Graeme C. Black

Active 1957–2025

123
Papers
19,988
Citations
76
h-index
119
i10-index

Citations

Citations per year for Graeme C. Black1963: 1 citations1973: 1 citations1977: 2 citations1987: 1 citations1989: 1 citations1990: 1 citations1992: 1 citations1993: 1 citations1995: 4 citations1996: 4 citations1997: 6 citations1998: 5 citations1999: 5 citations2000: 15 citations2001: 10 citations2002: 34 citations2003: 51 citations2004: 90 citations2005: 101 citations2006: 107 citations2007: 96 citations2008: 121 citations2009: 106 citations2010: 116 citations2011: 121 citations2012: 154 citations2013: 152 citations2014: 178 citations2015: 210 citations2016: 217 citations2017: 197 citations2018: 185 citations2019: 548 citations2020: 651 citations2021: 666 citations2022: 521 citations2023: 326 citations2024: 863 citations2025: 497 citations2026: 64 citations1964–1972: no citations, so these years are not shown1974–1976: no citations, so these years are not shown1978–1986: no citations, so these years are not shown1988: no citations, so this year is not shown1991: no citations, so this year is not shown1994: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,576 citing papers, 23.4% of this breakdownUnited Kingdom: 1,241 citing papers, 11.3% of this breakdownChina: 790 citing papers, 7.2% of this breakdownGermany: 683 citing papers, 6.2% of this breakdownCanada: 433 citing papers, 3.9% of this breakdownFrance: 426 citing papers, 3.9% of this breakdownNetherlands: 401 citing papers, 3.6% of this breakdownItaly: 395 citing papers, 3.6% of this breakdownAustralia: 375 citing papers, 3.4% of this breakdownJapan: 268 citing papers, 2.4% of this breakdownSpain: 260 citing papers, 2.4% of this breakdownSwitzerland: 216 citing papers, 2% of this breakdown
0%23.4%Other 26.7%

Fields

  • Biochemistry, Genetics and Molecular Biology56.5%
  • Medicine32.8%
  • Neuroscience3%
  • Immunology and Microbiology2.6%
  • Computer Science2.5%
  • Engineering0.5%
  • Other2.1%

Topics

  • Retinal Development and Disorders4.8%
  • Genomics and Rare Diseases3.3%
  • Retinal Diseases and Treatments3.1%
  • Wnt/β-catenin signaling in development and cancer2.9%
  • Retinal Imaging and Analysis1.9%
  • Bone Metabolism and Diseases1.7%
  • Other82.3%

Coauthors

All papers

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  1. A foundation model for generalizable disease detection from retinal images

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Usha Chakravarthy, Ruth Hogg, Euan Paterson, Jayne V. Woodside, Tünde Pető, Gareth J. McKay, Bernadette McGuinness, Paul J. Foster, Konstantinos Balaskas, Anthony P. Khawaja, Nikolas Pontikos, Jugnoo S. Rahi, Gerassimos Lascaratos, Praveen J. Patel, Michelle Chan, Sharon Chua, Alexander Day, Parul Desai, Cathy Egan, Marcus Fruttiger, David F. Garway‐Heath, Alison J. Hardcastle, Peng T. Khaw, Tony Moore, Sobha Sivaprasad, Nicholas G. Strouthidis, Dhanes Thomas, Adnan Tufail, Ananth C. Viswanathan, Bal Dhillon, Tom MacGillivray, Cathie Sudlow, Véronique Vitart, Alex S. F. Doney, Emanuele Trucco, Jeremy A. Guggeinheim, James E. Morgan, Christopher J. Hammond, Katie Williams, Pirro G. Hysi, Simon Harding, Yalin Zheng, Robert Luben, Philip J. Luthert, Zihan Sun, Martin McKibbin, Eoin O’Sullivan, Richard A. Oram, Mike Weedon, Christopher G. Owen, Alicja R. Rudnicka, Naveed Sattar, David Steel, Irene Stratton, Robyn J. Tapp, Max Yates, Axel Petzold, Savita Madhusudhan, André Altmann, Aaron Lee, Eric J. Topol, Alastair K. Denniston, Daniel C. Alexander, Pearse A. Keane - Nature 2023 cited by 925

  2. Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies

    Authors: , , , , , , - International Journal of Epidemiology 2019 cited by 1,400

  3. Whole-genome sequencing of patients with rare diseases in a national health system

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David R. Bentley, NIHR BioResource for the 100,000 Genomes Project, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan and 412 more - Nature, Nat. 2020 cited by 582

  4. Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2020 cited by 363

  5. Retinal layer segmentation in multiple sclerosis: a systematic review and meta-analysis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jonathan Calkwood, Christian Cordano, Fiona Costello, Ardith Courtney, Andrés Cruz-Herranz, Ricarda Diem, Avril Daly, Hélène Dollfus, Christina Fasser, Carsten Finke, Jette Lautrup Frederiksen, Elliot M. Frohman, Teresa C. Frohman, Elena García‐Martín, Inés González‐Suarez, Gorm Pihl-Jensen, Jennifer Graves, Ari Green, Joachim Havla, Bernhard Hemmer, Su‐Chun Huang, Jaime Imitola, Hong Jiang, David Keegan, Eric Kildebeck, Alexander Klistorner, Benjamin Knier, Scott Kolbe, Thomas Korn, Bart P. Leroy, Letizia Leocani, Dorothée Leroux, Netta Levin, Petra Lišková, Birgit Lorenz, Jana Lízrová Preiningerová, Elena H. Martínez‐Lapiscina, Janine Mikolajczak, Xavier Montalbán, Mark J. Morrow, Rachel Nolan, Timm Oberwahrenbrock, Frederike Cosima Oertel, Celia Oreja‐Guevara, Benjamin Osborne, Olivier Outteryck, Athina Papadopoulou, Friedemann Paul, Axel Petzold, Marius Ringelstein, Shiv Saidha, Bernardo Sánchez‐Dalmau, Jaume Sastre‐Garriga, Sven Schippling, Robert K. Shin, Neil Shuey, Kerstin Soelberg, Ahmed Toosy, R. Martinez Torres, Ángela Vidal‐Jordana, Pablo Villoslada, Amy Waldman, Owen White, Ann Ming Yeh, Sui H. Wong, Hanna Zimmermann - The Lancet Neurology 2017 cited by 568

  6. Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial

    Authors: , , , , , , , , , , , , , - The Lancet 2014 cited by 781

  7. LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , B. Floege, M. L. Halfhide, Bryan Hall, Raoul C. M. Hennekam, Tatsuo Hirose, Anneke Jans, Harald Jüppner, Chong Ae Kim, Kim M. Keppler‐Noreuil, A. Kohlschuetter, Didier Lacombe, Marie Lambert, Emmanuelle Lemyre, Tom G.W. Letteboer, Leena Peltonen, Raj Ramesar, Marta Romanengo, Hannu Somer, Elisabeth Steichen‐Gersdorf, B Steinmann, Beth Sullivan, Andrea Superti‐Furga, Walter Swoboda, M. J. van den Boogaard, Wim Van Hul, Miikka Vikkula, Marcela Votruba, Bernhard Zabel, Teresa García, Roland Baron, Bjørn R. Olsen, Matthew L. Warman - Cell 2001 cited by 2,248

  8. Germline selection shapes human mitochondrial DNA diversity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 305 more - Science 2019 cited by 251

  9. Retinal Optical Coherence Tomography Features Associated With Incident and Prevalent Parkinson Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tasanee Braithwaite, Roxana O. Carare, Usha Chakravarthy, Michelle Chan, Sharon Chua, Alexander Day, Parul Desai, Bal Dhillon, Andrew D. Dick, Alex S. F. Doney, Cathy Egan, Sarah Ennis, Marcus Fruttiger, John EJ Gallacher, David F. Garway‐Heath, Jane Whitney Gibson, Jeremy A. Guggeinheim, Christopher J. Hammond, Alison J. Hardcastle, Simon Harding, Ruth Hogg, Pirro G. Hysi, Peng T. Khaw, Gerassimos Lascaratos, Thomas J. Littlejohns, Andrew Lotery, Robert Luben, Philip J. Luthert, Tom MacGillivray, Sarah Mackie, Bernadette McGuiness, Gareth J. McKay, Marin McKibbin, Tony Moore, James E Morgan, Eoin O’Sullivan, Richard A. Oram, Christopher G. Owen, Euan Paterson, Tünde Pető, Alicja R. Rudnicka, Naveed Sattar, Jay Self, Panagiotis I. Sergouniotis, Sobha Sivaprasad, David Steel, Irene Stratton, Nicholas G. Strouthidis, Cathie Sudlow, Zihan Sun, Robyn J. Tapp, Dhanes Thomas, Emanuele Trucco, Adnan Tufail, Véronique Vitart, Ananth C. Viswanathan, Mike Weedon, Cathy Williams, Katie Williams, Jayne V. Woodside, MaxM. Yates, Jennifer Yip, Yalin Zheng - Neurology 2023 cited by 86

  10. Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William G. Newman - The American Journal of Human Genetics 2013 cited by 245

  11. Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Georgios Tsokolas, Paulo Stanga, Tsveta Ivanova, Muhannd El-Faouri, Sherif Shaarawy, Graeme C. Black, Janet L. Davis, Ninel Z. Gregori, Carlos E. Mendoza‐Santiesteban, Potyra R. Rosa, Kevin G. Evans, Rob Koenekoop, Dominik Fischer, Frank G. Holz, Kamron N. Khan, Jason Horowitz, Mark E. Pennesi, David G. Birch, Michael B. Gorin, Kim Stepien, Jacque Duncan, Tim Stout, Benjamin Bakall, Paul S. Bernstein, E.‐M. Sankila, Carel B. Hoyng, Camiel J.F. Boon, Isabelle Meunier - JAMA Ophthalmology 2023 cited by 62

  12. Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carel B. Hoyng, Stefan Mundlos, Musa M. Mhlanga, Frans P.M. Cremers, Michael E. Cheetham, Susanne Roosing, Alison J. Hardcastle - The American Journal of Human Genetics 2020 cited by 122

  13. Real-World Clinical Experience With Idebenone in the Treatment of Leber Hereditary Optic Neuropathy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Günther Rudolph, Oskars Mikazans, Magda Joana Silva, Xavier Llòria, Günther Metz, Thomas Klopstock - Journal of Neuro-Ophthalmology 2020 cited by 114

  14. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Van Vooren, Ronald J. Wapner, Andrew O.M. Wilkie, Caroline F. Wright, Anneke T. Vulto‐van Silfhout, Nicole de Leeuw, Bert B.A. de Vries, Nicole L. Washingthon, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa Haendel, Damian Smedley, Suzanna Lewis, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2013 cited by 837

  15. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney - Circulation Research 2019 cited by 198

  16. Genetic testing and diagnosis of inherited retinal diseases

    Authors: , , , , , - Orphanet Journal of Rare Diseases 2021 cited by 75

  17. Protein Kinase Cδ Deficiency Causes Mendelian Systemic Lupus Erythematosus With B Cell‐Defective Apoptosis and Hyperproliferation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pierre Lebon, Christophe Malcus, Yanick J. Crow, John Brognard, Nathalie Bonnefoy - Arthritis & Rheumatism 2013 cited by 198

  18. Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia

    Authors: , , , , , , , , , , , , , , , , - Nature Medicine 2018 cited by 186

  19. Molecular findings from 537 individuals with inherited retinal disease

    Authors: , , , , , , , , , , , , , , , - Journal of Medical Genetics 2016 cited by 168

  20. Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sébastien Jacquemont, Pierre‐Yves Jeannet, Rosalind J Jefferson, Ram Kumar, G Kutschke, Staffan Lundberg, Charles Marques Lourenço, Ramesh Mehta, Sakkubai Naidu, Ken K. Nischal, Luís Nunes, Katrin Õunap, Michel Philippart, Prab Prabhakar, Sarah Risen, Raphael Schiffmann, Calvin Soh, John B.P. Stephenson, Helen Stewart, Jon Stone, John Tolmie, Marjo S. van der Knaap, José Pedro Vieira, Catheline Vilain, Emma Wakeling, Vanessa Wermenbol, Andrea Whitney, Simon C. Lovell, Stefan Meyer, John H. Livingston, Gabriela M. Baerlocher, Graeme C. Black, Gillian Rice, Yanick J. Crow - Nature Genetics 2012 cited by 291

  21. UK Biobank retinal imaging grading: methodology, baseline characteristics and findings for common ocular diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paul J. Foster, Marcus Fruttiger, J. Gallacher, David F. Garway‐Heath, Jane Whitney Gibson, Jeremy A. Guggenheim, Christopher J. Hammond, Alison J. Hardcastle, Simon Harding, Ruth Hogg, Pirro G. Hysi, Pearse A. Keane, Peng T. Khaw, Anthony P. Khawaja, Gerassimos Lascaratos, Thomas J. Littlejohns, Andrew Lotery, Philip J. Luthert, Tom MacGillivray, Sarah Mackie, Bernadette McGuinness, Gareth J. McKay, Martin McKibbin, T. Moore, John Morgan, R. Oram, E. O'Sullivan, Christopher G. Owen, Prem N. Patel, Euan Paterson, Tünde Pető, Axel Petzold, Nikolas Pontikos, Jugnoo S. Rahi, Alicja R. Rudnicka, N. Sattar, Jay Self, P. Sergouniotis, Sobha Sivaprasad, David Steel, Irene Stratton, Nicholas G. Strouthidis, Cathie Sudlow, Zihan Sun, Robyn J. Tapp, Dhanes Thomas, Emanuele Trucco, Adnan Tufail, A. C. Viswanathan, V. Vitart, M. Weedon, Cathy Williams, C. H. Williams, Jayne V. Woodside, Max Yates, Jennifer Yip, Yingfeng Zheng, Jennifer Yip, Yingfeng Zheng - Eye 2022 cited by 35

  22. Mast cell infiltration of the choroid and protease release are early events in age-related macular degeneration associated with genetic risk at both chromosomes 1q32 and 10q26

    Authors: , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2022 cited by 29

  23. Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nigel Smith, Marcin Szynkiewicz, Alice Wiedeman, Carine Wouters, Leo Zeef, Jean‐Laurent Casanova, Keith B. Elkon, Anthony J. Janckila, Pierre Lebon, Yanick J. Crow - Nature Genetics 2011 cited by 259

  24. Assessment of Visual Function with Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Georgios Tsokolas, Tsveta Ivanova, Muhannd El-Faouri, Sherif Shaarawy, Graeme C. Black, Janet L. Davis, Ninel Z. Gregori, Carlos E. Mendoza‐Santiesteban, Andreas Lauer, Paul Yang, Steven T. Bailey, Rand Spencer, Gary E. Fish, Robert Wang, Deborah Y. Chong, Ashkan M. Abbey, Rajiv Anand, Albert A. MaGuire, Robert L. Roseman, Kaushik Hazariwala, Brandon Parrott, Kaushik Hazariwala, Brandon Parrott - Ophthalmology 2024 cited by 40