Manir Ali

6.1k citations

61 papers · 1.4k indexed · h-index 24

Ophthalmology top 2%
- Retinal Diseases and Treatments 10
- Glaucoma and retinal disorders 4
Radiology, Nuclear Medicine and Imaging top 5%
- Corneal surgery and disorders 6
- Corneal Surgery and Treatments 5
Genetics top 10%
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
Clinical Biochemistry top 10%
Endocrinology, Diabetes and Metabolism top 10%
- Diet, Metabolism, and Disease 6
Molecular Biology
- Retinal Development and Disorders 17

Co-authors: Chris F. Inglehearn Timothy M. Cox Peter Rellos Martin McKibbin Carmel Toomes P.M. Hocking Erica di Martino Alexander F. Markham
Cited by: Ophthalmology Radiology, Nuclear Medicine and Imaging Genetics
Journals: Investigative Ophthalmology & Visual Science (9 papers)Journal of Medical Genetics (3 papers)Human Mutation (3 papers)
Partner nations: United Kingdom United States Egypt

In The Last Decade

Manir Ali

60 papers receiving 1.4k citations

Peers

Countries citing papers authored by Manir Ali

Since Specialization

Citations

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

Fields of papers citing papers by Manir Ali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Manir Ali, 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 Manir Ali Line = papers co-authored together Manir Ali links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells Molecular Diagnosis & Therapy ·Ουρανία Τρέμμα,Christopher M. Watson,Ian Carr,Martin McKibbin,Laura A. Crinnion,Morag Taylor,Fernanda O. G. de Gaspi,Tracy Fletcher,Mohammed E. El‐Asrag,Manir Ali,Carmel Toomes,Chris F. Inglehearn	2023	4
2	Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK Genes ·А. Р. Мартюшева,Alejandro Schuller W,Martin McKibbin,Tassiara Almeida da Silva,Susanne Roosing,Yongxiang Shun,Manir Ali,Christopher M. Watson,David Steel,Frans P.M. Cremers,Chris F. Inglehearn,Nguyen Tac An,Carmel Toomes	2023	2
3	Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa PubMed Central ·Mohammed E. El‐Asrag,Marta Cortón,Martin McKibbin,Almudena Ávila‐Fernández,Moin Mohamed,Fiona Blanco‐Kelly,Carmel Toomes,Chris F. Inglehearn,Carmen Ayuso,Manir Ali	2022	8
4	Mutations in SLC38A8 and FOXD1 in patients with nystagmus and foveal hypoplasia. Investigative Ophthalmology & Visual Science ·Emma Lord,James A. Poulter,Andrew R. Webster,Panagiotis I. Sergouniotis,Kamron N. Khan,Paul J. Benke,Lee S. Friedman,Manir Ali,Chris F. Inglehearn,Carmel Toomes	2017	1
5	The effect of COMT Val158Met and DRD2 C957T polymorphisms on executive function and the impact of early life stress Brain and Behavior ·Kristel Klaus,Kevin Butler,Simon Durrant,Manir Ali,Chris F. Inglehearn,Timothy L. Hodgson,Humberto Gutiérrez,Kyla Pennington	2017	27
6	Specific Alleles of CLN7 / MFSD8 , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy Investigative Ophthalmology & Visual Science ·Kamron N. Khan,Mohammed E. El‐Asrag,Cristy A. Ku,Graham E. Holder,Martin McKibbin,Gavin Arno,James A. Poulter,Keren Carss,丽珍,Alessandro Mezzetti,Benjamin Bakall,Hendrik P. N. Scholl,F. Lucy Raymond,Carmel Toomes,Chris F. Inglehearn,Sun Zhanguo,Anthony T. Moore,Michel Michaelides,Andrew R. Webster,Manir Ali	2017	38
7	Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy JAMA Ophthalmology ·Rachel L. Taylor,Gavin Arno,James A. Poulter,Kamron N. Khan,François Hüe,Sarah Hull,Nikolas Pontikos,Simone Mantellini,Katherine R. Smith,Manir Ali,Carmel Toomes,Martin McKibbin,Jill Clayton‐Smith,Stephanie Grünewald,Michel Michaelides,Anthony T. Moore,Alison J. Hardcastle,Chris F. Inglehearn,Andrew R. Webster,Graeme C. Black	2017	32
8	Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in theDRAM2Gene Investigative Ophthalmology & Visual Science ·Panagiotis I. Sergouniotis,Martin McKibbin,Anthony G. Robson,Hanno J. Bolz,Elfride De Baere,Philipp L. Müller,Raoul Heller,Mohammed E. El‐Asrag,С Е Стешко,Vincent Plagnol,Carmel Toomes,Manir Ali,Graham E. Holder,Peter Charbel Issa,Bart P. Leroy,Chris F. Inglehearn,Andrew R. Webster	2015	12
9	Improved Response To Ranibizumab In Ex And Current Smokers With Age-related Macular Degeneration (AMD), But No Evidence That CFH, ARMS2/HTRA1 Or VEGF Genotypes Predict Treatment Outcome Investigative Ophthalmology & Visual Science ·Chris F. Inglehearn,Manir Ali,Richard Gale,Keerti. K. Choudhary,Lopes Da Cunha,Louise Downey,Paul D. Baxter,Martin McKibbin	2012	3
10	CFH,VEGFandHTRA1promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration British Journal of Ophthalmology ·Martin McKibbin,Manir Ali,Tiange Shen,Paul D. Baxter,Kil-Seong Kim,G. A. Williams,Keerti. K. Choudhary,Chris F. Inglehearn	2011	90
11	Ultrastructural changes in the retinopathy, globe enlarged (rge) chick cornea Journal of Structural Biology ·Craig Boote,Sally Hayes,Robert D. Young,Christina S. Kamma‐Lorger,P.M. Hocking,Ahmed Elsheikh,Chris F. Inglehearn,Manir Ali,Keith M. Meek	2009	29
12	Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment Cytogenetic and Genome Research ·Sabita K. Murthy,Anders O.H. Nygren,Yurie Arase,Jan P. Schouten,Saravanan Sujit Kaarthik,Z.Z. Liu,Manir Ali	2007	55
13	Collagen organization in the chicken cornea and structural alterations in the retinopathy, globe enlarged (rge) phenotype—An X-ray diffraction study Journal of Structural Biology ·Craig Boote,Sally Hayes,Simon Jones,Andrew J. Quantock,P.M. Hocking,Chris F. Inglehearn,Manir Ali,Keith M. Meek	2007	28
14	Analysis of Fcγ receptor haplotypes in rheumatoid arthritis: FCGR3A remains a major susceptibility gene at this locus, with an additional contribution from FCGR3B Arthritis Research & Therapy ·Ann W Morgan,Jennifer H. Barrett,Bridget Griffiths,Alina Schuckert,James Robinson,山本杏子,Manir Ali,Elizabeth A. Jones,Robert Old,Frédérique Ponchel,Arthur W. Boylston,R D Situnayake,Alexander F. Markham,Paul Emery,John D. Isaacs	2005	35
15	Congenital glaucoma and brain stem atrophy as features of Aicardi–Goutières syndrome American Journal of Medical Genetics Part A ·Yanick J. Crow,Ernesto García-López,M. C. Ciancimino,H. Ishikura,政剛仲谷,C. Geoffrey Woods,Manir Ali,John H. Livingston,Pierre Lebon,Menna Khalil,Meriel McEntagart,حمیدرضا گوهررستمی,R M Winter	2004	28
16	Overexpression of transcripts containing LINE-1 in the synovia of patients with rheumatoid arthritis Annals of the Rheumatic Diseases ·Manir Ali,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2003	18
17	Application of differential display to immunological research Journal of Immunological Methods ·Manir Ali,Alexander F. Markham,John D. Isaacs	2001	16
18	Rheumatoid arthritis synovial T cells regulate transcription of several genes associated with antigen-induced anergy Journal of Clinical Investigation ·Manir Ali,Frédérique Ponchel,Su Yanqun,M.J. Francis,Xia Wu,Adrienne Verhoef,Arthur W. Boylston,Douglas J. Veale,Paul Emery,Alexander F. Markham,Ramona Plebst,John D. Isaacs	2001	34
19	Fcγ receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groups Arthritis & Rheumatism ·Ann W Morgan,Bridget Griffiths,Frédérique Ponchel,Kiumars Farahbaksh,Manir Ali,Vania Meuli,Carma L. Sheely,R D Situnayake,Alexander F. Markham,Paul Emery,John D. Isaacs	2000	80
20	A newly identified aldolase B splicing mutation (G→C, 5′ intron 5) in hereditary fructose intolerance from New Zealand Human Mutation ·Manir Ali,MATTHIAS KAUFMANN,Timothy M. Cox	1996	6

About Manir Ali

Manir Ali is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging, Molecular Biology, Cell Biology and Developmental Biology, having authored 61 papers that have together received 1.4k indexed citations. Recurring topics across this work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (10 papers), Genomics and Rare Diseases (6 papers), Corneal surgery and disorders (6 papers), Diet, Metabolism, and Disease (6 papers), Corneal Surgery and Treatments (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Glaucoma and retinal disorders (4 papers). The work is most often cited by research in Ophthalmology (302 citations), Radiology, Nuclear Medicine and Imaging (356 citations), Genetics (277 citations), Clinical Biochemistry (67 citations) and Endocrinology, Diabetes and Metabolism (160 citations). Manir Ali has collaborated with scholars based in United Kingdom, United States and Egypt. Frequent co-authors include Chris F. Inglehearn, Timothy M. Cox, Peter Rellos, Martin McKibbin, Carmel Toomes, P.M. Hocking, Erica di Martino, Alexander F. Markham, John D. Isaacs and James A. Poulter. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Journal of Medical Genetics, Human Mutation, PLoS ONE and European Journal of Medical Genetics.

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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