Yates13
- Panagiotis I. Sergouniotis13
- Donna S. Mackay11
- Sarah Hull10
- Valentina Cipriani10
- Vanita Berry10
- Genevieve Wright9
- Kathleen A. Williamson9
- Veronica van Heyningen9
- Vincent Plagnol9
- Alice E. Davidson8
- Alison J. Hardcastle8
- Graeme C. Black8
- Humma Shahid8
- Peter J. Francis8
- Eamonn R. Maher7
全論文
- Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom
著者: Nikolas Pontikos, Gavin Arno, Neringa Jurkutė, Elena Schiff, Rola Ba‐Abbad, Samantha Malka, Ainoa Gimenez, Michalis Georgiou, Genevieve Wright, Monica Armengol, Hannah Knight, Menachem Katz, Mariya Moosajee, Patrick Yu‐Wai‐Man, Anthony T. Moore, Michel Michaelides, Andrew R. Webster, Omar A. Mahroo - Ophthalmology 2020 被引用: 258
- Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis
著者: James Bainbridge, Manjit Mehat, Venki Sundaram, Scott Robbie, Susie E. Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M. Mowat, Stuart G. Beattie, Peter J. Gardner, Kecia L. Feathers, Vy Luong, Suzanne Yzer, Kamaljit S. Balaggan, Ananth C. Viswanathan, Thomy de Ravel, Ingele Casteels, Graham E. Holder, Nick Tyler, Fred W. Fitzke, Richard G. Weleber, Marko Nardini, Anthony T. Moore, Debra A. Thompson, Simon M. Petersen‐Jones, Michel Michaelides, L. Ingeborgh van den Born, Andrew Stockman, Alexander J. Smith, Gary S. Rubin, Robin R. Ali - New England Journal of Medicine 2015 被引用: 737
- Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
著者: James Bainbridge, Alexander J. Smith, Susie S. Barker, Scott Robbie, Robert Henderson, Kamaljit S. Balaggan, Ananth C. Viswanathan, Graham E. Holder, Andrew Stockman, Nick Tyler, Simon M. Petersen‐Jones, Shomi S. Bhattacharya, Adrian J. Thrasher, Fred W. Fitzke, Barrie J. Carter, Gary S. Rubin, Anthony T. Moore, Robin R. Ali - New England Journal of Medicine 2008 被引用: 1,919
- OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
著者: Christiane Alexander, Marcela Votruba, Ulrike E. A. Pesch, Dawn L. Thiselton, Simone Mayer, Anthony T. Moore, Miguel Rodríguez, Ulrich Kellner, Beate Leo‐Kottler, Georg Auburger, Shomi S. Bhattacharya, Bernd Wissinger - Nature Genetics 2000 被引用: 1,319
- Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
著者: Keren Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Mégy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka, Vincent Plagnol, Christopher J. Penkett, Kathleen Stirrups, Roberta Rizzo, Genevieve Wright, Dragana Josifova, Maria Bitner‐Glindzicz, Richard H. Scott, Emma Clement, Louise Allen, Ruth Armstrong, Angela F. Brady, Jenny Carmichael, Manali Chitre, Robert Henderson, Jane A. Hurst, Robert E. MacLaren, Elaine Murphy, Joan Paterson, Elisabeth Rosser, Dorothy Thompson, Emma Wakeling, Willem H. Ouwehand, Michel Michaelides, Anthony T. Moore, Andrew R. Webster, F. Lucy Raymond, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhan O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Nichola Cooper, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi, Charu Deshpande, Lisa Devlin, Eleanor Dewhurst, Rainer Döffinger, Natalie Dormand, Elizabeth Drewe ほか 211 名 - The American Journal of Human Genetics 2016 被引用: 484
- Germline selection shapes human mitochondrial DNA diversity
著者: Wei Wei, Salih Tuna, Michael J. Keogh, Katherine R. Smith, Katherine R. Smith, Timothy J. Aitman, Phil L. Beales, David Bennett, Daniel P. Gale, Maria A. K. Bitner-Glindzicz, Graeme C. Black, Paul Brennan, Perry Elliott, Frances Flinter, R. Andrés Floto, Henry Houlden, Melita Irving, Ania Koziell, Eamonn R. Maher, Hugh S. Markus, Nicholas W. Morrell, William G. Newman, Irene Roberts, John A. Sayer, Kenneth G. C. Smith, Kenneth G. C. Smith, Jenny C. Taylor, Hugh Watkins, Andrew R. Webster, Andrew O.M. Wilkie, Catherine Williamson, NIHR BioResource–Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot, Sofie Ashford, Christopher J. Penkett, Kathleen Stirrups, Augusto Rendon, Willem H. Ouwehand, John R. Bradley, F. Lucy Raymond, Mark Caulfield, Ernest Turro, Patrick F. Chinnery, Aarnoud Huissoon, Abigail Crisp-Hihn, Adam Shaw, Adam J. Mead, Adam P. Levine, Adrian J. Thrasher, Agnieszka Bierżyńska, Ahamad Hassan, Ajith Kumar, Alba Sanchis‐Juan, Alex Richter, Allan Lawrie, Amy Frary, Andrea H. Németh, Andrea Olschewski, Andreas C. Themistocleous, Andrew C. Browning, Andrew Mumford, Andrew M. Schaefer, Andrew Marshall, Andrew O.M. Wilkie, Andrew Peacock, Andrew R. Harper, Andrew R. Webster, Andrew S.C. Rice, Angela Pyle, Ania Koziell, Anna M. Drazyk, Anne M. Kelly, Annette Wagner, Anthony Attwood, Anthony De Soyza, Anthony M. Vandersteen, Anthony T. Moore, Anton Vonk Noordegraaf, Anupama Rao, Archana Herwadkar, Arjan C. Houweling, Arjune Sen, Augusto Rendon, Austen Worth, Barbara Girerd, Bella Madan, Brian T. Wilson, Carmen Bugarin Diz, Carmen Treacy, Carole Brewer, Carolyn Campbell, Carolyn M. Millar, Catherine Roughley, Catherine Titterton, Catherine Williamson, Cecilia Compton, Cesare Danesino, Chantal Thys, Charaka Hadinnapola, Charu Deshpande ほか 305 名 - Science 2019 被引用: 251
- Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
著者: Neruban Kumaran, Anthony T. Moore, Richard G. Weleber, Michel Michaelides - British Journal of Ophthalmology 2017 被引用: 335
- Complement C3 Variant and the Risk of Age-Related Macular Degeneration
著者: John R.W. Yates, Tiina Sepp, Baljinder K. Matharu, Jane C. Khan, Deborah A. Thurlby, Humma Shahid, David Clayton, Caroline Hayward, Joanne Morgan, Alan F. Wright, Ana Maria Armbrecht, Baljean Dhillon, Ian J. Deary, Elizabeth Redmond, Alan C. Bird, Anthony T. Moore - New England Journal of Medicine 2007 被引用: 828
- Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes
著者: Kamron N. Khan, Omar A. Mahroo, Rehna Khan, Moin Mohamed, Martin McKibbin, Alan C. Bird, Michel Michaelides, Adnan Tufail, Anthony T. Moore - Progress in Retinal and Eye Research 2016 被引用: 228
- Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups
著者: David A. Parfitt, Amelia Lane, Conor M. Ramsden, Amanda‐Jayne F. Carr, Peter Munro, Katarina Jovanović, Nele Schwarz, Naheed Kanuga, Manickam Nick Muthiah, Sarah Hull, Jean‐Marc Gallo, Lyndon da Cruz, Anthony T. Moore, Alison J. Hardcastle, Peter Coffey, Michael E. Cheetham - Cell stem cell 2016 被引用: 303
- The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies
著者: Samantha R. De Silva, Gavin Arno, Anthony G. Robson, Ana Fakin, Nikolas Pontikos, Moin Mohamed, Alan C. Bird, Anthony T. Moore, Michel Michaelides, Andrew R. Webster, Omar A. Mahroo - Progress in Retinal and Eye Research 2020 被引用: 151
- Increased circulating levels of Factor H-Related Protein 4 are strongly associated with age-related macular degeneration
著者: Valentina Cipriani, Laura Lorés‐Motta, Fan He, Dina Fathalla, Viranga Tilakaratna, Selina McHarg, Nadhim Bayatti, İlhan E. Acar, Carel B. Hoyng, Sascha Fauser, Anthony T. Moore, John R.W. Yates, Eiko K. de Jong, B. Paul Morgan, Anneke I. den Hollander, Paul N. Bishop, Simon J. Clark - Nature Communications 2020 被引用: 106
- Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in Patients with X-Linked Retinoschisis
著者: Mark E. Pennesi, Paul Yang, David G. Birch, Christina Y. Weng, Anthony T. Moore, Alessandro Iannaccone, Jason Comander, Thiran Jayasundera, Jeffrey D. Chulay, Jeffrey Chulay, Deanine Halliman, Matthew Feinsod, Mark Pennesi, Paul Yang, David Birch, Lea Bennett, Christina Y. Weng, Tahira Scholle, Roomasa Channa, Laura Baker, Jay Stewart, Anthony Moore, Alessandro Iannaccone, Priyatham Mettu, Lejla Vajzovic, K. Thiran Jayasundera, Jason Comander, Neil Bressler, Byron Lam - Ophthalmology Retina 2022 被引用: 73
- Seven new loci associated with age-related macular degeneration
著者: Lars G. Fritsche, Wei Chen, Matthew Schu, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson, Donald J. Zack, Satoshi Arakawa, Valentina Cipriani, Stephan Ripke, Robert P. Igo, Gabriëlle H.S. Buitendijk, Xueling Sim, Daniel E. Weeks, Robyn H. Guymer, Joanna E. Merriam, Peter J. Francis, Gregory Hannum, Anita Agarwal, Ana Maria Armbrecht, Isabelle Audo, Tin Aung, Gaetano R. Barile, Mustapha Benchaboune, Alan C. Bird, Valentina Cipriani, Kari Branham, Matthew Brooks, Alexander J. Brucker, William H. Cade, Melinda Cain, Peter A. Campochiaro, Chi Chao Chan, Ching‐Yu Cheng, Emily Y. Chew, Kimberly Chin, Itay Chowers, David Clayton, Radu Cojocaru, Yvette P. Conley, Belinda K. Cornes, Mark J. Daly, Baljean Dhillon, Albert O. Edwards, Εvangelos Εvangelou, Jesen Fagerness, Henry Ferreyra, James S. Friedman, Ásbjörg Geirsdóttir, Ronnie George, Christian Gieger, Neel Gupta, Stephanie A. Hagstrom, Simon Harding, Christos Haritoglou, John R. Heckenlively, Frank G. Holz, Guy Hughes, John P. A. Ioannidis, Tatsuro Ishibashi, Peronne Joseph, Gyungah Jun, Eranga N Vithana, Nicholas Katsanis, Claudia N. Keilhauer, Jane C. Khan, Ivana K. Kim, Yutaka Kiyohara, Barbara E.K. Klein, Ronald Klein, Jaclyn L. Kovach, Igor Kozak, Clara J. Lee, Kristine E. Lee, Peter Lichtner, Andrew Lotery, Thomas Meitinger, Paul Mitchell, Saddek Mohand‐Saïd, Anthony T. Moore, Denise J. Morgan, Margaux A. Morrison, Chelsea E. Myers, Adam C. Naj, Yusuke Nakamura, Yukinori Okada, Anton Orlin, Maria Carolina Ortube, Mohammad Othman, Chris Pappas, Kyu Hyung Park, Gayle J. Pauer, Neal S. Peachey, Olivier Poch, Rinki Ratna Priya, Robyn Reynolds, Andrea J. Richardson, Raymond Ripp, Guenther Rudolph, Euijung Ryu ほか 56 名 - Nature Genetics 2013 被引用: 803
- Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy
著者: Jasdeep Gill, Michalis Georgiou, Angelos Kalitzeos, Anthony T. Moore, Michel Michaelides - British Journal of Ophthalmology 2019 被引用: 194
- Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
著者: Susanne Kohl, Ditta Zobor, Wei‐Chieh Chiang, Nicole Weisschuh, Jennifer Staller, Irene González-Menéndez, Stanley Chang, Susanne Beck, Marina Garcia Garrido, Vithiyanjali Sothilingam, Mathias W. Seeliger, Franco Stanzial, Francesco Benedicenti, Francesca Inzana, Elise Héon, Ajoy Vincent, Jill Beis, Tim M. Strom, Günther Rudolph, Susanne Roosing, Anneke I. den Hollander, Frans P.M. Cremers, Irma López, Huanan Ren, Anthony T. Moore, Andrew R. Webster, Michel Michaelides, Robert K. Koenekoop, Eberhart Zrenner, Randal J. Kaufman, Stephen H. Tsang, Bernd Wissinger, Jonathan H. Lin - Nature Genetics 2015 被引用: 216
- Association of ambient air pollution with age-related macular degeneration and retinal thickness in UK Biobank
著者: Sharon Chua, Alasdair Warwick, Tünde Pető, Konstantinos Balaskas, Anthony T. Moore, Charles Reisman, Parul Desai, Andrew Lotery, Baljean Dhillon, Peng T. Khaw, Christopher G. Owen, Anthony P. Khawaja, Paul J. Foster, Praveen J. Patel - British Journal of Ophthalmology 2021 被引用: 82
- Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies
著者: Malena Daich Varela, James Bellingham, Fabiana Louise Motta, Neringa Jurkutė, Jamie M. Ellingford, Mathieu Quinodoz, Kathryn Oprych, Michael Niblock, Lucas Janeschitz‐Kriegl, Karolina Kamińska, Francesca Cancellieri, Hendrik P. N. Scholl, Eva Lenassi, Elena Schiff, Hannah Knight, Graeme C. Black, Carlo Rivolta, Michael E. Cheetham, Michel Michaelides, Omar A. Mahroo, Anthony T. Moore, Andrew R. Webster, Gavin Arno - Human Molecular Genetics 2022 被引用: 32
- Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
著者: Pia Østergaard, Michael A. Simpson, Antonella Mendola, Pradeep Vasudevan, Fiona Connell, Andreas van Impel, Anthony T. Moore, Bart Loeys, Arash Ghalamkarpour, Alexandros Onoufriadis, Inés Martínez‐Corral, Sophie Devery, Jules G. Leroy, Lut Van Laer, Amihood Singer, Martin G. Bialer, Meriel McEntagart, Oliver Quarrell, Glen Brice, Richard C. Trembath, Stefan Schulte‐Merker, Taija Mäkinen, Miikka Vikkula, Peter Mortimer, Sahar Mansour, Steve Jeffery - The American Journal of Human Genetics 2012 被引用: 192
- Retinal Structure and Function in Achromatopsia
著者: Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill A. Cowing, Colin Han, Christopher S. Langlo, Ravinder Chana, Alice E. Davidson, Panagiotis I. Sergouniotis, James Bainbridge, Robin R. Ali, Alfredo Dubra, Gary S. Rubin, Andrew R. Webster, Anthony T. Moore, Marko Nardini, Joseph Carroll, Michel Michaelides - Ophthalmology 2013 被引用: 179
- An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data
著者: Valentina Cipriani, Nikolas Pontikos, Gavin Arno, Panagiotis I. Sergouniotis, Eva Lenassi, Penpitcha Thawong, Daniel Daniš, Michel Michaelides, Andrew R. Webster, Anthony T. Moore, Peter N. Robinson, Julius O.B. Jacobsen, Damian Smedley - Genes 2020 被引用: 70
- Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations
著者: Valentina Cipriani, Anna Tierney, John R. Griffiths, Verena Zuber, Panagiotis I. Sergouniotis, John R.W. Yates, Anthony T. Moore, Paul N. Bishop, Simon J. Clark, Richard D. Unwin - The American Journal of Human Genetics 2021 被引用: 52
- X linked retinoschisis.
著者: N D George, John R.W. Yates, Anthony T. Moore - British Journal of Ophthalmology 1995 被引用: 254
- Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease
著者: Kaoru Fujinami, Jana Zernant, Ravinder Chana, Genevieve Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Anthony G. Robson, Graham E. Holder, Rando Allikmets, Michel Michaelides, Anthony T. Moore - Ophthalmology 2014 被引用: 190
