1. Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients. Issue 12 (1st December 2018) Authors: Nallamilli, Babi Ramesh Reddy; Chakravorty, Samya; Kesari, Akanchha; Tanner, Alice; Ankala, Arunkanth; Schneider, Thomas; da Silva, Cristina; Beadling, Randall; Alexander, John J.; Askree, Syed Hussain; Whitt, Zachary; Bean, Lora; Collins, Christin; Khadilkar, Satish; Gaitonde, Pradnya; Dastur, R... Journal: Annals of clinical and translational neurology Issue: Volume 5:Issue 12(2018) Page Start: 1574 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study. Issue 4 (13th March 2015) Authors: Bello, Luca; Kesari, Akanchha; Gordish‐Dressman, Heather; Cnaan, Avital; Morgenroth, Lauren P.; Punetha, Jaya; Duong, Tina; Henricson, Erik K.; Pegoraro, Elena; McDonald, Craig M.; Hoffman, Eric P. Journal: Annals of neurology Issue: Volume 77:Issue 4(2015:Apr.) Page Start: 684 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Molecular Diagnostics. (3rd September 2013) Authors: Kesari, Akanchha; Dalal, Ashwin; Lal, Girdhari; Pandey, Sachchida Nand Journal: BioMed research international Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Muscular Dystrophy: Disease Mechanisms and Therapies. (24th August 2015) Authors: Pandey, Sachchida Nand; Kesari, Akanchha; Yokota, Toshifumi; Pandey, Gouri Shankar Journal: BioMed research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects. Issue 2 (30th November 2016) Authors: Punetha, Jaya; Kesari, Akanchha; Hoffman, Eric P.; Gos, Monika; Kamińska, Anna; Kostera‐Pruszczyk, Anna; Hausmanowa‐Petrusewicz, Irena; Hu, Ying; Zou, Yaqun; Bönnemann, Carsten G.; JȨdrzejowska, Maria Journal: Muscle & nerve Issue: Volume 55:Issue 2(2017) Page Start: 277 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Osteopontin is linked with AKT, FoxO1, and myostatin in skeletal muscle cells. Issue 6 (13th August 2017) Authors: Nghiem, Peter P.; Kornegay, Joe N.; Uaesoontrachoon, Kitipong; Bello, Luca; Yin, Ying; Kesari, Akanchha; Mittal, Priya; Schatzberg, Scott J.; Many, Gina M.; Lee, Norman H.; Hoffman, Eric P. Journal: Muscle & nerve Issue: Volume 56:Issue 6(2017) Page Start: 1119 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy. Issue 12 (15th October 2020) Authors: Nallamilli, Babi Ramesh Reddy; Chakravorty, Samya; Kesari, Akanchha; Bean, Lora; Hegde, Madhuri Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 12(2020) Page Start: 2541 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗