C.F. Inglehearn

2.1k citations

34 papers · 1.3k indexed · h-index 19

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
Cellular and Molecular Neuroscience top 5%
- Photoreceptor and optogenetics research

Papers in

Ophthalmology 8
- Retinal Diseases and Treatments 6
Cellular and Molecular Neuroscience 11
- Photoreceptor and optogenetics research 11

Co-authors: Alan C. Bird Marcelle Jay G. B. Arden Shoumo Bhattacharya R. Bashir Douglas H. Lester T J Keen Shomi S. Bhattacharya
Journals: British Journal of Ophthalmology (7 papers)Investigative Ophthalmology & Visual Science (6 papers)Genomics (3 papers)Nature Genetics (2 papers)Cells Tissues Organs (2 papers)
Partner nations: United Kingdom United States Mexico

In The Last Decade

C.F. Inglehearn

33 papers receiving 1.3k citations

Peers

Countries citing papers authored by C.F. Inglehearn

Since Specialization

Citations

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

Fields of papers citing papers by C.F. Inglehearn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C.F. Inglehearn. 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 C.F. Inglehearn. The network helps show where C.F. Inglehearn may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities Frontiers in Physiology ·Claire E. L. Smith, Jennifer Kirkham, Peter F. Day, Lady Bliss, Roger Mattsson, James A. Poulter, C.F. Inglehearn, Alan J. Mighell, Steven J. Brookes	2017	21
2	The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway Disease Models & Mechanisms ·Zakia A. Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, C.F. Inglehearn, Carmel Toomes, Colin A. Johnson, Daniel J. Jagger	2015	38
3	The D153del Mutation in GNB3 Gene Causes Tissue Specific Signalling Patterns and an Abnormal Renal Morphology in Rge Chickens PLoS ONE ·Hemanth Tummala, Stewart Fleming, P.M. Hocking, Daniel Wehner, ครรชิต สงฆ์สุวรรณ, Manir Ali, C.F. Inglehearn, Nikolai Zhelev, Douglas H. Lester	2011	9
4	Hypomaturation Amelogenesis Imperfecta due to <i>WDR72</i> Mutations: A Novel Mutation and Ultrastructural Analyses of Deciduous Teeth Cells Tissues Organs ·Walid El‐Sayed, Richard F. Shore, David Parry, C.F. Inglehearn, Alan J. Mighell	2010	30
5	Ultrastructural Analyses of Deciduous Teeth Affected by Hypocalcified Amelogenesis Imperfecta from a Family with a Novel Y458X FAM83H Nonsense Mutation Cells Tissues Organs ·Walid El‐Sayed, Richard F. Shore, David Parry, C.F. Inglehearn, Alan J. Mighell	2009	37
6	Confirmation of a Locus for Primary Congenital Glaucoma (PCG) on Chromosome 14q24 in a Pakistani Pedigree Investigative Ophthalmology & Visual Science ·Adam Booth, DEAN KARLAN, Gareth Williams, Edwin Antonio Gutiérrez Rodríguez, Carmel Toomes, Malcolm Brain, Yasmin Abdul Rashid, 武徳落合, C.F. Inglehearn	2008	1
7	Jalili Syndrome - Cone-Rod Dystrophy (CRD) and Amelogenesis Imperfecta (AI); Six Families and Consistent Linkage to 2q11 Investigative Ophthalmology & Visual Science ·C.F. Inglehearn, Walid El‐Sayed, Richard F. Shore, Weijia Li, Hélène Dollfus, Román Carlos, Daniela Rodríguez Urbano, David Mansfield, A. T. Moore, Alan J. Mighell	2008	1
8	The natural history of OPA1-related autosomal dominant optic atrophy British Journal of Ophthalmology ·Amy Cohn, Carmel Toomes, Alex W. Hewitt, Lisa S. Kearns, C.F. Inglehearn, Jamie E. Craig, David A. Mackey	2008	53
9	Characterization of Compound Knockin Prpf3/Prpf8 Mice Investigative Ophthalmology & Visual Science ·John J. Graziotto, C.F. Inglehearn, Eric A. Pierce	2007	1
10	Investigation of Candidate Loci for Familial Nonsyndromic Human Strabismus Investigative Ophthalmology & Visual Science ·Jinglan Tan, Keerti. K. Choudhary, G. A. Williams, Alejandra Suazo-Santibáñez, Eamonn Sheridan, Chris Wickham, Carmel Toomes, Brendan T. Barrett, David B. Elliott, C.F. Inglehearn	2005	0
11	Mutations in LRP5 or FZD4 underlie the common FEVR locus on chromosome 11q13 Investigative Ophthalmology & Visual Science ·Carmel Toomes, H.M. Bottomley, Richard M. Jackson, Katherine V. Towns, David A. Mackey, Jamie E. Craig, Kevin Gregory-Evans, Louise Downey, 马继贤, C.F. Inglehearn	2004	3
12	Retinitis pigmentosa: Genes, Proteins and Prospects Developments in ophthalmology ·권빈, Luthfy Arwiya, C.F. Inglehearn	2003	81
13	Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q. British Journal of Ophthalmology ·Kevin Gregory-Evans, Mai Al-Maghtheh, F.W. Fitzke, Anthony T. Moore, M Jay, C.F. Inglehearn, G. B. Arden, Alan C. Bird	1995	35
14	Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion Nature Genetics ·Kevin Gregory-Evans, Alan Fryer, C.F. Inglehearn, Josephine Duvall-Young, Joanne L. Whittaker, Cheryl Y. Gregory, Rachel Butler, Neil D. Ebenezer, David M. Hunt, E. Crowston	1994	93
15	A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family Human Molecular Genetics ·Mai Al-Maghtheh, Richard Kim, Alison J. Hardcastle, C.F. Inglehearn, S.S. Bhattacharya	1994	23
16	Molecular genetics of inherited retinal degenerations Current Opinion in Genetics & Development ·Susan Lindsay, C.F. Inglehearn, Ann Curtis, Shomi S. Bhattacharya	1992	11
17	Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP Genomics ·R. Bashir, C.F. Inglehearn, T J Keen, Janet C. Lindsey, Hurbert Kazoora, Patrick Jelinsky, A. Stephenson, Aaron K. Jackson, Marcelle Jay, A.C. Bird, S.S. Papiha, S.S. Bhattacharya	1992	4
18	Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation. British Journal of Ophthalmology ·Anthony T. Moore, F.W. Fitzke, C.M. Kemp, G. B. Arden, T J Keen, C.F. Inglehearn, Shoumo Bhattacharya, Alan C. Bird	1992	62
19	Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site Genomics ·T J Keen, C.F. Inglehearn, Douglas H. Lester, R. Bashir, M Jay, Alan C. Bird, Barrie Jay, Shoumo Bhattacharya	1991	129
20	no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneity Genomics ·C.F. Inglehearn, M Jay, Douglas H. Lester, R. Bashir, Barrie Jay, Alan C. Bird, Alan F. Wright, H.J. Evans, S.S. Papiha, Shoumo Bhattacharya	1990	28

About C.F. Inglehearn

C.F. Inglehearn is a scholar working on Ophthalmology, Cellular and Molecular Neuroscience, Molecular Biology, Radiology, Nuclear Medicine and Imaging and Oral Surgery, having authored 34 papers that have together received 1.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (21 papers), Photoreceptor and optogenetics research (11 papers), Retinal Diseases and Treatments (6 papers), Retinopathy of Prematurity Studies (6 papers), RNA regulation and disease (4 papers), Bone and Dental Protein Studies (4 papers), Advanced biosensing and bioanalysis techniques (4 papers) and dental development and anomalies (3 papers). The work is most often cited by research in Ophthalmology (410 citations), Cellular and Molecular Neuroscience (363 citations), Molecular Biology (1.2k citations), Cell Biology (216 citations) and Radiology, Nuclear Medicine and Imaging (142 citations). C.F. Inglehearn has collaborated with scholars based in United Kingdom, United States and Mexico. Frequent co-authors include Alan C. Bird, Marcelle Jay, G. B. Arden, Shoumo Bhattacharya, R. Bashir, Douglas H. Lester, T J Keen, Shomi S. Bhattacharya, Fred W. Fitzke and John J. Wroblewski. Their work appears in journals such as British Journal of Ophthalmology, Investigative Ophthalmology & Visual Science, Genomics, Nature Genetics and Cells Tissues Organs.

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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