1. A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts‐1 in north Indian kindred. Issue 2 (18th April 2018) Authors: Vellarikkal, S.K.; Jayarajan, R.; Verma, A.; Ravi, R.; Senthilvel, V.; Kumar, A.; Saini, L.; Gulati, S.; Lal, M.; Mathur, A.; Chhetri, M.K.; Faruq, M.; Scaria, V.; Sivasubbu, S. Journal: Clinical genetics Issue: Volume 94:Issue 2(2018) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. AB0188 Systematic Analysis of the Oral Microbiome in Primary SjÖgren's Syndrome Suggest Enrichment of Distinct Microbes. (9th June 2015) Authors: Sandhya, P.; Sharma, D.; Vellarikkal, S.K.; Surin, A.K.; Jayarajan, R.; Verma, A.; Dixit, V.; Sivasubbu, S.; Danda, D.; Scaria, V. Journal: Annals of the rheumatic diseases Issue: Volume 74(2015)Supplement 2 Page Start: 953 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Development of a clinical diagnostic matrix for characterizing inherited epidermolysis bullosa. (1st June 2017) Authors: Yenamandra, V.K.; Moss, C.; Sreenivas, V.; Khan, M.; Sivasubbu, S.; Sharma, V.K.; Sethuraman, G. Journal: British journal of dermatology Issue: Volume 176:Number 6(2017) Page Start: 1624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Development of a clinical diagnostic matrix for characterizing inherited epidermolysis bullosa. (5th May 2017) Authors: Yenamandra, V.K.; Moss, C.; Sreenivas, V.; Khan, M.; Sivasubbu, S.; Sharma, V.K.; Sethuraman, G. Journal: British journal of dermatology Issue: Volume 176:Number 6(2017) Page Start: 1624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Utility of whole‐exome sequencing in detecting novel compound heterozygous mutations in COL7A1 among families with severe recessive dystrophic epidermolysis bullosa in India – implications on diagnosis, prognosis and prenatal testing. (14th August 2018) Authors: Mahajan, R.; Vellarikkal, S.K.; Handa, S.; Verma, A.; Jayarajan, R.; Kumar, A.; De, D.; Kaur, J.; Panigrahi, I.; Vineeth, V.S.; Sivasubbu, S.; Scaria, V. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 32:Number 12(2018) Page Start: e433 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Whole‐exome sequencing solves diagnostic dilemma in a rare case of sporadic acrokeratosis verruciformis. (26th January 2015) Authors: Gupta, A.; Sharma, Y.K.; Vellarikkal, S.K.; Jayarajan, R.; Dixit, V.; Verma, A.; Sivasubbu, S.; Scaria, V. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 30:Number 4(2016:Apr.) Page Start: 695 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗