1. A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield. Issue 2 (17th December 2014) Authors: Ankala, Arunkanth; da Silva, Cristina; Gualandi, Francesca; Ferlini, Alessandra; Bean, Lora J. H.; Collins, Christin; Tanner, Alice K.; Hegde, Madhuri R. Journal: Annals of neurology Issue: Volume 77:Issue 2(2015:Feb.) Page Start: 206 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Ancestral founder mutations in calpain‐3 in the Indian Agarwal community: Historical, clinical, and molecular perspective. Issue 6 (11th May 2013) Authors: Ankala, Arunkanth; Kohn, Jordan N.; Dastur, Rashna; Gaitonde, Pradnya; Khadilkar, Satish V.; Hegde, Madhuri R. Journal: Muscle & nerve Issue: Volume 47:Issue 6(2013:Jun.) Page Start: 931 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical Applications and Implications of Common and Founder Mutations in Indian Subpopulations. Issue 1 (27th November 2014) Authors: Ankala, Arunkanth; Tamhankar, Parag M.; Valencia, C. Alexander; Rayam, Krishna K.; Kumar, Manisha M.; Hegde, Madhuri R. Journal: Human mutation Issue: Volume 36:Issue 1(2015:Jan.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover Image, Volume 176A, Number 8, August 2018. Issue 8 (22nd August 2018) Authors: Ankala, Arunkanth; Jain, Nieraj; Hubbard, Baker; Alexander, John J.; Shankar, Suma P. Journal: American journal of medical genetics Issue: Volume 176:Issue 8(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diagnostic overview of blood‐based dysferlin protein assay for dysferlinopathies. Issue 3 (16th June 2014) Authors: Ankala, Arunkanth; Nallamilli, Babi R.; Rufibach, Laura E.; Hwang, Esther; Hegde, Madhuri R. Journal: Muscle & nerve Issue: Volume 50:Issue 3(2014:Sep.) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evolving genetic heterogeneity of facioscapulohumeral muscular dystrophy. (9th June 2020) Authors: Johnson, Nicholas E.; Ankala, Arunkanth Journal: Neurology Issue: Volume 94:Number 23(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic and Epigenetic Determinants of Low Dysferlin Expression in Monocytes. Issue 8 (24th June 2014) Authors: Gallardo, Eduard; Ankala, Arunkanth; Núñez‐Álvarez, Yaiza; Hegde, Madhuri; Diaz‐Manera, Jordi; Luna, Noemí De; Pastoret, Ana; Suelves, Mònica; Illa, Isabel Journal: Human mutation Issue: Volume 35:Issue 8(2014:Aug.) Page Start: 990 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗
9. Genetic variation in dihydropyrimidine dehydrogenase (DPYD) gene in a healthy adult Indian population. (January 2015) Authors: Iyer, Sandhya N.; Singhal, Rekha S.; Hegde, Madhuri R.; Ankala, Arunkanth Journal: Annals of human biology Issue: Volume 42:Number 1(2015:Jan./Feb.) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of a novel nemaline myopathy‐Causing mutation in the troponin T1 (TNNT1) gene: A case outside of the old order amish. Issue 5 (17th February 2015) Authors: Marra, Jonathan D.; Engelstad, Kristin E.; Ankala, Arunkanth; Tanji, Kurenai; Dastgir, Jahannaz; De Vivo, Darryl C.; Coffee, Bradford; Chiriboga, Claudia A. Journal: Muscle & nerve Issue: Volume 51:Issue 5(2015:May) Page Start: 767 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗