ScholarIQanswers from OpenAlex & ORCID
Anthony T. Moore
ResearcherPublications, citations & collaboration network
Anthony T. Moore is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Anthony T. Moore have?
ScholarIQindexed works
Anthony T. Moore has 389 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Anthony T. Moore have?
ScholarIQcitation count
Anthony T. Moore has 22,547 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Anthony T. Moore?
ScholarIQh-index
Anthony T. Moore has an h-index of 76 in OpenAlex.
What is the i10-index of Anthony T. Moore?
ScholarIQi10-index
Anthony T. Moore has an i10-index of 253 in OpenAlex.
What is the ORCID of Anthony T. Moore?
ScholarIQorcid
The ORCID for Anthony T. Moore is on the source record.
What is the OpenAlex record for Anthony T. Moore?
ScholarIQopenalex
The OpenAlex for Anthony T. Moore is on the source record.
What are the most-cited papers on Anthony T. Moore?
ScholarIQmost cited works
Seven new loci associated with age-related macular degeneration
Lars G. Fritsche, Bernhard H. F. Weber, Wei Chen, Xueling Sim, Gonçalo R. Abecasis, Matthew Schu, Gyungah Jun, Lindsay A. Farrer, Brian L. Yaspan, Jonathan L. Haines, Yi Yu, Kimberly Chin, Robyn Reynolds, Johanna M. Seddon, Guðmar Þorleifsson, Hreinn Stefánsson, Kāri Stefánsson, Unnur Þorsteinsdóttir, Donald J. Zack, Isabelle Audo, José‐Alain Sahel, Thierry Léveillard, Peter A. Campochiaro, Satoshi Arakawa, Michiaki Kubo, Valentina Cipriani, Alan C. Bird, Anthony T. Moore, Andrew R. Webster, John R.W. Yates, Stephan Ripke, Mark J. Daly, Robert P. Igo, Peronne Joseph, Barbara Truitt, Sudha K. Iyengar, Gabriëlle H.S. Buitendijk, André G. Uitterlinden, Cornelia M. van Duijn, Johannes R. Vingerling, Caroline C. W. Klaver, Daniel E. Weeks, Robyn H. Guymer, Melinda Cain, Andrea J. Richardson, Tien Yin Wong, Paul N. Baird, Jie Jin Wang, Joanna E. Merriam, Gaetano R. Barile, R. Theodore Smith, Rando Allikmets, Peter J. Francis, Michael L. Klein, Gregory Hannum, Anita Agarwal, Ana Maria Armbrecht, Baljean Dhillon, Saddek Mohand‐Saïd, Tin Aung, Ching‐Yu Cheng, Belinda K. Cornes, Eranga N. Vithana, Mustapha Benchaboune, Paul N. Bishop, Kari Branham, John R. Heckenlively, Mohammad Othman, Anand Swaroop, Matthew Brooks, Radu Cojocaru, James S. Friedman, Neel Gupta, Rinki Ratna Priya, Alexander J. Brucker, William H. Cade, Adam C. Naj, William K. Scott, Margaret A. Pericak‐Vance, Hendrik P. N. Scholl, Chi Chao Chan, Emily Y. Chew, Itay Chowers, David Clayton, Jane C. Khan, Humma Shahid, Yvette P. Conley, Albert O. Edwards, Εvangelos Εvangelou, Jesen Fagerness, Henry Ferreyra, Guy Hughes, Igor Kozak, Clara J. Lee, Ming Zhang, Ling Zhao, Kang Zhang, Ásbjörg Geirsdóttir, Haraldur Sigurðsson, Ronnie George
Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis
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
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
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
Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
Neruban Kumaran, Anthony T. Moore, Richard G. Weleber, Michel Michaelides