1. A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians. Issue 12 (27th November 2013) Authors: Negi, Sapna; Juyal, Garima; Senapati, Sabyasachi; Prasad, Pushplata; Gupta, Aditi; Singh, Shalini; Kashyap, Sujit; Kumar, Ashok; Kumar, Uma; Gupta, Rajiva; Kaur, Satbir; Agrawal, Suraksha; Aggarwal, Amita; Ott, Jurg; Jain, Sanjay; Juyal, Ramesh C.; Thelma, B. K. Journal: Arthritis and rheumatism Issue: Volume 65:Issue 12(2013:Dec.) Page Start: 3026 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians. Issue 12 (December 2013) Authors: Negi, Sapna; Juyal, Garima; Senapati, Sabyasachi; Prasad, Pushplata; Gupta, Aditi; Singh, Shalini; Kashyap, Sujit; Kumar, Ashok; Kumar, Uma; Gupta, Rajiva; Kaur, Satbir; Agrawal, Suraksha; Aggarwal, Amita; Ott, Jurg; Jain, Sanjay; Juyal, Ramesh C.; Thelma, B. K. Journal: Arthritis and rheumatism Issue: Volume 65:Issue 12(2013:Dec.) Page Start: 3026 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease. (March 2021) Authors: Kumar, Sumeet; Abbas, Masoom M.; Govindappa, Shyla T.; Muthane, Uday B.; Behari, Madhuri; Pandey, Sanjay; Juyal, Ramesh C.; Thelma, B.K. Journal: Parkinsonism & related disorders Issue: Volume 84(2021) Page Start: 61 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Early Onset Parkinson's disease due to DJ1 mutations: An Indian study. (November 2016) Authors: Abbas, Masoom M.; Govindappa, Shyla T.; Sudhaman, Sumedha; Thelma, B.K.; Juyal, Ramesh C.; Behari, Madhuri; Muthane, Uday B. Journal: Parkinsonism & related disorders Issue: Volume 32(2016) Page Start: 20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Targeted Deep Resequencing Identifies MID2 Mutation for X‐Linked Intellectual Disability with Varied Disease Severity in a Large Kindred from India. Issue 1 (21st October 2013) Authors: Geetha, Thenral S.; Michealraj, Kulandaimanuvel Antony; Kabra, Madhulika; Kaur, Gurjit; Juyal, Ramesh C.; Thelma, B.K. Journal: Human mutation Issue: Volume 35:Issue 1(2014:Jan.) Page Start: 41 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗