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Whole exome sequencing in a multi-generation family from India reveals a genetic variation c.10C>T (p.Gln4Ter) in keratin 5 gene associated with Dowling-Degos disease.
Virmani N, Vellarikkal SK, Verma A, Jayarajan R, Sakhiya J, Desai C, Sivasubbu S, Scaria V. Virmani N, et al. Among authors: verma a. Indian J Dermatol Venereol Leprol. 2018 May-Jun;84(3):344-346. doi: 10.4103/ijdvl.IJDVL_268_17. Indian J Dermatol Venereol Leprol. 2018. PMID: 29600799 Free article. No abstract available.
Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of India.
Behera BK, Das P, Maharana J, Paria P, Mandal SN, Meena DK, Sharma AP, Jayarajan R, Dixit V, Verma A, Vellarikkal SK, Scaria V, Sivasubbu S, Rao AR, Mohapatra T. Behera BK, et al. Among authors: verma a. Genome Announc. 2015 Jan 8;3(1):e01321-14. doi: 10.1128/genomeA.01321-14. Genome Announc. 2015. PMID: 25573926 Free PMC article.
Erratum for Behera et al., Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of India.
Behera BK, Das P, Maharana J, Paria P, Mandal SN, Meena DK, Sharma AP, Jayarajan R, Dixit V, Verma A, Vellarikkal SK, Scaria V, Sivasubbu S, Rao AR, Mohapatra T. Behera BK, et al. Among authors: verma a. Genome Announc. 2015 Feb 19;3(1):e00123-15. doi: 10.1128/genomeA.00123-15. Genome Announc. 2015. PMID: 25700399 Free PMC article. No abstract available.
Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
Gupta A, Sharma Y, Deo K, Vellarikkal S, Jayarajan R, Dixit V, Verma A, Scaria V, Sivasubbu S. Gupta A, et al. Among authors: verma a. F1000Res. 2015 Jul 31;4:446. doi: 10.12688/f1000research.6779.1. eCollection 2015. F1000Res. 2015. PMID: 26594337 Free PMC article.
Chamber Specific Gene Expression Landscape of the Zebrafish Heart.
Singh AR, Sivadas A, Sabharwal A, Vellarikal SK, Jayarajan R, Verma A, Kapoor S, Joshi A, Scaria V, Sivasubbu S. Singh AR, et al. Among authors: verma a. PLoS One. 2016 Jan 27;11(1):e0147823. doi: 10.1371/journal.pone.0147823. eCollection 2016. PLoS One. 2016. PMID: 26815362 Free PMC article.
Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa.
Karuthedath Vellarikkal S, Jayarajan R, Verma A, Nair S, Ravi R, Senthivel V, Sivasubbu S, Scaria V. Karuthedath Vellarikkal S, et al. Among authors: verma a. F1000Res. 2016 May 17;5:900. doi: 10.12688/f1000research.8380.2. eCollection 2016. F1000Res. 2016. PMID: 27408687 Free PMC article.
Application of whole exome sequencing in elucidating the phenotype and genotype spectrum of junctional epidermolysis bullosa: A preliminary experience of a tertiary care centre in India.
Yenamandra VK, Vellarikkal SK, Kumar M, Chowdhury MR, Jayarajan R, Verma A, Scaria V, Sivasubbu S, Ray SB, Dinda AK, Kabra M, Kaur P, Sharma VK, Sethuraman G. Yenamandra VK, et al. Among authors: verma a. J Dermatol Sci. 2017 Apr;86(1):30-36. doi: 10.1016/j.jdermsci.2016.12.020. Epub 2016 Dec 29. J Dermatol Sci. 2017. PMID: 28087116
Case Report: Whole exome sequencing identifies a novel frameshift insertion c.1325dupT (p.F442fsX2) in the tyrosine kinase domain of BTK gene in a young Indian individual with X-linked agammaglobulinemia.
Rawat A, Karuthedath Vellarikkal S, Verma A, Jayarajan R, Gupta A, Singh S, Chopra A, Kumar R, Scaria V, Sivasubbu S. Rawat A, et al. Among authors: verma a. F1000Res. 2016 Nov 14;5:2667. doi: 10.12688/f1000research.9472.2. eCollection 2016. F1000Res. 2016. PMID: 28928935 Free PMC article.
5,960 results