Louise Ocaka

2.0k total citations
30 papers, 1.2k citations indexed

About

Louise Ocaka is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Louise Ocaka has authored 30 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Ophthalmology. Recurrent topics in Louise Ocaka's work include Retinal Development and Disorders (7 papers), Retinal Diseases and Treatments (6 papers) and Glaucoma and retinal disorders (5 papers). Louise Ocaka is often cited by papers focused on Retinal Development and Disorders (7 papers), Retinal Diseases and Treatments (6 papers) and Glaucoma and retinal disorders (5 papers). Louise Ocaka collaborates with scholars based in United Kingdom, Mexico and United States. Louise Ocaka's co-authors include Neil D. Ebenezer, Shomi S. Bhattacharya, Ordan J. Lehmann, Roger A. Hitchings, Chiara Bacchelli, Peng T. Khaw, Tim Jordan, Annette Payne, Brian J. Clark and Sue Povey and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and Ophthalmology.

In The Last Decade

Louise Ocaka

28 papers receiving 1.2k citations

Peers

Countries citing papers authored by Louise Ocaka

Since Specialization

Citations

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

Fields of papers citing papers by Louise Ocaka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Ocaka

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Ocaka. A scholar is included among the top collaborators of Louise Ocaka 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 Louise Ocaka. Louise Ocaka 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

#	Work	Indexed citations
1	Genetic variant of TTLL11 gene and subsequent ciliary defects are associated with idiopathic scoliosis in a 5-generation UK family 2021 ·Scientific Reports ·(unknown), Scott B. Patten, José Antonio Aragon-Martin, Louise Ocaka, Michael A. Simpson, Anne H. Child, Florina Moldovan	17
2	The genetic landscape of crystallins in congenital cataract 2020 ·Orphanet Journal of Rare Diseases ·Vanita Berry, (unknown), Nikolas Pontikos, Michalis Georgiou, Jing Yu, Louise Ocaka, Anthony T. Moore, Roy A. Quinlan, Michel Michaelides	34
3	Novel missense variants in the RNF213 gene from a European family with Moyamoya disease 2019 ·Human Genome Variation ·Andrey Gagunashvili, Louise Ocaka, Daniel Kelberman, Pinki Munot, Chiara Bacchelli, Philip L. Beales, Vijeya Ganesan	10
4	Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children 2018 ·Journal of Medical Genetics ·Lamia Mestek, Emma Clement, Wendy D. Jones, Suzanne Drury, Louise Ocaka, Andrey Gagunashvili, Polona Le Quesne Stabej, Chiara Bacchelli, (unknown), Shamima Rahman, Lucy Jenkins, Jane A. Hurst, Maria Bitner‐Glindzicz, Mark Peters, Philip L. Beales, Hywel Williams	89
5	An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes 2017 ·Orphanet Journal of Rare Diseases ·Polona Le Quesne Stabej, Chela James, Louise Ocaka, Mehmet Tekman, Stephanie Grünewald, Emma Clement, Horia Stanescu, Robert Kleta, Deborah Morrogh, Alistair Calder, Hywel Williams, Maria Bitner‐Glindzicz	14
6	COLEC10 is mutated in 3MC patients and regulates early craniofacial development 2017 ·PLoS Genetics ·Mustafa M. Munye, Anna Dı́az-Font, Louise Ocaka, Maiken L. Henriksen, Melissa Lees, Angela Brady, Dagan Jenkins, Jenny Morton, Søren Hansen, Chiara Bacchelli, Philip L. Beales, Víctor Hernández-Hernández	60
7	Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay 2017 ·Journal of Inherited Metabolic Disease ·Emma Reid, Hywel Williams, Glenn Anderson, (unknown), Kling Chong, Chela James, Louise Ocaka, (unknown), Cheryl Hemingway, Daniel Little, Richard J. P. Brown, Alasdair Parker, Simon Holden, Emma Footitt, Shamima Rahman, Paul Gissen, Philippa B. Mills, Peter T. Clayton	15
8	STAG3 truncating variant as the cause of primary ovarian insufficiency 2015 ·European Journal of Human Genetics ·(unknown), Polona Le Quesne Stabej, Hywel Williams, Chela James, Mehmet Tekman, Horia Stanescu, Robert Kleta, Louise Ocaka, Francesco Lescai, Helen L. Storr, Maria Bitner‐Glindzicz, Chiara Bacchelli, Gerard S. Conway	42
9	The use of whole-exome sequencing to disentangle complex phenotypes 2015 ·European Journal of Human Genetics ·(unknown), Hywel Williams, John R. Hurst, Louise Ocaka, Chela James, C. Pao, Estelle Chanudet, Francesco Lescai, Horia Stanescu, Robert Kleta, Elisabeth Rosser, Chiara Bacchelli, Philip L. Beales	11
10	Seizures Due to a KCNQ2 Mutation: Treatment with Vitamin B6 2015 ·JIMD Reports ·Emma Reid, Hywel Williams, Polona Le Quesne Stabej, Chela James, Louise Ocaka, Chiara Bacchelli, Emma Footitt, Stewart Boyd, Maureen Cleary, Philippa B. Mills, Peter T. Clayton	19
11	Detailed Phenotypic and Genotypic Characterization of Bietti Crystalline Dystrophy 2014 ·Ophthalmology ·Stephanie Halford, Gerald Liew, Donna S. Mackay, Panagiotis I. Sergouniotis, Richard Holt, Suzanne Broadgate, Emanuela V. Volpi, Louise Ocaka, Anthony G. Robson, Graham E. Holder, Anthony T. Moore, Michel Michaelides, Andrew R. Webster	72
12	Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel 2007 ·Journal of Medical Genetics ·Louise Ocaka, (unknown), (unknown), Neil D. Ebenezer, Glen Brice, Timothy Morley, Meenu Mehta, T. John O'Dowd, J L Weber, Alison J. Hardcastle, Anne H. Child	58
13	Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2 2005 ·Gene ·Suzanne Broadgate, Louise Ocaka, (unknown), Michelle Gaasenbeek, J. Paul Chapple, Michael E. Cheetham, Brian J. Clark, David M. Hunt, Stephanie Halford	42
14	Chromosomal localization, genomic organization and evolution of the genes encoding human phosphatidylinositol transfer protein membrane-associated (PITPNM) 1, 2 and 3 2004 ·Cytogenetic and Genome Research ·Louise Ocaka, C. Mirella Spalluto, David I. Wilson, David M. Hunt, Stephanie Halford	17
15	Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma 2002 ·Human Genetics ·Tin Aung, Louise Ocaka, Neil D. Ebenezer, Alex Morris, Glen Brice, Anne H. Child, Roger A. Hitchings, Ordan J. Lehmann, Shomi S. Bhattacharya	47
16	Linkage analysis of a large Amish pedigree with glaucoma. 2001 ·UCL Discovery (University College London) ·(unknown), (unknown), (unknown), Neil D. Ebenezer, Louise Ocaka, (unknown), (unknown), (unknown), (unknown)	1
17	Assignment<footref rid="foot01"><sup>1</sup></footref> of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids 2001 ·Cytogenetic and Genome Research ·Stephanie Halford, James Bellingham, Louise Ocaka, M. Fox, Stephen L. Johnson, F. Foster, David M. Hunt	9
18	A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene 2001 ·Human Genetics ·Tin Aung, Louise Ocaka, Neil D. Ebenezer, Alex Morris, Michael Krawczak, Dawn L. Thiselton, Christiane Alexander, Marcela Votruba, Glen Brice, Anne H. Child, Peter J. Francis, Roger A. Hitchings, Ordan J. Lehmann, Shomi S. Bhattacharya	106
19	An analysis of ABCR mutations in British patients with recessive retinal dystrophies. 2000 ·PubMed ·Myrto Papaioannou, Louise Ocaka, David Bessant, Noemi Lois, Alan C. Bird, Annette Payne, Shomi S. Bhattacharya	55
20	Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma 2000 ·The American Journal of Human Genetics ·Ordan J. Lehmann, Neil D. Ebenezer, Tim Jordan, Margaret Fox, Louise Ocaka, Annette Payne, Bart P. Leroy, Brian J. Clark, Roger A. Hitchings, Sue Povey, Peng T. Khaw, Shomi S. Bhattacharya	129

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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