Graeme C. Black

24.3k total citations · 2 hit papers
212 papers, 8.8k citations indexed

About

Graeme C. Black is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Graeme C. Black has authored 212 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 138 papers in Molecular Biology, 89 papers in Genetics and 57 papers in Ophthalmology. Recurrent topics in Graeme C. Black's work include Retinal Development and Disorders (67 papers), Retinal Diseases and Treatments (34 papers) and Connexins and lens biology (26 papers). Graeme C. Black is often cited by papers focused on Retinal Development and Disorders (67 papers), Retinal Diseases and Treatments (34 papers) and Connexins and lens biology (26 papers). Graeme C. Black collaborates with scholars based in United Kingdom, United States and Netherlands. Graeme C. Black's co-authors include Rahat Perveen, Andrew R. Webster, Forbes Manson, Yingjuan Liu, Mun‐Kit Choy, Bernard Keavney, Sen Chen, Liesl Zühlke, Ningxiu Li and Jill Clayton‐Smith and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Medicine.

In The Last Decade

Graeme C. Black

207 papers receiving 8.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

2019 713 citations Graeme C. Black et al. profile →
Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial

2014 622 citations Graeme C. Black, Andrew Lotery et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Graeme C. Black United Kingdom	48	5.3k	2.7k	2.1k	1.4k	865	212	8.8k
Carmen Ayuso Spain	50	5.7k 1.1×	2.2k 0.8×	1.9k 0.9×	707 0.5×	641 0.7×	351	9.0k
Elias I. Traboulsi United States	45	3.8k 0.7×	2.1k 0.8×	3.2k 1.5×	1.3k 1.0×	472 0.5×	289	7.5k
Richard A. Lewis United States	62	7.1k 1.3×	3.9k 1.4×	4.9k 2.3×	2.4k 1.8×	901 1.0×	255	13.1k
Fowzan S. Alkuraya Saudi Arabia	59	6.8k 1.3×	4.6k 1.7×	899 0.4×	556 0.4×	574 0.7×	385	11.5k
Birgit Lorenz Germany	40	4.8k 0.9×	1.1k 0.4×	3.0k 1.4×	1.6k 1.2×	413 0.5×	249	6.8k
Paul A. Overbeek United States	64	9.6k 1.8×	3.2k 1.2×	843 0.4×	873 0.6×	502 0.6×	166	13.0k
Brenda L. Gallie Canada	61	6.0k 1.1×	1.6k 0.6×	6.0k 2.8×	1.1k 0.8×	944 1.1×	250	12.8k
Albert M. Maguire United States	53	7.5k 1.4×	3.1k 1.1×	4.7k 2.2×	2.3k 1.7×	838 1.0×	183	10.2k
Robert F. Mullins United States	61	7.3k 1.4×	1.9k 0.7×	7.3k 3.4×	4.2k 3.0×	504 0.6×	259	13.2k
Ursula Schlötzer‐Schrehardt Germany	63	3.6k 0.7×	1.0k 0.4×	6.6k 3.1×	5.3k 3.9×	582 0.7×	308	13.4k

Countries citing papers authored by Graeme C. Black

Since Specialization

Citations

This map shows the geographic impact of Graeme C. Black's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Graeme C. Black with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Graeme C. Black more than expected).

Fields of papers citing papers by Graeme C. Black

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Graeme C. Black. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Graeme C. Black. The network helps show where Graeme C. Black may publish in the future.

Co-authorship network of co-authors of Graeme C. Black

This figure shows the co-authorship network connecting the top 25 collaborators of Graeme C. Black. A scholar is included among the top collaborators of Graeme C. Black based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Graeme C. Black. Graeme C. Black is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

McCarron, Éamon P, Andrew Bentley, Peter Woolfson, et al.. (2025). Genetic Insights and Diagnostic Challenges in Highly Attenuated Lysosomal Storage Disorders. Genes. 16(8). 915–915. 1 indexed citations

Jalil, Assad, Mariantonia Ferrara, Neil R. A. Parry, et al.. (2025). Real-world outcomes of Voretigene Neparvovec: a single-centre consecutive case series. Eye. 39(7). 1356–1363. 1 indexed citations

Lin, Siying, Anthony G. Robson, Dorothy Thompson, et al.. (2024). Non‐syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activity. Clinical Genetics. 106(4). 505–511. 1 indexed citations

Green, David J., Vincent Michaud, Eulalie Lasseaux, et al.. (2024). The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism. Nature Communications. 15(1). 8436–8436. 3 indexed citations

Stępień, Karolina M., Christopher Campbell, Stephanie Barton, et al.. (2023). Clinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy. Orphanet Journal of Rare Diseases. 18(1). 265–265. 6 indexed citations

Bárta, Tomáš, Graeme C. Black, Rahat Perveen, et al.. (2023). MIR204 n. 37C >T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early‐onset cataracts and congenital glaucoma. Clinical Genetics. 104(4). 418–426. 4 indexed citations

Sergouniotis, Panagiotis I., Vincent Michaud, Eulalie Lasseaux, et al.. (2023). A multilayered approach to the analysis of genetic data from individuals with suspected albinism. Journal of Medical Genetics. 60(12). 1245–1249. 1 indexed citations

Jalil, Assad, Tsveta Ivanova, George Moussa, Neil R. A. Parry, & Graeme C. Black. (2022). Retinal gene therapy in RPE-65 gene mediated inherited retinal dystrophy. Eye. 37(9). 1874–1877. 10 indexed citations

Sergouniotis, Panagiotis I., Simon Ramsden, Andrew Lotery, et al.. (2022). Assessing the Pathogenicity of In-Frame CACNA1F Indel Variants Using Structural Modeling. Journal of Molecular Diagnostics. 24(12). 1232–1239. 1 indexed citations

10.

Ellingford, Jamie M., Panagiotis I. Sergouniotis, Simon Ramsden, et al.. (2021). Improving the clinical interpretation of missense variants in X linked genes using structural analysis. Journal of Medical Genetics. 59(4). 385–392. 3 indexed citations

11.

Sergouniotis, Panagiotis I., Stephanie Barton, Simon Ramsden, et al.. (2020). Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar. European Journal of Human Genetics. 28(9). 1274–1282. 15 indexed citations

12.

Low, Sancy, Alice E. Davidson, Maria Papadopoulos, et al.. (2019). A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutations. Eye. 34(3). 577–583. 7 indexed citations

13.

Conte, Iván, Kristen D. Hadfield, Sara Barbato, et al.. (2015). MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma. Proceedings of the National Academy of Sciences. 112(25). E3236–45. 84 indexed citations

14.

Murray, Philip, Dan Hanson, Adam Stevens, et al.. (2013). 3-M syndrome: a growth disorder associated with IGF2 silencing. Endocrine Connections. 2(4). 225–235. 17 indexed citations

15.

Leroy, Bart P., Niki Hart‐Holden, B. A. Lafaut, et al.. (2004). Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC). Investigative Ophthalmology & Visual Science. 45(10). 3683–3683. 163 indexed citations

16.

Jamieson, Robyn V., Rahat Perveen, P. H. Glenister, et al.. (2003). A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding. Human Molecular Genetics. 12(6). 585–594. 45 indexed citations

17.

Munier, Francis L., Béatrice E. Frueh, Philippe Othenin‐Girard, et al.. (2002). BIGH3 mutation spectrum in corneal dystrophies.. PubMed. 43(4). 949–54. 178 indexed citations

18.

Ridgway, Anouk, Saeed Akhtar, Francis L. Munier, et al.. (2000). Ultrastructural and molecular analysis of Bowman's layer corneal dystrophies: an epithelial origin?. PubMed. 41(11). 3286–92. 48 indexed citations

19.

Black, Graeme C., et al.. (1996). Leber's hereditary Optic neuropathy:heteroplasmy is likely ot be significant in the expression of LHON in families with the 3460 ND1 mutation. Journal of Ophthalmology. 80. 1 indexed citations

20.

Black, Graeme C. & E. H. Linfoot. (1957). Spherical aberration and the information content of optical images. Proceedings of the Royal Society of London A Mathematical and Physical Sciences. 239(1219). 522–540. 73 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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