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Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.
Nallamilli BRR, Chakravorty S, Kesari A, Tanner A, Ankala A, Schneider T, da Silva C, Beadling R, Alexander JJ, Askree SH, Whitt Z, Bean L, Collins C, Khadilkar S, Gaitonde P, Dastur R, Wicklund M, Mozaffar T, Harms M, Rufibach L, Mittal P, Hegde M. Nallamilli BRR, et al. Among authors: ankala a. Ann Clin Transl Neurol. 2018 Dec 1;5(12):1574-1587. doi: 10.1002/acn3.649. eCollection 2018 Dec. Ann Clin Transl Neurol. 2018. PMID: 30564623 Free PMC article.
Molecular diagnosis of Duchenne muscular dystrophy.
Nallamilli BR, Ankala A, Hegde M. Nallamilli BR, et al. Among authors: ankala a. Curr Protoc Hum Genet. 2014 Oct 1;83:9.25.1-29. doi: 10.1002/0471142905.hg0925s83. Curr Protoc Hum Genet. 2014. PMID: 25271841
Gamut of genetic testing for neonatal care.
Ankala A, Hegde MR. Ankala A, et al. Clin Perinatol. 2015 Jun;42(2):217-26, vii. doi: 10.1016/j.clp.2015.02.001. Epub 2015 Mar 31. Clin Perinatol. 2015. PMID: 26042901 Review.
Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis.
Dastur RS, Gaitonde PS, Kachwala M, Nallamilli BRR, Ankala A, Khadilkar SV, Atchayaram N, Gayathri N, Meena AK, Rufibach L, Shira S, Hegde M. Dastur RS, et al. Among authors: ankala a. Ann Indian Acad Neurol. 2017 Jul-Sep;20(3):302-308. doi: 10.4103/aian.AIAN_129_17. Ann Indian Acad Neurol. 2017. PMID: 28904466 Free PMC article.
Genomic technologies and the new era of genomic medicine.
Ankala A, Hegde M. Ankala A, et al. J Mol Diagn. 2014 Jan;16(1):7-10. doi: 10.1016/j.jmoldx.2013.11.001. Epub 2013 Nov 21. J Mol Diagn. 2014. PMID: 24269227 Free article. No abstract available.
34 results