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1دورية أكاديمية
المؤلفون: Mohd Hussain Shah, Manojkumar Kumaran, Prakash Chermakani, Mohideen Abdul Kader, R Ramakrishnan, Subbiah R Krishnadas, Bharanidharan Devarajan, Periasamy Sundaresan
المصدر: Indian Journal of Ophthalmology, Vol 69, Iss 9, Pp 2461-2468 (2021)
مصطلحات موضوعية: arghef40 gene, genetic heterogeneity, primary open-angle glaucoma, rpgrip1 south indian, whole-exome sequencing, Ophthalmology, RE1-994
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Rajendran Kadarkarai Raj, Pankaja Dhoble, Rupa Anjanamurthy, Prakash Chermakani, Manojkumar Kumaran, Bharanidharan Devarajan, Periasamy Sundaresan
المصدر: Eye and Vision, Vol 7, Iss 1, Pp 1-10 (2020)
مصطلحات موضوعية: Stargardt, ABCA4, Macular degeneration, Yellow white flecks, Mutation detection, South Indian population, Ophthalmology, RE1-994
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2326-0254
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3دورية أكاديمية
المصدر: BMC Bioinformatics, Vol 20, Iss 1, Pp 1-11 (2019)
مصطلحات موضوعية: Whole exome sequencing, Simulated exome data, Human reference genome, Variant calling pipelines, SNVs and InDels, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5
وصف الملف: electronic resource
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المؤلفون: Manojkumar Kumaran, Bharanidharan Devarajan
المصدر: Genetics in Medicine. :100862
مصطلحات موضوعية: Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0faf9fdd7dddd378595efb650295f143
https://doi.org/10.1016/j.gim.2023.100862 -
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المؤلفون: Mohideen Abdul Kader, Renagappa Ramakrishnan, Subbiah. R. Krishnadas, Manojkumar Kumaran, Prakash Chermakani, Mohd Hussain Shah, Periasamy Sundaresan, Bharanidharan Devarajan
المصدر: Indian Journal of Ophthalmology, Vol 69, Iss 9, Pp 2461-2468 (2021)
Indian Journal of Ophthalmologyمصطلحات موضوعية: Candidate gene, primary open-angle glaucoma, genetic structures, Glaucoma, arghef40 gene, genetic heterogeneity, Tonometry, Ocular, symbols.namesake, Exome Sequencing, Genetic variation, Humans, Medicine, rpgrip1 south indian, whole-exome sequencing, Family history, Eye Proteins, Gene, Intraocular Pressure, Exome sequencing, Genetics, Sanger sequencing, Special Focus, Glaucoma, Original Article, business.industry, Genetic heterogeneity, RE1-994, medicine.disease, eye diseases, Ophthalmology, Mutation, symbols, sense organs, business, Glaucoma, Open-Angle
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المؤلفون: Gowhar Shafi, Manoj Dongare, Atul Bharde, Moubeen Fauzul, Kanchan Hariramani, Alain D’Souza, Bhagwat Jadhav, Trupti Kad, Sangeeta Prajapati, Vikas Jadhav, ManojKumar Kumaran, Sumit Haldar, Vatsal Mehra, Sujit Joshi, Gourishankar Aland, Richa Dave, Sreeja Jayant, Aravindan Vasudevan, Mohan Uttarwar, Jayant Khandare
المصدر: Cancer Research. 83:PR007-PR007
مصطلحات موضوعية: Cancer Research, Oncology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::81c8cc9697aeb8d187ecf846a5bdd40b
https://doi.org/10.1158/1538-7445.metastasis22-pr007 -
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المؤلفون: Manojkumar Kumaran, Bharanidharan Devarajan
المصدر: Bioinformatics and Human Genomics Research ISBN: 9781003005926
Bioinformatics and Human Genomics Researchمصطلحات موضوعية: Computational biology, Biology, Exome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2b7c3a7adcd4cd8fe2e8d3b8735dccef
https://doi.org/10.1201/9781003005926-7 -
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المؤلفون: Bharanidharan Devarajan, Roopam Duvesh, Jayant Kumar, Ayyasamy Vanniarajan, Manojkumar Kumaran, Susmita Chowdhury, Periasamy Sundaresan, Rupa Anjanamurthy
مصطلحات موضوعية: Proband, Genetics, Ophthalmology, Retinal Disorder, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Genotype, Biology, Phenotype, Genetics (clinical), Retinal Dystrophies, Autosomal recessive bestrophinopathy, Exome sequencing
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7203e3ea992bd81b0efd129d11d706
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المؤلفون: Bharanidharan Devarajan, Rupa Anjanamurthy, Periasamy Sundaresan, Manojkumar Kumaran, Rajendran Kadarkarai Raj, Prakash Chermakani, Pankaja Dhoble
المصدر: Eye and Vision
Eye and Vision, Vol 7, Iss 1, Pp 1-10 (2020)مصطلحات موضوعية: 0301 basic medicine, genetic structures, Stargardt, ABCA4, Genetic analysis, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, lcsh:Ophthalmology, medicine, Missense mutation, Exome sequencing, Genetic association, South Indian population, Sanger sequencing, Genetics, biology, Yellow white flecks, Genetic heterogeneity, Research, Macular degeneration, medicine.disease, eye diseases, Mutation detection, Stargardt disease, 030104 developmental biology, lcsh:RE1-994, 030221 ophthalmology & optometry, symbols, biology.protein