Naheed Kanuga

2.5k citations

34 papers · 2.0k indexed · h-index 24

Ophthalmology top 1%
- Retinal Diseases and Treatments 6
Molecular Biology top 5%
- Retinal Development and Disorders 17
- Connexins and lens biology 4
- CRISPR and Genetic Engineering 3
- Fungal and yeast genetics research 3
Cellular and Molecular Neuroscience top 5%
- Photoreceptor and optogenetics research 5
Cell Biology top 5%
- Cellular transport and secretion 5
- Endoplasmic Reticulum Stress and Disease 4
Neurology top 10%

Co-authors: Michael E. Cheetham John Greenwood Peter Adamson Alison J. Hardcastle Peter Coffey Philip J. Luthert Mònica Aguilà Ignacio A. Romero
Cited by: Ophthalmology Molecular Biology Cellular and Molecular Neuroscience
Journals: Human Molecular Genetics (8 papers)Gene (2 papers)Investigative Ophthalmology & Visual Science (2 papers)
Partner nations: United Kingdom Mexico Germany

In The Last Decade

Naheed Kanuga

34 papers receiving 2.0k citations

Peers

Countries citing papers authored by Naheed Kanuga

Since Specialization

Citations

This map shows the geographic impact of Naheed Kanuga'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 Naheed Kanuga with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Naheed Kanuga more than expected).

Fields of papers citing papers by Naheed Kanuga

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Naheed Kanuga. 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 Naheed Kanuga. The network helps show where Naheed Kanuga may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Naheed Kanuga, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Naheed Kanuga Line = papers co-authored together Naheed Kanuga links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa Human Molecular Genetics ·Dimitra Athanasiou,Mònica Aguilà,James Bellingham,Naheed Kanuga,Peter Adamson,Michael E. Cheetham	2017	74
2	Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups Cell stem cell ·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	2016	233
3	Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration Human Molecular Genetics ·Dimitra Athanasiou,Mònica Aguilà,Lin Dai,Kieron South,James Bellingham,Dalila Bevilacqua,Peter Munro,Naheed Kanuga,Francesca E. Mackenzie,Adam M. Dubis,Anastasios Georgiadis,Anna B. Graca,R. A. Pearson,Robin R. Ali,Sanae Sakami,Krzysztof Palczewski,Michael Y. Sherman,Philip J. Reeves,Michael E. Cheetham	2016	41
4	The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa Cell Death and Disease ·David A. Parfitt,A. S. Chan,Caroline McCulley,Dalila Bevilacqua,Hugo F. Mendes,Dimitra Athanasiou,Sergey S. Novoselov,Naheed Kanuga,Peter Munro,Peter Coffey,Bernadett Kalmár,Linda Greensmith,Michael E. Cheetham	2014	53
5	Molecular Chaperone Mediated Late-Stage Neuroprotection in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis PLoS ONE ·Sergey S. Novoselov,W. V. Purcell,Anna L. Gray,James R. Dick,Naheed Kanuga,Bernadett Kalmár,Linda Greensmith,Michael E. Cheetham	2013	46
6	Hsp90 inhibition protects against inherited retinal degeneration Human Molecular Genetics ·Mònica Aguilà,Dalila Bevilacqua,Caroline McCulley,Nele Schwarz,Dimitra Athanasiou,Naheed Kanuga,Sergey S. Novoselov,Clemens Lange,Robin R. Ali,James Bainbridge,Carlos Gias,Peter Coffey,Pere Garriga,Michael E. Cheetham	2013	69
7	Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) Human Molecular Genetics ·Tom R. Webb,David A. Parfitt,J.C. Gardner,顕成檜,I A Aziz,Alice E. Davidson,Ilaria Zito,Dawn L. Thiselton,Young-Kyung Cho,Maria Apergi,Wei You,Naheed Kanuga,Michel Michaelides,Michael E. Cheetham,Michael B. Gorin,Alison J. Hardcastle	2012	122
8	The Inherited Blindness Protein AIPL1 Regulates the Ubiquitin-Like FAT10 Pathway PLoS ONE ·John S. Bett,Naheed Kanuga,憲則松本,Gunter Schmidtke,Marcus Groettrup,Michael E. Cheetham,Jacqueline van der Spuy	2012	13
9	A Novel Missense Mutation in Both OPN1LW and OPN1MW Cone Opsin Genes Causes X-Linked Cone Dystrophy (XLCOD5) Advances in experimental medicine and biology ·Jessica C. Gardner,Tom R. Webb,Naheed Kanuga,Anthony G. Robson,Graham E. Holder,Andrew Stockman,Caterina Ripamonti,Neil D. Ebenezer,Olufunmilola A. Ogun,Sophie Devery,Genevieve Wright,Eamonn R. Maher,Michael E. Cheetham,Anthony T. Moore,Michel Michaelides,Alison J. Hardcastle	2011	2
10	The Nance–Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology Human Molecular Genetics ·Simon P. Brooks,Margherita Coccia,Hao Tang,Naheed Kanuga,Laura M. Machesky,Maryse Bailly,Michael E. Cheetham,Alison J. Hardcastle	2010	55
11	X-Linked Cone Dystrophy Caused by Mutation of the Red and Green Cone Opsins The American Journal of Human Genetics ·Jessica C. Gardner,Tom R. Webb,Naheed Kanuga,Anthony G. Robson,Graham E. Holder,Andrew Stockman,Caterina Ripamonti,Neil D. Ebenezer,Olufunmilola A. Ogun,Sophie Devery,Genevieve Wright,Eamonn R. Maher,Michael E. Cheetham,Anthony T. Moore,Michel Michaelides,Alison J. Hardcastle	2010	37
12	Blue cone monochromacy: causative mutations and associated phenotypes. PubMed ·Jessica C. Gardner,Michel Michaelides,Graham E. Holder,Naheed Kanuga,Tom R. Webb,J. D. Mollon,Anthony T. Moore,Alison J. Hardcastle	2009	51
13	X-linked cataract and Nance-Horan syndrome are allelic disorders Human Molecular Genetics ·Margherita Coccia,Simon P. Brooks,Tom R. Webb,Moisés H. Sandoval,Hans-Christoph Graf v. Seherr-Thoss,Victoria Murday,Eric M. Mangum,Emil Schönaich-Carolath,Teresia Wangensteen,Ruth Riise,Anand Saggar,Soo‐Mi Park,Naheed Kanuga,Peter J. Francis,Eamonn R. Maher,Anthony T. Moore,Isabelle Russell‐Eggitt,Alison J. Hardcastle	2009	50
14	Adeno-Associated Virus Gene Transfer to Mouse Retina Human Gene Therapy ·Robin R. Ali,Martin Reichel,Mahesh de Alwis,Naheed Kanuga,Christine Kinnon,Roland J. Levinsky,David M. Hunt,Shomi S. Bhattacharya,Adrian J. Thrasher	1998	114
15	Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse Current Eye Research ·Robin R. Ali,Martin Reichel,Naheed Kanuga,Peter Munro,Robert Alexander,Alan R. Clarke,Philip J. Luthert,Shomi S. Bhattacharya,David M. Hunt	1998	20
16	Co-injection of adenovirus expressing CTLA4-Ig prolongs adenovirally-mediated lacZ reporter gene expression in the mouse retina. UCL Discovery (University College London) ·(unknown),Katherine Vanessa Franco Mejía,David Baker,Andrew P. Byrnes,(unknown),Naheed Kanuga,David M. Hunt,(unknown)	1997	1
17	In vivo gene delivery to the mouse retina UCL Discovery (University College London) ·Robin R. Ali,G. Kliest,ChangHoon Shin,Naheed Kanuga,David M. Hunt,董来成	1996	1
18	The influence of the Ustilago maydis REC1 gene on plasmid-chromosome recombination Current Genetics ·Geoffrey R. Banks,Naheed Kanuga,John Ealing,Ad Spanos,David W. Holden	1992	3
19	The Ustilago maydis pyr3 gene: sequence and transcriptional analysis Gene ·Ad Spanos,Naheed Kanuga,David W. Holden,Geoffrey R. Banks	1992	15
20	Cloning the REC1 gene of Ustilago maydis Current Genetics ·David W. Holden,Ad Spanos,Naheed Kanuga,Geoffrey R. Banks	1991	9

About Naheed Kanuga

Naheed Kanuga is a scholar working on Ophthalmology, Cell Biology and Molecular Biology, having authored 34 papers that have together received 2.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (6 papers), Photoreceptor and optogenetics research (5 papers), Cellular transport and secretion (5 papers), Endoplasmic Reticulum Stress and Disease (4 papers), Connexins and lens biology (4 papers), CRISPR and Genetic Engineering (3 papers) and Fungal and yeast genetics research (3 papers). The work is most often cited by research in Ophthalmology (496 citations), Molecular Biology (1.6k citations) and Cellular and Molecular Neuroscience (425 citations). Naheed Kanuga has collaborated with scholars based in United Kingdom, Mexico and Germany. Frequent co-authors include Michael E. Cheetham, John Greenwood, Peter Adamson, Alison J. Hardcastle, Peter Coffey, Philip J. Luthert, Mònica Aguilà, Ignacio A. Romero, T. A. Bailey and Dimitra Athanasiou. Their work appears in journals such as Human Molecular Genetics, Gene, Investigative Ophthalmology & Visual Science, Current Genetics and Proceedings of the National Academy of Sciences.

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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